Kandhare Amit D, Bandyopadhyay Debasish, Thakurdesai Prasad A
Department of Scientific Affairs, Indus Biotech Private Limited 1, Rahul Residency, Off Salunke Vihar Road, Kondhwa Pune 411048 Maharashtra India
Oxidative Stress and Free Radical Biology Laboratory, Department of Physiology, University of Calcutta, University College of Science and Technology Kolkata 700 009 India.
RSC Adv. 2018 Sep 18;8(57):32401-32416. doi: 10.1039/c8ra05204b.
: Obesity is a complex, chronic metabolic disorder and its prevalence is increasing throughout most of the world. Low molecular weight galactomannans-based standardized fenugreek seed extract (LMWGAL-TF) has previously shown anti-diabetic and anti-hyperlipidemic potential. : To evaluate the efficacy and mechanism of action of LMWGAL-TF in treating high fat diet (HFD)-induced obesity and hyperlipidemia in mice. : Male C57BL/6 mice were fed the HFD for 12 weeks and were co-administered with LMWGAL-TF (10, 30 and 100 mg kg, p.o.). Variables measured were behavioral, biochemical, molecular and histopathological. In a separate experiment, copper-ascorbate (Cu-As)-induced mitochondrial oxidative damage was evaluated. : The HFD-induced increase ( < 0.001) in body weight, fat mass, lean mass, adipose tissue (brown, mesenteric, epididymal and retroperitoneal) and liver weight was significantly attenuated ( < 0.001) by LMWGAL-TF (30 and 100 mg kg). The HFD-induced elevated levels of serum lipid, interleukins (ILs)-6 and leptin were significantly decreased ( < 0.001) by LMWGAL-TF (30 and 100 mg kg). Elevated fatty acid synthase (FASn), IL-6, leptin and transcriptional regulator interacting with the PHD-bromodomain 2 (TRIP-Br2) mRNA expression in brown adipose tissue (BAT), liver, and epididymal fat were significantly down-regulated ( < 0.001) by LMWGAL-TF (30 and 100 mg kg). Additionally, HFD-induced histological alterations in skeletal muscle, liver, white adipose tissue (WAT) and BAT were also reduced by LMWGAL-TF. Furthermore, the Cu-As-induced alteration in mitochondria oxidative stress (lipid peroxidation, protein carbonylation, glutathione, glutathione reductase, glutathione peroxidase, isocitrate dehydrogenase and α-ketoglutarate dehydrogenase) in skeletal muscle and BAT was significantly ( < 0.001) ameliorated by LMWGAL-TF (2, 4 and 6 mg mL) treatment. It also reduced the Cu-As-induced mitochondrial swelling. : LMWGAL-TF showed its beneficial effect in reducing HFD-induced obesity down-regulation of FASn, IL-6, leptin, and TRIP-Br2 in mice.
肥胖是一种复杂的慢性代谢紊乱疾病,在世界大部分地区其患病率都在上升。基于低分子量半乳甘露聚糖的标准化胡芦巴籽提取物(LMWGAL-TF)此前已显示出抗糖尿病和抗高血脂的潜力。
为了评估LMWGAL-TF治疗高脂饮食(HFD)诱导的小鼠肥胖和高脂血症的疗效及作用机制。
雄性C57BL/6小鼠喂食高脂饮食12周,并同时给予LMWGAL-TF(10、30和100毫克/千克,口服)。测量的变量包括行为、生化、分子和组织病理学方面的。在另一个实验中,评估了铜-抗坏血酸盐(Cu-As)诱导的线粒体氧化损伤。
LMWGAL-TF(30和100毫克/千克)显著减轻了高脂饮食诱导的体重、脂肪量、瘦体重、脂肪组织(棕色、肠系膜、附睾和腹膜后)及肝脏重量的增加(P<0.001)。LMWGAL-TF(30和100毫克/千克)显著降低了高脂饮食诱导的血清脂质、白细胞介素(ILs)-6和瘦素水平的升高(P<0.001)。LMWGAL-TF(30和100毫克/千克)显著下调了棕色脂肪组织(BAT)、肝脏和附睾脂肪中脂肪酸合酶(FASn)、IL-6、瘦素以及与PHD-溴结构域2相互作用的转录调节因子(TRIP-Br2)的mRNA表达(P<0.001)。此外,LMWGAL-TF还减轻了高脂饮食诱导的骨骼肌、肝脏、白色脂肪组织(WAT)和BAT中的组织学改变。此外,LMWGAL-TF(2、4和6毫克/毫升)治疗显著改善了Cu-As诱导的骨骼肌和BAT中线粒体氧化应激(脂质过氧化、蛋白质羰基化、谷胱甘肽、谷胱甘肽还原酶、谷胱甘肽过氧化物酶、异柠檬酸脱氢酶和α-酮戊二酸脱氢酶)的改变(P<0.001)。它还减少了Cu-As诱导的线粒体肿胀。
LMWGAL-TF在减轻高脂饮食诱导的肥胖方面显示出有益作用,其机制可能与下调小鼠体内的FASn、IL-6、瘦素和TRIP-Br2有关。