期刊文献+

缺血性脑卒中与CYP450代谢途径的研究进展

Advances in research on ischemic stroke and CYP450 metabolic pathway
下载PDF
导出
摘要 缺血性脑卒中是危害人类健康的主要疾病之一。近年研究发现,多不饱和脂肪酸(PUFA)及其经细胞色素P450 (cytochrome P450,CYP)途径代谢的产物参与缺血性脑卒中的生理病理过程。血浆中ω-3多不饱和脂肪酸(ω-3 PUFA)、20-羟基二十碳四烯酸(20-HETE)和环氧二十碳三烯酸(EETs)浓度水平可反映疾病的预后,对CYP450途径代谢酶进行诱导或抑制可改善神经功能。此外,CYP2C19基因型与氯吡格雷抗血小板治疗效果及复发性缺血性脑卒中有关,因而鉴定基因型和选择合理治疗方案尤为重要。本文就缺血性脑卒中与CYP450代谢途径相关研究进展进行综述。 Ischemic stroke is one of the major diseases that endanger human health in the world. In recent years, studies have found that polyunsaturated fatty acids(PUFA) and its products metabolized by the cytochrome P450(CYP450) pathway are involved in the physiological and pathological processes of cerebral ischemic stroke. Not only the prognosis of the disease can be predicted by detecting the plasma concentration levels of ω-3 Polyunsaturated fatty acid(ω-3 PUFA), 20-hydroxyeicosatetraenoic acid(20-HETE), and epoxyeicosatrienoic acids(EETs), but also the CYP450 pathway metabolic enzyme can be induced or inhibited to change the concentration of related products, thereby improving the neurological function. In addition, the CYP2C19 genotype is associated with the effect of clopidogrel antiplatelet therapy and recurrent ischemic stroke, so it is important for identifying genotypes and selecting a reasonable treatment regimen. This article reviews the research progress of ischemic stroke and CYP450 metabolic pathway.
作者 徐思敏 陈煜森 XU Si-min;CHEN Yu-sen(Department of Neurology, the Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, Guangdong, CHINA)
出处 《海南医学》 CAS 2019年第14期1868-1873,共6页 Hainan Medical Journal
关键词 缺血性脑卒中 细胞色素P450 20-羟基二十碳四烯酸 环氧二十碳三烯酸 Ω-3多不饱和脂肪酸 氯吡格雷 Ischemic stroke Cytochrome P450 20-hydroxyeicosatetraenoic acid Epoxyeicosatrienoic acids ω-3 Polyunsaturated fatty acid Clopidogrel
  • 相关文献

参考文献2

二级参考文献47

  • 1Kelly RP, Close SL, Farid NA, Witers K J, Shen L, Natanegara F, et al. Pharmacokinetics and pharmacodynamics following maintenance doses of prasugrel and clopidogrel in Chinese carriers of CYP2C19 variants. BrJ Clin Pharmaco12012; 73: 93-105.
  • 2Boggon R, van Staa TP, Timmis A, Hemingway H, Ray KK, Begg A, et al. Clopidogrel discontinuation after acute coronary syndromes: frequency, predictors and associations with death and myocardial infarction -- a hospital registry - primary care linked cohort (MINAP- GPRD). Eur Heart J 2011; 32: 2376-86.
  • 3Perry CG, Shuldiner AR. Pharmacogenomics of anti-platelet therapy: how much evidence is enough for clinical implementation? J Hum Genet 2013: 58: 339-45.
  • 4Nguyen TA, Diodati JG, Pharand C. Resistance to clopidogrel: a review of the evidence. J Am Coil Cardiol 2005; 45: 1157-64.
  • 5Serebruany VL, Steinhubl SR, Berger PB, Malinin AI, Bhatt DL, Topoi EJ. Variability in platelet responsiveness to clopidogrel among 544 individuals. J Am Coil Cardiol 2005; 45: 246-51.
  • 6Ford NF. Clopidogrel resistance: pharmacokinetic or pharmaco- genetic? J Clin Pharmacol 2009; 49: 506-12.
  • 7Hasan MS, Basri HB, Hin LP, Stanslas J. Genetic polymorphisms and drug interactions leading to clopidogrel resistance: why the Asian population requires special attention. Int J Neurosci 2013; 123: 143-54.
  • 8Jiang XL, Samant S, Lesko U, Schmidt S. Clinical pharmacokinetics and pharmacodynamics of clopidogrel. Clin Pharmacokinet 2015; 54: 147 - 66.
  • 9Kazui M, Nishiya Y, Ishizuka 1, Hagihara K, Farid NA, Okazaki O, et al. Identification of the human cytochrome P450 enzymes involved in the two oxidative steps in the bioactivation of clopidogrel to its pharmacologically active metabolite. Drug Metab Dispos 2010; 38: 92-9.
  • 10Wang XD, Deng XY, Chen J, Li JL, Chen X, Zhao LZ, et al. Single nucleotide polymorphisms of the pregnane X receptor gene in Han Chinese and a comparison with other ethnic populations. Pharma- cology 2008; 81: 350-4.

共引文献45

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部