20-HETE contributes to the acute fall in cerebral blood flow after subarachnoid hemorrhage in the rat
Open Access
- 1 April 2002
- journal article
- Published by American Physiological Society in American Journal of Physiology-Heart and Circulatory Physiology
- Vol. 282 (4) , H1556-H1565
- https://doi.org/10.1152/ajpheart.00924.2001
Abstract
This study examined the effects of blocking the formation of 20-hydroxyeicosatetraenoic acid (20-HETE) on the acute fall in cerebral blood flow after subarachnoid hemorrhage (SAH) in the rat. In vehicle-treated rats, regional cerebral blood flow (rCBF) measured with laser-Doppler flowmetry fell by 30% 10 min after the injection of 0.3 ml of arterial blood into the cisterna magna, and it remained at this level for 2 h. Pretreatment with inhibitors of the formation of 20-HETE, 17-octadecynoic acid (17-ODYA; 1.5 nmol intrathecally) and N-hydroxy- N′-(4-butyl-2-methylphenyl)formamidine (HET0016; 10 mg/kg iv), reduced the initial fall in rCBF by 40%, and rCBF fully recovered 1 h after induction of SAH. The concentration of 20-HETE in the cerebrospinal fluid rose from 12 ± 2 to 199 ± 17 ng/ml after SAH in vehicle-treated rats. 20-HETE levels averaged only 15 ± 11 and 39 ± 13 ng/ml in rats pretreated with 17-ODYA or HET0016, respectively. HET0016 selectively inhibited the formation of 20-HETE in rat renal microsomes with an IC50of 50 of 42, 125, and 100 nM, respectively. These results indicate that 20-HETE contributes to the acute fall in rCBF after SAH in rats.Keywords
This publication has 41 references indexed in Scilit:
- Angiotensin II releases 20-HETE from rat renal microvesselsAmerican Journal of Physiology-Renal Physiology, 2000
- Epidemiology of Aneurysmal Subarachnoid Hemorrhage in Australia and New ZealandStroke, 2000
- 16(R)-hydroxy-5,8,11,14-eicosatetraenoic acid, a new arachidonate metabolite in human polymorphonuclear leukocytesBiochemical Pharmacology, 2000
- Contribution of 20-HETE to Vasodilator Actions of Nitric Oxide in the Cerebral MicrocirculationStroke, 1999
- 20-HETE agonists and antagonists in the renal circulationAmerican Journal of Physiology-Renal Physiology, 1999
- Mechanisms of cerebral vasospasm in subarachnoid haemorrhagePharmacology & Therapeutics, 1995
- Cortical Blood Flow and Cerebral Perfusion Pressure in a New Noncraniotomy Model of Subarachnoid Hemorrhage in the RatStroke, 1995
- Initial and recurrent bleeding are the major causes of death following subarachnoid hemorrhage.Stroke, 1994
- BQ-123, a peptidic endothelin ETA receptor antagonist, prevents the early cerebral vasospasm following subarachnoid hemorrhage after intracisternal but not intravenous injectionLife Sciences, 1993
- The Biphasic Response of Cerebral Vasospasm in Experimental Subarachnoid HemorrhageJournal of Neurosurgery, 1968