Effects of gonadotropin-releasing hormone pulse-frequency modulation on luteinizing hormone, follicle-stimulating hormone and testosterone secretion in hypothalamo/pituitary-disconnected rams.

The effects of changes in pulse frequency of exogenously infused gonadotropin-releasing hormone (GnRH) were investigated in 6 adult surgically hypothalamo/pituitary-disconnected (HPD) gonadal-intact rams. Ten-minute sampling in 16 normal animals prior to HPD showed endogenous luteinizing hormone (LH) pulses occurring every 2.3 h with a mean pulse amplitude of 1.11 +/- 0.06 (SEM) ng/ml. Mean testosterone and follicle-stimulating hormone (FSH) concentrations were 3.0 +/- 0.14 ng/ml and 0.85 +/- 0.10 ng/ml, respectively. Before HPD, increasing single doses of GnRH (50-500 ng) elicited a dose-dependent rise of LH, 50 ng producing a response of similar amplitude to those of spontaneous LH pulses. The effects of varying the pulse frequency of a 100-ng GnRH dose weekly was investigated in 6 HPD animals; the pulse intervals explored were those at 1, 2, and 4 h. The pulsatile GnRH treatment was commenced 2-6 days after HPD when plasma testosterone concentrations were in the castrate range (less than 0.5 ng/ml) in all animals. Pulsatile LH and testosterone secretion was reestablished in all animals in the first 7 days by 2-h GnRH pulses, but the maximal pulse amplitudes of both hormones were only 50 and 62%, respectively, of endogenous pulses in the pre-HPD state. The plasma FSH pattern was nonpulsatile and FSH concentrations gradually increased in the first 7 days, although not to the pre-HPD range. Increasing GnRH pulse frequency from 2- to 1-hour immediately increased the LH baseline and pulse amplitude. As testosterone concentrations increased, the LH responses declined in a reciprocal fashion between Days 2 and 7. FSH concentration decreased gradually over the 7 days at the 1-h pulse frequency. Slowing the GnRH pulse to a 4-h frequency produced a progressive fall in testosterone concentrations, even though LH baselines were unchanged and LH pulse amplitudes increased transiently. FSH concentrations were unaltered during the 4-h regime. These results show that 1) the pulsatile pattern of LH and testosterone secretion in HPD rams can be reestablished by exogenous GnRH, 2) the magnitude of LH, FSH, and testosterone secretion were not fully restored to pre-HPD levels by the GnRH dose of 100 ng per pulse, and 3) changes in GnRH pulse frequency alone can influence both gonadotropin and testosterone secretion in the HPD model.

[1]  R. Short,et al.  Seasonal breeding: nature's contraceptive. , 1980, Recent progress in hormone research.

[2]  I. Clarke,et al.  Pituitary gland function after disconnection from direct hypothalamic influences in the sheep. , 1983, Neuroendocrinology.

[3]  B. Schanbacher,et al.  Hypothalamic control of the post-castration rise in serum LH concentration in rams. , 1984, Journal of reproduction and fertility.

[4]  J. Levine,et al.  Simultaneous measurement of luteinizing hormone-releasing hormone and luteinizing hormone release in unanesthetized, ovariectomized sheep. , 1982, Endocrinology.

[5]  J. Marshall,et al.  Pulsatile gonadotropin secretion during the human menstrual cycle: evidence for altered frequency of gonadotropin-releasing hormone secretion. , 1984, The Journal of clinical endocrinology and metabolism.

[6]  I. Clarke,et al.  Effects on plasma luteinizing hormone and follicle-stimulating hormone of varying the frequency and amplitude of gonadotropin-releasing hormone pulses in ovariectomized ewes with hypothalamo-pituitary disconnection. , 1984, Neuroendocrinology.

[7]  I. Clarke,et al.  THE TEMPORAL RELATIONSHIP BETWEEN GONADOTROPIN RELEASING HORMONE (GnRH) AND LUTEINIZING HORMONE (LH) SECRETION IN OVARIECTOMIZED EWES1 , 1982 .

[8]  G. Lamming,et al.  The induction of ovulation and luteal function in seasonally anoestrous ewes treated with small-dose multiple injections of Gn-RH. , 1982, Journal of reproduction and fertility.

