The term diabetes mellitus is used to describe a variety of chronic metabolic disorders characterised by elevated blood glucose levels now afflicting 3 % of the world population(Reference Gianni, Mohn and Chiarelli1, Reference Craig, Hattersley and Donaghue2). Diabetes mellitus can broadly be classified into two main types based on individual aetiologies. Type 1 diabetes (T1D) that accounts for approximately 5–10 % of all cases of diabetes, is an inflammatory autoimmune disease in which pancreatic insulin-producing β-cells are selectively destroyed by cells of the immune system(Reference Tisch and McDevitt3) culminating in a state of hypoinsulinaemia and hyperglycaemia(Reference Daaboul and Schatz4). Type 2 diabetes (T2D) that is estimated to represent 90–95 % of all cases is due to β-cell failure or various degrees of insulin resistance(Reference Watson and Miller5). The only possible cure for T1D is control of the T cell autoimmunity against β-cells together with recovery and/or replacement of the destroyed β-cell mass. Over many years, various immunomodulatory regimens were tested with the aim of blocking autoimmunity against β-cell mass and promoting β-cell preservation. Despite considerable progress in the management of T1D with conventional drugs, a single effective immune-based therapeutic approach has not been identified so far(Reference Craig, Hattersley and Donaghue2, Reference Mastrandrea, Yu and Behrens6–Reference Rother, Brown and Morales9). This provides an impetus for the development of new therapeutic strategies using various animal models(Reference Shoda, Young and Ramanujan10, Reference Stosic-Grujicic, Cvetkovic and Mangano11). However, any single animal model is unlikely to address the issue of population heterogeneity, so the application of different models has been instructive about many diverse scenarios that might occur in human T1D(Reference Stosić-Grujicić, Cvjetićanin and Stojanović12).
Benefits of the Mediterranean-style diet have been known for centuries, and it has been traditionally used to prevent and treat different metabolic disorders. Phenolic components of commonly consumed foods, such as red wine and virgin olive oil, or components of other olive (Olea europaea) organs, such as leaves, rich in these constituents, have been shown to possess strong antioxidant and anti-inflammatory properties(Reference Perona, Cabello-Moruno and Ruiz-Gutierrez13). The chemical composition of dry olive leaf extract (DOLE) is very complex, comprising oleuropein, caffeic acid, luteolin, luteolin-7-O-glucoside, apigenin-7-O-glucoside, quercetin, chrysoeriol and others(Reference Dekanski, Janicijevic-Hudomal and Tadic14). Due to all these useful active ingredients, olive oil and olive leaf constituents have been used increasingly as complementary and alternative medicine to improve metabolic disorders(Reference Ramírez-Tortosa, Suárez and Gómez15–Reference Panagiotakos and Polychronopoulos19). Some of these beneficial effects include reactive oxygen species scavenge, inhibition of LDL oxidation, production of NO, down-regulation of adhesion molecules and inhibition of inflammatory cytokines(Reference Visioli, Bellosta and Galli20–Reference Bitler, Viale and Damaj22). It has also been reported that constituents of olive leaves have anti-hyperglycaemic and insulin-sensitising activities, suggesting a beneficial metabolic effect in T2D(Reference Al-Azzawie and Alhamdani23–Reference Eidi, Eidi and Darzi26). However, the development of therapeutic approaches for T1D has been neglected in favour of efforts to advance therapies for the larger T2D population.
In view of the increasing prevalence, there is a growing need to develop integrated approaches towards prevention and treatment of T1D by exploring potentials offered by traditional phytotherapies as alternative and/or supplementary therapy. Recently, we have shown that DOLE-enriched diet ameliorated central nervous system autoimmunity in rats through reduction of proinflammatory cytokine production, which implied that this extract had a potent immunomodulatory effect(Reference Miljkovic, Dekanski and Miljkovic27). Therefore, in the present study we investigated the effects of commercially available standardised DOLE on pancreatic islet (Panc)-directed autoimmunity. For this purpose, we used two models of T1D: cyclophosphamide (CY)-accelerated diabetes in non-obese diabetic (NOD) mice(Reference Brode, Raine and Zaccone28); multiple low-dose streptozotocin (MLDS)-induced diabetes in susceptible mouse strains(Reference Like and Rossini29), because hyperglycaemia and insulitis can be easily induced in a relatively short period of time in a high percentage of animals. In both the disease models, inflammatory autoreactive T cells and macrophages mediate the autoimmune status, causing islet β-cell destruction either directly or through secretion of proinflammatory cytokines and free radicals(Reference Bach30). However, in contrast to MLDS-induced diabetes, CY-induced diabetes in NOD mice is based on selective elimination of inhibitory cells that would otherwise prevent development of the disease(Reference Brode, Raine and Zaccone28). Therefore, the ultimate translational objective is to use both of these animal models to test the hypothesis that DOLE protects against T1D development and to determine potential mechanisms involved in this protective effect.
Materials and methods
Reagents
Standardised to 18–26 % of oleuropein, DOLE EFLA® 943 was purchased from Frutarom Switzerland Ltd (Wädenswil, Switzerland). The extract was manufactured from the dried leaves of O. europaea L., applying an ethanol (80 % m/m) extraction procedure. After a patented filtration process (EFLA® Hyperpure), the crude extract was dried. Furthermore, stability and microbiological purity were confirmed by the manufacturer. The extract was standardised to 19·8 % of oleuropein content by the manufacturer. It was further phytochemically analysed for the presence of various components in the previous report of Dekanski and collaborators. There it was detected that the extract contained oleuropein (19·8 %), total flavonoids (0·29 %), including luteoline-7-O-glucoside (0·04 %), apigenine-7-O-glucoside (0·07 %) and quercetin (0·04 %), as well as tannins (0·52 %) and caffeic acid (0·02 %)(Reference Dekanski, Janicijevic-Hudomal and Tadic14). All other reagents were purchased from Sigma (St Louis, MO, USA) unless otherwise noted.
