The farnesoid X receptor (FXR) regulates bile acid, lipid and glucose metabolism. Here we show that treatment of mice with glycine-β-muricholic acid (Gly-MCA) inhibits FXR signalling exclusively in intestine, and improves metabolic parameters in mouse models of obesity. Gly-MCA is a selective high-affinity FXR inhibitor that can be administered orally and prevents, or reverses, high-fat diet-induced and genetic obesity, insulin resistance and hepatic steatosis in mice. The high-affinity FXR agonist GW4064 blocks Gly-MCA action in the gut, and intestine-specific Fxr-null mice are unresponsive to the beneficial effects of Gly-MCA. Mechanistically, the metabolic improvements with Gly-MCA depend on reduced biosynthesis of intestinal-derived ceramides, which directly compromise beige fat thermogenic function. Consequently, ceramide treatment reverses the action of Gly-MCA in high-fat diet-induced obese mice. We further show that FXR signalling in ileum biopsies of humans positively correlates with body mass index. These data suggest that Gly-MCA may be a candidate for the treatment of metabolic disorders.
Obesity is associated with chronic diseases such as type 2 diabetes mellitus, cardiovascular diseases, hepatosteatosis and cancer1. A chronic imbalance between energy intake and energy expenditure causes obesity for which there is no safe and effective drug therapy2. Bariatric surgery, such as Roux-en-Y gastric bypass and vertical sleeve gastrectomy, are among the most effective surgical treatments for obesity3,4.
Farnesoid X receptor (FXR, NR1H4), a member of the nuclear receptor superfamily of transcription factors5, is an important sensor and regulator of bile acid, lipid and glucose metabolism6. FXR agonists obeticholic acid and fexaramine were found to improve metabolic profiles in obese mouse models7,8. Others reported that FXR whole-body knockout mice on a high-fat diet (HFD) displayed metabolic improvement4,9,10. These results suggest that FXR has complex roles in the pathogenesis of metabolic dysfunction, and its activity in liver, intestine, adipose tissue and kidney, could possibly exert different effects on metabolism; thus specific inhibition of FXR needs to be evaluated. Recent studies in which mice on a HFD were treated with the gut microbiota-modifying agent tempol or antibiotics, suggested that inhibition of intestinal FXR signalling could be of benefit in amelioration of obesity, insulin resistance and non-alcoholic fatty liver disease10,11. This led to the search for a compound that could inhibit FXR signalling specifically in the intestine.
Here a new orally available, small molecule, intestine-specific FXR inhibitor, glycine-β-muricholic acid (Gly-MCA), a bile acid that is not hydrolyzed by gut bacterial bile salt hydrolase (BSH), was developed. Oral administration of Gly-MCA to mice prevents and treats diet-induced and genetic obesity, along with insulin resistance and hepatic steatosis without systemic, hepatic or intestinal toxicities. Specific inhibition of a novel intestinal FXR-ceramide axis produced striking metabolic improvement after Gly-MCA treatment. Mechanistic studies revealed that FXR regulates genes involved in ceramide synthesis, and that ceramides mediate the metabolic effects of Gly-MCA. Specific inhibition of intestinal FXR may be a reasonable therapeutic strategy for the treatment of human metabolic disorders.
FXR signalling in obese human intestine
FXR signalling was activated in distal ileum biopsies from obese individuals as indicated by an increase in mRNAs encoded by Fxr and the FXR target genes small heterodimer partner (Shp) and fibroblast growth factor 19 (Fgf19; Fig. 1a). Ileal mRNA levels for Fxr, Shp and Fgf19 were also positively correlated with body mass index (BMI; Fig. 1b–d). Thus, suppression of intestinal FXR signalling might be a novel therapeutic target. However, antagonism of FXR as a therapeutic strategy has not been considered due to the potential for cholestasis. Recently, tauro-β-muricholic acid (T-β-MCA) was reported to antagonize FXR signalling in the intestine10,12 and this inhibition was correlated with improved metabolic function10. However, T-β-MCA is rapidly hydrolyzed by gut bacterial BSH, and thus cannot reach concentrations that inhibit gut-specific FXR signalling in vivo. This led to the search for small-molecule inhibitors of FXR to treat metabolic dysfunction.
Identification of an intestine-selective FXR inhibitor
Molecular modelling13 was carried out to find derivatives of T-β-MCA that could inhibit FXR leading to the identification of Gly-MCA as inhibitor or possible direct antagonist of FXR (Supplementary Fig. 1a–f and Table 1). To validate inhibition of FXR by Gly-MCA, the HEK293T cell line was transiently co-transfected with a chimeric receptor construct and reporter gene and treated with increasing concentrations of the FXR agonist GW4064 in the presence of vehicle, Gly-MCA, deoxycholic acid (DCA), T-β-MCA, T-α-MCA, β-MCA or α-MCA. Gly-MCA substantially inhibited the FXR transactivation activity induced by GW4064 (Supplementary Fig. 2a). In the human intestinal cell line, Caco-2 cells, 100 μM of the FXR agonist chenodeoxycholic acid (CDCA) caused a fourfold increase in mRNA levels for theFXR target gene Shp, while Gly-MCA inhibited the induction of Shp mRNA by CDCA (Supplementary Fig. 2b). Similarly, induction of the FXR target genes Shp and Fgf19 by GW4064 were blocked by Gly-MCA (Supplementary Fig. 2c,d). To determine whether Gly-MCA would be stable in the gut, it was subjected to faecal BSH enzyme activity derived from the gut microbiota. Indeed, Gly-MCA was resistant to hydrolysis by BSH, in contrast to T-β-MCA that was rapidly hydrolyzed (Supplementary Fig. 2e). The question arose as to whether Gly-MCA inhibited FXR signalling in vivo. To reflect its potential clinical use, bacon-flavoured dough pills were produced for the oral administration of Gly-MCA (dose of 0, 1, 10 and 50 mg kg−1). The Shp and Fgf15 (Fgf19 in human) mRNAs in ileum were decreased to 0.447±0.087 (P=0.019) and 0.364±0.089 (P=0.015), respectively, at a dose of 10 mg kg−1 Gly-MCA for 24 h compared with vehicle (Fig. 1e). Moreover, the higher dose of Gly-MCA (50 mg kg−1) did not further inhibit FXR signalling in ileum (Fig. 1e). Gly-MCA did not cause any liver toxicity at each of the doses compared with vehicle, as revealed by serum aminotransferase (ALT) and aspartate aminotransferase (AST) levels (Fig. 1f,g). Pharmacokinetic analysis further showed that Gly-MCA levels in liver, which were almost undetectable, were much lower than in ileum (Fig. 1h,i). These results indicated that Gly-MCA via oral administration, was not significantly absorbed into liver or was rapidly metabolized in the liver. Conversely, Gly-MCA mainly accumulates in ileum where it can selectively inhibit intestinal FXR signalling. These studies identified Gly-MCA as a novel, potent, stable and orally available intestinal FXR inhibitor.
