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Involvement of microbiota and short-chain fatty acids on non-alcoholic steatohepatitis when induced by feeding a hypercaloric diet rich in saturated fat and fructose

Published online by Cambridge University Press:  08 April 2022

Iñaki Milton-Laskibar
Affiliation:
Precision Nutrition and Cardiometabolic Health Program, IMDEA Food Institute (Madrid Institute for Advanced Studies), Campus of International Excellence (CEI) UAM+CSIC, Spanish National Research Council, Madrid, Spain CIBEROBN Physiopathology of Obesity and Nutrition, Institute of Health Carlos III (ISCIII), Madrid, Spain
Laura Judith Marcos-Zambrano
Affiliation:
Computational Biology Group, Precision Nutrition and Cancer Research Program, IMDEA Food Institute, Madrid, Spain
Saioa Gómez-Zorita
Affiliation:
CIBEROBN Physiopathology of Obesity and Nutrition, Institute of Health Carlos III (ISCIII), Madrid, Spain Nutrition and Obesity group, Department of Pharmacy and Food Science, Faculty of Pharmacy, Lucio Lascaray Research Center, University of the Basque Country (UPV/EHU), Vitoria-Gasteiz, Spain BIOARABA Health Research Institute, Vitoria-Gasteiz, Spain
Enrique Carrillo de Santa Pau
Affiliation:
Computational Biology Group, Precision Nutrition and Cancer Research Program, IMDEA Food Institute, Madrid, Spain
Alfredo Fernández-Quintela
Affiliation:
CIBEROBN Physiopathology of Obesity and Nutrition, Institute of Health Carlos III (ISCIII), Madrid, Spain Nutrition and Obesity group, Department of Pharmacy and Food Science, Faculty of Pharmacy, Lucio Lascaray Research Center, University of the Basque Country (UPV/EHU), Vitoria-Gasteiz, Spain BIOARABA Health Research Institute, Vitoria-Gasteiz, Spain
Jose Alfredo Martínez
Affiliation:
CIBEROBN Physiopathology of Obesity and Nutrition, Institute of Health Carlos III (ISCIII), Madrid, Spain
María Puy Portillo*
Affiliation:
CIBEROBN Physiopathology of Obesity and Nutrition, Institute of Health Carlos III (ISCIII), Madrid, Spain Nutrition and Obesity group, Department of Pharmacy and Food Science, Faculty of Pharmacy, Lucio Lascaray Research Center, University of the Basque Country (UPV/EHU), Vitoria-Gasteiz, Spain BIOARABA Health Research Institute, Vitoria-Gasteiz, Spain
*
Corresponding author. Email: mariapuy.portillo@ehu.eus

Abstract

Consumption of high-energy-yielding diets, rich in fructose and lipids, is a factor contributing to the current increase in non-alcoholic fatty liver disease prevalence. Gut microbiota composition and short-chain fatty acids (SCFAs) production alterations derived from unhealthy diets are considered putative underlying mechanisms. This study aimed to determine relationships between changes in gut microbiota composition and SCFA levels by comparing rats featuring diet-induced steatohepatitis with control counterparts fed a standard diet. A high-fat high-fructose (HFHF) feeding induced higher body, liver and mesenteric adipose tissue weights, increased liver triglyceride content and serum transaminase, glucose, non-HDL-c and MCP-1 levels. Greater liver malondialdehyde levels and glutathione peroxidase activity were also observed after feeding the hypercaloric diet. Regarding gut microbiota composition, a lowered diversity and increased abundances of bacteria from the Clostridium sensu stricto 1, Blautia, Eubacterium coprostanoligenes group, Flavonifractor, and UBA1819 genera were found in rats featuring diet-induced steatohepatitis, as well as higher isobutyric, valeric and isovaleric acids concentrations. These results suggest that hepatic alterations produced by a hypercaloric HFHF diet may be related to changes in overall gut microbiota composition and abundance of specific bacteria. The shift in SCFA levels produced by this unbalanced diet cannot be discarded as potential mediators of the reported hepatic and metabolic alterations.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s), 2022. Published by Cambridge University Press on behalf of The Nutrition Society

Introduction

Obesity is a chronic metabolic disease featuring an excessive body fat accumulation that may impair health status and life expectancy (WHO, 2020). The prevalence of obesity has worldwide exponentially increased in the last decades, becoming one of the most prevalent chronic non-communicable diseases, which is expected to affect more than 1-billion people by the year 2025 (World obesity, 2021). Obesity leads to the development of other pathological conditions and morbid manifestations, such as diabetes, cardiovascular diseases, hypertension, certain types of cancer and non-alcoholic fatty liver disease (NAFLD; Blüher, Reference Blüher2019; Silveira et al., Reference Silveira, Kliemann, Noll, Sarrafzadegan and de Oliveira2021). Indeed, obesity is currently considered as one of the main causes of early deaths in most developed countries (Blüher, Reference Blüher2019).

Sedentary lifestyle habits and/or excessive energy intake are usually the main contributors to the development of this multifactorial disease. Moreover, endogenous factors such as genetic predisposition (mainly single nucleotide polymorphisms) and altered gut microbiota composition are also involved (Hwalla and Jaafar, Reference Hwalla and Jaafar2021). In this scenario, the food industry has modified the composition of a wide variety of foods and foodstuffs, exchanging calories coming from fat (the most energy-yielding nutrient) for those coming from different sugars in order to reduce their energy density and thus the energy intake of consumers. Unfortunately, this strategy not only has not been effective in blunting the aforementioned obesity prevalence increase, but it has contributed to the increase in added dietary fructose consumption, which has been related to NAFLD development (Softic et al., Reference Softic, Cohen and Kahn2016). Indeed, once fructose is absorbed in the intestine, the majority of this monosaccharide in the portal vein enters the liver for subsequent metabolic utilization (Hannou et al., Reference Hannou, Haslam, Mckeown and Herman2018). Within the liver, fructose is known to impair hepatic lipid metabolism by enhancing de novo lipogenesis, as well as reducing hepatic fatty acid oxidation, which may result in hepatic lipid accumulation (Hannou et al., Reference Hannou, Haslam, Mckeown and Herman2018). Moreover, it must be noted that fructose can also induce further dysfunction in the liver (inflammation, oxidative stress and mitochondrial dysfunction), thus contributing to the onset and progression of NAFLD from relatively benign conditions (hepatic steatosis) towards more harmful ones (steatohepatitis, cirrhosis and hepatocellular carcinoma; Jegatheesan and De Bandt, Reference Jegatheesan and De Bandt2017). Of note, high-fructose intake is also known to induce hepatic insulin resistance due to enhanced fatty acid synthesis and decreased oxidation (resulting in mitochondrial dysfunction), increased reactive oxygen species (ROS) production and/or endoplasmic reticulum stress induction (Softic et al., Reference Softic, Meyer, Wang, Gupta, Batista, Lauritzen, Fujisaka, Serra, Herrero, Willoughby, Fitzgerald, Ilkayeva, Newgard, Gibson, Schilling, Cohen and Kahn2019; Wang et al., Reference Wang, Sun, Zeng, Zhou, Li, Jo, Molero and Ye2015).

Moreover, the relationship between fructose and NAFLD is not restricted to the effects exerted by the sugar in the liver (Jegatheesan et al., Reference Jegatheesan, Beutheu, Ventura, Sarfati, Nubret, Kapel, Waligora-Dupriet, Bergheim, Cynober and De Bandt2016). Indeed, gut microbiota composition and permeability alterations have been reported in trials conducted in rodents fed diets rich in fructose (Jegatheesan et al., Reference Jegatheesan, Beutheu, Ventura, Sarfati, Nubret, Kapel, Waligora-Dupriet, Bergheim, Cynober and De Bandt2016). In this context, the “multiple hit” theory, which is currently used to describe NAFLD development, considers gut microbiota alteration as one of the potential mechanisms underlying this morbid liver condition (Buzzetti et al., Reference Buzzetti, Pinzani and Tsochatzis2016). In addition, the alterations induced by fructose in gut microbiota composition can also impair the metabolite profile produced by intestinal bacteria (Buzzetti et al., Reference Buzzetti, Pinzani and Tsochatzis2016). Among them, much attention has been paid to short-chain fatty acids (SCFAs) due to their effects on energy metabolism or immune response, as well as their ability to act as signalling molecules (Chakraborti, Reference Chakraborti2015). These lipid species are the product of indigestible carbohydrate fermentation by intestinal bacteria (Aragonès et al., Reference Aragonès, González-García, Aguilar, Richart and Auguet2019), and when gut microbiota dysbiosis occurs, their concentration may be impaired, affecting hepatic lipid metabolism (Alves-Bezerra and Cohen, Reference Alves-Bezerra and Cohen2017).

