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一氧化氮合酶抑制对猫局灶性缺血期间脑血流量和损伤体积的影响。

Effect of nitric oxide synthase inhibition on cerebral blood flow and injury volume during focal ischemia in cats.

作者信息

Nishikawa T, Kirsch J R, Koehler R C, Bredt D S, Snyder S H, Traystman R J

机构信息

Department of Anesthesiology and Critical Care Medicine, Johns Hopkins Medical Institutions, Baltimore, Md.

出版信息

Stroke. 1993 Nov;24(11):1717-24. doi: 10.1161/01.str.24.11.1717.

Abstract

BACKGROUND AND PURPOSE

We tested the hypothesis that inhibition of nitric oxide synthase activity in brain before ischemia alters cerebral blood flow and decreases brain injury after 4 hours of middle cerebral artery occlusion in cats.

METHODS

Halothane-anesthetized cats underwent 4 hours of left middle cerebral artery occlusion after they were randomly assigned to receive either intravenous N omega-nitro-L-arginine methyl ester, at a dose that completely inhibited cortical nitric oxide synthase activity (10 mg/kg, n = 10), or an equal volume of diluent (10 mL saline, n = 10). Serial blood flow measurements were made with radiolabeled microspheres, and injury volume was measured by triphenyltetrazolium staining.

RESULTS

Blood flow to caudate nucleus and inferior temporal cortex decreased to the same extent in both groups during middle cerebral artery occlusion. Somatosensory evoked potential amplitude was reduced to less than 10% of baseline values in both groups. Injury volume of ipsilateral caudate nucleus in cats pretreated with nitroarginine (52 +/- 5%, mean +/- SE) was less (P < .05) compared with the saline group (80 +/- 4%), whereas ipsilateral cerebral hemispheric injury volume was similar between the two groups (30 +/- 6% and 32 +/- 4% of hemisphere in saline and nitroarginine groups, respectively).

CONCLUSIONS

These results suggest that inhibition of nitric oxide synthase decreases caudate injury volume at 4 hours of middle cerebral artery occlusion without an alteration in distribution of cerebral blood flow.

摘要

背景与目的

我们检验了这样一个假设,即在猫大脑中动脉闭塞4小时前抑制一氧化氮合酶活性会改变脑血流量并减少脑损伤。

方法

将氟烷麻醉的猫随机分为两组,一组静脉注射Nω-硝基-L-精氨酸甲酯,剂量为完全抑制皮质一氧化氮合酶活性的剂量(10mg/kg,n = 10),另一组注射等体积的稀释剂(10mL生理盐水,n = 10)。之后对两组猫进行4小时的左大脑中动脉闭塞。用放射性微球进行连续血流量测量,并用三苯基四氮唑染色测量损伤体积。

结果

在大脑中动脉闭塞期间,两组的尾状核和颞下回皮质血流量下降程度相同。两组体感诱发电位幅度均降至基线值的10%以下。用硝基精氨酸预处理的猫同侧尾状核损伤体积(52±5%,平均值±标准误)低于生理盐水组(80±4%)(P <.05),而两组同侧大脑半球损伤体积相似(生理盐水组和硝基精氨酸组分别占半球的30±6%和32±4%)。

结论

这些结果表明,在大脑中动脉闭塞4小时时,抑制一氧化氮合酶可减少尾状核损伤体积,而不会改变脑血流量分布。

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