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亚慢性氟哌啶醇治疗可降低大鼠黑质中速激肽的体内释放。

Subchronic haloperidol treatment decreases the in vivo release of tachykinins in rat substantia nigra.

作者信息

Lindefors N, Brodin E, Ungerstedt U

机构信息

Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Eur J Pharmacol. 1989 Feb 14;161(1):95-8. doi: 10.1016/0014-2999(89)90185-4.

Abstract

Microdialysis combined with sensitive radioimmunoassays was used to measure the in vivo release of substance P (SP) and neurokinin A (NKA) in the rat substantia nigra. The effect of acute and subchronic haloperidol treatment (0.5 mg/kg) on the basal and potassium-evoked release was studied. No significant effect was observed after a single injection. However, pretreatment with haloperidol for 10 days decreased the potassium-induced release of SP and NKA by 25 and 27%, respectively. The basal overflow of NKA was reduced by 29%, while no significant effect could be seen on the basal release of SP.

摘要

采用微透析技术结合灵敏的放射免疫分析法,测定大鼠黑质中P物质(SP)和神经激肽A(NKA)的体内释放情况。研究了急性和亚慢性氟哌啶醇治疗(0.5mg/kg)对基础释放和钾诱发释放的影响。单次注射后未观察到显著影响。然而,氟哌啶醇预处理10天分别使钾诱导的SP和NKA释放减少了25%和27%。NKA的基础溢出减少了29%,而对SP的基础释放未观察到显著影响。

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