Ventura C, Muscari C, Spampinato S, Bernardi P, Caldarera C M
Peptides. 1987 Jul-Aug;8(4):695-9. doi: 10.1016/0196-9781(87)90045-3.
In isolated rat hearts, the infusion for 10 min of 10(-10), 10(-8) or 10(-6) M (-)naloxone affected the cardiac function by markedly increasing the coronary pressure and by reducing both the heart rate and the developed tension. A lower dose of (-)naloxone (10(-11) M) or a dose of 10(-6) M (+)naloxone, did not modify the cardiac function. Morphine (10(-6) or 10(-5) M) and 10(-10), 10(-8) or 10(-6) M methionine-enkephalin or leucine-enkephalin, both significantly reduced the coronary pressure of the isolated rat hearts, during the first 4-6 min of perfusion, but the coronary pressure progressively increased above the control value in the last 4 min of perfusion. Each opioid also influenced the mechanical activity of the isolated rat heart, by significantly lowering both the heart rate and the developed tension. (-)Naloxone, at all the doses tested, was only able to antagonise the hypotensive effect induced by the opioids on the coronary pressure and was ineffective in counteracting the negative inotropic and chronotropic effects produced by each opioid. The perfusion in the presence of (+)naloxone (even at a dose of 10(-6) M) did not affect the opioid-induced changes on both the coronary pressure and the mechanical performance of the isolated heart.
在离体大鼠心脏中,灌注10分钟10(-10)、10(-8)或10(-6)M的(-)纳洛酮会影响心脏功能,显著增加冠状动脉压力,同时降低心率和心肌收缩张力。较低剂量的(-)纳洛酮(10(-11)M)或10(-6)M的(+)纳洛酮则不会改变心脏功能。吗啡(10(-6)或10(-5)M)以及10(-10)、10(-8)或10(-6)M的甲硫氨酸脑啡肽或亮氨酸脑啡肽,在灌注的最初4 - 6分钟内均显著降低离体大鼠心脏的冠状动脉压力,但在灌注的最后4分钟内冠状动脉压力逐渐升高至高于对照值。每种阿片类药物还通过显著降低心率和心肌收缩张力来影响离体大鼠心脏的机械活动。在所测试的所有剂量下,(-)纳洛酮仅能拮抗阿片类药物对冠状动脉压力的降压作用,而无法抵消每种阿片类药物产生的负性肌力和负性变时作用。在(+)纳洛酮存在下(即使剂量为10(-6)M)进行灌注,并不会影响阿片类药物对离体心脏冠状动脉压力和机械性能的改变。