The Endocrinology of Human Parturition

Definitive modifications of the endocrine milieu of pregnancy herald the onset of parturition in many mammalian species. It is understandable, therefore, that much research has been conducted to examine the role of the sex steroid hormones in the maintenance of human pregnancy, the initiation of parturition, and thence the onset of labor. The endocrine changes that accompany human pregnancy are massive; indeed, it is not generally appreciated that the hormonal modifications that obtain in women during gestation are much greater and, in many respects, more diverse than those in all other mammalian species studied, including subhuman primates. In spite of these endocrine alterations in human pregnancy and notwithstanding recognized hormonal changes that precede parturition in most mammals, the endocrine changes in human pregnancy that participate in the initiation of parturition, if such exist, have not been discovered.

[1]  M. Casey,et al.  Parathyroid hormone-related protein and human myometrial cells: action and regulation 1 This investigation was supported, in part, by USPHS Grants 5-P50-HD-11149 and 1-R01-HD33283-01. 1 , 1997, Molecular and Cellular Endocrinology.

[2]  F. Pipkin,et al.  Differential Sensitivity of Human Nonpregnant and Pregnant Myometrium to Calcitonin Gene-Related Peptide , 1997, The Journal of the Society for Gynecologic Investigation: JSGI.

[3]  M. Casey,et al.  Transforming growth factor-beta inhibits progesterone-induced enkephalinase expression in human endometrial stromal cells. , 1996, The Journal of clinical endocrinology and metabolism.

[4]  S. Thompson,et al.  The human myometrium expresses multiple isoforms of the corticotropin-releasing hormone receptor. , 1995, The Journal of clinical endocrinology and metabolism.

[5]  V. Paspaliaris,et al.  Steroid regulation of parathyroid hormone-related protein expression and action in the rat uterus , 1995, The Journal of Steroid Biochemistry and Molecular Biology.

[6]  M. Silver Placental progestagens in the sheep and horse and the changes leading to parturition. , 2009, Experimental and clinical endocrinology.

[7]  C. Rao,et al.  Direct regulation of human myometrial contractions by human chorionic gonadotropin. , 1994, The Journal of clinical endocrinology and metabolism.

[8]  R. van Aarde,et al.  Progestin content and biosynthetic potential of the corpus luteum of the African elephant (Loxodonta africana). , 1994, Journal of reproduction and fertility.

[9]  C. Rao,et al.  Human myometrial chorionic gonadotropin/luteinizing hormone receptors in preterm and term deliveries. , 1994, The Journal of clinical endocrinology and metabolism.

[10]  D. Crankshaw,et al.  Effects of some naturally occurring prostanoids and some cyclooxygenase inhibitors on the contractility of the human lower uterine segment in vitro. , 1994, Canadian journal of physiology and pharmacology.

[11]  N. Milton,et al.  The human myometrial CRH receptor: G proteins and second messengers , 1994, Molecular and Cellular Endocrinology.

[12]  G. Thorburn A speculative review of parturition in the mare. , 2010, Equine veterinary journal. Supplement.

[13]  M. Casey,et al.  Human Parturition: Distinction Between the Initiation of Parturition and the Onset of Labor , 1993 .

[14]  N. Milton,et al.  The identification of a human myometrial corticotropin-releasing hormone receptor that increases in affinity during pregnancy. , 1993, The Journal of clinical endocrinology and metabolism.

[15]  W. Vale,et al.  Corticotropin releasing hormone-binding protein (CRH-BP): plasma levels decrease during the third trimester of normal human pregnancy. , 1993, The Journal of clinical endocrinology and metabolism.

[16]  S. J. Rzucidlo,et al.  Extragonadal gonadotropin receptors, their distribution and function. , 1992, Journal of physiology and pharmacology : an official journal of the Polish Physiological Society.

[17]  A. Broadus,et al.  Stretch-induced parathyroid hormone-related peptide gene expression in the rat uterus. , 1992, The Journal of biological chemistry.

[18]  S. Uzan,et al.  Plasma calcitonin gene-related peptide during gestation , 1992, The Lancet.

[19]  M. Thiede,et al.  Parathyroid hormone-related protein in the rat urinary bladder: a smooth muscle relaxant produced locally in response to mechanical stretch. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[20]  M. Casey,et al.  Transforming growth factor-beta 1 stimulation of parathyroid hormone-related protein expression in human uterine cells in culture: mRNA levels and protein secretion. , 1992, The Journal of clinical endocrinology and metabolism.

[21]  L. Johnson,et al.  Ornithine decarboxylase in large bowel mucosa: regulation by gastrin, secretin and EGF. , 1992, Journal of physiology and pharmacology : an official journal of the Polish Physiological Society.