Gly-MCA reduces obesity and metabolic syndrome in obese mice
To determine whether inhibition of intestinal FXR could be a therapeutic target for HFD-induced obesity, insulin resistance and hepatic steatosis, and to confirm that this transcription factor is a suitable drug target, mice fed a chow diet or a HFD were orally administered with Gly-MCA. Chronic Gly-MCA treatment did not affect the body weights of mice fed a chow diet (Supplementary Fig. 3a). In contrast, Gly-MCA treatment substantially prevented weight gain produced after a HFD (Supplementary Fig. 3b). The absolute fat mass and the fat/lean mass ratio, measured by NMR, were substantially decreased in HFD-fed mice after 9 weeks of treatment with Gly-MCA compared with vehicle-treated mice (Supplementary Fig. 3c). To explore the mechanism of reduced adiposity in Gly-MCA-treated mice, cumulative food intake and energy expenditure using an energy balance technique (TEEbal: food energy intake and body composition change) were measured. Food intake was comparable between the two groups (Supplementary Fig. 3d). Gly-MCA treatment substantially increased energy expenditure, which could contribute to the decreased HFD-induced body weight gain compared with vehicle treatment (Supplementary Fig. 3e).
To clarify the role of Gly-MCA in obesity-related glucose homoeostasis, glucose and insulin tolerance tests (GTT and ITT, respectively) were performed. GTT revealed that Gly-MCA-treated mice displayed substantially reduced blood glucose levels after glucose loading compared with vehicle-treated mice (Supplementary Fig. 3f,g). ITT demonstrated that insulin sensitivity was substantially increased after Gly-MCA treatment (Supplementary Fig. 3h). Fasting serum insulin levels of Gly-MCA-treated mice were lower than vehicle-treated mice (Supplementary Fig. 3i). These results indicated that Gly-MCA prevented mice from HFD-induced obesity and insulin resistance. Liver histology indicated a marked reduction in hepatic lipid droplets with no apparent cholestasis, inflammation and necrosis after Gly-MCA treatment of mice fed a HFD for 9 weeks (Supplementary Fig. 4a), which was reflected by lower liver weights (Supplementary Fig. 4b). Hepatic triglyceride contents decreased to ∼51%, although serum triglyceride levels remained unchanged in mice treated with Gly-MCA compared with vehicle (Supplementary Fig. 4c,d). These results indicated that Gly-MCA treatment protected mice from HFD-induced hepatic steatosis.
To exclude the possibility that the effects of Gly-MCA on metabolic disorders were due to non-specific toxicological effects, serum ALT and AST were measured. Gly-MCA treatment dramatically decreased these enzyme levels compared with vehicle-treated mice (Supplementary Fig. 4e,f), thus indicating that Gly-MCA at the dose employed was not hepatotoxic, but actually decreased HFD-induced hepatic toxicity. To assess potential gastrointestinal toxicity, faecal lipocalin 2 (LCN-2), a sensitive and non-invasive biomarker for intestinal toxicity and inflammation, was measured14. Gly-MCA did not increase faecal LCN-2 levels (Supplementary Fig. 4g), indicating that Gly-MCA did not induce intestinal inflammation.
To evaluate the effects of Gly-MCA on obese mice, C57BL/6N mice were fed a HFD for 12 weeks, and then treated with Gly-MCA. Administration of Gly-MCA daily to obese mice fed a HFD, resulted in reduced body weight as compared with vehicle treatment (Fig. 2a). Fat mass and the fat/lean mass ratio were substantially decreased in Gly-MCA-treated obese mice compared with vehicle-treated mice after 5 weeks of treatment (Supplementary Fig. 5a). Cumulative food intake remained similar between the two groups (Supplementary Fig. 5b). Indirect calorimetry indicated that Gly-MCA treatment significantly increased energy expenditure (Fig. 2b,c). GTT demonstrated that the response to glucose challenge is substantially improved in Gly-MCA-treated obese mice (Fig. 2d). Moreover, ITT revealed that Gly-MCA ameliorated insulin sensitivity (Fig. 2e). Administration of Gly-MCA decreased fasting serum insulin levels of obese mice fed a HFD (Fig. 2f). Liver histology indicated the loss of hepatic lipid droplets with no apparent cholestasis, inflammation and necrosis after Gly-MCA treatment (Fig. 2g). Gly-MCA treatment also reduced liver weights and hepatic triglyceride levels (Fig. 2h,i), and Gly-MCA-treated obese mice displayed reduced serum ALT and AST levels (Supplementary Fig. 5c,d), and faecal LCN-2 levels were similar between Gly-MCA-treated and vehicle-treated mice (Supplementary Fig. 5e). Mice returned to their original weights 4–5 weeks after removal of Gly-MCA (Supplementary Fig. 5f), indicating that Gly-MCA produced reversible weight loss in obese mice. In another model of genetic obesity, leptin receptor-deficient (db/db) mice, Gly-MCA administration daily for 6 weeks reduced body weight (Supplementary Fig. 6a), fat mass and the fat/lean mass ratio compared with vehicle-treated mice (Supplementary Fig. 6b). Liver histology indicated a significant decrease in hepatic lipid droplets with no observed cholestasis, inflammation and necrosis after Gly-MCA treatment (Supplementary Fig. 6c). Gly-MCA treatment decreased liver weights and hepatic triglyceride contents, whereas serum triglyceride levels were unchanged (Supplementary Fig. 6d–f). Gly-MCA treatment substantially decreased serum ALT and AST levels, while faecal LCN-2 levels were unchanged (Supplementary Fig. 6g–i), thus indicating that Gly-MCA was not toxic to liver and intestine of the db/db mice, and actually reduced hepatic lipid toxicity in this mouse model.
Gly-MCA inhibits FXR signalling in ileum, but not liver
The accumulation of Gly-MCA in the ileum is much greater than in liver in Gly-MCA-treated mice in the different models tested (Fig. 3a, Supplementary Figs 8a and 9a). Gly-MCA treatment inhibited FXR signalling, as revealed by a decrease in Shp and Fgf15 mRNAs in the ileum, but not in the liver of the mice concurrently fed a HFD (Fig. 3b,c). Certain bile acids are known to activate TGR5 and PXR signalling pathways15, and therefore the effect of Gly-MCA on TGR5 and PXR signalling pathways was evaluated. Luciferase reporter assays indicated that Gly-MCA failed to activate TGR5 signalling (Supplementary Fig. 7a). Furthermore, the expression of mRNAs encoded by the Tgr5 and Glp1 genes in the ileum remained similar after Gly-MCA treatment in the mice fed a HFD (Supplementary Fig. 7b). Gly-MCA treatment did not alter ileum cAMP levels and serum GLP-1 levels of the mice fed a HFD (Supplementary Fig. 7c,d). In addition, PXR mRNAs and PXR target gene mRNAs Cyp3a11 and Mdr1 in the ileum were comparable between vehicle- and Gly-MCA-treated mice fed a HFD (Supplementary Fig. 7e). These observations indicated that Gly-MCA had no effects on the Tgr5–Glp1 pathway and PXR signalling, and that Gly-MCA is an intestine-specific FXR inhibitor circumventing the potential adverse outcomes that would result from liver FXR antagonism.
