Article(id=1322927743607899091, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926217711726961, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2025.08.029, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793340152885, onlineDateStr=2026-10-30, pubDate=1754755200000, pubDateStr=2025-08-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793340152885, onlineIssueDateStr=2026-10-30, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793340152885, creator=13701087609, updateTime=1793340152885, updator=13701087609, issue=Issue{id=1322926217711726961, tenantId=1146029695717560320, journalId=1255847919539208197, year='2025', volume='43', issue='8', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1754755200000', pubDateStr='2025-08-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=0, createTime=1793339789083, creator='13701087609', updateTime=1793340517761, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322929274071679978, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926217711726961, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322929274071679979, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926217711726961, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=145, endPage=148, ext={EN=ArticleExt(id=1322927743817614292, articleId=1322927743607899091, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Exploring Relationship between Ferroptosis and Parkinson´s Disease Based on Blood Turbidity Theory, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Blood turbidity refers to a pathological phenomenon where blood either loses its purity or its circulation due to various internal and external factors,or it can refer to a pathological product resulting from a disease.Parkinson´s disease(PD)is a chronic,progressive neurodegenerative disease,and its prevalence is increasing annually alongside the aging of the population.Many medical practitioners consider that patients with PD are primarily characterized by deficiency of liver and kidney syndrome as the root cause,along with symptoms such as wind,phlegm,fire,stasis and toxicity.As PD progresses,there is a disruption in the balance between the turbid and the clear elements;blood turbidity is generated and accumulates,obstructing the meridians and collaterals,and causing internal organ dysfunction,which ultimately leads to the emergence or exacerbation of PD symptoms.Therefore,the article posits that blood turbidity stagnation is a fundamental pathogenic change in PD.Numerous studies have established that ferroptosis,an iron-dependent form of regulated cell death characterized by lipid peroxidation,is closely associated with the development of PD.The abnormal accumulation of iron and lipids is a pathological hallmark of ferroptosis and represents one of the microscopic manifestations of blood turbidity.The continuous accumulation of iron and lipids leads to the gradual damage and demise of dopaminergic neurons,thereby contributing to the progression of PD.The blood turbidity theory offers a novel perspective for elucidating the mechanisms of PD and guiding its clinical prevention and treatment.Guided by the theory of blood turbidity,this paper proposes a treatment approach that involves activating blood circulation and resolving blood stasis,detoxifying and resolving the turbidity,as well as harmonizing meridians to restore the clear.It also integrates the clinical research to achieve a synergistic intervention in PD,targeting ferroptosis as an entry point,and employing Western pharmaceuticals to reduce side effects or dosages,thereby increasing the treatment effectiveness.
, authors=Qiying LIU
1, Yansai ZHAO
1, Tao QIU
2, authorsList=Qiying LIU, Yansai ZHAO, Tao QIU, authorCompany=null, correspAuthors=Tao QIU, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1322927744316736469, articleId=1322927743607899091, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=基于血浊理论探讨铁死亡与帕金森病的关系, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
血浊是指血液循行失常,失去其清纯状态的一种病理现象或其产生的病理产物。帕金森病(Parkinson’s disease,PD)是一种慢性进行性神经退行性疾病,随着人口老龄化的加重,其患病率正逐年上升。多位医家认为PD患者多为本虚标实之证,以肝肾亏虚为病之本,以风、痰、火、瘀、毒为病之标。随着PD的进展,清浊升降失常,血浊内生,蓄积于内,阻滞经络,脏腑功能失调,最终导致PD临床症状的出现或加重。故认为血浊留滞为PD的基本病机变化。多项研究发现铁死亡作为一种铁依赖性的以脂质过氧化为特点的细胞死亡形式,与PD的发生发展密切相关。铁、脂的异常积累是铁死亡的病理特征,也是血浊的微观体现之一,随着铁、脂的持续积累,多巴胺能神经元逐渐受损死亡,促使PD的进展。血浊理论的提出为解释PD的机制以及指导PD的临床防治提供了新思路。在血浊理论指导下,提出活血化瘀、解毒化浊、和脉复清的治法,同时结合临床研究,以铁死亡为切入点,配合西药使用实现对PD的协同干预,减少西药的使用剂量或不良反应,提高治疗的有效率。
, authors=刘绮瑛
1, 赵艳赛
1, 裘涛
2, authorsList=刘绮瑛, 赵艳赛, 裘涛, authorCompany=null, correspAuthors=裘涛, authorNote=
刘绮瑛(1999-),女,浙江杭州人,硕士在读,研究方向:中西医结合神经内科。
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