Type 1 diabetes induction and in vivo treatment protocols
All experimental procedures were approved by the Institutional Animal Care and Use Committee at the Institute for Biological Research ‘Siniša Stanković’, University of Belgrade and run in accordance to the requirements of the European Union regarding handling of experimental animals. Specific pathogen-free inbred C57BL/6, CBA/H and NOD/ShiLtJ mice were provided by the Central Animal House Facility of our institute. Mice were maintained under conventional conditions with free access to a standard laboratory chow and potable water. Animals and feed were regularly checked by appropriate microbiological examinations, which showed that the animals were not infected with common mouse pathogens and that the feed was free of microbiological contamination.
Immunoinflammatory T1D was induced in male mice of the C57BL/6 and CBA/H strains with multiple low doses of streptozotocin (MLDS, 40 mg/kg body weight (b.wt.), intraperitoneal (i.p.) for five consecutive days) as described previously(Reference Cvetkovic, Al-Abed and Miljkovic31). The mice were age-matched (8–12 weeks of age) with b.wt. ranging from 25 to 30 g. Treatment with DOLE was per oral (p.o.) by gavage in 0·2 ml of PBS (100 mg/kg b.wt. per d, divided into two daily doses), or i.p. (40 mg/kg b.wt per d), given as a prevention regimen (days − 5–21 of diabetes post induction (p.i.)) or as a reversal regimen (days 5–21 p.i.). Control MLDS-induced mice were treated with an equivalent amount of vehicle. A group of non-diabetic control mice were treated i.p. with DOLE only. The mice subjected to morphological examination of pancreatic glands and ex vivo analyses were sacrificed on day 15 p.i., unless otherwise stated. Each experimental group used for in vivo analyses consisted of six to seven mice per group, whereas for ex vivo analyses each experimental group had four to five mice per group.
For induction of T1D with CY, nulliparous non-pregnant non-diabetic female NOD mice, 8–10 weeks old (b.wt. range 20–25 g) were injected twice with the drug at a dose of 300 mg/kg b.wt., i.p., with a 2-week interval between the injections. DOLE was administered i.p. (40 mg/kg b.wt. per d), or p.o. (100 mg/kg b.wt. per d, divided into two daily doses) as a continuous treatment until the end of the experiments, starting 1 d after the first diabetogenic challenge with CY. Control mice were i.p. administered with an equivalent amount of vehicle or left untreated. The number of mice used for every experiment was seven to sixteen per group.
Both in MLDS- and CY-induced diabetes, blood samples were taken from the tail tip of non-fasting mice for blood glucose determination, with a handheld glucometer (GlucoSure Plus; ApexBio, Hsinchu, Taiwan, ROC). Mice were considered hyperglycaemic when blood glucose concentration exceeded 10 mmol/l (for MLDS induction) and 8·8 mmol/l (for CY induction).
The dose of DOLE used in the present study was calculated according to a clinical study in which DOLE at 1000 mg daily (divided in two doses) effectively reduced blood pressure(Reference Perrinjaquet-Moccetti, Busjahn and Schmidlin32). We used the metabolic body size or food intake rather than b.wt. as the criterion for extrapolation of the dosage from human subjects to mice(Reference Rucker33). The estimated quantity of DOLE expressed per unit of human diet was 20 mg/g of dry food. For the mouse, this consumption corresponded to a DOLE dose of 100 mg/kg. Moreover, our previous results indicated that a similar amount (80 mg/kg) was very effective in experimentally induced gastric lesions in rats(Reference Dekanski, Janicijevic-Hudomal and Tadic14), as well as for preventing experimental autoimmune encephalomyelitis in rats(Reference Miljkovic, Dekanski and Miljkovic27).
Histology and immunohistochemistry
For histological analysis, pancreases were placed in formalin and embedded in paraffin. Five-micrometer sections were prepared from different levels (200 μm apart), stained with haematoxylin and eosin and examined for the presence of mononuclear cell infiltration by light microscopy. Multiple independent sections were analysed at varying depths for each pancreas in a blind fashion. At least twenty islets per pancreas were graded for insulitis according to an arbitrary scale as follows: 0, intact islets; 1, area of mononuclear cell infiltration within an islet < 25 %; 2, 25–50 %; 3, >50 %; 4, small retracted islets with some residual infiltrates. The mean score for each group was calculated by dividing the total score by the number of islets examined. Representative islets were photographed using a Zeiss microscope at 200 × magnification.
Immunohistochemical analyses were performed on 5 μm paraffin thick transverse sections of pancreas. After deparaffinisation, tissue sections were treated using a microwave antigen retrieval procedure in 0·01 m sodium citrate buffer. After blocking endogenous peroxidase, slides were incubated for 1 h with the appropriate dilution of primary antibodies, followed by the Rabbit ExtrAvidin peroxidase staining kit according to the manufacturer's instructions. Primary antibodies were rabbit anti-nitrotyrosine (1:500), and rabbit anti-inducible NO synthase (iNOS; 1:400). Staining was developed with diaminobenzidine (DakoCytomation, Carpinteria, CA, USA), and sections were counterstained with haematoxylin. A minimum of twenty islets per animal were analysed for each marker.
Cell preparations and culture
Pancreatic lymph nodes (PLN), spleens, resident peritoneal cells (PC) and pancreata were collected from individual MLDS-induced mice or from CY-induced NOD mice treated with DOLE or its vehicle, on day 15 of diabetes p.i. Resident PC were collected by peritoneal lavage with cold PBS. To isolate PLN cells and splenocytes (Spl), organs were mechanically disrupted, passed through 40 μm nylon mesh filter and collected by centrifugation. Erythrocytes from single cell suspensions were lysed using erthrocytes lysis buffer (eBioscience, San Diego, CA, USA). Pancreata were used for isolation of the Panc by collagenase digestion, as previously described(Reference Stosić-Grujicić, Cvjetićanin and Stojanović12), followed by handpicking. Cell culture supernatants, used for detection of cytokine and NO production were obtained by culturing the cells (1 × 106 PC, 5 × 106 Spl or 3 × 106 PLN cells) in twenty-four-well culture plates in 1 ml of Roswell Park Memorial Institute-1640 containing 5 % fetal calf serum, 2 mm-glutamine, 0·01 % sodium pyruvate, 5 × 10− 5 m-2-mercaptoethanol and antibiotics (culture medium). After 48 h incubation at 37°C in a humidified atmosphere with 5 % CO2, media were harvested for cytokine and NO assay.
