门冬氨酸钾减轻大鼠可控性皮质打击伤引起的脑损伤

目的门冬氨酸钾(potassium aspartate,PA)作为一种电解质补充剂,在临床上广泛使用。以往的研究发现门冬氨酸钾在脑缺血/再灌注大鼠中对细胞凋亡有神经保护的作用。本研究将探讨门冬氨酸钾对创伤性脑损伤(traumatic brain injury,TBI)是否有保护作用。方法 TBI通过大鼠可控性皮质打击伤(controlled cortical impact,CCI)产生。门冬氨酸钾组或溶剂对照组在CCI发生后30 min以腹腔注射给予生理盐水或62.5 mg/kg剂量的PA,观察脑血流灌注量,改良神经功能缺损评分(modified Neurological Severity S...

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Bibliographic Details
Published in中国卒中杂志 Vol. 12; no. 6; pp. 489 - 495
Main Author 顾漪 赵育梅 苏玉金
Format Journal Article
LanguageChinese
Published 首都医科大学 2017
中枢神经系统损伤北京市重点实验室
首都医科大学附属北京天坛医院
100050 北京北京市神经外科研究所神经药物室
国家神经系统疾病临床研究中心
国家神经系统疾病临床研究中心%北京市神经外科研究所神经病理室
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ISSN1673-5765
DOI10.3969/j.issn.1673-5765.2017.06.005

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Summary:目的门冬氨酸钾(potassium aspartate,PA)作为一种电解质补充剂,在临床上广泛使用。以往的研究发现门冬氨酸钾在脑缺血/再灌注大鼠中对细胞凋亡有神经保护的作用。本研究将探讨门冬氨酸钾对创伤性脑损伤(traumatic brain injury,TBI)是否有保护作用。方法 TBI通过大鼠可控性皮质打击伤(controlled cortical impact,CCI)产生。门冬氨酸钾组或溶剂对照组在CCI发生后30 min以腹腔注射给予生理盐水或62.5 mg/kg剂量的PA,观察脑血流灌注量,改良神经功能缺损评分(modified Neurological Severity Score,m NSS)和皮质损伤体积,并检测脑水肿以及脑组织三磷腺苷(adenosine triphosphate,ATP)、乳酸含量和钠钾ATP酶活性。结果在CCI引起的大鼠皮质损伤中,与溶剂对照组相比,急性给予62.5 mg/kg剂量的PA治疗可以明显改善神经功能缺损(P〈0.05),降低皮质损伤体积(P〈0.01),减轻脑水肿(P〈0.05)。此外,与溶剂对照组相比,门冬氨酸钾治疗组显著减少ATP缺失(P〈0.01),降低乳酸含量(P〈0.05),并增加钠钾ATP酶的活性(P〈0.05)。结论 PA能通过增加ATP含量和钠钾ATP酶的活性并降低脑水肿,对TBI具有神经保护作用。这为PA在临床脑损伤时的应用提供了实验证据。
Bibliography:11-5434/R
Aspartic acid; Brain injury; Controlled cortical impact; Ischemia; Na+/K+-ATPase
GU Yi, ZHAO Yu-Mei, SU Yu-Jin.(Department of Pharmacology, Beijing Neurosurgieal Institute, Beijing Tiantan Hospital, Capital Medical University Beijing Key Laboratory of Central Nervous, System Injury, China National Clinical Research Center for Neurological Diseases, Beijing 100050, China)
Objective Potassium aspartate (PA), as an electrolyte supplement, is widely used in clinical practice. Previous study found PA had neuroprotective effects against apoptosis after cerebral ischemia/reperfusion in rats. This study is to investigate whether PA has protective effects on traumatic brain injury. Methods Traumatic brain injury (TBI) was induced by controlled cortical impact (CCI) in rats. Vehicle treatment group or potassium aspartate treatment group were administered saline via intraperitoneal injection or PA at the dose of 62.5 mg/kg at 30 minutes after onset of CCI. The brain blood perfusion, modified Neurological Severity
ISSN:1673-5765
DOI:10.3969/j.issn.1673-5765.2017.06.005