In this scenario, the aim of this study was to determine the relationship between changes in gut microbiota composition and SCFA levels induced by a high-fat, high-fructose (HFHF) feeding in rats. Likewise, the role played by SCFAs in the development of steatohepatitis was also analysed.

Material and methods

Animals, diets and experimental design

This study was conducted using 20 six-week-old male Wistar rats (Envigo, Barcelona, Spain), and all the experimental procedures were carried out in agreement with the Ethical Committee of the University of the Basque Country (document reference CUEID CEBA/30/2010), according to the European regulations (European Convention-Strasburg 1986, Directive 2003/65/EC and Recommendation 2007/526/EC).

Rats were housed in polycarbonate metabolic cages (Tecniplast Gazzada, Buguggiate, Italy) in an air-conditioned room (22°C) with a 12-hour light/dark cycle. After a 6-day adaptation period, the animals were randomly distributed into two groups of ten animals each: the control group, in which animals were fed a standard diet (AIN-93G, OpenSource Diets, Denmark, D10012G) and the HFHF group, in which animals were fed an HFHF diet (OpenSource Diets, Denmark, D09100301; Supplementary Table S1). These experimental conditions were maintained for 8 weeks and animals had free access to food and water throughout this time frame. Once the whole experimental period was completed, animals were sacrificed after overnight fasting under anaesthesia (chloral hydrate) by cardiac exsanguination.

Body weight and food intake were monitored daily. Faecal samples were collected and processed as explained elsewhere (Milton-Laskibar et al., Reference Milton-Laskibar, Marcos-Zambrano, Gómez-Zorita, Fernández-Quintela, Carrillo de Santa Pau, Martínez and Portillo2021). Serum was obtained by blood sample centrifugation after clotting (1,000 g for 10 minutes, at 4ºC). Liver, as well as different white adipose tissue depots (subcutaneous, epididymal, perirenal and mesenteric) were dissected, weighed and immediately frozen in liquid nitrogen. Fresh faecal samples were collected at the end of the intervention period, prior to the overnight fasting. To do so, the animals were taken one at a time and housed in a clean, single cage to separately obtain faeces directly after defecation induced by a soft abdominal massage. All samples were stored at –80ºC until analysis.

Determination of liver triacylglycerol content and blood markers

Total liver lipids were extracted following the method described by Folch et al. (Reference Folch, Lees and Sloane Stanley1957), dissolved in isopropanol and subsequently measured using a commercial spectrophotometric kit (SpinReact, Girona, Spain). Commercially available spectrophotometric kits were also used to determine serum glucose (Biosystems, Barcelona, Spain), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels. An enzyme-linked immunosorbent assay kit was used to measure serum monocyte chemoattractant protein-1 (MCP-1; Abyntek, Derio, Spain) levels.

Hepatic oxidative stress markers

A commercial thiobarbituric acid reactive substances (TBARSs) assay kit (Cayman Chemical¸ Ann Arbor, MI, USA) was used to analyse lipid peroxidation in rat liver lysates. The malondialdehyde (MDA) and TBARS adduct resulting from their reaction in an acid medium was measured using an Infinite 200Pro plate reader (Tecan, Männedorf, Zürich, Switzerland). The obtained results were expressed as μg MDA/mg of tissue.

The activity of catalase (CAT) was studied as described elsewhere (Gómez-Zorita et al., Reference Gómez-Zorita, González-Arceo, Trepiana, Aguirre, Crujeiras, Irles, Segues, Bujanda and Portillo2020) following the method described by Aebi (Reference Aebi1984), measuring the H2O2 disappearance spectrophotometrically at a wavelength of 240 nm. Catalase activity was expressed as nmol/min/μg of protein. Glutathione peroxidase (GPx) activity was measured spectrophotometrically in liver lysates using a commercial kit (Biovision, Milpitas, CA, USA) and following the manufacturers’ instructions in an Infinite 200Pro plate reader. Results were expressed as GPx U/mg of protein.

SCFA analysis

Faecal samples (about 30 mg of faeces) were directly weighted to a 1.5-mL LoBind Eppendorf tube and mixed with 10 μL of internal standard mixture (BA-LAB, PA-LAB and AA-LAB) and 990 μL of a methanol:water (50:50) mixture. Samples were vortexed for 5 minutes and centrifuged (5 minutes, 15,000 rpm at 4ºC). A volume of 80 μL of the supernatant was mixed with 10 μL BHA 0.1M and 10 μL EDC 0.25M. Then, samples were vortexed and incubated at room temperature for 1 hour in darkness. After incubation, the faecal extract was diluted 20-fold in 50 per cent aqueous MeOH. 200μL of diluted sample was extracted by 600 μL of diethyl ether and 10 minutes of vigorous shaking. Then, samples were centrifuged (5 minutes, 15,000 rpm at 4ºC), and 40 μL of the upper organic layer was transferred and evaporated to dryness using an StarlettePlus-E (SPE)-dryer. The residual was reconstituted in 200 μL of 50 per cent aqueous MeOH, briefly vortexed and centrifuged (5 minutes, 15,000 rpm at 4ºC) prior to 1-μL injection on LC-MS/MS (Zeng and Cao, Reference Zeng and Cao2018).

The chromatographic separation was performed with a gradient, which was 0.1 per cent formic acid in water with 10 mM of ammonium formate for mobile phase A and 0.1 per cent formic acid in methanol:isopropanol (9:1 v/v) for mobile phase B. The column temperature was set at 45ºC, and the injection volume was 1 μL. The source parameters were optimised operating in positive electrospray ionisation to obtain the maximum response. The validation of the analytical methodology was carried out by analysing a faecal sample pool by standard addition, using the internal standards mentioned above. The quality parameters determined were linearity, limit of detection (MLD), limit of quantification (MQL) and both intraday and interday precision (repeatability and intermediate precision, respectively).

Faecal DNA extraction and 16S rRNA gene amplification for microbiota composition analysis

DNA extraction was performed in fresh faecal samples collected at the end of the intervention period using the QIAamp DNA stool MiniKit according to the manufacturer´s instructions (QIAGEN, Hilden, Germany). The variable V3 and V4 regions of the bacterial 16S ribosomal RNA gene (16S rRNA) were amplified from the faecal DNA and sequenced with the Illumina MiSeq platform (2 × 300). Briefly, amplicon preparation was performed using the 16S Metagenomic Sequencing Library Preparation Protocol (Illumina, San Diego, CA, USA), which includes overhang adapter sequences for compatibility with Illumina index and sequencing adapters. Amplicon size was subsequently verified by electrophoresis (LabChip GX; PerkinElmer, Waltham, MA, USA). DNA libraries for 16S rRNA amplicons sequencing were prepared with the Nextera XT DNA Library Preparation Kit (Nextera XT; Illumina) according to the manufacturer’s instructions.