In vitro suppression assay
The in vitro interaction between PC and Spl was assessed by co-culture. To measure proliferation, Spl (5 × 105 per well) were co-cultured with different numbers of PC (1 × 103–1 × 104). Cells were plated in ninety-six-well flat-bottom plates in culture medium and stimulated with 1 μg/ml concanavalin A. After 48 h in co-culture, 37·5 kBq (1 μCi) of [3H]thymidine (ICN, Costa Mesa, CA, USA) was added to each well, and cells were harvested 18 h later. Incorporated radioactivity was measured in a liquid scintillation counter (Beckman Coulter, Fullerton, CA, USA).
Assessment of insulin and cytokines
For estimation of insulin concentration, non-fasted mice were bled from the orbital plexus. Serum was obtained and examined for mouse insulin using an ELISA kit (Mercodia, Uppsala, Sweden) according to the manufacturer's instructions. Cytokines in both serum and cell culture supernatants were determined by sandwich ELISA using MaxiSorp plates (Nunck, Rochild, Denmark) and anti-mouse paired antibodies according to the manufacturer's instructions. Samples were analysed in duplicate for murine IL-17, IL-1β, TNF-α (BD Pharmingen, San Diego, CA, USA), IL-6, IL-10 (eBioscience), interferon (IFN)-γ and IL-4 (R&D, Minneapolis, MN, USA). The results were calculated using standard curves made on the basis of known concentrations of the appropriate recombinant cytokines.
Assay of nitric oxide release
Nitrite accumulation, as an indirect measure of NO release, was determined in cell culture supernatants using the Griess reaction. In brief, triplicate aliquots of cell-free supernatants were mixed with an equal volume of Griess reagent (a 1:1 mixture of 0·1 % naphthylethylenediamine dihydrochloride and 1 % sulphanilamide in 5 % H3PO4). The absorbance at 570 nm was determined in a microplate reader (LKB 5060-006; LKB, Vienna, Austria) and compared to a standard curve for NaNO2.
RNA isolation and real-time PCR
Total RNA was extracted from a pool of freshly isolated Spl, PLN cells and PC (5 × 106) or Panc from each experimental group using a mi-Total RNA Isolation Kit (Metabion, Martinsried, Germany) according to the manufacturer's instructions. RNA (1 μg) was reverse transcribed using Moloney murine leukaemia virus RT and random hexamer primers (both from Fermentas, Vilnius, Lithuania). PCR amplification of cDNA (1 μl per 20 μl of PCR) was carried out in an ABI PRISM 7000 Sequence Detection System (Applied Biosystems, Warrington, UK) using SYBRGreen PCR master mix (Applied Biosystems) as follows: 10 min at 50°C for deoxy-uridine triphosphate activation; 10 min at 95°C for initial denaturation of cDNA followed by forty cycles (15 s of denaturation at 95°C and 60 s for primer annealing and chain extension step). Primer pairs (Metabion, Munich, Germany) were: IL-17, 5′-GGG AGA GCT TCA TCT GT-3′ and 5′-GAC CCT GAA AGT GAA GGG-3′ (GenBank accession no. NM 010552.3); IFN-γ, 5′-CAT CAG CAA CAA CAT AAG CGT CA-3′ and 5′-CTC CTT TTC CGC TTC CTG A-3′ (GenBank accession no. NM 008337.2); TNF-α, 5′-CCA CGT AGC AAA CCA C-3′ and 5′-TGG GTG AGG AGC ACG TAG T-3′ (GenBank accession no. NM 013693.2); IL-4, 5′-ATC CTG CTC TTC TTT CTC G-3′ and 5′-GAT GCT CTT TAG GCT TTC C-3′ (GenBank accession no. NM 021283.1); IL-10, 5′-TGT GAA AAT AAG AGC AAG GCA GTG-3′ and 5′-CAT TCA TGG CCT TGT AGA CAC C-3′ (GenBank accession no. NM 010548·1); IL-1β, 5′-TGT CGT TGC TTG GTT CTC CTT-3′ and 5′-GCT GAA AGC TCT CCA CCT CAA TG-3′ (GenBank accession no. NM 008361.3); iNOS, 5′-CCA TAA TAC TGG TTG ATG AAC T-3′ and 5′-AAG CTA AAT CCT ACC AAA GTG A-3′ (GenBank accession no. NM 010927.2); insulin, 5′-CCA TCA GCA AGC AGG TTA T-3′ and 5′-GGG TGT GTA GAA GAA GCC A-3′ (GenBank accession no. NM 008386.3); β-actin, 5′-GGA CCT GAC AGA CTA CC-3′ and 5′-GGC ATA GAG GTC TTT ACG G-3′ (NM 007393.2). Data were quantitatively analysed using SDS 2.1 software (Applied Biosystems). The expression of these genes was calculated according to the formula: 2− (C ti− C ta), where C ti is the cycle threshold of the gene of interest and C ta is the cycle threshold value of β-actin. The obtained values of the samples from MLDS group were arbitrarily attributed a value of one (an arbitrary unit). The efficiency of real time PCR was in the optimal range of 90–110 % (slope of standard curves 3·1–3·6) for all of the primer pairs used.
