The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.
The effects of adrenocorticotropin and prolactin on adrenal dehydroepiandrosterone secretion in the baboon fetus
Abstract
The present study was designed to determine whether PRL, in addition to ACTH, stimulates adrenal secretion of dehydroepiandrosterone (DHA) in vivo at midgestation in the baboon fetus (Papio anubis). On day 100 of gestation (term = day 184), fetuses were exteriorized, and a constant infusion of saline (0.1 ml/min) was initiated via a fetal femoral vein. Forty minutes later, a bolus injection of 30 nmol ACTH/ml saline (n = 5), 40 nmol ovine PRL/ml saline (n = 4), or 1 ml saline (n = 5) was administered via the fetal femoral venous catheter. ACTH (0.15 nmol/min.0.1 ml saline), PRL (0.20 nmol/min.0.1 ml saline), or saline (0.1 ml/min) was then infused for an additional 25 min. Blood samples were obtained from the contralateral fetal femoral vein and the maternal saphenous vein immediately before and after peptide infusion and from the umbilical vein and artery at the end of the infusion. Fetal serum DHA concentrations (range, 9-11 micrograms/100 ml) were significantly increased (P less than 0.05) by PRL and ACTH, but not by saline. In contrast, fetal concentrations of cortisol (15-20 micrograms/100 ml) and DHA sulfate (DHAS; 13-18 micrograms/100 ml) were not altered by infusion of test substances into the fetus. The maternal concentrations of F (49-61 micrograms/100 ml) and DHAS (19-22 micrograms/100 ml) exceeded (P less than 0.05) respective values in the fetus, whereas DHA concentrations (2-3 micrograms/100 ml) in the mother were lower (P less than 0.05) than those in fetal serum. The serum concentrations of DHA, DHAS, and cortisol in the mother were not altered by PRL or ACTH. Regardless of the treatment, concentrations of DHA and DHAS in umbilical vein were lower (P less than 0.05) than those in the umbilical artery. These findings indicate that PRL as well as ACTH are effective in vivo in stimulating serum DHA concentrations in fetal baboons at midgestation. The greater concentration of DHA in umbilical artery vs. umbilical vein as well as the lack of response in maternal DHA concentrations indicate that the site of action of PRL and ACTH is the fetal adrenal. Therefore, we conclude that at midgestation, there is the potential for multifactorial regulation of baboon fetal adrenal androgen production and that PRL, in addition to ACTH, can function as a fetal adrenocorticotropic factor in vivo.
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“Concerning this point, experiments in the baboon foetus at midgestation have shown that both ACTH and PRL can stimulate DHEA production in the foetal adrenal 7 .”
From ACTH and prolactin synergistically and selectively regulate CYP17 expression and adrenal androgen production in human foetal adrenal organ cultures (2023) · cites this paper as [7]
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Cites
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Fetal Plasma Prolactin Levels1
Winters, A. J., COLSTON, C., MacDonald, P. C., & Porter, J. C. (1975) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-41-3-626 · Cited by 127
Walsh, S. W., Norman, R. L., & Novy, M. J. (1979) · Endocrinology · doi:10.1210/endo-104-6-1805 · Cited by 83
Endocrine functions of the human fetus and placenta
Diczfalusy, E. (1974) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(74)90305-6 · Cited by 79
Maternal-Fetal ACTH Relationship in Man
Allen, J. P., COOK, D. M., Kendall, J. W., & McGILVRA, R. (1973) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-37-2-230 · Cited by 75
Regulation and Function of the Primate Fetal Adrenal Gland and Gonad
Jaffe, R. B., Serón‐Ferré, M., Crickard, K., Koritnik, D. R., Mitchell, B. F., & Huhtaniemi, I. T. (1981) · Elsevier eBooks · doi:10.1016/b978-0-12-571137-1.50007-4 · Cited by 74
The Regulation of Transplacental Cortisol- Cortisone Metabolism by Estrogen in Pregnant Baboons*
Pepe, G. J., Waddell, B. J., STAHL, S. J., & Albrecht, E. D. (1988) · Endocrinology · doi:10.1210/endo-122-1-78 · Cited by 63
Albrecht, E. D., Haskins, A. L., & Pepe, G. J. (1980) · Endocrinology · doi:10.1210/endo-107-3-766 · Cited by 57
Pepe, G. J., & Albrecht, E. D. (1984) · Endocrinology · doi:10.1210/endo-115-5-1946 · Cited by 55
EXCRETION OF URINARY OESTROGENS IN PREGNANT PATIENTS TREATED WITH CORTISONE AND ITS ANALOGUES
Brown, J. B., Beischer, N. A., & Smith, M. (1968) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1968.tb01599.x · Cited by 54
Cited by
Sorted by citations
Actions of Placental and Fetal Adrenal Steroid Hormones in Primate Pregnancy*
