Metabolomics Study on the Effects of Salvianolic Acid B and Borneol for Treating Cerebral Ischemia in Rats by Ultra-Performance Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry

被引:15
作者
Duan, Wenting [1 ]
Wang, Lin [2 ]
Lv, Jianzhuang [1 ]
Gao, Kai [3 ]
Lu, Yiqing [1 ]
Qin, Shaobo [1 ]
Ma, Xin [1 ]
Li, Jiankang [3 ]
Ge, Xingli [1 ]
机构
[1] Xian 1 Hosp, Dept Cardiol, Xian 710002, Shaanxi, Peoples R China
[2] Xian 1 Hosp, Dept Med Lab, Xian, Shaanxi, Peoples R China
[3] Air Force Med Univ, Xijing Hosp, Dept Pharm, Xian 710032, Shaanxi, Peoples R China
关键词
Sal B; borneol; cerebral ischemia; metabolomics; neuroprotection; UPLC-Q; TOF-MS; INJURY; PHARMACOKINETICS; MILTIORRHIZA; INFLAMMATION; MEDICINES; MODEL;
D O I
10.1089/rej.2018.2099
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Salviae miltiorrliza-borneol Jun-Shi coupled-herbs have been widely used for treatment of ischemia stroke. Salvianolic acid B was the most abundant and bioactive compound of Salviae miltiorrliza and used for prevention and treatment of cerebrovascular diseases. However, the scientific intension and compatible mechanism of Salvianolic acid B - borneol combination were still unknown. A metabolomics study approach based on ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-Q/TOF-MS) combined with a pathological study has been applied to study the metabolic disturbances of cerebral ischemia and evaluate the efficacies of Sal B and Sal B/borneol against cerebral ischemia in middle cerebral artery occlusion (MCAO) rats. The neuroprotection of Sal B and Sal B/borneol was reversed through the evaluation of neurological deficits, infarct volume, and neuronal apoptosis in MCAO model. The metabonomic analysis revealed that the MCAO-induced cerebral ischemia could be ameliorated by Sal B through improving the energy metabolism, lipids metabolism, inflammatory responses, and oxidant stress. Borneol could enhance the neuroprotective effects, was associated with the increased concentration of Sal B, and attenuate the function of sphingolipid metabolism pathway in cerebral ischemia rats. These findings perhaps clarify the mechanism of neuroprotective effects of treating ischemia stroke by Sal B or Sal B/borneol preliminarily through metabolomics and push the quality promotion and the composition of borneol/Sal B in secondary development of prescription.
引用
收藏
页码:313 / 324
页数:12
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