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作 者:朱琳[1] 付蕾[1] 王学彪 李玉民 范儒堂 吕荷叶[3] 李良晨[1]
机构地区:[1]河南医科大学,郑州450052 [2]中原油田总医院 [3]河南省胸科医院
出 处:《河南医学研究》1999年第3期193-196,共4页Henan Medical Research
基 金:国家自然科学基金
摘 要:目的: 对比研究多巴胺1(DA1) 和多巴胺2(DA2) 受体激动剂对兔冠状动脉和肾动脉cAMP生成量的影响。方法: 以cAMP生成量为生化指标,观察了DA1 及DA2 受体激动剂对兔冠状动脉及肾动脉AC活性的影响。结果: 发现DA1 受体激动剂Fenoldopam(FODA) 及DA2 受体激动剂NnpropylNnbutyldoparnine(PBDA) 均可剂量依赖性增加冠状动脉及肾动脉cAMP的生成量。然而,肾动脉cAMP的生成量均显著高于冠状动脉cAMP 的生成量,选择性DA1 受体阻断剂SCH23390 能够阻断FODA及PBDA所引起的cAMP生成量的增加,而DA2 受体阻断剂domperidone 则对PBDA 的这一作用没有影响。心得安阻断β受体后,FODA仍可显著增加cAMP的生成量,但增加的程度却明显降低。结论: 兔肾动脉及冠状动脉上都存在有刺激AC活性的DA1 受体,但冠状动脉DA1 受体的位点数比肾动脉DA1 位点数要少得多;冠状动脉DA1 受体的作用比肾动脉要弱。Objective: The purpose of this study is to reserch the effects of D 1 and D 2 receptor agonists on rabbit coronary and renal arteries.Methods: cAMP content were measured as a biomedical index of DA receptor function. Results: It was found that both the selective D 1 receptor agonist, fenoldopam, and the D 2 receptor agonist, propyl propyl butyl doparnine(PBDA), induced a dose related increases in cAMP formation in coronary and renal arteries; however, the magnitude of increase in the renal artery was remarkably greater than that in the coronary artery. The stimulator effect on AC activity of fenoldopam was significanly more potent than that of PBDA. The selective D 1 receptor antagonist, SCH 23390, blocked fenoldopam and PBDA induced cAMP production, while the selective D 2 receptor antagonist, domperidone, was without effect on the increase of cAMP elicited by PBDA. After β adrenergic blockade with propranolol, fenoldopam still increased the cAMP level significantly but to a much lesser degree.Conclusion: The existence of postsynaptic D 2 receptors associated with stimulation of AC activity in both renal and coronary arteries. However, there are much fewer receptor sites in the coronary artery than in the renal atrery, suggesting less physiological importance of such receptors in the coronary artery than in the renal artery.
分 类 号:R331.33[医药卫生—人体生理学]
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