Flow cytometry
Cells (3 × 105 per sample) were stained for surface markers with 0·5 μg of fluorescein isothiocyanate conjugate-labelled anti-CD4, anti-CD8 or F4/80 antibody (eBioscience). Treg cells were detected by a Mouse Regulatory T cell Staining Kit (PE-Cy5 Foxp3 FJK-16s, fluorescein isothiocyanate conjugate CD4, PE CD25) according to the manufacturer's instructions (eBioscience). Appropriate isotype controls with the same fluorophore were used (eBioscience). Stained cells were detected on FACSCalibur and analysed by CellQuest Pro software (BD Biosciences, San Diego, CA, USA).
Statistical analysis
The results are provided as means and standard deviations. Statistical analysis of differences was made using one-way ANOVA, followed by Student–Newman–Keuls test for multiple comparisons, or Student's t-test, as appropriate. The Spearman ρ value was calculated to determine the type of correlation ( − 1–0 = inverse correlation). Differences in diabetes incidence were analysed by Fisher's exact probability test. The statistical package used was Primer, version 1.0 (McGraw-Hill, Columbus, OH, USA). P < 0·05 was considered to be significant.
Results
Treatment with dry olive leaf extract reduces clinical signs of multiple low-dose streptozotocin-induced diabetes
Diabetes was induced with MLDS in two T1D-susceptible inbred mouse strains, C57BL/6 and CBA/H. In order to avoid direct interference with the initial streptozotocin action upon β-cells by DOLE, i.p. treatment with the extract was started 24 h after completion of MLDS administration (reversal regimen). Control mice that were challenged with MLDS and received vehicle i.p., developed persistent late onset hyperglycaemia over a 2-week period after MLDS injections (Fig. 1(a) and (b)). Although MLDS induced different degrees of hyperglycaemia in the two mouse strains, DOLE treatment (40 mg/kg b.wt.) led to a clear reduction in blood glucose levels in both strains (Fig. 1(a) and (b)). The extract showed a similar protective effect when given p.o. (100 mg/kg b.wt. per d, divided into two daily doses; Fig. 1(a)). Moreover, in mice treated with DOLE by a preventive regimen, diabetes was avoided (not shown). In addition, when a control non-diabetic group of mice was treated with DOLE i.p. for 5 weeks, the animals remained normoglycaemic for the entire period of observation (not shown), indicating that DOLE acts via the immune system, rather than through metabolic pathways. Importantly, prolonged treatment (for 7 weeks) with the extract appeared to be well tolerated by the mice as judged from their behaviour and general appearance (data not shown). Moreover, DOLE treatment did not affect b.wt. gain of treated mice (Fig. 1(c)), suggesting that the extract does not induce toxicity in mice.
Effect of dry olive leaf extract (DOLE) treatment on hyperglycaemia and body weight (b.wt.) of multiple low-dose streptozotocin (MLDS)-treated mice. (a) Plasma glucose levels in control CBA/H mice or (b) C57BL/6 mice, receiving MLDS (40 mg/kg per d for five consecutive days), or mice treated with MLDS and DOLE, administered intraperitoneally (i.p.) or per orally (p.o.) from days 5 to 21. (c) Percentage change in b.wt. from the start of the experiment determined in the mice described in (a). Results from a representative experiment are presented as the means and standard deviations for six to seven mice per group. *P < 0·05 refers to corresponding control MLDS mice. (a) –⋄–, MLDS; –■–, MLDS+i.p. DOLE; –▲–, MLDS+p.o. DOLE. (b) –⋄–, MLDS; –■–, MLDS+i.p. DOLE. (c) –⋄–, MLDS; –■–, MLDS+i.p. DOLE; –▲–, MLDS+ p.o. DOLE.
The effects of dry olive leaf extract on pathohistological changes and insulin gene expression in the pancreas and on insulin concentration in the serum
Concordant with the clinical status, histological examination of pancreatic specimens showed that administration of DOLE abrogated the development of the MLDS-induced destructive autoimmune process. Whereas most of the islets of control diabetic mice exhibited insulitis (mean grade1·7 at day 15 p.i.) and subsequently lost clear margins as a result of β-cell depletion (mean grade 2·6 at day 42 p.i.; Fig. 2(a)), at the end of the study the islets of DOLE-treated mice appeared normal, with no signs of inflammation or destruction (Fig. 2(b)). The mean histological grade of DOLE-treated mice did not exceed 0·5 during the whole investigation period. Also, the total number of islets was reduced in control diabetic mice, when compared with DOLE-treated mice (data not shown). In agreement with pathohistological findings, a decrease in the expression of insulin transcripts, as well as lower systemic insulin levels were found in vehicle-treated v. DOLE-treated mice (Fig. 2(c) and (d)).
Histopathology and insulin expression of pancreatic islets (Panc) and serum insulin of multiple low-dose streptozotocin (MLDS)-treated mice. (a and b) Light micrographs showing morphological profiles of Panc by day 42 after disease induction (haematoxylin and eosin staining): (a) control MLDS-induced and (b) dry olive leaf extract (DOLE)-treated MLDS-induced C57BL/6 mice. (c) Insulin gene expression and (d) serum insulin concentration in mice described in Fig. 1(b), sacrificed on day 15 post induction. Gene expression is presented in arbitrary units, and the actual value (2− (C ti− C ta)) for the gene expression was 0·013. Results from a representative experiment are presented as the means and standard deviations for four to five mice per group. *P < 0·05 refers to corresponding control MLDS mice.
Dry olive leaf extract counteracts accelerated diabetogenesis induced by cyclophosphamide challenge in non-obese diabetic mice
Since CY-induced diabetes in NOD mice differs in many aspects from MLDS-induced diabetes, mainly due to the selective effect of the compound on Treg function(Reference Brode, Raine and Zaccone28), we further examined whether DOLE has a beneficial effect in this model of autoimmune diabetogenesis, as well. As expected, approximately 80 % of the control mice treated with vehicle developed an acute form of diabetes within 2 weeks of the CY injections (Table 1). In contrast, DOLE treatment, given either i.p. or by oral gavage every day from day 1 of CY treatment, completely abolished the diabetogenic process, since none of the DOLE-treated mice developed hyperglycaemia (Table 1). Concurring with the clinical findings, histological studies of pancreases showed that DOLE treatment reduced the extensive leucocyte infiltration observed in mice treated with vehicle (Fig. 3(a) and (b)). While control mice developed severe destructive insulitis (Fig. 3(a)), either intact islets or stationary peri-insulitis were mostly observed in DOLE-treated mice, as exemplified in Fig. 3(b). Consistent with these findings, DOLE-treated mice retained their capacity to secrete insulin, as revealed by higher serum insulin concentrations in these animals (Fig. 3(c)).
