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复方草药制剂SMK001对链脲佐菌素诱导的糖尿病大鼠的抗糖尿病活性:治疗研究

Anti-diabetic activity of SMK001, a poly herbal formula in streptozotocin induced diabetic rats: therapeutic study.

作者信息

Kim Jong Dae, Kang Seock Man, Seo Bu Il, Choi Hae Yun, Choi Hong Sik, Ku Sae Kwang

机构信息

College of Oriental Medicine, Daegu Haany University, Gyeongsan, Republic of Korea.

出版信息

Biol Pharm Bull. 2006 Mar;29(3):477-82. doi: 10.1248/bpb.29.477.

DOI:10.1248/bpb.29.477
PMID:16508149
Abstract

The therapeutic anti-diabetic effect of SMK001, a poly herbal formula was evaluated in the streptozotocin (STZ; 60 mg/kg, single intraperitoneal injection) induced diabetic rats. For therapeutic study, test articles were orally dosed once a day from 21 d after STZ-dosing at 100, 200 and 500 mg/kg/5 ml dosage levels for 4 weeks. The body weight changes, blood and urine glucose level changes were monitored with changes on the pancreas weight, and after sacrifice, the histopathological changes of pancreas and the changes of insulin- and glucagon-producing cells were also observed by immunohistochemistry. The results were compared to that of glibenclamide 5 mg/kg-dosing group. Significantly (p<0.01 or p<0.05) decrease of body weight, blood and urine glucose levels were detected in STZ-induced diabetic animals with disruption and disappearance of pancreatic islets. In addition, significantly (p<0.01) increase of glucagon- and decrease of insulin-producing cells were detected in STZ induced diabetic rats. However, these diabetic changes were significantly (p<0.01 or p<0.05) and dose dependently decreased in SMK001-dosing groups, and SMK001 100 mg/kg showed more favorable effects compared to that of glibenclamide 5 mg/kg. Based on these results, it is considered that SMK001 has favorable effect to inhibit the changes on the blood and urine glucose levels, body weight and the histopathological changes of pancreas in STZ induce diabetes.

摘要

对一种多草药配方SMK001在链脲佐菌素(STZ;60毫克/千克,单次腹腔注射)诱导的糖尿病大鼠中的抗糖尿病治疗效果进行了评估。在治疗研究中,从STZ给药后第21天起,以100、200和500毫克/千克/5毫升的剂量水平,每天口服给药一次,持续4周。监测体重变化、血糖和尿糖水平变化以及胰腺重量变化,在处死动物后,还通过免疫组织化学观察胰腺的组织病理学变化以及胰岛素和胰高血糖素产生细胞的变化。将结果与格列本脲5毫克/千克给药组进行比较。在STZ诱导的糖尿病动物中,检测到体重、血糖和尿糖水平显著(p<0.01或p<0.05)下降,胰岛出现破坏和消失。此外,在STZ诱导的糖尿病大鼠中,检测到胰高血糖素产生细胞显著(p<0.01)增加,胰岛素产生细胞减少。然而,在SMK001给药组中,这些糖尿病变化显著(p<0.01或p<0.05)且呈剂量依赖性降低,与格列本脲5毫克/千克相比,SMK001 100毫克/千克显示出更有利的效果。基于这些结果,认为SMK001对抑制STZ诱导的糖尿病中血糖和尿糖水平变化、体重以及胰腺组织病理学变化具有有利作用。

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