""""""""Flow-induced dilation"""""""" (often referred to as """"""""upstream dilation"""""""") of arteries and arterioles is an important mechanism for maintaining vascular homeostasis in the peripheral circulation. When blood flow increases in an artery or arteriole, the vessel dilates. This """"""""flow-induced dilation"""""""" functions to maintain appropriate perfusion through a tissue bed by maintaining an optimum perfusion pressure across the bed. In the cerebral circulation, flow-induced effects are not well understood. In fact, there is not a consensus that flow-induced dilations even occur. The confusion and lack of consensus in the cerebral circulation could be due to multiple mechanisms responsible for flow-induced dilations. Furthermore, different mechanisms might occur at different levels of the cerebral circulatory tree. Two general hypotheses will be tested: (1) Flow-induced dilations occur at all levels of the vascular tree in the cerebral circulation (large arteries, smaller arteries, and arterioles). The mechanisms for flow-induced dilations are different at the different levels of the vascular tree. Specific hypotheses include experiments testing whether shear stress causes (a) release of an EDRF, (b) an elaboration of endothelial ATP as an autocrine/paracrine vasodilator (c) an elaboration of RBC ATP as an paracrine vasodilator (d) intravascular ATP delivery to the endothelium is a regulator of vasodilation (2) Pathological conditions such as ischemia/reperfusion impair """"""""flow-induced dilations"""""""" at all levels of the cerebral circulatory tree. These hypothesis will be tested using isolated, pressurized, and perfused rat cerebral arteries and arterioles. The study of flow-induced dilations along the entire length of a vascular tree in a single organ is unique. Furthermore, consideration of multiple mechanisms provides a novel approach to the study of flow-induced dilations. After considering and testing these hypotheses, a clearer understanding of flow-induced effects in the cerebral circulation will be obtained. Furthermore, insight into the consequences of ischemia/reperfusion on flow-induced dilations in the cerebral circulation could lead to a therapeutic strategy for improving maintenance of cerebral perfusion after stroke.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS037250-01
Application #
2504348
Study Section
Neurology A Study Section (NEUA)
Program Officer
Jacobs, Tom P
Project Start
1997-12-15
Project End
2001-11-30
Budget Start
1997-12-15
Budget End
1998-11-30
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Anesthesiology
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Marrelli, Sean P; Eckmann, Maxim S; Hunte, Michael S (2003) Role of endothelial intermediate conductance KCa channels in cerebral EDHF-mediated dilations. Am J Physiol Heart Circ Physiol 285:H1590-9
You, Junping; Marrelli, Sean P; Bryan Jr, Robert M (2002) Role of cytoplasmic phospholipase A2 in endothelium-derived hyperpolarizing factor dilations of rat middle cerebral arteries. J Cereb Blood Flow Metab 22:1239-47
Schildmeyer, Lisa A; Bryan Jr, Robert M (2002) Effect of NO on EDHF response in rat middle cerebral arteries. Am J Physiol Heart Circ Physiol 282:H734-8
Golding, Elke M; Marrelli, Sean P; You, Junping et al. (2002) Endothelium-derived hyperpolarizing factor in the brain: a new regulator of cerebral blood flow? Stroke 33:661-3
You, J; Edvinsson, L; Bryan Jr, R M (2001) Neuropeptide Y-mediated constriction and dilation in rat middle cerebral arteries. J Cereb Blood Flow Metab 21:77-84
Bryan Jr, R M; Steenberg, M L; Marrelli, S P (2001) Role of endothelium in shear stress-induced constrictions in rat middle cerebral artery. Stroke 32:1394-400
Marrelli, S P (2001) Mechanisms of endothelial P2Y(1)- and P2Y(2)-mediated vasodilatation involve differential [Ca2+]i responses. Am J Physiol Heart Circ Physiol 281:H1759-66
Golding, E M; You, J; Robertson, C S et al. (2001) Potentiated endothelium-derived hyperpolarizing factor-mediated dilations in cerebral arteries following mild head injury. J Neurotrauma 18:691-7
Golding, E M; Kepler, T E (2001) Role of estrogen in modulating EDHF-mediated dilations in the female rat middle cerebral artery. Am J Physiol Heart Circ Physiol 280:H2417-23
Bryan Jr, R M; Marrelli, S P; Steenberg, M L et al. (2001) Effects of luminal shear stress on cerebral arteries and arterioles. Am J Physiol Heart Circ Physiol 280:H2011-22

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