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新生大鼠前脑去甲肾上腺素的6-羟基多巴胺损伤并不能消除性腺激素操纵行为效应的关键期。

Neonatal 6-hydroxydopamine lesion of forebrain norepinephrine does not eliminate critical period for behavioral effects of gonadal hormone manipulation.

作者信息

Pappas B A, Armstrong B

出版信息

Brain Res. 1986 May;391(2):310-4. doi: 10.1016/0165-3806(86)90299-3.

Abstract

Newborn rats were injected s.c. with 6-hydroxydopamine to deplete forebrain norepinephrine (NE) or with the vehicle. The males were then castrated at 4 days and the females injected with testosterone at 5 days of age. Both sexes were tested for female-like sexual responsiveness to a stud male at 6 months of age. The loss of forebrain NE did not prevent the feminization of the males due to castration or the masculinization of the females due to testosterone. This result contraindicates a general permissive-requisite role for forebrain NE for the mammalian brain's plasticity during its critical periods.

摘要

给新生大鼠皮下注射6-羟基多巴胺以耗尽前脑去甲肾上腺素(NE),或注射赋形剂。然后,雄性大鼠在4日龄时进行阉割,雌性大鼠在5日龄时注射睾酮。在6月龄时,对两性进行测试,观察其对雄性种鼠的雌性样性反应。前脑NE的缺失并未阻止因阉割导致的雄性大鼠雌性化或因睾酮导致的雌性大鼠雄性化。这一结果与前脑NE在关键期对哺乳动物大脑可塑性具有普遍许可-必要作用的观点相矛盾。

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