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大鼠延髓A5区降压、降心率效应的机制及其与A1区之比较

MECHANISMS UNDERLYING DEPRESSOR AND BRADYCARDIA EFFECTS OF A5-EXCITATION (COMPARED WITH THAT OF A1-EXCITATION) IN RATS

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【作者】 魏东顾蕴辉

【Author】 WEI DONG AND GU(KU) YUN-HUI(Department of Physiology, Beijing Medical University, Beijing)

【机构】 北京医科大学生理教研室北京医科大学生理教研室

【摘要】 在与上一篇论文(关于A1区)相同的条件下,(1) 用谷氨酸钠兴奋大鼠A5区,和A1区类似,也产生明显的降压、降心率效应。(2) 切断双侧颈迷走神经也明显衰减兴奋A5区的心血管作用。(3) 将不同受体阻断剂注入延髓头端腹外侧区对兴奋A5区引起的降压,降心率反应之影响,与A1区比较有所不同:酚妥拉明、心得安、纳洛酮和荷包牡丹碱均能明显衰减A5区的降压、降心率效应(心得安和荷包牡丹碱甚至反转之),表明除α-,β-,GABA受体之外,阿片受体也中介A5区的降压降心率作用。

【Abstract】 Experiments were performed under the same condition described in the accompanying paper. (1) Injection of sodium L-glutamate (Glu) into A5 area of rat induced depressor and bradycardia responses, as Glu-injection into A1 aera did. (2) Bilateral vagotomy also markedly attenuated the cardiovascular effect of Glu-injection into A5. (3) Influences of the receptor blockers injected into rostral ventrolateral medulla (RVL) on the depressor and bradycardia responses of Glu-injection into A5 were slightly different from those of the same receptor blockers administered into RVL: phentolamine,propranolol, naloxone and bicuculline all markedly reduced the depressor and bradycardia effects of As-excitation (propranolol and bicuculline even reversed these effects). These results indicate that not only α-β-, GABA receptors, but also opiate receptors mediate the depressor and bradycardia effects of A5.

【基金】 自然科学基金
  • 【文献出处】 生理学报 ,Acta Physiological Sinica , 编辑部邮箱 ,1989年05期
  • 【被引频次】5
  • 【下载频次】17
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