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中脑边缘多巴胺耗竭可逆转苯丙胺对听觉惊吓前脉冲抑制的破坏作用。

Amphetamine disruption of prepulse inhibition of acoustic startle is reversed by depletion of mesolimbic dopamine.

作者信息

Swerdlow N R, Mansbach R S, Geyer M A, Pulvirenti L, Koob G F, Braff D L

机构信息

Department of Psychiatry, University of California, San Diego, La Jolla 92093.

出版信息

Psychopharmacology (Berl). 1990;100(3):413-6. doi: 10.1007/BF02244616.

Abstract

Previous studies have demonstrated that dopamine (DA) agonists disrupt sensorimotor gating as measured by prepulse inhibition (PPI) of the acoustic startle response (ASR) in rats; other reports suggest that this stimulant-induced disruption of PPI may reflect drug-induced increases in ASR amplitude rather than changes in sensorimotor gating. In the current study, 6-hydroxydopamine lesions that depleted dopamine from the nucleus accumbens, olfactory tubercles and anterior striatum reversed the disruption of PPI caused by amphetamine (AMPH), but did not disrupt AMPH potentiation of ASR baseline. These findings strongly suggest that increased mesolimbic DA activity is one substrate of the AMPH-induced disruption of PPI; in contrast, AMPH potentiation of baseline startle amplitude may be independent of mesolimbic DA activation.

摘要

先前的研究表明,多巴胺(DA)激动剂会破坏大鼠听觉惊吓反应(ASR)的前脉冲抑制(PPI)所测量的感觉运动门控;其他报告表明,这种兴奋剂诱导的PPI破坏可能反映了药物诱导的ASR幅度增加,而非感觉运动门控的变化。在当前研究中,6-羟基多巴胺损伤使伏隔核、嗅结节和前纹状体中的多巴胺耗竭,逆转了苯丙胺(AMPH)引起的PPI破坏,但并未破坏AMPH对ASR基线的增强作用。这些发现强烈表明,中脑边缘DA活性增加是AMPH诱导的PPI破坏的一个底物;相比之下,AMPH对基线惊吓幅度的增强作用可能与中脑边缘DA激活无关。

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