Bousselmame R, Eustache M, Michael-Titus A, Costentin J
Unité de Neuropsychopharmacologie Expérimentale, U.R.A. 1170 du C.N.R.S., Faculté de Médecine et Pharmacie de Rouen, Saint Etienne du Rouvray, France.
Neuropharmacology. 1991 Aug;30(8):865-70. doi: 10.1016/0028-3908(91)90120-z.
The enkephalinase inhibitor thiorphan was infused intracerebroventricularly in rats during 14 days (25 micrograms/5 microliters/hr), inducing an average inhibition of cerebral enkephalinase of about 65%. Animals were tested during the infusion for their response to acetorphan, a parenterally active derivative of thiorphan. When administered intravenously on day 8 of the infusion, acetorphan (5 mg/kg) significantly increased locomotion in chronic saline-infused rats but not in animals receiving thiorphan. Furthermore, when injected at the same dose on day 10, acetorphan did not modify the latency to jump, in the hot plate test, in thiorphan-treated rats, whereas it elicited a significant analgesia in chronic saline-treated controls. These data show that the effects induced by the administration of an enkephalinase inhibitor were diminished after a period of chronic inhibition of the enzyme, suggesting the development of tolerance.
在14天内(25微克/5微升/小时)向大鼠脑室内注入脑啡肽酶抑制剂硫喷妥,导致脑内脑啡肽酶平均抑制约65%。在注入过程中测试动物对阿醋托芬的反应,阿醋托芬是硫喷妥的一种胃肠外活性衍生物。在注入第8天静脉注射时,阿醋托芬(5毫克/千克)可显著增加慢性注入生理盐水大鼠的活动,但对接受硫喷妥的动物无此作用。此外,在第10天以相同剂量注射时,阿醋托芬在硫喷妥处理的大鼠的热板试验中并未改变跳跃潜伏期,而在慢性注入生理盐水处理的对照组中则引起显著的镇痛作用。这些数据表明,在对该酶进行一段时间的慢性抑制后,给予脑啡肽酶抑制剂所诱导的效应减弱,提示耐受性的产生。