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通过颈内动脉输注癸酸钠实现大鼠血脑屏障的分级可逆开放。

Graded reversible opening of the rat blood-brain barrier by intracarotid infusion of sodium caprate.

作者信息

Preston Edward, Slinn Jacqueline, Vinokourov Inna, Stanimirovic Danica

机构信息

Cerebrovascular Research Group, Institute for Biological Sciences, Building M54, 1200 Montreal Road, National Research Council of Canada, Ottawa, Ontario, Canada K1A 0R6.

出版信息

J Neurosci Methods. 2008 Mar 15;168(2):443-9. doi: 10.1016/j.jneumeth.2007.11.004. Epub 2007 Nov 19.

Abstract

The fatty acid salt, sodium caprate (C10) is a well recognized drug absorption enhancer in intestine because of its ability to widen tight junctions in the epithelial cell lining. Caprate's potential usefulness to similarly alter the blood-brain barrier (BBB) tight junctions of brain vasculature and enhance CNS drug delivery has undergone little investigation. Adult SD rats were anesthetized and C10 was infused into the left internal carotid artery (dosing parameters: 10-30 mM, 1 or 2 ml min(-1), for 0.5-1.5 min). Beginning 5 or 60 min after infusion an i.v. bolus of [3H]mannitol was allowed to circulate for 30 min and degree of BBB leakiness measured as magnitude of the transfer constant (Ki, nl g(-1)s(-1)) for blood to brain mannitol permeation determined from brain and plasma samples. In initial experiments identical C10 infusions caused dramatic BBB opening in some rats, e.g., 10-fold increase in Ki, but not in others. Higher dosing produced consistent opening measured 5-35 or 60-90 min post-infusion but was also toxic as shown by severe brain edema and cardio-respiratory failure. The variable effect of moderate doses was attributed to the fact that arterial blood pressure markedly increased during C10 infusion and may have altered the flow dynamics of cerebrovascular caprate distribution from rat to rat. We modified the procedure by temporarily withdrawing blood to produce hypovolemia and systemic arterial hypotension during C10 infusion. Caprate infusions of 15-25 mM, 2 ml min(-1) for 1 min, produced reliable dose-related openings that lasted as much as an hour, were reversible, and accompanied by little or moderate edema, depending on dose. These findings confirm an earlier report showing that intracarotid caprate infusion opens the BBB but also show that control of the temporary hypertensive response produced by intracarotid caprate infusion is key to tailoring the dosage to consistently achieve graded, reversible BBB opening.

摘要

脂肪酸盐癸酸钠(C10)是一种广为人知的肠道药物吸收促进剂,因为它能够扩大上皮细胞内衬中的紧密连接。癸酸盐对类似改变脑血管的血脑屏障(BBB)紧密连接并增强中枢神经系统药物递送的潜在用途尚未得到充分研究。将成年SD大鼠麻醉,然后将C10注入左颈内动脉(给药参数:10 - 30 mM,1或2 ml min(-1),持续0.5 - 1.5分钟)。在输注后5或60分钟开始,静脉注射[3H]甘露醇推注,使其循环30分钟,并根据脑和血浆样本测定血脑屏障渗漏程度,以血脑甘露醇渗透的转运常数(Ki,nl g(-1)s(-1))大小来衡量。在最初的实验中,相同的C10输注在一些大鼠中引起了显著的血脑屏障开放,例如,Ki增加了10倍,但在其他大鼠中则没有。更高剂量的输注在输注后5 - 35分钟或60 - 90分钟时产生了一致的开放,但也有毒性,表现为严重脑水肿和心肺功能衰竭。中等剂量的可变效应归因于在C10输注期间动脉血压显著升高,这可能改变了大鼠之间脑血管癸酸盐分布的流动动力学。我们修改了实验程序,在C10输注期间通过暂时抽血产生血容量不足和全身性动脉低血压。15 - 25 mM、2 ml min(-1)持续1分钟的癸酸盐输注产生了可靠的剂量相关开放,持续长达1小时,是可逆的,并且根据剂量不同伴有轻微或中度水肿。这些发现证实了早期的一份报告,即颈内输注癸酸盐会打开血脑屏障,但也表明控制颈内输注癸酸盐产生的暂时性高血压反应是调整剂量以始终实现分级、可逆性血脑屏障开放的关键。

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