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生长抑素迅速诱导的超微结构变化可能会抑制雌激素预处理的大鼠腺垂体中催乳素的释放。

Ultrastructural changes rapidly induced by somatostatin may inhibit prolactin release in estrogen-primed rat adenohypophysis.

作者信息

Saunders S L, Reifel C W, Shin S H

出版信息

Cell Tissue Res. 1983;232(1):21-34. doi: 10.1007/BF00222371.

Abstract

Apart from the known hypothalamic controls, which have been well documented, a myriad of compounds both endogenous and exogenous have proved effective in influencing secretion of prolactin (PRL). Recent studies have shown that somatostatin (SRIF), when injected intra-atrially as a bolus, is able to inhibit PRL secretion in vivo. However, the inhibitory effect of SRIF occurs only in adenohypophyses previously primed with estradiol. This research was undertaken to examine the ultrastructural effects of that inhibition using male Sprague-Dawley rats primed for three weeks with subcutaneous implants of estradiol. Within 2 min of injection of SRIF (1 mg/kg), the adenohypophyses were removed and processed for electron microscopy. We found dramatic changes in the estradiol-primed mammotrophs, including 1) an apparent rearrangement of rough endoplasmic reticulum (RER) into concentric cisternae, and 2) the appearance of intracellular bodies closely associated with granules. These changes were not observed in non-estradiol-primed male rats injected with SRIF which is consistent with the fact that in the normal male rats, SRIF failed to inhibit PRL secretion. These findings suggest that SRIF causes reorganization of cellular organelles so that PRL granules are sequestered thereby inhibiting secretion of PRL.

摘要

除了已被充分记录的已知下丘脑控制机制外,大量内源性和外源性化合物已被证明可有效影响催乳素(PRL)的分泌。最近的研究表明,生长抑素(SRIF)以大剂量心房内注射时,能够在体内抑制PRL分泌。然而,SRIF的抑制作用仅发生在先前用雌二醇预处理过的腺垂体中。本研究采用皮下植入雌二醇预处理三周的雄性Sprague-Dawley大鼠,以检查这种抑制作用的超微结构效应。在注射SRIF(1mg/kg)后2分钟内,取出腺垂体并进行电子显微镜处理。我们发现,在经雌二醇预处理的乳腺营养细胞中发生了显著变化,包括:1)粗面内质网(RER)明显重排为同心池;2)出现与颗粒紧密相关的细胞内小体。在注射SRIF的未用雌二醇预处理的雄性大鼠中未观察到这些变化,这与正常雄性大鼠中SRIF未能抑制PRL分泌的事实一致。这些发现表明,SRIF导致细胞器重组,从而使PRL颗粒被隔离,进而抑制PRL分泌。

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