Gly-MCA reduces intestinal and serum ceramides levels
FXR is the central sensor and regulator of the biosynthesis and enterohepatic recycling of bile acids16. Metabolomics analysis revealed that T-α-MCA and T-β-MCA levels of ileum and liver, and T-β-MCA levels of gall bladder were moderately increased, while serum levels of taurine-conjugated bile acids remained unchanged in Gly-MCA-treated mice concurrently fed a HFD compared with vehicle (Fig. 3d–g). Similar results were obtained after Gly-MCA treatment in established obese mice fed a HFD or db/db mice (Supplementary Figs 8b–d and 9b–e). Hepatic cholesterol 7α-hydroxylase (CYP7A1) regulates T-α-MCA and T-β-MCA synthesis, and sterol 12α-hydroxylase (CYP8B1) is required for taurocholic acid (TCA) synthesis17,18. Previous studies demonstrated that the intestinal Fxr–fgf15 signalling pathway regulates Cyp7a1, but not Cyp8b1 (ref. 19). Consistently, Cyp7a1 mRNA levels were substantially induced after Gly-MCA treatment, but Cyp8b1 mRNA levels were similar between the two groups, which resulted in the increase of T-α-MCA and T-β-MCA levels (Supplementary Fig. 7f, Fig. 3d). Lipidomics analysis showed that ileum ceramides, especially the most abundant C16:0 ceramide, were substantially reduced, accompanied by lower serum ceramides levels in Gly-MCA-treated mice compared with vehicle-treated mice concurrently fed a HFD (Fig. 3h,i). Similar results were obtained after Gly-MCA treatment in mice made obese with a HFD or db/db mice (Supplementary Figs 8e,f and 9f,g). Expression of ceramide synthesis-related gene mRNAs Sptlc2, Sptlc3, Cers2, Cers4, Degs1, Degs2, Smpd3 and Smpd4 were substantially downregulated in ileum of Gly-MCA-treated mice compared with vehicle-treated mice fed a HFD for 9 weeks, but not in liver and white adipose tissue (WAT; Fig. 3j, Supplementary Fig. 7g,h). The mRNAs from ceramide catabolism-related genes, for example, Sgms1, Sgms2, and Acer2, remained similar in ileum, liver and WAT between the two groups (Fig. 3j, Supplementary Fig. 7g,h). Fgf21 recently emerged as a regulator of energy metabolism and alters ceramides in an adiponectin-dependent manner20. However, Gly-MCA did not affect hepatic Fgf21 mRNA (Supplementary Fig. 7i).
Intestinal FXR is required for Gly-MCA-decreased ceramides
To uncover the mechanism by which intestinal FXR regulates ceramide synthesis-related genes, wild-type (WT; Fxrfl/fl) and intestine-specific Fxr-null (FxrΔIE) mice fed a chow diet were treated with the FXR agonist TCA for 24 h. Fxr gene expression was almost absent in the ileum of FxrΔIE mice, and there was no activation of FXR signalling by the natural agonist TCA, as revealed by measurements of the FXR target gene Shp and Fgf15 mRNAs in FxrΔIE mice in contrast to the robust activation of these genes in Fxrfl/fl mice (Fig. 4a). Sptlc2, Cers4, Degs2, Smpd3 and Smpd4 mRNAs were also induced in the ileum after TCA treatment in Fxrfl/fl mice, but not in FxrΔIE mice (Fig. 4b). Gly-MCA inhibited TCA-activated FXR signalling in the ileum (Fig. 4c), and further blunted TCA-induced Sptlc2, Cers4, Degs2, Smpd3 and Smpd4 mRNAs in the ileum of WT mice (Fig. 4d). Earlier-published intestinal chromatin immunoprecipitation-sequencing data for FXR21 revealed FXR binding peaks near the Sptlc2, Degs2 and Smpd3 genes, and inverted repeat 1 consensus binding motifs for FXR were observed in the FXR-binding peak regions of Sptlc2 and Smpd3 genes (http://bit.ly/1W9cvJf). These results suggested that Sptlc2 and Smpd3 were potential target genes of FXR in ileum, which was confirmed by promoter–reporter gene studies showing that FXR directly activated the Sptlc2 and Smpd3 promoters (C.N.B., unpublished observations). Further, TCA significantly increased the ileal SMPD3 enzyme activities in Fxrfl/fl mice, but not in FxrΔIE mice fed a chow diet (Fig. 4e). The induction of ileal SMPD3 enzyme activities by TCA was significantly inhibited by Gly-MCA treatment in WT mice fed a chow diet (Fig. 4f). Gly-MCA decreased the SPTLC2 protein levels and the SMPD3 enzyme activities in ileum of the mice fed a HFD (Fig. 3k,l). The full western blot for Fig. 3k is found in Supplementary Fig. 17.
To further clarify the role of intestinal FXR in the Gly-MCA-improved metabolic dysfunctions, Fxrfl/fl mice and FxrΔIE mice fed a HFD were treated with vehicle and Gly-MCA. Gly-MCA prevented HFD-induced body weight gain in Fxrfl/f mice, but not in FxrΔIE mice (Fig. 5a). The fat mass and fat/lean mass ratios of Gly-MCA-treated Fxrfl/fl mice were substantially decreased to levels similar to those in FxrΔIE mice (Fig. 5b). FxrΔIE mice displayed ameliorated glucose intolerance and insulin resistance, and were unresponsive to the metabolic benefits of Gly-MCA treatment (Fig. 5c–e). Liver histology showed that Gly-MCA substantially decreased hepatic lipid droplets in Fxrfl/fl mice, but had no effects on FxrΔIE mice (Supplementary Fig. 10a). The liver weights and hepatic triglyceride contents in Gly-MCA-treated Fxrfl/fl mice, and vehicle-treated FxrΔIE mice, were substantially lower compared with vehicle-treated Fxrfl/fl mice (Supplementary Fig. 10b,c). These results indicated that Gly-MCA did not further improve obesity, insulin resistance and hepatic steatosis beyond that was achieved in FxrΔIE mice.
Ceramide reverses the beneficial metabolic effects of Gly-MCA
To further evaluate the role of the intestinal FXR–ceramide axis in the Gly-MCA-improved metabolic disorders, the FXR agonist GW4064 (10 mg kg−1) or C16:0 ceramide were administered to Gly-MCA-treated mice fed a HFD. Ceramide treatment was found not to affect the pharmacokinetic profile of Gly-MCA (C.X., unpublished observations). GW4064 or ceramide treatment reversed the reduction in body weight gain in Gly-MCA-treated mice (Fig. 6a). The response to glucose and insulin challenge in Gly-MCA-treated mice was blunted after GW4064 or ceramide treatment (Fig. 6b–d). Liver histology indicated that GW4064 or ceramide treatment increased hepatic lipid droplets in Gly-MCA-treated mice (Fig. 6e). Hepatic triglyceride levels were also increased to similar levels in the vehicle group after GW4064 or ceramide treatment of the Gly-MCA-treated mice (Fig. 6f). GW4064 or ceramide treatment reversed ileum and serum ceramides levels, which were decreased by Gly-MCA administration (Supplementary Fig. 11a,b).
