Proliferative responses of normal rat ventral prostate in organ culture: Effects of testosterone and its metabolites in chemically defined medium

The Prostate ◽  
1985 ◽  
Vol 7 (4) ◽  
pp. 419-428 ◽  
Author(s):  
Lynn J. Buchanan ◽  
Andrew C. Riches
1975 ◽  
Vol 80 (4) ◽  
pp. 761-774 ◽  
Author(s):  
Risto Johansson

ABSTRACT In an organ type tissue culture of the rat ventral prostate in a chemically defined medium insulin (0.08 IU/ml) stimulated the synthesis of RNA within 6–12 h, the synthesis of protein within 6–12 h and the synthesis of DNA within 2–4 days. Testosterone (10−8 m) stimulated these synthetic processes somewhat more slowly: the synthesis of RNA within 12–24 h, protein within 12–24 h and DNA at 4 days. Rather high concentrations of insulin were needed while testosterone was effective at a physiological concentration. Prolactin (1000 ng/ml) stimulated the synthesis of RNA and protein, but not DNA, when added together with either testosterone or insulin, but was completely ineffective when added alone. The response times resembled those of insulin. The lower concentrations of prolactin were ineffective. Growth hormone, luteinizing hormone and follicle stimulating hormone did not stimulate the synthesis of RNA, protein or DNA even when added with testosterone. The results confirm the findings of the numerous in vivo experiments that the hypophyseal hormone prolactin has a direct effect on the ventral prostate.


PLoS ONE ◽  
2018 ◽  
Vol 13 (2) ◽  
pp. e0192884 ◽  
Author(s):  
Hiroyuki Sanjo ◽  
Mitsuru Komeya ◽  
Takuya Sato ◽  
Takeru Abe ◽  
Kumiko Katagiri ◽  
...  

1983 ◽  
Vol 207 (2) ◽  
pp. 279-288 ◽  
Author(s):  
Paula Martikainen ◽  
Jyrki Suominen

1989 ◽  
Vol 120 (1) ◽  
pp. 43-49 ◽  
Author(s):  
Paula Martikainen ◽  
Jyrki Suominen ◽  
Kimmo Vihko

Abstract. The usefulness of plasminogen activators (PAs) in the follow-up of the secretory function of the prostate in culture, as well as the hormonal control of these secretory proteins was studied. Organ culture of rat ventral prostate was used as an experimental model. PA secreted into the culture medium during the two weeks' culture period was of the urokinase-type in all culture conditions, as determined by zymography. The highest activities at the end of culture were found in the involuting prostate in cultures without any hormones. As the epithelial component is strongly reduced in the involuted explants, these high activities were suggested to be derived from stroma. Corticosterone (10−7 mol/l) and insulin (80 U/l) reduced significantly the secretion of PA, and this reduction was attenuated when the favourable effect of these hormones on the maintenance of morphology and tissue weight was taken into account. Testosterone (10−7 mol/l) increased significantly the secretion of PA in all hormone-treated cultures, which could be due to the increased secretory activity of the epithelium. Interactions between the hormones were significant, i.e. the effects of the hormone combinations were different and could not be calculated from the separate effects of these hormones. Even though the general growth and function of the prostate is strictly androgen-controlled, these results suggest that the control of PA secretion is multihormonal.


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