Since the ban on antibiotic feed additives in the European Union (EU) in 2006, research in alternative substances has gained in importance. In particular for growing broilers and for weaned pigs, several feed additives have been investigated with regard to the prevention of diarrhoea and to increasing general performance and health. Besides pre- and/or probiotics and organic acids, phytogenic substances are most commonly used for this purpose. Phytogenic feed additives comprise a heterogenous group of plant-derived products including herbs, spices, essential oils or other preparations. In particular, labiatae plant oils from Origanum vulgare, Thymus vulgaris and Rosmarinus officinalis have been reported to promote the performance and health of poultry via three different mechanisms(Reference Windisch, Schedle and Plitzner1).
The first mechanism suggests that essential oils (EO) positively affect the growth and performance of chickens by improving feed palatability, secretion of digestive enzymes and nutrient digestibility. Data regarding this topic are, however, not consistent(Reference Halle, Thomann and Bauermann2–Reference Cross, McDevitt and Hillman5).
The second mechanism suggests that the EO of labiatae plants exert antibiotic-like bactericidal and/or bacteriostatic effects on several pathogenic intestinal micro-organisms. Most of the studies in this context have been carried out in vitro, frequently in the context of food safety of meat products. For instance, carvacrol, the main monoterpene compound in oregano- and thymbra spicata oil, exhibited a distinct bactericidal activity against Escherichia coli, including an enterohaemorrhagic strain(Reference Burt, Vlielander and Haagsman6, Reference Burt, van der Zee and Koets7), Salmonella enterica (Reference Burt, Fledderman and Haagsman8), Staphylococcus epidermis and S. aureus, and numerous other bacteria(Reference Kiliç9). However, the limitation of the bactericidal effects of EO was demonstrated in an experiment with Caco-2 cells. The addition of oregano oil (Oo) and thyme oil (To) to the culture media in a concentration (0·05 %) that strongly inhibited the growth of enteroinvasive E. coli also was harmful to the cells, whereas lower EO concentrations (0·01 %), causing no cell damage, exhibited a drastically reduced bactericidal activity(Reference Fabian, Sabol and Domaracká10). However, the in vivo bactericidal activity of the EO from labiatae plants in vivo is in doubt. Whereas two trials with growing broilers reported that even low dietary concentrations of carvacrol (100 mg/kg)(Reference Horosová, Bujnáková and Kmet11) and thymol (15 mg/kg)(Reference Tiihonen, Kettunen and Bento12) had a bactericidal activity against E. coli and Clostridiae, or influenced the growth of Lactobacillae positively(Reference Horosová, Bujnáková and Kmet11–Reference Jamroz, Wiliczkiewicz and Wertelecki13), in another study an even higher concentration of Oo (1000 mg/kg) failed to influence bacterial counts in faeces and in caecal chymus(Reference Westendrap, Klaus and Halle4).
The third mechanism suggests that the EO of labiatae plants positively affect animal health by direct antioxidant effects based on the high availability of the phenolic terpenes carvacrol and thymol. The TROLOX® equivalent, also referred to as Trolox equivalent antioxidant capacity (TEAC), is a common method to study the antioxidant potential of antioxidant compounds in comparison to the water-soluble vitamin E derivative TROLOX® as the reference substance. In vitro testing of the TEAC value (mmol TROLOX®/g DM) of ethanolic extracts of twenty-six spices showed that oregano had the highest antioxidant potential within labiatae plants (TEAC value: 100·7), followed by rosemary (38·8) and thyme (38·1)(Reference Shan, Cai and Sun14).
Beside the EO of labiatae plants, similar mechanisms improving the performance and health of farm animals have been reported for Zingiberaceae plant extracts, particularly for turmeric (Curcuma longa L.). Comparable to labiatae oils, turmeric oil (Cuo) contains a highly active terpene, the sesquiterpene ar-turmerone. Ar-turmerone has been demonstrated to evolve a strong bactericidal activity against several micro-organisms(Reference Negi, Jayaprakasha and Jagan Mohan Rao15). The limited direct antioxidant activity of Cuo (TEAC value: approximately 25·5)(Reference Sacchetti, Maietti and Muzzoli16) compared to labiatae oils derives from the fact that ar-turmerone is not a phenolic terpene.
Broccoli extract, containing the isothiocyanate sulforaphane (SFN) in the form of its glucosinolate precursor glucoraphanin, is a phytogenic substance that has not yet been studied as a feed additive, and it is not yet permitted in the EU. In human nutrition, broccoli extract and SFN are generally accepted dietary supplements exerting a high anti-carcinogenic potential, in particular against intestinal cancers(Reference Clarke, Dashwood and Ho17). The safety of broccoli extract has been proven for humans(Reference Shapiro, Fahey and Dinkova-Kostova18). Promising results for SFN have also been published with regard to a strong bactericidal activity against various pathogenic intestinal micro-organisms(Reference Aires, Mota and Saavedra19). The anti-carcinogenic effects of turmeric and of SFN are based on the induction of genes with an ‘antioxidant response element’ (ARE) in their DNA promoter. ARE containing genes include xenobiotic- and antioxidant enzymes such as glutathione-S-transferases (GST), epoxide hydrolases, aflatoxin B1 aldehyde reductases (AFAR), haeme oxygenases (HMOX), thioredoxin reductase (TrxR) and cytosolic Cu/Zn-superoxide dismutase (Cu/Zn SOD) 1(Reference Chauhan20–Reference Gowda, Ledoux and Rottinghaus26).
ARE gene induction depends on the transcription factor ‘nuclear factor erythroid 2-related factor 2’ (Nrf2). When the cells are protected sufficiently against oxidative stress, Nrf2 is associated with the Kelch-like erythroid CNC (cap-‘n’-collar) homologue-associated protein 1 (Keap1) in the cytosol. Oxidative stress or electrophiles like SFN or terpenes modify Keap1 at redox-sensitive –SH-groups(Reference Hong, Freeman and Liebler27), leading to Nrf2 liberation and its nuclear translocation. Subsequently, Nrf2 binds to the ARE promoter sequence of the aforementioned xenobiotic- and antioxidant enzymes and initiates the up-regulation of their gene expression(Reference Surh28).
In contrast to a number of studies that have investigated the beneficial effects of phytogenic feed additives via the mechanisms (1)–(3), their indirect antioxidant potential via the induction of xenobiotic- and antioxidant enzymes has not been studied in farm animals till now. To the best of our knowledge, only one trial has reported on the induction of xenobiotic enzymes by thyme in mouse liver(Reference Sasaki, Wada and Tanaka29).
Consequently, we aimed to study the induction of ARE-regulated xenobiotic- and antioxidant enzymes by various EO from labiatae plants in the intestine and the liver of fast-growing broiler chickens. We used broccoli sprouts extract and Cuo as reference substances, both having a proven impact on ARE gene expression. Moreover, we studied the effects of broccoli extract, not yet permitted as a feed additive in the EU, on performance parameters.
Methods and materials
Bird husbandry and diets
The protocol of the broiler study was approved by the Regional Council of Halle and by the Animal Welfare Committee of the Martin Luther University Halle-Wittenberg (record token: 45.202-3-559 MLU). Further, a certificate of exemption for feeding the broccoli sprouts extract, not yet permitted to be used as a feed additive in the EU, was attested by the veterinary administrative office, Saxony Anhalt, Halle (record token: 203.2.1/22·10).
