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胆囊收缩素对中脑边缘通路多巴胺调节作用的行为学证据。

Behavioral evidence for cholecystokinin modulation of dopamine in the mesolimbic pathway.

作者信息

Crawley J H

出版信息

Prog Clin Biol Res. 1985;192:131-8.

PMID:4080706
Abstract

Cholecystokinin octapeptide sulfate (CCK) injected bilaterally into the nucleus accumbens significantly potentiated dopamine-induced hyperlocomotion and apomorphine-induced stereotypy. CCK had no effect alone on locomotion or stereotypy, suggesting that this peptide acts as a neuromodulator. CCK did not potentiate dopamine or apomorphine when injected into the caudate nucleus, where CCK and DA are located in separate neurons, indicating that CCK potentiation of dopamine is specific for the mesolimbic pathway, where CCK and dopamine co-exist in the same neuron. Unsulfated CCK had no effect alone or in conjunction with dopamine or apomorphine, suggesting that the facilitory effect of CCK on dopamine-mediated behaviors is specific for the sulfated form of CCK.

摘要

双侧注射到伏隔核的硫酸缩胆囊素八肽(CCK)显著增强了多巴胺诱导的运动亢进和阿扑吗啡诱导的刻板行为。CCK单独对运动或刻板行为没有影响,表明该肽作为一种神经调节剂发挥作用。当注射到尾状核时,CCK不会增强多巴胺或阿扑吗啡的作用,在尾状核中CCK和多巴胺位于不同的神经元中,这表明CCK对多巴胺的增强作用对中脑边缘通路具有特异性,在该通路中CCK和多巴胺共存于同一神经元中。未硫酸化的CCK单独或与多巴胺或阿扑吗啡联合使用均无作用,表明CCK对多巴胺介导行为的促进作用对CCK的硫酸化形式具有特异性。

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