温病湿热证线粒体氧化损伤、能量代谢及中药干预机制研究
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摘要
温病湿热证是临床常见病证,湿热既是中医特有的致病原因,又是具有广泛临床基础的中医病证,涉及多系统、多器官、多组织的病变。岭南气候、地理、饮食习惯及体质因素致使岭南地区湿热病证易发、多发。在岭南地区研究温病湿热证具有重要的意义。目前研究已表明湿热证致病机制与免疫、炎症、水通道蛋白、幽门螺杆菌、胃肠动力功能、内毒素、氧化损伤、微生态、微量元素、血脂代谢及能量代谢等密切相关,并不局限于某一脏腑或某一靶点。本课题通过临床研究与实验研究相结合的思路,从线粒体氧化损伤及能量代谢的角度探讨温病湿热证的发病机制,并采用清热化湿中药进行干预,探讨其部分作用机制。
     目的:
     本研究以鼠肝炎病毒(MHV-A59)为生物致病因子,建立“肥甘饮食+外湿热环境+鼠肝炎病毒感染”温病湿热证模型,观察温病湿热证肝线粒体超微结构、超氧化物歧化酶(SOD)、谷胱甘肽过氧化酶(GSH-PX)、丙二醛(MDA)、膜电位、ATP酶活力、ATP含量、四种呼吸链复合物Ⅰ、Ⅱ、Ⅲ、Ⅳ活性,从温病湿热证小鼠肝脏线粒体氧化损伤及能量代谢的角度探讨湿热证的发病机制,并采用清热化湿中药进行干预,反证其致病机制,初步探讨清热化湿法的作用机理。临床探讨外感湿热证患者外周血SOD、GSH-PX和MDA的变化是对实验研究的补充与佐证。
     方法:
     1、文献研究,采用评述的方法,整理温病湿热证动物模型的研究现状,湿热证证候本质研究概况,线粒体氧化损伤和能量转换的现代研究,归纳湿热证与线粒体氧化、能量代谢的相关性研究和MHV的研究进展,以期理清本实验的研究思路。
     2、实验研究,本实验所选用的均为4周龄左右的雄性BALB/c小鼠。①温病湿热证模型的建立:动物随机分为4组:正常对照组(正常饮食、饮水)、单纯湿热组(肥甘饮食+外湿热环境造模)、单纯病毒组(单纯小鼠肝炎病毒MHV-A59造模)和模型组(肥甘饮食+外湿热环境+小鼠肝炎病毒造模),检测小鼠血清TG、肝功能ALT、AST水平及肝组织病理切片,观察动物症状及体征。②在模型成功的基础上探讨温病湿热证的致病机制:动物随机分为4组:正常对照组、单纯湿热组、单纯病毒组和模型组,电镜观察各组线粒体超微结构,检测各组小鼠肝线粒体SOD、GSH-PX、MDA、膜电位、ATP酶活力、ATP含量、四种呼吸链复合物Ⅰ、Ⅱ、Ⅲ、Ⅳ活性的变化。③清热化湿中药的对温病湿热证的干预机制:动物随机分为4组:模型组、蒿芩清胆汤组(模型组用蒿芩清胆汤治疗),甘露消毒丹组(模型组用甘露消毒丹治疗)、西药组(模型组用易善复胶囊治疗):检测各组小鼠肝线粒体SOD、GSH-PX、MDA、MDA、膜电位、ATP酶活力、ATP含量、四种呼吸链复合物Ⅰ、Ⅱ、Ⅲ、Ⅳ活性的变化。
     3、临床研究,30例辨证属外感湿热证作为治疗组,病例来源于广州市中医医院门诊,同时期随机检测25例健康体检者作为对照组。比色法测定血清SOD、GSH-PX、MDA水平变化,治疗组运用蒿芩清胆汤治疗3日,复测上述指标,观察蒿芩清胆汤的干预作用。对照组不使用药物治疗。
     结果:
     1.温病湿热证动物模型方面,与正常组比较,温病湿热证模型小鼠出现了活动量、饮食量均明显减少、部分动物不进食,粪便及排泄物粘滞或稀溏、明显增多,小鼠体重减轻,肛温升高,出现肢体瘫痪和追尾征,毛发蓬松,无光泽。动物这些症状与体征符合温病湿热证的发病特点。模型组甘油三酯(TG)升高,脂肪代谢紊乱,与正常组和单纯病毒组比较,差异有显著性(P<0.01)。模型组光镜下见小鼠肝脏可见空泡样变、炎性细胞浸润,100%存在小叶内炎症,并可见脂肪样变、点状坏死、灶状坏死、碎屑样坏死。正常组和单纯病毒组小鼠肝脏未见脂肪变性。这些表现基本符合温病湿热证的病理特征。
     2.线粒体氧化损伤方面,温病湿热证模型组肝脏线粒体SOD活性和GSH-PX活性降低,MDA含量升高,膜电位降低,与正常组、单纯湿热组和单纯病毒组比较,均有显著性差异(P<0.01或P<0.05)。说明温病湿热证动物模型体内脂质过氧化物含量升高,相关抗氧化酶浓度和活性降低,线粒体功能受到损伤。蒿芩清胆汤与甘露消毒丹均能够提高温病湿热证模型组小鼠肝线粒体SOD、GSH-PX活性,提高清除自由基的防御体系功能,降低MDA含量,清除自由基,提高线粒体膜电位,与模型组比较具有显著性差异。(P<0.01)。提示清热化湿中药治疗温病湿热证,通过提高清除自由基的防御体系和减少自由基生成两方面作用,达到提高线粒体抗氧化功能及减少氧化损伤,保护线粒体功能。在与模型组比较,西药易善复在提高SOD、GSH-PX活性及膜电位方面无显著性差异,但在降低MDA含量方面差异有显著性(P<0.05)。本研究结果提示,清热化湿中药干预温病湿热证模型线粒体氧化损伤的机理主要表现在提高SOD、GSH-PX活性及膜电位,提高自由基消除的防御体系,减少自由基生成,降低MDA含量,清除已生成的自由基,提高膜电位。
