Melo L G, Sonnenberg H
Department of Physiology, University of Toronto, Ontario, Canada.
Regul Pept. 1995 Dec 7;60(1):79-87. doi: 10.1016/0167-0115(95)00127-3.
Release of atrial natriuretic factor (ANF) from the heart is primarily affected by myocyte stretch. In addition, ANF release can be modulated by a variety of hormones and neurotransmitters, but the mechanisms involved in such modulation are not completely understood. In the present study, we investigated the effect of inhibition of cyclooxygenase activity on release of ANF from the isolated, spontaneously beating rat heart: (1) during basal conditions; and (2) in response to arginine vasopressin (AVP), acetylcholine (ACh) and angiotensin II (ANG II), in order to determine if cardiac prostaglandin synthesis is involved in modulation of basal and hormone-mediated ANF secretion. Basal secretion in the time controls remained stable for the duration of the experiment. AVP, ACh and ANG II reduced basal secretion significantly by 58 +/- 4%, 51 +/- 6% and 26 +/- 8%, respectively, independently of concomitant changes in coronary flow and heart rate. Inhibition of cyclooxygenase with indomethacin (1 x 10(-5) M) decreased basal ANF release by 38 +/- 6%, indicating that basal secretion requires prostaglandin production. The effects of AVP, ACh and ANG II were maintained during perfusion with indomethacin, suggesting a common mechanism of action which operates via inhibition of cyclooxygenase. Based on our previous findings that the effects of indomethacin, AVP and ACh are overcome by inhibition of NO/EDRF synthesis, we suggest a common mechanism of action by means of which NO/EDRF mediates the effects of these agents by inhibiting cyclooxygenase activity.
心房利钠因子(ANF)从心脏的释放主要受心肌细胞牵张的影响。此外,ANF的释放可受到多种激素和神经递质的调节,但其调节机制尚未完全明确。在本研究中,我们研究了抑制环氧化酶活性对离体自发搏动大鼠心脏ANF释放的影响:(1)在基础条件下;(2)对精氨酸加压素(AVP)、乙酰胆碱(ACh)和血管紧张素II(ANG II)的反应,以确定心脏前列腺素合成是否参与基础和激素介导的ANF分泌调节。在实验过程中,时间对照组的基础分泌保持稳定。AVP、ACh和ANG II分别使基础分泌显著降低58±4%、51±6%和26±8%,与冠状动脉血流和心率的伴随变化无关。用吲哚美辛(1×10⁻⁵ M)抑制环氧化酶使基础ANF释放降低38±6%,表明基础分泌需要前列腺素的产生。在吲哚美辛灌注期间,AVP、ACh和ANG II的作用得以维持,提示存在一种通过抑制环氧化酶起作用的共同作用机制。基于我们之前的发现,即吲哚美辛、AVP和ACh的作用可通过抑制NO/EDRF合成而被克服,我们提出一种共同的作用机制,即NO/EDRF通过抑制环氧化酶活性介导这些药物的作用。