Gly-MCA induces the ‘browning’ function of beige fat in scWAT via inhibition of the intestinal FXR-ceramide axis
The beige fat in subcutaneous WAT (scWAT) and brown fat were found to make an important contribution to the maintenance of energy balance and thermogenesis22,23,24. To explore the mechanism that Gly-MCA increased energy expenditure, mRNA levels for beige fat thermogenic-associated genes were measured. Gly-MCA markedly induced expression of mRNAs encoding Ucp1, Ppargc1a, Prdm16, Cox7a, Slc27a1, Cd137, and Klhl13 in scWAT of Fxrfl/fl mice, but not in FxrΔIE mice concurrently fed a HFD (Fig. 7a). Immunohistochemistry further confirmed that UCP1+ beige adipocytes in scWAT of Fxrfl/fl mice were increased after Gly-MCA treatment, whereas no further increase was noted in FxrΔIE mice treated with Gly-MCA (Fig. 7b). In contrast, Gly-MCA treatment failed to activate brown fat biogenesis related genes in interscapular brown fat of Fxrfl/fl mice or FxrΔIE mice (Supplementary Fig. 12a). Gly-MCA had no effects on the TGR5-DIO2 signalling pathway as revealed by the similar Tgr5 and Dio2 mRNA expression levels in beige fat, and brown fat of Fxrfl/fl or FxrΔIE mice between vehicle and Gly-MCA treatment (Fig. 7c, Supplementary Fig. 12b). The β-sympathetic nerve-activated β-adrenergic receptors-cAMP signals exert an important role in the thermogenesis of brown fat and beige fat. Gly-MCA treatment did not alter the cAMP levels in beige fat and brown fat (Fig. 7d, Supplementary Fig. 12c). Moreover, beige fat thermogenic-associated mRNA expression was markedly induced after Gly-MCA treatment at both 29.5 and 5 °C (Supplementary Fig. 13a,b), suggesting that Gly-MCA increased beige fat thermogenesis independent of the activation of β-sympathetic nervous system. Instead, the increase of beige fat thermogenic related mRNAs in Gly-MCA-treated mice concurrently fed a HFD was markedly blunted after GW4064 or ceramide treatment (Fig. 7e). These results implied that inhibition of intestinal FXR-ceramides axis result in improvement of beige fat thermogenesis after Gly-MCA administration.
To further rule out the possibility that reduced body weight contributed to the observed beneficial metabolic effects of Gly-MCA and to establish a causal relationship between beige fat thermogenesis improvement and body weight loss, mice on a HFD were treated with Gly-MCA for 5 days when no alteration of body weight was noted (Fig. 8a). Gly-MCA substantially inhibited FXR signalling in ileum, but not in liver (Fig. 8b,c). The Sptlc2, Degs2, Smpd3 and Smpd4 mRNAs were decreased in ileum, but not in liver and scWAT after 5 days of Gly-MCA treatment of mice on a HFD (Fig. 8d–f). Gly-MCA significantly lowered SMPD3 enzyme activity in ileum (Fig. 8g). Lipidomics analysis revealed that ileum ceramides were decreased, accompanied by lower portal vein and systematic vein ceramides in Gly-MCA-treated mice compared with vehicle-treated mice (Fig. 8h–j). Gly-MCA-induced expression of Ucp1, Ppargc1a, Prdm16, Cox7a and Klhl13 mRNAs in beige fat, in parallel with an increase of metabolic rate and similar food intake (Fig. 9a–d). These results demonstrated that the improvement of beige fat thermogenesis via inhibition of the intestinal FXR–ceramide axis might be causal rather than due simply to weight loss.
Ceramides impaired beige fat thermogenesis in vitro
To evaluate direct effects of ceramide on beige fat function, induced beige adipocytes25 were stimulated by ceramides in vitro. Ceramide treatment substantially suppressed expression of Ucp1, Ppargc1a, Cox7a, Cd40 and Cd137 mRNAs in beige adipocytes in a dose- and time-dependent manner (Fig. 10a,b). Since mitochondrial respiration rates are used to estimate the ‘browning’ function of beige fat26, oxygen consumption rate (OCR) analysis was determined. Ceramide treatment markedly decreased basal and maximal respiration of beige adipocytes in a dose-dependent manner (Fig. 10c,d). No cell toxicity was noted at any indicated doses of the ceramides after 24 h treatment (Fig. 10e).
Gly-MCA reduces serum inflammatory cytokine levels
Gly-MCA was also observed to decrease the levels of mRNAs encoding inflammatory cytokines such as IL-1β, MCP-1, MIP-1α and IL-17, and the adipokine leptin in scWAT of Fxrfl/fl mice, but not in FxrΔIE mice fed a HFD (Supplementary Fig. 14a,b). Consistent with this result, IL-1β, MCP-1, MIP-1α, IL-17 and leptin were lower after Gly-MCA treatment in Fxrfl/fl mice, and no further decrease was noted in FxrΔIE mice treated with Gly-MCA on a HFD (Supplementary Fig. 14c,d). Five days of Gly-MCA treatment decreased Mcp-1 mRNA levels but not Il-1β, and Mip-1α mRNA levels that were reduced on Gly-MCA treatment (Supplementary Fig. 14e). Thus, decreased Mcp-1 expression might contribute to the improvement of insulin sensitivity after Gly-MCA.
Ceramides levels modulate Gly-MCA improvement of hepatic steatosis
Gly-MCA substantially decreased the expression of mRNAs encoded by fatty acid synthesis-related genes such as Srebp1c, Cidea, Fasn and Elovl6 in the liver of Fxrfl/fl mice, whereas no further decrease was noted in FxrΔIE mice treated with Gly-MCA (Supplementary Fig. 15a). GW4064 or ceramide treatment reversed the Srebp1c, Cidea, Fasn and Elovl6 mRNA levels in Gly-MCA-treated mice (Supplementary Fig. 15b). Expression of hepatic mRNAs encoded by triglyceride formation related genes such as Dgat1 and Dgat2 remained unchanged after Gly-MCA treatment (Supplementary Fig. 15a,b). These results indicated that Gly-MCA treatment downregulated the Srebp1c–cidea pathway through inhibition of the intestinal FXR–ceramide axis.
Increasing evidence points to intestinal FXR as a major regulator of metabolic disorders4,9,27. Notably, constitutive signalling of intestinal FXR as a result of bile acid agonists produced in liver appears to aggravate obesity, insulin resistance and fatty liver, and thus antagonism of intestinal FXR may be a reasonable therapeutic strategy. Gly-MCA was identified as a new orally available, intestinal-selective FXR inhibitor that circumvents the side effects of hepatic FXR inhibition that would result in increased cholestasis as found in Fxr-null mice16. Gly-MCA prevented and treated metabolic dysfunction resulting from HFD treatment and genetic obesity via the inhibition of intestinal FXR signalling. No inhibition of hepatic FXR signalling was noted and no cholestasis was observed in Gly-MCA-treated mice. Mechanistically, a decrease in intestinal-derived ceramides, as a result of lower ceramide synthesis-related genes by inhibition of FXR, likely mediates the resolution of the HFD-induced obesity and hepatic steatosis by Gly-MCA, although at this time it is uncertain whether ceramides affect insulin resistance. Ceramide injection reversed the effects of Gly-MCA on HFD-fed WT mice, and the associated metabolically favourable phenotype of HFD-fed FxrΔIE mice, although it should be noted that they have no metabolic abnormalities found in HFD-fed WT mice. FXR was found to directly regulate ceramide metabolism in intestine as revealed by the increase of Sptlc2 mRNA and the corresponding protein, and the upregulation of Smpd3 mRNA and enzyme activity in the intestine, and FXR activation of the Sptlc2 and Smpd3 promoters. More importantly, the reduced degree of portal vein ceramides (from intestine) was greater than that from the systematic vein ceramides (38% reduced versus 25% reduced for portal vein ceramides levels and systematic vein ceramides levels, respectively). In addition, no alterations were observed for ceramide catabolism-related genes in ileum, liver and WAT. Thus, the serum ceramide changes after Gly-MCA treatment mainly come from intestine metabolism. The site of reduced ceramide synthesis, the intestine and the partial reduction of ceramides through suppression of intestinal FXR signalling, is rather fortuitous, since major reductions in ceramides might cause central nervous system toxicity and skin toxicity since spingolipids are important constituents of these organs28,29.
