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Topic:Steroid Hormones

Steroid hormones in horses are biologically active compounds that are synthesized from cholesterol and play a significant role in various physiological processes. These hormones include glucocorticoids, mineralocorticoids, and sex steroids such as estrogens, androgens, and progestogens. They are involved in regulating metabolism, immune function, electrolyte balance, and reproductive functions. The levels of steroid hormones can be influenced by factors such as age, sex, stress, and disease states. Understanding their regulatory mechanisms and effects is essential for managing equine health and performance. This page compiles peer-reviewed research studies and scholarly articles that explore the synthesis, regulation, and physiological roles of steroid hormones in horses.
Effect of stress on steroid hormone levels in racehorses.
Australian veterinary journal    February 1, 1982   Volume 58, Issue 2 70-71 doi: 10.1111/j.1751-0813.1982.tb02692.x
Baker HW, Baker ID, Epstein VM, Hudson B.Cortisol and testosterone were measured by radioimmunoassay in plasma samples from race horses. None of 6 stressed male horses had low cortisol levels but testosterone levels (0.81 +/- 0.15 nmol/l) were significantly lower than in healthy horses (1.86 +/- 0.31 nmol/l). The conclusion was made that adrenocortical insufficiency is not a common association of stress in race horses. The reduction in testosterone levels is probably a nonspecific response similar to that seen in other species.
Effects of injected ovarian steroids on reproductive patterns and performance in post-partum mares.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 199-204 
Loy RG, Evans MJ, Pemstein R, Taylor TB.Treatment of foaling mares with 150 mg progesterone and 10 mg oestradiol daily beginning within 12 h of parturition resulted in a delay of ovulation (15.6 +/- 2.6 days compared with 10.3 +/- 2.4 days in untreated mares). When mares were mated after this 5.3-day delay there was no advantage in reproductive performance over that of mares mated according to a conventional management system. Gonadotrophin secretion was inhibited during treatment but the following secretory patterns were similar to those of normal oestrous periods.
Isolation and identification of steroids from gonadal vein blood of the fetal horse.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 383-387 
Raeside JI, Gofton N, Liptrap RM, Milne FJ.Direct connection of the artery of a fetal ovary to the carotid artery of the mare allowed collection of a large volume of blood over a 30-min period. Extraction of steroids and their fractionation was followed by separation of the steroids by alumina adsorption chromatography, and Sephadex LH-20 and Celite partition chromatography. Further resolution of the material by HPLC led to the identification of dehydroepiandrosterone (DHA) by nuclear magnetic resonance and mass spectrometry. Other compounds were isolated, which remain to be identified fully, but in the 8th month of pregnancy the princ...
Effects of exogenous steroids on serum FSH and LH, and on follicular development in cyclic mares.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 205-212 
Evans MJ, Loy RG, Taylor TB, Barrows SP.Cyclic mares were given daily i.m. injections of 150 mg progesterone (Group P, N = 4), 150 mg progesterone and 10 mg oestradiol-17 beta (Group PE, N = 3), 10 mg oestradiol-17 beta (Group E, N = 3) or cottonseed oil vehicle (Group C, N = 4), from the day after ovulation (Day 1) to Day 28. Blood samples were collected daily, and the ovaries were palpated every 1-2 days. Serum FSH and LH concentrations were measured in all samples, and means determined for 7 consecutive 4-day periods throughout treatment. Comparisons within each steroid treatment group between time periods and comparisons between...
Glucocorticoid suppression of oestrus, follicles, LH and ovulation in the mare.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 247-251 
Asa CS, Ginther OJ.Dexamethasone, a synthetic glucocorticoid, was administered (30 mg/day) from Day 10 after ovulation to assess the involvement of the adrenal glands in the ovulatory cycle. Only 1 of 8 mares treated in this way exhibited behavioural oestrus, compared to 7 of 8 control mares. Mean maximum LH concentration and follicle size were significantly reduced. Ovulation occurred in 1 and possibly in 2 other treated mares, compared to all 8 control mares. The results demonstrated that dexamethasone can interfere with ovulation and associated events in the mare, but the mechanism of action is uncertain.