[9]  G. Lincoln Use of a pulsed infusion of luteinizing hormone releasing hormone to mimic seasonally induced endocrine changes in the ram. , 1979, The Journal of endocrinology.

[10]  E. Knobil,et al.  The neuroendocrine control of the menstrual cycle. , 1980, Recent progress in hormone research.

[11]  J. Clements,et al.  Elevated plasma levels of pro-opiomelanocortin-derived peptides in sheep following hypothalamo-pituitary disconnection. , 1986, Neuroendocrinology.

[12]  J. Findlay,et al.  Regulation of gonadotrophin secretion in rams from birth to sexual maturity. I. Plasma LH, FSH and testosterone levels. , 1976, Journal of reproduction and fertility.

[13]  G. Lincoln Hypothalamic Control of the Testis in the Ram , 1978 .

[14]  L. Wildt,et al.  Frequency and amplitude of gonadotropin-releasing hormone stimulation and gonadotropin secretion in the rhesus monkey. , 1981, Endocrinology.

[15]  D. Baird,et al.  Gonadotrophic control of follicular development and function during the oestrous cycle of the ewe. , 2019, Journal of reproduction and fertility. Supplement.

[16]  S. Legan,et al.  Does the seasonal increase in estradiol negative feedback prevent luteinizing hormone surges in anestrous ewes by suppressing hypothalamic gonadotropin-releasing hormone pulse frequency? , 1985, Biology of reproduction.

[17]  R. Drongowski,et al.  Ontogeny of pulsatile luteinizing hormone and testosterone secretion in male lambs. , 1978, Endocrinology.

[18]  H. Burger,et al.  Radioimmunoassay for luteinizing hormone-releasing hormone (LHRH): its application to the measurement of LHRH in ovine and human plasma. , 1975, Endocrinology.

[19]  J. Findlay,et al.  Regulation of gonadotrophin secretion in rams from birth to sexual maturity. II. Response of the pituitary-testicular axis to LH-RH infusion. , 1976, Journal of reproduction and fertility.

[20]  W. Bremner,et al.  Feedback effects of the testis on pituitary responsiveness to luteinizing hormone-releasing hormone infusions in the ram. , 1980, Endocrinology.

[21]  I. Clarke,et al.  The temporal relationship between gonadotropin releasing hormone (GnRH) and luteinizing hormone (LH) secretion in ovariectomized ewes. , 1982, Endocrinology.

[22]  D. Davidson,et al.  A radioimmunoassay for testosterone in various biological fluids without chromatography. , 1978, Journal of steroid biochemistry.

[23]  I. Clarke,et al.  GnRH pulse frequency determines LH pulse amplitude by altering the amount of releasable LH in the pituitary glands of ewes. , 1985, Journal of reproduction and fertility.

[24]  B. Bindon,et al.  Pituitary gonadotrophins in Booroola and control Merino sheep. , 1984, Journal of reproduction and fertility.

[25]  D. Loriaux,et al.  Studies of the role of sex steroids in the feedback control of FSH concentrations in men. , 1973, The Journal of clinical endocrinology and metabolism.

[26]  W. H. Moger Impact of Pulsatile Administration of Gonadotropin‐Releasing Hormone on the Pituitary‐Testicular Axis of the Immature Rat , 1982 .

[27]  J. Kinder,et al.  Testosterone feedback on FSH secretion in male sheep. , 1982, Journal of reproduction and fertility.

[28]  W. Crowley,et al.  The physiology of gonadotropin-releasing hormone (GnRH) secretion in men and women. , 1985, Recent progress in hormone research.

[29]  J. Marshall,et al.  Pulsatile gonadotropin-releasing hormone in gonadotropin deficient and normal men: suppression of follicle-stimulating hormone responses by testosterone. , 1981, The Journal of clinical endocrinology and metabolism.

[30]  D. W. Denman,et al.  Male sexual development in the monkey. II. Cross-sectional analysis of pulsatile hypothalamic-pituitary secretion in castrated males. , 1983, The Journal of clinical endocrinology and metabolism.

[31]  G. Hodgen,et al.  Pulsatile pituitary gonadotropin secretion during maturation of the dominant follicle in monkeys: estrogen positive feedback enhances the biological activity of LH. , 1981, Endocrinology.