Inhibition of diabetes by dry olive leaf extract (DOLE) in cyclophosphamide (CY)-treated non-obese diabetic mice (NOD)*
p.o., per orally; i.p., intraperitoneally.
* Diabetes was induced in euglycaemic female NOD mice by CY, as described in ‘Materials and methods’, and development of the disease was monitored within 2 weeks post induction of diabetes.
† The incidence of diabetes in each group was compared using Fisher's exact probability test.
‡ The mice were treated with DOLE p.o. (100 mg/kg per d, divided in two daily doses) from the first injection of CY till the end of the experiment.
§ The mice were treated with DOLE i.p. (40 mg/kg per d) from the first injection of CY till the end of the experiment.
∥ The mice were left untreated.
¶ The mice were treated with vehicle i.p. from the first injection of CY till the end of the experiment.
Histopathology of pancreatic islets and serum insulin of cyclophosphamide (CY)-treated mice. (a and b) Representative examples of the light microscopic evaluation of the islets of Langerhans after 2 weeks of CY-accelerated diabetes: (a) vehicle-treated and (b) dry olive leaf extract (DOLE)-treated CY-accelerated non-obese diabetic (NOD) mice. (c) Serum insulin concentration of the mice described in (a) and (b). Results from a representative experiment are presented as the means and standard deviations for four to five mice per group. *P < 0·05 refers to corresponding control CY-accelerated NOD mice.
In vivo treatment with dry olive leaf extract differentially modulates systemic and local nitric oxide production
To elucidate the mechanisms by which DOLE treatment prevents disease onset, functional ex vivo studies were performed during early progression of the disease induced by CY or MLDS (days 7 and 15 of diabetes induction, respectively) on both peripheral compartments and the pancreas. First, we examined production of NO. In CY-induced NOD mice, the production of NO by PC obtained from mice that had received DOLE treatment p.o. was significantly up-regulated in comparison with control diabetic mice, as revealed by nitrite formation by these cells (Fig. 4(a)). Similarly, peripheral immune cells, present in the peritoneal cavity, spleen and PLN of DOLE-treated MLDS-induced mice produced much more NO in comparison with cells from vehicle-treated animals (Fig. 4(b)). In line with these results, iNOS expression in peripheral compartments was also significantly higher in mice that had received DOLE compared with vehicle-treated diabetic control mice (Fig. 4(c)). In contrast, nitrite accumulation in cell culture supernatants of the Panc isolated from DOLE-treated mice was significantly reduced when compared with islets of control diabetic mice (Fig. 4(b)), whereas local iNOS staining of pancreatic sections was barely detectable (Fig. 4(d)). Concordantly, immunostaining for nitrotyrosine, a collective marker for oxidative and nitrative stress, was less prominent in pancreata of DOLE-treated v. vehicle-treated diabetic mice (Fig. 4(e)).
Effect of dry olive leaf extract (DOLE) treatment on nitric oxide generation in lymphoid tissues and pancreatic islets, inducible nitric oxide synthase (iNOS) expression in lymphoid tissues, presence of iNOS and nitrotyrosine in pancreatic islets (Panc). (a) Peritoneal cells (PC) were isolated from control and DOLE-treated cyclophosphamide (CY)-accelerated non-obese diabetic (NOD) mice and nitrite accumulation was measured in the 48 h culture supernatants of cells. (b) Nitrite accumulation in the 48 h culture supernatants of PC, splenocytes (Spl), pancreatic lymph node cells (PLNC) and Panc of control and DOLE-treated multiple low-dose streptozotocin (MLDS)-induced C57BL/6 mice (□, MLDS; ■, MLDS+DOLE). (c) Inducible NO synthase (iNOS) mRNA expression in the cells of the mice (□, MLDS; ■, MLDS+DOLE) described in (b). Gene expression is presented in arbitrary units, and the actual values (2− (C ti− C ta)) for iNOS gene expression were 0·00 087 for PC, 0·000093 for Spl and 0·000052 for PLNC (d). Immunostaining for iNOS and (e) nitrotyrosine of Panc of the mice described in (b). (a–c) Results from one of three separate experiments with similar results are given as the means and standard deviations for five mice per group. *P < 0·05 refers to corresponding control (a) CY-accelerated NOD mice, or (b and c) MLDS mice.
In vivo treatment with dry olive leaf extract induces in vitro nitric oxide-mediated suppressor function of peritoneal cells
In order to examine whether DOLE-induced up-regulation of peripheral NO production influences T cell activation, we performed a suppression assay of the conventional T cell response to mitogen. To this, different concentrations of PC isolated from DOLE-treated or vehicle-treated MLDS-treated mice were co-cultured with normal untreated lymph node-derived lymphocytes stimulated in vitro with concanavalin A. In contrast to PC derived from vehicle-treated mice, PC obtained from DOLE-treated animals displayed dose-dependent suppressive effects on T cell proliferation (Fig. 5(a)). Moreover, a clear negative correlation (r − 0·81, P < 0·05; linear regression) was observed between the dose-dependent increase in NO production (Fig. 5(b)) and the concomitant reduction in [3H]thymidine incorporation (Fig. 5(a)). To determine whether alteration of the PC subsets ratio following DOLE treatment might contribute to the observed suppression of T cell response, phenotype analysis of cell populations within the peritoneal cavity was performed. Administration of DOLE did not significantly alter the percentage of CD4+ cells (11·0 (sd 3·0) v. 9·1 (sd 2·6) for control and DOLE-treated mice, respectively) or CD8+ cells (8·3 (sd 1·9) v. 7·7 (sd 2·7) for control and DOLE-treated mice, respectively), but it significantly increased the frequency of F4/80+ cells, i.e. macrophages (43·9 (sd 1·6) v. 53·6 (sd 7·0) for control and DOLE-treated mice, respectively; P = 0·040) among PC. Although there was no significant increase in the absolute PC number at the two time points examined, a trend towards greater absolute cell number was noted in the DOLE-treated group (Table 2), suggesting immigration of cells into the peritoneum as an explanation for the increase in absolute cell number.