Androgens, behaviour and fertility control in feral stallions.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 79-87 
Turner JW, Kirkpatrick JF.This field study of feral stallions in Montana and Idaho examines and correlates the seasonal pattern of plasma androgens and specific sociosexual behaviour and reports the effect of a long-acting androgenic steroid on this behaviour and on fertility. Plasma testosterone was measured by competitive protein binding assay in samples obtained by jugular venepuncture from captured animals. In samples taken from 34 sexually mature stallions in 6 different months during the year, a definite seasonal pattern in testosterone was present, with a peak in May (3.04 +/- 0.63 ng/ml) and a nadir in December...
Identification of stage-specific and hormonally induced polypeptides in the uterine protein secretions of the mare during the oestrous cycle and pregnancy.
Journal of reproduction and fertility    January 1, 1982   Volume 64, Issue 1 199-207 doi: 10.1530/jrf.0.0640199
Zavy MT, Sharp DC, Bazer FW, Fazleabas A, Sessions F, Roberts RM.Uterine secretions were obtained on Days 4, 8, 12, 14, 16, 18 and 20 of the oestrous cycle and early pregnancy. Acid phosphatase activity was significantly affected by day of the cycle, reaching a maximum at days 12-14 during the luteal phase and then declining to almost undetectable levels, by Day 20. In pregnant animals, activity continued to increase beyond Day 14. Two-dimensional polyacrylamide gel electrophoresis showed that albumin was a major component. However, a number of unique proteins of non-serum origin appeared in mid-cycle but had disappeared by Day 20. One of these was a basic ...
Effect of prolonged administration of anabolic and androgenic steroids on reproductive function in the mare.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 213-218 
Turner JE, Irvine CH.Administration to mares of the anabolic steroid, methandriol, at the maximum recommended dose (300 mg every 3 weeks) for 1 1/2 years had no effect on reproductive characteristics except for suppression of GnRH-induced LH release and a tendency to suppress basal LH levels and the height of the ovulatory LH surge. A 4-fold increase in dosage caused marked suppression of basal LH, the LH surge, and GnRH-induced LH release. Other reproductive responses were minimally affected. There were no behavioural effects, and no changes in weight occurred when mares were compared with matched controls. Small...
Changes in equine follicular aromatase activity during transition from winter anoestrus.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 225-233 
Seamans KW, Sharp DC.Follicular aromatase activity during sexual resurgence after the winter anoestrus was investigated in 3 groups of 5 Pony mares. Group ET was studied during the early transition period, Group LT in late transition and Group C in full breeding condition. Granulosa and theca cells were incubated for 3 h with 3H-labelled androstenedione or progesterone. Analysis of the free oestrogenic products was by high performance liquid chromatography (HPLC) and recrystallization revealed highly variable oestrogen production in both cell types from mares in all 3 groups. Only oestrone and oestradiol peaks wer...
Dehydroepiandrosterone synthesis by the fetal foal and its importance as an oestrogen precursor.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 389-397 
Pashen RL, Sheldrick EL, Allen WR, Flint AP.The gonads of the fetal horse were found to be relatively devoid of 3 beta-hydroxysteroid dehydrogenase and other enzymes which metabolize dehydroepiandrosterone (DHA). In short-term in-vitro incubation experiments fetal liver converted DHA to the potential equilin precursor, 7 alpha-hydroxy DHA. DHA was converted to oestrone when incubated with extracts of horse placenta but 7 alpha-hydroxy DHA was not converted to equilin. Levels of DHA measured in peripheral blood of mares throughout pregnancy paralleled those of equilin and oestrone, and DHA concentrations fell rapidly after fetal gonadect...
