Analyze Diet

Journal of steroid biochemistry.

Discontinued
Periodical
Biochemistry
Steroids
Publisher:
Pergamon Press.. Oxford : Pergamon Press
Frequency: Eighteen no. a year
Country: England
Language: English
Start Year:1969 - 1990
Identifiers
ISSN:0022-4731 (Print)
0022-4731 (Linking)
NLM ID:0260125
(DNLM):J39580000(s)
(OCoLC):01799893
Coden:JSTBBK
Classification:W1 JO904M
Concentration decrease of corticosteroid binding globulin (CBG) in plasma of the mare throughout pregnancy.
Journal of steroid biochemistry    January 1, 1990   Volume 35, Issue 1 121-125 doi: 10.1016/0022-4731(90)90155-l
Martin B, Silberzahn P.A significant decrease of CBG binding capacity in plasma of the mare throughout pregnancy was demonstrated using equilibrium dialysis and gel equilibration methods. As indicated with immunoelectrophoresis experiments, the pregnancy related fall of CBG binding capacity was linked to an actual decrease in blood CBG concentration. This result contrasts sharply with data on most other mammalian species, with the exception of the gestating rhesus monkey.
Androgen and 19-norandrogen aromatization by equine and human placental microsomes.
Journal of steroid biochemistry    November 1, 1989   Volume 33, Issue 5 949-954 doi: 10.1016/0022-4731(89)90245-8
Dintinger T, Gaillard JL, Moslemi S, Zwain I, Silberzahn P.The ability of equine and human placental microsomes to aromatize testosterone and 19-nortestosterone was studied. When 3 microM [1 beta,2 beta-3H]testosterone was used as substrate, the specific activity of equine placental microsomal aromatase was 2.5 times higher than that of the human microsomal enzyme. Although 19-nortestosterone was aromatized 67 times more rapidly by equine than by human aromatase, we found that equine aromatase exhibited a markedly weaker affinity for this substrate than did the human enzyme. Competitive inhibition of testosterone aromatization by 19-nortestosterone oc...
Regulation of ovarian function by catecholestrogens: current concepts.
Journal of steroid biochemistry    October 1, 1989   Volume 33, Issue 4A 489-501 doi: 10.1016/0022-4731(89)90033-2
Spicer LJ, Hammond JM.Development of the ovarian follicle(s) destined for ovulation appears to be a process in which antral follicles undergo a recruitment, selection and subsequent dominance phase. Several intraovarian or autocrine/paracrine regulatory mechanisms have been evoked to explain these processes. One of these potential autocrine/paracrine regulators is a catecholestrogen, 2-hydroxy-estradiol (2-OH-E2). Evidence implicating 2-OH-E2 as an autocrine/paracrine regulator of follicular function is reviewed. Studies have shown 2-OH-E2 to be present in nanomolar concentrations in fluid of human and equine folli...
Synthesis and aromatization of 19-norandrogens in the stallion testis.
Journal of steroid biochemistry    April 1, 1989   Volume 32, Issue 4 537-544 doi: 10.1016/0022-4731(89)90387-7
Dintinger T, Gaillard JL, Zwain I, Bouhamidi R, Silberzahn P.The results of the measurement of 19-nortestosterone in the testiscular artery and vein of the stallion, the very low levels of this steroid in the peripheral blood of geldings and the similar patterns of increase in the peripheral levels of 19-nortestosterone and testosterone after hCG stimulation, show that 19-nortestosterone, like testosterone, is essentially synthesized in the testis. This testicular origin was confirmed by the ability of testicular tissue to synthesize 19-norandrogens from [4-14C]androgens in vitro. 19-Nortestosterone was 50% conjugated in the peripheral blood and almost ...
Aromatization of testosterone and 19-nortestosterone by a single enzyme from equine testicular microsomes. Differences from human placental aromatase.
Journal of steroid biochemistry    January 1, 1988   Volume 29, Issue 1 119-125 doi: 10.1016/0022-4731(88)90385-8
Silberzahn P, Gaillard JL, Quincey D, Dintinger T, Al-Timimi I.A single enzyme in the stallion testis was able to aromatize both testosterone and nortestosterone. This enzyme had a much lower affinity for nortestosterone than for testosterone. In contrast to human placental estrogen synthetase, this enzyme aromatized testosterone and 19-nortestosterone with similar efficiency. The differences observed (effects of monovalent cations, inhibition of androstenedione aromatization by testosterone and 19-nortestosterone and, above all, rate of norandrogen aromatization) suggest that the aromatase in the horse testis is not the same as that in the human placenta...
Equilin and equilenin biosynthesis. Stereochemistry of aromatization of 3-hydroxy-3,5,7-androstatrien-17-one by horse placenta.
Journal of steroid biochemistry    January 1, 1987   Volume 26, Issue 1 137-143 doi: 10.1016/0022-4731(87)90042-2
Numazawa M, Osawa Y.The metabolic pathway leading to equilin and equilenin biosynthesis in the pregnant mare is different from that of estrone and estradiol and it is apparently cholesterol-independent. The precise precursors and intermediates and the stereomechanism of equine placental aromatization have not been established. [1,2-3H, 4-14C]3-Hydroxy-3,5,7-androstatrien-17-one was synthesized as a potential substrate and the 3H-distribution was analyzed by biochemical and chemical derivatization methods. The substrate was converted to equilin, equilenin and Heard's ketone by horse placental microsomes with a sp....