In vitro suppressor function and nitric oxide generation of peritoneal cells (PC). (a and b) PC were collected from dry olive leaf extract (DOLE)-treated or vehicle-treated multiple low-dose streptozotocin (MLDS)-induced mice on day 15 of diabetes post induction. These cells were co-cultured at the indicated concentrations with 3 × 105 cervical lymph node cells (LNC) prepared from healthy untreated mice, along with 1 μg/ml concanavalin A. (a) Proliferation of LNC was assessed 66 h later by incorporation of [3H]-thymidine over the last 18 h of culture. Data points show the mean thymidine incorporation counts and standard deviations for triplicate wells (–⋄–, MLDS; –■–, MLDS+DOLE). (b) Nitrite accumulation in the culture supernatant was measured after 48 h of cultivation. Horizontal line: LNC alone. *P < 0·05 refers to corresponding control MLDS mice. cpm, Cycles per minute.
(Mean values and standard deviations)
MLDS, multiple low doses of streptozotocin; PC, peritoneal cells; PLNC, pancreatic lymph node cells; i.p., intraperitoneally; p.i., post induction.
* MLDS was administered i.p. to C57BL/6 mice at a daily dose of 40 mg/kg per d for 5 d (four mice per group per experiment).
† DOLE was administered i.p. at a daily dose of 40 mg/kg per d from day 5 of MLDS diabetes p.i. (four mice per group per expt).
‡ Cells were obtained after 14 d (Expts 1 and 2) or 38 d (Expt 3) of diabetes p.i.
In vivo treatment with dry olive leaf extract modulates cytokine production
Because proinflammatory cytokines contribute to T1D pathogenesis, we examined whether DOLE treatment may influence MLDS-induced cytokine production in the spleen. Spleens were collected 15 d after diabetes induction, and cytokine expression and release were assayed ex vivo without further stimulation. The results clearly showed that Spl (Fig. 6(a)) isolated from DOLE-treated mice released significantly reduced amounts of proinflammatory cytokines, including IFN-γ, IL-17 and TNF-α compared with control diabetic animals. Moreover, we also evaluated cytokine gene expression in both experimental groups and found that IFN-γ expression in the spleen of DOLE-treated mice was decreased when compared with that in the vehicle-treated group, whereas there was no significant difference between the two groups regarding the other cytokines examined (Fig. 6(b)). Also, it was important to find out if DOLE had an effect on Treg cell frequency in peripheral lymphoid tissues. To that extent the percentage of CD4+CD25+FoxP3+ (i.e. Treg) cells among PLN cells was determined in both MLDS- and CY-induced diabetes. DOLE did not induce a significant alteration in Treg percentage in either the MLDS model (11·5 (sd 1·2) v. 9·9 (sd 2·2) for control and DOLE-treated mice, respectively) or the CY model (14·6 (sd 0·6) v. 14·0 (sd 1·6)). Also, the absolute cellularity of PLN was not affected by treatment with DOLE in either MLDS-induced diabetes (Table 2) or CY-accelerated diabetes in NOD mice (1·88 (sd 0·78) v. 1·92 (sd 0·62), in millions, for control and DOLE-treated mice, respectively).
Effect of dry olive leaf extract (DOLE) treatment on cytokine profile in splenocytes (Spl). Cytokine concentration in culture supernatants (□, MLDS; ■, LDS+DOLE) (a) and cytokine gene expression (b) of Spl from vehicle-treated and DOLE-treated multiple low-dose streptozotocin (MLDS)-induced C57BL/6 mice after 48 h of cultivation. Gene expression is presented in arbitrary units, and the actual values (2− (C ti− C ta)) for the analysed cytokines were as follows: 0·000017 for IL-17; 0·000090 for IL-6; 0·0052 for TNF-α; 0·000037 for IL-4; 0·00 045 for IL-10; 0·013 for IL-1β; 0·0021 for interferon-γ (IFN-γ). Data are means and standard deviations of four experiments, each with four to five mice per group. *P < 0·01 refers to corresponding control MLDS mice.
Discussion
The present study is the first demonstration that O. europaea-derived components, present in DOLE, confer protection from T1D by interfering with an islet-directed autoimmune response. This interference was reflected in NO-mediated suppression of T lymphocyte proliferation and lower production of proinflammatory cytokines (TNF-α, IFN-γ and IL-17) in the peripheral lymphoid compartments as well as less oxidative and nitrative damage within the pancreas.
