Kumar Puttanarasaiah Mahesh, Venkataranganna Marikunte V, Manjunath Kirangadur, Viswanatha Gollapalle L, Ashok Godavarthi
Department of Biotechnology, Padmashree Institute of Information Sciences, Bengaluru, Karnataka, India.
Connexios Life Sciences Pvt. Ltd., Bengaluru, Karnataka, India.
J Intercult Ethnopharmacol. 2016 Mar 1;5(2):146-52. doi: 10.5455/jice.20160224051727. eCollection 2016 Mar-Apr.
The present study was undertaken to evaluate the effect of methanolic leaf extract of Gymnema sylvestre (MLGS) on glucose transport (GLUT) and insulin resistance in vitro.
Peroxisome proliferator-activated receptor-gamma (PPAR-γ) and GLUT-4 expression were assessed in L6 myotubes for concluding the GLUT activity, and adiponectin and leptin expression was studied in 3T3 L1 murine adipocyte cell line to determine the effect of MLGS (250-750 μg/ml) on insulin resistance.
The findings of the experiments have demonstrated a significant and dose-dependent increase in glucose uptake in all the tested concentrations of MLGS, further the glucose uptake activity of MLGS (750 μg/ml) was at par with rosiglitazone (50 μg/ml). Concomitantly, MLGS has shown enhanced GLUT-4 and PPAR-γ gene expressions in L6 myotubes. Furthermore, cycloheximide (CHX) had completely abolished the glucose uptake activity of MLGS when co-incubated, which further confirmed that glucose uptake activity of MLGS was linked to enhanced expression of GLUT-4 and PPAR-γ. In addition, in another experimental set, MLGS showed enhanced expression of adiponectin and leptin, thus confirms the ameliorative effect of MLGS on insulin resistance.
These findings suggest that MLGS has an enhanced glucose uptake activity in L6 myotubes, and ameliorate the insulin resistance in 3T3 L1 murine adipocyte cell line in vitro.
本研究旨在评估匙羹藤甲醇叶提取物(MLGS)对体外葡萄糖转运(GLUT)和胰岛素抵抗的影响。
在L6肌管中评估过氧化物酶体增殖物激活受体γ(PPAR-γ)和GLUT-4的表达以推断GLUT活性,并在3T3 L1小鼠脂肪细胞系中研究脂联素和瘦素的表达,以确定MLGS(250 - 750μg/ml)对胰岛素抵抗的影响。
实验结果表明,在所有测试浓度的MLGS中,葡萄糖摄取均有显著且剂量依赖性的增加,此外,MLGS(750μg/ml)的葡萄糖摄取活性与罗格列酮(50μg/ml)相当。同时,MLGS在L6肌管中显示出增强的GLUT-4和PPAR-γ基因表达。此外,当与放线菌酮(CHX)共同孵育时,其完全消除了MLGS的葡萄糖摄取活性,这进一步证实了MLGS的葡萄糖摄取活性与GLUT-4和PPAR-γ表达增强有关。另外,在另一组实验中,MLGS显示出脂联素和瘦素表达增强,从而证实了MLGS对胰岛素抵抗的改善作用。
这些发现表明,MLGS在L6肌管中具有增强的葡萄糖摄取活性,并在体外改善3T3 L1小鼠脂肪细胞系中的胰岛素抵抗。