The 16S rRNA gene sequence data were processed using the Quantitative Insights Into Microbial Ecology program (QIIME 2; Bolyen et al., Reference Bolyen, Rideout, Dillon, Bokulich, Abnet, Al-Ghalith, Alexander, Alm, Arumugam, Asnicar, Bai, Bisanz, Bittinger, Brejnrod, Brislawn, Brown, Callahan, Caraballo-Rodríguez, Chase, Cope, Da Silva, Diener, Dorrestein, Douglas, Durall, Duvallet, Edwardson, Ernst, Estaki, Fouquier, Gauglitz, Gibbons, Gibson, Gonzalez, Gorlick, Guo, Hillmann, Holmes, Holste, Huttenhower, Huttley, Janssen, Jarmusch, Jiang, Kaehler, Kang, Keefe, Keim, Kelley, Knights, Koester, Kosciolek, Kreps, Langille, Lee, Ley, Liu, Loftfield, Lozupone, Maher, Marotz, Martin, McDonald, McIver, Melnik, Metcalf, Morgan, Morton, Naimey, Navas-Molina, Nothias, Orchanian, Pearson, Peoples, Petras, Preuss, Pruesse, Rasmussen, Rivers, Robeson, Rosenthal, Segata, Shaffer, Shiffer, Sinha, Song, Spear, Swafford, Thompson, Torres, Trinh, Tripathi, Turnbaugh, Ul-Hasan, van der Hooft, Vargas, Vázquez-Baeza, Vogtmann, von Hippel, Walters, Wan, Wang, Warren, Weber, Williamson, Willis, Xu, Zaneveld, Zhang, Zhu, Knight and Caporaso2019). Low-quality reads were filtered, and chimeric sequences were removed afterwards. Clean reads were clustered as amplicon sequence variants (ASVs) using DADA2 (Callahan et al., Reference Callahan, McMurdie, Rosen, Han, Johnson and Holmes2016) and annotated with the SILVA v.132 16S rRNA gene reference database (Quast et al., Reference Quast, Pruesse, Yilmaz, Gerken, Schweer, Yarza, Peplies and Glöckner2013). The relative abundance of each ASV and alpha diversity (Shannon, Chao and Simpson indexes) were calculated using the phyloseq R package (McMurdie and Holmes, Reference McMurdie and Holmes2013). Weighted UniFrac distances were used to calculate Beta-diversity and then visualised with principal coordinate analysis (PCoA). Statistical significance was determined by permutational multivariate analysis of variance (PERMANOVA) with 999 random permutations using the function adonis from the vegan R package (version 2.5.7; Dixon, Reference Dixon2003). We performed Linear Discriminant Analysis effect size (LEfSe) to identify the bacterial taxa differentially enriched in different bacterial communities and establish microbial biomarkers (Segata et al., Reference Segata, Izard, Waldron, Gevers, Miropolsky, Garrett and Huttenhower2011).

Statistical analysis

Descriptive results are presented as mean ± SEM. Statistical analyses were performed using SPSS 24.0 (SPSS, Chicago, IL, USA). In the current analysis, all variables, with the exception of microbiome variables, were normally distributed according to the Shapiro-Wilks test. Data were tested by an independent Student’s t-test, being p < 0.05 values considered as statistically significant. In the case of differences in the abundance of taxa, statistical analysis was performed with the Kruskal–Wallis test. Significance was also set up at the p < 0.05 level.

Correlations between differentially enriched bacterial taxa and the studied SCFAs, and phenotypic and inflammatory parameters were estimated by Spearman’s rank method, using the Microbiome package in R (available at https://microbiome.github.io/tutorials/; accessed 28 May 2021). The correlation was assessed as Coefficient ≥ 0.2 and FDR ≤ 0.05.

Results

Body weight, liver weight, adipose tissue weights, liver triacylglycerol content and serum parameters

As shown in Figure 1A, the body weights of the animals fed the HFHF diet became significantly higher than those observed in the control group since the second week of the study and remained until the end of the experimental period (Week 8). Higher liver weights were also found in the animals of the HFHF group in comparison to the animals in the control group (Figure 1B). Indeed, this same pattern was also found regarding liver triacylglycerol content, where the values found in the HFHF group were significantly higher than those in the control group (Table 1). As far as the weight of different adipose deposits is concerned, significant differences were only found in the case of mesenteric adipose tissue. In this case, the values observed in the HFHF group were significantly higher than those found in the control group (Figure 1C). In turn, no significant changes were found between the two groups regarding visceral adipose tissue nor total adipose tissue weights, although non-statistically significant trends were found in both cases (p < 0.1) towards increased weights in the HFHF group.

Figure 1 Body weight evolution (A), liver weights (B), weights of different adipose tissue depots (C) and serum transaminase levels (D) of rats fed the experimental diets for 8 weeks. Values are means ± SEM (n = 10). Statistical analyses were performed using unpaired Student’s t-test. *The level of probability was set up at p < 0.05 as statistically significant, and # was used to represent values of p < 0.1. ALT, alanine aminotransferase; AST, aspartate aminotransferase; AT, adipose tissue; C, control group; HFHF, high-fat high-fructose fed animals; VAT, visceral adipose tissue.

Table 1. Serum glucose, insulin, non-HDL-c and MCP-1 levels, TyG index, hepatic triglyceride content, MDA content, and activities of CAT and GPx in the liver of rats fed on the experimental diets for 8 weeks.

Notes: Values are means ± SEM (n = 10). Statistical analyses were performed using unpaired Student’s t-test.

Abbreviations: CAT, catalase; GPx, glutathione peroxidase; HDL-c, high-density lipoprotein cholesterol; MCP-1, monocyte chemoattractant protein-1; MDA, malondialdehyde; TyG, triglyceride-glucose index; NS, not significant.

* p < 0.05.

** p < 0.01.

With regard to serum parameters, the fasting serum glucose level observed in the animals from the HFHF group was significantly higher in comparison to that found in the control group (Table 1). Serum non-high-density lipoprotein cholesterol (non-HDL-c), which was calculated by subtracting serum high-density lipoprotein cholesterol (HDL-c) levels from total serum cholesterol levels, was significantly increased in the HFHF group compared to the control group. Finally, the analysis of serum MCP-1 levels revealed that this parameter was significantly increased in the HFHF group in comparison to the control group (Table 1).

Hepatic oxidative stress markers

The hepatic oxidative stress analysis revealed that the amounts of MDA found in the liver samples of animals in the HFHF group were significantly greater than those found in the animals in the control group (Table 1). In addition, while no changes were observed between the two groups regarding CAT activity, a higher GPx activation was observed in the livers of the animals in the HFHF group compared to those in the control group (Table 1).

SCFA analysis

Among all the studied SCFAs, significant differences were found in isobutyric, isovaleric and valeric acids, whose faecal concentrations were significantly greater in the HFHF group compared to the control group (Table 2).

Table 2. Concentration of SCFAs in faecal samples of rats fed on the experimental diets for 8 weeks.

Notes: Values are means ± SEM (n = 10). Statistical analyses were performed using unpaired Student’s t-test.

* p < 0.05.

** p < 0.01.

Abbreviation: NS, not significant.

Dietary induced shifts in microbiota composition

To understand the underlying mechanisms by which HFHF diet contributed to hepatic damage, the effects of dietary strategies on the gut microbiota composition were explored. As measured by β-diversity, there was a significant difference in overall microbial composition between the two experimental groups (p < 0.001, PERMANOVA). Figure 2 shows PCoA using the weighted UniFrac distance matrix. The microbiota of HFHF group was clearly separated from that of the control group.

Figure 2 Principal coordinate analysis (PCoA) weighted UniFrac plot. Components PCoA1 and PCoA2 are shown (p < 0.001, PERMANOVA). All samples are connected to the centroid (shown as a point). C, control group, represented in red circles; HFHF, high-fat high-fructose fed animals, represented in blue triangles.

A significant decrease in alpha diversity was observed in the HFHF group, as showed by the Chao1 index (C = 73.2 and HFHF = 57.2; p < 0.01; Figure 3A). In addition to the overall microbial composition, gut microbiota was evaluated at different levels to establish differences in the abundance of microbial taxa according to both dietary groups, and to select those bacteria which can represent potential microbial biomarkers of each condition by performing a LEfSe analysis (Figure 3B,C). In the case of the animals in the control group, the most abundant bacteria were from the Class Clostridia, order Clostridiales, family Ruminococcaceae (particularly the Ruminiclostridium 9, Ruminococacceae UCG 005 and Ruminococacceae UCG 014 genera), as well as bacteria from Class Clostridia (Lachnospiraceae UCG 004 and Coprococcus 3 genera) and phylum Tenericutes (Anaeroplasma and Mollicutes RF39 genera) were observed. Another genus of less-described bacteria (ie. Muribaculaceae uncultured and Lachnospiraceae UCG 004) was also characteristic of this group.

