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选择性非肽类神经降压素受体拮抗剂SR 48692对小鼠和大鼠两种多巴胺依赖性行为反应的影响。

Effects of SR 48692, a selective non-peptide neurotensin receptor antagonist, on two dopamine-dependent behavioural responses in mice and rats.

作者信息

Poncelet M, Souilhac J, Gueudet C, Terranova J P, Gully D, Le Fur G, Soubrié P

机构信息

Sanofi Recherche, Neuropsychiatry Department, Montpellier, France.

出版信息

Psychopharmacology (Berl). 1994 Oct;116(2):237-41. doi: 10.1007/BF02245067.

Abstract

One major mechanism underlying the central action of neurotensin is an interaction with the function of dopamine (DA)-containing neurons. In addition, direct or indirect DA agonists have been reported to promote neurotensin release. We have found that SR 48692, a non-peptide neurotensin receptor antagonist (0.04-0.64 mg/kg orally), antagonizes (50-65%) yawning induced by apomorphine (0.07 mg/kg SC) or bromocriptine (2 mg/kg IP) in rats, and turning behaviour induced by intrastriatal injection of apomorphine (0.25 micrograms), (+) SKF 38393 (0.1 micrograms), bromocriptine (0.01 ng) or (+) amphetamine (10 micrograms) in mice. Other apomorphine-induced effects in mice and rats such as climbing, hypothermia, hypo- and hyper-locomotion, penile erections and stereotypies were not significantly modified by SR 48692. Taken together, these data suggest that neurotensin may play a permissive role in the expression of some but not all behavioural responses to DA receptor stimulation.

摘要

神经降压素中枢作用的一个主要机制是与含多巴胺(DA)的神经元功能相互作用。此外,据报道直接或间接的DA激动剂可促进神经降压素释放。我们发现,SR 48692,一种非肽类神经降压素受体拮抗剂(口服剂量为0.04 - 0.64 mg/kg),可拮抗(50 - 65%)阿扑吗啡(皮下注射0.07 mg/kg)或溴隐亭(腹腔注射2 mg/kg)诱导的大鼠打哈欠,以及纹状体内注射阿扑吗啡(0.25微克)、(+)SKF 38393(0.1微克)、溴隐亭(0.01纳克)或(+)苯丙胺(10微克)诱导的小鼠旋转行为。SR 48692对阿扑吗啡在小鼠和大鼠中诱导的其他效应,如攀爬、体温过低、运动减少和增加、阴茎勃起及刻板行为,没有显著影响。综上所述,这些数据表明神经降压素可能在对DA受体刺激的某些而非所有行为反应的表达中起允许作用。

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