A total of 240 male Ross-308 broiler chickens (1 d old) (mean body weight: 41·9 (se 0·57) g) were obtained from a hatchery (Geflügelhof Möckern ZN (Zucht and Nutzvieh) der Lohmann & Co. AG, Möckern, Germany) and fed a commercial starter diet (Landkornstarter, DEUKA, Könnern, Germany) without phytogenic feed additives for 14 d. On day 15, the birds were assigned to the six experimental groups of forty birds each, with a mean live weight of 442 (se 14·7) g. Broilers were kept in a stainless-steel cage battery in groups of eight birds per cage and fed the experimental diets for 21 d. The experimental design included five cages of eight birds per diet. The broilers had free access to their diets and water. During the experiment, temperature, humidity and lighting were controlled. The temperature was gradually reduced from 34°C on day 1 to 19°C on day 35. The lighting regime consisted of a 12 h light–4 h dark–4 h light–4 h dark cycle. The light intensity of 20 lux and all other housing conditions were in accordance with the recommendations for poultry of the Society for Laboratory Animal Science(30). During the 21 d experimental period, the control (Con) group was fed a diet, meeting the nutritional requirements of growing broilers, without a phytogenic additive. Minerals, vitamins and essential amino acids were added to all diets as recommended for broilers by the Society of Nutrition Physiology(31) and the National Research Council(32). The diet of group SFN contained 3000 mg/kg broccoli sprouts extract providing 75·0 mg/kg SFN, whereas 150·0 mg/kg of the essential oils from C. longa (Cuo), T. vulgaris (To), O. vulgare (Oo) and rosemary oil (R. officinalis, Ro) were added to the diets of the other four experimental groups The active ingredients in the broccoli sprouts extract and the EO, as provided by the manufacturers, had the following concentrations (g/100 g = %): broccoli sprouts extract (SFN, 5·00), Cuo (ar-turmerone, 30·0), Oo (carvacrol, 65·0), To (thymol, 49·0) and Ro (1,8-cineole, 46·0). Premixes of all phytogenic feed additives were prepared in 20 g wheat bran and 10 g sunflower oil and added to 970 g of the basal diet (Table 1). All diets were pelleted with a pellet mill using a 3 mm dye. Feed intake and individual live weight were recorded once a week. Feed conversion was calculated from the ratio of feed intake (g) and weight gain (g). On day 35, the broilers were killed after stunning for organ sampling (liver, small-intestine mucosa and colon). Small-intestine mucosa samples were taken from a 15 cm jejunal segment located 10 cm distal to the duodenum. Colon tissue was taken from a 10 cm segment located distal to the caecum.
Composition of the basal diet*
AME, apparent metabolisable energy; CP, crude protein
* The complete diets had the following nutrient contents according to the National Research Council recommendations for poultry(32) and did not differ between the diets: DM (analysed), 91 %; gross energy (analysed), 17·25 MJ/kg; AMEN-corrected (calculated), 12·88 MJ/kg (the deviation in AMEN-corrected between basal and complete diet resulted from adding the different phytogenic feed additives in terms of premixes as described in Methods and materials); crude fat (analysed), 66·4 g/kg DM; CP (analysed), 201 g/kg DM; fibre (analysed), 41·0 g/kg DM; crude ash (analysed), 59·8 g/kg DM.
† Premix supplied the following according to the supplier (BASU-Mineralfutter GmbH, Bad Sulza, Germany; per kg of complete diet): Ca, 2·3 g; vitamin A, 3·6 g (as retinyl acetate); cholecalciferol, 0·008 mg; vitamin E, 38·22 g (as dl-α-tocopheryl acetate); vitamin K3, 2 mg; thiamine, 2 mg; riboflavin, 6·6 mg; vitamin B6, 5 mg; vitamin B12, 0·02 mg; niacin, 99 mg; folic acid, 1 mg; biotin, 0·15 mg; Ca-d-panthothenate, 15 mg; choline chloride, 0·7 g; Cu, 5 mg; Zn, 51 mg; Fe, 60 mg; Mn, 71 mg; I, 0·6 mg; Se, 0·2 mg.
RNA preparation and real-time RT-PCR assay including stability analysis of four selected reference genes in the jejunal mucosa, colon and liver
Relative mRNA expression levels were measured for GSTα, HMOX1, TrxR1, microsomal epoxide hydrolase 1 (EPHX1), cytosolic epoxide hydrolase 2 (EPHX2), AFAR, cytochrome P450, family 1, subfamily A, polypeptide 1 (CYP1A1) and ATP-binding cassette, sub-family C (cystic fibrosis transmembrane conductance regulator multidrug resistance-associated protein; CFTR/MRP), member 2 (ABCC2). Therefore, total RNA was isolated from the liver, jejunal mucosa and colon of four birds per repetition and the experimental group (n 120, half the number of experimental birds) using Trizol® reagent (Invitrogen GmbH, Darmstadt, Germany), according to the manufacturer's protocol. RNA concentration and purity were evaluated photometrically at 260 and 280 nm. Additionally, RNA quality was controlled by checking the integrity of the 18S- and 28S-ribosomal RNA bands and by controlling the absence of genomic DNA. In brief: following the denaturation of 4·5 μl of diluted RNA (0 5 μg/μl) with 2·0 μl 5 × gel running buffer, 3·5 μl formaldehyde and 10 μl formamide at 70°C for 10 min, the samples were chilled on ice. Then, 1·0 μl of a ethidium bromide solution (1·0 μg/μl) and 2·0 μl of sample loading buffer were added and the samples were run in 1·2 % agarose gels, containing 2·2 m-formaldehyde and visualised under a UV-imager (Syngene, Cambridge, UK). Subsequently, 1·5 μg of the RNA of two birds per treatment were pooled and subjected to reverse transcription using a commercial complementary DNA synthesis kit (RevertAid™ First Strand synthesis kit; Fermentas GmbH, St Leon-Rot, Germany). In this manner, n 10 complementary DNA pools per treatment were generated and could be subjected to mRNA expression analysis by real-time detection PCR (RT-PCR) using a Rotorgene 6000 apparatus (Corbett Research/QIAGEN GmbH, Hilden, Germany). The complementary DNA obtained by reverse transcription (20 μl) was diluted 2·5-fold (final volume 50 μl) with diethylpyrocarbonate-treated sterile water. The standard PCR protocol consisted of an initial denaturation step (95°C, 3 min), followed by 25–32 amplification cycles (denaturation: 95°C, 25 s, annealing: 60°C, 30 s, and elongation: 72°C, 55 s). Subsequent to the identification of the correct length of the amplification products in 1·2 % agarose gels, relative quantification of mRNA expression was performed using the ΔΔC t method(Reference Livak and Schmittgen33). In accordance with the current guidelines for the proper determination of gene expression data in various tissues (MIQE guidelines)(Reference Bustin, Benes and Garson34), a set of four reference genes was selected and their expression stability (M) was ranked according to the standard procedure(Reference Vandesompele, De Preter and Pattyn35). Acid ribosomal protein 1 (ARP1), glycerine aldehyde-3-phosphate dehydrogenase (GAPDH), elongation factor 1α (ELFA) and β-actin were selected as capable reference genes reported in current literature(Reference Hosseini, Sauerwein and Mielenz36, Reference Olsvik, Lie and Mykkeltvedt37), and their expression (C t values) was measured in the jejunum, the colon and the liver. The treatment independent expression stability (M) was determined by calculating the C t ratios of one gene with all the other genes. Subsequently, the standard deviation of the logarithmically transformed ratios was calculated and plotted(Reference Vandesompele, De Preter and Pattyn35). According to their expression stability M, indicated by a decrease of standard deviation, a ranking of the most stable reference genes was compiled for each tissue investigated. The best set of housekeeping genes was used for normalisation of the expression data of the target genes. The expression values of the target genes were normalised using the arithmetic mean of the C t values of ARP1 and β-actin in the jejunal mucosa, of GAPDH and ELFA in the colon, and of GAPDH and β-actin in the liver.
