Department of Biochemistry, Centre for Biological Sciences, K. S. Rangasamy College of Arts and Science (Autonomous), Namakkal Dt, Tiruchengode, Tamil Nadu, 637215, India.
Department of Biotechnology, Vikrama Simhapuri University, Nellore, Andhra Pradesh, 524003, India.
Mol Cell Biochem. 2018 May;442(1-2):143-154. doi: 10.1007/s11010-017-3199-2. Epub 2017 Oct 9.
The present study evaluated the effects of asiatic acid (AA), a pentacyclic triterpenoid from Centella asiatica on lipid metabolism parameters in a rat model of obesity induced using a high fat diet (HFD) for 42 days. AA (20 mg/kg body weight [BW]) was administered orally once daily for 42 days, and an orlistat-treated group of rats (10 mg/kg BW) was included for comparison. Changes in BW, blood glucose levels, insulin resistance and leptin, adiponectin, amylase, and lipase levels in the blood; lipid profiles of plasma; liver antioxidants levels; and acetyl CoA carboxylase(ACC), uncoupling protein-2 (UCP2), and carnitine palmitoyltransferase-1 (CPT1) mRNA expression were observed in the experimental rats. Our results revealed that AA (20 mg/kg BW), similar to orlistat, reduced the increase in BW; increased bone mineral contents and bone mineral densities; reduced blood glucose levels, insulin resistance, leptin, plasma lipid levels; increased adiponectin, amylase, lipase levels in the blood; showed antioxidant activity; and altered mRNA expression of lipid metabolism-related genes, including ACC, UCP 2, and CPT 1, in the HFD-fed rats. From these results, we concluded that AA possesses significant anti-obesity potential through the suppression of BW gain, lipid lowering action, development of insulin and leptin sensitivity, antioxidant activity, and increased mRNA expression of lipid metabolism-related genes.
本研究评估了积雪草酸(AA)对高脂肪饮食(HFD)诱导肥胖大鼠模型脂质代谢参数的影响。AA(20mg/kg 体重)每天口服给药一次,共 42 天,并纳入奥利司他治疗组大鼠(10mg/kg BW)进行比较。观察实验大鼠体重(BW)、血糖水平、胰岛素抵抗和瘦素、脂联素、淀粉酶和脂肪酶水平的变化;血浆脂质谱;肝抗氧化剂水平;以及乙酰辅酶 A 羧化酶(ACC)、解偶联蛋白 2(UCP2)和肉毒碱棕榈酰转移酶 1(CPT1)mRNA 表达的变化。结果表明,AA(20mg/kg BW)与奥利司他相似,可减少 BW 的增加;增加骨矿物质含量和骨密度;降低血糖水平、胰岛素抵抗、瘦素、血浆脂质水平;增加血液中的脂联素、淀粉酶和脂肪酶水平;表现出抗氧化活性;并改变 HFD 喂养大鼠与脂质代谢相关的基因(包括 ACC、UCP2 和 CPT1)的 mRNA 表达。从这些结果中,我们得出结论,AA 通过抑制 BW 增加、降低血脂作用、增加胰岛素和瘦素敏感性、抗氧化活性和增加与脂质代谢相关的基因的 mRNA 表达,具有显著的抗肥胖潜力。