Petersen J S, DiBona G F
Department of Internal Medicine, University of Iowa College of Medicine, Iowa City 52242.
Hypertension. 1994 Jun;23(6 Pt 2):924-30. doi: 10.1161/01.hyp.23.6.924.
To examine whether furosemide elicits a cardiorenal reflex response via stimulation of cardiac afferents, furosemide was administered intrapericardially in sinoaortic denervated rats. The role of vagal afferents was evaluated by intrapericardial (IPC) administration of furosemide before and after bilateral vagotomy. The role of cardiac sympathetic afferents was examined by IPC administration of furosemide before and after IPC lidocaine blockade in rats with bilateral vagotomy. Low-dose furosemide (10 micrograms) elicited renal sympathoinhibition, whereas high-dose furosemide (1000 micrograms) produced a rapid and transient change in efferent renal sympathetic nerve activity of either inhibitory (19/49, or 39%) or excitatory (30/49, or 61%) nature. The responses were not affected by vagotomy but were abolished by IPC lidocaine blockade. In rats with a renal sympathoinhibitory response to IPC administration of 1000 micrograms furosemide, both the hypotensive and sympathoinhibitory responses were inhibited by indomethacin, whereas indomethacin did not affect reflex responses in rats showing a renal sympathoexcitatory response to IPC injection of 1000 micrograms furosemide. We conclude that furosemide elicits a nonuniform reflex response mediated via cardiac sympathetic afferents of which the renal sympathoinhibitory response is dependent on intact cyclooxygenase function.
为了研究呋塞米是否通过刺激心脏传入神经引发心肾反射反应,在去窦弓神经支配的大鼠心包腔内注射呋塞米。通过在双侧迷走神经切断术前和术后心包腔内注射呋塞米来评估迷走神经传入神经的作用。通过在双侧迷走神经切断的大鼠心包腔内注射利多卡因阻断前后心包腔内注射呋塞米来研究心脏交感神经传入神经的作用。低剂量呋塞米(10微克)引起肾交感神经抑制,而高剂量呋塞米(1000微克)使肾交感神经传出神经活动迅速发生短暂变化,性质为抑制性(19/49,或39%)或兴奋性(30/49,或61%)。这些反应不受迷走神经切断术的影响,但心包腔内注射利多卡因阻断可消除这些反应。在对心包腔内注射1000微克呋塞米有肾交感神经抑制反应的大鼠中,消炎痛可抑制降压反应和交感神经抑制反应,而消炎痛对心包腔内注射1000微克呋塞米表现出肾交感神经兴奋反应的大鼠的反射反应没有影响。我们得出结论,呋塞米引发一种通过心脏交感神经传入神经介导的不均匀反射反应,其中肾交感神经抑制反应依赖于完整的环氧化酶功能。