Therapeutic Efficacy of Neuro AiD™ (MLC 601), a Traditional Chinese Medicine, in Experimental Traumatic Brain Injury

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作者
Ming-Che Tsai
Ching-Ping Chang
Syue-Wei Peng
Kai-Sheng Jhuang
Yi-Hsien Fang
Mao-Tsun Lin
Thomas Chang-Yao Tsao
机构
[1] Chung Shan Medical University,Institute of Medicine and School of Medicine
[2] Chung Shan Medical University Hospital,Department of Emergency Medicine
[3] Southern Taiwan University of Science and Technology,Department of Biotechnology
[4] Taipei Medical University,Graduate Institute of Medical Sciences, College of Medicine
[5] National Chung Cheng University,Department of Life Science, Institute of Molecular Biology, Institute of Biomedical Science
[6] Chi Mei Medical Center,Department of Medical Research
[7] Chung Shan Medical University Hospital and Chung Shan Medical University,Division of Thoracic Medicine
来源
关键词
Astragalosides; Traumatic brain injury; Microglia; Tumor necrosis factor-α;
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学科分类号
摘要
Traumatic brain injury (TBI) causes increased release of several mediators from injured and dead cells and elicits microglial activation. Activated microglia change their morphology, migrate to injury sites, and release tumor necrosis factor-alpha (TNF-α) and others. In this study we used a controlled fluid percussion injury model of TBI in the rat to determine whether early (4 h post-injury) or late (4 days post-injury) treatment with MLC 601, a Traditional Chinese Medicine, would affect microglial activation and improve recovery. MLC 601 was chosen for this study because its herbal component MLC 901 was beneficial in treating TBI in rats. Herein, rats with induced TBI were treated with MLC 601 (0.2–0.8 mg/kg) 1 h (early treatment) or 4 day post-injury (late treatment) and then injected once daily for consecutive 2 days. Acute neurological and motor deficits were assessed in all rats the day before and 4 days after early MLC 601 treatment. An immunofluorescence microscopy method was used to count the numbers of the cells colocalized with neuron- and apoptosis-specific markers, and the cells colocalized with microglia- and TNF-α-specific markers, in the contused brain regions 4 days post-injury. An immunohistochemistry method was used to evaluate both the number and the morphological transformation of microglia in the injured areas. It was found that early treatment with MLC 601 had better effects in reducing TBI-induced cerebral contusion than did the late therapy with MLC 601. Cerebral contusion caused by TBI was associated with neurological motor deficits, brain apoptosis, and activated microglia (e.g., microgliosis, amoeboid microglia, and microglial overexpression of TNF-α), which all were significantly attenuated by MLC 601 therapy. Our data suggest that MLC 601 is a promising agent for treatment of TBI in rats.
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页码:45 / 54
页数:9
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