Figure 3 Linear discriminant analysis (LDA) integrated with effect size (LEfSe). Cladogram representing the differentially abundant taxonomic groups (LDA score > 4, p < 0.001) (A), microbial diversity according to Chao1, Shannon and Simpson indexes (B) and histogram representing the 20 most abundant genera (C) in rats fed on the experimental diets for 8 weeks. C, control group, represented in red; HFHF, high-fat high-fructose fed animals, represented in green.

As far as the rats fed the HFHF diet (HFHF group) are concerned, bacteria from the phylum Firmicutes, class Bacilli, (particularly the Lactococcus genus), as well as bacteria from the class Clostridia, particularly the genera Clostridium sensu stricto 1, Blautia, Eubacterium coprostanoligenes group, Flavonifractor and the uncharacterized genus UBA1819 genera were the most abundant ones. Interestingly, these changes found in the HFHF group occurred despite at class (Clostridia) and order (Clostridiales) levels, the relative abundances in the control group were greater (Figure 3C). In addition, bacteria from the class Erysipelotrichia (particularly genus Fecalitalea) were also overrepresented in the animals from the HFHF group.

A correlation analysis looking for an association between the observed microbial biomarkers and the changes reported in phenotypic and biochemical parameters, SCFA abundances and markers of hepatic oxidative stress in the liver was conducted. A negative correlation was found between bacteria enriched in the control group fed with a standard diet (Ruminococcaceae UCG 005, Ruminococcaceae UCG 014 and Ruminiclostridium 9) and liver weight, transaminase (ALT) and non-HDL-c levels. On the other hand, bacteria found in HFHF group (Clostridium sensu stricto 1, Clostridiaceae 1) was correlated positively with liver weight, non-HDL-c and GPx (Table 3 and Supplementary Figure S1)

Table 3. Significant correlations between the relative abundance (%) of microbial biomarkers selected after LEfSe analysis A and several phenotypic and metabolic parameters in rats fed on the experimental diets for 8 weeks.

Abbreviations: ALT, alanine aminotransferase; GPx, glutathione peroxidase; HDL-c, high-density lipoprotein cholesterol.

Discussion

The worldwide increase in NAFLD prevalence has converted this morbid liver condition in a global health problem, becoming the most common hepatic alteration not only in adults, but also in children (DiStefano and Shaibi, Reference DiStefano and Shaibi2021; Masarone et al., Reference Masarone, Federico, Abenavoli, Loguercio and Persico2014). NAFLD encompasses a wide spectrum of liver alterations, from a relatively benign steatosis to more harmful situations such as cirrhosis or hepatocellular carcinoma (Engin, Reference Engin2017). Besides excessive lipid accumulation in the liver, events such as oxidative stress, inflammation and fibrosis are involved in the progression of hepatic damage (Brunt et al., Reference Brunt, Wong, Nobili, Day, Sookoian, Maher, Bugianesi, Sirlin, Neuschwander-Tetri and Rinella2015). High-fat intake, a common feature of “westernised diets,” is considered among the triggering factors of NAFLD development. In this regard, excessive dietary fat intake (specially saturated fats) can alter hepatic lipid metabolism, impairing the balance between liver lipid “input” (plasma fatty acid uptake and de novo lipogenesis) and “output” (mitochondrial fatty acid oxidation and very-low-density lipoprotein release), thus resulting in an excessive liver lipid accumulation (Lian et al., Reference Lian, Zhai, Li and Wang2020). Additionally, much attention has also been paid to added fructose intake as another factor leading to NAFLD development. The consumption of this sugar has increased in the last decades concomitantly with the expansion of NAFLD (DiStefano and Shaibi, Reference DiStefano and Shaibi2021). Indeed, excessive fructose consumption may not only increase hepatic lipid accumulation, but also produce liver inflammation and fibrosis, leading to the development of non-alcoholic steatohepatitis (Jegatheesan and De Bandt, Reference Jegatheesan and De Bandt2017).

In accordance with these facts, in the present study, rats fed with the HFHF diet showed increased liver weight and triglyceride content, which were accompanied by an increase in the levels of serum transaminases (ALT and AST), commonly used as markers of liver function impairment (Sattar et al., Reference Sattar, Forrest and Preiss2014). Moreover, alterations in glycaemic control (higher fasting glucose) and dyslipidaemia (higher non-HDL-c levels) were also found in these same animals. These observations are in agreement with the available scientific literature, where fructose derived alterations in glucose and lipid metabolisms have been described (Softic et al., Reference Softic, Stanhope, Boucher, Divanovic, Lanaspa, Johnson and Kahn2020; Stanhope et al., Reference Stanhope, Medici, Bremer, Lee, Lam, Nunez, Chen, Keim and Havel2015).

In addition, the enhanced hepatic MDA content found in the rats fed the HFHF diet suggests that a greater ROS production occurred in these animals, which in turn resulted in higher lipid peroxidation. Moreover, the enhanced GPx activity found in the same rats points towards a higher antioxidant response, most likely as an attempt to revert the oxidative damage produced by the HFHF diet. Additionally, the higher circulating MCP-1 levels found in the HFHF group could be expected since the involvement of this cytokine in liver damage progression has been previously reported (Glass et al., Reference Glass, Henao, Patel, Guy, Gruss, Syn, Moylan, Streilein, Hall, Diehl and Abdelmalek2018; Kirovski et al., Reference Kirovski, Dorn, Huber, Moleda, Niessen, Wobser, Schacherer, Buechler, Wiest and Hellerbrand2011).

Traditionally, the so-called “two hit” theory has been used to describe the events resulting in NAFLD. According to this theory, the “first hit” is originated by insulin resistance mediated excessive hepatic lipid accumulation due to enhanced de novo lipogenesis and altered fatty acid transport, whereas the “second hit” accounts for hepatic oxidative stress, inflammation and mitochondrial dysfunction. All these events would lead to NAFLD development, as well as progression to nonalcoholic steatohepatitis (NASH) (Engin, Reference Engin2017). However, this theory has been considered as too simplistic, and thus the “multiple hit” theory has been proposed, which, besides the aforementioned mechanisms, also considers the alterations in gut microbiota composition as one of the contributing factors (Buzzetti et al., Reference Buzzetti, Pinzani and Tsochatzis2016).

In the present study, the HFHF diet not only led to a decreased microbial α-diversity as revealed by lowered values in the Chao1 index, but it also affected the abundances of specific gut bacteria. Similar results were previously reported in Wistar rats fed a diet rich in fat and sucrose (45 and 17 per cent of the total energy as fat and sucrose, respectively) for 6 weeks (Etxeberria et al., Reference Etxeberria, Arias, Boque, Macarulla, Portillo, Martínez and Milagro2015). Indeed, bacteria from Ruminococcaceae family, known to be inversely correlated with NAFLD in humans (Astbury et al., Reference Astbury, Atallah, Vijay, Aithal, Grove and Valdes2020), were abundant in the control group and significantly diminished in the animals fed the HFHF diet. In addition, the abundance of several bacteria genera that have been related to liver alterations, such as Clostridium sensu stricto 1 or Blautia, were increased in the HFHF group. Interestingly, these changes occurred despite at class (Clostridia) and order (Clostridiales) levels the abundances in these bacteria were greater in the control group. These findings suggest that the negative effects elicited by the HFHF feeding affects the overall gut microbiota diversity, and therefore the abundance of specific bacteria. The results obtained in this study regarding gut microbiota composition are in good accordance with those reported by other authors using rodent models fed with unbalanced experimental diets (Chen et al., Reference Chen, Sun, Bai and Zhi2019; Daniel et al., Reference Daniel, Gholami, Berry, Desmarchelier, Hahne, Loh, Mondot, Lepage, Rothballer, Walker, Böhm, Wenning, Wagner, Blaut, Schmitt-Kopplin, Kuster, Haller and Clavel2014; Duparc et al., Reference Duparc, Plovier, Marrachelli, Van Hul, Essaghir, Ståhlman, Matamoros, Geurts, Pardo-Tendero, Druart, Delzenne, Demoulin, van der Merwe, van Pelt, Bäckhed, Monleon, Everard and Cani2017; Leal-Díaz et al., Reference Leal-Díaz, Noriega, Torre-Villalvazo, Torres, Alemán-Escondrillas, López-Romero, Sánchez-Tapia, Aguilar-López, Furuzawa-Carballeda, Velázquez-Villegas, Avila-Nava, Ordáz, Gutiérrez-Uribe, Serna-Saldivar and Tovar2016). One of the limitations of this study is that the 16S rRNA analysis of gut microbiota composition was only carried out at one timepoint, using faecal samples collected at the end of the study. The main reason for not collecting faecal samples at previous time points (at the beginning of the study) is that after the adaptation period, the animals were randomly distributed in the experimental groups assuming that there were no differences between both experimental groups at baseline. Other limitation is the lack of resolution at species level of amplicon sequencing allowing characterisation of microbial changes only to genus level, and the representation of less characterised genera such as UBA1819.

