Michaud Nadine, Couture Réjean
Département de Physiologie, Faculté de Médecine, Université de Montréal, C.P. 6128, Succursale centre-ville, Montréal, Qué, Canada H3C 3J7.
Neuropeptides. 2003 Dec;37(6):345-54. doi: 10.1016/j.npep.2003.09.003.
This study examined the intracerebroventricular (i.c.v.) effects of three selective tachykinin receptor antagonists on the cardiovascular and behavioural responses induced by naloxone-precipitated morphine withdrawal in rats. I.c.v. injection of naloxone (10 microg) to morphine pre-treated rats (i.c.v. for 5 days) induced an immediate increase in blood pressure ( approximately 10 mmHg) and behavioural activity (sniffing > rearing > face washing approximately grooming approximately wet dog shake) without causing significant heart rate changes. The prior i.c.v. injection of the NK(1) receptor antagonist (6.5 nmol LY306740) reduced face washing and grooming during morphine withdrawal. NK(2) and NK(3) receptor antagonists (6.5 nmol SR48968 and R820) did not affect behavioural effects, yet the co-injection of the three tachykinin antagonists reduced all behavioural activity. The pressor response was not affected by the selective inhibition of NK(1) and NK(3) receptors while both blood pressure and heart rate were markedly enhanced by SR48968 during morphine withdrawal. The potentiating effect of SR48968 was prevented following simultaneous blockade of the three tachykinin receptors. In addition to confirming the involvement of central tachykinins in behavioural manifestations to morphine withdrawal, data suggest a modulatory function for tachykinins, especially the NK(2) receptor, in brain autonomic control of blood pressure and heart rate in supraspinal noloxone-precipitated withdrawal.
本研究考察了三种选择性速激肽受体拮抗剂对纳洛酮诱发的大鼠吗啡戒断心血管和行为反应的脑室内(i.c.v.)效应。对预先经i.c.v.注射吗啡5天的大鼠i.c.v.注射纳洛酮(10微克),可立即引起血压升高(约10 mmHg)和行为活动增加(嗅探>竖尾>洗脸>梳理毛发>湿狗样抖动),但心率无显著变化。预先i.c.v.注射NK(1)受体拮抗剂(6.5纳摩尔LY306740)可减少吗啡戒断期间的洗脸和梳理毛发行为。NK(2)和NK(3)受体拮抗剂(6.5纳摩尔SR48968和R820)不影响行为效应,但三种速激肽受体拮抗剂共同注射则可抑制所有行为活动。NK(1)和NK(3)受体的选择性抑制不影响升压反应,而SR48968在吗啡戒断期间可显著提高血压和心率。同时阻断三种速激肽受体后,可防止SR48968的增强作用。除了证实中枢速激肽参与吗啡戒断的行为表现外,数据还表明速激肽,尤其是NK(2)受体,在脊髓上纳洛酮诱发的戒断过程中对脑自主控制血压和心率具有调节作用。