Abstract

BackgroundRats fed a high-fat and high-sucrose (HF) diet develop hepatic steatosis and hyperlipidemia. There are several reports that a change in nutritional status affects hepatic levels of drug-metabolizing enzymes. Synthetic inulin is a dietary component that completely evades glucide digestion. Supplementing a HF diet with inulin ameliorates hypertriglycemia and hepatic steatosis, but not hypercholesterolemia. This study aimed at distinguishing the effects of synthetic inulin and 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor (statin), which inhibit cholesterol biosynthesis.MethodsWe examined effects of co-treatment with synthetic inulin (5%) and fluvastatin (0, 4, and 8 mg/kg, per os) on body weight, epidydimal white adipose tissue weight, serum and hepatic lipid profiles, and hepatic cytochrome P450 (CYP) mRNA and protein profiles in rats fed a standard diet or a HF diet for 3 weeks.ResultsTreatment with the synthetic inulin (5%) or fluvastatin at 4 mg/kg (lethal dose in rats fed the HF diet, 8 mg/kg) ameliorated the elevation in hepatic triacylglycerol and total cholesterol levels in rats fed the HF diet. Whereas co-treatment with the inulin (5%) and fluvastatin (4 mg/kg) had a tendency to more strongly suppress the elevation in serum levels of very low density lipoprotein triacylglycerol than either treatment alone, no additive or synergistic effect was found in decrease in hepatic lipid levels. Hepatic levels of CYP1A1/2 and CYP2E1 mRNA and protein and methoxyresorufin O-demethylase and ethoxyresorufin O-deethylase activities were reduced in rats fed the HF diet. The synthetic inulin alleviated the reduction in hepatic levels of CYP1A1/2 and CYP2E1 mRNA and protein more strongly than fluvastatin, and no synergistic effects were observed on co-treatment. Furthermore, hepatic levels of aryl hydrocarbon receptor mRNA were decreased in rats fed the HF diet and recovered to near normal values with the intake of dietary inulin, which correlated with change in CYP1A1/2.ConclusionsDietary inulin alone was effective to prevent the development of hepatic steatosis, ameliorate nutritional effects, and alleviate the hepatic change in the expression of CYP1A1/2 and CYP2E1, while co-treatment with statin did not have additive or synergistic effects and statin may cause adverse effects in rats fed the HF diet.

Highlights

  • Rats fed a high-fat and high-sucrose (HF) diet develop hepatic steatosis and hyperlipidemia

  • Fisher et al [8] reported that the expression of CYP2E1 significantly decreased with the progression of human nonalcoholic fatty liver disease (NAFLD) from simple fatty liver to the more severe nonalcoholic steatohepatitis (NASH), and the expression of CYP1A2, CYP2C19, CYP2B6 and CYP3A4 tended to decrease with increasing severity of NAFLD

  • Since the synthetic inulin did not suppress the elevation in serum cholesterol levels of rats fed a HF diet, we investigated the influence of co-treatment with the synthetic inulin and fluvastatin on the health of rats fed a HF diet and the changes in hepatic cytochrome P450 (CYP) expression caused by fatty liver

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Summary

Introduction

Rats fed a high-fat and high-sucrose (HF) diet develop hepatic steatosis and hyperlipidemia. Fisher et al [8] reported that the expression of CYP2E1 significantly decreased with the progression of human nonalcoholic fatty liver disease (NAFLD) from simple fatty liver (steatosis) to the more severe NASH, and the expression of CYP1A2, CYP2C19, CYP2B6 and CYP3A4 tended to decrease with increasing severity of NAFLD. These observations were not consistent with reports of increased CYP2E1 expression in livers from patients with NAFLD [9,10] Nutritional factors such as starvation, fasting and a highlipid diet have been reported to modulate liver microsomal CYP composition, leading to the altered hepatic metabolism of drugs, carcinogens, steroid hormones, and fatty acids, little is known about whether the suppression of lipid accumulation in fatty liver alleviates the changes in hepatic CYP composition. It is worth investigating how to suppress the changes in hepatic CYP composition associated with hepatic steatosis, which is proposed to be the setting for more severe liver diseases such as nonalcoholic steatohepatitis with histologic signs of fibrosis and necroinflammation through to cirrhosis, terminal liver failure and hepatocellular carcinoma [11]

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