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[AH-9的降血糖作用]

[The hypoglycemic effect of AH-9].

作者信息

Jiang Z, Xie M

机构信息

Institute of Materia Medica, CAMS and PUMC, Beijing.

出版信息

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1993 Aug;15(4):235-41.

PMID:8168201
Abstract

AH-9 is an acylhydrazine compound with hypoglycemic effects in normal mice, alloxan-induced diabetic mice and spontaneously diabetic KK mice. In terms of equi-molar doses (0.3 mmol/kg po), AH-9 was found to be more potent than phenfornin and glicalazide (diamicron) in normal mice. Insulin resistance was shown to be improved in spontaneously diabetic KK mice and hydrocortisone-induced insulin resistant mice after treatment with AH-9. The LD 50 of AH-9 given orally to mice was found to be 956 mg/kg (about 18 times its effective dose). Studies on the hypoglycemic mechanism of AH-9 (insulin release, insulin receptor and post-receptor) showed that AH-9 did not influence serum insulin levels in mice. But, in in vivo experiments, AH-9 appeared to promote the capacity and affinity of insulin receptors in mouse liver plasma membranes. AH-9 was also found to antagonize the elevation of blood glucose level and liver glycogen content caused by alanine injection. AH-9 was shown to enhance the conversion of U-14C-glucose to 14CO2 in mouse epididymal fat tissue in vitro. According to the above results, the hypoglycemic action of AH-9 might be due to: 1) increasing the capacity and affinity of insulin receptors; 2) directly enhancing glucose aerobic oxidation; and 3) inhibiting gluconeogenesis.

摘要

AH-9是一种酰肼化合物,对正常小鼠、四氧嘧啶诱导的糖尿病小鼠和自发性糖尿病KK小鼠均有降血糖作用。在等摩尔剂量(0.3 mmol/kg口服)下,发现AH-9在正常小鼠中比苯乙双胍和格列齐特(达美康)更有效。在自发性糖尿病KK小鼠和氢化可的松诱导的胰岛素抵抗小鼠中,用AH-9治疗后胰岛素抵抗得到改善。给小鼠口服AH-9的半数致死量为956 mg/kg(约为其有效剂量的18倍)。对AH-9降血糖机制(胰岛素释放、胰岛素受体和受体后机制)的研究表明,AH-9不影响小鼠血清胰岛素水平。但是,在体内实验中,AH-9似乎能提高小鼠肝细胞膜上胰岛素受体的能力和亲和力。还发现AH-9能拮抗丙氨酸注射引起的血糖水平升高和肝糖原含量增加。在体外实验中,AH-9能增强小鼠附睾脂肪组织中U-14C-葡萄糖向14CO2的转化。根据上述结果,AH-9的降血糖作用可能是由于:1)增加胰岛素受体的能力和亲和力;2)直接增强葡萄糖有氧氧化;3)抑制糖异生。

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