Besides gut microbiota composition, the different metabolic products that are produced by intestinal bacteria have also gain interest as mediators of microbioma-host crosstalk (Bashiardes et al., Reference Bashiardes, Shapiro, Rozin, Shibolet and Elinav2016). Among them, SCFAs have received much attention since these metabolites are known to be involved in the maintenance of body weight and energy homeostasis or glucose and lipid metabolism, as well as being related to NAFLD development (Bashiardes et al., Reference Bashiardes, Shapiro, Rozin, Shibolet and Elinav2016). In this regard, SCFAs may protect against NAFLD, improving gut barrier integrity, reducing visceral adipose tissue accumulation and derived excessive fatty acid entrance into the liver, as well as by directly exerting anti-inflammatory effects once having reached the liver (Dai et al., Reference Dai, Hou, Zhang, Liu, Li, Wang, Wang and Cao2020).

Acetate, propionate and butyrate are the three major volatile SCFAs produced by gut bacteria and are known to participate in a variety of processes (Deleu et al., Reference Deleu, Machiels, Raes, Verbeke and Vermeire2021). In the case of the liver, studies conducted in rodents and humans have described hepato-protective effects for these SCFAs. Several mechanisms of action have been described to date regarding the effects of SCFAs in liver protection (Dangana et al., Reference Dangana, Omolekulo, Areola, Olaniyi, Soladoye and Olatunji2020) including the modulation of visceral adipose tissue fat accumulation and lipid metabolism. Moreover, the improvement produced by these SCFAs in gut barrier function is also potentially responsible for their hepato-protective effects. Additionally, the activation of nod-like receptor family pyrin domain containing 3 inflammasome and resulting release of interleukin 18 produced by acetate, butyrate and propionate has also been described to improve gut barrier integrity (Macia et al., Reference Macia, Tan, Vieira, Leach, Stanley, Luong, Maruya, McKenzie, Hijikata, Wong, Binge, Thorburn, Chevalier, Ang, Marino, Robert, Offermanns, Teixeira, Moore, Flavell, Fagarasan and Mackay2015). Despite the well characterised hepato-protective effects of acetate, propionate and butyrate, no differences on their levels were found between the control and HFHF groups. As far as the enhanced faecal level of isobutyric acid found in the HFHF group of our study, it could be considered as expected since increased faecal level of this bacterial product has been found in patients with NAFLD (Da Silva et al., Reference Da Silva, Teterina, Comelli, Taibi, Arendt, Fischer, Lou and Allard2018; Jumpertz et al., Reference Jumpertz, Le DS, Trinidad, Bogardus, Gordon and Krakoff2011). In addition, a greater level of isobutyric acid has been reported in faecal samples of subjects with hypercholesterolemia in the study reported by Granado-Serrano et al. (Reference Granado-Serrano, Martín-Garí, Sánchez, Riart Solans, Berdún, Ludwig, Rubió, Vilaprinyó, Portero-Otín and Serrano2019), where a positive correlation between faecal isobutyric acid level and serum low-density lipoprotein cholesterol level was observed. Moreover, in that study, a higher faecal isovaleric acid concentration was also found in patients with hypercholesterolemia, which fits well with the results of our study, where the rats fed the HFHF diet showed the same effect (Granado-Serrano et al., Reference Granado-Serrano, Martín-Garí, Sánchez, Riart Solans, Berdún, Ludwig, Rubió, Vilaprinyó, Portero-Otín and Serrano2019). However, in our case, no correlation was found between the level of this SCFA and non-HDL-c-levels. As valeric acid is concerned, the studies addressing the effects of this SCFA in liver steatosis are scarce.

In order to better understand the potential associations between the studied microbial measurements and the phenotypical, biochemical and SCFA levels, correlation studies were carried out. According to the results obtained, bacteria from the Ruminococcaceae family could be considered as markers of low liver weight and/or serum transaminase and non-HDL-c levels, since negative correlations were found in the control group between these bacteria and the aforementioned markers. These results could be explained because these bacteria have been related to gastrointestinal health in humans due to their effect in the maintenance of intestinal structure and functions, such as permeability, nutrient uptake and immunocompetence (Rajilić‐Stojanović and de Vos, Reference Rajilić‐Stojanović and de Vos2014; Tang et al., Reference Tang, Yao, Xia, Yang, Chen, Zhou and Liu2018). As far as the positive correlations found in the HFHF group between Clostridium sensu stricto 1 and Clostridiaceae 1 with parameters such as non-HDL-c and GPx, these results are in line with data reported in studies in humans, in which the abundance of these bacteria was positively correlated with HDL-c molecule diameter (Vojinovic et al., Reference Vojinovic, Radjabzadeh, Kurilshikov, Amin, Wijmenga, Franke, Ikram, Uitterlinden, Zhernakova, Fu, Kraaij and van Duijn2019). However, other studies have also reported negative correlations of these bacteria with markers such as liver stiffness measurement and controlled attenuation parameter in humans (Lanthier et al., Reference Lanthier, Rodriguez, Nachit, Hiel, Trefois, Neyrinck, Cani, Bindels, Thissen and Delzenne2021). Indeed, reductions in abundance have been related to the development of liver fibrosis in patients with severe steatosis (Lanthier et al., Reference Lanthier, Rodriguez, Nachit, Hiel, Trefois, Neyrinck, Cani, Bindels, Thissen and Delzenne2021). Therefore, despite Clostridium sensu stricto 1 and Clostridiaceae 1 are indicators of less healthy microbiota (Yang et al., Reference Yang, Lee, Lu, Chou and Wang2019), further studies are warranted in order to better understand this apparent discrepancy. With regard to SCFAs, despite significant differences in their levels were found between the control and HFHF groups, no correlations were found with gut microbiota composition. These outcomes may result unexpected, especially for rats in the control group whose faeces revealed a greater presence of butyrate-producing bacteria such as Ruminococcaceae, but without an actual change of the levels of butyrate. Similarly, increased acetate levels could also been expected in the animals fed the HFHF diet since a relationship between this SCFA and metabolic syndrome has been proposed through a microbiota-brain axis (Perry et al., Reference Perry, Peng, Barry, Cline, Zhang, Cardone, Petersen, Kibbey, Goodman and Shulman2016). In this scenario, it could be hypothesised that the observed changes in gut microbiota composition were not big enough to shift the production of certain SCFA. In this regard, a longer experimental period could have resulted in a clearer relationship between shifts in gut microbiota composition and SCFA levels.

In conclusion, the current study demonstrates that the alterations induced by a high-energy diet rich in saturated fat and fructose in the liver, as well as the impairment of several metabolic markers involved in glycaemic control and lipid homeostasis, may be related, at least in part, to changes in overall gut microbiota composition and the abundance of specific bacteria derived by this dietary pattern since several mechanisms of action have been characterised (increased gut permeability, enhanced bacterial translocation and production/release of pro-inflammatory mediators or inflammation of adipose tissue and liver) linking the two events (Deleu et al., Reference Deleu, Machiels, Raes, Verbeke and Vermeire2021). Nevertheless, further determinations are warranted to better elucidate/confirm this hypothesis. As far as SCFA is concerned, the differences found between the experimental groups were not extensive despite the significant changes induced by the HFHF diet in gut microbiota richness and diversity. It seems that under these experimental conditions, the role played by SCFAs in diet-induced steatohepatitis development seems limited and may not be associated with gut microbiota shifts.

