Endogenous opioids could represent a significant vasoactive component in the cerebral circulation. The opioids are intrinsic modulators of the cerebral circulation. I will test the hypothesis that opioids act on the cerebral circulation directly as well as indirectly by interacting with neural stimuli and prostanoids. To test these hypotheses, three specific aims will be addressed: 1) characterize the relationship between cerebral opioid concentrations and cerebral hemodynamics during control conditions and during a condition that changes cerebral vascular resistance, namely hemorrhagic hypotension; 2) determine the functional significance of the relationship between cerebral opioids and the cerebral circulation; and 3) investigate the mechanisms by which endogenous opioids affect cerebral hemodynamics by determining the interaction of opioids with other important vascular regulators such as the prostanoid, vasopressin, and adrenergic nervous systems. Both the """"""""closed"""""""" cranial window and radiolabelled microspheres methods will be used in these experiments. Using the cranial window, the investigator can: 1) directly observe and measure diameters of cerebral resistance vessels, 2) perivascularly apply opioids and other drugs, and 3) sample cortical periarachnoid cerebrospinal fluid, and measure opioid, vasopressin, catecholamine, and prostanoid levels via HPLC and radioimmunoassay. To complement the window experiments, radiomicrospheres will be used to allow study of distribution of cerebral blood flow and cerebral oxygen consumption. This investigation will explore mechanisms involved in the regulation of the cerebral circulation during normal and pathologic conditions and will provide new information in an area where little data are available. These experimental findings may be of clinical relevance and lead to therapies that improve outcome in stressed individuals.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
1R29HL042939-01
Application #
3472672
Study Section
Experimental Cardiovascular Sciences Study Section (ECS)
Project Start
1989-08-01
Project End
1994-07-31
Budget Start
1989-08-01
Budget End
1990-07-31
Support Year
1
Fiscal Year
1989
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
Leffler, C W; Mirro, R; Shanklin, D R et al. (1994) Light/dye microvascular injury selectively eliminates hypercapnia-induced pial arteriolar dilation in newborn pigs. Am J Physiol 266:H623-30
Leffler, C W; Mirro, R; Armstead, W M et al. (1992) Topical arachidonic acid restores pial arteriolar dilation to hypercapnia of postischemic newborn pig brain. Am J Physiol 263:H746-51