化瘀通络法通过SATB1/HDAC1/HDAC3转录网络调控脑缺血神经保护的分子机制

批准号:
82004086
项目类别:
青年科学基金项目
资助金额:
24.0 万元
负责人:
贤明华
依托单位:
学科分类:
中西医结合基础理论
结题年份:
2023
批准年份:
2020
项目状态:
已结题
项目参与者:
贤明华
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中文摘要
化瘀通络法常用于治疗缺血性脑卒中,且具有确切临床疗效,尤其在神经功能损伤恢复上。鉴于化瘀通络相关研究多集中在血管系统角度并已取得一定研究成果,但对神经元保护研究尚缺乏深入机制探讨,难以全面阐明化瘀通络科学内涵。前期研究采用临床疗效确切的化瘀通络方丹红注射液为探针,通过高通量蛋白质组学等方法,筛选出了与缺血性脑卒中病理过程密切相关的特殊富含AT序列结合蛋白(SATB1)。据此新发现,继续深入研究其在缺血性脑卒中病理过程神经保护所扮演角色,对于进一步提高对缺血性脑卒中的病理认识,并为发现治疗新靶点、从神经元层面阐明“化瘀通络”新的科学内涵尤为必要。本项目拟建立体内小鼠MCAO模型和体外神经元细胞OGD模型,从动物、细胞、分子水平围绕上述科学问题而开展研究,其不仅有助于发现缺血性脑卒中干预的新机制,也有利于阐明“化瘀通络” 神经元层面的科学内涵。
英文摘要
Blood-stasis-removing and collateral-activating therapies is commonly used in the treatment of ischemic stroke, and has definite clinical efficacy, especially in the recovery of neurological damage. In view of the fact that the research related to blood-stasis-removing and collateral-activating therapies focuses on the vascular system and has achieved certain research results, there is still no in-depth mechanism for the research of neuron protection, and it is difficult to fully clarify the scientific connotation of blood-stasis-removing and collateral-activating therapies. In the previous study, Danhong injection, which was the representative prescription of blood-stasis-removing and collateral-activating therapies, was used as a probe with high clinical efficacy. High-throughput proteomics and other methods were used to screen out special AT-sequence-binding proteins (SATB1) that are closely related to the pathological process of ischemic stroke . Based on this new discovery, continue to further study its role in neuroprotection in the pathological process of ischemic stroke, to further improve the pathological understanding of ischemic stroke, and to clarify from the neuron level for the discovery of new therapeutic targets. The new scientific connotation of "blood-stasis-removing and collateral-activating therapies" is especially necessary. This project intends to establish an in vivo mouse MCAO model and an in vitro neuronal cell OGD model, and conduct research on the above scientific issues from the animal, cellular, and molecular levels, which not only helps to discover new mechanisms for ischemic stroke intervention, but also it is helpful to clarify the scientific connotation of "blood-stasis-removing and collateral-activating therapies" at neuron level.
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专利列表
DOI:10.1016/j.phrs.2022.106230
发表时间:2022-05-06
期刊:PHARMACOLOGICAL RESEARCH
影响因子:9.3
作者:Liang, Jiayin;Zhang, Yutong;Wang, Shumei
通讯作者:Wang, Shumei
DOI:10.1039/d2fo02367a
发表时间:2022
期刊:Food & Function
影响因子:6.1
作者:Jiayin Liang;Jiale Cai;Yutong Zhang;Meixia Xie;Xiaoshi Li;Tao Hu;Shengwang Liang;Minghua Xian;Shumei Wang
通讯作者:Shumei Wang
DOI:10.1007/s12035-022-03075-z
发表时间:2022-10
期刊:Molecular Neurobiology
影响因子:5.1
作者:S. Zhan;Jiayin Liang;Huiting Lin;Jiale Cai;Xinxin Yang;Hongwei Wu;Junying Wei;Shumei Wang;Minghua Xian
通讯作者:S. Zhan;Jiayin Liang;Huiting Lin;Jiale Cai;Xinxin Yang;Hongwei Wu;Junying Wei;Shumei Wang;Minghua Xian
DOI:10.1016/j.jep.2022.115281
发表时间:2022-05-04
期刊:JOURNAL OF ETHNOPHARMACOLOGY
影响因子:5.4
作者:Xian,Minghua;Shen,Lin;Wang,Shumei
通讯作者:Wang,Shumei
DOI:10.1039/d1fo01144h
发表时间:2021-06-28
期刊:FOOD & FUNCTION
影响因子:6.1
作者:Xian, Minghua;Cai, Jiale;Wang, Shumei
通讯作者:Wang, Shumei
三棱素A靶向ASAP2介导ERK1/2/JUNB/ATF3调控脑缺血小胶质细胞极化的机制研究
- 批准号:--
- 项目类别:省市级项目
- 资助金额:15.0万元
- 批准年份:2024
- 负责人:贤明华
- 依托单位:
化瘀通络法通过SATB1/JUNB介导“氨基酸代谢网-小胶质细胞极化”调控脑缺血神经功能恢复的机制研究
- 批准号:82374172
- 项目类别:面上项目
- 资助金额:49万元
- 批准年份:2023
- 负责人:贤明华
- 依托单位:
国内基金
海外基金