The primers used in PCR and their gene bank accession numbers were as follows:
ARP1 (X13876.1), primer forward (5′ → 3′): ATC GAC ATC GGA AGC CTC AT, primer reverse (5′ → 3′): GAC CAA AGC CCA TGT CAT CA; GAPDH (NM204305.1), primer forward (5′ → 3′): CCT CTC TGG CAA AGT CCA AG, primer reverse (5′ → 3′): TCT CCA TGG TGG TGA AGA CA; ELFA (L00677.1), primer forward (5′ → 3′): ACC TCT GCG TCT GCC TCT TC, primer reverse (5′ → 3′): TTC GCT AAG GGC TTC ATG GT; β-actin (LO8165), primer forward (5′ → 3′): ATG AAG CCC AGA GCA AAA GA, primer reverse (5′ → 3′): GGG GTG TTG AAG GTC TCA AA; GSTα (NM001001777), primer forward (5′ → 3′): TTC TCT CCA CCT GAG GCA AAG, primer reverse (5′ → 3′): GGC TTC CAT GAG CTG AAC ATC; HMOX1 (NM205344), primer forward (5′ → 3′): CTG GAG AAG GGT TGG CTT TCT, primer reverse (5′ → 3′): GAA GCT CTG CCT TTG GCT GTA; TrxR1 (NM001030762), primer forward (5′ → 3′): AGT CAT TTC TGG CCA CTG GAA, primer reverse (5′ → 3′): TTGGTGATGGACAGAGTGGTG; EPHX1 (XM419497), primer forward (5′ → 3′): CAA GTG ATG CTT GGG GCT TAC, primer reverse (5′ → 3′): ACC TGC AGT GTC TGG TTT GGT; EPHX2 (NM001033645), primer forward (5′ → 3′): GAA AGC CCT TAT CCG TTC CAC, primer reverse (5′ → 3′): GGT CTC ATG TTC CGG TAC CAA; AFAR (XM417628·2), primer forward (5′ → 3′): CAA ACT GCA GGG TTC TCT TGG, primer reverse (5′ → 3′): GAA GTA GTT GGG GCA GTC GTG; CYP1A1 (NM205146), primer forward (5′ → 3′): GAAGATTCAGGCAGAGCTGGA, primer reverse (5′ → 3′): AGT AGC CAT TCA GCA CCG TGT; ABCC2 (XM421698), primer forward (5′ → 3′): CCG CAG CAT CAG TAC ACA GAG, primer reverse (5′ → 3′): GAA GGA AAA GCC CAA ACC AAC.
Differential superoxide dismutase activity in the liver
The differential measurement of SOD activity (total SOD, mitochondrial Mn SOD (Mn SOD) and Cu/Zn SOD) in the jejunum and the liver was assayed using a photometric standard procedure in which the inhibition of pyrogallol (1,2,3-trihydroxybenzol) autoxidation by the SOD activity of the samples is recorded(Reference Marklund and Marklund38). Following this, 1:5 (w/v) crude homogenates of the liver were prepared in 0·1 m-potassium phosphate buffer (pH 6·5). The formation of purpurogallin by pyrogallol oxidation was measured for 3 min at 420 nm. Each determination included a blank without the liver homogenate. Here, one unit of SOD activity was defined as the 50 % inhibition of pyrogallol autoxidation to purpurogallin by the samples' SOD activity. The determination of Mn SOD was carried out as previously mentioned, in 50 mm-Tris succinate buffer, containing additionally 100 mm-potassium cyanide to inhibit Cu/Zn SOD. Activity of Cu/Zn SOD was calculated from the difference of total SOD and Mn SOD activity. Data were normalised to 1 mg of protein. Organ sample pools were generated in an analogous manner as described for mRNA expression. The SOD activity of each sample pool (n 10) was measured in duplicate.
Glutathione peroxidase 1 activity in the liver and combined activity of glutathione peroxidases 1 and 2 in the jejunum
The activity of liver cytosolic glutathione peroxidase (GPx1) and the combined activity of GPx1 and gastrointestinal glutathione peroxidase (GPx2) in the jejunal cytosolic supernatant were measured spectrophotometrically (Ultrospec 3300 pro; Amersham Pharmacia Biotech, Freiburg, Germany) at 340 nm using the assay protocol coupled to glutathione reductase and NADPH(Reference Lawerence and Burk39). NADPH oxidation, which is proportional to glutathione peroxidase (GPx)-dependent peroxide reduction, was recorded for 3 min. For both enzymes, H2O2 was used as substrate. Here, one unit of GPx1 and of combined GPx1- and GPx2 activity was defined as 1 μmol NADPH oxidised per min and normalised to 1 mg protein. Organ sample pools were generated in an analogous manner as described for mRNA expression. GPx activity of each sample pool (n 10) was measured in duplicate.
Trolox equivalent antioxidant capacity=TROLOX® equivalent in the essential oils, the jejunal mucosa and the liver
TEAC in 1:5 (w/v) crude homogenates of the liver and of the jejunal mucosa as well as of the essential oils used in the study was measured using the method originally described by Miller et al. (Reference Miller, Rice-Evans and Davies40) with modifications of Wang et al. (Reference Wang, Chu and Chu41). The method is based on monitoring the inhibition of 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid (ABTS) radical formation spectrophotometrically at 600 nm and 20°C for 15 min. The reaction mixture contained PBS buffer, ABTS reagent (0·15 mm), H2O2 (0·1 mm) and metmyoglobin (2·50 μm). Since TROLOX® inhibitory capacity decreases progressively with time, the sample TEAC values were calculated by comparison to the TEAC values of a TROLOX® standard curve (concentration range: 0–21·0 μm). The comparisons were done for the linear range of the reaction. Mean TEAC values for the liver and the jejunal mucosa were calculated as the arithmetic mean of the individual TEAC values measured after 3, 5 and 10 min. Before the determination of the TEAC values of the EO, a dilution with 70 % (v/v) ethanol was carried out. The TEAC values of the samples were expressed in μmol TROLOX® equivalent per g organ fresh matter or mmol TROLOX® equivalent per 100 g essential oil. Organ samples were pooled in an analogous manner as described for mRNA expression. The TEAC value of each sample pool (n 10) was measured in duplicate.
2-Thiobarbituric acid-reactive substances in the liver
2-Thiobarbituric acid-reactive substances (TBARS) were measured in the liver of the broilers as a parameter of lipid peroxidation according to a modified protocol from Wong et al. (Reference Wong, Knight and Hopfer42). TBARS concentration was measured in liver samples subsequent to the provocation of lipid peroxidation with FeSO4 in order to test their antioxidant capacity. Then, 25 μl of the 1:5 (w/v) liver crude homogenates were mixed with 375 μl H3PO4 (0·44 m) in sealable glass tubes. After the addition of 25 μl FeSO4 solution (0·05 m), 200 μl aqua bidest and 125 μl 0·6 % 2-thiobarbituric acid, the samples were incubated in a thermo block at 100°C for 60 min. Determination of the blank was carried out, using 25 μl of potassium phosphate buffer (0·1 m) instead of the liver homogenate. Following the incubation at 100°C, the samples were chilled on ice and 750 μl of methanolic NaOH (10 ml of 1 m-NaOH+90 ml methanol) were added. After thorough vortexing and centrifugation at 4000 g at 4°C for 10 min, the extinction was measured spectrophotometrically at 532 nm. Sample TBARS concentrations were calculated from a calibration curve prepared with 1,1,3,3,-tetraethoxypropane in a concentration range of 0·60–1·20 μm. TBARS concentration of each sample pool (n 10) was measured in duplicate.