Acknowledgement

The SCFA analyses were performed with the equipment of the Centre for Omic Sciences (COS), Joint Unit of the Universitat Rovira i Virgili and Eurecat.

Supplementary Materials

To view supplementary material for this article, please visit http://doi.org/10.1017/gmb.2022.2.

Disclosure statement

The authors declare no conflict of interest.

Author contributions

Conceptualisation: M.P.P., J.A.M. and I.M.-L.; Data curation: I.M.-L., L.J.M.-Z., S.G.-Z., E.C.S.P. and A.F.-Q.; Formal analysis: I.M.-L., L.J.M.-Z. and E.C.S.P.; Funding acquisition: M.P.P.; Investigation: M.P.P., J.A.M., I.M.-L., L.J.M.-Z., S.G.-Z. and A.F.-Q.; Methodology: I.M.-L., S.G.-Z. and M.P.P.; Writing – original draft: M.P.P., J.A.M. and I.M.-L; Writing – review & editing: I.M.-L., L.J.M.-Z., S.G.-Z., E.C.S.P., A.F.-Q., M.P.P. and J.A.M.

Funding

I.M.-L. acknowledges financial support from the Juan de la Cierva Programme-Training Grants of the Spanish State Research Agency of the Spanish Ministerio de Ciencia e Innovación y Ministerio de Universidades (FJC2019-038925-I). L.J.M.-Z. has a Juan de la Cierva Grant (IJC2019-042188-I) from the Spanish State Research Agency of the Spanish Ministerio de Ciencia e Innovación y Ministerio de Universidades. This research was funded by the Ministerio de Economía y Competitividad-Fondo Europeo de Desarrollo Regional (grant number AGL-2015-65719-R MINECO/FEDER, UE), Instituto de Salud Carlos III CIBERobn (grant number CB12/03/30007) and University of the Basque Country (grant number GIU 18/173).

Footnotes

I.M.-L. and L.J.M.-Z. contributed equally to this work.

