This PPG continues to be a group of interrelated projects focused primarily on the potential cardiovascular benefits of soy phytoestrogen supplementation/treatment. Potential benefits of soy phytoestrogens (SPEs) for breast and uterus of females and of prostate of males constitute a secondary focus. The research is directed toward males and pre and postmenopausal females. In Project 1, the investigators will intensify their pharmacologic studies of the soy phytoestrogens (SPEs) by addressing four questions: 1. What is the peptide fraction of soy protein that is required for the phytoestrogens (isoflavones) to have their effect on lipid metabolism? 2. Are there differences in the effects of soy phytoestrogen preparations that are predominately genistein or predominately daidzein? 3. What is the relationship between dose of soy phytoestrogens and their metabolic effects? 4. What are the longer term effects of the """"""""optimal"""""""" soy treatment? The major objective of Project 2 is to assess the usefulness of soy phytoestrogens in primary cardioprotection of adult male monkeys. Also, the study will address directly whether long-term soy consumption is without adverse effects on the reproductive system, cognition, social and sexual behavior and function and determine if it has favorable effects on the prostate gland. Postmortem assessments will be made of atherosclerosis extent and arterial expression of estrogen receptors (alpha and beta). In addition, immunohistochemical and histomorphometric markers of prostatic hyperplasia and neoplasia will be studied as will histomorphometric markers of mammary gland hyperplasia and neoplasia. Project 3 is a comprehensive, periclinical study that will determine whether treatment with SPEs inhibits the progression of coronary and carotid artery atherosclerosis and improves coronary artery dilator responses in high risk, subordinate premenopausal monkeys. Furthermore, the study will determine whether SPEs inhibit or potentiate proliferation and estrogenic responses in the endometrium and mammary tissue of premenopausal monkeys, and whether SPEs adversely affect or improve bone development and peak bone mass in these females.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL045666-10
Application #
6389158
Study Section
Special Emphasis Panel (ZHL1-PPG-R (F2))
Program Officer
Ershow, Abby
Project Start
1991-01-01
Project End
2005-03-31
Budget Start
2001-04-01
Budget End
2002-03-31
Support Year
10
Fiscal Year
2001
Total Cost
$2,129,434
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Pathology
Type
Schools of Medicine
DUNS #
937727907
City
Winston-Salem
State
NC
Country
United States
Zip Code
27157
Register, Thomas C; Appt, Susan E; Clarkson, Thomas B (2016) Atherosclerosis and Vascular Biologic Responses to Estrogens: Histologic, Immunohistochemical, Biochemical, and Molecular Methods. Methods Mol Biol 1366:517-532
Meléndez, Giselle C; Register, Thomas C; Appt, Susan E et al. (2015) Beneficial effects of soy supplementation on postmenopausal atherosclerosis are dependent on pretreatment stage of plaque progression. Menopause 22:289-96
Silverstein, Marnie G; Kaplan, Jay R; Appt, Susan E et al. (2014) Effect of soy isoflavones on thyroid hormones in intact and ovariectomized cynomolgus monkeys (Macaca fascicularis). Menopause 21:1136-42
Eyster, K; Appt, S; Chalpe, A et al. (2014) Effects of equol on gene expression in female cynomolgus monkey iliac arteries. Nutr Metab Cardiovasc Dis 24:423-7
Eyster, Kathleen M; Appt, Susan; Chalpe, Abha et al. (2014) Effects of estradiol on transcriptional profiles in atherosclerotic iliac arteries in ovariectomized cynomolgus macaques. Menopause 21:143-52
Sophonsritsuk, Areepan; Appt, Susan E; Clarkson, Thomas B et al. (2013) Differential effects of estradiol on carotid artery inflammation when administered early versus late after surgical menopause. Menopause 20:540-7
Schnatz, Peter F; Nudy, Matthew; O'Sullivan, David M et al. (2012) The quantification of vitamin D receptors in coronary arteries and their association with atherosclerosis. Maturitas 73:143-7
Schnatz, Peter F; Vila-Wright, Sharon; Jiang, Xuezhi et al. (2012) The association between plasma 25-hydroxyvitamin D3 concentrations, C-reactive protein levels, and coronary artery atherosclerosis in postmenopausal monkeys. Menopause 19:1074-80
Schnatz, Peter F; Nudy, Matthew; O'Sullivan, David M et al. (2012) Coronary artery vitamin D receptor expression and plasma concentrations of 25-hydroxyvitamin D: their association with atherosclerosis. Menopause 19:967-73
Wood, Charles E; Stavisky, Ronda C; Nowak, Jette et al. (2012) Stimulatory adrenocortical effects of a selective estrogen receptor modulator in ovariectomized female macaques. Toxicol Pathol 40:55-61

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