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大鼠黑质内注射吗啡和脑啡肽类似物FK 33-824诱导的对侧转圈行为

Contralateral circling behaviour induced by intranigral injection of morphine and enkephalin analogue FK 33-824 in rats.

作者信息

Kaakkola S

出版信息

Acta Pharmacol Toxicol (Copenh). 1980 Nov;47(5):385-93. doi: 10.1111/j.1600-0773.1980.tb01577.x.

Abstract

Contralateral circling behaviour induced by intranigral injection of morphine or an enkephalin analogue, FK 33-824, was studied in rats. Both morphine (0.625-10.0 micrograms) and FK 33-824 (1.25-40.0 ng) evoked the same kind of contralateral circling behaviour when injected into the substantia nigra. FK 33-824 was about 1000 times more potent than morphine and its effect lasted a little longer. Pretreatment with naloxone (5 mg/kg subcutaneously or 1 microgram intranigrally) almost completely blocked the circling induced by intranigral morphine or FK 33-824. The lesion of the ipsilateral nigrostriatal dopaminergic pathway with 6-hydroxydopamine significantly antagonized both morphine- and FK 33-824-induced circling. Pretreatment with d-amphetamine (1 mg/kg intraperitoneally) significantly increased the intensity of the circling induced by morphine or FK 33-824, and pretreatment with haloperidol (0.5 mg/kg subcutaneously) attenuated this intensity. Pretreatment with pilocarpine (10 mg/kg intraperitoneally) or mecamylamine (2 mg/kg intraperitoneally) inhibited the circling, whereas pretreatment with atropine (10 mg/kg intraperitoneally) or nicotine (0.2 mg/kg subcutaneously) increased morphine- and FK 33-824-induced circling. Pretreatment with muscimol (0.5 mg/kg subcutaneously) did not significantly increase morphine-induced circling but tended to increase FK 33-824-induced circling. Pretreatment with bicuculline (3 mg/kg intraperitoneally) slightly but significantly inhibited both morphine- and FK 33-824-induced circling. Pretreatment with strychnine (0.25 mg/kg intraperitoneally) did not modify the circling induced by morphine or FK 33-824. The results show that the contralateral circling behaviour induced by intranigral injection of morphine and FK 33-824 seems to be mediated by the activation of the dopaminergic nigrostriatal system.

摘要

研究了在大鼠中,经黑质内注射吗啡或脑啡肽类似物FK 33 - 824所诱导的对侧转圈行为。当将吗啡(0.625 - 10.0微克)和FK 33 - 824(1.25 - 40.0纳克)注射到黑质时,二者均诱发了同一种对侧转圈行为。FK 33 - 824的效力比吗啡强约1000倍,且其作用持续时间稍长。用纳洛酮(皮下注射5毫克/千克或黑质内注射1微克)预处理几乎完全阻断了黑质内注射吗啡或FK 33 - 824所诱导的转圈行为。用6 - 羟基多巴胺损伤同侧黑质纹状体多巴胺能通路可显著拮抗吗啡和FK 33 - 824所诱导的转圈行为。用右旋苯丙胺(腹腔注射1毫克/千克)预处理可显著增强吗啡或FK 33 - 824所诱导的转圈行为强度,而用氟哌啶醇(皮下注射0.5毫克/千克)预处理则减弱了这种强度。用毛果芸香碱(腹腔注射10毫克/千克)或美加明(腹腔注射2毫克/千克)预处理可抑制转圈行为,而用阿托品(腹腔注射10毫克/千克)或尼古丁(皮下注射0.2毫克/千克)预处理则增强了吗啡和FK 33 - 824所诱导的转圈行为。用蝇蕈醇(皮下注射0.5毫克/千克)预处理并未显著增强吗啡所诱导的转圈行为,但倾向于增强FK 33 - 824所诱导的转圈行为。用荷包牡丹碱(腹腔注射3毫克/千克)预处理轻微但显著地抑制了吗啡和FK 33 - 824所诱导的转圈行为。用士的宁(腹腔注射0.25毫克/千克)预处理并未改变吗啡或FK 33 - 824所诱导的转圈行为。结果表明,黑质内注射吗啡和FK 33 - 824所诱导的对侧转圈行为似乎是由多巴胺能黑质纹状体系统的激活介导的。

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