STEROIDOGENIC EFFECTS OF LUTEINIZING HORMONE AND PROLACTIN ON THE RAT OVARY IN VIVO

1967 ◽  
Vol 38 (4) ◽  
pp. 423-430 ◽  
Author(s):  
K. YOSHINAGA ◽  
SUSAN A. GRIEVES ◽  
R. V. SHORT

SUMMARY Progesterone and 20α-dihydroprogesterone were measured in the ovarian venous blood of rats in early pro-oestrus, late dioestrus, day 5 of pseudopregnancy, and in androgen-treated animals with persistent oestrus. Little progesterone was secreted in early pro-oestrus or persistent oestrus (0·1 μg./hr.), but the secretion rose in dioestrus (2·1 μg./hr.) and in pseudopregnancy (7 μg./hr.). The 20α-dihydroprogesterone secretion was low in the persistent oestrous group; in all the other groups it was 1·5–3 μg./hr. Treatment with luteinizing hormone increased progesterone secretion within 30 min. in pro-oestrus and persistent oestrus, had no significant effect in dioestrus, and depressed it markedly in pseudopregnancy. It appeared to have no significant effect on 20α-dihydroprogesterone secretion except during pseudopregnancy, when it was depressed. Treatment with prolactin produced no effect within 30 min.in pro-oestrous, dioestrous or pseudopregnant animals.

1970 ◽  
Vol 65 (2) ◽  
pp. 244-260 ◽  
Author(s):  
Andre Rado ◽  
John A. McCracken ◽  
David T. Baird

ABSTRACT The autotransplanted ovary of the ewe was perfused in vivo via the ovarian artery with either 14C or 3H labelled C19 steroids. 17β-Oestradiol was the major phenolic steroid isolated in ovarian venous blood from either testosterone or androstenedione. Smaller amounts of oestrone were obtained but there was no 17α-oestradiol, oestriol nor conjugated oestrogens isolated. The yield of oestrogen was approximately ten fold greater from androstenedione than from testosterone suggesting that the main route of oestrogen biosynthesis in the ovine ovary is via the former steroid. The effect of infusing luteinizing hormone (LH) at the rate of 10 μg per hour on the conversion of androstenedione to 17β-oestradiol was measured in 5 experiments. In 2 experiments, when the steady state was not achieved, the increasing rate of conversion was halted. On the other hand LH resulted in a temporary increase followed by a decrease in the rate of conversion in the remaining 3 experiments in which there was a constant rate of conversion in the control samples. These results are compatible with the concept that LH stimulates the aromatisation of androstenedione to oestrogens by the ovary in vivo.


1991 ◽  
Vol 69 (9) ◽  
pp. 1288-1293 ◽  
Author(s):  
Yallampalli Chandrasekhar ◽  
David T. Armstrong

Serum and ovarian progesterone levels and in vitro production of progesterone by preovulatory follicles were measured on proestrus in pregnant mare's serum gonadotropin (PMSG) primed immature rats in which the luteinizing hormone (LH) surge and ovulation were blocked by administration of the antiandrogen hydroxyflutamide. Serum progesterone levels observed at 12:00 on proestrus were significantly elevated, twofold above those observed in vehicle-treated controls, by in vivo administration of 5 mg hydroxyflutamide 4 h earlier. In control rats, proestrous progesterone did not increase until 16:00, in parallel with rising LH levels of the LH surge. No LH surge occurred in the hydroxyflutamide-treated rats, ovulation was blocked, and serum progesterone declined throughout the afternoon of proestrus, from the elevated levels present at 12:00. Administration of human chorionic gonadotropin (hCG) at 11:00 advanced the elevation of serum progesterone by 2 h in vehicle-treated controls and prevented the decline in progesterone levels in hydroxyfiutamide-treated rats. The patterns of change in ovarian tissue concentrations with time and treatment were essentially similar to those observed for serum progesterone. In in vitro experiments, progesterone secretion during 24 h culture of preovulatory follicles obtained on PMSG-induced proestrus was significantly increased, sixfold, by addition to the culture media of 370 μM but not of 37 μM hydroxyflutamide. Testosterone (50 nM) and hCG (20 mIU/mL) caused 26- and 14-fold increases, respectively, in progesterone secretion by cultured follicles. Hydroxyflutamide significantly reduced the stimulatory effect of testosterone but not of hCG on progesterone secretion in vitro. These results suggest that the antiandrogen hydroxyflutamide stimulates progesterone secretion, both in vivo and in vitro, through an initial androgen-agonistic action, before its antagonistic action is expressed. Its androgen-antagonistic action is responsible for its ability to inhibit testosterone-induced progesterone secretion in vitro. Its failure to reduce hCG-stimulated progesterone secretion in vivo and in vitro indicates that the latter stimulation is exerted independently of, and not as a consequence of, androgen action. The decrease in serum progesterone levels on the afternoon of proestrus therefore appears to be a consequence rather than a cause of the absence of an LH surge in the hydroxyflutamide-treated rats. It is concluded that the inhibitory effect of hydroxyflutamide on the preovulatory LH surge and ovulation is due not to inhibition of progesterone secretion at the ovarian level but most likely to neuroendocrine site(s) of action of the inhibitor.Key words: antiandrogen, hydroxyflutamide, progesterone, luteinizing hormone, ovulation, human chorionic gonadotropin.


