Notizen: The Accessory Sex Glands as the Repository for Juvenile Hormone in Male Cecropia Moths

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.

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.


2019 ◽  
Vol 134 ◽  
pp. 104-111 ◽  
Author(s):  
Funda Eşki ◽  
Nebi Çetin ◽  
Sema Uslu ◽  
Barış Atalay Uslu ◽  
Sait Şendağ ◽  
...  

1971 ◽  
Vol 26 (12) ◽  
pp. 1270-1276 ◽  
Author(s):  
Manfred Metzler ◽  
Karl Heinz Dahm ◽  
Dietrich Meyer ◽  
Herbert Röller

In adult males of the giant silk moth Hyalophora cecropia (L.) the amount of juvenile hormone (JH) extractable from the abdomens increases sharply between the first and fourth day of adult life; 4-8 day-old moths contain up to 6 μg. During the biosynthesis, L-methionine provides the ester methyl group of both JH and its lower homologue JH-II. It does not contribute to the formation of the carbon skeleton. Farnesol, farnesyl pyrophosphate, and propionate are not utilized. Mevalonate is extensively incorporated into trans,trans-farnesol, but not into the sesquiterpene-like hormone. This result indicates that JH is not synthesized via mevalonate in the adult moths. Label of 2-14C-acetate was recovered in both JH and farnesol; the incorporation rate, however, was very small. The label of JH was located in the carbon skeleton.


1987 ◽  
Vol 113 (1) ◽  
pp. 111-116 ◽  
Author(s):  
R. F. A. Weber ◽  
M. P. Ooms ◽  
J. T. M. Vreeburg

ABSTRACT The effects of hyperprolactinaemia on serum levels of LH were investigated in adult male rats of the R × U strain. Hyperprolactinaemia was induced by three pituitary grafts under the kidney capsule, transplanted on day 0 of each experiment. Special attention was paid to the contribution of prolactin-stimulated testes, adrenals and corticosterone. In experiment 1, hyperprolactinaemia significantly reduced the serum concentrations of LH in intact rats. In spite of a significant increase in the serum levels of corticosterone, serum testosterone was not significantly affected by hyperprolactinaemia. The weights of both the adrenals and accessory sex glands were significantly increased at autopsy. In experiment 2, treatment with 10 mg corticosterone s.c. daily from day 14 to day 28 after pituitary grafting significantly reduced serum levels of both LH and testosterone. The suppression of testosterone in the hyperprolactinaemic corticosterone-treated animals was significantly less than in the corticosterone-treated control animals. The weights of the accessory sex glands were significantly increased in the hyperprolactinaemic animals. In experiment 3, rats were adrenalectomized and half of them were substituted with corticosterone. Serum testosterone levels significantly increased in both hyperprolactinaemic adrenalectomized rats and in adrenalectomized corticosterone-treated animals without any significant effect on serum LH. Again the weights of the accessory sex glands were significantly increased in the hyperprolactinaemic animals. In experiment 4, rats were adrenalectomized, gonadectomized and corticosterone treated on day 0 and then implanted with a 2, 1·5 or 1 cm silicone elastomer capsule containing testosterone. On day 28 after pituitary grafting, LH levels were significantly suppressed in animals with a 2 or 1·5 cm testosterone implant. The weights of the accessory sex glands were not increased in the hyperprolactinaemic animals. These results show that in the male rat the inhibitory effects of hyperprolactinaemia on serum LH levels may be due to (1) increased sensitivity of the hypothalamic-pituitary axis to the negative feedback action of testosterone by prolactin and by the prolactin-stimulated corticosterone secretion and (2) stimulation of testicular testosterone secretion by prolactin, which can also explain the increased weights of the accessory sex glands. Even in the presence of high serum concentrations of corticosterone, stimulation of testicular testosterone secretion by prolactin was observed. J. Endocr. (1987) 113,111–116


Sign in / Sign up

Export Citation Format

Share Document