Prostaglandins are synthetized by cerebral vessels and tissues and have vasoactive effects. Their role in control of cerebral blood (CBF), however, is controversial. We propose to examine systematically the role played by prostaglandins in control of the cerebral circulation. Studies are designed to determine whether prostaglandins are involved in maintenance of resting CBF and in cerebrovascular dilatation during hypercapnia, and whether prostaglandins limit constrictor effects of sympathetic nerves on cerebral arteries. several new approaches will be used. First, regional and total CBF will be measured with microspheres. Second, CBF will be measured continuously using a new method developed recently by the applicant. Cerebral blood flow is determined from measurements of diameter and blood velocity in pial artery. Third, efficacy and specificity of inhibition of prostaglandin synthesis in cerebral arteries and tissues by cyclooxygenase inhibitors will be examined using the cranial window method. An added feature of these studies is that experiments will be performed on awake animals when possible. It is expected that administration of cyclooxygenase inhibitors will not afect CBF during normocapnia dn hypercapnia in awake rabbits. Due to species differences, however, prostaglandins may contribute to regulation of CBF under these conditions in awake rats. In other studies, it is expected tht inhibition of prostaglandin synthesis will unmask constrictor effects of smpathetic nerves on CBF. These studies will provide new information on regulation of CBF.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL030260-06
Application #
3341324
Study Section
Experimental Cardiovascular Sciences Study Section (ECS)
Project Start
1982-08-01
Project End
1989-06-30
Budget Start
1988-07-01
Budget End
1989-06-30
Support Year
6
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Tennessee Health Science Center
Department
Type
Schools of Medicine
DUNS #
941884009
City
Memphis
State
TN
Country
United States
Zip Code
38163
Dutta, Somhrita; Rutkai, Ibolya; Katakam, Prasad V G et al. (2015) The mechanistic target of rapamycin (mTOR) pathway and S6 Kinase mediate diazoxide preconditioning in primary rat cortical neurons. J Neurochem 134:845-56
Rutkai, Ibolya; Katakam, Prasad V G; Dutta, Somhrita et al. (2014) Sustained mitochondrial functioning in cerebral arteries after transient ischemic stress in the rat: a potential target for therapies. Am J Physiol Heart Circ Physiol 307:H958-66
Katakam, Prasad V G; Gordon, Angellica O; Sure, Venkata N L R et al. (2014) Diversity of mitochondria-dependent dilator mechanisms in vascular smooth muscle of cerebral arteries from normal and insulin-resistant rats. Am J Physiol Heart Circ Physiol 307:H493-503
Busija, David W; Katakam, Prasad V (2014) Mitochondrial mechanisms in cerebral vascular control: shared signaling pathways with preconditioning. J Vasc Res 51:175-89
Carvalho, Cristina; Katz, Paige S; Dutta, Somhrita et al. (2014) Increased susceptibility to amyloid-? toxicity in rat brain microvascular endothelial cells under hyperglycemic conditions. J Alzheimers Dis 38:75-83
Katakam, Prasad V G; Wappler, Edina A; Katz, Paige S et al. (2013) Depolarization of mitochondria in endothelial cells promotes cerebral artery vasodilation by activation of nitric oxide synthase. Arterioscler Thromb Vasc Biol 33:752-9
Wappler, Edina A; Institoris, Adam; Dutta, Somhrita et al. (2013) Mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures. PLoS One 8:e63206
Nautiyal, Manisha; Katakam, Prasad V G; Busija, David W et al. (2012) Differences in oxidative stress status and expression of MKP-1 in dorsal medulla of transgenic rats with altered brain renin-angiotensin system. Am J Physiol Regul Integr Comp Physiol 303:R799-806
Institoris, Adam; Lenti, Laura; Domoki, Ferenc et al. (2012) Cerebral microcirculatory responses of insulin-resistant rats are preserved to physiological and pharmacological stimuli. Microcirculation 19:749-56
Katakam, Prasad V G; Snipes, James A; Steed, Mesia M et al. (2012) Insulin-induced generation of reactive oxygen species and uncoupling of nitric oxide synthase underlie the cerebrovascular insulin resistance in obese rats. J Cereb Blood Flow Metab 32:792-804

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