Effects of pituitary-testicular axis suppression in utero and during the early neonatal period with a long-acting luteinizing hormone-releasing hormone analog on genital development, somatic growth, and bone density in male cynomolgus monkeys in the first 6 months of life.

The specific role of late fetal and early neonatal gonadotropins and/or sex steroids on genital development, linear growth, and bone mass accretion remains unclear. To investigate this, we attempted to selectively suppress pituitary-testicular activation from midgestation through early infancy with a long-acting LHRH agonist (LHRHA), D-Trp6,Pro9-NEt-LHRH, in microspheres. The agonist was injected sc on days 72-81 in utero, on day 1 of life, and 3 months postnatally in male cynomolgus monkeys. Control animals were treated with placebo. We then examined the consequences of such an intervention in the first 6 months of life. In the LHRHA-treated animals, marked suppression of plasma testosterone and gonadotropin levels were evident in the first 3 months of life compared to control values. The mean testicular volumes of the LHRHA group were significantly lower at birth and in the first 2 months of life than those of the placebo group (P less than 0.05). However, by 4 months of age, the mean testicular volumes of the two groups were comparable. Similarly, the mean stretched phallic lengths of the LHRH approximately A group were significantly lower than those of the placebo group throughout the first 6 months of life (P less than 0.05). By contrast, LHRHA treatment had no effect on somatic growth, as mean body weights, total body lengths, and trunk lengths of the two groups were similar over the first 6 months of life. Mean bone widths and densities of the distal third of the left radius and the left midfemur were similar in the two groups at 1 and 6 months of life. We conclude that pituitary-testicular axis suppression with a long-acting LHRHA in utero and during early infancy results in markedly stunted penile and testicular growth without affecting general somatic growth and bone density of appendicular cortical bone in the cynomolgus monkey in the first 6 months of life. Thus, an intact fetal and neonatal pituitary-testicular axis is critical for normal genital growth. However, the sex steroid requirement for maintenance of bone mineral content of appendicular cortical bone may be lower than that necessary for normal genital development.

[1]  R. Cabrera,et al.  Validation of single photon absorptiometry in estimating bone mineral mass in rhesus monkey skeletons. , 1989, Puerto Rico health sciences journal.

[2]  K. Wallen,et al.  Blockade of neonatal activation of the pituitary-testicular axis: effect on peripubertal luteinizing hormone and testosterone secretion and on testicular development in male monkeys. , 1989, The Journal of clinical endocrinology and metabolism.

[3]  C. Bardin,et al.  Reversal of testicular function after prolonged suppression with an LHRH agonist in rhesus monkeys. , 1987, Journal of andrology.

[4]  K. Wallen,et al.  Blockade of neonatal activation of the pituitary-testicular axis with continuous administration of a gonadotropin-releasing hormone agonist in male rhesus monkeys. , 1984, The Journal of clinical endocrinology and metabolism.

[5]  F. Cassorla,et al.  Effects of the luteinizing hormone-releasing hormone (LHRH) analog D-Trp6-Pro9-NEt-LHRH on the pituitary-gonadal axis of prepubertal rhesus monkeys. , 1984, Biology of reproduction.

[6]  D. Collins,et al.  Influence of continuous gonadotropin-releasing hormone (GnRH) agonist treatment on luteinizing hormone and testosterone secretion, the response to GnRH, and the testicular response to human chorionic gonadotropin in male rhesus monkeys. , 1984, The Journal of clinical endocrinology and metabolism.

[7]  D. W. Denman,et al.  Male sexual development in the monkey. I. Cross-sectional analysis of pulsatile hypothalamic-pituitary-testicular function. , 1983, The Journal of clinical endocrinology and metabolism.

[8]  R. Mazess,et al.  An Accurate and Reproducible Absorptiometric Technique for Determining Bone Mineral Content in Newborn Infants , 1983, Pediatric Research.