1970 ◽  
Vol 120 (1) ◽  
pp. 145-150 ◽  
Author(s):  
A. P. F. Flint

Methods are described for the assay and partial purification of mevalonate kinase from superovulated rat ovary. The total activity of mevalonate kinase in superovulated rat ovary was 1.6±0.14units/g wet wt.; it was unchanged by the administration of luteinizing hormone in vivo. The Km of a partially purified preparation of mevalonate kinase for dl-Mevalonate was 3.6±0.5μm; its Km for MgATP2− was 120±7.7μm. The enzyme was inhibited by geranyl pyrophosphate and farnesyl pyrophosphate, but not by isopentenyl pyrophosphate or 3,3′-dimethylallyl pyrophosphate. dl-mevalonate 5-phosphate inhibited at high concentrations. With both geranyl pyrophosphate and farnesyl pyrophosphate the inhibition was competitive with respect to MgATP2−. The Ki for inhibition by geranyl pyrophosphate was 1.3±0.2μm; the Ki for inhibition by farnesyl pyrophosphate was 1.0±0.3μm. These findings are discussed with reference to the control by luteinizing hormone of steroidogenesis from acetate.


1967 ◽  
Vol 37 (2) ◽  
pp. 139-146 ◽  
Author(s):  
BARBARA J. WHITEHOUSE ◽  
G. P. VINSON ◽  
P. A. JANSSENS

SUMMARY Incubation of hamster adrenal tissue in Krebs bicarbonate Ringer solution gave rapid conversion of added [4-14C]cortisol to cortisone. Moreover, incubation in Ringer solution with [4-14C]progesterone as precursor invariably yielded cortisone in greater amounts than cortisol. On the other hand it has been confirmed that cortisol is the major free ultraviolet absorbing steroid in the adrenal venous blood of the hamster. Incubation of adrenal tissue with [4-14C]progesterone in hamster whole blood gave relatively greater amounts of cortisol which were more in keeping with the findings in vivo. This suggested that the blood contains factors which affect the cortisone-cortisol equilibrium by modifying adrenal enzyme activity. Some reduction of [3H] cortisone to cortisol was also observed during incubation with blood alone.


1973 ◽  
Vol 58 (3) ◽  
pp. 387-391 ◽  
Author(s):  
D. B. CRIGHTON

SUMMARY A synthetic decapeptide gonadotrophin releasing factor was tested for effects on the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) using an ovine pituitary incubation system. The effects of other synthetic peptides used at similar doses were studied. The synthetic decapeptide consistently provoked significant increases in the LH content of the incubation medium at doses equal to or in excess of 0·5 ng/flask (0·2 ng/ml medium). Significant increases in the FSH content of the incubation medium at doses equal to or in excess of 0·25 ng/flask (0·1 ng/ml medium) were observed. The other synthetic peptides failed to influence LH or FSH release in vitro even at a dose 20–40 times greater. The results demonstrate that the decapeptide releases both LH and FSH from sheep pituitary tissue, suggesting that it may play a role in the release of both hormones in vivo in the sheep.