Olive tree constituents have long been known as anti-diabetic herbal agents in the metabolic syndrome and T2D, due to their antioxidant(Reference Vissers, Zock and Katan16) and glucose-lowering effects associated with insulin-sensitising activity, increased peripheral glucose utilisation and improved insulin release(Reference Said, Fulder and Khalil25, Reference Eidi, Eidi and Darzi26, Reference Gonzalez, Zarzuelo and Gamez34–Reference Jemai, Bouaziz and Fki37). The anti-diabetic properties of O. europaea L. leaf constituents were evaluated in several experimental models of ‘toxic’ forms or dietary-induced T2D(Reference Al-Azzawie and Alhamdani23, Reference Sato, Genet and Strehle24, Reference Eidi, Eidi and Darzi26, Reference Gonzalez, Zarzuelo and Gamez34, Reference Bennani-Kabchi, Fdhil and Cherrah38, Reference Coskun, Kanter and Korkmaz39). To our knowledge, this is the first study on the effects of O. europaea-derived components in T1D in two established mouse models: MLDS-induced immunoinflammatory diabetes; CY-accelerated NOD diabetes. We used the MLDS-induced diabetes model, as the autoimmune process is initiated by minor chemical destruction of β-cells and shedding of target autoantigens, in contrast to the non-immune ‘toxic’ form of diabetes induced by a single high dose of streptozotocin. As a consequence, immune cells respond to self β-cell antigens so progression of hyperglycaemia and insulitis evolves during a 2-week period(Reference Stosic-Grujicic, Cvetkovic and Mangano11, Reference Like and Rossini29). Alternatively, CY-induced diabetes was used because it is known that the autoimmune response directed against pancreatic β-cells relies on selective depletion of Treg cells(Reference Brode, Raine and Zaccone28). We showed that in both models, DOLE efficiently counteracted diabetogenesis, indicating that the suppressive effect on the islet-directed T cell immune response is most likely mediated by common events and independently of Treg cells. In support of this is our finding that there was no difference in the frequency of Treg cells within PLN in vehicle- and DOLE-treated mice in which diabetes was induced with CY. The common effect of DOLE in MLDS- and CY-induced diabetes was an increase of NO generation in peripheral lymphoid tissues. This finding is of importance for understanding the beneficial effect of DOLE in diabetes, as it is well known that NO produced in lymphoid tissues has immunoregulatory functions, including anti-proliferative, pro-apoptotic and cytokine-shifting effects on T cells during their activation(Reference Albina, Abate and Henry40–Reference Lemaire, Guittet and Vesin42). In addition, PC isolated from DOLE-treated mice, but not PC isolated from vehicle-treated mice, were able to inhibit proliferation of mitogen-activated T cells. Importantly, the observed inhibition was inversely proportional to the level of NO produced in these co-cultures. One possible explanation for the enhanced capacity of PC to produce NO is the observed increase in frequency of cells responsible for its production among PC, i.e. of F4/80+ macrophages. Together, our findings suggest that DOLE acts through up-regulation of NO in peripheral lymphoid tissues, which consequently leads to limitation of T cell activation and finally to restriction of the autoimmune attack upon pancreatic β-cells. The capacity of DOLE to up-regulate NO generation by lymphoid cells is in accordance with the previously reported amplifying effects of the O. europaea bioactive component, oleuropein, on the release of NO and the expression of iNOS by macrophages during the response to endotoxin challenge in vitro (Reference Visioli, Bellosta and Galli20). However, several studies showed that O. europaea-derived components, such as flavonoids and phenols, are capable of inhibiting inflammation through inhibition of NO production and increasing antioxidant enzyme activity(Reference Bitler, Viale and Damaj22, Reference Al-Azzawie and Alhamdani23, Reference Briante, Patumi and Terenziani35, Reference Visioli, Poli and Galli36). Although, we do not report inhibition of NO production in peripheral compartments by DOLE treatment, we do show that DOLE inhibits NO synthesis in pancreatic β-cells. This again is very important for the anti-diabetogenic effect of DOLE, as it is recognised that NO released in Panc is mostly cytotoxic and leads to dysfunction and destruction of insulin-producing cells(Reference Stassi, De Maria and Trucco43, Reference Pearl-Yafe, Kaminitz and Yolcu44). Damaging effects of NO may be attributable to the reaction with superoxide anions to yield peroxynitrite, a potent nitrating and nitrosylating agent. Since oxidative stress in diabetes coexists with reduced antioxidant status of the pancreas, which can further increase the deleterious effects of free radicals, it is tempting to speculate that DOLE has a protective effect in diabetes at least partly, through decreasing local oxidative and nitrative damage. Indeed, reduced immunostaining of DOLE-treated Panc for nitrotyrosine, a collective marker for reactive oxygen species and reactive nitrogen species(Reference Ischiropoulos, Zhu and Chen45), further supported this assumption.
The other important factor influenced by DOLE is the cytokine profile of Spl. We showed that, under the influence of the extract, typical pro-inflammatory cytokines IFN-γ, TNF-α and IL-17 were down-regulated in MLDS-induced diabetes. On the contrary, anti-inflammatory cytokine (IL-4 and IL-10) generation was unaffected by DOLE. Therefore, it seems that DOLE promotes a profile shift of Spl cytokine production from pro-inflammatory to anti-inflammatory, or from Th1/Th17 to Th2. The importance of Th1 cells and IFN-γ, as well as of TNF-α for autoimmune diabetes pathology has been described in many papers(Reference Pearl-Yafe, Kaminitz and Yolcu44). According to the current understanding of T1D pathogenesis, initial injury to the islets leads to the presentation of exposed autoantigens on antigen-presenting cells to autoreactive T cells within the regional lymph nodes. The antigen-presenting cells stimulate effector Th1 cells which produce IFN-γ, and this cytokine activates additional macrophages and polymorphonuclear cells. These cells release IL-1β, TNF-α and NO, which are directly toxic to β-cells. Moreover, the antigen-presenting cells promote CD8+T cells which use FasL, perforin/granzyme and TNF-α to trigger β-cell apoptosis(Reference Pearl-Yafe, Kaminitz and Yolcu44). The role of Th17 cells and their signature cytokine IL-17 in diabetes is still not clear. It has been suggested that Th17 cells are important for the development of diabetes in NOD mice and that IL-17-directed therapy could be useful in the treatment of the disease(Reference Emamaullee, Davis and Merani46). It has also been shown that islet-reactive Th17 cells primarily function by promoting inflammation, and that their conversion to Th1 cells in lymphopenic hosts results in diabetes(Reference Martin-Orozco, Chung and Chang47). Importantly, IFN-γ seems indispensable for Th17-induced diabetes, whereas Th17 cells play an accessory role by promoting inflammation produced by Th1 or CD8+T cells. In the line with these results, in both MLDS-induced and human diabetes, inflammatory infiltrates are composed of both IFN-γ- and IL-17-producing cells(Reference Stosić-Grujicić, Cvjetićanin and Stojanović12, Reference Miljkovic, Cvetkovic and Momcilovic48, Reference Tesmer, Lundy and Sarkar49). Moreover, it was suggested that IL-17 cooperates with TNF-α in inflammation associated with autoimmunity(Reference Hartupee, Liu and Novotny50). Having in mind all of the findings mentioned above, inhibition of IFN-γ, TNF-α and IL-17 by DOLE in regional lymphoid tissue, the place of initiation and perpetuation of the diabetogenic process, seem to be a valid explanation for the beneficial effect of the extract in T1D. Importantly, we have recently demonstrated the efficiency of DOLE in experimental autoimmune encephalomyelitis, an animal model of multiple sclerosis(Reference Miljkovic, Dekanski and Miljkovic27). There, the application of the extract also led to down-regulation of IFN-γ and IL-17 production during the disease course. Thus, it seems that DOLE counteracts pathogenic autoimmune responses dependent on IFN-γ and IL-17-producing cells.
