Hemicastration causes and testosterone prevents enhanced uptake of [3H] thymidine by Sertoli cells in testes of immature rats.
Hemicastration causes and testosterone prevents enhanced uptake of [3H] thymidine by Sertoli cells in testes of immature rats.
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半去势会导致未成熟大鼠睾丸中支持细胞对 [3H] 胸苷的增强摄取,而睾酮会阻止其增强。
DOI:
10.1095/biolreprod30.1.263
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发表时间:
1984
影响因子:
3.6
通讯作者:
Salisbury,RL
中科院分区:
文献类型:
--
作者:
Orth,JM;Higginbotham,CA;Salisbury,RL
Rat pups were hemicastrated and uptake of [3H] thymidine by Sertoli cells in the remaining testis was compared to that in testes of sham-operated pups at intervals of from 8 h to 21 days after surgery. Labeled thymidine was administered subcutaneously 2 h before sacrifice. Testes were processed for light microscope autoradiography and the percent of Sertoli cell nuclei that had incorporated [3H] thymidine was determined by scoring nuclei in tissue sections as labeled or unlabeled. The percentage of cells labeled was increased in hemicastrates over intact controls by 8 h after surgery and testicular hypertrophy became apparent in hemicastrates by the following day. Labeling of Sertoli cells in hemicastrates remained elevated for 4 days and then returned to normal. When plasma levels of gonadotropins were measured in both groups 4 days after surgery, follicle-stimulating hormone (FSH) was found to be more than twice normal in hemicastrates while luteinizing hormone (LH) was unchanged. The effect of testosterone on the response of Sertoli cells to hemicastration was also examined. In hemicastrates, 2 days of androgen therapy depressed, and an additional 2 days abolished, the proliferative response of the Sertoli cells. Our findings suggest that increased proliferation of Sertoli cells within the remaining testis is involved in the enlargement of the testis that follows hemicastration. They also imply that prevention of compensatory hypertrophy by testosterone involves interference with this response of Sertoli cells in some way. Finally, our data implicate FSH in control of Sertoli cell proliferation in vivo in immature rats.
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影响因子:
4.8
作者:
V. Ramirez;C. Sawyer
通讯作者:
C. Sawyer
DOI:
--
发表时间:
1956
期刊:
影响因子:
--
作者:
Grant Jh
通讯作者:
Grant Jh
DOI:
10.1530/jrf.0.0210537
发表时间:
1970
期刊:
Journal of reproduction and fertility
影响因子:
--
作者:
D. S. Liang;M. D. Liang
通讯作者:
M. D. Liang
影响因子:
4.8
作者:
OJEDA, SR;RAMIREZ, VD
通讯作者:
RAMIREZ, VD
影响因子:
3.6
作者:
SOLARI, AJ;FRITZ, IB
通讯作者:
FRITZ, IB