Effect of PGF-2 alpha on LH receptors in the equine corpus luteum.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 235-245 
Roser JF, Evans JW, Mikuckis GM, Adams TE, Hughes JP.As quantified by Scatchard analysis, a 27 000 g crude luteal membrane fraction contained a single population of unoccupied LH receptors characterized by high affinity, ka = 0.647 +/- 0.158 X 10(11) M-1 and low binding capacity, Rt = 4.91 +/- 0.78 X 10(-11) M/mg membrane fraction. Acceptable hormonal specificity, reversibility, saturability, high affinity and tissue specificity indicated that the binding protein was a physiological receptor. To ensure that the methods used for Scatchard analysis were valid, hCG was characterized for specific activity and maximum bindability, non-specific bindin...
Secretion of free and conjugated steroids by the horse testis into lymph and venous blood.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 123-127 
Setchell BP, Cox JE.In 3 testes of 2 adult Pony stallions under halothane anaesthesia, catheters were inserted into a vein and a lymphatic vessel in the spermatic cord and into a vein on the surface of the testis. Lymph and venous blood were collected from the catheters in the cord and p-aminohippurate (2% w/v, 0 . 1 ml/min) was infused into the vein on the testis to determine blood flow by dilution. After 1 h, 6000 i.u. hCG was injected i.v. and collections continued for 45 min. The testes weighed 126-176 g. Lymph flow was 20-150 microliter/min before hCG and 100-270 microliter/min after hCG; the range of blood ...
Control of ovulation in mares in the early breeding season with ovarian steroids and prostaglandin.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 219-224 
Taylor TB, Pemstein R, Loy RG.Two trials were conducted to (1) determine the degree of control of ovulation achieved by treating mares in late winter with progesterone and oestradiol-17 beta combined after prior exposure to an artificially increased photoperiod, and (2) to examine the effectiveness of such a procedure incorporated into equine breeding farm management systems. Following a 15-day treatment of 150 mg progesterone and 10 mg oestradiol-17 beta daily with 10 mg PGF-2 alpha on the last day of steroid treatment, 27 of 31 mares ovulated on Days 8-14 after the last injection in one trial. Conception rate for mares m...
Concentrations of progesterone, 17 alpha-hydroxyprogesterone and 20 alpha-dihydroprogesterone in the plasma of mares during pregnancy and at parturition.
Journal of reproduction and fertility    November 1, 1981   Volume 63, Issue 2 443-448 doi: 10.1530/jrf.0.0630443
Seren E, Tamanini C, Gaiani R, Bono G.Plasma concentrations of progesterone and 17 alpha-hydroxyprogesterone were high in the 2nd and 3rd months of gestation, but 20 alpha-dihydroprogesterone increased from a level of 2 ng/ml, during the first 3 months, to 10-15 ng/ml during months 5-10, to reach 80-120 ng/ml during the last 30 days before foaling.
Prostaglandin F2alpha in the equine endometrium: steroid modulation and production capacities during the estrous cycle and early pregnancy.
Biology of reproduction    October 1, 1981   Volume 25, Issue 3 581-589 doi: 10.1095/biolreprod25.3.581
Vernon MW, Zavy MT, Asquith RL, Sharp DC.No abstract available
Anabolic steroids in the horse.
Journal of the American Veterinary Medical Association    August 1, 1981   Volume 179, Issue 3 278-280 
Beroza GA.No abstract available
Studies related to the metabolism of anabolic steroids in the horse: the identification of some 16-oxygenated metabolites of testosterone and a study of the phase II metabolism.
Xenobiotica; the fate of foreign compounds in biological systems    May 1, 1981   Volume 11, Issue 5 323-331 doi: 10.3109/00498258109045311
Dumasia MC, Houghton E.1. Isomers of 3,17-dihydroxyandrostan-16-one, 3,16-dihydroxyandrostan-17-one and androstane-3,16,17-triol have been identified as urinary metabolites of testosterone in the horse. 2. Following XAD-2 extraction of urine samples, Sephadex LH-20 chromatography was used to separate the extract into conjugate groups. Metabolites obtained after hydrolysis of the conjugates have been investigated by g.l.c.-mass spectrometry. 3. Testosterone, 3,17-dihydroxyandrostan-16-one and 3,16-dihydroxyandrostan-17-one were found only in the sulphate fraction. 5 alpha-Androstane-3 beta,17 beta-diol, and two isome...
