(Stroke. 1995;26:2103-2111.)
© 1995 American Heart Association, Inc.
Articles |
From the Laboratory for Research in Neonatal Physiology, Department of Physiology and Biophysics, University of Tennessee, Memphis.
Correspondence to Charles W. Leffler, PhD, Department of Physiology and Biophysics, University of Tennessee at Memphis, 894 Union Ave, Memphis, TN 38163. E-mail cleffler@ physiol.utmem.edu.
Background and Purpose Both light/dye endothelial injury and indomethacin treatment inhibit hypercapnia-induced cerebral prostacyclin synthesis and pial arteriolar dilation in newborn pigs. Topical iloprost can allow hypercapnia-induced dilation of pial arterioles to occur in piglets treated with indomethacin. We addressed the hypothesis that prostacyclin receptor activation with iloprost can return the ability of pial arterioles with endothelial injury to respond to hypercapnia. We also examined whether the endothelial dependence and the permissive role of prostacyclin extended to histamine-induced dilation or are specific for hypercapnia.
Methods Experiments used chloralose-anesthetized
piglets equipped with closed cranial windows. Hypercapnia
(PaCO2
80 mm Hg) and topically applied
histamine (10-6 and 10-5 mol/L) dilated pial
arterioles. Dilations in response to both stimuli were abolished by
light/dye treatment.
Results Simultaneous topical treatment with iloprost (10-12 mol/L, which caused no residual dilation, returned dilation of pial arterioles to both hypercapnia and histamine. On removal of iloprost, responses were again absent and returned with readdition of iloprost to the cortical cerebrospinal fluid. Neither isoproterenol nor sodium nitroprusside returned responses to hypercapnia after light/dye treatment.
Conclusions These data add further support to the hypothesis that prostacyclin represents an important endothelial-derived signal in the newborn pig cerebral circulation that can permit appropriate responses by adjacent smooth muscle in response to specific stimuli.
Key Words: cerebral circulation histamine hypercapnia prostacyclins pigs
This article has been cited by other articles:
![]() |
F. Domoki, B. Kis, K. Nagy, E. Farkas, D. W. Busija, and F. Bari Diazoxide preserves hypercapnia-induced arteriolar vasodilation after global cerebral ischemia in piglets Am J Physiol Heart Circ Physiol, July 1, 2005; 289(1): H368 - H373. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Pourcyrous, H. S. Bada, K. E. Blaho, M. M. Randolph, H. Parfenova, T. D. Mandrell, K. Arheart, S. B. Korones, and C. W. Leffler Chronic Prenatal Exposure to Cocaine Alters Cerebrovascular Responses in Newborn Pigs Experimental Biology and Medicine, September 1, 2004; 229(8): 819 - 825. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Zhang and C. W. Leffler Compensatory role of NO in cerebral circulation of piglets chronically treated with indomethacin Am J Physiol Regulatory Integrative Comp Physiol, February 1, 2002; 282(2): R400 - R410. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. P. Willis and C. W. Leffler Endothelial NO and prostanoid involvement in newborn and juvenile pig pial arteriolar vasomotor responses Am J Physiol Heart Circ Physiol, December 1, 2001; 281(6): H2366 - H2377. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. A. Parkinson, H. Parfenova, and C. W. Leffler Phospholipase C Activation by Prostacyclin Receptor Agonist in Cerebral Microvascular Smooth Muscle Cells Experimental Biology and Medicine, January 1, 2000; 223(1): 53 - 58. [Abstract] [Full Text] |
||||
![]() |
C. W. Leffler, L. Balabanova, and K. K. Williams cAMP production by piglet cerebral vascular smooth muscle cells: pHo, pHi, and permissive action of PGI2 Am J Physiol Heart Circ Physiol, November 1, 1999; 277(5): H1878 - H1883. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. P. Willis and C. W. Leffler NO and prostanoids: age dependence of hypercapniaand histamine-induced dilations of pig pial arterioles Am J Physiol Heart Circ Physiol, July 1, 1999; 277(1): H299 - H307. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.-S. Bolz and U. Pohl Indomethacin enhances endothelial NO release -- evidence for a role of PGI2 in the autocrine control of calcium-dependent autacoid production Cardiovasc Res, December 1, 1997; 36(3): 437 - 444. [Abstract] [Full Text] [PDF] |
||||
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1995 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |