Neuroendocrine function in adult female transgenic mice expressing the human growth hormone gene.

Adult female transgenic mice expressing the human GH (hGH) gene with mouse metallothionein-I promoter are sterile. To evaluate the hypothalamic-pituitary function in these animals, adult female transgenic mice and nontransgenic normal littermates were ovariectomized. On days 7 and 8 after ovariectomy, mice were injected with either oil or primed with 0.5 micrograms estradiol benzoate (EB) in oil, 24 h later treated with 10 micrograms EB/100 g body wt and a day later bled for measurements of FSH, LH, and PRL levels. Plasma gonadotropin and PRL levels were also measured in ovary-intact transgenic and normal siblings at estrus. Additional ovariectomized EB-treated transgenic mice and normal siblings were injected with either saline or GnRH in saline (1 ng/g body wt) and were bled 15 min later for determination of circulating hormone levels. At estrus, in transgenic mice, circulating FSH and PRL levels were significantly lower (FSH:P less than 0.001; PRL:P less than 0.025), but plasma LH concentrations were higher (P less than 0.001) than those in nontransgenic mice. As expected, ovariectomy significantly increased (P less than 0.001) circulating FSH and LH levels in both groups of mice relative to ovary-intact animals, but the increase in plasma LH levels was attenuated in transgenic mice. The suppressive effect of estrogen on circulating FSH and LH levels were similar in transgenic and nontransgenic mice. Treatment with GnRH significantly increased plasma FSH and LH levels in both transgenic and normal mice. However, the plasma FSH and LH responses to GnRH administration were significantly reduced (P less than 0.001) in transgenic mice. The results of these studies indicate that adult female transgenic mice expressing the hGH gene are hypoprolactinemic. Yet due to PRL-like activity of hGH, the gonadotropin secretion is altered. Thus, endogenously secreted hGH modulates the hypothalamic-pituitary function of adult female transgenic mice bearing the hGH gene.

[1]  T. Wagner,et al.  Interactions of human growth hormone and prolactin on pituitary and Leydig cell function in adult transgenic mice expressing the human growth hormone gene. , 1991, Biology of reproduction.

[2]  N. Ben-Jonathan,et al.  Acute stimulation of prolactin release by estradiol: mediation by the posterior pituitary. , 1990, Endocrinology.

[3]  D. Moore,et al.  Glucocorticoid regulation of human growth hormone expression in transgenic mice and transiently transfected cells. , 1989, The Journal of endocrinology.

[4]  R. Palmiter,et al.  Expression of insulin-like growth factor I in transgenic mice with elevated levels of growth hormone is correlated with growth. , 1988, Endocrinology.

[5]  R. Palmiter,et al.  Progress on gene transfer in farm animals. , 1987, Veterinary immunology and immunopathology.

[6]  A. Bartke,et al.  Prolactin modulates the gonadotropin response to the negative feedback effect of testosterone in immature male rats. , 1987, Endocrinology.

[7]  D. Moore,et al.  Human growth hormone as a reporter gene in regulation studies employing transient gene expression , 1986, Molecular and cellular biology.

[8]  M. Culler,et al.  Evidence that pulsatile follicle-stimulating hormone secretion is independent of endogenous luteinizing hormone-releasing hormone. , 1986, Endocrinology.

[9]  R. Palmiter,et al.  Partial correction of murine hereditary growth disorder by germ-line incorporation of a new gene , 1984, Nature.

[10]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[11]  R. Palmiter,et al.  Metallothionein-human GH fusion genes stimulate growth of mice. , 1983, Science.

[12]  Michael G. Rosenfeld,et al.  Dramatic growth of mice that develop from eggs microinjected with metallothionein–growth hormone fusion genes , 1982, Nature.

[13]  D. Sarkar,et al.  Damage to hypothalamic dopaminergic neurons is associated with development of prolactin-secreting pituitary tumors. , 1982, Science.

[14]  N. Schwartz,et al.  Characterization of the FSH-suppressing activity in follicular fluid. , 1982, Recent progress in hormone research.

[15]  B. McEwen,et al.  Steroid receptor levels in intact and ovariectomized estrogen-treated rats: an examination of quantitative, temporal and endocrine factors influencing the efficacy of an estradiol stimulus. , 1981, Neuroendocrinology.

[16]  S. Ojeda,et al.  Activation of growth hormone short loop negative feedback delays puberty in the female rat. , 1981, Endocrinology.

[17]  W. Vale,et al.  Antireproductive effects of a potent GnRH antagonist in the female rat. , 1981, Endocrinology.

[18]  J. C. Porter,et al.  Role of estrogen in the dopaminergic control of prolactin secretion. , 1981, Endocrinology.

[19]  D. Kleinberg,et al.  Evidence that human growth hormone is a potent lactogen in primates. , 1980, The Journal of clinical endocrinology and metabolism.

[20]  D. Herbert,et al.  Early response of the dopaminergic tuberoinfundibular neurons to anterior pituitary homografts. , 1980, Neuroendocrinology.

[21]  J. Hustin,et al.  Inhibin: from concept to reality. , 1979, Vitamins and hormones.

[22]  S. Wiegand,et al.  Persistent estrus and blockade of progesterone-induced LH release follows lesions which do not damage the suprachiasmatic nucleus. , 1978, Endocrinology.

[23]  H. Fraser,et al.  Changes in the ovaries of rats after immunization against luteinizing hormone releasing hormone. , 1978, The Journal of endocrinology.

[24]  S. Ojeda,et al.  Developmental patterns of plasma and pituitary growth hormone (GH) in the female rat. , 1977, Endocrinology.

[25]  J. Clemens,et al.  Studies on the role of the preoptic area in the control of reproductive function in the rat. , 1976, Endocrinology.

[26]  D. Johnson,et al.  Stress-induced gonadotropin and prolactin secretory patterns. , 1976, Neuroendocrinology.

[27]  P. Kalra,et al.  The effects of hypothalamic lesions on the release of gonadotropins and prolactin in response to estrogen and progesterone treatment in female rats. , 1972, Endocrinology.

[28]  C. Sawyer,et al.  Pituitary prolactin secretion in female rats made persistently estrous or diestrous by hypothalamic deafferentation. , 1972, Endocrinology.

[29]  A. Bingel Estrous Cyclicity in Mice Housed in the Presence or Absence of Males , 1972, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[30]  A. Schally,et al.  Effect of Pentobarbital and Ether Stress on Serum Prolactin Levels in Rats 1 , 1971, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[31]  J. Meites,et al.  Effects of Ether and Pentobarbital on Serum Prolactin and LH Levels in Proestrous Rats , 1970, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.