ULTRASTRUCTURAL AND CYTOCHEMICAL STUDIES OF THE EFFECTS OF PROLACTIN ON THE LATERAL PROSTATE AND THE SEMINAL-VESICLE OF THE CASTRATED GUINEA-PIG

被引:4
|
作者
TAM, CC [1 ]
WONG, YC [1 ]
TANG, F [1 ]
机构
[1] UNIV HONG KONG, FAC MED, DEPT PHYSIOL, HONG KONG, HONG KONG
关键词
PROLACTIN; LATERAL PROSTATE; SEMINAL VESICLE; THIAMINE PYROPHOSPHATASE; RADIOIMMUNOASSAY; MORPHOMETRY; GUINEA PIG (DUNKIN HARTLEY);
D O I
10.1007/BF00381885
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Administration of ovine prolactin to castrated guinea pigs for 2 weeks induced hypertrophy of secretory cells in the lateral prostate when compared with the castrated controls. This was accompanied by an apparent increase in the number of profiles of granular endoplasmic reticulum and well developed Golgi complexes with dilated cisternae. An increase in the number of low-contrast electron-dense secretory granules was observed 4 weeks after prolactin treatment. In the seminal vesicle, dilatation and degranulation of granular endoplasmic reticulum and an apparent decrease in the number of secretory granules were observed 4 weeks after prolactin administration. Following castration and 2 weeks after prolactin treatment, thiamine pyrophosphatase (TPPase)-reaction product was mainly confined to 1-2 trans cisternae of the Golgi complexes in secretory cells of the lateral prostate and the seminal vesicle. In both glands, a reduction of TPPase activity was observed 2 weeks following prolactin administration, and the reaction product was totally absent after prolonged treatment for 4 weeks. The present study has provided morphological evidence that prolactin is capable of stimulating the secretory function of the lateral prostate while exerting some inhibitory effects on the seminal vesicle of the castrated guinea pig. In both glands, TPPase activity, and hence the process of glycosylation was inhibited after prolactin administration. The results from radioimmunoassay indicated that the action of prolactin on these glands could be a direct effect and not mediated through testosterone.
引用
收藏
页码:105 / 112
页数:8
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