Information on myometrial and fetal adrenocortical activity in non-human primates is important in understanding fetal responses to various stresses and involvement of the fetal hypothalamo- hypophyseal-adrenal axis (HHAA) in initiation of labor.
Our Specific Aims Are: I)a) To identify lateral ventricle coordinates in the fetal rhesus monkey brain at 120 d.G.A. to enable placement of laternal venticular catheters (LVC); b) to perform immunocytochemistry for AVP and CRF containing neurons of the fetal rhesus hypothalamus in control and experimental fetuses. II) To determine the roles and interactions of CRF1-41 and AVP in the increased production of fetal androgen in response to instrumentation. We will use specific antagonists to CRF1-41 and AVP administered separately and together to the fetal LVC. III) To determine the roles and interactions of CRF1-41 and AVP in the increased production of fetal ACTH that we hypothesize will occur during fetal hypoxemia. IV) To determine the roles and interactions of CRF1-41 and AVP in the growth of the fetal adrenal cortex and increased fetal plasma androgen concentrations observed prior to parturition. V) To obtain a better understanding of the various factors involved in regulation of the primate myometrium. We will use fetectomized pregnant rhesus monkeys from Ia in which fetuses have been removed but placentas left in situ. We will investigate the role of estrogen in the fetectomized pregnant monkey. We will study regulation of the primate myometrium by uterine stretch, AAM and CAT in vivo. VI) To study the interrelationship of steroids, AAM and CAT in the control of the non-pregnant primate uterus in vivo. Labor is a multifactorial process with interconnected positive and negative feedback loops. Most studies on control of the fetal adrenal, parturition and myometrial function have been performed in sheep. Differences in fetal and maternal endocrinology between primates and sheep dictate that a clear understanding of control of the fetal HHAA in humans awaits firm experimental data in non-human primates.

Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Cornell University
Department
Type
DUNS #
City
Ithaca
State
NY
Country
United States
Zip Code
14850
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Spradling-Reeves, Kimberly D; Glenn, Jeremy P; Lange, Kenneth J et al. (2018) The non-human primate kidney transcriptome in fetal development. J Med Primatol 47:157-171
Huber, Hillary F; Li, Cun; Nathanielsz, Peter W (2018) 2D:4D digit ratio is not a biomarker of developmental programming in baboons (Papio hamadryas species). J Med Primatol 47:78-80
Kuo, A H; Li, J; Li, C et al. (2018) Poor perinatal growth impairs baboon aortic windkessel function. J Dev Orig Health Dis 9:137-142
Kuo, Anderson H; Li, Cun; Mattern, Vicki et al. (2018) Sex-dimorphic acceleration of pericardial, subcutaneous, and plasma lipid increase in offspring of poorly nourished baboons. Int J Obes (Lond) 42:1092-1096
Light, Lydia E O; Bartlett, Thad Q; Poyas, Annica et al. (2018) Maternal activity, anxiety, and protectiveness during moderate nutrient restriction in captive baboons (Papio sp.). J Med Primatol :
Kuo, A H; Li, J; Li, C et al. (2017) Prenatal steroid administration leads to adult pericardial and hepatic steatosis in male baboons. Int J Obes (Lond) 41:1299-1302
Proffitt, J Michael; Glenn, Jeremy; Cesnik, Anthony J et al. (2017) Proteomics in non-human primates: utilizing RNA-Seq data to improve protein identification by mass spectrometry in vervet monkeys. BMC Genomics 18:877
Muralimanoharan, Sribalasubashini; Li, Cun; Nakayasu, Ernesto S et al. (2017) Sexual dimorphism in the fetal cardiac response to maternal nutrient restriction. J Mol Cell Cardiol 108:181-193
Li, Cun; Jenkins, Susan; Mattern, Vicki et al. (2017) Effect of moderate, 30 percent global maternal nutrient reduction on fetal and postnatal baboon phenotype. J Med Primatol 46:293-303

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