The biotransformation and urinary excretion of dexamethasone in equine male castrates.
Journal of steroid biochemistry    October 1, 1986   Volume 25, Issue 4 547-553 doi: 10.1016/0022-4731(86)90401-2
Dumasia MC, Houghton E, Moss MS, Chakraborty J, Marks V.The pro-drugs of dexamethasone, a potent glucocorticoid, are frequently used as anti-inflammatory steroids in equine veterinary practice. In the present study the biotransformation and urinary excretion of tritium labelled dexamethasone were investigated in cross-bred castrated male horses after therapeutic doses. Between 40-50% of the administered radioactivity was excreted in the urine within 24 h; a further 10% being excreted over the next 3 days. The urinary radioactivity was largely excreted in the unconjugated steroid fraction. In the first 24 h urine sample, 26-36% of the total dose was...
Estrogen metabolites in equine ovarian follicles: gas chromatographic-mass spectrometric determinations in relation to follicular ultrastructure and progestin content.
Journal of steroid biochemistry    April 1, 1985   Volume 22, Issue 4 501-505 doi: 10.1016/0022-4731(85)90169-4
Silberzahn P, Almahbobi G, Dehennin L, Merouane A.Equine follicular fluid was aspirated at various developmental stages (viable, preovulatory and atretic) determined by ultrastructural study. Estrogens and progestins were analyzed by gas chromatography-mass spectrometry associated with stable isotope dilution. Progesterone and 17-hydroxyprogesterone were the principal progestins of the preovulatory and viable follicles. Among the catechol estrogens, 2-hydroxy-estradiol was particularly abundant in the preovulatory follicle and its definitive identification was made by the scan of a full mass spectrum.
Estrogens in seminal plasma of human and animal species: identification and quantitative estimation by gas chromatography-mass spectrometry associated with stable isotope dilution.
Journal of steroid biochemistry    November 1, 1982   Volume 17, Issue 5 567-572 doi: 10.1016/0022-4731(82)90017-6
Reiffsteck A, Dehennin L, Scholler R.Estrone, 2-methoxyestrone and estradiol-17 beta have been definitely identified in seminal plasma of man, bull, boar and stallion by high resolution gas chromatography associated with selective monitoring of characteristic ions of suitable derivatives. Quantitative estimations were performed by isotope dilution with deuterated analogues and by monitoring molecular ions of trimethylsilyl ethers of labelled and unlabelled compounds. Concentrations of unconjugated and total estrogens are reported together with the statistical evaluation of accuracy and precision.
Species specificity of estrogen biosynthesis in pregnancy. Immunochemical difference of placental NADPH-cytochrome c (P-450) reductase in human, baboon and horse.
Journal of steroid biochemistry    December 1, 1981   Volume 15 449-452 doi: 10.1016/0022-4731(81)90313-7
Osawa Y, Higashiyama T, Nakamura T.NADPH-cytochrome c (P-450) reductases from human placental aromatase II and from horse placental microsomes were solubilized and purified to show a single band of 83,000 daltons in SDS-polyacrylamide gel electrophoresis. Rabbits were immunized with purified human placental aromatase II NADPHcytochrome c (P-450) reductase. The resulting antibodies (Reduc-Ab) were used to examine the species specificity of estrogen biosynthesis and the reductase activity in humans, baboons, horses and rats. Rcduc-Ab suppressed androstenedione aromatase activity in human, baboon and horse placental microsomes wit...
The measurement of oestrone, equilin and dehydroepiandrosterone in the peripheral plasma of pregnant pony mares by radioimmunoassay.
Journal of steroid biochemistry    November 1, 1978   Volume 9, Issue 11 1065-1069 doi: 10.1016/0022-4731(78)90033-x
Rance TA, Park BK.Oestrone, equilin and dehydroepiandrosterone were measured by radioimmunoassay in peripheral plasma from five pony mares; samples were taken from day 60 of pregnancy at approximately weekly intervals through to parturition. Of the three steroids measured, dehydroepiandrosterone showed the most consistent pattern of secretion. DHA concentrations remained low until day 105, increased rapidly from day 120 and attained maximum values between days 168–210; levels declined to day 300, but there was considerable variation between mares in DHA patterns prior to parturition. There was great variation...
A preovulatory rise of dehydroepiandrosterone in the mare measured by radioimmunoassay.
Journal of steroid biochemistry    September 1, 1976   Volume 7, Issue 9 677-681 doi: 10.1016/0022-4731(76)90065-0
Rance TA, Park BK, Rowe PH, Dean PD.A radioimmunoassay procedure was developed for the measurement of dehydroepiandrosterone (DHA) in peripheral serum in nonpregnant mares. The synthesis and conjugation of 3beta-hydroxy-5-androsten-19-al-17-one 19(0-carboxymethyl) oxime is described. Antisera were developed against this antigen and characterized. The most specific antiserum was used to measure DHA. Concentrations of DHA were greatest immediately before ovulation.