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PMID: 3730489 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Morphological and histological study of castration-induced degeneration and androgen-induced regeneration in the mouse prostate.

Biology of reproduction ·Vol. 34 ·No. 5 ·1986-06-00 ·Pages 973-83

Sugimura Y, Cunha GR, Donjacour AA

Abstract

Degenerative and regenerative changes in the ductal architecture of the ventral and dorsolateral prostates (VP and DLP) of the adult mouse were investigated in microdissected specimens over a time-course of 14 days following castration and subsequently during 14 days of administration of testosterone propionate. After castration, about 35% of the ductal tips and branch-points were lost in distal regions (usually near the capsule) in both prostatic lobes. By contrast, in more proximal regions of the prostate (closer to the urethra), the ducts survived in an atrophic condition. The ductal morphology that had been lost in the distal regions completely regenerated after testosterone propionate was administered to the castrated males. In the VP, androgen replacement simply returned the gland to its former size with moderate ductal distension; in the DLP, excessive epithelial infoldings and ductal distension were elicited in the distal regions of the ducts after 14 days of treatment with testosterone propionate. These results suggest that androgenic responsiveness and dependency are different in distal versus proximal ducts. Distal ducts are exquisitely androgen-dependent and androgen-sensitive; in proximal regions, androgen-dependency is not as strict.

MeSH Terms
Animals Male Mice Mice, Inbred BALB C Orchiectomy Prostate/drug effects,pathology,physiology Regeneration Testosterone/pharmacology Time Factors
Chemicals
Testosterone
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sugimura Y
Cunha G R
Donjacour A A
Article Info
Journal
Biology of reproduction
Abbr.
Biol Reprod
ISSN
0006-3363
Published
1986-06-00
Pages
973-83
Language
English
Region
United States
NLM ID
0207224
Subset
IM
Grants
NIADDK NIH HHS · AM/CA32157 · United States
NCI NIH HHS · CA05388 · United States
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