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二甲双胍在非胰岛素依赖型糖尿病中的作用机制。

Mechanism of metformin action in non-insulin-dependent diabetes.

作者信息

Jackson R A, Hawa M I, Jaspan J B, Sim B M, Disilvio L, Featherbe D, Kurtz A B

出版信息

Diabetes. 1987 May;36(5):632-40. doi: 10.2337/diab.36.5.632.

DOI:10.2337/diab.36.5.632
PMID:3552795
Abstract

The mechanism of action of metformin was studied by comparing glucose turnover before and after a 75-g oral glucose load in 10 nonobese men with non-insulin-dependent diabetes mellitus (NIDDM) during metformin and placebo therapy by the combined application of the forearm and double-isotope techniques. During the study, 9 of the 10 patients were regularly receiving glibenclamide therapy. In 5 of the men, the first study was performed during metformin therapy, and the second study was done during placebo administration; in the other 5 subjects, the order was reversed. The interval between the studies was at least 3 mo. The metformin dosage was 1 g twice daily in 9 of the patients and 850 mg thrice daily in the 10th subject. In the basal state, metformin administration reduced plasma glucose levels from 172 +/- 14 to 103 +/- 9 mg/dl (P less than .005), hepatic glucose output (HGO) from 2.67 +/- 0.15 to 2.20 +/- 0.20 mg X kg-1 X min-1 (P less than .02), and forearm glucose uptake (FGU) from 0.106 +/- 0.18 to 0.039 +/- 0.016 mg X 100 ml-1 forearm X min-1 (P less than .005), whereas insulin (23 +/- 6 microU/ml) and lactate (1.56 +/- 0.18 mM) levels were unchanged. Although the oral glucose tolerance curve (OGTC) was significantly lowered by metformin, the incremental area under the curve and the insulin response were unchanged. The systemic appearance of ingested glucose was unaffected by metformin; 64 +/- 2% of the load was recovered peripherally in 3 h.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过联合应用前臂和双同位素技术,在10名非肥胖的非胰岛素依赖型糖尿病(NIDDM)男性患者中,比较了二甲双胍治疗期和安慰剂治疗期口服75克葡萄糖负荷前后的葡萄糖周转率,以此研究二甲双胍的作用机制。研究期间,10名患者中有9名规律接受格列本脲治疗。5名男性患者的首次研究在二甲双胍治疗期进行,第二次研究在安慰剂给药期进行;另外5名受试者顺序相反。两次研究间隔至少3个月。9名患者的二甲双胍剂量为每日2次,每次1克,第10名受试者剂量为每日3次,每次850毫克。在基础状态下,服用二甲双胍使血浆葡萄糖水平从172±14降至103±9毫克/分升(P<0.005),肝葡萄糖输出量(HGO)从2.67±0.15降至2.20±0.20毫克·千克⁻¹·分钟⁻¹(P<0.02),前臂葡萄糖摄取量(FGU)从0.106±0.18降至0.039±0.016毫克·100毫升⁻¹前臂·分钟⁻¹(P<0.005),而胰岛素(23±6微单位/毫升)和乳酸(1.56±0.18毫摩尔)水平未改变。尽管二甲双胍使口服葡萄糖耐量曲线(OGTC)显著降低,但曲线下增量面积和胰岛素反应未改变。摄入葡萄糖的全身表现不受二甲双胍影响;3小时内64±2%的负荷在外周被回收。(摘要截短于250字)

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