Δ53β hydroxysteroid dehydrogenase activity of the rat corpus luteum exhibits positive substrate-binding co-operativity: A continuous monitoring microdensitometric study with unfixed ovarian tissue sections

1987 ◽  
Vol 5 (4) ◽  
pp. 255-261 ◽  
Author(s):  
M. Gordon ◽  
W. R. Robertson
Keyword(s):  
Corpus Luteum ◽  
Dehydrogenase Activity ◽  
Continuous Monitoring ◽  
Ovarian Tissue ◽  
Substrate Binding ◽  
Hydroxysteroid Dehydrogenase ◽  
Tissue Sections

A quantitative relationship between conceptus number and ovarian steroid dehydrogenase activity in pregnant rats

1984 ◽  
Vol 101 (3) ◽  
pp. 285-288
Author(s):  
F. Miyauchi ◽  
H. Kato ◽  
H. Yamashita ◽  
K. Ueda ◽  
H. Tamura ◽  
...  
Keyword(s):  
Corpus Luteum ◽  
Dehydrogenase Activity ◽  
Ovarian Tissue ◽  
Quantitative Relationship ◽  
Hydroxysteroid Dehydrogenase ◽  
Ovarian Steroid ◽  
Serum Progesterone ◽  
Pregnant Rats ◽  
Placental Hormone ◽  
Steroid Dehydrogenase

ABSTRACT The effects of a conceptus-derived substance on the activity of 3β-hydroxysteroid dehydrogenase (3β-HSD) and 20α-HSD in the ovary were studied in the rat. On day 7 of pregnancy (day 1 = insemination), rats were laparotomized and the desired number of conceptuses was aspirated from the uterus; thus, rats carrying one, two, three, four, five to seven or eight to ten conceptuses were prepared. They were autopsied on day 15 and 3β-HSD and 20α-HSD activity in the corpus luteum (CL) or non-luteal ovarian tissue (NLO) was determined. Conceptus number was directly related to 3β-HSD and inversely related to 20α-HSD activity in the CL. The serum progesterone level and CL weight were also directly related to conceptus number. Neither 3β-HSD nor 20α-HSD activity in the NLO was affected by conceptus number. These results indicated that 3β-HSD and 20α-HSD in the CL are probably regulated by placental hormone secreted in proportion to the number of conceptuses; in the NLO these enzymes may be controlled by a different mechanism. J. Endocr. (1984) 101, 285–288

3β-HYDROXYSTEROID DEHYDROGENASE ACTIVITY IN THE HUMAN FOETAL ADRENAL CORTEX

1965 ◽  
Vol 48 (3) ◽  
pp. 423-428 ◽  
Author(s):  
M. Niemi ◽  
A. H. Baillie
Keyword(s):  
Dehydrogenase Activity ◽  
Adrenal Cortex ◽  
Substrate Binding ◽  
Hydroxysteroid Dehydrogenase ◽  
List Type ◽  
Histochemical Reaction ◽  
Enzyme Substrate ◽  
Human Male ◽  
Foetal Life ◽  
Free Steroid

ABSTRACT 3β-Hydroxysteroid dehydrogenase activity was studied histochemically in the adrenal cortex of ten human male foetuses, ranging in crownrump length from 3.0 cm to 18.3 cm, with the following steroids: 3β-hydroxy-pregn-5-en-20-one (pregnenolone). 3β,17α-dihydroxy-pregn-5-en-20-one (17α-hydroxypregnenolone). 3β-hydroxy-androst-5-en-17-one (DHA). 3β,17β-dihydroxy-androst-5-ene (androstenediol). 3β-sulphoxy-pregn-5-en-20-one (pregnenolone sulphate). 3β-sulphoxy-17α-hydroxy-pregn-5-en-20-one (17α-hydroxy-pregnenolone sulphate) 3β-sulphoxy-androst-5-en-17-one (DHAsulphate). 3β-hydroxy-5α-androstan-17-one (epiandrosterone). After incubation with pregnenolone, 17α-hydroxypregnenolone, DHA and androstenediol a positive histochemical reaction was obtained in the inner part of the »definitive« cortex and throughout the foetal cortex of all adrenals studied. Initially very weak, the reaction became strongly positive about the twelfth week of foetal life. Pregnenolone sulphate and 17α-hydroxypregnenolong sulphate also gave a histochemical reaction in all the adrenals investigated, but DHA sulphate differed significantly from the free steroid by giving a very poor reaction. Formazan deposition followed incubation with epiandrosterone in all adrenals used and this may imply that a δ5 configuration is not necessary for enzyme-substrate binding.

scholarly journals Participation of intraluteal progesterone and prostaglandin F2 alpha in LH-induced luteolysis in pregnant rat

1998 ◽  
Vol 156 (2) ◽  
pp. 253-259 ◽  
Author(s):  
CO Stocco ◽  
RP Deis
Keyword(s):  
Corpus Luteum ◽  
Dehydrogenase Activity ◽  
Subcutaneous Administration ◽  
Hydroxysteroid Dehydrogenase ◽  
Good Evidence ◽  
Pregnant Rats ◽  
Pregnant Rat ◽  
Prostaglandin F2 Alpha

