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二甲双胍对内脏床葡萄糖代谢的影响。

Effect of metformin on glucose metabolism in the splanchnic bed.

作者信息

Bailey C J, Wilcock C, Day C

机构信息

Department of Pharmaceutical Sciences, Aston University, Birmingham.

出版信息

Br J Pharmacol. 1992 Apr;105(4):1009-13. doi: 10.1111/j.1476-5381.1992.tb09093.x.

Abstract
  1. Use of the antihyperglycaemic agent, metformin, is often associated with a small rise in circulating lactate. This study investigates the source of the lactate and examines the effect of metformin on glucose metabolism by the intestine and liver of rats. 2. Changes in plasma glucose and lactate were measured in the inferior vena cava (IVC), hepatic portal vein (HPV), hepatic vein (HV) and aorta (A) after intrajejunal administration of metformin (50 and 250 mg kg-1) without and with glucose (2 g kg-1). 3. Metformin 250 mg kg-1 reduced the hyperglycaemic response to a glucose challenge, associated with a greater reduction of glucose concentrations in the HPV (average decrease of 33% at 60 and 120 min) than at other sites. 4. Both doses of metformin increased lactate concentrations in the glucose-loaded state: the highest concentration (2.5 fold increase) was recorded in the HPV 60 min after administration of 250 mg kg-1 metformin, with a high lactate concentration persisting in the HV at 120 min. Metformin 250 mg kg-1 also increased lactate concentrations in the basal state, with highest concentrations (2 fold increase) in the HPV. 5. Two hours after intrajejunal administration of metformin, 50 mg kg-1, rings of tissue from the small intestine showed an average 22% decrease in glucose oxidation ([14C]-glucose conversion to 14CO2) and a 10% increase in lactate production. Since glucose metabolism in the gut is predominantly anaerobic, metformin caused an overall 9.5% increase of intestinal glucose utilization.6. Metformin, 10-6 and I0- mol 1', did not significantly alter glucose oxidation or lactate production by isolated hepatocytes, but a very high concentration of metformin (102 mol 1') increased lactate production by 60%.7. The results support the view that metformin increased intestinal glucose utilization and lactate production by the intestine. Under basal conditions there was net extraction of lactate by the liver but not after an enteral glucose load.
摘要
  1. 抗高血糖药物二甲双胍的使用通常会使循环乳酸水平略有升高。本研究调查了乳酸的来源,并研究了二甲双胍对大鼠肠道和肝脏葡萄糖代谢的影响。2. 在空肠内给予二甲双胍(50和250mg kg-1),分别在有无葡萄糖(2g kg-1)的情况下,测量下腔静脉(IVC)、肝门静脉(HPV)、肝静脉(HV)和主动脉(A)中的血糖和乳酸变化。3. 二甲双胍250mg kg-1减轻了对葡萄糖刺激的高血糖反应,与HPV中葡萄糖浓度的降低幅度(60和120分钟时平均降低33%)相比,其他部位的降低幅度更大。4. 两种剂量的二甲双胍均会使葡萄糖负荷状态下的乳酸浓度升高:给予250mg kg-1二甲双胍60分钟后,HPV中的乳酸浓度最高(升高2.5倍),120分钟时HV中的乳酸浓度仍维持在较高水平。二甲双胍250mg kg-1还会使基础状态下的乳酸浓度升高,HPV中的浓度最高(升高2倍)。5. 空肠内给予二甲双胍50mg kg-1两小时后,小肠组织环显示葡萄糖氧化([14C] -葡萄糖转化为14CO2)平均降低22%,乳酸生成增加10%。由于肠道中的葡萄糖代谢主要是无氧代谢,二甲双胍使肠道葡萄糖利用率总体提高了9.5%。6. 10-6和10-5mol 1-1的二甲双胍对分离的肝细胞的葡萄糖氧化或乳酸生成没有显著影响,但非常高浓度的二甲双胍(10-2mol 1-1)使乳酸生成增加了60%。7. 结果支持以下观点:二甲双胍增加了肠道葡萄糖利用率和肠道乳酸生成。在基础条件下,肝脏会净摄取乳酸,但肠内葡萄糖负荷后则不会。

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