|本期目录/Table of Contents|

[1]彭金玲,边育红,王丽,等.马兜铃酸肾毒性的研究进展[J].环球中医药,2013,6(01):59-0.
 PENG Jin ling,BIAN Yu hong,WANG Li,et al.Research progress of Aristolochic acid renal toxicity[J].,2013,6(01):59-0.
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马兜铃酸肾毒性的研究进展()
     
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《环球中医药》[ISSN:1006-6977/CN:61-1281/TN]

卷:
第6卷
期数:
2013年01期
页码:
59-0
栏目:
综述
出版日期:
2013-01-06

文章信息/Info

Title:
Research progress of Aristolochic acid renal toxicity
作者:
彭金玲;边育红;王丽;李金奎;
Author(s):
PENG JinlingBIAN YuhongWANG Liet al.
Immunization Branch, Second People’s Hospital of EPI, Fengrun District, Tangshan City, Hebei Province,Tangshan 063400,China
关键词:
马兜铃酸肾毒性马兜铃酸肾病发病机制
Keywords:
Aristolochic acidRenal toxicityAristolochic acid nephropathyPathogenesis 
分类号:
R96
DOI:
-
文献标志码:
A
摘要:
马兜铃酸(AA)为硝基菲类有机酸类化合物,是马兜铃、关木通、细辛、广防己等植物的主要成分。马兜铃酸药理作用广泛,有抗感染、抗癌、增强细胞免疫及终止妊娠等功能。目前,含有马兜铃酸的中药或中成药广泛应用于风湿及泌尿系统等多种疾病,由于服用含有马兜铃酸成分的中药而引起的肾脏损害报道日益增加,马兜铃酸肾毒性作用越来越受到人们的重视。本文总结了近年来马兜铃酸化学结构、毒理作用基础及临床研究,并对其肾毒理作用机制进行综述,使其为临床合理应用含有马兜铃酸的中药或中成药制剂提供参考。通过设计安全有效的药用剂型,严格控制用药剂量和时间,避免长期或大剂量服用,预防并减少毒性作用,将使该药在临床上得到更广泛应用。
Abstract:
Aristolonic acid is a nitro phenanthrene organic acid compound found as a main component of Aristolochia, Guan mutong, Asarum, Aristolochia Fangchi and many other medicinal plants. Aristolochic acid is widely used in the pharmaceutical industry due to its anti infection, anti tumor, abortifacient and cellular immunity enhancing properties. Present uses of Aristolochic acid containing Chinese medicine are for the treatment of rheumatic and urinary system diseases. However, there have been increased reports on kidney damage as a result of using Aristolochic acid containing drugs, which, leads to increased research in the field. It is necessary and crucial to provide proper reference for safer clinical use of Chinese traditional medicines with Aristolochic acid components. This paper therefore focuses on the structure, toxicological effects and clinical applications of Aristolochic acid as well as its renal toxicological mechanisms. We therefore conclude that, due to the beneficial medicinal properties of Aristolochic acid, it is necessary to design a safer and effective pharmaceutical dosage formulation and strictly control drug dose and time as well as duration of drug use in order to reduce its toxic effect, thereby increasing its clinical application.

参考文献/References:

