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NMDA 受体阻断对高渗性血脑屏障破坏大鼠脑氧耗的影响。

Effects of blockade of NMDA receptors on cerebral oxygen consumption during hyperosmolar BBB disruption in rats.

机构信息

Department of Anesthesia, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, New Brunswick, NJ 08901-1977, USA.

出版信息

J Neurol Sci. 2013 Mar 15;326(1-2):29-34. doi: 10.1016/j.jns.2013.01.006. Epub 2013 Jan 26.

Abstract

Hyperosmolar blood-brain barrier (BBB) disruption has been reported to increase cerebral O2 consumption. This study was performed to test whether blockade of N-methyl-d-aspartate (NMDA) receptor would affect cerebral O2 consumption during hyperosmolar BBB disruption. A competitive NMDA receptor antagonist CGS-19755 10mg/kg was injected iv 15min before intracarotid infusion of 25% mannitol. Twelve min after BBB disruption, the BBB transfer coefficient (Ki) of (14)C-α-aminoisobutyric acid ((14)C-AIB) was measured. Regional cerebral blood flow (rCBF), regional arteriolar and venular O2 saturation (SaO2 and SvO2 respectively), and O2 consumption were determined using (14)C-iodoantipyrine autoradiography and cryomicrospectrophotometry in alternate slices of the brain tissue. The Ki of (14)C-AIB was markedly increased with hyperosmolar mannitol in both the control (5.8×) and the CGS treated rats (5.2×). With BBB disruption, the O2 consumption was significantly increased (+39%) only in the control but not in the CGS treated rats and was significantly lower (-29%) in the CGS treated than the control rats. The distribution of SvO2 was significantly shifted to the higher concentrations with CGS treatment. Our data demonstrated an increase of O2 consumption by hyperosmolar BBB disruption and attenuation of the increase with NMDA blockade without affecting the degree of BBB disruption.

摘要

高渗性血脑屏障(BBB)破坏已被报道会增加脑氧消耗。本研究旨在测试 N-甲基-D-天冬氨酸(NMDA)受体阻断是否会影响高渗性 BBB 破坏期间的脑氧消耗。在颈内动脉输注 25%甘露醇前 15 分钟,静脉注射竞争性 NMDA 受体拮抗剂 CGS-19755(10mg/kg)。BBB 破坏后 12 分钟,测量(14)C-α-氨基异丁酸((14)C-AIB)的 BBB 转移系数(Ki)。使用(14)C-碘安替比林放射自显影和组织切片的低温显微镜分光光度法,测定局部脑血流(rCBF)、局部动静脉氧饱和度(SaO2 和 SvO2)和氧消耗。在对照(5.8×)和 CGS 处理大鼠(5.2×)中,高渗甘露醇均明显增加了(14)C-AIB 的 Ki。BBB 破坏后,仅在对照组中,氧消耗显著增加(+39%),而在 CGS 处理组中则没有增加,并且 CGS 处理组的氧消耗显著低于对照组(-29%)。SvO2 的分布在 CGS 处理后明显向较高浓度转移。我们的数据表明,高渗性 BBB 破坏会增加氧消耗,并通过 NMDA 阻断来减弱这种增加,而不影响 BBB 破坏的程度。

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