     3.线粒体能量代谢方面,与正常组比较,单纯湿热组、模型组ATP酶活力和ATP含量均明显下降。其中,模型组下降最为显著,有非常显著性差异(P<0.01)。ATP酶活性下降提示能量分解和利用减少,ATP含量降低提示能量生成不足。研究结果说明单纯湿热组和模型组能量代谢障碍,ATP生成和分解利用下降。这种现象在模型组表现最为显著。与模型组比较,甘露消毒丹组与蒿芩清胆汤组ATP酶活力和ATP含量均升高最显著(P<0.01),提示清热化湿中药能提高温病湿热证线粒体ATP酶活性,促进能量的合成,促进ATP合成,改善线粒体的能量代谢障碍。
     模型组呼吸链复合物Ⅰ、Ⅱ、Ⅲ、Ⅳ活性降低,与正常组比较有显著性差异(P<0.01),说明模型组可能存在严重的能量代谢障碍和线粒体功能的障碍。蒿芩清胆汤组和甘露消毒丹组呼吸链复合物Ⅰ、Ⅱ、Ⅲ、Ⅳ活性升高,与模型组比较有显著性差异(P<0.01或P<0.05),提示清热化湿中药治疗温病湿热证,通过提高呼吸链复合物Ⅰ、Ⅱ、Ⅲ、Ⅳ活性,促进ATP的生成和分解利用,能改善线粒体能量代谢。
     4.临床研究方面,与正常组比较,急性上呼吸道病毒感染湿热证患者外周血清SOD和GSH-PX活性降低(P<0.01),而MDA含量显著升高(P<0.01);经蒿芩清胆汤治疗后,患者血清SOD和GSH-PX活性显著升高(P<0.01或P<0.05),MDA含量明显降低(P<0.01)。
     结论:
     1.以MHV-A59为生物致病因子,结合肥甘饮食及湿热外环境的复合因素构建的动物模型,可以作为温病湿热证动物模型之一,也是对病证结合动物模型的一种新的探索。
     2.温病湿热证存在线粒体氧化损伤及能量代谢障碍,使用清热化湿中药治疗后能改善氧化损伤,提高膜电位,促进能量的生成和利用,有利于恢复细胞的正常功能。因此,线粒体氧化损伤及能量代谢障碍可能是温病湿热证发病机制之一。
     3.蒿芩清胆汤和甘露消毒丹均能在一定程度上改善温病湿热证线粒体氧化损伤,保护线粒体的功能,改善能量代谢,反证了温病湿热证的上述致病机制。清热化湿中药治疗温病湿热证具有改善细胞氧化损伤,促进能量代谢功能。
     4.外感湿热证患者机体存在氧化应激损伤,抗氧化酶系功能降低。蒿芩清胆汤能够改善急性上呼吸道病毒感染湿热证机体氧化损伤。
Background:
     Damp-heat syndrome of seasonal febrile disease is common clinical disease, involving pathological changes of many systems and organs and tissues. Because of the special climate, geography, food habit and constitution factors in Ling Nan Area, damp-heat disease is common and easy, so it is important significance to study damp-heat syndrome in Ling Nan Area. The current researches demonstrate that pathogenesis of damp-heat syndrome of seasonal febrile disease is not limited to one entrails or target, it is related to immunologic function, inflammation, aquaporins, helicobacter pylori, gastrointestinal motility, endotoxin, oxidative damage, microecology, trace elements, blood lipid metabolism and energy metabolism, etc. On the basis of clinical and experimental research, we explore the pathogenesis of damp-heat syndrome of seasonal febrile disease from oxidative damage and energy metabolism of mitochondria and effects of Chinese herbs.