[9]  C. Bardin,et al.  Sertoli cell maturation is impaired by neonatal passive immunization with antiserum to luteinizing hormone-releasing hormone. , 1983, Endocrinology.

[10]  W. Vale,et al.  Reversible inhibition of testicular steroidogenesis and spermatogenesis by a potent gonadotropin-releasing hormone agonist in normal men: an approach toward the development of a male contraceptive. , 1981, The New England journal of medicine.

[11]  C. Polychronakos,et al.  Perinatal activity of the hypothalamic-pituitary-gonadal axis in the lamb. III. LH, testosterone and prolactin secretory pattern in newborn lambs. , 1981, Hormone research.

[12]  A. Hsueh,et al.  Gonadotropin-releasing hormone and its agonist inhibit testicular luteinizing hormone receptor and steroidogenesis in immature and adult hypophysectomized rats. , 1980, Endocrinology.

[13]  J. Money,et al.  Micropenis. I. Criteria, etiologies and classification. , 1980, The Johns Hopkins medical journal.

[14]  K. Catt,et al.  Luteinizing hormone-releasing hormone-induced regulation of gonadotropin and prolactin receptors in the rat testis. , 1979, Endocrinology.

[15]  G. Hodgen,et al.  Fetal or maternal hypophysectomy in rhesus monkeys (Macaca mulatta): effects on the development of testes and other endocrine organs. , 1977, Biology of reproduction.

[16]  H. Safaii,et al.  Permanent impairment of testicular development after transient immunological blockade of endogenous luteinizing hormone releasing hormone in the neonatal rat. , 1977, Endocrinology.

[17]  L. Birnbaumer,et al.  Adenylyl cyclase activities in ovarian tissues. II. Regulation of responsiveness to LH, FSH, and PGE1 in the rabbit. , 1976, Endocrinology.

[18]  G. Ross,et al.  A new radioimmunoassay for follicle-stimulating hormone in macaques: ovulatory menstrual cycles. , 1976, Endocrinology.

[19]  K. Catt,et al.  In vitro bioassay of LH in human serum: the rat interstitial cell testosterone (RICT) assay. , 1976, The Journal of clinical endocrinology and metabolism.

[20]  M. Grumbach,et al.  Congenital hypopituitarism associated with neonatal hypoglycemia and microphallus: four cases secondary to hypothalamic hormone deficiencies. , 1975, The Journal of pediatrics.

[21]  M. Tseng,et al.  Effects of fetal decapitation on the structure and function of Leydig cells in rhesus monkeys (Macaca mulatta). , 1975, The American journal of anatomy.

[22]  J. Winter,et al.  Pituitary-gonadal relations in infancy. I. Patterns of serum gonadotropin concentrations from birth to four years of age in man and chimpanzee. , 1975, The Journal of clinical endocrinology and metabolism.

[23]  J. Jowsey,et al.  Osteoporosis in ovarian dysgenesis. , 1974, The Journal of pediatrics.

[24]  J. Winter,et al.  Studies on human sexual development. II. Fetal and maternal serum gonadotropin and sex steroid concentrations. , 1974, The Journal of clinical endocrinology and metabolism.

[25]  M. Forest,et al.  Hypophyso-gonadal function in humans during the first year of life. 1. Evidence for testicular activity in early infancy. , 1974, The Journal of clinical investigation.

[26]  D. Hess,et al.  Radioimmunoassay of testosterone during fetal development of the rhesus monkey. , 1973, Endocrinology.

[27]  G. Abraham CHAPTER 21 – Radioimmunoassay of Plasma Steroid Hormones , 1973 .

[28]  B. Goldman,et al.  Serum gonadotropin concentrations in intact and castrated neonatal rats. , 1971, Endocrinology.

[29]  S. Shapiro,et al.  An Analysis of Variance Test for Normality (Complete Samples) , 1965 .

[30]  L. Zondek,et al.  Observations on the testis in anencephaly with special reference to the Leydig cells. , 1965, Biologia neonatorum. Neo-natal studies.