Protein concentration of samples
Protein concentration in the liver cytosol, jejunal mucosa, colonic tissue and in the samples for liver immunoblot analysis of Nrf2 was determined using the standard method of Bradford(Reference Bradford43), adapted to the needs for measurement in a ninety-six-well plate reader.
Immunoblot analysis of nuclear factor erythroid 2-related factor 2 in whole liver cell lysate
For the analysis of Nrf2 protein expression in whole liver cell lysate 1:10 (w/v), liver homogenates were prepared in a non-reducing radioimmuno precipitation assay (RIPA) lysis buffer (50 mm-Tris–HCl, 150 mm-NaCl, 1 mm-phenylmethylsulphonylfluoride, 1 mm-EDTA, 1·0 % sodium desoxycholate, 0·1 % SDS and 1 % TritonX-100, pH 7·4). Then, 60 μg of protein were separated according to the standard method(Reference Laemmli44) under non-reducing conditions on 10 % SDS-polyacrylamide gels (50 mA, 4°C, 2 h). Separated proteins were transferred onto a polyvinylidene membrane (PALL Biotrace 0·45 μm™; Pall GmbH, Dreieich, Germany) by semi-dry blotting (25 min at a constant 6 V (approximately 60 mA)). After blocking the membranes overnight at 4°C in Tris-buffered saline-Tween (TBST) (20 mm-Tris–HCl, 150 mm-NaCl, 0·1 % Tween 20, pH 7·6) containing 5 % non-fat dry milk and 0·2 % bovine serum albumin, the analysis was continued by a 12 h incubation with the first antibody, a polyclonal anti-rabbit-Nrf2 antibody (Abcam, ab 31 163), in TBS (1:1000) followed by a 1 h incubation with the secondary antibody (1:3000) linked to horseradish peroxidase (Goat Anti-Rabbit IgG-h+I). Subsequent to three washes with TBST, the protein bands were detected using an ECL-kit (GE Healthcare Europe GmbH, Freiburg, Germany). Optical density of the 57 kDa band, representing active Nrf2, and of the 101 kDa band, representing ubiquitinated Nrf2 (http://www.abcam.com/index.html?pageconfig = reviews&intAbID = 31 163), were evaluated with a Phoretix TotalLab TL100 imager (BioStep GmbH, Jahnsdorf, Germany) after scanning the membranes with the biostep Bio-Imaging Systems F-ChemiBIS 3·2M luminescence reader (Berthold Technologies, Bad Wildbad, Germany). The intensity of the Nrf2 bands was normalised to β-actin, carried along as the standard. Moreover, the ratio of active Nrf2:ubiquitinated Nrf2 was calculated. Whole liver tissue protein pools (n 10) were generated in an analogous manner as described for mRNA expression. Immunoblot analysis was carried out in duplicate for four selected sample pools.
Statistical analysis
Data are presented as means with their standard errors (except for Table 6 and related remarks). Following assurance of the normality of distribution (Shapiro–Wilk test and Kolmogorov–Smirnov test) and the homogeneity of variances (Levene's test), the data were analysed with SPSS 19.0 (SPSS, Inc., Chicago, IL, USA) for Windows using the one-way ANOVA procedure. If variances were homogenous, significant differences between means (P < 0·05) were evaluated with the least significant difference-test; if not, the Games Howell test was used. Box plots for the analysis of reference gene stability were generated with SPSS 19.0 for Windows (SPSS, Inc.). Other figures were prepared with Microsoft Excel (version 2003; Microsoft Corporation, Redmond, WA, USA).
Results
Performance parameters (feed intake, body weight, weight gain, feed conversion)
All birds showed no clinical abnormalities during the whole experiment, and no broilers were lost. Both in the initial feeding period (days 1–14) on the commercial starter diet and in the experimental period on diets with the phytogenic feed additives, feed intake did not differ between groups (Table 2). Weight gain between groups was not different in the initial feeding period and in the first 2 weeks of the experimental period (Table 4).
(Mean values with their standard errors)
Con, control; SFN, sulforaphane; Cuo, turmeric oil; Oo, oregano oil; To, thyme oil; Ro, rosemary oil.
* For details of diets and procedures, see the Methods and materials section.
However, in week 5 (days 29–35), broilers of the Cuo group showed a significantly reduced weight gain compared to group Con and to all the other experimental groups with phytogenic feed additives (SFN, Oo, To, Ro). The lower weight gain of group Cuo compared to group Con was also apparent when weight gain data for the experimental period (days 15–35) and the whole experiment (days 1–35) were compared. Broilers of the Oo group produced a significantly lower weight gain over the whole experimental period (days 1–35) compared to Con broilers (Tables 3 and 4). Consequently, broilers of groups Cuo and Oo had a reduced feed conversion compared to Con birds (Table 5). Although no statistical significances could be analysed, broilers of the other groups receiving diets with phytogenic feed additives (SFN, To, Ro) also showed an overall somewhat lower performance than Con broilers, as indicated by weight gain and feed conversion.
(Mean values with their standard errors)
Con, control; SFN, sulforaphane; Cuo, turmeric oil; Oo, oregano oil; To, thyme oil; Ro, rosemary oil.
a,b Mean values with unlike superscript letters within a column were significantly different in the least significant difference test or the Games Howell test (P < 0·05).
* For details of diets and procedures, see the Methods and materials section.
(Mean values with their standard errors)
Con, control; SFN, sulforaphane; Cuo, turmeric oil; Oo, oregano oil; To, thyme oil; Ro, rosemary oil.
a,b Mean values with unlike superscript letters within a column were significantly different in the least significant difference test or the Games Howell test (P < 0·05).
* For details of diets and procedures, see the Methods and materials section.
(Mean values with their standard errors)
Con, control; SFN, sulforaphane; Cuo, turmeric oil; Oo, oregano oil; To, thyme oil; Ro, rosemary oil.
a,b Mean values with unlike superscript letters within a column were significantly different in the least significant difference test or the Games Howell test (P < 0·05).
* For details of diets and procedures, see the Methods and materials section.
Selection of reference genes
Table 6 shows the medians of the C t values of the four selected reference genes GAPDH, ARP1, ELFA and β-actin in the jejunal mucosa, the colon and the liver with their individual standard deviations. Calculation of the percentual standard deviation revealed the following results: In the jejunum, the C t values of β-actin produced the highest percentual standard deviation from the median ( ± 7·58 %), whereas that of ARP1 ( ± 6·21 %) was the lowest. Jejunal GAPDH (7·47 %) and ELFA ( ± 7·08 %) showed the highest C t values, with intermediate values for the percentual standard deviation. In the colon, the following percentual standard deviations were calculated: GAPDH ( ± 5·55 %), ARP1 ( ± 6·46 %), ELFA ( ± 4·67 %) and β-actin ( ± 6·18 %). Data for the liver percentual standard deviation were: ± 4·70 % for GAPDH, ± 10·4 % for ARP1, ± 6·42 % for ARP1 and ± 3·61 % for β-actin.
(Medians and standard deviations)
GAPDH, glycerine aldehyde-3-phosphate dehydrogenase; ARP1, acid ribosomal protein 1; ELFA, elongation factor 1α.
* Within a line indicates the most stable reference genes for the different tissues. Average expression stability (M) of remaining reference genes was calculated by stepwise exclusion of the least stable pair of reference genes in the jejunal mucosa, colon and liver. Sample pools (n 60) for all groups, corresponding to ten sample pools per dietary treatment were analysed.
† For details of diets and procedures, see the Methods and materials section.
To select the most stable pair of reference genes, expression stability (M) was recalculated after repetitive exclusion of the worst performing gene. The most stable pairs of reference genes after successive exclusion were ARP1 and β-actin in the jejunal mucosa, GAPDH and ELFA in the colon, and GAPDH and β-actin in the liver (Table 6).