     Objective:
     The research established mouse model of damp-heat syndrome of seasonal febrile disease through richly fatty and sweet diet, humid heat environment and infected by MHV-A59, in which MHV-A59 was used as biological pathogenic factor. The research studied the pathogenesis of damp-heat syndrome of seasonal febrile disease from oxidative damage and energy metabolism of mitochondrion in the model mouse, by observing the ultramicrostructure, superoxide dismutase(SOD), glutathione proxidase (GSH-PX), malondialdehyde(MDA), membrane potential, ATPase activity, ATP concent and activities of respiratory chain complexⅠ、Ⅱ、Ⅲ、Ⅳin the hepatic mitochondrion of mice model of damp-heat syndrome of seasonal febrile disease. The research certificated the pathogenesis of damp-heat syndrome of seasonal febrile disease by treatment with Decoction of Hao qin qing dan and Decoction of Gan lu xiaodu, observed the treatment mechanism of clearing away heat and dampness. It was supplementary and evidence for pathogenesis of damp-heat syndrome of seasonal febrile disease by studing SOD, GSH-PX and MDA of peripheral blood of patients with exogenous damp-heat disease.
     Methods:
     1. Literature research:on the basis of the approach of evaluating and reviewing articles, we proposed to arrange the study state of animal model of damp-heat syndrome of seasonal febrile disease, study the survey of essence of damp-heat syndrome, the modern study of oxidative damage and energy metabolism of mitochondrion, sum up the study progression of MHV and the relationship between therapy of clearing away heat and dampness and oxidative damage and energy metabolism of mitochondrion.
     2. Experimental research:①establishment of damp-heat syndrome of seasonal febrile disease model. four-weeks-old male mice of BALB/c was divided randomly into four groups:control group(normal diet), simple damp-heat syndrome group(richly fatty, sweet diet and humid heat environment), simple virus infection group (normal diet and virus infection) and model group (richly fatty, sweet diet, humid heat environment and infected by MHV-A59), The triglyceride (TG), the indexes of liver function ALT、AST and Hepatic histopathology in mice were detected by biochemistry and ELISA. In the experiment we observed the symptom and sign of mice.②pathogenesis of damp-heat syndrome of seasonal febrile disease:four-weeks-old mice of BALB/c was divided randomly into four groups:control group, simple damp-heat syndrome group, simple virus infection group and model group. The ultramicrostructure of hepatic mitochondria in each group was observed with electronic microscope and the change of SOD, GSH-PX, MDA, membrane potential, ATPase activity, ATP content and activities of respiratory chain complexⅠ、Ⅱ、Ⅲ、Ⅳin the hepatic mitochondrion of mice were detected.③The pathogenesis of treating damp-heat syndrome of seasonal febrile disease with the decoction of clearing away heat and dampness:four-weeks-old mice of BALB/c were divided into four groups randomly, model group, Hao qin qing dan decoction group (mice of model group were treated by Decoction of Hao qin qing dan), Gan lu xiao du decoction group(mice of model group were treated by Decoction of Gan lu xiao du), western medicine group (mice of model group were treated by Polyene Phosphatidylcholine Capsules).The change of SOD, GSH-PX,MDA, membrane potential, ATPase activity, ATP content and activities of respiratory chain complexⅠ、Ⅱ、Ⅲ、Ⅳin the hepatic mitochondrion of mice were detected
     3. Clinical research:The 30 patients of exogenous damp-heat syndrome as the test group were from out-patient clinic of guangzhou hospital of Chinese medicine. There were 25 healthy people undergoing medical examination as control group. The level of SOD, GSH-PX and MDA of patients and healthy people were detected by colorimetry. The patients were treated by Decoction of Hao qin qing dan for three days. Then we detected the level of SOD, GSH-PX and MDA again. Healthy people without treatment.