Effects of etiocholanolone and prednisolone on intravascular granulocyte kinetics in horses.
American journal of veterinary research    April 1, 1981   Volume 42, Issue 4 626-628 
Carakostas MC, Moore WE, Smith JE, Johnson D.The functional capacity of the marrow granulocyte reserve (MGR) in 4 adult horses was studied, using 51Cr-labeled leukocytes. The mean increase in the peripheral granulocyte count following injections of etiocholanolone (0.3 mg/kg) was 870 granulocytes/mm3, and the mean increase following prednisolone administration (200 mg) was 5,880 granulocytes/mm3. Etiocholanolone failed to mobilize the MGR and decreased the rate of granulocyte egress from the blood. Prednisolone rapidly mobilized the MGR and markedly decreased the granulocyte specific activity during the first 3 hours after injection.
Oestrogen biosynthesis in the pregnant mare.
The Journal of endocrinology    January 1, 1981   Volume 89 Suppl 19P-32P 
Bhavnani BR.No abstract available
Sexual behavior, seminal pH and accessory sex gland weights in geldings administered testosterone and(or) estradiol-17 beta.
Journal of animal science    December 1, 1980   Volume 51, Issue 6 1358-1366 doi: 10.2527/jas1981.5161358x
Thompson DL, Pickett BW, Squires EL, Nett TM.Sixteen stallions were castrated and 30 days later assigned to one of four treatments: (1) testosterone propionate (175 microgram/kg body weight), (2) 17 beta-estradiol-3-benzoate (44 micrograms/kg body weight), (3) a combination of both steroids or, (4) vehicle only. These dosage were administered every other day for 18 days. The dosages were then doubled and continued for 20 days. Concentrations of testosterone and estradiol in serum decreased rapidly after castration and stabilized within about 6 hours. Mean concentrations of testosterone and estradiol maintained by the steroids were 1.4 an...
Studies related to the metabolism of anabolic steroids in the horse: the identification of some 16-oxygenated metabolites of 19-nortestosterone.
Xenobiotica; the fate of foreign compounds in biological systems    May 1, 1980   Volume 10, Issue 5 381-390 doi: 10.3109/00498258009033771
Houghton E, Dumasia MC.1. The metabolism of 19-nor[4-14C]testosterone in a thoroughbred horse has been studied and neutral urinary metabolites obtained after enzyme hydrolysis have been investigated by g.l.c.-mass spectrometry. 2. 3-Hydroxyestran-17-one, 17 alpha- and 17 beta-nortestosterone, estrane-3,17-diol (two isomers), 3,16-dihydroxyestran-17-one (two isomers), 3,17-dihydroxyestran-16-one (two isomers) and estrane-3,16,17-triol were identified in the neutral urinary extracts.
A perspective on anabolics.
New Zealand veterinary journal    May 1, 1980   Volume 28, Issue 5 85 doi: 10.1080/00480169.1980.34704
No abstract available
Dexamethasone suppression of sexual behavior in the ovariectomized mare.
Hormones and behavior    March 1, 1980   Volume 14, Issue 1 55-64 doi: 10.1016/0018-506x(80)90015-x
Asa CS, Goldfoot DA, Carcia MC, Ginther OJ.No abstract available
Levels of deoxycorticosterone and 21-hydroxy-5 alpha-pregnane-3,20-dione in the peripheral circulation of the prepartum and postpartum mare.
Biology of reproduction    September 1, 1979   Volume 21, Issue 2 433-437 doi: 10.1095/biolreprod21.2.433
Fleeger JL, Harms PG, Dunn EL, Atkins DT.No abstract available
Adrenal-testis interaction in the stallion.
