Study on the activities of testes and accessory sex glands after losulazine treatment in rats

1994 ◽  
Vol 73 (3) ◽  
pp. 175-183 ◽  
Author(s):  
A RAY ◽  
S CHATTERJEE ◽  
N BISWAS
Keyword(s):  
1983 ◽  
Vol 96 (3) ◽  
pp. 407-416 ◽  
Author(s):  
R. Jones ◽  
P. R. Riding ◽  
M. G. Parker

The relative importance of testosterone and prolactin in regulating growth and protein synthesis in rat accessory sex glands has been investigated. Protein synthesis was measured by incubating tissue minces in vitro with [35S]methionine and analysing labelled proteins on polyacrylamide gels containing sodium dodecyl sulphate. Plasma prolactin was assayed by radioimmunoassay. Results showed that castration for 8 days significantly reduced wet weights and total protein synthesis in the ventral prostate, dorsolateral prostate and caput epididymidis, but that these effects could be reversed by exogenous testosterone. Similarly, the specific incorporation of [35S]methionine into four polypeptides in the ventral prostate, two polypeptides in the dorsolateral prostate and two polypeptides in the caput epididymidis was lowered by castration but markedly stimulated by testosterone. Acute or chronic administration of 2-bromo-α-ergocryptine to animals in combination with testosterone had no significant effect on any of the parameters measured, although the drug reduced circulating prolactin to undetectable levels. In addition, exogenous prolactin given alone, or in combination with testosterone, to hypophysectomized rats had no effect on general or specific protein synthesis. The induction of hyperprolactinaemia in immature or mature rats with pituitary homographs had no effect on testosterone-stimulated growth of any accessory gland, although it caused a significant stimulation of total protein synthesis in the dorsolateral prostate and coagulating glands. However, this was a generalized effect as it did not increase the specific incorporation of [35S]methionine into androgen-dependent proteins. The results do not indicate a major role for prolactin in regulating androgen responsiveness of male accessory sex glands in the rat.


1981 ◽  
Vol 36 (7-8) ◽  
pp. 579-585 ◽  
Author(s):  
Martin G. Peter ◽  
Paul D. Shirk ◽  
Karl H. Dahm ◽  
Herbert Roller

Abstract The accessory sex glands (ASG) of adult male Cecropia contain an enzyme that methylates juvenile hormone acids (JH-acids) in the presence of S-adenosyl-L-methionine (SAM). The methyltransferase is highly specific. The reaction rates decrease in the order JH-I-acid, JH-II-acid and JH-III-acid; in each case the natural enantiomer is esterified predominantly. Methyltrans­ ferase activity with the same substrate specificity was also demonstrated in adult female corpora allata (CA). Male CA have only marginal methyltransferase activity. The CA of male H. cecropia contain substantial amounts of JH-I-acid and JH-II-acid (minimum: 5 pmol/pair). When kept in organ culture, they release JH-acids into the medium. Radiolabeled propionate and mevalonate are incorporated efficiently into the carbon skeletons of the JH-acids. The enzyme system performing these transformations cannot be forced to produce JH-III-acid even in the presence of high mevalonate concentrations, though homomevalonate may enhance biosynthesis of JH-I-acid and JH-II-acid more than tenfold. It becomes evident that the regulation of JH titer balances with regard to the homologous structures during insect development is not merely a question of the availability of low molecular weight precursors, but in addition that of highly specific enzymes acting as regulatory entities in the later steps of the biosynthetic sequence.


1976 ◽  
Vol 31 (3-4) ◽  
pp. 199-200 ◽  
Author(s):  
Paul Shirk ◽  
Karl Dahm ◽  
Herbert Roller

Abstract Gas chromatographic determinations, bioassays, and radio­ labelling experiments show that the juvenile hormone in adult male Hyalophora cecropia is accumulated exclusively in the accessory sex glands. Moths do not store measurable quantities of juvenile hormone if their accessory sex glands are removed shortly after adult eclosion.


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