     Results:
     1.In the research of establishment of damp-heat syndrome of seasonal febrile disease model:Compared to control group, the mice in model group showed some features such as drinking less water, eat less food, viscous and more plentiful excretion, weight loss, rectal temperature going up, bulky hair, etc. These signs and symptoms were closely related to the features of damp-heat syndrome of seasonal febrile disease. The level of TG obviously risen up compared to control group and simple virus infection group (p<0.01). The liver of the mice under microscope in model group showed vacuolating chang, inflammatory cell infiltration,100% leaflet inflammation, hepatic steatosis, necrosi. Hepatic steatosis was not existing in control group and simple virus infection group. These pathological changes were closely related to basically pathological features of damp-heat syndrome of seasonal febrile disease.
     2. In the research of oxidative damage of mitochondria:The level of SOD, GSH-PX and membrane potential decline and MDA risen up in model group obviously compared to control group, simple damp-heat syndrome group and simple virus infection group (P<0.01 or P<0.05). These show that lipid peroxidation content risen up and relative antioxidase activity decreased, mitochondrion function was injured in damp-heat syndrome of seasonal febrile disease model. Decoction of Hao qin qing dan and Decoction of Gan lu xiao du could improve the activities of SOD, GSH-PX and membrane potential in the hepatic mitochondria of damp-heat syndrome of seasonal febrile disease, improve the function of defense system scavenging free radicals, at the same time,they reduced MDA content and scavenged the free radicals. The difference was significant compared to model group (p<0.01) These findings indicate that Chinese herbs of clearing away heat and dampness can reinforce mitochondria function of antioxidation and reduce the injure of oxidation to protect mitochondrion though improving the function of defense system scavenging free radicals and reducing the production of free radicals. There is no significant difference in improving the activities of SOD, GSH-PX and membrane potential in the hepatic mitochondrion between model group and western medicine group, but western medicine group obviously ruduce MDA content compared to model group(P<0.05). The research result indicate that the mechanism of Chinese herbs clearing away heat and dampness was to improve the activities of SOD, GSH-PX and mitochondrial membrane potential, improve the function of defense system, reduce the production of free radicals, remove the producted free radicals in treatment of damp-heat syndrome of seasonal febrile disease.
     3. In the research of energy metabolism:The level of ATPase activity and ATP content obviously decline in model group and simple damp-heat syndrome group compared to control group, specially in model group (P<0.01).The decreasement of ATPase activity indicates that energy decomposition and utilization decrease. The decreasement of ATP content indicates that energy product Insufficiently. The research result indicate that energy metabolize disorderly and the production and utilization of ATP decrease in damp-heat syndrome of seasonal febrile disease. Chinese herbs clearing away heat and dampness could improve the ATPase activity and ATP content obviously compared to model group (P<0.01), improve energy metabolic disorders and promote the production of energy.
     Activities of respiratory chain complexⅠ、Ⅱ、Ⅲ、Ⅳin the hepatic mitochondrion of mice from model of damp-heat syndrome of seasonal febrile disease decline obviously compared to control group (p<0.01), which illustrate that serious energy metabolic disorders and dysfunction of mitochondrion may esist in damp-heat syndrome of seasonal febrile disease. Activities of complexⅠ、Ⅱ、Ⅲ、Ⅳin Hao qin qing dan decoction group and Gan lu xiao du decoction group obviously risen up compared to model group (p<0.05 or p<0.01). The research result indicate that Chinese herbs clearing away heat and dampness could improve the activities of complexⅠ、Ⅱ、Ⅲ、Ⅳ, in order to promote the production and utilization of energy, improve the energy metabolism of mitochondrion.
     4. clinical research:Compared to healthy people, the level of Peripheral blood SOD, GSH-PX of patients obviously decreased (p<0.01) and MDA rised up (p<0.01), there were significant differences. The level of Peripheral blood SOD, GSH-PX of patients who treated by decoction of Hao qin qing dan obviously rised (p<0.01 or p<0.05), and MDA obviously decreased (p<0.01).
     Conclusion:
     1.A new mouse model of damp-heat syndrome of seasonal febrile disease was duplicated by richly fatty and sweet diet, humid heat environment and MHV-A59. MHV-A59 was a biological pathogenic factor in the model which possessed characteristics of the illness and syndrome.
     2.Oxidative damage and energy metabolic disorders exist in damp-heat syndrome of seasonal febrile disease. Chinese herbs clearing away heat and dampness could reduce oxidative damage and improve production and utilization of energy, which was in favor of recovery of normal function of cell. So, oxidative damage and energy metabolic disorders in mitochondrion may be one of the pathogenesis of damp-heat syndrome of seasonal febrile disease.
     3. Both decoction of Hao qin qing dan and decoction of Gan lu xiao du could reduce oxidative damage of mitochondrion to a certain extent in the damp-heat syndrome of seasonal febrile disease, protect the function of mitochondrion, improve the energy metabolism. These proof the pathogenesis of damp-heat syndrome of seasonal febrile disease discussed above. Chinese herbs of clearing away heat and dampness could reduce oxidative damage of mitochondrion and promote the production and utilization of energy.
