Geng Jian-Liang, Aa Ji-Ye, Feng Si-Qi, Wang Shu-Yao, Wang Pei, Zhang Yue, Ouyang Bing-Chen, Wang Jian-Kun, Zhu Ye-Jin, Huang Wen-Zhe, Wang Zhen-Zhong, Xiao Wei, Wang Guang-Ji
Key Laboratory of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China.
Jiangsu Kanion Modern Chinese Medicine Institute, Nanjing 210017, China; State Key Laboratory of Pharmaceutical New-Tech for Chinese Medicine, Jiangsu Kanion Pharmaceutical Co., Ltd., Lianyungang 222001, China.
J Pharm Biomed Anal. 2017 Aug 5;142:190-200. doi: 10.1016/j.jpba.2017.04.031. Epub 2017 Apr 23.
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.
脑缺血再灌注(I/R)损伤通常是缺血性中风后导致死亡和残疾的原因。银杏内酯注射液(GIn)是一种由银杏二萜内酯提取物组成的标准制剂,临床上用于脑梗死恢复期的神经保护治疗。然而,对其治疗机制仍缺乏了解。在本研究中,采用基于气相色谱-质谱联用(GC-MS)的代谢组学方法结合多变量数据分析(MVDA),探讨GIn在短暂性大脑中动脉闭塞(tMCAO)诱导的局灶性缺血性中风大鼠模型中的神经保护作用。代谢组学分析揭示了一系列构成脑I/R病理事件基础的代谢紊乱。GIn可通过调节多种代谢途径,如糖酵解、三羧酸循环、磷酸戊糖途径(PPP)、γ-氨基丁酸(GABA)分流和脂质代谢,逆转I/R诱导的脑代谢偏差。此外,静脉给药后,tMCAO大鼠脑组织中GIn的主要生物活性成分比正常大鼠更容易分布,这表明在I/R病理状态下,脑组织对银杏内酯的暴露增加可能通过直接作用于脑而促进了GIn的神经保护作用。本研究为我们了解脑I/R损伤的代谢变化及GIn的临床应用提供了有价值的信息。