[1]蒋贵仲, 陈灵.中药中马兜铃酸的毒性研究进展[J].中国农学通报,2008,24(9):8487.
[2]陈孟兰,朱正兰.马兜铃属植物的药理作用研究进展[J].武汉生物工程学院学报,2007,3(1):5962.
[3]张万明,马淑兰.马兜铃酸及含有马兜铃酸中药的研究概述[J].河北北方学院学报,2007,23(6):3538.
[4]戴小慧.对含马兜铃酸类中药引起毒性反应的情况分析[J].浙江中医药大学学报,2009,33(3):427428.
[5]王勇,邓晓春.马兜铃酸结构多样性及其复方毒性研究进展[J].中草药,2006,37(8):附3附5.
[6]郭永超,林哲绚,李慧,等.三种马兜铃酸类化合物对HK2细胞的毒性比较[J].癌变·畸变·突变,2006,18(2):8892.
[7]Balachandran P, Wei F, Lin RC, et al.Structure activity relationships of aristolochic acid analogues: toxicity in cultured renal epithelial cells [J].Kidney Int, 2005,67(5):17971805.
[8]杜贵友,方文贤.有毒中药现代研究与合理应用[M].北京:人民卫生出版社, 2003:2125.
[9]刘金渊,曾汉基.大量煎服关木通致急性肾功能衰竭死亡1例[J].中国中药杂志,1994,19(11):692693.
[10]李锋,程庆砾,董柯,等.对13例木通中毒导致急性肾功能衰竭的分析[J].中国中药杂志,1999,24(7):435437.
[11]Li Yang,Xiaomei Li,Haiyan Wang.Possible mechanisms explaining the tendency towards interstitial fibrosis in aristolochic acidinduced acute tubular necrosis[J]. Nephrol Dial Transplant, 2007,22:445456.
[12]于敏,赵伟,刘晓玲,等.马兜铃酸肾病的发病机制临床特点及防治[J].中华中医药学刊,2009,27(2):257259.
[13]夏爱军,梁园.含马兜铃酸中药引起的肾脏损害及其防治[J]. 解放军药学学报,2008,24(3):282283.
[14]陆再英,钟南山.内科学[M]. 7版.北京:人民卫生出版社,2008:329332.
[15]王树祥,马洪波,路群,等.慢性马兜铃酸肾病与恶性肿瘤关系的研究[J].山东医药,2009,49(33):7374.
[16]周颖,黄丽华,梁雁,等.服含马兜铃酸中药患者肾移植术后发生继发肿瘤风险的调查[J]. 药物不良反应杂志,2009, 11(1):912.
[17]Reiko Inagi. Endoplasmic reticulum stress as a progression factor for kidney injury[J]. Pharmacology,2010,10(2):156165.
[18]Nobuhiko Hiramatsua, Ayumi Kasaia, Shuqi Du, et al. Rapid, transient induction of ER stress in the liver and kidney after acute exposure to heavy metal: Evidence from transgenic sensor mice[J]. Federation of European Biochemical Societies, 2007, 581(10):20552059.
[19]Katsoulieris E, Mabley JG,Samai M, et al. Lipotoxicity in renal proximal tubular cells: Relationship between endoplasmic reticulum stress and oxidative stress pathways[J]. Free Radical Biology & Medicine, 2010,48(12):16541662.
[20]Shaohua Zhu, Yan Wang, Jing Jin, et al. Endoplasmic reticulum stress mediates aristolochic acid Iinduced apoptosis in human renal proximal tubular epithelial cells[J]. Toxicology in Vitro,2012,26(5):663671.
[21]Xie J, Guo Q. Apoptosis antagonizing transcription factor protects renal tubule cells against oxidative damage and apoptosis induced by ischemiareperfusion[J].J Am Soc Nephrol,2006,17(12):33363346.
[22]季文萱,黄俊彦,孟冬梅,等. 马兜铃酸对肾小管上皮细胞氧化应激效应的作用[J]. 山东医药,2011,51(25):98100.
[23]李振雪,耿成燕,姜丽萍,等.关木通水煎剂致大鼠肾毒性及DNA损伤机制[J]. 毒理学杂志,2007,21(6):444446.
[24]Lebeau C, Debelle FD, Arlt VM, et al. Early proximal tubule injury in experimental aristolochic acid nephropathy: functional and histological studies [J]. Nephrol Dial Transplant, 2005,20 (11): 23212332.
[25]Wan Chana,Hao Yuea,Wing Tat Poon.Quantification of aristolochic acidderived DNA adducts in rat kidney and liver by using liquid chromatographyelectrospray ionization mass spectrometry[J]. Mutation Research,2008,646(12):1724.
[26]Cronin AJ,Maidment G,Cook T,et al.Aristolochic acid as acausative factor in a case of Chinese herbal nephropathy[J].Nephrol Dial Transplant,2002,17(3):524525.