     4.Oxidative damage and antioxidant enzyme system function deficiency exists in the body with damp-heat syndrome of seasonal febrile disease. Decoction of Hao qin qing dan could reduce the oxidative damage in treating viral upper respiratory infection of damp-heat syndrome
引文
[1]郭金龙.湿阻证病理造型的实验研究[J].中医杂志,1988,(8):59
    [2]王新华.温病湿热证病理造型及实验研究[J].广州中医学院学报,1990,(3):82
    [3]程方平.湿温病湿重于热证病理模型研究[J].湖北中医学院学报,1999,1(3):25
    [4]刘国强,温病卫气营血证候动物实验研究.陕西人民教育出版社,1992,172.
    [5]吴仕九,杨运高,杨钦河,等.清热利湿法对湿热证动物模型的影响[J].中国中西医结合脾胃杂志,1999,7(4):200
    [6]吴智兵.温病湿热证发病机理的实验研究[J].广州:广州中医药大学,1999.1
    [7]刘晓鹰,杜恒,王文广,等.IgA肾病湿热证模型的研制[J].中华中医药学刊,2008,26(9):1847—1849
    [8]佟丽 陈江华 吴仕九,等.多因素所致温病湿热证模型大鼠红细胞免疫功能的变化[J].中国免疫学杂志,1999,(15):366-368
    [9]杨春波,傅肖岩,柯晓.慢性胃炎脾胃湿热证的免疫组织化学研究[J].中国中西医结合脾胃杂志,1998,6(2):6
    [10]林群莲,葵师敏.胃十二指肠疾病患者外周血T淋巴细胞亚群的观察及与中医证型的关系[J].中国中西医结合脾胃杂志,1997,5(1):23.
    [11]陈晴清,张静.脾胃湿热证与Th1/Th2细胞平衡的相关研究[J].内科,2007:2(4):589
    [12]李俊,王佳勇,罗笠,等.消化性溃疡活动期脾胃湿热证胃液及血前列腺素E2水平研究[J].中国中西医结合脾胃杂志,2000,8(1):23.
    [13]金敬善.胃十二指肠疾病血、尿PGE2和PGF10含量及其与中医证型的关系[J].中医杂志,1992,33(7):429.
    [14]朱辟疆,施荣华,刘永平.慢性肾小球疾病湿热证血浆及尿白介素-6的改变[J].浙江中西医结合杂志,1999,9(2):75
    [15]陈更新,劳绍贤,黄志新,等.中药对脾胃湿热证患者胃黏膜水通道蛋白3、4基因表达的影响[J].中国中西医结合杂志,2005,25(3):199—202
    [16]张诗军,劳绍贤,周正,等.慢性浅表性胃炎脾胃湿热证与水通道蛋白3基因表达的相关性研究[J].中医杂志,2004;45(11):852
    [17]吴仕九,廖礼兵.湿热证大鼠肾内髓及尿液中水通道蛋白AQP2含量的变化[J].中国中医药科技,2003;10(1):4
    [18]周正,劳绍贤,黄志新,等.脾胃湿热证与水通道蛋白4基因表达的关系[J].中国中西医结合消化杂志,2004,12(2):7
    [19]罗云坚,黄穗平,陈慧,等.慢性胃炎中医证候与胃窦十二指肠运动及胃炎程度的 相关性[J].广州中医药大学学报,2000,17(3):241.
    [20]杨春波,傅肖岩,柯晓,等.慢性胃炎脾胃湿热证的免疫组织化学研究[J].中国中西医结合脾胃杂志,1998,6(2):68.
    [21]杨春波,柯晓,李秀娟,等.脾胃湿热证的临床研究[J].福建中医学院学报,1999,9(4):1
    [22]陈朝元,王岩.幽门螺杆菌与慢性萎缩性胃炎及其证型的关系[J].中医药学刊,2002,20(6):828
    [23]陆敏,赵卡冰,沈洪,等.幽门螺杆菌相关性慢性胃炎中医辨证分型与胃泌素的关系[J].中国中西医结合消化杂志,2004,12(1):21
    [24]崔琦珍,黄志新,劳绍贤,等.慢性浅表性胃炎脾胃虚实证钡条胃排空功能观察[J].现代中西医结合杂志,2000,9(22):2193
    [25]李长生,周祝谦,于红.胃脘痛中医辨证分型的X线征象[J].山东中医学院学报,1994,18(1):3
    [26]周燕萍,高清华,李华锋,等.3种温病治法对温病湿热证模型血浆ETX血清TNF-IL-1影响的对比研究[J].中医药学刊.2006,24(8):1567-1568
    [27]常淑枫,萧照岑,陈爽白.三仁汤对温病湿热证大鼠血浆内毒素廓清作用机制研究[J].四川中医,2003,21(11):21.