The increasing interest in olive tree (O. europaea) constituents is mainly attributed to its antioxidant effects, due to the high concentration of phenolic compounds. In addition to their activities as antioxidants, some phenolics have been shown to possess anti-inflammatory activity(Reference Bitler, Viale and Damaj22). This is supported by experiments in which phenolic compounds significantly decreased the production of pro-inflammatory mediators, such as TNF-α, IL-1β and PGE2 (Reference Carluccio, Siculella and Ancora21, Reference Blonska, Czuba and Krol51–Reference Zunino, Storms and Stephensen53). Feeding NOD mice diets rich in polyphenols derived from grape was recently found to decrease the autoimmune inflammatory process associated with T1D(Reference Zunino, Storms and Stephensen53). Here we add that DOLE, rich in phenolic compound oleuropein inhibits inflammation in T1D and protects mice from disease progression. Two observations of particular relevance from the clinical point of view are the apparently low toxicity of DOLE, as demonstrated by the lack of characteristic b.wt. loss that occurs in MLDS-induced diabetes, and the equal efficacy of the extract given either i.p. or p.o. to prevent the disease. Therefore, our finding that DOLE applied orally to mice suppressed T1D, show that oral administration of phenolic compounds could be a feasible way of treating subjects suffering from diabetes. However, the proper evaluation of DOLE efficiency in the treatment of patients with newly diagnosed T1D will require preclinical studies in animals with established disease carried out under a therapeutic regimen of application. Nonetheless, the capacity of DOLE to counteract the diabetogenic effects of MLDS even when applied as a reversal regimen, started 1 d after the last toxin dose had been given, is encouraging for translation of these findings to a clinical setting.
Regarding DOLE, it has to be emphasised that it is a mixture of various chemicals with potential bioreactivity(Reference Dekanski, Janicijevic-Hudomal and Tadic14). Therefore, the putative immunomodulating effects of other primary and secondary compounds of DOLE cannot be excluded. Indeed, oleanolic, ursolic and maslinic acids, three main olive leaf triterpenic compounds(Reference Sanchez-Avila, Priego-Capote and Ruiz-Jimenez54) were recently shown to contribute to the anti-diabetic effect of olive leaves(Reference Sato, Genet and Strehle24, Reference Jang, Yee and Choi55, Reference Liu, Sun and Duan56). Further, although as a consequence of gentle processing of olive leaf constituents the phenolic component of DOLE contains almost exclusively oleuropein, it has to be understood that the extract constituents are extensively metabolised in the body. As a consequence, the single phenol products of oleuropein breakdown tyrosol and hydroxytyrosol may contribute to its health-promoting properties, as well. In line with such a possibility, numerous studies have clearly demonstrated that these compounds exhibit beneficial health effects in various oxidative stress associated disorders due to their antioxidant and anti-inflammatory activities(Reference Bitler, Viale and Damaj22, Reference Briante, Patumi and Terenziani35, Reference Visioli, Poli and Galli36, Reference Lory, Incani and Deiana57, Reference Andrikopoulos, Kaliora and Assimopoulou58). Therefore, the effect of DOLE on T1D should not be attributed only to the phenolic fraction – oleuropein, but also to other components, such as triterpenic compounds (oleanolic acid, maslinic and ursolic acid), tannins and flavonoids, as well as to oleuropein metabolites. To that extent, it is of importance to investigate the individual effect of each compound on the T1D course. However, the obvious advantage of DOLE is that it is an easily attainable product of olive leaves, not requiring purification of any fractions of the extract before application in T1D models, and possibly for human subjects.
In conclusion, we have provided evidence that olive leaf constituents are effective inhibitors of T1D. The results also suggest that the inhibitory effect of DOLE may be due, at least in part, to the NO-mediated suppression of T lymphocyte proliferation and lower production of proinflammatory cytokines (IFN-γ, IL-17 and TNF-α) in the spleen, and subsequent blockade of β-cell destruction. Though the active components and precise mode of action of DOLE are not yet ascertained, its powerful anti-diabetogenic activity, along with the safety profile observed in vivo, suggest that it would be worth undertaking additional studies to explore the possibility that DOLE possesses the desired therapeutic properties applicable to human T1D.
Acknowledgements
The study was supported by the Serbian Ministry of Science (grant 143029B).The contributions of the authors were as follows: T. C. and I. S. carried out in vivo treatments, conducted glucose, insulin and cytokine analyses, performed real-time PCR and conducted gene expression analyses. D. M. conducted flow cytometry analysis, contributed to data analysis and helped to write the manuscript. D. D. planned and carried out the feeding experiments. S. S.-G. designed the study, performed the cell proliferation assay, conducted histology and immunohistochemistry analyses, coordinated the project and wrote the manuscript. The authors would like to thank Boško Milovanović, Geographical Institute – Serbian Academy of Sciences and Arts for the help with statistical analysis of our data. None of the authors has any conflicts of interest.
