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有证据表明,多巴胺能催乳素抑制因子机制仅调节大鼠哺乳期间催乳素分泌的消耗 - 转化阶段,而非释放阶段。

Evidence that the dopaminergic prolactin-inhibiting factor mechanism regulates only the depletion-transformation phase and not the release phase of prolactin secretion during suckling in the rat.

作者信息

Grosvenor C E, Mena F, Whitworth N S

出版信息

Endocrinology. 1980 Feb;106(2):481-5. doi: 10.1210/endo-106-2-481.

Abstract

We have compared the effectiveness of stalk-median eminence (SME) extracts, dopamine, and bromocriptine (CB-154) in inhibiting the release of PRL into the plasma during suckling when injected before depletion with that when the injections were given after the pituitary stores of PRL had been depleted and transformed by 10 min of suckling. We found that a single injection of either neutralized acidic extracts of SME at a dose of one or two SME equivalents per rat or 625 ng dopamine effectively prevented both the depletion of PRL within the pituitary and the subsequent rise in plasma PRL when given 1-3 min before the onset of suckling. Likewise, a single injection of bromocriptine (0.5 mg) given 20-30 min before the onset of suckling totally blocked pituitary depletion and the subsequent release of PRL into the circulation. However, the PRL concentration rose normally in the plasma in response to suckling when either SME extract or bromocriptine was given after PRL depletion had first been effected by prior short term (10 min) suckling. These data indicate that the depletion-transformation phase but not the release phase (into the circulation) of PRL secretion is under inhibitory control by a dopaminergic PRL-inhibiting factor system.

摘要

我们比较了茎-正中隆起(SME)提取物、多巴胺和溴隐亭(CB-154)在哺乳期抑制催乳素(PRL)释放到血浆中的效果,比较了在垂体PRL储存被耗尽之前注射与在垂体PRL储存被10分钟的哺乳耗尽并转化后注射的情况。我们发现,在哺乳开始前1-3分钟给予每只大鼠一剂一或两个SME当量的中和酸性SME提取物或625 ng多巴胺,能有效防止垂体中PRL的耗尽以及随后血浆PRL的升高。同样,在哺乳开始前20-30分钟给予一剂溴隐亭(0.5 mg),能完全阻止垂体耗尽以及随后PRL释放到循环中。然而,当在先前短期(10分钟)哺乳首先导致PRL耗尽后给予SME提取物或溴隐亭时,血浆中的PRL浓度会因哺乳而正常升高。这些数据表明,PRL分泌的耗尽-转化阶段而非释放阶段(进入循环)受多巴胺能PRL抑制因子系统的抑制性控制。

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