References

Aebi, H (1984) Catalase in vitro. Methods in Enzymology 105, 121126.CrossRefGoogle ScholarPubMed
Alves-Bezerra, M and Cohen, DE (2017) Triglyceride metabolism in the liver. Comprehensive Physiology 8(1), 18.Google ScholarPubMed
Aragonès, G, González-García, S, Aguilar, C, Richart, C, Auguet, T (2019) Gut microbiota-derived mediators as potential markers in nonalcoholic fatty liver disease. BioMed Research International 2019, 8507583. https://doi.org/10.1155/2019/8507583CrossRefGoogle ScholarPubMed
Astbury, S, Atallah, E, Vijay, A, Aithal, GP, Grove, JI and Valdes, AM (2020) Lower gut microbiome diversity and higher abundance of proinflammatory genus Collinsella are associated with biopsy-proven nonalcoholic steatohepatitis. Gut Microbes 11(3), 569580.CrossRefGoogle ScholarPubMed
Bashiardes, S, Shapiro, H, Rozin, S, Shibolet, O, Elinav, E (2016) Non-alcoholic fatty liver and the gut microbiota. Molecular Metabolism 5(9),782794.CrossRefGoogle ScholarPubMed
Blüher, M (2019) Obesity: Global epidemiology and pathogenesis. Nature Reviews. Endocrinology 15, 288298.CrossRefGoogle ScholarPubMed
Bolyen, E, Rideout, JR, Dillon, MR, Bokulich, NA, Abnet, CC, Al-Ghalith, GA, Alexander, H, Alm, EJ, Arumugam, M, Asnicar, F, Bai, Y, Bisanz, JE, Bittinger, K, Brejnrod, A, Brislawn, CJ, Brown, CT, Callahan, BJ, Caraballo-Rodríguez, AM, Chase, J, Cope, EK, Da Silva, R, Diener, C, Dorrestein, PC, Douglas, GM, Durall, DM, Duvallet, C, Edwardson, CF, Ernst, M, Estaki, M, Fouquier, J, Gauglitz, JM, Gibbons, SM, Gibson, DL, Gonzalez, A, Gorlick, K, Guo, J, Hillmann, B, Holmes, S, Holste, H, Huttenhower, C, Huttley, GA, Janssen, S, Jarmusch, AK, Jiang, L, Kaehler, BD, Kang, KB, Keefe, CR, Keim, P, Kelley, ST, Knights, D, Koester, I, Kosciolek, T, Kreps, J, Langille, MGI, Lee, J, Ley, R, Liu, YX, Loftfield, E, Lozupone, C, Maher, M, Marotz, C, Martin, BD, McDonald, D, McIver, LJ, Melnik, AV, Metcalf, JL, Morgan, SC, Morton, JT, Naimey, AT, Navas-Molina, JA, Nothias, LF, Orchanian, SB, Pearson, T, Peoples, SL, Petras, D, Preuss, ML, Pruesse, E, Rasmussen, LB, Rivers, A, Robeson, MS, Rosenthal, P, Segata, N, Shaffer, M, Shiffer, A, Sinha, R, Song, SJ, Spear, JR, Swafford, AD, Thompson, LR, Torres, PJ, Trinh, P, Tripathi, A, Turnbaugh, PJ, Ul-Hasan, S, van der Hooft, JJJ, Vargas, F, Vázquez-Baeza, Y, Vogtmann, E, von Hippel, M, Walters, W, Wan, Y, Wang, M, Warren, J, Weber, KC, Williamson, CHD, Willis, AD, Xu, ZZ, Zaneveld, JR, Zhang, Y, Zhu, Q, Knight, R and Caporaso, JG (2019) Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2. Nature Biotechnology 37, 852857.CrossRefGoogle ScholarPubMed
Brunt, EM, Wong, VW, Nobili, V, Day, CP, Sookoian, S, Maher, JJ, Bugianesi, E, Sirlin, CB, Neuschwander-Tetri, BA and Rinella, ME (2015) Nonalcoholic fatty liver disease. Nature Reviews Disease Primers 1, 15080. https://doi.org/10.1038/nrdp.2015.80CrossRefGoogle ScholarPubMed
Buzzetti, E, Pinzani, M and Tsochatzis, EA (2016) The multiple-hit pathogenesis of non-alcoholic fatty liver disease (NAFLD). Metabolism 65(8), 10381048.CrossRefGoogle Scholar
Callahan, BJ, McMurdie, PJ, Rosen, MJ, Han, AW, Johnson, AJA and Holmes, SP (2016) DADA2: High-resolution sample inference from illumina amplicon data. Nature Methods 13(7), 581583.CrossRefGoogle ScholarPubMed
Chakraborti, CK (2015) New-found link between microbiota and obesity. World Journal of Gastrointestinal Pathophysiology 6(4), 110119.CrossRefGoogle ScholarPubMed
Chen, Y, Sun, H, Bai, Y and Zhi, F (2019) Gut dysbiosis-derived exosomes trigger hepatic steatosis by transiting HMGB1 from intestinal to liver in mice. Biochemical and Biophysical Research Communications 509(3), 767772.CrossRefGoogle ScholarPubMed
Dangana, EO, Omolekulo, TE, Areola, ED, Olaniyi, KS, Soladoye, AO and Olatunji, LA (2020) Sodium acetate protects against nicotine-induced excess hepatic lipid in male rats by suppressing xanthine oxidase activity. Chemico-Biological Interactions 316, 108929.CrossRefGoogle ScholarPubMed
Dai, X, Hou, H, Zhang, W, Liu, T, Li, Y, Wang, S, Wang, B and Cao, H (2020) Microbial metabolites: Critical regulators in NAFLD. Frontiers in Microbiology 11, 567654. https://doi.org/10.3389/fmicb.2020.567654CrossRefGoogle ScholarPubMed
Daniel, H, Gholami, AM, Berry, D, Desmarchelier, C, Hahne, H, Loh, G, Mondot, S, Lepage, P, Rothballer, M, Walker, A, Böhm, C, Wenning, M, Wagner, M, Blaut, M, Schmitt-Kopplin, P, Kuster, B, Haller, D and Clavel, T (2014) High-fat diet alters gut microbiota physiology in mice. The ISME Journal 8(2), 295308.CrossRefGoogle ScholarPubMed
Da Silva, HE, Teterina, A, Comelli, EM, Taibi, A, Arendt, BM, Fischer, SE, Lou, W and Allard, JP (2018) Nonalcoholic fatty liver disease is associated with dysbiosis independent of body mass index and insulin resistance. Scientific Reports 8(1), 1466.CrossRefGoogle ScholarPubMed
Deleu, S, Machiels, K, Raes, J, Verbeke, K and Vermeire, S (2021) Short chain fatty acids and its producing organisms: An overlooked therapy for IBD? eBioMedicine 66, 103293.CrossRefGoogle ScholarPubMed
DiStefano, JK and Shaibi, GQ (2021) The relationship between excessive dietary fructose consumption and paediatric fatty liver disease. Pediatric Obesity 16(6), e12759. https://doi.org/10.1111/ijpo.12759CrossRefGoogle ScholarPubMed
Dixon, P (2003) VEGAN, a package of R functions for community ecology. Journal of Vegetation Science 14, 927930.CrossRefGoogle Scholar
Duparc, T, Plovier, H, Marrachelli, VG, Van Hul, M, Essaghir, A, Ståhlman, M, Matamoros, S, Geurts, L, Pardo-Tendero, MM, Druart, C, Delzenne, NM, Demoulin, JB, van der Merwe, SW, van Pelt, J, Bäckhed, F, Monleon, D, Everard, A and Cani, PD (2017) Hepatocyte MyD88 affects bile acids, gut microbiota and metabolome contributing to regulate glucose and lipid metabolism. Gut 66(4), 620632.CrossRefGoogle ScholarPubMed
Engin, A (2017) Non-alcoholic fatty liver disease. Advances in Experimental Medicine and Biology 960, 443467.CrossRefGoogle ScholarPubMed
Etxeberria, U, Arias, N, Boque, N, Macarulla, MT, Portillo, MP, Martínez, JA, Milagro, FI (2015) Reshaping faecal gut microbiota composition by the intake of trans-resveratrol and quercetin in high-fat sucrose diet-fed rats. The Journal of Nutritional Biochemistry 26(6), 651660.CrossRefGoogle ScholarPubMed
Folch, J, Lees, M and Sloane Stanley, GH (1957) A simple method for the isolation and purification of total lipids from animal tissues. The Journal of Biological Chemistry 226(1), 497509.CrossRefGoogle ScholarPubMed
Glass, O, Henao, R, Patel, K, Guy, CD, Gruss, HJ, Syn, WK, Moylan, CA, Streilein, R, Hall, R, Diehl, AM and Abdelmalek, MF (2018) Serum interleukin-8, osteopontin, and monocyte chemoattractant protein 1 are associated with hepatic fibrosis in patients with nonalcoholic fatty liver disease. Hepatology Communications 2(11), 13441355.CrossRefGoogle ScholarPubMed
Gómez-Zorita, S, González-Arceo, M, Trepiana, J, Aguirre, L, Crujeiras, AB, Irles, E, Segues, N, Bujanda, L and Portillo, MP (2020) Comparative effects of pterostilbene and its parent compound resveratrol on oxidative stress and inflammation in steatohepatitis induced by high-fat high-fructose feeding. Antioxidants (Basel) 9(11), 1042. https://doi.org/10.3390/antiox9111042CrossRefGoogle ScholarPubMed
Granado-Serrano, AB, Martín-Garí, M, Sánchez, V, Riart Solans, M, Berdún, R, Ludwig, IA, Rubió, L, Vilaprinyó, E, Portero-Otín, M and Serrano, JCE (2019) Faecal bacterial and short-chain fatty acids signature in hypercholesterolemia. Scientific Reports 9, 1772. https://doi.org/10.1038/s41598-019-38874-3CrossRefGoogle ScholarPubMed
Hannou, SA, Haslam, DE, Mckeown, NM and Herman, MA (2018) Fructose metabolism and metabolic disease. The Journal of Clinical Investigation 128(2), 545555.CrossRefGoogle ScholarPubMed
Hwalla, N and Jaafar, Z (2021) Dietary management of obesity: A review of the evidence. Diagnostics (Basel) 11(1), 24.CrossRefGoogle Scholar
Jegatheesan, P, Beutheu, S, Ventura, G, Sarfati, G, Nubret, E, Kapel, N, Waligora-Dupriet, AJ, Bergheim, I, Cynober, L and De Bandt, JP (2016) Effect of specific amino acids on hepatic lipid metabolism in fructose-induced non-alcoholic fatty liver disease. Clinical Nutrition 35(1), 175182.CrossRefGoogle ScholarPubMed
Jegatheesan, P and De Bandt, JP (2017) Fructose and NAFLD: The multifaceted aspects of fructose metabolism. Nutrients 9(3), 230.CrossRefGoogle ScholarPubMed
Jumpertz, R, Le DS, TPJ, Trinidad, C, Bogardus, C, Gordon, JI and Krakoff, J (2011) Energy-balance studies reveal associations between gut microbes, caloric load, and nutrient absorption in humans. The American Journal of Clinical Nutrition 94(1), 5865.CrossRefGoogle ScholarPubMed
Kirovski, G, Dorn, C, Huber, H, Moleda, L, Niessen, C, Wobser, H, Schacherer, D, Buechler, C, Wiest, R and Hellerbrand, C (2011) Elevated systemic monocyte chemoattractrant protein-1 in hepatic steatosis without significant hepatic inflammation. Experimental and Molecular Pathology 91(3), 780783.CrossRefGoogle ScholarPubMed
Lanthier, N, Rodriguez, J, Nachit, M, Hiel, S, Trefois, P, Neyrinck, AM, Cani, PD, Bindels, LB, Thissen, JP and Delzenne, NM (2021) Publisher correction: Microbiota analysis and transient elastography reveal new extra-hepatic components of liver steatosis and fibrosis in obese patients. Scientific Reports 11(1), 6123. https://doi.org/10.1038/s41598-021-85083-yCrossRefGoogle ScholarPubMed
Leal-Díaz, AM, Noriega, LG, Torre-Villalvazo, I, Torres, N, Alemán-Escondrillas, G, López-Romero, P, Sánchez-Tapia, M, Aguilar-López, M, Furuzawa-Carballeda, J, Velázquez-Villegas, LA, Avila-Nava, A, Ordáz, G, Gutiérrez-Uribe, JA, Serna-Saldivar, SO and Tovar, AR (2016) Aguamiel concentrate from Agave salmiana and its extracted saponins attenuated obesity and hepatic steatosis and increased Akkermansia muciniphila in C57BL6 mice. Scientific Reports 6, 34242. https://doi.org/10.1038/srep34242CrossRefGoogle ScholarPubMed
Lian, CY, Zhai, ZZ, Li, ZF and Wang, L (2020) High fat diet-triggered non-alcoholic fatty liver disease: A review of proposed mechanisms. Chemico-Biological Interactions 330, 109199. https://doi.org/10.1016/j.cbi.2020.109199CrossRefGoogle ScholarPubMed
Macia, L, Tan, J, Vieira, AT, Leach, K, Stanley, D, Luong, S, Maruya, M, McKenzie, CI, Hijikata, A, Wong, C, Binge, L, Thorburn, AN, Chevalier, N, Ang, C, Marino, E, Robert, R, Offermanns, S, Teixeira, MM, Moore, RJ, Flavell, RA, Fagarasan, S and Mackay, CR (2015) Metabolite-sensing receptors GPR43 and GPR109A facilitate dietary fibre-induced gut homeostasis through regulation of the inflammasome. Nature Communications 6, 6734.CrossRefGoogle ScholarPubMed
Masarone, M, Federico, A, Abenavoli, L, Loguercio, C and Persico, M (2014) Non alcoholic fatty liver: Epidemiology and natural history. Reviews on Recent Clinical Trials 9(3), 126133.CrossRefGoogle ScholarPubMed
McMurdie, PJ and Holmes, S (2013) Phyloseq: An R package for reproducible interactive analysis and graphics of microbiome census data. PLoS One 8(4), e61217. https://doi.org/10.1371/journal.pone.0061217CrossRefGoogle Scholar
Milton-Laskibar, I, Marcos-Zambrano, LJ, Gómez-Zorita, S, Fernández-Quintela, A, Carrillo de Santa Pau, E, Martínez, JA and Portillo, MP (2021) Gut microbiota induced by Pterostilbene and resveratrol in high-fat-high-fructose fed rats: Putative role in steatohepatitis onset. Nutrients 13(5), 1738. https://doi.org/10.3390/nu13051738CrossRefGoogle ScholarPubMed
Perry, RJ, Peng, L, Barry, NA, Cline, GW, Zhang, D, Cardone, RL, Petersen, KF, Kibbey, RG, Goodman, AL and Shulman, GI (2016) Acetate mediates a microbiome-brain-β-cell axis to promote metabolic syndrome. Nature 534(7606), 213217.CrossRefGoogle ScholarPubMed
Quast, C, Pruesse, E, Yilmaz, P, Gerken, J, Schweer, T, Yarza, P, Peplies, J and Glöckner, FO (2013) The SILVA ribosomal RNA gene database project: Improved data processing and web-based tools. Nucleic Acids Research 41, D590D596.CrossRefGoogle ScholarPubMed
Rajilić‐Stojanović, M and de Vos, WM (2014) The first 1000 cultured species of the human gastrointestinal microbiota. FEMS Microbiology Reviews 38(5), 9961047.CrossRefGoogle ScholarPubMed
Sattar, N, Forrest, E and Preiss, D (2014) Non-alcoholic fatty liver disease. BMJ 349, g4596. https://doi.org/10.1136/bmj.g4596CrossRefGoogle ScholarPubMed
Segata, N, Izard, J, Waldron, L, Gevers, D, Miropolsky, L, Garrett, WS and Huttenhower, C (2011) Metagenomic biomarker discovery and explanation. Genome Biology 12(6), R60. https://doi.org/10.1186/gb-2011-12-6-r60CrossRefGoogle ScholarPubMed
Silveira, EA, Kliemann, N, Noll, M, Sarrafzadegan, N and de Oliveira, C (2021) Visceral obesity and incident cancer and cardiovascular disease: An integrative review of the epidemiological evidence. Obesity Reviews 22(1), e13088.CrossRefGoogle ScholarPubMed
Softic, S, Cohen, DE and Kahn, CR (2016) Role of dietary fructose and hepatic de novo lipogenesis in fatty liver disease. Digestive Diseases and Sciences 61(5), 12821293.CrossRefGoogle ScholarPubMed
Softic, S, Meyer, JG, Wang, GX, Gupta, MK, Batista, TM, Lauritzen, HPMM, Fujisaka, S, Serra, D, Herrero, L, Willoughby, J, Fitzgerald, K, Ilkayeva, O, Newgard, CB, Gibson, BW, Schilling, B, Cohen, DE and Kahn, CR (2019) Dietary sugars alter hepatic fatty acid oxidation via transcriptional and post-translational modifications of mitochondrial proteins. Cell Metabolism 30(4), 735753.CrossRefGoogle ScholarPubMed
Softic, S, Stanhope, KL, Boucher, J, Divanovic, S, Lanaspa, MA, Johnson, RJ and Kahn, CR (2020) Fructose and hepatic insulin resistance. Critical Reviews in Clinical Laboratory Sciences 57(5), 308322.CrossRefGoogle ScholarPubMed
Stanhope, KL, Medici, V, Bremer, AA, Lee, V, Lam, HD, Nunez, MV, Chen, GX, Keim, NL and Havel, PJ (2015) A dose-response study of consuming high-fructose corn syrup-sweetened beverages on lipid/lipoprotein risk factors for cardiovascular disease in young adults. The American Journal of Clinical Nutrition 101(6), 11441154.CrossRefGoogle ScholarPubMed
Tang, W, Yao, X, Xia, F, Yang, M, Chen, Z, Zhou, B and Liu, Q (2018) Modulation of the gut microbiota in rats by Hugan Qingzhi tablets during the treatment of high-fat-diet-induced nonalcoholic fatty liver disease. Oxidative Medicine and Cellular Longevity 2018, 7261619. https://doi.org/10.1155/2018/7261619CrossRefGoogle ScholarPubMed
Vojinovic, D, Radjabzadeh, D, Kurilshikov, A, Amin, N, Wijmenga, C, Franke, L, Ikram, MA, Uitterlinden, AG, Zhernakova, A, Fu, J, Kraaij, R and van Duijn, CM (2019) Relationship between gut microbiota and circulating metabolites in population-based cohorts. Nature Communications 10(1), 5813.CrossRefGoogle ScholarPubMed
Wang, H, Sun, RQ, Zeng, XY, Zhou, X, Li, S, Jo, E, Molero, JC and Ye, JM (2015) Restoration of autophagy alleviates hepatic ER stress and impaired insulin signalling transduction in high fructose-fed male mice. Endocrinology 156(1), 169181.CrossRefGoogle ScholarPubMed
WHO (2020) Obesity and overweight. 6 June 2021 Available at https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight.Google Scholar
World Obesity (2021) Prevalence of obesity. Available at https://www.worldobesity.org/about/about-obesity/prevalence-of-obesityGoogle Scholar
Yang, WY, Lee, Y, Lu, H, Chou, CH and Wang, C (2019) Analysis of gut microbiota and the effect of lauric acid against necrotic enteritis in Clostridium perfringens and Eimeria side-by-side challenge model. PLoS One 14(5), e0205784.CrossRefGoogle ScholarPubMed
Zeng, M and Cao, H (2018) Fast quantification of short chain fatty acids and ketone bodies by liquid chromatography-tandem mass spectrometry after facile derivatization coupled with liquid-liquid extraction. Journal of Chromatography B 1083, 137145.CrossRefGoogle ScholarPubMed
Figure 0

