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降血糖磺酰脲类药物对犬心血管系统的直接作用。

Direct effect of hypoglycemic sulphonylureas on the cardiovascular system of dogs.

作者信息

Ballagi-Pordány G, Koltai M Z, Aranyi Z, Pogátsa G

机构信息

National Institute of Cardiology, Research Department, Budapest, Hungary.

出版信息

Diabetes Res Clin Pract. 1991 Jan;11(1):47-52. doi: 10.1016/0168-8227(91)90140-9.

Abstract

The effects of first generation sulphonylurea compounds carbutamide, gliclazide and tolbutamide as well as second generation compounds glibenclamide and glipizide on the cardiovascular system were investigated in dogs. Six dogs received each compound intravenously at cumulative dose levels of 74, 296, 1184 mumol/kg of carbutamide and tolbutamide, 0.4, 2.0, 10.0 mumol/kg of glibenclamide and glipizide, and 16, 48 and 144 mumol/kg of gliclazide. Mean arterial blood pressure, myocardial contractile force, cardiac output and heart rate were measured. The rate of change of myocardial contractile force development (positive dF/dt), as well as of myocardial relaxation (negative dF/dt) were measured. The first generation sulphonylureas were found, in dogs, to exert a positive inotropic effect in contrast to second generation compounds. The clinical importance of our findings may be in the potential for the malfunction of the cardiovascular system (based on cardiopathy, neuropathy, atherosclerosis, and obesity), developing in diabetes, to be further impaired by the first generation sulphonylureas. Therefore, second generation sulphonylureas should be preferred in the therapy of type 2 diabetics, if satisfactory metabolic control cannot be achieved by dietary management alone and sulphonylurea treatment becomes necessary.

摘要

在犬类动物中研究了第一代磺酰脲类化合物氨磺丁脲、格列齐特和甲苯磺丁脲以及第二代化合物格列本脲和格列吡嗪对心血管系统的影响。六只犬分别静脉注射每种化合物,氨磺丁脲和甲苯磺丁脲的累积剂量水平为74、296、1184 μmol/kg,格列本脲和格列吡嗪为0.4、2.0、10.0 μmol/kg,格列齐特为16、48和144 μmol/kg。测量平均动脉血压、心肌收缩力、心输出量和心率。测量心肌收缩力发展的变化率(正dF/dt)以及心肌舒张的变化率(负dF/dt)。结果发现,与第二代化合物相比,第一代磺酰脲类化合物在犬类动物中具有正性肌力作用。我们的研究结果的临床意义可能在于,糖尿病中发生的心血管系统功能障碍(基于心脏病、神经病变、动脉粥样硬化和肥胖)有可能因第一代磺酰脲类化合物而进一步受损。因此,如果仅通过饮食管理无法实现满意的代谢控制且必须进行磺酰脲类治疗,那么在2型糖尿病的治疗中应首选第二代磺酰脲类药物。

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