We examined the participation of the intraluteal levels of progesterone (P4) and prostaglandin F2 alpha (PGF2 alpha) in the induction of luteolysis by LH and its relationship with the induction of the 20 alpha-hydroxysteroid dehydrogenase activity (20 alpha-HSD). Subcutaneous administration of four doses of 10 microgram ovine LH (oLH) at 0800, 0900, 1000 and 1100 h on day 19 of pregnancy induced a decrease in the activity of the enzyme 3 beta-HSD 24 and 48 h after treatment and an increase in luteal 20 alpha-HSD activity 48 h after oLH treatment when compared with control rats. Intraluteal and serum P4 levels were lower than control values 24 and 48 h after oLH treatment, with a significant increase in luteal PGF2 alpha content and a decrease in corpus luteum (CL) weight 48 h after oLH treatment. Intrabursal ovarian (i.b.) treatment with an inhibitor of PG's biosynthesis (diclofenac) (70 microgram/ovary) or P4 (3 microgram/ovary) on day 20 of pregnancy, prevented the increase in 20 alpha-HSD activity observed 48 h after oLH treatment, without any effect on 3 beta-HSD activity. The i.b. administration of P4 prevented the increase in intraluteal PGF2 alpha content induced by oLH treatment and the increases in 20 alpha-HSD activity and intraluteal PGF2 alpha content observed in control animals on day 21 of pregnancy. The inhibition of PG biosynthesis also prevents the decrease in intraluteal and serum P4 level induced by oLH. These results provide good evidence of the important participation of intraluteal P4 and PGF2 alpha on the oLH-induced luteolysis in pregnant rats. We also found the P4 produced by the CL is involved, in part, in the regulation of luteal PG synthesis. Thus, the early decline in 3 beta-HSD activity and the consequent fall in intraluteal P4 content, may trigger the synthesis of PGs and thereafter the increase in luteal 20 alpha-HSD activity to establish luteolysis.

scholarly journals A HISTOCHEMICAL METHOD FOR THE DEMONSTRATION OF 20α-HYDROXYSTEROID DEHYDROGENASE ACTIVITY IN RAT OVARIES

1964 ◽  
Vol 12 (9) ◽  
pp. 670-673 ◽  
Author(s):  
KÁROLY BALOGH
Keyword(s):  
Enzyme Activity ◽  
Corpus Luteum ◽  
Dehydrogenase Activity ◽  
Present Method ◽  
Hydroxysteroid Dehydrogenase ◽  
Microscopic Level ◽  
Corpora Lutea ◽  
Endocrine Glands ◽  
Progesterone Metabolism ◽  
Rat Ovary

20α-Hydroxysteroid dehydrogenase activity was localized histochemically in the corpus luteum of the rat by using Nitro-BT as an indicator. Intensive enzyme activity was obseryed in the corpus luteum cells, especially during involution. The placenta and corpora lutea of pregnancy failed to reveal enzyme activity during the last week of gravidity. Other tissues, including endocrine glands, liver and kidneys were also negative. The Present method offers a possibility to identify the sites of progesterone metabolism in the rat ovary at the microscopic level.

3β-HYDROXYSTEROID DEHYDROGENASE IN THE ADRENAL GLAND AND PLACENTA

1965 ◽  
Vol 31 (3) ◽  
pp. 227-NP ◽  
Author(s):  
A. H. BAILLIE ◽  
E. H. D. CAMERON ◽  
K. GRIFFITHS ◽  
D. McK. HART
Keyword(s):  
Adrenal Gland ◽  
Dehydrogenase Activity ◽  
Adrenal Glands ◽  
Hydroxysteroid Dehydrogenase ◽  
Histochemical Demonstration ◽  
Zona Fasciculata ◽  
Histochemical Reaction ◽  
Tissue Sections ◽  
Adrenal Zona Fasciculata ◽  
Human Placentae

SUMMARY 3β-Hydroxysteroid dehydrogenase activity was studied histochemically in human, monkey, and rat adrenal glands and in human placentae. Tissue sections were incubated separately with each of the following substrates: (1) 3β-hydroxypregn-5-en-20-one (pregnenolone); (2) sodium 3β-sulphoxypregn-5-en-20-one (pregnenolonesulphate); (3) 3β-acetoxypregn-5-en-20 one (pregnenoloneacetate); (4) 3β,16α-dihydroxypregn-5-en-20-one (16α-hydroxypregnenolone); (5) 3β,17α-dihydroxypregn-5-en-20-one (17α-hydroxypregnenolone); (6) ammonium 3β-sulphoxy-17α-hydroxypregn-5-en-20-one (17α-hydroxypregnenolone ammonium sulphate); (7) 3β-hydroxyandrost-5-en-17-one (DHA); (8) 3β-sulphoxyandrost-5-en-17-one (DHA sulphate); (9) 3β-acetoxyandrost-5-en-17-one (DHA acetate); (10) androst-5-ene-3β, 17β-diol (androstenediol). The histochemical results obtained with pregnenolone and DHA as substrates resemble those described by other workers. Using pregnenolone sulphate and 17α-hydroxypregnenolone sulphate, a strong histochemical reaction with diformazan deposition was found in the zona fasciculata of the adrenals of all species and in the placental syntrophoblast. With DHA sulphate an extremely weak histochemical reaction was obtained with the adrenal zona fasciculata, monoformazan only being deposited. The syntrophoblast, however, showed intense 3β-hydroxysteroid dehydrogenase activity when incubated with DHA sulphate. These results accord with recent findings regarding the secretion and metabolism of 3β-sulphoxysteroids. A strong histochemical reaction was also obtained in both adrenal and placental tissues using 17α-hydroxypregnenolone, 16α-hydroxypregnenolone, androstenediol, pregnenolone acetate, and DHA acetate. These steroids have not previously been described as substrates for the histochemical demonstration of 3β-hydroxysteroid dehydrogenase in the adrenal or placenta.

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