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蛙皮素对大鼠苯丙胺诱导行为及脑区多巴胺释放的不同影响。

Differential effects of ceruletide on amphetamine-induced behaviors and regional dopamine release in the rat.

作者信息

Kihara T, Ikeda M, Matsubara K, Matsushita A

机构信息

Division of Pharmacology, Shionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan.

出版信息

Eur J Pharmacol. 1993 Jan 19;230(3):271-7. doi: 10.1016/0014-2999(93)90561-u.

Abstract

This study concerned the effects of ceruletide, a cholecystokinin (CCK)-related peptide, on amphetamine-stimulated behaviors (hyperlocomotion and stereotypy) and amphetamine-induced dopamine (DA) release from the striatum and the nucleus accumbens of the rat. Also, behavioral alterations due to ceruletide administration were compared with the change in DA release from these areas. Ceruletide 160 micrograms/kg s.c., attenuated hyperlocomotion induced by amphetamine, 1 mg/kg and 3 mg/kg s.c., but had no effect on amphetamine-induced stereotypy. Results from in vivo microdialysis experiments showed that s.c. administration of ceruletide caused a significant inhibition of the amphetamine-induced increase in DA release in the nucleus accumbens but not in the striatum. These neurochemical inhibitory effects of ceruletide disappeared completely with bilateral subdiaphragmatic vagotomy. However, infusion of 1 microM of ceruletide into the nucleus accumbens through the dialysis probe had no effect on amphetamine-induced DA release. These results suggest that the inhibitory effect of peripheral administration of ceruletide on amphetamine-induced hyperlocomotion is closely related to the change in DA release from the nucleus accumbens. In the nucleus accumbens, systemically administered ceruletide acts initially on the peripheral organs and influences the activity of DA terminals via an unknown path related to the vagus. Ceruletide had different actions on the dopaminergic system in the striatum and that in the nucleus accumbens.

摘要

本研究关注促胰液素(一种与胆囊收缩素(CCK)相关的肽)对苯丙胺刺激行为(活动亢进和刻板行为)以及苯丙胺诱导的大鼠纹状体和伏隔核中多巴胺(DA)释放的影响。此外,将促胰液素给药引起的行为改变与这些区域DA释放的变化进行了比较。皮下注射160微克/千克促胰液素可减弱皮下注射1毫克/千克和3毫克/千克苯丙胺诱导的活动亢进,但对苯丙胺诱导的刻板行为无影响。体内微透析实验结果表明,皮下注射促胰液素可显著抑制苯丙胺诱导的伏隔核中DA释放增加,但对纹状体无此作用。促胰液素的这些神经化学抑制作用在双侧膈下迷走神经切断术后完全消失。然而,通过透析探针向伏隔核内注入1微摩尔促胰液素对苯丙胺诱导的DA释放无影响。这些结果表明,外周给予促胰液素对苯丙胺诱导的活动亢进的抑制作用与伏隔核中DA释放的变化密切相关。在伏隔核中,全身给药的促胰液素最初作用于外周器官,并通过与迷走神经相关的未知途径影响DA终末的活性。促胰液素对纹状体和伏隔核中的多巴胺能系统有不同作用。

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