Abstract

Background and purpose: Russelioside B (RB) is a pregnane glycoside obtained from Caralluma quadrangula; a herb with antidiabetic, anti-inflammatory, and antihyperlipidemic activities. The present experiment tested the possible role of RB in controlling weight gain in rats fed on high fat (HF) diet.Methods: RB was separated from the n-butanol fraction of the crude methanolic extract by chromatographic separation on a Si gel column according to the procedures described previously. The experiment of the biological assessment of RB used 32 male Wistar rats (4 groups, n = 8). Group 1 rats were fed with a palatable normal diet. Group 2, 3, and 4 were fed on HF diet for 16 weeks. Group 2 served as the HF diet control group while Group 3 and 4 received daily oral doses of RB (25 and 50 mg/kg) during the last four weeks. Animals’ parameters like weight gain, fasting level of blood sugar, serum lipids, and serum liver enzyme activities were measured. Liver or adipose tissue weight was divided by the rat’s body weight and multiplied by 100 to obtain the liver or adipose tissue index, respectively. Adipose tissues were processed for histopathological examination, measurement of mRNA expression of visfatin, leptin, adiponectin, uncoupling protein-1 (UCP-1), and carnitine palmitoyl transferase-1 (CPT-1). Furthermore, serum levels of insulin, interleukin-6 (IL-6), IL-1β, tumor necrosis factor-α (TNF-α), leptin, resistin, and adiponectin were assessed using ELISA kits.Results: Rats fed with the HF diet exhibited significant body weight gain, abnormal liver function, disturbed lipid profile, and greater serum level of pro-inflammatory cytokines in addition to greater insulin resistance, adipose tissue and liver indices. Further, rats fed with the HF diet displayed upregulations in the expression of visfatin and leptin with downregulations in the expression of adiponectin, UCP-1, and CPT-1 compared to normal rats. Interestingly, RB (25 or 50 mg/kg) favorably modulated the measured parameters.Conclusion: Data from this study documented the beneficial role of RB in diminishing weight gain, improving the inflammatory perturbations and energy expenditure in HF diet fed rats. Therefore, RB might be a promising candidate for obesity.

Highlights

  • Diet-induced obesity (DIO) and insulin resistance are clinical executions of metaflammatory derangements foreboding type-2 diabetes mellitus (Wellen and Hotamisligil, 2005)

  • DIO is associated with increased inflammatory markers (Hosseinzadeh-Attar et al, 2016) and perturbations of adipose secretory hormones (Trayhurn and Beattie, 2001; Simons et al, 2007)

  • The current study aimed to examine the potential role of Russelioside B (RB) in controlling weight gain associated with high fat (HF) feeding in rats focusing on the influence of RB on adipose tissue expression for adipokines as well as energy expenditure

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Summary

Introduction

Diet-induced obesity (DIO) and insulin resistance are clinical executions of metaflammatory derangements foreboding type-2 diabetes mellitus (Wellen and Hotamisligil, 2005). DIO is associated with increased inflammatory markers (Hosseinzadeh-Attar et al, 2016) and perturbations of adipose secretory hormones (adiponectin, visfatin, resistin, and leptin) (Trayhurn and Beattie, 2001; Simons et al, 2007). UCP-1 is sited within the inner mitochondrial membrane where it increases energy dissipation via uncoupling of mitochondrial oxidation of substrates producing heat instead of ATP (Bargut et al, 2016). Carnitine palmitoyl transferase (CPT-1) is sited at the outer membrane of the mitochondria and it is the rate-determining step in fatty acid β-oxidation. Its role is to shuttle long-chain fatty acids from the cytoplasm to the mitochondrial inner membrane for further catabolism and energy production (Zammit, 2008). The present experiment tested the possible role of RB in controlling weight gain in rats fed on high fat (HF) diet

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