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Benjakul supplementation improves hepatic fat metabolism in high-fat diet-induced obese rats

机译:Benjakul补充改善了高脂饮食诱导的肥胖大鼠的肝脂肪代谢

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Purpose: To evaluate the effects of Benjakul water extract (BWE) supplementation for the prevention of hepatic fat metabolic dysfunction in a rat obesity model induced by a high-fat diet (HFD). Methods: Forty male outbred Sprague-Dawley rats were separated into six groups according to diet composition and treatment: control, HFD, and HFD supplemented with Benjakul extraction at low and high dose (41.3 and 413 mg/kg/day, respectively). After 4 weeks, blood biochemical parameters (i.e., hepatic 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) enzyme and liver histological features) were examined. Subsequently, hepatic gene ex pression of sterol regulatory element binding protein-1 (SREBP-1) and nuclear factor-kappa B (NF-kB) were investigated. Results: Low and high doses of BWE showed significant prevention of abdominal fat accumulation (p 0.05) and inhibited hypercholesterolemia without restoring triglyceride (TG) and lipoprotein-cholesterol (LDL-C) in serum compared to rats fed HFD alone. BWE hindered hepatic fat accumulation via suppression of SREBP-1 ex pression and HMGCR activity in HFD-induced obese rats, while significantly promoting NF-kB down regulation (p 0.05). Conclusion: BWE may be a novel prophylactic strategy for preventing metabolic syndrome and to protect against steatosis due to its regulatory effects on lipid homeostasis.
机译:目的:评估Benjakul水提取物(BWE)对预防高脂饮食(HFD)诱导的大鼠肥胖模型预防肝脂代谢功能障碍的影响。方法:根据饮食成分和治疗,将四十名男性郊外Sprague-Dawley大鼠分为六组:对照,HFD和HFD,在低剂量和高剂量(分别为41.3和413mg / kg /天)。检查4周后,检查血液生化参数(即,肝3-羟基-3-甲基戊齐芳基还原酶(HMGCR)酶和肝脏组织学特征)。随后,研究了甾醇调节元素结合蛋白-1(SrebP-1)和核因子-Kappa(NF-KB)的肝基因。结果:低剂量的BWE显示出腹部脂肪积累(P <0.05)的显着预防,并抑制了与单独喂养HFD大鼠的大鼠血清中的甘油三酯(TG)和脂蛋白 - 胆固醇(LDL-C)的高胆固醇血症。通过抑制HFD诱导的肥胖大鼠的Srebp-1 Ex压力和HMGCR活性,抑制了肝脂肪积累,同时显着促进NF-KB下调调节(P <0.05)。结论:BWE可能是一种用于预防代谢综合征的新型预防策略,并由于其对脂质稳态的调节作用而保护脂肪变性。

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