    [28]徐萌,高云飞,吴仕九.清香散对湿热证大鼠的抗氧化和肝细胞凋亡作用[J].中药材,2001,24(6):420—421
    [29]江月斐,劳绍贤,邝枣园,等.腹泻型肠易激综合征脾胃湿热证肠道菌群的变化[J].中国中西医结合杂志,2006,26(3):218—220
    [30]江月斐,劳绍贤,邝枣园,等.腹泻型肠易激综合征脾胃湿热证舌苔微生态的初步研究[J].陕西中医学院学报,2005,28(2):5—5
    [31]刘立,杨运高,吴仕九,等.湿热证动物模型微量元素、维生素E变化及清香散的调节作用[J].广东微量元素科学,2002,9(7):33
    [32]祁建生,李秀娟,杨春波等.慢性胃炎脾胃虚实证红细胞游离Ca2+及膜Ca2+-Mg2+-ATPase研究[J].中国中西医结合脾胃杂志,1999,7(1):16.
    [33]祁建生,李秀娟,杨春波.红细胞膜Na+-K+-ATPase活性与慢性胃炎中医辨证分型关系的研究[J].新中医,1999,31(1):34.
    [34]周燕萍,高清华,李华锋,等.3种温病治法对温病湿热证模型血脂影响的对比研究[J].中医药学刊,2006,24(2):368
    [35]佟丽,吴仕九,陈江华.湿热证患者免疫功能及自由基水平变化的研究[J].中国实验临床免疫学杂志,1999,11(4):48—50
    [36]黄秀深.中焦湿阻证大鼠红细胞膜Na+-K+-ATP酶活性研究[J].成都中医药大学学报,2000,4(23):23—24
    [37]程方平,刘松林,李云海.温病湿热证大鼠模型肝线粒体Na+-K+-ATP酶活力变化的对比研究[J].浙江中医药大学学报,2008,32(2):174—175
    [38]祁建生,杨春渡,汪碧萍,等.慢性胃炎脾胃湿热证红细胞膜Na+—K+-ATPase与血清DBHase关系探讨[J].新中医,2001,33(10):30—31
    [39]Bos EC, Heijnen L, Luytjes W, Spaan WJ. Mutational analysis of the murine corona virus spike protein:effect on cell-to-cell fusion [J]. Virology, 1995; 214(2):453-463
    [40]Gombold JL, Hingley ST, Weiss SR. Fusion-defective mutants of mouse hepatitis virus A59 contain a mutation in the spike protein cleavage signal [J]. Virol,1993:67(8):4504
    [41]Navass, Seo SH, Chua MM, et al. Murine corona virus spike protein determines the ability of the virus to replicate in the lixter and cause hepatitis [J]. Jviml,2001:75:2452-2457
    [42]Dandekar AA, Anghelina D, Perlman S. Bystander CD8 T-cell mediated demye-lination is interferon-gamma-dependent in a coronavirus model of multiple sclerosis[J]. Am J Pathol,2004;164:363-369
    [43]Lane TE, Liu MT, Chen BP, et al. A central role for CD4(1) T cells and RANTES in virus-induced central nervous system in-flammation and demyelynation. J Virol,2000,74:1415-1424.
    [44]高诚,邵伟娟,潘漪清,等.RT-PCR方法在小鼠肝炎病毒检测中的初步应用[J].上海实验动物科学,1999,19(4):207~209。
    [45]王英,邵伟娟,高俊,等.小鼠肝炎病毒以不同途径感染4个品系小鼠的比较[J].上海交通大学学报(农业版),2005;23(2):126
    [46]Leparc-Goffart, I., S. T. Hingley, M. M. Chua, X. Jiang, E. Lavi, and S. R.Weiss. Altered pathogenesis of a mutant of the murine corona virus MHV-A59 is associated with a Q159L amino acid substitution in the spike protein [J]. Virology,1997;239:1-10
    [47]Phillips, J. J., M. M. Chua, G. F. Rall, and S. R.Weiss. Murine corona virus spike glycoprotein mediates degree of viral spread, inflammation, and virus-induced immuneopathology in the central nervous system [J]. Virology,2002:301:109-120
    [48]Fahey James R. An over view of diagnostic tests for MHV detection. Jax communication,2000;5(4):1-3
    [49]杨帮玲,胡柏林,史晋,等.小鼠肝炎病毒抗体Dot-ELISA诊断试剂盒的研制[J].中国实验动物学杂志,1997;7(2):65-68
    [50]Yamada YK, Yabe M, Takimoto K, et al. Application of nested polymerase chain reaction to detection of mouse hepatitis virus in fecal specimens during a natural outbreak in an immunodeficient mouse colony [J].Exp An im,1998; 47(4):261-264
    [52]刘叶.清热化湿透表法干预小鼠流感病毒性肺炎湿热证免疫损伤的机理研究[M].广州中医药大学2008年博士毕业论文.
