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β-(酪氨酰9)促黑素-(9-18)对用阿托品或普萘洛尔预处理的大鼠主动回避和旷场行为的影响。

The effect of beta-(Tyr9)melanotropin-(9-18) on the active avoidance and open-field behavior on rats pretreated with atropine or propranolol.

作者信息

Vécsei L, Bollók I, Telegdy G, Coy D H, Schally A V

出版信息

Pharmacol Res Commun. 1984 Apr;16(4):369-79. doi: 10.1016/s0031-6989(84)80005-3.

Abstract

beta-(Tyr9)melanotropin-(9-18) inhibited the extinction of active avoidance behavior. The muscarinic cholinergic blocker atropine did not influence the peptide-induced inhibition, whereas the beta-receptor blocker propranolol decreased it. Furthermore, the peptide increased the ambulation of the animals. Neither the muscarinic blocker nor the beta-blocker had any action on this effect of beta-(Tyr9)melanotropin-(9-18). Atropine markedly decreased the defecation of the animals, and this effect was not influenced by the peptide. The results suggest that the beta-receptors play an important role in the inhibition of extinction induced by the peptide, however, the actions on the open-field activity are mediated by different mechanisms.

摘要

β-(酪氨酰9)促黑素-(9-18)抑制主动回避行为的消退。毒蕈碱型胆碱能阻滞剂阿托品不影响该肽诱导的抑制作用,而β受体阻滞剂普萘洛尔则降低这种抑制作用。此外,该肽增加了动物的走动。毒蕈碱阻滞剂和β阻滞剂对β-(酪氨酰9)促黑素-(9-18)的这种作用均无影响。阿托品显著减少动物的排便,且该作用不受该肽的影响。结果表明,β受体在该肽诱导的消退抑制中起重要作用,然而,对旷场活动的作用是由不同机制介导的。

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The interaction between beta-[Tyr9]melanotropin-(9-18), haloperidol and amphetamine in different behavior tests of rats.
Pharmacol Biochem Behav. 1982 Jul;17(1):15-8. doi: 10.1016/0091-3057(82)90255-6.

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