Neuroprotective effects of the novel polyethylene glycol-hemoglobin conjugate SB1 on experimental cerebral thromboembolism in rats

被引:6
作者
Ji, Hyeong-Jin
Chai, Hee-Youl
Nahm, Sang-Soep
Lee, Junhee
Bae, Gun Won
Nho, Kwang
Kim, Yun-Bae
Kang, Jong-Koo
机构
[1] Chungbuk Natl Univ, Coll Vet Med, Cheongju 361763, South Korea
[2] Chungbuk Natl Univ, Vet Med Res Inst, Cheongju 361763, South Korea
[3] SunBio Inc, Anyang 431060, South Korea
基金
新加坡国家研究基金会;
关键词
hemoglobin; polyethylene glycol conjugate; stroke; neuroprotection; CROSS-LINKED HEMOGLOBIN; HYPERVOLEMIC-HEMODILUTION; INFARCT VOLUME; BRAIN-INJURY; ISCHEMIA; MODEL; STROKE; TRANSFUSION; SUBSTITUTES; INHIBITION;
D O I
10.1016/j.ejphar.2007.02.061
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
SunBio1 (SB1) is a novel polyethylene glycol-bovine hemoglobin conjugate. It is a small molecule that shows high oxygen-delivery capacity, and exhibits extended plasma half-life compared to hemoglobin alone, thus reducing renal toxicity. The aim of the present study was to evaluate potential neuroprotective effects of SB1 using a rat middle cerebral artery occlusion model. The middle cerebral artery of male Sprague-Dawley rats was occluded with a thrombotic blood clot and SB1 was administered via intra-arterial infusion 5 min after the operation. Brain tissue was harvested after 2 It, and cerebral infarct volumes were calculated from coronal sections stained with 2,3,5-triphenyltetrazolium chloride. Three to 6 days after the procedure, sub-groups of animals were subjected to an open field test and the Morris water maze to assess locomotor activity and learning/memory function. Thrombotic blood clots induced extensive brain infarction and edema; however, these were significantly reduced in SB1 treated animals. In addition, SB1 treatment increased locomotor activity in open field tests, and improved the learning/memory deficits caused by the thromboembolism. These results suggest that SB1 has neuroprotective effects against ischemic brain injury caused by thromboembolism. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 87
页数:5
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