Pietra C, Poggesi E, Angelico P, Guarneri L, Testa R
Pharmacology Department, RECORDATI S.p.A., Milan, Italy.
Pharmacol Res. 1990 Jul-Aug;22(4):421-32. doi: 10.1016/1043-6618(90)90749-4.
It has been suggested that tricyclic antidepressants such as imipramine, might exert their anti-enuretic action by a blockade of muscarinic receptors in the detrusor muscle of the urinary bladder. We have therefore investigated the effects of two tricyclic (imipramine and nortriptyline) and three atypical (citalopram, amineptine and mianserin) antidepressants on the micturition reflex and muscarinic receptors in rats. The micturition reflex pathway was monitored indirectly by recording the rhythmic intravesical pressure waves which occurred when the bladder was distended and maintained under constant saline-volume. The activity of the antidepressants was correlated to their potencies as antagonists of [3H]QNB binding to rat brain (mainly M1 receptors) and bladder (mainly M2 receptors) membranes, as well as antagonists of carbachol-induced contractions of rat bladder strips. Only imipramine and citalopram dose dependently inhibited the voiding contractions, whereas nortriptyline, imipramine and mianserin (in order of potency) were active both in binding studies and as competitive antagonists of carbachol-induced bladder contractions, but were inactive in inhibiting the micturition reflex. The present data seem to suggest that affinities for muscarinic receptors are unrelated to the inhibition of micturition reflex.
有人提出,三环类抗抑郁药如丙咪嗪,可能通过阻断膀胱逼尿肌中的毒蕈碱受体来发挥其抗遗尿作用。因此,我们研究了两种三环类抗抑郁药(丙咪嗪和去甲替林)和三种非典型抗抑郁药(西酞普兰、安非他明和米安色林)对大鼠排尿反射和毒蕈碱受体的影响。通过记录膀胱在恒量生理盐水充盈并维持时出现的节律性膀胱内压波来间接监测排尿反射通路。抗抑郁药的活性与其作为[3H]QNB与大鼠脑(主要是M1受体)和膀胱(主要是M2受体)膜结合的拮抗剂的效力相关,也与其作为卡巴胆碱诱导的大鼠膀胱条收缩的拮抗剂的效力相关。只有丙咪嗪和西酞普兰剂量依赖性地抑制排尿收缩,而去甲替林﹑丙咪嗪和米安色林(按效力顺序)在结合研究中以及作为卡巴胆碱诱导的膀胱收缩的竞争性拮抗剂均有活性,但在抑制排尿反射方面无活性。目前的数据似乎表明,对毒蕈碱受体的亲和力与排尿反射的抑制无关。