Expression of antioxidant response element-regulated xenobiotic-and antioxidant enzymes in the jejunum, the colon and the liver
The analysed normalised gene expression pattern of selected ARE-regulated xenobiotic-and antioxidant enzymes depended on the phytogenic feed additive and on the organ investigated. The jejunal expression of all ARE-regulated genes was up-regulated by the reference additives SFN and Cuo compared to group Con (Table 7, jejunum), with significant changes for HMOX1 (average factor: 1·73), EPHX1 (average factor: 2·10) and AFAR (average factor: 2·10). Among the labiatae oils, only Ro effected a significant up-regulation of HMOX1, EPHX1 and TrxR1 compared to group Con, whereas Oo and To produced no significant changes. In the colon, the expression pattern originating from feeding the phytogenic feed additives differed distinctly from the jejunal profile (Table 7, colon). The number of ARE-regulated genes influenced by the reference additives SFN and Cuo was distinctly lower in the colon than in the jejunum. AFAR was the only colonic gene showing a significant up-regulation by SFN addition to the diet (factor: 1·82) compared to the Con group. Cuo solely increased colonic TrxR1 expression by the factor 2·41. Ro influenced the expression of colonic ARE-regulated genes most powerful, including HMOX1 (factor: 1·98), EPHX1 (factor: 1·32) and TrxR1 (factor: 2·31). Interestingly, Oo and To that remained without a significant influence on the jejunal expression of ARE-regulated genes had the highest impact on colonic TrxR1 expression (average factor: 3·52). In addition, colonic AFAR expression also responded significantly to Oo treatment (factor: 1·96). In contrast to our expectations, both the reference additives SFN and Cuo and the labiatae oils Oo, To and Ro caused a more or less pronounced down-regulation of the mRNA expression of the ARE-regulated enzymes in the liver of the broilers (Table 7, liver). In particular, Cuo and Ro decreased the mRNA concentrations of the antioxidant enzymes HMOX1 and TrxR1, and that of the epoxide metabolising enzymes EPHX1 and 2 to a level of 40–50 % of that analysed in the Con group (Table 7, liver). Cuo additionally reduced GSTα expression significantly. In groups SFN, Oo and To, the expression of HMOX1, EPHX1 and EPHX2 was down-regulated by 15–40 % of the Con level, whereas TrxR1 expression was not influenced (Table 7, liver).
(Mean values with their standard errors of the mRNA abundance relative to group Con=1·0 (n 10 pools of two animals per experimental group))
SFN, sulforaphane; Cuo, turmeric oil; Oo, oregano oil; To, thyme oil; Ro, rosemary oil; GSTα, glutathione-S-transferase α HMOX1, haeme oxygenase 1; EPHX1, microsomal epoxide hydrolase; EPHX2, cytosolic epoxide hydrolase; AFAR, aflatoxin B1 aldehyde reductase; TrxR1, thioredoxin reductase 1; CYP1A1, cytochrome P450 family 1 subfamily A polypeptide 1; ABCC2, ATP-binding cassette subfamily C member 2.
a,b,c,d Mean values with unlike superscript letters within a row indicate significant differences in the least significant difference test or the Games Howell test (P < 0·05). The superscript ‘a’ was assigned to group Con.
* For details of diets and procedures, see the Methods and materials section.
To judge the changes in the whole xenobiotic metabolising system, we have additionally measured the gene expression of the phase I cytochrome P450 enzyme CYP1A1 and that of the phase III ATP-binding-cassette exporter ABCC2, both having a proven function in mycotoxin detoxification (Table 7, liver). Cuo that caused the strongest down-regulation of all ARE-regulated enzymes also reduced the expression of CYP1A1 and ABCC2 most potently. Similarly for the other phytogenic additives (SFN, Oo, To and Ro), their efficacy on CYP1A1 and ABCC2 mRNA reduction corresponded well to their impact on the down-regulation of the xenobiotic- and antioxidant enzymes investigated. This specific result suggests a down-regulation of the complete liver xenobiotic metabolising machinery by the phytogenic feed additives.
Differential jejunal- and liver superoxide dismutase activity
Total SOD activity comprises the activity of the cytosolic Cu/Zn enzyme (Cu/Zn SOD) and of the mitochondrial Mn enzyme (Mn SOD). Cu/Zn SOD is an antioxidant enzyme with an ARE sequence in its DNA promoter. Total jejunal SOD activity was increased significantly by all phytogenic additives, whereas it was decreased to a greater or lesser extent in the liver (Table 8), as analogously observed for gene expression of the xenobiotic- and antioxidant enzymes. Accordingly, the raise in jejunal SOD activity was based to a higher percentage on an increased Cu/Zn SOD activity than on changes of Mn SOD. The opposite way around, total SOD activity and, in particular, that of Cu/Zn SOD activity were reduced by the phytogenic substances in the liver.
(Mean values with their standard errors, n 10 pools of two animals per experimental group)
Cu/Zn SOD, cytosolic Cu–Zn SOD; Mn SOD, mitochondrial Mn SOD.
a,b,c Mean values with unlike superscript letters within a row were significantly different in the least significant difference test or the Games Howell test (P < 0·05).
* For details of diets and procedures, see the Methods and materials section.
Combined cytosolic glutathione peroxidase- and gastrointestinal glutathione peroxidase activity in the jejunum and liver cytosolic glutathione peroxidase activity
In the intestine, cytosolic GPx activity comprises the activity of GPx1 and that of GPx2, whereas cytosolic GPx activity in all other organs is restricted to GPx1 action. Both GPx1 and GPx2 sensitively respond to oxidative stress with an up-regulation. Comparably to Cu/Zn SOD, GPx2 also has an ARE in its DNA promoter. As probably observed for Cu/Zn SOD, all phytogenic feed additives increased GPx activity in the jejunum to a different extent, but in contrast effected a significant reduction of liver GPx activity (Table 8).
Immunoblot analysis of nuclear factor erythroid 2-related factor 2 regulation in the liver
All phytogenic feed additives decreased protein abundance of active Nrf2 in whole liver homogenate by 20–39 % compared to group Con. In contrast, relative protein concentration of ubiquitinated Nrf2 was 2·20- to 3·60-fold higher in the liver of broilers receiving any phytogenic feed additive compared to Con broilers. As a consequence, in broilers fed phytogenic feed additives, the ratio of active Nrf2:ubiquitinated Nrf2 decreased to 28–40 % of that in Con broilers (Fig. 1(A) and (B)).
Nuclear factor erythroid 2-related factor 2 (Nrf2) protein expression in whole liver lysate of growing broilers fed diets containing different phytogenic additives for 21 d. (A) Representative immunoblot of ubiquitinated Nrf2 ( = Nrf2 marked with ubiquitin for proteasomal degradation, 101 kDa, upper lane), active Nrf2 (57 kDa, middle lane) and β-actin (42 kDa, lower lane), selected from four pools of whole liver tissue homogenate per experimental group. Immunoblot analysis for each protein pool was performed in duplicate. (B) Nrf2 protein expression and ratio of active:ubiquitinated Nrf2 in whole liver lysate of growing broilers fed diets containing different phytogenic additives for 21 d relative to group Con = 1·0. Values are means, with their standard errors represented by vertical bars of active and ubiquitinated Nrf2 protein abundance relative to group Con = 1·0 and the ratio of active Nrf2:ubiquitinated Nrf2 relative to group Con = 1·0 (n 4 pools of two animals per experimental group). a,b,c Mean values with unlike letters were significantly different in the least significant difference test or the Games Howell test (P < 0·05). The letter ‘a’ was assigned to group Con. For details of diets and procedures, see the Methods and materials section. 