Obese humans were found to have increased FXR expression and FXR signalling in the intestine as compared with lean controls. While a cause–effect relationship was not established, these data suggest that since FXR is activated in human obesity, and that gut-specific inhibition may be a promising human therapy. Supporting this view, the bile acid sequestrant colesevelam, a clinically-used anti-diabetes drug, was found to improve glucose homoeostasis partially through inhibition of FXR signalling30,31. Colesevelam also improved insulin resistance via altering TGR5–GLP-1 signalling in DIO-mice and rats32,33.
HFD-fed mice given Gly-MCA had improved insulin sensitivity and resolution of fatty liver, and thus the question arises whether these improved metabolic endpoints are the result of lower obesity. However, mice on a HFD for 5 days without any significant weight change had improved insulin resistance. There might be two potential mechanisms to explain this result. First, the increased beige fat function via inhibition of intestinal-derived ceramides might lead to improved insulin resistance in Gly-MCA-treated mice. Supporting this view, beige fat is not only a fat-burning organ but also impacts glucose homoeostasis24,34. Second, 5 days of Gly-MCA treatment significantly decrease Mcp-1 mRNA expression in scWAT. Others found that MCP-1 promotes adipose tissue inflammation and insulin resistance35,36. However, the precise mechanism by which Gly-MCA improved insulin sensitivity remains unclear. Resolution of fatty livers in obese mice treated with Gly-MCA may also be independent of the obese phenotype since HFD-induced obese mice or genetically obese db/db mice displayed reduced steatosis with Gly-MCA, although these mice, even with weight loss, were still obese. Hepatic steatosis is positively correlated with hypertriglyceridemia. Surprisingly, Gly-MCA improved HFD-induced hepatic triglyceride contents but not serum triglyceride levels. The downregulation of hepatic lipogenesis-related mRNAs Srebp1c, Cidea, Fasn and Elovl6 mainly led to decreased HFD-induced hepatic triglyceride accumulation after Gly-MCA treatment. It is well known that hepatic triglyceride secretion plays an important role in maintenance of serum triglyceride homoeostasis. Gly-MCA treatment did not affect the expression of hepatic triglyceride secretion-related genes such as Mttp and Apob (C.X. and C.J., unpublished observations). This result might partially explain the difference between liver and serum triglyceride levels after Gly-MCA treatment. Consistent with these findings, liver-specific CYP7A1 transgenic mice displayed reduced hepatic triglyceride levels and the unchanged serum triglyceride levels compared with WT mice37.
Ursodeoxycholic acid (UDCA), a bile acid metabolite, is used for the treatment of liver dysfunction, notably non-alcoholic fatty liver disease, non-alcoholic steatohepatitis and primary biliary cirrhosis38,39. Treatment with UDCA (28–35 mg kg−1 per day) for 1 year exerts beneficial metabolic profiles40. Three-week administration of UDCA at 20 mg kg−1 per day reduced serum AST, γ-glutamyl transferase, free fatty acids, total cholesterol and low-density lipoprotein cholesterol41. Hepatic gene expression changes and altered bile acid metabolites suggested that UDCA might be an inhibitor of FXR signalling; however, direct evidence that UDCA is an FXR antagonist was not presented. Others demonstrated that tauroursodeoxycholic acid (TUDCA), a UDCA derivative, exerts metabolic benefits as a chemical chaperone to inhibit endoplasmic reticulum (ER) stress in mice and human42,43. Interestingly, TUDCA antagonizes FXR activation by synthetic agonist GW4064, and TUDCA is rapidly hydrolyzed by gut bacterial BSH (C.X. and A.D.P., unpublished observations), suggesting that high doses of TUDCA might inhibit FXR signalling, resulting in improved insulin resistance.
A recent study revealed that the gut-restricted FXR agonist fexaramine, at much higher doses (100mgkg−1, administered by gavage) than those used for Gly-MCA (10mgkg−1, administered by pill), decreased diet-induced body weight gain and its associated metabolic dysfunction in the diet-induced obese mouse model8. However, in contrast to the present study, the effects of fexaramine appear to be driven in part by the activation of TGR5, whereas Gly-MCA works exclusively through the inhibition of intestinal FXR, with no effects on TGR5 signalling.
Emerging studies revealed that beige fat recruitment plays a significant role in whole-body energy metabolism23,44. Gly-MCA enhanced the browning of beige fat as a result of inhibition of the intestinal FXR-ceramide axis, and increased energy expenditure was evident even before significant weight loss was evident. Beige fat thermogenesis is sufficient to increase energy expenditure34. Supporting this view, activation of beige fat, but not classic brown fat, increased metabolic rates leading to decreased obesity45,46,47. Conversely, mice with selective inhibition of beige fat, displayed an increased susceptibility to HFD-induced body weight gain24. Other studies demonstrated that thermogenic adipose tissues from adult humans mainly express beige adipocyte-selective markers and not the classic brown adipocyte-related markers34,48. Genome-wide analyses based on global RNA sequencing further, indicated that beige adipocytes exist in supraclavicular regions of adult humans49. 18F-FDG-PET/CT analyses revealed that thermogenic adipocytes are undetectable under basal conditions, while prolonged cold treatment dramatically elicited thermogenic adipocytes accompanied by increased energy expenditure and improvement of insulin sensitivity50,51. Collectively, the existence of beige adipocytes in adult humans provides an attractive therapeutic target for obesity-related metabolic disease.
Lower intestinal-derived ceramides contributed to the metabolic benefits of Gly-MCA. In support of these findings, recent studies revealed that ceramides are correlated with obesity and insulin resistance20,52,53. Thus, it would be interesting to determine the effects of Gly-MCA on regulating body temperature in the cold. The expression of beige fat thermogenic-related genes were markedly induced by Gly-MCA treatment under thermoneutral, room temperature and cold conditions. Gly-MCA-treated mice displayed a higher core body temperature compared with vehicle-treated mice after cold stimulation (C.X. and C.J., unpublished observations). In addition, Gly-MCA had no effects on cAMP levels in both beige and brown fat. These results suggested that Gly-MCA treatment restored beige fat thermogenesis, likely independent of β-sympathetic nervous system activation. Thus, reduction of intestinal-derived ceramides largely mediated the Gly-MCA-increased energy expenditure. However, the mechanism by which ceramides compromise beige fat thermogenesis remains unclear. Fortuitously, ceramides are only partially reduced in mice treated with Gly-MCA and thus no toxicities would be expected nor are they observed in tissues dependent on ceramides such as neurons and skin. However, long-term studies are warranted to determine safety during chronic treatment.
Oral administration of a new chemical entity Gly-MCA prevents and reverses obesity-related metabolic dysfunctions. It is proposed that any compound that is orally administered, specifically inhibits intestinal FXR and has no effects on liver FXR signalling, would have utility in the therapy of patients with metabolic disorders.
Materials and reagents
Bile acids were ordered from Steraloids, Inc., (Newport, RI) and Sigma-Aldrich (St Louis, MO), and T-β-MCA-d5 sodium salt was from Toronto Research Chemicals, Inc., (Toronto, Ontario). C16:0, C18:0, C20:0, C22:0, C24:0 and C24:1 ceramides were obtained from Avanti Polar Lipids. HFD (60 kcal % fat) were purchased from Bio-Serv (Frenchtown, NJ). Gly-MCA was synthesized as according to the Supplementary Fig. 16.
