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β-抑制蛋白2在可卡因诱导的奖赏行为中起关键作用。

[β-arrestin2 plays a critical role in reward behaviors induced by cocaine].

作者信息

Yin Xu-Ming, Huang Bing, Ma Lan, Liu Xing

机构信息

Pharmacology Research Center, Shanghai Medical College, Fudan University, Shanghai 200032, China.

出版信息

Sheng Li Xue Bao. 2013 Apr 25;65(2):178-84.

Abstract

Besides its role in desensitization and internalization of receptors, β-arrestin2 facilitates G protein-independent signaling through its ability to scaffold various signaling molecules. β-arrestin2 is widely distributed in the central nervous system, and mediates signal transduction of brain circuit. The aim of the present study was to investigate the role of β-arrestin2 in reward behaviors induced by cocaine. We assessed the conditioned place preference (CPP) induced by low (10 mg/kg), moderate (20 mg/kg) and high (30 mg/kg) doses of cocaine in Arrb2(-/-) mice and Arrb2(+/+) controls. In the Arrb2(-/-) mice, moderate and high, but not low, dose of cocaine induced pronounced increases of CPP scores, which were higher than those in the Arrb2(+/+) mice. Moreover, cocaine-induced locomotor activity was significantly lower in Arrb2(-/-) mice than that of Arrb2(+/+) littermate controls. Taken together, our results suggest a potential role of β-arrestin2 in the cocaine-induced rewarding behaviors.

摘要

除了在受体脱敏和内化过程中发挥作用外,β-抑制蛋白2还通过其搭建各种信号分子支架的能力促进不依赖G蛋白的信号传导。β-抑制蛋白2广泛分布于中枢神经系统,并介导脑回路的信号转导。本研究的目的是探讨β-抑制蛋白2在可卡因诱导的奖赏行为中的作用。我们评估了低剂量(10毫克/千克)、中等剂量(20毫克/千克)和高剂量(30毫克/千克)可卡因在Arrb2基因敲除小鼠和野生型对照小鼠中诱导的条件性位置偏爱(CPP)。在Arrb2基因敲除小鼠中,中等剂量和高剂量而非低剂量的可卡因诱导CPP得分显著增加,且高于野生型小鼠。此外,Arrb2基因敲除小鼠中可卡因诱导的运动活性显著低于其野生型同窝对照小鼠。综上所述,我们的结果表明β-抑制蛋白2在可卡因诱导的奖赏行为中具有潜在作用。

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