Equine veterinary journal    July 1, 1979   Volume 11, Issue 3 195-198 doi: 10.1111/j.2042-3306.1979.tb01341.x
Cox JE, Jawad NM.The authors describe the short and long term effects of synthetic adrenocorticotrophin and of cortisol on peripheral plasma testosterone concentrations in 2 stallions. A single injection of either hormone temporarily raised plasma testosterone concentrations but repeated injection (twice daily for 5 days) depressed plasma testosterone concentrations. Cessation of treatment was followed by a rise in plasma testosterone to concentrations higher than those in the pretreatment period. These findings are briefly discussed.
Studies related to the metabolism of anabolic steroids in the horse: testosterone.
Xenobiotica; the fate of foreign compounds in biological systems    May 1, 1979   Volume 9, Issue 5 269-279 doi: 10.3109/00498257909038730
Houghton E, Dumasia MC.1. After intramuscular administration of [4-14C]testosterone to two cross-bred gelded horses, 45% of the radioactivity was excreted in urine in 96 h. Small amounts of urinary activity could still be detected at 200 h. 2. Neutral metabolites obtained after both enzyme and acid hydrolysis of urine samples have been investigated by g.l.c.-mass spectrometry. 3. 5 alpha-Androstane-3 beta, 17 alpha-diol was found only in the enzyme-hydrolysable extract and testosterone only in the acid-hydrolysable extract. 5 alpha-Androstane-3 beta, 17 beta-diol and 3 beta-hydroxy-5 alpha-androstan-17-one were foun...
Adrenal gland function in the horse: effect of dexamethasone on hydrocortisone secretion and blood cellularity and plasma electrolyte concentrations.
American journal of veterinary research    May 1, 1979   Volume 40, Issue 5 727-729 
Eiler H, Oliver J, Goble D.No abstract available
A precursor role for DHA in a feto-placental unit for oestrogen formation in the mare.
Journal of reproduction and fertility. Supplement    January 1, 1979   Issue 27 493-497 
Raeside JI, Liptrap RM, McDonell WN, Milne FJ.Plasma levels of total oestrogens and dehydroepiandrosterone (DHA) were measured by radioimmunossay in samples taken from various blood vessels in both maternal and fetal compartments in 11 Pony mates. High concentrations of oestrogens (greater than 100 ng/ml of plasma), expressed as oestrone equivalents, were found in the fetal circulation. On both the fetal and maternal sides, oestrogen concentrations were lower in blood going to than from the placenta. DHA concentrations, on the other hand, were higher in blood flowing to the placenta from the fetus. The fetal gonads were seen as the source...
Episodic nature of the delta 4-ene and delta 5-ene steroidogenic pathways and their relationship to the adreno-gonadal axis in stallions.
Journal of reproduction and fertility. Supplement    January 1, 1979   Issue 27 67-71 
Ganjam VK.Changes in the daily secretory patterns of testosterone and other 17 beta-hydroxyandrogen, total oestrogens and total corticoids were investigated in 7 stallions. Pulsatile fluctuations in plasma hormone levels were found in the serial blood samples collected hourly for 24 h in all animals. The plasma profiles indicated that corticoids, oestrogens and androgens were secreted episodically at all times in stallions. A significant correlation was observed between the precursor and products of delta 4-ene and delta 5-ene pathways and in inverse correlation (r = -0.68; P less than 0.01) was observe...
The source of the 5-alpha-pregnanes that occur during gestation in mares.
Journal of reproduction and fertility. Supplement    January 1, 1979   Issue 27 511-519 
Moss GE, Estergreen VL, Becker SR, Grant BD.[1,2,6,7-3H]Progesterone was injected into the uterine artery of umbilical vein of 4 pregnant Ponies to determine whether 5 alpha-pregnane-3,20-dione (DHP), 20 alpha-hydroxy-5 alpha-pregnan-3-one (20 alpha-ol), and 3 beta-hydroxy-5 alpha-pregnan-20-one (3 beta-ol) are produced by the placenta, fetus, or mare during late gestation. Plasma samples were collected from indwelling catheters in the uterine artery and vein and the umbilical artery and vein at frequent intervals until 6 h after isotope injection. The plasma samples were extracted with organic solvents and the respective pregnanes were...
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