The biopsies of the distal ileum mucosa tissue were obtained from 66 individuals who underwent colonoscopy. The ages of the subjects ranged from 18 to 67 years, and all had a BMI between 17.9 and 32.1 kg m−2. In these subjects, lean subjects (n=36), BMI are under 25 kg m−2, obese subjects (n=30), BMI are equal or over 25 kg m−2. The demographic characteristics were similar at baseline between the groups (Supplementary Table 2). All individuals fulfilled the following inclusion criteria: (1) no significant alcohol consumption (the definition of significant alcohol consumption has been inconsistent and ranged from >1 alcoholic beverage (10 g of alcohol per one drink unit) per day to >40 g per day); (2) no significant acute or chronic inflammatory disease; (3) no medical history of hypertension (that is, systolic blood pressure <140 mm Hg and diastolic blood pressure <85 mm Hg); (4) no clinical evidence of either cardiovascular or peripheral artery disease; (5) no thyroid dysfunction; (6) no gastrointestinal disease; and (7) no pregnancy. The study was approved by Conjoint Health Research Ethics Board of Peking University People’s Hospital, and written informed consents were given all subjects before participation in this study.
HFD (60% kcal from fat) was purchased from Bio-Serv, Inc. Male 6- to 8-week-old intestine-specific Fxr-null (FxrΔIE)19 mice and control (Fxrfl/fl) mice were on a C57BL/6N genetic background, after backcrossing with C57BL/6N mice for over 10 generations. For the Gly-MCA study, Gly-MCA was custom synthesized. For oral administration of Gly-MCA (0.25 mg Gly-MCA per pill, dose of 10 mg kg−1), bacon-flavoured dough pills were produced by adding Gly-MCA to the dough and then formulating the pills by use of a tablet triturate mold (Gallipot, St. Paul, MN)54. Mice were trained to eat the dough pills before the study. For the prevention of obesity, insulin resistance and hepatic steatosis, male WT C57BL/6 N mice, 6 to 8 weeks old, were fed a HFD (Bio-Serv, Frenchtown, NJ; 60 kcal% fat) and were orally administered with vehicle (control pills) or Gly-MCA (0.25 mg per pill per day, dose10 mg kg−1). For the therapy of obesity, obese C57BL/6N mice, induced by a HFD for 12 weeks, were administered (0.25 mg Gly-MCA per pill, dose of 10 mg kg−1). Leptin receptor-deficient db/db mice, 6 to 8 weeks old, fed a chow diet, were administered Gly-MCA (0.25 mg per pill per day, or 10 mg kg−1 once per day). To investigate the role of intestine FXR in ceramide synthesis, 6- to 8-week-old male littermate Fxrfl/fl and FxrΔIE mice were fed a chow diet and administered TCA (400 mg kg−1, in saline) by gavage. To determine whether the action of Gly-MCA was FXR dependent, 6- to 8-week-old male Fxrfl/fl and FxrΔIE mice, were fed a HFD and orally administered vehicle (control pills) or Gly-MCA (0.25 mg per pill per day, dose 10 mg kg−1). For the GW4064 (10 mg kg−1) and ceramide turnover study, male 6-week-old C57BL/6N mice fed a HFD were divided into four groups: vehicle, Gly-MCA (0.25 mg per pill per day, dose 10 mg kg−1), GW4064+Gly-MCA (each pill contained 0.25 mg GW4064 and 0.25 mg Gly-MCA, each dose10 mg kg−1) and injected with ceramide (see below)+Gly-MCA (0.25 mg per pill per day, dose 10 mg kg−1) groups treated for 5 weeks. C16:0 ceramide (Avanti Polar Lipids) was dissolved in saline with 0.5% sodium carboxymethyl cellulose and 5% Tween 80. The mice were administered C16:0 ceramide at a dose of 10 mg kg−1 per day by intraperitoneal (i.p.) injection. Saline with 0.5% sodium carboxymethyl cellulose and 5% Tween 80 was injected to controls. For the short-time treatment, male 6-week-old C57BL/6N mice fed a HFD were orally administered with vehicle (control pills) or Gly-MCA (0.25 mg per pill per day, dose 10 mg kg−1) for 5 days. Mice were housed individually in their home cages. Cumulative food intake and TEEbal were measured for 1 week for vehicle and Gly-MCA-treated mice fed a HFD for 6 to 7 weeks. The following equation was used to calculate TEEbal:
Metabolizable energy intake is defined as grams of food ingested per 24 h multiplied by the metabolizable energy for the HFD. ΔSomatic fat energy is calculated as final fat mass energy minus initial fat mass energy. ΔSomatic lean energy is calculated as final lean mass energy minus initial lean mass energy55. For thermal neutral temperature exposure experiments, male 6-week-old C57BL/6N mice fed a HFD were orally administered with vehicle (control pills) or Gly-MCA (0.25 mg per pill per day, dose10 mg kg−1) at 29.5 °C for 2 weeks. For cold stimulation experiments, male 6-week-old C57BL/6N mice fed a HFD were orally administered with vehicle (control pills) or Gly-MCA (0.25 mg per pill per day, dose 10 mg kg−1) at 22 °C for 5 days and then acutely moved to 5 °C for another 1 day. All mice were randomly assigned to experimental groups and the groups showed no difference in body weight gain before treatment. All mouse studies were performed in accordance with the Institute of Laboratory Animal Resources guidelines and approved by the NCI Animal Care and Use Committee.
Indirect calorimetry was performed on obese mice fed a HFD for 12 weeks and then treated with vehicle or Gly-MCA (10 mg kg−1) concurrently on a HFD for 2 weeks using a 12-chamber Environment Controlled CLAMS (Columbus Instruments, Columbus, OH). After 48-h acclimatization, mice were monitored for 24 h at 22 °C and then for the following 24 h at thermoneutrality (29.5 °C) for recording data. During testing, food and water were provided ad libitum and Gly-MCA was administered via oral gavage.
For the GTT, mice were fasted for 16 h, blood was drawn, and mice injected i.p. with 1 g kg−1 glucose. For the ITT, mice were fasted for 4 h, blood was drawn and then were injected with insulin (Eli Lilly, Washington, DC), i.p. at a dose of 1 U kg−1 body weight. Blood samples were taken from the tail at 15, 30, 60 and 90 min after injection, and glucose concentration was measured using a Glucometer (Bayer, Pittsburgh, PA).
Hematoxylin and eosin staining were performed on formalin-fixed paraffin-embedded sections using a standard protocol. At least three discontinuous liver sections were evaluated for each mouse.
Hepatic lipids were extracted using a 2:1 chloroform–methanol solution. Liver triglycerides were measured with a triglyceride colorimetric assay kit, according to the manufacturer’s recommendation (Bioassay Systems, Hayward, CA).
Caco-2 (ATCC HTB-37) cells were induced to differentiate using the following the method56: the cells were cultured in DMEM with 10% fetal bovine serum (FBS). The medium was changed once every 3 days. The cells were grown to 100% confluence, and then maintain 1 day. The cells were harvested with trypsin, diluted 1:3 and then seeded in a new plate, which was considered as one passage. After 50 passages, the differentiated Caco-2 cells were verified by mRNA expression of FXR and its target genes. The differentiated Caco-2 cells were incubated for 8 h with DMEM media with 1% FBS, and then exposed to Gly-MCA/CDCA/GW4064 for 24 h. HEK293T (ATCC CRL-3216) cells used for the luciferase report assays were obtained from the ATCC (Manassas, VA). The mycoplasma contamination tests on Caco-2 (ATCC HTB-37) and HEK293T (ATCC CRL-3216) were negative.
