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基于(1)H NMR 代谢组学和 NF-κB 通路的羟基红花黄色 A 的神经保护作用的系统综合研究。

A Systematic, Integrated Study on the Neuroprotective Effects of Hydroxysafflor Yellow A Revealed by (1)H NMR-Based Metabonomics and the NF-κB Pathway.

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China ; School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100102, China.

出版信息

Evid Based Complement Alternat Med. 2013;2013:147362. doi: 10.1155/2013/147362. Epub 2013 Apr 22.

Abstract

Hydroxysafflor yellow A (HSYA) is the main active component of the Chinese herb Carthamus tinctorius L.. Purified HSYA is used as a neuroprotective agent to prevent cerebral ischemia. Injectable safflor yellow (50 mg, containing 35 mg HSYA) is widely used to treat patients with ischemic cardiocerebrovascular disease. However, it is unknown how HSYA exerts a protective effect on cerebral ischemia at the molecular level. A systematical integrated study, including histopathological examination, neurological evaluation, blood-brain barrier (BBB), metabonomics, and the nuclear factor-κB (NF-κB) pathway, was applied to elucidate the pathophysiological mechanisms of HSYA neuroprotection at the molecular level. HSYA could travel across the BBB, significantly reducing the infarct volume and improving the neurological functions of rats with ischemia. Treatment with HSYA could lead to relative corrections of the impaired metabolic pathways through energy metabolism disruption, excitatory amino acid toxicity, oxidative stress, and membrane disruption revealed by (1)H NMR-based metabonomics. Meanwhile, HSYA treatment inhibits the NF-κB pathway via suppressing proinflammatory cytokine expression and p65 translocation and binding activity while upregulating an anti-inflammatory cytokine.

摘要

羟基红花黄色素 A(HSYA)是中药红花的主要活性成分。纯化的 HSYA 用作神经保护剂,以预防脑缺血。注射用红花黄色素(50mg,含 HSYA35mg)广泛用于治疗缺血性心脑血管病患者。然而,HSYA 如何在分子水平上发挥对脑缺血的保护作用尚不清楚。本研究采用系统的整合研究方法,包括组织病理学检查、神经学评估、血脑屏障(BBB)、代谢组学和核因子-κB(NF-κB)通路,从分子水平阐明 HSYA 神经保护的病理生理机制。HSYA 可以穿过血脑屏障,显著减少大鼠脑缺血的梗死体积,改善其神经功能。通过(1)H NMR 代谢组学揭示的能量代谢紊乱、兴奋性氨基酸毒性、氧化应激和膜破坏,HSYA 治疗可导致代谢途径的相对纠正。同时,HSYA 治疗通过抑制促炎细胞因子的表达和 p65 易位及结合活性,同时上调抗炎细胞因子,抑制 NF-κB 通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8aa/3654365/3f3e8619261a/ECAM2013-147362.001.jpg

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