Figure 1 Body weight evolution (A), liver weights (B), weights of different adipose tissue depots (C) and serum transaminase levels (D) of rats fed the experimental diets for 8 weeks. Values are means ± SEM (n = 10). Statistical analyses were performed using unpaired Student’s t-test. *The level of probability was set up at p < 0.05 as statistically significant, and # was used to represent values of p < 0.1. ALT, alanine aminotransferase; AST, aspartate aminotransferase; AT, adipose tissue; C, control group; HFHF, high-fat high-fructose fed animals; VAT, visceral adipose tissue.

Figure 1

Table 1. Serum glucose, insulin, non-HDL-c and MCP-1 levels, TyG index, hepatic triglyceride content, MDA content, and activities of CAT and GPx in the liver of rats fed on the experimental diets for 8 weeks.

Figure 2

Table 2. Concentration of SCFAs in faecal samples of rats fed on the experimental diets for 8 weeks.

Figure 3

Figure 2 Principal coordinate analysis (PCoA) weighted UniFrac plot. Components PCoA1 and PCoA2 are shown (p < 0.001, PERMANOVA). All samples are connected to the centroid (shown as a point). C, control group, represented in red circles; HFHF, high-fat high-fructose fed animals, represented in blue triangles.

Figure 4

Figure 3 Linear discriminant analysis (LDA) integrated with effect size (LEfSe). Cladogram representing the differentially abundant taxonomic groups (LDA score > 4, p < 0.001) (A), microbial diversity according to Chao1, Shannon and Simpson indexes (B) and histogram representing the 20 most abundant genera (C) in rats fed on the experimental diets for 8 weeks. C, control group, represented in red; HFHF, high-fat high-fructose fed animals, represented in green.

Figure 5

Table 3. Significant correlations between the relative abundance (%) of microbial biomarkers selected after LEfSe analysis A and several phenotypic and metabolic parameters in rats fed on the experimental diets for 8 weeks.

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