The angiotensin II type 1-receptor blocker candesartan increases cerebral blood flow, reduces infarct size, and improves neurologic outcome after transient cerebral ischemia in rats

被引:95
作者
Engelhorn, T
Goerike, S
Doerfler, A
Okorn, C
Forsting, M
Heusch, T
Schulz, T
机构
[1] Essen Univ, Sch Med, Dept Neuroradiol, D-45122 Essen, Germany
[2] Essen Univ, Inst Pathophysiol, D-45122 Essen, Germany
关键词
experimental ischemia; MCA infarction; reperfusion; AT1-receptor blocker; LDF; radioactive microspheres;
D O I
10.1097/00004647-200404000-00012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The goal of the present study was to test the impact of administration time of the angiotensin II type 1-receptor blocker candesartan on cerebral blood flow (CBF), infarct size, and neuroscore in transient cerebral ischemia. Therefore, 1-hour middle cerebral artery occlusion (MCAO) was followed by reperfusion. Rats received 0.5-mg/kg candesartan intravenously 2 hours before MCAO (pretreatment), 24 hours after MCAO, every 24 hours after MCAO, or 2 hours before and every 24 hours after MCAO. Infarct size (mm(3)) and a neuroscore at day 7 were compared with controls. CBF was quantified by radiolabeled microspheres and laser-Doppler flowmetry. Compared with controls (95 8). infarct size in candesartan-treated groups was smaller (59 5, 68 10, 28 3, and 15 +/- 3, respectively P < 0.05). Although there was no difference in neuroscore between pretreatment and controls (1.55 +/- 0.18, 1.80 +/- 0.13). other treatment regimens resulted in improved neuroscores (1.33 +/- 0.16. 1.11 +/- 0.11, 0.73 +/- 0.15; P < 0.05). CBF in pretreated animals at 0.5 hours after MCAO was significantly higher than in controls (0.58 +/- 0.09 mL (.) g(-1) min(-1) and 44% +/- 7% of baseline compared with 0.49 +/- 0.06 mL (.) g(-1) min(-1) and 37% +/- 6%, microspheres and laser-Doppler flowmetry; P < 0.05). Thus, candesartan reduces infarct size even if administered only during reperfusion. Apart from pretreatment, other treatment regimens result in significantly improved neuroscores. In the acute phase of cerebral ischemia, candesartan increases CBF.
引用
收藏
页码:467 / 474
页数:8
相关论文
共 38 条
[11]  
Iadecola C, 1997, J NEUROSCI, V17, P9157
[12]   Protective effects of candesartan cilexetil (TCV-116) against stroke, kidney dysfunction and cardiac hypertrophy in stroke-prone spontaneously hypertensive rats [J].
Inada, Y ;
Wada, T ;
Ojima, M ;
Sanada, T ;
Shibouta, Y ;
Kanagawa, R ;
Ishimura, Y ;
Fujisawa, Y ;
Nishikawa, K .
CLINICAL AND EXPERIMENTAL HYPERTENSION, 1997, 19 (07) :1079-1099
[13]   Infarct size reduction by AT1-receptor blockade through a signal cascade of AT2-receptor activation, bradykinin and prostaglandins in pigs [J].
Jalowy, A ;
Schulz, R ;
Dörge, H ;
Behrends, M ;
Heusch, G .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 32 (06) :1787-1796
[14]   TEMPORAL THRESHOLDS FOR NEOCORTICAL INFARCTION IN RATS SUBJECTED TO REVERSIBLE FOCAL CEREBRAL-ISCHEMIA [J].
KAPLAN, B ;
BRINT, S ;
TANABE, J ;
JACEWICZ, M ;
WANG, XJ ;
PULSINELLI, W .
STROKE, 1991, 22 (08) :1032-1039
[15]   Effects of TCV-116 on expression of NOS and adrenomedullin in failing heart of Dahl salt-sensitive rats [J].
Kobayashi, N ;
Nishikimi, T ;
Horinaka, S ;
Ishimitsu, T ;
Matsuoka, H .
ATHEROSCLEROSIS, 2001, 156 (02) :255-265
[16]   Temporal evolution of ischemic injury evaluated with diffusion-, perfusion-, and T2-weighted MRI [J].
Li, FH ;
Silva, MD ;
Sotak, CH ;
Fisher, M .
NEUROLOGY, 2000, 54 (03) :689-696
[17]   EFFECT OF BRAIN EDEMA ON INFARCT VOLUME IN A FOCAL CEREBRAL-ISCHEMIA MODEL IN RATS [J].
LIN, TN ;
HE, YY ;
WU, G ;
KHAN, M ;
HSU, CY .
STROKE, 1993, 24 (01) :117-121
[18]   REVERSIBLE MIDDLE CEREBRAL-ARTERY OCCLUSION WITHOUT CRANIECTOMY IN RATS [J].
LONGA, EZ ;
WEINSTEIN, PR ;
CARLSON, S ;
CUMMINS, R .
STROKE, 1989, 20 (01) :84-91
[19]   TISSUE-PLASMINOGEN ACTIVATOR FOR ACUTE ISCHEMIC STROKE [J].
MARLER, JR ;
BROTT, T ;
BRODERICK, J ;
KOTHARI, R ;
ODONOGHUE, M ;
BARSAN, W ;
TOMSICK, T ;
SPILKER, J ;
MILLER, R ;
SAUERBECK, L ;
JARRELL, J ;
KELLY, J ;
PERKINS, T ;
MCDONALD, T ;
RORICK, M ;
HICKEY, C ;
ARMITAGE, J ;
PERRY, C ;
THALINGER, K ;
RHUDE, R ;
SCHILL, J ;
BECKER, PS ;
HEATH, RS ;
ADAMS, D ;
REED, R ;
KLEI, M ;
HUGHES, S ;
ANTHONY, J ;
BAUDENDISTEL, D ;
ZADICOFF, C ;
RYMER, M ;
BETTINGER, I ;
LAUBINGER, P ;
SCHMERLER, M ;
MEIROSE, G ;
LYDEN, P ;
RAPP, K ;
BABCOCK, T ;
DAUM, P ;
PERSONA, D ;
BRODY, M ;
JACKSON, C ;
LEWIS, S ;
LISS, J ;
MAHDAVI, Z ;
ROTHROCK, J ;
TOM, T ;
ZWEIFLER, R ;
DUNFORD, J ;
ZIVIN, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (24) :1581-1587
[20]   MIDDLE CEREBRAL-ARTERY OCCLUSION IN RATS - A NEUROLOGICAL AND PATHOLOGICAL EVALUATION OF A REPRODUCIBLE MODEL [J].
MENZIES, SA ;
SMITH, RR ;
HOFF, JT ;
BETZ, AL .
NEUROSURGERY, 1992, 31 (01) :100-107