Pepe, G. J., & Albrecht, E. D. (1995) · Endocrine Reviews · doi:10.1210/edrv-16-5-608 · Cited by 491
Regulation of the Primate Fetal Adrenal Cortex*
Pepe, G. J., & Albrecht, E. D. (1990) · Endocrine Reviews · doi:10.1210/edrv-11-1-151 · Cited by 209
Adrenal Androgens in Humans and Nonhuman Primates: Production, Zonation and Regulation
Nguyen, A. D., & Conley, A. J. (2008) · KARGER eBooks · doi:10.1159/000134765 · Cited by 92
Endocrine and Morphological Maturation of the Fetal and Neonatal Adrenal Cortex in Baboons*
Ducsay, C. A., Hess, D. L., McClellan, M. C., & Novy, M. J. (1991) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-73-2-385 · Cited by 47
Nguyen, A. D., Mapes, S. M., Corbin, C. J., & Conley, A. J. (2008) · Journal of Endocrinology · doi:10.1677/joe-08-0337 · Cited by 38
Tal, R., Taylor, H. S., Burney, R. O., Mooney, S., & Giudice, L. C. (2015) · Europe PMC (PubMed Central) · Cited by 30
O'Connell, Y., McKenna, T. J., & Cunningham, S. K. (1994) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(94)90150-3 · Cited by 30
Pepe, G. J. (1998) · Human Reproduction Update · doi:10.1093/humupd/4.4.406 · Cited by 24
The involvement of prolactin in the regulation of adrenal cortex function in pigs
Kamińska, B., Opałka, M., Ciereszko, R. E., & Dusza, L. (2000) · Domestic Animal Endocrinology · doi:10.1016/s0739-7240(00)00076-x · Cited by 21
Ketamine inhibits fetal ACTH responses to cerebral hypoperfusion
Powers, M. J., & Wood, C. E. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00300.2006 · Cited by 20
“Other stress-induced hormones, such as prolactin, may also stimulate fetal adrenocortical activation or participate in the increase of adrenal sensitivity to ACTH (37; 62).”
BackgroundPepe, G. J., & Albrecht, E. D. (1991) · Endocrinology · doi:10.1210/endo-128-5-2395 · Cited by 20
Kim, S. Y., Sung, Y. A., Ko, K. S., Cho, B. Y., Lee, H. K., Koh, C. S., & Min, H. K. (1993) · The Korean Journal of Internal Medicine · doi:10.3904/kjim.1993.8.1.8 · Cited by 18
Giussani, D. A., Winter, J. A., Jenkins, S. L., Tame, J. D., Abrams, L. M., Ding, X. Y., & Nathanielsz, P. W. (1998) · Endocrinology · doi:10.1210/endo.139.6.6044 · Cited by 16
Berghorn, K. A., Albrecht, E. D., & Pepe, G. J. (1991) · Endocrinology · doi:10.1210/endo-129-3-1424 · Cited by 14
Billiar, R. B., Rohan, R. M., Henson, M. C., Smith, P. R., & Babischkin, J. S. (1992) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.75.5.1345 · Cited by 10
The Roles of Growth Hormone, Prolactin, and Placental Lactogen in Human Fetal Development
Freemark, M. (1999) · Humana Press eBooks · doi:10.1007/978-1-59259-697-3_5 · Cited by 9
Prado, N. A., Krcmarik, M. D., Paris, S., Larry, L., & Brown, J. L. (2023) · Theriogenology Wild · doi:10.1016/j.therwi.2023.100062 · Cited by 7
Regulation of Baboon Fetal Pituitary Prolactin Expression by Estrogen1
Pepe, G. J., Lynch, T. J., Davies, W. A., & Albrecht, E. D. (2009) · Biology of Reproduction · doi:10.1095/biolreprod.108.072785 · Cited by 6
“Moreover, there are several studies showing that prolactin regulates aspects of fetal adrenal development, including growth [15] and androgen production by the fetal zone [19, 20].”
BackgroundWood, C. E., & KELLER-WOOD, M. E. (2011) · Neonatology · doi:10.1159/000324431 · Cited by 4
Schneider, G., Ruggiero, C., Renault, L., Doghman-Bouguerra, M., Durand, N., Hingrai, G., Dijoud, F., Plotton, I., & Lalli, E. (2023) · European Journal of Endocrinology · doi:10.1093/ejendo/lvad118 · Cited by 3
Ayata, M., Yamane, T., Okamoto, S., Li, W., TerActa, N., & Matsumoto, K. (1989) · Journal of Steroid Biochemistry · doi:10.1016/0022-4731(89)90518-9 · Cited by 2
Metadata
- Authors
- PEPE, G. J., WADDELL, B. J., & ALBRECHT, E. D.
- Affiliations
- University of Maryland, Baltimore (US)
- Venue
- Endocrinology
- Publisher
- The Endocrine Society
- Published
- 1988-02
- Volume
- 122
- Issue
- 2
- Pages
- 646-650
- ISSN
- 0013-7227 (ISSN-L)
- 1945-7170
- OpenAlex
- W2022815472
- Cited by
- 21
- References
- 34
- Citations by year
- 2023: 2 · 2015: 1
- FWCI
- 1.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrinology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Abbott Laboratories
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD13294)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
- Keywords
- ACTH, prolactin, dehydroepiandrosterone, fetal adrenal gland, gestational age, fetal cortisol, dehydroepiandrosterone sulfate, umbilical circulation, fetal steroidogenesis
- MeSH terms
- Adrenal Glands, Adrenocorticotropic Hormone, Animals, Dehydroepiandrosterone, Female, Hydrocortisone, Papio, Pregnancy, Prolactin, Reference Values, Dehydroepiandrosterone Sulfate
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