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High-probability grants
According to our matching algorithm, Christopher P. Pawela is the likely recipient of the following grants.
| Years |
Recipients |
Code |
Title / Keywords |
Matching
score |
| 2015 |
Pawela, Christopher Paul |
R56Activity Code Description:
To provide limited interim research support based on the merit of a pending R01 application while applicant gathers additional data to revise a new or competing renewal application. This grant will underwrite highly meritorious applications that if given the opportunity to revise their application could meet IC recommended standards and would be missed opportunities if not funded. Interim funded ends when the applicant succeeds in obtaining an R01 or other competing award built on the R56 grant. These awards are not renewable. |
Fmri Studies of Cerebrovascular Structure and Function in Low-Renin Hypertension @ Medical College of Wisconsin
? DESCRIPTION (provided by applicant): Hypertension is the quintessential multisystem disease and is influenced by a wide range of factors including genetics and the environment. Chronic hypertension causes reduced vascular function, reduced blood flow, damaged cerebral autoregulation, and is a known risk factor for ischemic stroke and vascular-associated cognitive decline. Blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI) is sensitive to changes in cerebrovascular hemodynamic function. Strong preliminary rodent fMRI data demonstrate a diminished cerebrovascular BOLD hyperemic response to forepaw sensory stimulation in salt- induced hypertensive Dahl Salt-Sensitive (SS) rats, a widely-used animal model of low-renin hypertension. Clinically, salt-induced low-renin hypertension accounts for 25% of all essential hypertensive patients, but 75% in African Americans. Additional fMRI experiments revealed an earlier and increased cerebral hemodynamic response to vasodilation by CO2 challenge in hypertensive SS rats. Our data suggests that neurovascular coupling is impaired in low-renin salt-induced hypertension since the diminished BOLD response is neuronal in origin and CO2 acts directly on the vasculature bypassing the neurovascular unit. Mechanistically, we hypothesize that salt-sensitive hypertension leads to vessel endothelium dysfunction through damage by oxidative stress. Free radicals reduce the bioavailability of nitric oxide, a key factor in neurovascular coupling. Our hypothesis is based on our previous work in isolated blood vessels of hypertensive SS rats. We have also shown in isolated vessel preparations that these hypertensive vascular phenotypes are associated with the SS Renin allele. Our proposed research plan has three goals: 1) Characterize the neurovascular uncoupling in salt-induced hypertension. 2) Define the sensitivity and selectivity of the brain BOLD fMRI signal to chronic hypertension. 3) Determine the influence of the SS Renin gene allele on phenotypic differences in the BOLD signal in salt-induced hypertension. These goals will be pursued in three Specific Aims. Aim 1: we will simultaneously measure evoked neural activity and BOLD fMRI response in SS and in Brown Norway salt- resistant normotensive rats. Aim 2: we will relate BOLD signal characteristics (e.g. intensity) and physiological factors (e.g. cerebral blood volume) to salt-induced hypertension. Aim 3: we will examine the influence of the Renin gene on the phenotypic variation in BOLD signal in genetically modified rat strains under both low and high-salt consumption. This project will build a platform methodology for resolving the influence of vascular genes on the BOLD signal and lead to potential BOLD fMRI biomarkers for hypertensive cerebral blood flow changes that precede ischemic stroke. Since hypertension affects 1 of every 3 Americans, this work will additionally impact interpretation of human fMRI exams.
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