| Literature DB >> 28514718 |
Jian-Liang Geng1, Ji-Ye Aa1, Si-Qi Feng1, Shu-Yao Wang2, Pei Wang1, Yue Zhang1, Bing-Chen Ouyang1, Jian-Kun Wang1, Ye-Jin Zhu1, Wen-Zhe Huang2, Zhen-Zhong Wang2, Wei Xiao3, Guang-Ji Wang4.
Abstract
Cerebral ischemia-reperfusion (I/R) injury usually contributes to mortality and disability after ischemic stroke. Ginkgolides injection (GIn), a standard preparation composed of ginkgo diterpene lactones extract, is clinically used for neuroprotective treatment on reconvalescents of cerebral infarction. However, the understanding about its therapeutic mechanism is still lacking. In this study, a gas chromatography-mass spectrometry (GC-MS) based metabolomic approach coupled with multivariate data analysis (MVDA) was applied to explore the neuroprotective effects of GIn in a rodent model of focal ischemic stroke induced by transient middle cerebral artery occlusion (tMCAO). Metabolomic profiling revealed a series of metabolic perturbations that underlie the cerebral I/R pathological events. GIn can reverse the I/R induced brain metabolic deviations by modulating multiple metabolic pathways, such as glycolysis, Krebs cycle, pentose phosphate pathway (PPP), γ-aminobutyrate (GABA) shunt and lipid metabolism. Moreover, the main bioactive components of GIn were distributed to brain tissue much more easily in tMCAO rats than in normal rats after an intravenous administration, suggesting that the increased cerebral exposure to ginkgolides in I/R pathological condition potentially facilitated the neuroprotective effects of GIn by directly targeting at brain. The present study provided valuable information for our understanding about metabolic changes of cerebral I/R injury and clinical application of GIn.Entities:
Keywords: Cerebral exposure level; Cerebral ischemia–reperfusion injury; Ginkgolides injection; Metabolomic profiling; Neuroprotection
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Year: 2017 PMID: 28514718 DOI: 10.1016/j.jpba.2017.04.031
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935