, Nfr2 active; 
, Nrf2 ubiquitinated; 
, active:ubiquitinated. Con, control; SFN, sulforaphane; Cuo, turmeric oil; Oo, oregano oil; To, thyme oil; Ro, rosemary oil.
Trolox equivalent antioxidant capacity=TROLOX® equivalent in the essential oils and the liver
The analysed TEAC values (mmol per 100 ml) of the essential oils were as follows: Cuo: 90·7 (se 1·81), Oo: 120 (se 10·1), To: 116 (se 8·72) and Ro: 156 (se 21·1) (Fig. 2). A TEAC value for sulforphane or its glucosinolate precursor glucoraphanin could not be analysed since these compounds possess no direct antioxidant effects. Jejunal TEAC (μmol per g of organ) was 3- to 7-fold lower than that in the liver (jejunum: Con 29·4 (se 9·61), SFN 174 (se 36·6), Cuo 343 (se 22·9), Oo 392 (se 31·0), To 446 (se 43·1), Ro 364 (se 59·8); liver: Con 282 (se 28·0), SFN 680 (se 52·2), Cuo 494 (se 34·9), Oo 992 (se 57·4), To 1129 (se 87·1), Ro 764 (se 115)). All phytogenic feed additives raised the jejunal and liver TEAC values significantly compared to group Con. The TEAC values of Oo and To directly reflected the TEAC values analysed in the jejunum and in the liver of the broilers. Cuo which had a distinctly lower TEAC value than the labiatae oils (Oo, To and Ro) had a distinctly higher influence on the jejunal TEAC than on the liver TEAC. Feeding Ro, with the highest analysed TEAC, resulted in a lower liver TEAC than Oo- and To feeding, whereas its influence on the jejunal TEAC was comparable to that of Oo and To. SFN, having no direct antioxidant activity, increased the jejunal and liver TEAC significantly less than the labiatae oils (Oo, To and Ro).
Trolox equivalent antioxidant capacity (TEAC) values of essential oils (
) and TEAC values in jejunal (○) mucosa and the liver (□) of fast-growing broilers fed diets containing different phytogenic additives for 21 d. Values are means, with their standard errors represented by vertical bars (n 10 pools of two animals per experimental group). a,b,c,d Mean values with unlike letters were significantly different in the least significant difference (LSD) test or the Games Howell test for the jejunal TEAC values (P < 0·05). A,B,C,D Mean values with unlike letters were significantly different in the LSD test or the Games Howell test for the liver TEAC values (P < 0·05). For details of diets and procedures, see the Methods and materials section. Con, control; SFN, sulforaphane; Cuo, turmeric oil; Oo, oregano oil; To, thyme oil; Ro, rosemary oil.
Concentration of thiobarbituric acid-reactive substances in the liver
All the phytogenic feed additives tested, effected a reduction of Fe-induced lipid peroxidation in the liver of the broilers compared to the Con group (Fig. 3). Cuo feeding thereby had the strongest effect, reducing TBARS by nearly 60 % compared to group Con. To and Ro as well as SFN produced an intermediate protection against the Fe-provoked lipid peroxidation (reduction of about 40 %), whereas Oo showed the smallest effect in comparison (reduction of about 20 %).
Thiobarbituric acid-reactive substances (TBARS) after iron provocation in the liver of fast-growing broilers fed diets containing different phytogenic additives for 21 d. Values are means, with their standard errors represented by vertical bars (n 10 pools of two animals per experimental group). a,b,c Mean values with unlike letters were significantly different in the least significant difference test or the Games Howell test (P < 0·05). For details of diets and procedures, see the Methods and materials section.
Discussion
Performance parameters (feed intake, body weight, weight gain, feed conversion)
As mentioned in the introduction, the effects of phytogenic feed additives, and in particular of labiatae oils on the performance parameters of broilers are subject to a controversial discussion. Whereas one study reported on the beneficial effects of extremely high dietary concentrations of oregano leaves (up to 20 g/kg = 20 kg/tonne) and Oo (up to 1·0 g/kg = 1·0 kg/tonne) on weight gain and feed conversion(Reference Halle, Thomann and Bauermann2), other studies showed no effects(Reference Basmacioğlu Malayoğlu, Baysal and Misirlioğlu3) or even opposite effects on these parameters(Reference Cross, McDevitt and Hillman5). In the last mentioned study, the influence of Oo, To and Ro on the performance of broilers was studied. In this study, Oo and Ro impaired weight gain and feed conversion compared to control broilers, whereas To influenced these parameters positively. Our results are partially in accordance with these results(Reference Cross, McDevitt and Hillman5). Although we could not confirm an improvement of performance by To addition to the diet, weight gain was reduced to a lesser extent by To compared to Oo and Ro (Table 2). In studies on the effects of turmeric on aflatoxin-metabolising enzymes, the addition of 500 g/t turmeric powder to the diets of Cobb × Cobb broilers reduced body weight gain and feed conversion of these birds compared to the Con(Reference Gowda, Ledoux and Rottinghaus26, Reference Yarru, Settivari and Gowda45). Our results for Cuo confirm these results (Table 2), with the difference that the Cobb × Cobb broilers(Reference Vieira, Olmos and Berres46) had a somewhat higher weight gain and a better feed conversion than our Ross-308 broilers(Reference Yarru, Settivari and Gowda45, Reference Gowda, Ledoux and Rottinghaus47). Broccoli extract (SFN), not yet permitted as a feed additive in the EU, in our trial also influenced the performance parameters of the broilers, slightly negative compared to group Con (Table 2). However, this effect reached only a magnitude comparable to that of To. Feasible negative effects of broccoli extract on performance may derive from the goitrogenic potential of isothiocyanates. However, studies with human subjects have proven that even high dietary concentrations of SFN affect thyroid metabolism only negligibly(Reference Shapiro, Fahey and Dinkova-Kostova18, Reference McMillan, Spinks and Fenwick48).
Weight gain and feed conversion are the two most important goals in today's animal nutrition. Frequently both parameters are associated with general animal health. Our present results and the outcome of a number of the aforementioned studies(Reference Halle, Thomann and Bauermann2, Reference Basmacioğlu Malayoğlu, Baysal and Misirlioğlu3, Reference Vieira, Olmos and Berres46) suggest that phytogenic feed additives do not meet the criteria acting as mere growth promoters. However, in these studies, including our present experiment, the animals were not subjected to a challenge with pathogenic micro-organisms or toxic substances. It can be assumed that the threat of infections and the challenge with feed contaminants increase under practical feeding conditions with a high stocking rate. Experiments in which broilers were infected with Eimeria tenella or fed aflatoxin-containing diets, Oo or turmeric powder counteracted the depressed feed intake and growth(Reference Gowda, Ledoux and Rottinghaus26, Reference Yarru, Settivari and Gowda45, Reference Giannenas, Florou-Paneri and Papazahariadou49). Moreover, the exclusive addition of phytogenic substances as growth promoters to animal feed may be less effective than combinations with feed enzymes(Reference Windisch, Schedle and Plitzner1, Reference Halle, Thomann and Bauermann2) or probiotics(Reference Clarke and Mullin50).