    [53]李华锋.从NF-κB、AQP4及T细胞免疫探讨温病湿热证的致病机制[M].广州中医药大学2008年博士毕业论文.
    [54]王瑾,陈宜鸿,赵志玲.中医温病湿热证动物模型实验的研究[J].解放军药学报,2002:18(4):209-211
    [55]吴仕九,杨运高,佟丽,等.中医湿热证证候模型的应用研究[J].中医杂志,2001;42(9):553-559
    [56]吴仕九,杨运高,杨钦河,等.清热祛湿法对湿热证动物模型的影响[J].中国中西医结合杂志,1999:9(4):200-201
    [57]吴仕九,廖礼兵,文小敏,等.温病湿热证湿热量化的相关性实验研究[J].中医杂志,2003;44(9):688
    [58]程方平.湿温病湿重于热证病理模型研究[J].湖北中医学院学报,1999;1(3):25
    [59]陈爽白,常淑枫,肖照岑,等.湿热证大鼠模型的复制及三仁汤对其影响的实验观察[J].天津中医,2002,19(2):38
    [60]周燕萍,高清华,李华锋,等.3种温病治法对温病湿热证模型血脂影响的对比研究[J].中医药学刊,24(2):368—369
    [61]ClairceLS, Pagadigorria FM, AnaMK, eta.l Effects of methotrexate on calcium flux in rat liver mitochondria, microsomes and plasmamembrane vesicles. Comparative Biochemistry and Physiology, PartC,2006; 143:340-348
    [62]姜洪华,周福生,廖荣鑫,等.不同病种的脾气虚证患者吸收细胞线粒体超微结构的观察[J].厂西医学,2008,29(4):548—549。
    [63]Blum J, Fridovich I. Inactivation of glutathione peroxidase by superoxide radical. Arch Biophys,1985;240:500
    [64]D I browski A, Konturek SJ, Konturek JW, Gabryelewicz A. Role of oxidative stree in the pathogennsis of caerulein-induced acute pancreatitis. Eur J Pharmacol,1999;377:1-11
    [65]Ide T, Tsutsui H, Kinugawa S, Utsumi H, Hatori N, Uchida, Arimura K, Egashira K,Takeshita A. Mitochondirial electron transport complex Ⅰ is a potential source of oxygen free radicals in the failing myocardium. Cir Res,1999:85:357-363
    [66]Beckman JS, Beckman TM,Chen J, Marshall PA.Apparent hydroxyl radical production byperoxynitrite:Implications for endothelial injuey from nitricoxide and superoxide. Proc. Natl. Acad. Sci. USA,1990;87:1620-1624
    [67]Candeias LP, Patel KB, Stratford MRL, Wardman P. Free hydroxyl radicals Are formad on reaction between the neutrophil-derived species superoxide anion And hypochlorus acid FEBS Lett,1993;1:151-153
    [68]Aawyer DB, Colucci WS. Mitochondrial axidative stress in heart failuer: "oxygen wastage" reviseted.Cire Res,2000:86:119-120
    [69]Wallace DC. Mitochondrial diseases in man and mouse. Science,1999, 283:11482-1488
    [70]IshiiM, ShimizuS, NawataS, Kiuchi Y, Yamamoto T.Involvement of reactive oxygen species and nitric oxide in gastric ischemia-reperfusion injury in rats:protective effect of tetrahydrobiopterin. Dig Dis Sci,2000:45:93-98
    [71]IshiiM, ShimiznS, NawataS, et al. Involvement of reactive oxygen species and nitric oxide in gastric ischemia-reperfusion injury in rats:protective effect of tetrahydrobiopterin. Dig Dis Sci,2000:45:93-98
    [72]Koc A, Duru M, CiraliK H,et al Protective agent erdosteine, against cisplatin-induced heatic oxidant injury in rats. Mol Cell Biochem,2005, 278(1-2):79-84
    [73]张旭辉,裴国献,魏宽海.高温高湿环境吠肢体火器伤后超氧化物歧化酶和丙二醛含量的变化[J].第一军医大学学报,2002,22(4):331
    [74]李权超,何英强,谭终意,等.湿热应激对小鼠脂质过氧化反应的影响[J].解放军预防医学杂志,1997,15(5):353