Stromal vascular cells (SVCs) were isolated from inguinal subcutaneous fat pads of normal male Sprague-Dawley rats (160–180 g). The fat pads were minced and digested in serum-free DMEM containing 0.8 mg ml−1 type I collagenase and 1% defatted BSA, for 60 min at 37 °C in a water bath shaken at 120 cycles per min. The digestion mixture was filtered through 80 and 400 steel mesh to remove debris and floating primary adipocytes. SVCs fractions containing adipose precursor cells residing in the digestion mixture were collected by centrifugation at 800 g for 10 min and plated in DMEM/F-12 (1:1) plus 10% FBS. Then, SVCs were differentiated into adipocytes in DMEM/F-12 (1:1) (10% FBS), supplemented with 5 μg ml−1 insulin, 33 μM biotin and 200 pM triiodothyronine. On differentiated day 2, the cells were treated with 1 μM rosiglitazone for another 5 days to differentiate into beige adipocyte. After 7 days of differentiation, cultured beige adipocytes were used for the next series of experiments26.
Mitochondrial OCR assay
Primary SVCs were isolated from inguinal fat of s.d. rats. Subconfluent SVC cultures were trypsinized and seeded into 24-well plates (Seahorse XF24 extracellular flux analyser) and then differentiated into beige adipocytes. OCR of adipocytes in the basal state and in response to respiratory chain modulators were measured with XF Cell Mito Stress Test Kit (Seahorse Bioscience, North Billerica, MA) by use of a XF24 Flux Analyzer. The following modulators were injected sequentially: (1) Oligomycin (1 μM), (2) FCCP (1 μM), (c) Rotenone (1 μM) and Antimycin A (1 μM). OCR rates were calculated and analysed using the Seahorse XF24 v18.104.22.168 software.
Cell viability was determined using the Cell Counting Kit-8 assay (CCK-8, Dojindo Molecular Technologies, Gaithersburg, MD). A 100 μl aliquot of serum-free medium containing 10% CCK-8 was added to each well. The plates were incubated at 37 °C for 120 min, and absorbance measured at 450 nm. The absorbance of the treated cells was compared with that of the control cells exposed only to the vehicle, and thus were considered as 100% viable.
Hydrolysis efficiency of Gly-MCA and T-β-MCA
Faecal proteins were prepared from faeces pellets (0.5 g) in pH 7.4 PBS (5.0 ml) using sonication. Incubations were carried out in 3 mM sodium acetate buffer, pH 5.2, containing 0.1 mg ml−1 faecal protein and 50 μM TβMCA-d5 or Gly-MCA in a final volume of 200 μl. After a 20 min incubation at 37 °C, the reactions were stopped by plunging the samples into dry ice. Acetonitrile (100 μl) was directly added to the reaction mix. After centrifuging at 14,000 g for 20 min, 5 μl of the supernatant was transferred to an auto sampler vial and subjected to analysis by use of a UPLC system coupled with a XEVO triple–quadrupole tandem mass spectrometer (Waters Corp., Milford, MA).
Grace L. Guo supplied the PGL4-Shp-TK firefly luciferase construct and human FXR expression plasmid. Paul A. Dawson provided the human ASBT expression plasmid, and Makoto Miyazaki and Kristina Schoonjans gifted the pCMVSPORT6/hTGR5 and cAMP response element-driven luciferase reporter plasmids. The Cignal CRE Reporter Assay kit (LUC) was purchased from QIAGEN. HEK293T cells were co-transfected with: (1) a chimeric receptor construct in which the carboxy terminal portions of human FXR (containing the native ligand-binding domain and AF2 transactivation domain) was fused to an amino terminal GAL4 DNA-binding domain under regulatory control of the constitutively active SV40 promoter; (2) a firefly luciferase reporter plasmid driven by the UAS GAL4 DNA response element; and (3) a Renilla luciferase reporter gene (pRL-luciferase; Promega; Madison, WI) as a transfection efficiency control. The plasmids were transfected into cells using X-tremeGENE HP DNA Transfection Reagent (Roche). The cells were lysed, and luciferase activities measured with the Dual Luciferase Reporter Assay kit (Promega Corp., Madison, WI) and a Tecan GeniosPro luminescent plate reader (Research Triangle Park, NC).
Quantification of faecal LCN-2
Frozen faecal samples were homogenized in PBS containing 0.1% Tween-20 (100 mg ml−1), vibrated for 20 min, and then centrifuged at 14,000 g for 10 min. Supernatants were collected and analysed with a mouse LCN-2 ELISA kit (R&D Systems, Minneapolis, MN).
Determination of sphingomyelinase activity
Frozen intestine samples were homogenized in PBS containing 0.1% BSA, and then centrifuged at 18,000 g for 5 min. Supernatants were collected and analysed with a Colorimetric Sphingomyelinase Assay kit (Sigma-Aldrich).
Frozen intestine and subcutaneous adipose tissue samples were homogenized in 0.1 M HCl, and then centrifuged at 18,000 g for 5 min. Supernatants were collected and analysed with a mouse cAMP Direct Immunoassay kit (Abcam, Cambridge, MA).
Assessment of serum cytokine and adipokine levels
Serum cytokine and adipokine levels were evaluated using the Milliplex MAP mouse cytokine/chemokine panel, rat/mouse hormone panel and mouse adiponectin panel on a Luminex (Bio-Plex 200) platform (Milliplex, Millipore, Luminex Corp., Austin, TX). Analysis was performed by Eve Technologies (Calgary, Alberta, Canada).
The intestine mucosa was gently scraped and liver were flash frozen in liquid nitrogen and were stored at −80 °C until RNA was prepared. RNA was extracted from frozen intestine and liver using TRIzol reagent (Invitrogen, Carlsbad, CA). Complementary DNA was synthesized from 1 μg total RNA using Superscript II reverse transcriptase (Invitrogen, Carlsbad, CA). Quantitative PCR primers were designed with qPrimerDepot, and the sequences are shown in the Supplementary Table 3. Messenger RNA levels were normalized to 18S ribosomal RNA and expressed as fold change relative to the control group.
Intestine protein extracts were prepared, separated and transferred to a PVDF membrane. The membrane was incubated with antibody against SPTLC2 (LS-B9514, LifeSpan Biosciences, Inc., Seattle, WA) at 1:1000 dilution. Signals obtained were normalized to β-ACTIN (Abcam). For quantitation of the western blot bands, the blots were scanned and analysed using ImageJ software (National Institutes of Health, Bethesda, MD).