Antioxidant response element-regulated xenobiotic- and antioxidant enzymes, Trolox equivalent antioxidant capacity in the intestine
To the best of our knowledge, our data have shown for the first time that labiatae oils have differentiated and promising effects on ARE-regulated xenobiotic- and antioxidant enzymes and on antioxidant capacity in the intestine and the liver of fast-growing broilers. This assertion is also appropriate for Cuo which is permitted as a feed additive in the EU and for broccoli sprouts extract which is currently only accredited as a dietary supplement for humans. Due to their known impact on the induction of ARE-regulated genes, we have applied the aforementioned phytogenic substances as the reference additives in our study. For turmeric and SFN(Reference Li, Hullar and Beresford51) derived from glucoraphanin cleavage by intestinal microbial β-glucosidases, our data regarding their impact on the induction of intestinal ARE-regulated xenobiotic- and antioxidant enzymes are in agreement with recent literature. A number of cell culture studies and in vivo studies with human subjects and laboratory animals have demonstrated the potential of turmeric and SFN on the induction of ARE-regulated genes in the intestine(Reference Petri, Tannergren and Holst22, Reference Pool-Zobel, Veeriah and Böhmer52–Reference Yeh, Chiu and Yen54). In humans, turmeric and SFN predominantly have been established as preventive agents against intestinal cancers. Their safety has been verified(Reference Shapiro, Fahey and Dinkova-Kostova18, Reference McMillan, Spinks and Fenwick48, Reference Joshi, Ghaisas and Vaidya55). In farm animals, having a short life span and needed for food production, the application of potent inductors of ARE-regulated genes rather aims on their efficiency to strengthen the intestinal barrier against toxic feed-derived substances or endogenously produced toxic metabolites and thereby impeding their absorption into the organism. In our trial, Cuo and SFN both induced a similar pattern of ARE-regulated genes in the small intestine (Table 7, jejunum) with a particular focus on HMOX1, EPHX 1 and 2, and on AFAR(Reference Gowda, Ledoux and Rottinghaus26, Reference Yarru, Settivari and Gowda45).
Further, our results have shown an effect of labiatae oils (Oo, To, Ro) on the expression of intestinal ARE-regulated genes. The labiatae oils induced a differential expression pattern depending on the oil and on the intestinal segment investigated (Table 7; jejunum, colon). Within the labiatae oils, Oo and To effected a smaller increase in jejunal ARE-regulated enzymes compared to Ro. In the colon, feeding the phytogenic substances resulted in a more individual induction pattern. In the colon, all the additives induced TrxR1 possessing both, antioxidant properties, and a key role in DNA-synthesis(Reference Arnér and Holmgren56) to a higher extent than in the jejunum. Whereas SFN and Oo increased the colonic AFAR expression potently, Ro had a high impact on HMOX1 expression. The exact mechanisms by which EO and SFN influence ARE-regulated genes differentially have not been studied to date. It can be speculated that the different main terpene compounds of EO and SFN modify Keap1 at sensor –SH-groups by individual chemical reactions(Reference Hong, Freeman and Liebler27). Moreover, the number of ARE and that of other transcription-factor-regulated elements in the promoter region differ between the single xenobiotic- and antioxidant enzymes investigated(Reference Wang, Tomso and Chorley57). That terpenes increase the expression and activity of ARE-regulated enzymes has been demonstrated(Reference Miyakoshi, Yamaguchi and Takagaki23, Reference Jäger, Scheffler and Schmellenkamp58, 59). In contrast to carvacrol (oregano) and thymol (thyme)(Reference Shan, Cai and Sun14), the main terpenes of Cuo (ar-turmerone) and of Ro (1,8 cineole)(Reference Sacchetti, Maietti and Muzzoli16, Reference Erkan, Ayranci and Ayranci60), accounting for 30–50 % (v/v) of these oils, have no antioxidant phenolic groups in their molecular structure. For this reason, sesquiterpenes like ar-turmerone (turmeric) or terpenes with an epoxide function like 1,8 cineole (rosemary) may induce ARE-regulated genes more powerful than phenolic monoterpenes(Reference Miyakoshi, Yamaguchi and Takagaki23). On the other hand, the phenolic monoterpenes exert a higher direct antioxidant potential(Reference Sacchetti, Maietti and Muzzoli16). In this context, our results for the TEAC values of the oils and of jejunal mucosa are of interest (Fig. 2). The TEAC value of a tissue comprises direct antioxidant effects and that of the antioxidant enzymes increased by secondary mechanisms. In our study, the broccoli-derived isothiocyanate SFN, having no direct antioxidant properties, produced the lowest increase in jejunal TEAC compared to group Con. From this fact, it can be concluded that the increase in jejunal TEAC in group SFN mainly bases on the induction of ARE-regulated antioxidant enzymes. For Cuo showing an intermediate effect on jejunal TEAC, it can be assumed that both, its moderate direct antioxidant effect and the powerful induction of ARE-regulated antioxidant enzymes by ar-turmerone(Reference Miyakoshi, Yamaguchi and Takagaki23, Reference Jäger, Scheffler and Schmellenkamp58, 59) have contributed to jejunal TEAC modulation (Fig. 2). Oo and To contain high concentrations of the antioxidant phenolic terpenes carvacrol and thymol(Reference Shan, Cai and Sun14). In contrast, both oils have induced ARE-regulated enzymes only moderately. Therefore, the high jejunal TEAC values of Oo and To may mainly result from their high carvacrol and thymol content (Fig. 2). To complicate matters, Ro had the highest TEAC value within the labiatae oils. Additionally, Ro powerfully induced intestinal ARE-regulated genes (Table 7; jejunum, colon). However, its influence on jejunal TEAC was not stronger than that of Oo and To. This conflicting result could have two causes: on the one hand, the non-antioxidant epoxy-terpene 1,8 cineole(Reference Jäger, Scheffler and Schmellenkamp58) may have produced a strong induction of ARE-regulated antioxidant enzymes. On the other hand, Ro additionally contains small amounts of the phenolic diterpenes carnosic acid, carnosol and epirosmanol coming along with a high direct antioxidant activity(Reference Shan, Cai and Sun14, Reference Erkan, Ayranci and Ayranci60), which may limit the further induction of ARE-regulated antioxidant enzymes. In summary, our data showed a differentiated response of intestinal ARE-regulated genes to dietary treatment with the phytogenic additives SFN, Cuo, Oo, To and Ro. Future studies with tissue cultures and other farm animal species should focus on the examination of the individual xenobiotic-and antioxidant enzyme induction pattern of EO, and in particular, on the examination of their pure main terpenes and of SFN. In those studies, the added concentration of the oils should be standardised to their main terpenes. The results of those investigations may contribute to the creation of new and optimised mixtures of phytogenic feed additives.
Nuclear factor erythroid 2-related factor 2, antioxidant response element-regulated xenobiotic- and antioxidant enzymes, Trolox equivalent antioxidant capacity and thiobarbituric acid-reactive substances in the liver
In contrast to our expectations and to data from other studies(Reference Hu, Xu and Shen25, Reference Lii, Liu and Cheng61, Reference El-Ashmawy, Ashry and El-Nahas62), SFN and Cuo, the reference substances in our experiment, as well as the labiatae oils, generally reduced the expression of ARE-regulated genes in the liver (Table 7, liver). Nevertheless, data from other trials feeding diets supplemented with curcumin, quercetin and catechin to mice and rats support our findings regarding a down-regulation of xenobiotic- and antioxidant enzymes in the liver(Reference Wiegand, Boesch-Saadatmandi and Regos63, Reference Schrader, Schiborr and Frank64). This effect may have two reasons:
(1) The dietary concentration of both reference additives was too low to produce an induction of ARE-regulated genes also in the liver.
(2) The antioxidant protection achieved by the induction of ARE-regulated genes in the intestine acted as a barrier and protected the organism against the uptake of toxic xenobiotics and against oxidative stress.
