Biotechnology High School of Sfax (ISBS), Soukra Km 4.5, P.O. Box 261, Sfax 3052, Tunisia.
J Physiol Biochem. 2011 Mar;67(1):121-8. doi: 10.1007/s13105-010-0056-0. Epub 2010 Nov 16.
Diabetes mellitus, with its attendant disorders and dysfunctional behaviors, constitutes a growing concern to the population of the world. With this concern in mind, the present study investigated the anti-diabetic and hypolipedimic potential of 17β-estradiol (called E2), particularly in terms of its inhibitory effects on maltase, sucrase, lactase, and lipase activities in the intestine of surviving diabetic rats. The findings revealed that this supplement helped protect the β cells of the rats from death and damage. Interestingly, E2 induced considerable decreases of 29%, 46%, 42%, and 84% in the activities of intestinal maltase, lactase, sucrase, and lipase, respectively. The E2 extract also decreased the glucose, triglyceride, and total cholesterol rates in the plasma of diabetic rats by 39%, 27%, and 53%, respectively, and increased the HDL-cholesterol level by 74%, which helped maintain the homeostasis of blood lipid. When compared to those of the untreated diabetic rats, the superoxide dismutase, catalase, and glutathione peroxidase levels in the pancreas of the rats treated with this supplement were also enhanced by 330%, 170%, and 301%, respectively. A significant decrease was also observed in the lipid peroxidation level and lactate dehydrogenase activity in the pancreas of diabetic rats after E2 administration. Overall, the findings presented in this study demonstrate that E2 has both a promising potential with regard to the inhibition of intestinal maltase, sucrase, lactase, and lipase activities, and a valuable hypoglycemic and hypolipidemic function, which make it a potential strong candidate for industrial application as apharmacological agent for the treatment and prevention of hyperlipidemia, obesity, and cardiovascular diseases.
糖尿病及其伴随的紊乱和功能障碍行为,是全世界人口日益关注的问题。考虑到这一关注点,本研究调查了 17β-雌二醇(称为 E2)的抗糖尿病和降血脂潜力,特别是其对存活糖尿病大鼠肠道中麦芽糖酶、蔗糖酶、乳糖酶和脂肪酶活性的抑制作用。研究结果表明,这种补充剂有助于保护大鼠的β细胞免受死亡和损伤。有趣的是,E2 诱导肠道麦芽糖酶、乳糖酶、蔗糖酶和脂肪酶的活性分别显著降低 29%、46%、42%和 84%。E2 提取物还使糖尿病大鼠血浆中的葡萄糖、甘油三酯和总胆固醇水平分别降低 39%、27%和 53%,并使 HDL-胆固醇水平升高 74%,有助于维持血液脂质的体内平衡。与未治疗的糖尿病大鼠相比,用这种补充剂治疗的大鼠胰腺中的超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶水平也分别提高了 330%、170%和 301%。E2 给药后,糖尿病大鼠胰腺中的脂质过氧化水平和乳酸脱氢酶活性也显著降低。总的来说,本研究的结果表明,E2 具有抑制肠道麦芽糖酶、蔗糖酶、乳糖酶和脂肪酶活性的巨大潜力,同时具有降血糖和降血脂的作用,使其成为治疗和预防高血脂症、肥胖症和心血管疾病的潜在强力候选药物。