    [75]李亚洁,王影,翟惠敏,等.复合营养素对湿热复合创伤应激大鼠脂质过氧化反应的影响[J].中国危重病急症医学,2004,16(1):52
    [76]FallCP, Bennett JP Jr. Visualization of cyclosporin A and Ca2+ sensitive cyclical mitochondrial depolarizations in cell culture[J]. Biochim BiophyActa,1999,1410(1):77
    [77]GollaopudiS, McCormickMJ, Gupta S. Changes in mitochondrial membrane potential and mitochondrial mass occur independent of the activation of caspase-8 and caspase-3 during CD95-mediated apoptosis in peripheral blood T cells [J].Int J Onco,1 2003,22 (3):597-600
    [78]KroemerG, Reed JC. Mitochondrial control of cell death[J]. NatMed,2000, 6 (5):513-519
    [79]Makani S, Gollapudi S, Yel L, et al. Biochemical and molecular basis of thimerosal-induced apoptosis in T cells:a major role of mitochondrial pathway [J] Genes Immun,2002,3 (5):270-389
    [80]梁佩燕,曾耀英,王通,等.地塞米松影响小鼠胸腺细胞线粒体膜电势变化研究[J].中国病理生理杂志,2005,21(5):962.
    [81]孙萍,翟佳滨.蒿芩清胆汤临床应用及实验研究进展[J].中国中医急症,2008,17(9):1286—1287
    [82].Sipos I, TretterL, ViziVA. Quantitative relationship between inhibition of respiratory complexes and formation of reactive oxygen species in isolated nerve terminals[J]. Neurochem,2003; 84:112-8
    [83]滕海林,岳炳德,管英俊.Na+-K+-ATP酶与糖尿病血管并发症[J].解剖科学进展,2003,9(1):85—87
    [84]Hackenbrock CK, BaueAE, Johnson D, et a.l Lateral diffusion and electron transfer in the mitochondria innermembrane. Trends Biochem Sc, i 2005;6(12):151 - 158
    [85]Slater EC,TodaK, Kayano K, et a.1 A hypothesis for the michanism of respiratory chain phosphorylation not involving the electrochemical gradient of protons as obligatory intermedicate. Biochem Biophys Acta,2005;811:217
    [86]黄秀深.中焦湿阻证大鼠红细胞膜Na+-K+-ATP酶活性研究[J].成都中医药大学学报,2000,4(23):23-24
    [87]郭明阳.温病湿热证湿重于热动物模型的研究[J].成都中医药大学学报,2003,1(26):34-36.
    [88]郭遂群.老年NIDDDM病患者氧化损伤、抗氧化能力和血糖控制[J].国外医学临床生物学与检验学分册,1999,20(2):88.
    [89]柳君泽.高文祥,曹利飞,等.低压缺氧大鼠脑线粒体内腺苷酸含量及能荷的变化[J].第三军医大学学报.2003,25(24):2165—2168
    [90]Fukai T, Siegfried MR, Ushio-Fukai M, et al. Regulation of the vascular excellular superoxide dismutase by nitric oxide and exercise training. Clin Invest,2000,105 (11):1631-1639.
    [91]熊正英,唐量.DTT、Tau和Vc对小鼠运动耐力、心肌自由基代谢及血清GOT活性影响的比较研究[J].中国运动医学杂志,2001,20(4):370-373.
    [92]Graziewicz M A, Day B J, Copeland W C. The mitochondrial DNA polymerase as a target of oxidative damage[J]. Nucleic Acids Res,2002,30(13): 2817-2824.
    [93]Tanaka S, Takehashi M, Matoh N, et al. Generation of reactive oxygen species and activation of NF-kappaBbynon-Abeta component of Alzheimer's disease amyloid[J]. J Neurochem,2002,82(2):305-315.
    [94]张诗君,马翠玉,陈泽雄,等.自由基与黄腻苔的关系及清热化湿中药治疗的影响[J].实用中医药杂志,1995, (5):29—30
    [95]莫日根,韩雪梅,新燕等.蒿芩清胆汤抗流感病毒的实验研究[J].中医研究,2005;5(1):516-518.
    [96]彭胜权.传染性非典型性肺炎的中医辨证论治[J].上海中医药杂志,2003;37(5):3-4.
    [97]邓铁涛.论中医诊治非典型性肺炎[J].新中医,2003;35(6):3—5.