Murugan Pidaran, Pari Leelavinothan, Rao Chippada Appa
Department of Biochemistry, Faculty of Science, Annamalai University, Annamalainagar 608 002, India.
J Biosci. 2008 Mar;33(1):63-72. doi: 10.1007/s12038-008-0022-y.
Curcumin is the most active component of turmeric. It is believed that curcumin is a potent antioxidant and anti-inflammatory agent. Tetrahydrocurcumin (THC) is one of the major metabolites of curcumin, and exhibits many of the same physiological and pharmacological activities as curcumin and, in some systems, may exert greater antioxidant activity than curcumin. Using circulating erythrocytes as the cellular mode, the insulin-binding effect of THC and curcumin was investigated. Streptozotocin (STZ)-nicotinamide-induced male Wistar rats were used as the experimental models. THC (80 mg/kg body weight) was administered orally for 45 days. The effect of THC on blood glucose, plasma insulin and insulin binding to its receptor on the cell membrane of erythrocytes were studied. Mean specific binding of insulin was significantly lowered in diabetic rats with a decrease in plasma insulin. This was due to a significant decrease in mean insulin receptors. Erythrocytes from diabetic rats showed a decreased ability for insulin-receptor binding when compared with THC-treated diabetic rats. Scatchard analysis demonstrated that the decrease in insulin binding was accounted for by a decrease in insulin receptor sites per cell, with erythrocytes of diabetic rats having less insulin receptor sites per cell than THC-treated rats. High affinity (K d1), low affinity (K d2) and kinetic analyses revealed an increase in the average receptor affinity of erythrocytes from THC-treated rats compared with those of diabetic rats. These results suggest that acute alteration of the insulin receptor on the membranes of erythrocytes occurred in diabetic rats. Treatment with THC significantly improved specific insulin binding to the receptors, with receptor numbers and affinity binding reaching near-normal levels. Our study suggests the mechanism by which THC increases the number of total cellular insulin binding sites resulting in a significant increase in plasma insulin. The effect of THC is more prominent than that of curcumin.
姜黄素是姜黄中最具活性的成分。人们认为姜黄素是一种强效抗氧化剂和抗炎剂。四氢姜黄素(THC)是姜黄素的主要代谢产物之一,具有许多与姜黄素相同的生理和药理活性,并且在某些系统中,其抗氧化活性可能比姜黄素更强。以循环红细胞作为细胞模型,研究了THC和姜黄素的胰岛素结合效应。采用链脲佐菌素(STZ)-烟酰胺诱导的雄性Wistar大鼠作为实验模型。口服给予THC(80mg/kg体重),持续45天。研究了THC对血糖、血浆胰岛素以及胰岛素与红细胞细胞膜上受体结合的影响。糖尿病大鼠的胰岛素平均特异性结合显著降低,同时血浆胰岛素减少。这是由于平均胰岛素受体显著减少所致。与经THC处理的糖尿病大鼠相比,糖尿病大鼠的红细胞胰岛素受体结合能力降低。Scatchard分析表明,胰岛素结合的减少是由于每个细胞胰岛素受体位点的减少,糖尿病大鼠红细胞的每个细胞胰岛素受体位点比经THC处理的大鼠少。高亲和力(K d1)、低亲和力(K d2)和动力学分析显示,与糖尿病大鼠相比,经THC处理的大鼠红细胞的平均受体亲和力增加。这些结果表明,糖尿病大鼠红细胞膜上的胰岛素受体发生了急性改变。THC治疗显著改善了胰岛素与受体的特异性结合,受体数量和结合亲和力达到接近正常水平。我们的研究提示了THC增加细胞总胰岛素结合位点数量从而导致血浆胰岛素显著增加的机制。THC的作用比姜黄素更显著。