[27]Hylke de Jonge,Yves Vanrenterghem. Aristolochic acid: the common culprit of Chinese herbs nephropathy and Balkan endemic nephropathy[J].Nephrol Dial Transplant,2008,23(1):3941.
[28]尹广,刘正钊,刘志红,等. 肾脏基础疾病对马兜铃酸肾病临床表现及病理改变的影响[J]. 西南国防医药,2010,20(2):135137.
[29]左巍,刘亚革,王继红,等.大鼠马兜铃酸肾病模型中炎性细胞浸润的特点及意义[ J].细胞与分子免疫学杂志, 2005, 21(6): 757759.
[30]孙建新. 小鼠马兜铃酸肾病免疫病理机制的初步探讨[D].苏州:苏州大学,2008:2427.
[31]Pozdzik A, Salmon J, Husson CP, et al. Patterns of interstitial inflammation during the evolution of renal injury in experimental aristolochic acid nephropathy[J]. Nephrol Dial Transplant, 2008, 23(8): 24802491.
[32]周雯静.马兜铃酸肾毒性的研究及其思考[J].光明中医,2008,23(9):13871388.
[33]余晓霞,李胜,陶静莉,等. 不同浓度马兜铃酸对肾小管上皮细胞的毒性作用以及骨形成蛋白7的抗凋亡作用[J]. 广东医学,2011,32(7):821823.
[34]Li J,Zhang L,Jiang Z,et al.Toxicities of aristolochic acid I and aristololactam I in cultured renal epithelial cells[J].Toxicol In Vitro,2010,24(4):10921097.
[35]熊静悦,谭正怀.马兜铃酸的主要毒性作用及其相关机制[J].四川中医,2011,29(9):3942.
[36]Wang Y,Zhang Z,Shen H, et al. TGFβ1/Smad7 signaling stimulates renal tubulointerstitial fibrosis induced by AAI[J]. J Recept Signal TransductRes, 2008, 28(4):413428.
[37]Yang L, Li X, Wang H. Possible mechanisms explaining the tendency towards interstitial fibrosis in aristolochic acid induced acute tubular necrosis[J]. Nephrol Dial Transplant, 2007, 22(2): 445456.
[38]牛效清,陈楠,刘中柱,等.慢性马兜铃酸肾病患者血清TGFβ1、BMP7的改变[J].黑龙江医药科学,2012,35(2):3435.
[39]Wen YJ,Qu L,Li XM.Ischemic injury underlies the pathogenesis of aristolochic acidinduced acute kidney injury[J].Transl Res,2008,152(1):3846.
[40]张林,孙东,尹忠诚,等.急性马兜铃酸肾病大鼠肾脏微血管损伤的研究[J].山东医药,2010,50(39):3638.
[41]Xiao Y,Ge M,Xue X,et al.Hepatic cytochrome P450s metabolize aristolochic acid and reduce its kidney toxicity [J].Kidney Int,2008,73(11):12311239.
[42]陈敏,宫丽崑,任进. 代谢酶在马兜铃酸肾病中的作用[J].中草药,2012,43(2):388392.
[43]M. Stiborová, M. Rupertová a, E. Frei. Cytochrome P450 and peroxidasemediated oxidation of anticancer alkaloid ellipticine dictates its antitumor efficiency[J]. Biochimica et Biophysica Acta,2011,1814(1):175185.
[44]Stiborova M,Mareis J,Frei E,et al.The human carcinogen aristolochic acid I is activated to form DNA adducts by human NAD(P)H:quinone oxidoreductase without the contribution of acetyltransferases or sulfotransferases[J].Environ Mol Mutagen,2011,52(6):448459.
[45]Lord GM, Hollstein M, Arlt VM, et al. DNA adducts and p53 mutations in a patient with aristolochic acidassociated nephropathy[J].Am J Kidney Dis,2004,43(4): e11e17.
[46]Katerina Levova, Michaela Moserova, Daniel W. Nebert et al. NAD(P)H:quinone oxidoreductase expression in Cyp1aknockout and CYP1Ahumanized mouse lines and its effect on bioactivation of the carcinogen aristolochic acid I [J]. Toxicol Appl Pharmacol,2012,265(3):360367.

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备注/Memo

备注/Memo:
基金项目:国家自然科学基金(81072741)
作者单位:063400 河北省唐山市丰润区第二人民医院计划免疫科(彭金玲);天津中医药大学中医学院免疫教研室(边育红);天津市传染病医院制剂科(王丽);新探健康发展研究中心控烟项目办公室(李金奎)
作者简介:彭金玲(1968- ),本科,主治医师。研究方向:流行病学。Email:chaihuogun0423@yahoo.com.cn
通讯作者:边育红(1968- ),博士,硕士生导师,教授。研究方向:干细胞、表观遗传学。Email:bianyuhong_2012@163.com
更新日期/Last Update: 1900-01-01