1974 ◽  
Vol 75 (2) ◽  
pp. 368-378
Author(s):  
S. Dell'Acqua ◽  
S. Mancuso ◽  
M. G. Catelli ◽  
A. Bompiani

ABSTRACT Four human ovaries in mid-luteal phase have been perfused with tritium labelled cholesterol through the cannulated ovarian artery for thirty minutes. Three 15-min samples of ovarian venous blood have been collected, two during the perfusion and the third in the following 15 min. In two cases, 15 min after the beginning of the perfusion, highly purified human urinary LH was rapidly injected into the ovarian artery. The ovarian tissue and the three fractions of venous blood were analysed for phenolic and neutral steroids. In the ovarian tissue only progesterone (4-pregnene-3,20-dione), pregnenolone (3β-hydroxy-5-pregnen-20-one) and 17α-hydroxyprogesterone (17α-hydroxy-4-pregnene-3,20-dione) were isolated. The amount of progesterone isolated from the two ovaries injected with LH was five times higher as compared with the other two ovaries. No steroids were present in the samples of venous blood except in the two cases in which LH was injected, where progesterone was isolated only in the third sample. It is concluded that circulating cholesterol is utilized by the ovary at the mid-luteal phase for the synthesis of C21 steroids and that the presence of LH increases the production and the release of progesterone by the ovary.


1977 ◽  
Vol 72 (3) ◽  
pp. 379-383 ◽  
Author(s):  
K. M. HENDERSON ◽  
R. J. SCARAMUZZI ◽  
D. T. BAIRD

SUMMARY Corpora lutea of ewes bearing ovarian autotransplants were infused for 4 h with prostaglandin F2α (PGF2α) (10 μg/h), PGF2α + PGE2 (10 μg/h of each), PGE2 (10 μg/h) or saline on day 10 of the cycle. Ovarian venous blood obtained before, during, and up to 12 h after the infusion period, was assayed for progesterone. Prostaglandin F2α produced an immediate, rapid and sustained decline in progesterone secretion, but infusion of PGE2 together with PGF2α prevented the decline until after the infusion. Progesterone secretion was unaffected by infusion of PGE2 alone. Oestrous behaviour was observed in four out of seven animals infused with PGF2α but in only one out of six infused with PGF2α + PGE2. None of the animals infused with PGE2 alone or saline only came into heat.


1967 ◽  
Vol 39 (1) ◽  
pp. 27-35 ◽  
Author(s):  
D. A. STANSFIELD ◽  
A. P. FLINT

SUMMARY Judged from the exchange rate between luteal and plasma ascorbic acid there appears to be no compartmentalization of ascorbic acid within the corpus luteum. Evidence is presented to show that the uptake of ascorbic acid into slices of superovulated rat ovary is an energy-dependent process which is inhibited by luteinizing hormone (LH) by means of its stimulatory effect on progesterone synthesis. The results are discussed in relation to the adrenal cortex and methods involving ascorbic acid depletion used in the assay of corticotrophin and LH.


1973 ◽  
Vol 134 (2) ◽  
pp. 399-406 ◽  
Author(s):  
David T. Armstrong ◽  
Anthony P. F. Flint

Cholesterol ester-storage granules were isolated from luteinized rat ovary and rabbit ovarian interstitial tissue by centrifugal flotation and were investigated with regard to their structure and function. Cholesterol ester, protein, phospholipid and unesterified cholesterol accounted for the dry weight of granules from luteinized rat ovary. The protein and the phospholipid were resistant to removal by washing. Substrate specificities of nucleotide phosphatase and specific radioactivities of lipid-soluble P (determined after administration of [32P]Piin vivo) were the same in granules and in a microsomal fraction from the same tissue. After administration of [32P]Piin vivo, luteinizing hormone increased the specific radioactivity of lipid-soluble P in granules, mitochondria and the microsomal fraction. Since granules did not swell in hypo-osmotic media, whereas microsomal particles did, it is suggested that adherent phospholipid and protein in granule suspensions is unlikely to result from contamination with endoplasmic reticulum. Luteinizing hormone administered in vivo increased the phospholipid and unesterified cholesterol contents of isolated granules relative to their cholesterol ester content, and also tended to raise their protein content. This treatment decreased the ability of isolated granules to act as a substrate for cholesterol esterase in vitro and increased the activity of cholesterol esterase. Cycloheximide in vivo also raised the unesterified cholesterol/cholesterol ester ratio of isolated granules, and when administered with luteinizing hormone acted synergistically to bring about a further increase. These results are considered compatible with evidence obtained by microscopy which suggests that granules may be surrounded by a membrane, that they arise by pinching off from the endoplasmic reticulum, and that they shrink on trophic stimulation of the tissue.


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