Effect of 20-HETE inhibition on infarct volume and cerebral blood flow after transient middle cerebral artery occlusion (CROSBI ID 309697)
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Podaci o odgovornosti
Renic, Marija ; Klaus, Judith A ; Omura, Tomohiro ; Kawashima, Naoya ; Onishi, Michihito ; Miyata, Noriyuki ; Koehler, Raymond C ; Harder, David R ; Roman, Richard J
engleski
Effect of 20-HETE inhibition on infarct volume and cerebral blood flow after transient middle cerebral artery occlusion
This study examined the effects of an inhibitor of 20-hydroxyeicosatetraenoic acid (20-HETE) synthesis, N-(3-chloro-4-morpholin-4-yl)phenyl-N′- hydroxyimido formamide (TS-011), on infarct volume, volume at risk, cerebral blood flow (CBF), and levels of cytochrome P450 (CYP450) eicosanoids in the brain after transient occlusion of the middle cerebral artery (t-MCAO) in rats. TS-011 (0.1 mg/kg, iv) reduced cortical infarct volume by approximately 70% and total infarct volume by 55%. TS-011 had no effect on the volume at risk or CBF during or up to 30 mins after the ischemic period. TS-011 reduced the delayed fall in CBF seen 2 h after reperfusion. The levels of CYP450 eicosanoids were similar in the ischemic and contralateral hemispheres after t-MCAO. TS-011 reduced 20-HETE levels in cerebral tissue by 80% but had no effect on the levels of EETs. Administration of another 20-HETE inhibitor, HET0016 (0.01 to 1.0 mg/kg, iv) or a 20-HETE antagonist 20-hydroxyeicosa-6(Z), 15(Z)-dienoic acid (10mg/kg, iv) also reduced infarct size. Theseresults indicate that inhibitors of the synthesis or vasoconstrictor effects of 20-HETE reduce infarct size in rats after cerebral ischemia. The effects of TS-011 are not associated with changes in the area at risk or CBF and may be because of a potential protective effect in neurons subjected to ischemic stress.
20-HETE ; ischemic stroke ; cytochrome P450 ; cerebral blood flow ; eicosanoids
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Podaci o izdanju
29
2009.
629-639
objavljeno
0271-678X
10.1038/jcbfm.2008.156
Povezanost rada
Temeljne medicinske znanosti