[22]  R. Papka,et al.  Galanin and calcitonin gene-related peptide immunoreactivity in nerves of the rat uterus: Localization, colocalization, and effects on uterine contractility , 1991, Peptides.

[23]  B. Bagni,et al.  Circadian profile of plasma calcitonin gene-related peptide in healthy man. , 1991, The Journal of clinical endocrinology and metabolism.

[24]  L. Duong,et al.  Expression of the parathyroid hormone-related protein gene in the avian oviduct: potential role as a local modulator of vascular smooth muscle tension and shell gland motility during the egg-laying cycle. , 1991, Endocrinology.

[25]  M. Thiede,et al.  In vivo regulation of parathyroid hormone-related peptide messenger ribonucleic acid in the rat uterus by 17 beta-estradiol. , 1991, Endocrinology.

[26]  M. Leroy,et al.  Disappearance of human myometrial adenylate cyclase activation by prostaglandins at the end of pregnancy. Comparison with beta-adrenergic response. , 1991, Advances in prostaglandin, thromboxane, and leukotriene research.

[27]  A. Broadus,et al.  Intrauterine occupancy controls expression of the parathyroid hormone-related peptide gene in preterm rat myometrium. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[28]  J. Fahrenkrug,et al.  Peptide histidine methionine and vasoactive intestinal peptide: occurrence and relaxant effect in the human female reproductive tract. , 1989, Biology of reproduction.

[29]  J. Thompson,et al.  Parathyroid hormone as a smooth muscle relaxant. , 1989, Endocrine reviews.

[30]  J. Stevenson,et al.  Increased concentration of circulating calcitonin gene related peptide during normal human pregnancy. , 1986, British medical journal.

[31]  J. Fahrenkrug,et al.  Peptides PHI and VIP: comparison between vascular and nonvascular smooth muscle effect in rabbit uterus. , 1986, The American journal of physiology.

[32]  Y. Yiangou,et al.  The regional distribution of NPY-, PHM-, and VIP-containing nerves in the human female genital tract. , 1986, International journal of fertility.

[33]  T. Hökfelt,et al.  Calcitonin gene-related peptide inhibits spontaneous contractions in human uterus and fallopian tube. , 1985, Neuroscience letters.

[34]  H. Morris,et al.  Calcitonin gene-related peptide is a potent vasodilator , 1985, Nature.

[35]  J. Polak,et al.  Localisation and measurement of VIP in the genitourinary system of man and animals , 1984, Peptides.

[36]  B. Ottesen Vasoactive intestinal polypeptide as a neurotransmitter in the female genital tract. , 1983, American journal of obstetrics and gynecology.

[37]  J. Fahrenkrug,et al.  Vasoactive intestinal polypeptide (VIP) increases vaginal blood flow and inhibits uterine smooth muscle activity in women , 1983, European journal of clinical investigation.

[38]  J. Larsen,et al.  Vasoactive intestinal polypeptide and the female genital tract: relationship to reproductive phase and delivery. , 1982, American journal of obstetrics and gynecology.

[39]  S. Ashton,et al.  Effect of vasoactive intestinal polypeptide (VIP) on the in vitro and in vivo motility of the rabbit reproductive tract. , 1982, Fertility and sterility.

[40]  B. Ottesen Vasoactive intestinal polypeptide (VIP): effect on rabbit uterine smooth muscle in vivo and in vitro. , 1981, Acta physiologica Scandinavica.

[41]  J. Larsen,et al.  Effects of VIP in the female genital tract. , 1980, Endocrinologia japonica.

[42]  J. Fahrenkrug,et al.  Vasoactive intestinal polypeptide (VIP) inhibits prostaglandin-F2 alpha-induced activity of the rabbit myometrium. , 1980, Prostaglandins.

[43]  J. Fahrenkrug,et al.  Vasoactive intestinal polypeptide (VIP) inhibits oxytocin induced activity of the rabbit myometrium. , 1979, Acta physiologica Scandinavica.

[44]  A. Csapo,et al.  Indispensability of the human corpus luteum in the maintenance of early pregnancy. Luteectomy evidence. , 1978, Obstetrical & gynecological survey.

[45]  G. Thorbert Regional Changes in Structure and Function of Adrenergic Nerves in Guinea‐Pig Uterus During Pregnancy , 1978, Acta obstetricia et gynecologica Scandinavica. Supplement.

[46]  J. Marks,et al.  Massive Extraglandular Aromatization of Plasma Androstenedione Resulting in Feminization of a Prepubertal Boy , 1977 .

[47]  H. Kaihola,et al.  The relationship between the timing of luteectomy and the incidence of complete abortions. , 1974, American journal of obstetrics and gynecology.