This competing renewal application (R01 AG027678) will extend and expand on research that was responsive to RFA-AG-05-008 """"""""Biology of the Perimenopause: Impact on Health and Aging."""""""" Findings from the first award period demonstrate that: 1) endothelial function (endothelium-dependent dilation;EDD) becomes more impaired with declining ovarian function, and 2) oxidative stress is one of the underlying mechanisms involved in impaired EDD. The global aim of this renewal application is to determine the role of tetrahydrobiopterin (BH4;an essential cofactor for endothelial nitric oxide synthase (eNOS) and nitric oxide [NO] synthesis) and eNOS uncoupling as potential mediators of oxidative stress-related endothelial dysfunction with the menopause transition and aging in women. This will be assessed in Aim 1 using cross-sectional comparisons of healthy pre-, peri- and postmenopausal women. Endothelial function will be measured under basal conditions and following an acute increase in BH4.
Aim 2 will expand on the cross-sectional comparisons by using short-term (10 days) suppression of estrogen (E2) using gonadotropin releasing hormone antagonist [GnRHant] in pre-and perimenopausal women to determine the age-independent effects of E2 on EDD.
Aim 3 will examine the co-administration of BH4 and an anti-oxidant (ascorbic acid;AA) for the restoration of EDD. The primary hypotheses are that the reduced EDD in peri- and postmenopausal women, and in pre- and perimenopausal women following short-term E2 suppression, will increase in response to oral BH4. Secondary hypotheses predict that the reduced EDD in peri- and postmenopausal women (at baseline and with E2 suppression) will be associated with plasma and endothelial cell protein markers of BH4 biosynthesis and oxidative stress in vascular endothelial cells. A tertiary hypothesis is that the co-administration of BH4 an AA will restore EDD in peri-and postmenopausal women to levels of premenopausal women. To test these hypotheses, brachial artery EDD will be measured in: 1) pre-and early perimenopausal women before and after short-term E2 suppression (GnRHant) and add-back of either transdermal E2 or placebo;and 2) postmenopausal women at baseline. To determine possible mechanisms for endothelial dysfunction, EDD will also be measured after oral BH4 supplementation alone and during AA infusion. Insight into the molecular events underlying the decrease in EDD will be determined by assessing the changes in endothelial cell expression of proteins involved in the regulation of cellular and systemic adaptations to E2 deficiency including BH4 biosynthesis and oxidative stress. [The results from this research should expand our earlier findings and elucidate further the mechanisms that mediate endothelial dysfunction across the stages of the menopause transition and whether these processes are triggered by E2 deficiency. Understanding these mechanistic defects will help to inform the critical window of intervention and guide future sex-specific interventions and therapies for the maintenance of vascular function and prevention of future cardiovascular diseases.]

Public Health Relevance

The findings from this research should provide new information into determining the possible causes by which vascular health changes in relation to changes in hormone concentrations during the menopause transition, which may lead to the development of preventative and therapeutic strategies that could favorably modify these factors, and thus, prevent or slow changes in vascular health and decrease cardiovascular disease risk in women.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
High Priority, Short Term Project Award (R56)
Project #
2R56HL114073-06A1
Application #
8732808
Study Section
Clinical and Integrative Cardiovascular Sciences Study Section (CICS)
Program Officer
Maric-Bilkan, Christine
Project Start
2013-07-01
Project End
2014-08-31
Budget Start
2013-09-19
Budget End
2014-08-31
Support Year
6
Fiscal Year
2013
Total Cost
$650,795
Indirect Cost
$229,795
Name
University of Colorado Denver
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Hildreth, Kerry L; Ozemek, Cemal; Kohrt, Wendy M et al. (2018) Vascular dysfunction across the stages of the menopausal transition is associated with menopausal symptoms and quality of life. Menopause 25:1011-1019
Moreau, Kerrie L (2018) The intersection between gonadal function and vascular aging in women. J Appl Physiol (1985) :
Moreau, Kerrie L; Ozemek, Cemal (2017) Vascular Adaptations to Habitual Exercise in Older Adults: Time for the Sex Talk. Exerc Sport Sci Rev 45:116-123
Ozemek, Cemal; Hildreth, Kerry L; Groves, Daniel W et al. (2016) Acute ascorbic acid infusion increases left ventricular diastolic function in postmenopausal women. Maturitas 92:154-161
Moreau, Kerrie L; Hildreth, Kerry L (2014) Vascular Aging across the Menopause Transition in Healthy Women. Adv Vasc Med 2014: