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IV型磷酸二酯酶抑制剂BBB022对局灶性脑缺血中血脑屏障破坏的保护作用:一项定量研究。

Protection against blood-brain barrier disruption in focal cerebral ischemia by the type IV phosphodiesterase inhibitor BBB022: a quantitative study.

作者信息

Belayev L, Busto R, Ikeda M, Rubin L L, Kajiwara A, Morgan L, Ginsberg M D

机构信息

Cerebral Vascular Disease Research Center, Department of Neurology (D4-5), University of Miami School of Medicine, P.O. Box 016960, Miami, FL 33101, USA.

出版信息

Brain Res. 1998 Mar 23;787(2):277-85. doi: 10.1016/s0006-8993(97)01499-6.

Abstract

We examined the effect of BBB022, a type IV phosphodiesterase inhibitor, on blood-brain barrier (BBB) integrity after transient middle cerebral artery occlusion (MCAo) in rats. Male Sprague-Dawley rats were anesthetized with halothane and subjected to 120 min of temporary MCAo by retrograde intraluminal insertion of a nylon suture coated with poly-L-lysine. The drug (BBB022 in saline, 1 mg kg-1 h-1, i.v.) or vehicle (0.9% saline, 1-2 ml kg-1 h-1) was administered by infusion after the onset of MCAo. Four animal groups were studied: Groups A and B were treated by infusion of vehicle or drug over 5 h, and groups C and D over 48 h. Damage to the BBB was judged by extravasation of Evans blue (EB) dye, which was administered i.v. at 3 h after the onset of MCAo in groups A and B; and at 46 h in groups C and D. Fluorometric quantitation of EB was performed 1 or 2 h later in six brain regions. In the 5-h infusion series (group B), BBB022 decreased dye extravasation in the ipsilateral cortex, striatum and hemisphere (hemisphere mean+/-S.E.M. : 41.2+/-5.4 vs. 82.4+/-9.2 microg/g, p=0.005) compared to the vehicle-treated group (A). The 48-h infusion of BBB022 (group D) also decreased dye extravasation in the ipsilateral cortex (7.4+/-2. 5 vs. 29.0+/-8.3 microg/g, p=0.05), striatum (17.2+/-2.2 vs. 50. 8+/-12.1 microg/g, p=0.03) and hemisphere (30.7+/-4.0 vs. 93.2+/-18 microg/g, p=0.01) compared to the vehicle-treated group (C). BBB022 also significantly improved the neurological score at 3 and 5 h after MCAo (in the 5-h infusion group) and at 60 min, 24 h and 48 h (in the 48-h infusion group) compared to the vehicle groups. These data indicate that BBB022 prevents ischemic damage to the BBB after focal cerebral ischemia in rats.

摘要

我们研究了IV型磷酸二酯酶抑制剂BBB022对大鼠大脑中动脉短暂闭塞(MCAo)后血脑屏障(BBB)完整性的影响。雄性Sprague-Dawley大鼠用氟烷麻醉,通过逆行腔内插入涂有聚-L-赖氨酸的尼龙缝线进行120分钟的暂时性MCAo。在MCAo发作后通过输注给予药物(溶于生理盐水中的BBB022,1mg kg-1 h-1,静脉注射)或载体(0.9%生理盐水,1-2ml kg-1 h-1)。研究了四个动物组:A组和B组在5小时内输注载体或药物,C组和D组在48小时内输注。通过伊文思蓝(EB)染料外渗判断BBB的损伤,在A组和B组中,于MCAo发作后3小时静脉注射EB染料;在C组和D组中,于46小时静脉注射。1或2小时后在六个脑区进行EB的荧光定量分析。在5小时输注系列(B组)中,与载体处理组(A组)相比,BBB022减少了同侧皮质、纹状体和半球的染料外渗(半球平均值±标准误:41.2±5.4对82.4±9.2μg/g,p = 0.005)。与载体处理组(C组)相比,48小时输注BBB022(D组)也减少了同侧皮质(7.4±2.5对29.0±8.3μg/g,p = 0.05)、纹状体(17.2±2.2对50.8±12.1μg/g,p = 0.03)和半球(30.7±4.0对93.2±18μg/g,p = 0.01)的染料外渗。与载体组相比,BBB022在MCAo后3小时和5小时(在5小时输注组中)以及在60分钟、24小时和48小时(在48小时输注组中)也显著改善了神经学评分。这些数据表明,BBB022可预防大鼠局灶性脑缺血后BBB的缺血性损伤。

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