However, the second hypothesis seems to be more plausible, since we found a distinct up-regulation of SOD- and GPx enzyme activity by all phytogenic feed additives compared to the control in jejunal mucosa (Table 8). Intestinal GPx activity, measured with H2O2 as the substrate, comprises the activity of GPx1 and GPx2. GPx2 is an unusual selenoprotein, induced by both, a sufficient selenium status and by Nrf2(Reference Brigelius-Flohé, Müller and Menard65, Reference Müller, Banning and Brigelius-Flohé66). Both peroxidases underlie a coordinated regulation. In the case of lacking GPx2 activity, GPx1 is up-regulated to compensate reduced peroxide detoxification(Reference Florian, Krehl and Loewinger67). Numerous studies have demonstrated that the loss of both enzymes promotes the development of chronic inflammatory intestinal diseases. Moreover, it has been shown that GPx2 blocks the up-regulation of the proinflammatory inducible cyclo-oxygenase 2. Further, GPx2 impedes the aquaporin-mediated absorption of peroxides into the organism(Reference Esworthy, Kim and Larson68–Reference Wingler, Müller and Schmehl72).
Our second hypothesis that the increased intestinal barrier against pro-oxidants and inflammatory stress protects peripheral organs like the liver from oxidative stress is further supported by our findings for Nrf2(Reference Itho, Miramura and Yamamoto73) (Fig. 1(A) and (B)), SOD (Table 8), GPx1 (Table 8), TEAC (Fig. 2) and TBARS (Fig. 3). The coincident down-regulation of active Nrf2 (Fig. 1(A) and (B)) and xenobiotic- and antioxidant enzymes (Table 7, liver) on the one hand, and higher TEAC values (Fig. 2) accompanied by a reduced, provoked lipid peroxidation (Fig. 3) of all chickens receiving a phytogenic additive on the other, suggest that the livers of supplemented broilers had an increased antioxidative capacity and reduced oxidative stress, making the further induction of antioxidant enzymes dispensable(Reference Wiegand, Boesch-Saadatmandi and Regos63, Reference Schrader, Schiborr and Frank64). This particular result was also supported by the finding that protein abundance of ubiquitinated Nrf2 was significantly higher in broilers fed diets with phytogenic additives than in Con broilers (Fig. 1(A) and (B)). Contrarily it can be assumed that the livers of untreated Con broilers were exposed to higher oxidative stress, as indicated by the highest protein abundance of active Nrf2 and the lowest of ubiquitinated Nrf2. This, in turn, explains the higher expression of ARE-regulated xenobiotic-and antioxidant enzymes in Con broilers(Reference Itho, Miramura and Yamamoto73).
That feeding phytogenic feed additives protects peripheral organs from oxidative stress is confirmed by results from other studies reporting on reduced lipid peroxidation and increased storage stability of broiler meat and fat(Reference Lopez-Bote, Gray and Gomaa74–Reference Mirshekar, Dastar and Shabanpour76).
In contradiction to our results, a study with broilers found a distinct up-regulation of liver ARE-regulated genes (AFAR, EPHX1) due to feeding diets with turmeric powder. However, this response was triggered only by feeding aflatoxin simultaneously(Reference Yarru, Settivari and Gowda45). From this fact it can be concluded once again that the regulation of liver ARE genes by phytogenic substances presumably depends largely on the exposure of an organism to toxic substances and oxidative stress. In contrast, an optimum protection against oxidative stress counteracts the further induction of ARE-regulated xenobiotic- and antioxidant enzymes in peripheral organs(Reference Wiegand, Boesch-Saadatmandi and Regos63, Reference Schrader, Schiborr and Frank64).
An issue that should be addressed at the end of the discussion is the regulation of phase II, I and III enzymes in a unidirectional manner as analysed in our study (Table 7, liver). This aspect is very important to keep the balance between the single stages of xenobiotic metabolism(Reference Patterson, Gonzalez and Idle77) and to prevent the organism from damage. The simultaneous down-regulation of Cyp1A1 with an important function in mycotoxin activation(Reference Diaz, Murcia and Cepeda78), of the xenobiotic-and antioxidant phase II enzymes investigated(Reference McWalter, Higgins and McLellan79), and of ABCC2 responsible for the excretion of conjugated mycotoxin metabolites(Reference Videmanna, Mazallona and Prouillaca80), is a further indicator of a reduced exposure of the liver to toxic metabolites and oxidative stress. In summary, our results for the liver suggest that the induction of jejunal ARE-regulated genes and the increase in jejunal TEAC in the small intestine by phytogenic feed additives seem to act as a barrier against oxidative stress in the organism(Reference Te Velde, Pronk and de Kort71, Reference Wingler, Müller and Schmehl72). This protective function of essential oils and of broccoli extract is also of particular interest for human nutrition and with regard to inflammatory bowel disease in humans(Reference Esworthy, Kim and Larson68, Reference Esworthy, Aranda and Martín69, Reference Te Velde, Pronk and de Kort71), since we have used chickens as a single-stomached animal species in our study.
Conclusions
(1) On the one hand, our study confirmed results from the literature that phytogenic feed additives do not merely act as growth promoters under conditions without an infectious or toxic challenge.
(2) On the other hand, our results have demonstrated for the first time that broccoli extract, Cuo and the labiatae oils of oregano, thyme and rosemary influence the expression of ARE-regulated xenobiotic- and antioxidant enzymes. The up-regulation of these genes in the intestine seems to build a barrier against oxidative stress in the organism. In particular, the up-regulation of ARE-regulated genes in the small intestine may represent an attractive and new mechanism by which phytogenic feed additives improve the intestinal and general health of farm animals.
(3) However, different regulation patterns of the single phytogenic substances demonstrate the necessity for future research with regard to this issue. Understanding the different regulation patterns of single phytogenic feed additives may contribute to the development of optimised combinations of phytogenic substances in animal nutrition and to the use of these substances as dietary supplements for humans.
(4) Moreover, we have tested for the first time a broccoli sprouts extract containing SFN as a phytogenic feed additive in animal nutrition. Compared to the other additives tested, SFN did not show significant negative effects on the performance parameters under well-controlled housing conditions without a microbial or toxic challenge. Moreover, broccoli extract acted as a modulator of the aforementioned ARE-regulated genes. For this reason, broccoli extract, currently permitted only as a dietary supplement for humans, has turned out to be an attractive phytogenic feed additive for use in the future.
Acknowledgements
The present study was supported by the H. Wilhelm Schaumann Foundation, Hamburg by the provision of a non-recurring donation for the study and by funding Dipl. troph. Kristin Mueller with a doctoral scholarship. We thank Devakumari Hiller (Jarrow Deutschland GmbH, Berlin, Germany) for arranging the contact with Jarrow L. Rogovin from Jarrow Formulas, Los Angeles, CA, USA, who provided us with the broccoli seed extract. Further thanks are addressed to Dostofarm GmbH (Westerstede, Germany) for providing us with the Oo. Moreover, we thank our stockmen Olaf Hoedel and Detlev Barth for their help with the diet preparation, animal care and organ sampling. Thanks are also addressed to our Master's degree students Anke Markert and Kathrin Sinningen for their help with the analyses within the scope of their Master's theses. The contributions of the authors were as follows: K. M. assisted in planning the trial and blending the diets. Further, she participated in the broilers' care and organ sampling. She carried out all laboratory analyses and supervised the Master's degree students who had supported her with the analyses. Besides, K. M. carried out the data evaluation, other than writing voluminous sections of the manuscript. N. M. B. assisted K. M. in the laboratory analyses and helped in the preparation of the tables. H. K. was responsible for calculating the exact composition of the diets. A. S. M. planned the trial and participated in organ sampling and analyses. Further, he had drafted the applications for obtaining the licence for the animal study and the certificate of exemption for using the broccoli sprouts extract as a feed. A. S. M. contributed to supervising the data evaluation and manuscript writing. All authors declare that they have no conflicts of interest.
