Hicks K K, Seifen E, Stimers J R, Kennedy R H
Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock 72205, USA.
Am J Physiol. 1997 Oct;273(4):H1888-93. doi: 10.1152/ajpheart.1997.273.4.H1888.
Experiments were designed to determine whether insulin-dependent diabetes mellitus (IDDM) alters direct chronotropic effects of adrenergic and cholinergic agonists and whether the observed changes are associated with hyperglycemia or combined hyperglycemia and ketoacidosis. Diabetes was induced by intravenous administration of 45, 50, or 65 mg/kg streptozotocin (STZ). Rats treated with 65 mg/kg STZ had higher levels of blood glucose and ketones compared with the levels of the other groups. Right atria were isolated 12 wk after administration of STZ and bathed in Krebs-Henseleit solution. Basal spontaneous pacemaker rate was diminished in preparations isolated from diabetic rats. The maximum pacemaker rate observed during exposure to isoproterenol or norepinephrine was also depressed in preparations from diabetic animals; however, the increase in rate and half-maximal effective concentration values for each agent were not affected. The sensitivity to the negative chronotropic action of acetylcholine was enhanced by IDDM, whereas the response to carbachol (a cholinergic agonist not readily metabolized by acetylcholinesterase) was not changed. No significant differences were observed when we compared preparations isolated from diabetic animals with and without ketoacidosis. In summary, these data suggest 1) that IDDM is associated with a diminished basal spontaneous pacemaker without changes in the responsiveness to adrenergic and cholinergic receptor activation and 2) that ketoacidosis does not play a role in the observed alterations.
实验旨在确定胰岛素依赖型糖尿病(IDDM)是否会改变肾上腺素能和胆碱能激动剂的直接变时作用,以及观察到的变化是否与高血糖或合并的高血糖和酮症酸中毒有关。通过静脉注射45、50或65mg/kg链脲佐菌素(STZ)诱导糖尿病。与其他组相比,接受65mg/kg STZ治疗的大鼠血糖和酮水平更高。在注射STZ 12周后分离右心房,并置于Krebs-Henseleit溶液中。从糖尿病大鼠分离的标本中,基础自发起搏率降低。在暴露于异丙肾上腺素或去甲肾上腺素期间观察到的最大起搏率在糖尿病动物的标本中也降低;然而,每种药物的心率增加和半数最大有效浓度值不受影响。IDDM增强了对乙酰胆碱负性变时作用的敏感性,而对卡巴胆碱(一种不易被乙酰胆碱酯酶代谢的胆碱能激动剂)的反应没有改变。当我们比较有无酮症酸中毒的糖尿病动物分离的标本时,未观察到显著差异。总之,这些数据表明:1)IDDM与基础自发起搏率降低有关,而对肾上腺素能和胆碱能受体激活的反应性没有变化;2)酮症酸中毒在观察到的改变中不起作用。