Highlighted Paper selected by Editor-in-Chief : Protection of Tong-Qiao-Huo-Xue Decoction against Cerebral Ischemic Injury through Reduction Blood-Brain Barrier Permeability

DOI Web Site Web Site PubMed 被引用文献2件 参考文献23件
  • Li Lili
    Key Laboratory of Xin’an Medicine, Ministry of Education Institute for Pharmacodynamics and Safety Evaluation of Chinese Medicine, Anhui Academy of Chinese Medicine College of Pharmacy, Anhui University of Chinese Medicine
  • Wang Ning
    Key Laboratory of Xin’an Medicine, Ministry of Education Institute for Pharmacodynamics and Safety Evaluation of Chinese Medicine, Anhui Academy of Chinese Medicine College of Pharmacy, Anhui University of Chinese Medicine
  • Jin Qizhong
    Key Laboratory of Xin’an Medicine, Ministry of Education Institute for Pharmacodynamics and Safety Evaluation of Chinese Medicine, Anhui Academy of Chinese Medicine
  • Wu Qian
    Key Laboratory of Xin’an Medicine, Ministry of Education Institute for Pharmacodynamics and Safety Evaluation of Chinese Medicine, Anhui Academy of Chinese Medicine
  • Liu Yafang
    Key Laboratory of Xin’an Medicine, Ministry of Education Institute for Pharmacodynamics and Safety Evaluation of Chinese Medicine, Anhui Academy of Chinese Medicine College of Pharmacy, Anhui University of Chinese Medicine
  • Wang Yan
    Key Laboratory of Xin’an Medicine, Ministry of Education Institute for Pharmacodynamics and Safety Evaluation of Chinese Medicine, Anhui Academy of Chinese Medicine

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  • Protection of Tong-Qiao-Huo-Xue Decoction against Cerebral Ischemic Injury through Reduction Blood–Brain Barrier Permeability

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<p>Tong-Qiao-Huo-Xue Decoction (TQHXD) is a classical prescription in traditional Chinese medicine treating blood stagnation in the head and facial channels, especially cerebral ischemia. We investigate the effect of TQHXD on the expressions of related proteins of the blood–brain barrier (BBB) and analysis of constituents in the cerebrospinal fluid (CSF) on cerebral ischemic model rats. Here, we demonstrate that TQHXD protected the hippocampus neurons, reduced the opening of tight junction (TJ) and decreased the permeability of BBB by up-regulating ZO-1, occludin, claudin-5 expressions, down-regulating aquaporin-4 (AQP-4) and matrix metalloproteinase-9 (MMP-9) expressions. Meanwhile, we detected Muscone, ligustilide and hydroxysafflor yellow A in CSF on cerebral ischemic model rats. These compounds could be identified as the main active ingredients of TQHXD on protecting the damaged BBB. These results suggest that TQHXD could act as a potential neuroprotective agent against BBB damage for cerebral ischemia.</p>

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