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
[1]   EVALUATION OF 2, 3, 5-TRIPHENYLTETRAZOLIUM CHLORIDE AS A STAIN FOR DETECTION AND QUANTIFICATION OF EXPERIMENTAL CEREBRAL INFARCTION IN RATS [J].
BEDERSON, JB ;
PITTS, LH ;
GERMANO, SM ;
NISHIMURA, MC ;
DAVIS, RL ;
BARTKOWSKI, HM .
STROKE, 1986, 17 (06) :1304-1308
[2]   RAT MIDDLE CEREBRAL-ARTERY OCCLUSION - EVALUATION OF THE MODEL AND DEVELOPMENT OF A NEUROLOGIC EXAMINATION [J].
BEDERSON, JB ;
PITTS, LH ;
TSUJI, M ;
NISHIMURA, MC ;
DAVIS, RL ;
BARTKOWSKI, H .
STROKE, 1986, 17 (03) :472-476
[3]  
Bennai F, 1999, J AM SOC NEPHROL, V10, pS104
[4]  
CHANDLER LJ, 1995, AM J PHYSIOL, V268, P700
[5]   Blockade of central angiotensin AT1 receptors improves neurological outcome and reduces expression of AP-1 transcription factors after focal brain ischemia in rats [J].
Dai, WJ ;
Funk, A ;
Herdegen, T ;
Unger, T ;
Culman, J .
STROKE, 1999, 30 (11) :2391-2398
[6]   CONTINUOUS MEASUREMENT OF CEREBRAL CORTICAL BLOOD-FLOW BY LASER-DOPPLER FLOWMETRY IN A RAT STROKE MODEL [J].
DIRNAGL, U ;
KAPLAN, B ;
JACEWICZ, M ;
PULSINELLI, W .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1989, 9 (05) :589-596
[7]  
DORFLER A, 1997, AJNR, V18, P427
[8]   Decompressive craniectomy, reperfusion, or a combination for early treatment of acute "malignant" cerebral hemispheric stroke in rats? Potential mechanisms studied by MRI [J].
Engelhorn, T ;
Doerfler, A ;
Kastrup, A ;
Beaulieu, C ;
de Crespigny, A ;
Forsting, M ;
Moseley, ME .
STROKE, 1999, 30 (07) :1456-1462
[9]  
HACKE W, 1995, JAMA-J AM MED ASSOC, V274, P1017, DOI 10.1001/jama.274.13.1017
[10]   To what extent have functional studies of ischaemia in animals been useful in the assessment of potential neuroprotective agents? [J].
Hunter, AJ ;
Mackay, KB ;
Rogers, DC .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1998, 19 (02) :59-66