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胰岛素模拟物钒-聚(γ-谷氨酸)复合物对糖尿病大鼠模型的影响。

Effects of insulin-mimetic vanadyl-poly(gamma-glutamic acid) complex on diabetic rat model.

机构信息

Laboratory of Molecular Biology, School of Life Science, East China Normal University, 3663 Zhongshan North Road, Shanghai 200062, PR China.

出版信息

J Pharm Sci. 2010 Jul;99(7):3041-7. doi: 10.1002/jps.22071.

Abstract

Poly-gamma-glutamic acid (gamma-PGA) prepared by fermentation of microbe was used as drug carrier for vanadium sulfate to obtain vanadyl-poly-gamma-glutamic acid (VO-gamma-PGA) complex. The FI-IR spectrum of the complex demonstrated that the expected VO-gamma-PGA complex is formed by the coordination of VO(2+) through the side chain carboxylic groups of the gamma-PGA. Studies of the complex in treating type I diabetes were carried out on alloxan induced diabetes rats. The results of treating the rats in 2 weeks and then stopping administration for 10 days showed that VO-gamma-PGA can effectively lower blood glucose levels of diabetic rats during administration. But after ceasing treatment there were no differences between groups in blood glucose level and water intake. The results of oral glucose tolerance and some serum parameters also demonstrated that VO-gamma-PGA was more effective than vanadium sulfate in treating diabetic rats.

摘要

聚-γ-谷氨酸(γ-PGA)由微生物发酵制备,用作硫酸氧钒的药物载体,以获得氧钒-聚-γ-谷氨酸(VO-γ-PGA)复合物。该复合物的 FI-IR 光谱表明,预期的 VO-γ-PGA 复合物是通过 γ-PGA 的侧链羧酸基团与 VO(2+)的配位形成的。对复合物在治疗 I 型糖尿病方面的研究是在链脲佐菌素诱导的糖尿病大鼠上进行的。在 2 周的治疗后停止给药 10 天的结果表明,VO-γ-PGA 在给药期间可有效降低糖尿病大鼠的血糖水平。但停止治疗后,各组间血糖水平和饮水量无差异。口服葡萄糖耐量和一些血清参数的结果也表明,VO-γ-PGA 在治疗糖尿病大鼠方面比硫酸氧钒更有效。

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