For serum lipidomics, a 25 μl aliquot of serum was extracted with 100 μl of ice-cold chloroform:methanol (2:1, v/v) solution containing SM (17:0) and CER (17:0) (Avanti Polar Lipids, Alabaster, AL) at 2 μM as internal standards. The samples were vibrated for 30 s and then incubated for 5 min at room temperature. The organic and aqueous phases were separated by centrifugation at 13,000 g for 5 min. The lower organic phase was transferred to another clean tube and evaporated to dryness at room temperature under vacuum. The residue was dissolved in 25 μl of chloroform:methanol (1:1), followed by diluting with isopropanol:acetonitrile:H2O (2:1:1, v/v/v) containing 2 μM PC (17:0) before UPLC-MS analysis. For tissue lipidomics, about 50 mg tissue was accurately weighed and homogenized with 700 μl of methanol:H2O (4:3, v/v) solution and then extracted using 800 μl of chloroform containing SM (17:0) and CER (17:0) at 2 μM as internal standards. The homogenate was shaken and incubated at 37 °C for 20 min followed by centrifugation at 13,000 g for another 20 min. The lower organic phase was collected and evaporated to dryness under vacuum. The residue was then suspended with 100 μl of chloroform:methanol (1:1, v/v) solution and then diluted with isopropanol:acetonitrile:H2O (2:1:1, v/v/v) solution containing 2 μM PC (17:0) before injection. Lipidomics analysis was performed on an Acquity UPLC/Synapt QTOFMS system (Waters Corp., Milford, MA) equipped with an electrospray ionization (ESI) source. Separation was achieved on an Acquity UPLC CSH C18 column (100 × 2.1 mm internal diameter, 1.7 μm, Waters Corp.). The mobile phase was a mixture of acetonitrile/water (60/40, v/v, A) and isopropanol/acetonitrile (90/10, v/v, B), and both A and B contained 10 mM ammonium acetate and 0.1% formic acid. The gradient elution programme consisted of a 2 min linear gradient of 60% A to 57% A, to 50% A at 2.1 min*, a linear decrease to 46% A at 12 min, to 30% A at 12.1 min*, a linear decrease to 1% A at 18 min before returning to initial conditions at 18.5 min to equilibrate the column (*indicates ballistic gradient). The column temperature was maintained at 55 °C and the flow rate was 0.4 ml min−1. Mass spectrometry data were acquired in the both positive and negative ESI modes at a range of m/z 100–1,000.
Concentrations of bile acids were determined by an Acquity UPLC/Xevo G2 QTOFMS system (Waters Corp.) with an ESI source. An Acquity BEH C18 column (100 × 2.1 mm internal diameter, 1.7 μm, Waters Corp.) was applied for chromatographic separation. A mixture of 0.1% formic acid in water (A) and 0.1% formic acid in acetonitrile (B) was used as the mobile phase. The gradient elution was started from 80% A for 4 min, decreased linearly to 60% A over 11 min, to 40% A over the next 5 min, to 10% A for the succeeding 1 min, and finally increased to 80% A for 4 min to re-equilibrate the column. Column temperature was maintained at 45 °C, and the flow rate was 0.4 ml min−1. Mass spectrometry detection was operated in negative mode. A mass range of m/z 50–850 was acquired.
Synthesis of Gly-MCA
Synthesis of β-MCA 9 and Gly-MCA 10. β-MCA 9 was prepared as illustrated in the Supplementary Fig. 16 by following the literature procedure57. In general, esterification of the dihydroxy acid 1 with methanol under acid catalysis provides ester 2 in quantitative yield. Protection of the hydroxyl group in 3-position with ethyl chloroformate provided carbonate 3 in 79% yield. Oxidation of the 6-hydroxyl group with potassium chromate gave ketone 4 in quantitative yield. Bromination with 47% HBr solution gave bromo ketone 5, which upon reduction with NaBH4 gave bromohydrin 6, in 73% yield. Reductive dehydrobromination with zinc metal provides olefin 7 in about 80% yield. Cis-dihydroxylation with osmium tetroxide and N-methymorpholine N-oxide gave cis diol 8 in moderate yield followed by hydrolysis provided β-MCA 9 in quantitative yield. β-MCA 9 was conjugated to provide Gly-MCA 10 as shown in Supplementary Fig. 16. In brief, ethyl glycinate hydrochloride (1 mmol) was suspended in ethyl acetate (20 ml) containing triethylamine (0.3 ml). The reaction mixture was stirred at 25 °C for 1 h and reacted with β-MCA 9 (0.70 mmol) and EEDQ (1 mmol) by refluxing overnight. The resultant reaction mixture was poured over water (10 ml) and ethyl acetate (10 ml). The organic layer was separated, washed successively with 0.5 N NaOH (10 ml), water (10 ml), 0.5 N HCl (10 ml × 2), water (10 ml × 2), dried over Drierite, filtered and evaporated. The residue obtained was purified by column chromatography and methyl Gly-β-muricholic obtained was dissolved in boiling ethanol (15 ml) and hydrolyzed with 10% K2CO3 over a period of 1 h. The solvent was evaporated to half its volume, diluted with water (10 ml) and the aqueous solution was acidified to give Gly-MCA 10 as a white powder in 61% yield over 2 steps. 1H NMR spectra were recorded on a Bruker Avance II 500 MHz instrument equipped with a BBO probe and the chemical shifts are given as δ values with reference to tetramethylsilane as internal standard. melting point 224–226 °C; 1H NMR (500 MHz, CD3OD) 0.75 (s, 3H, 18-Me), 1.01 (d, 3H, J=6.5 Hz, 21-Me), 1.12 (s, 3H, 19-Me), 1.05–1.56 (m, 13H), 1.58–1.70 (m, 2H), 1.71–1.80 (m, 2H), 1.80–2.03 (m, 3H), 2.04–2.10 (m, 1H), 2.15–2.25 (m, 1H), 2.29–2.37 (m, 1H), 3.30–3.35 (m, 1H), 3.44–3.56 (m, 2H), 3.58–3.61 (m, 1H), 3.70–3.73 (m, 2H), 3.91 (s, 2H); 13C-NMR (125 MHz, CD3OD): d 175.75, 171.84, 75.81, 72.98, 70.47, 55.89, 55.17, 47.79, 43.43, 40.56, 40.06, 39.79, 38.17, 35.42, 35.37, 35.15, 33.57, 32.46, 31.74, 29.34, 28.22, 26.83, 24.78, 20.64, 17.69, 11.27; [M+H]+ calculated for C26H43NO6, 466.3169; found 466.3133; [M−H]- calculated for C26H43NO6, 464.3012, found 464.3055. Purity was determined to be >97%.
Sample sizes were chosen based on pilot experiments that ensured adequate statistical power with similar variances. Values that fell more than two s.d. from the mean were considered as outliers and were excluded from statistical analyses. Experimental values are presented as mean±s.d. Appropriate statistical analyses were applied, assuming a normal sample distribution. When comparing two groups, statistical significance was determined using two-tailed Student’s t-test. When more than two groups were investigated, one-way analysis of variance with Tukey’s correction was applied for comparisons between different preservation groups. P values of <0.05 were considered significant. The investigators involved in this study were not completely blinded during sample collection or data analysis. All data shown were representative results from at least three independent experiments.
How to cite this article: Jiang, C. et al. Intestine-selective farnesoid X receptor inhibition improves obesity-related metabolic dysfunction. Nat. Commun. 6:10166 doi: 10.1038/ncomms10166 (2015).
We thank Linda G. Byrd and John Buckley for technical assistance with the mouse studies. We thank Paul A. Dawson, Makoto Miyazaki and Kristina Schoonjans for recombinant plasmids and Jerry T. Thompson for assistance with the FXR reporter assays. This work was supported by the Intramural Research Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, and by the National Institutes of Environmental Health Sciences (ES022186 (A.D.P.)). This project was funded in part by grants from the National Natural Science Foundation of China (31401011 to C.J. and 81200626 to J.L.) and in part by a grant with the Pennsylvania Department of Health using Tobacco CURE Funds (to A.D.P.). The Pennsylvania Department of Health specifically disclaims responsibility for any analyses, interpretations or conclusions of this work.
Supplementary Figures 1-17, Supplementary Tables 1-3 and Supplementary Reference
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Biochemical Pharmacology (2019)