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免疫检查点抑制剂相关心肌炎小鼠模型的中医证候研究

刘恒 郭抒娟 王勇 葛菲 李伟利 张亚雯 吴云霞 张虞钦 李一琳 凌观静 卫岩

北京中医药大学学报2026,Vol.49Issue(2):157-167,11.
北京中医药大学学报2026,Vol.49Issue(2):157-167,11.DOI:10.3969/j.issn.1006-2157.2026.02.002

免疫检查点抑制剂相关心肌炎小鼠模型的中医证候研究

Traditional Chinese medicine syndromes in a mouse model of immune checkpoint inhibitor-associated myocarditis

刘恒 1郭抒娟 1王勇 2葛菲 1李伟利 1张亚雯 1吴云霞 1张虞钦 1李一琳 1凌观静 1卫岩1

作者信息

  • 1. 北京中医药大学中医学院 北京 100029
  • 2. 北京中医药大学中医学院 北京 100029||北京中医药大学东直门医院||证候与方剂基础研究北京市重点实验室||证候与方剂研究教育部重点实验室
  • 折叠

摘要

Abstract

Objective To establish a stable disease-syndrome combination model of immune checkpoint inhibitor-associated myocarditis(ICIM)and comprehensively evaluate its macroscopic manifestations and microscopic biomarkers to elucidate the dynamic evolution of traditional Chinese medicine(TCM)syndromes.Methods Twenty SPF male C57BL/6J mice were randomly divided into model and control groups,with 10 mice per group.From day 8,according to body weight,mice in the model group received intraperitoneal injections of in vivo anti-mouse programmed death 1(25 mg/kg)and cytotoxic T lymphocyte-associated antigen 4(25 mg/kg)monoclonal antibody.In contrast,mice in the control group received intraperitoneal injections of an isotype anti-mouse IgG2a antibody(50 mg/kg).Antibodies were administered once every 3 days for a total of five times.On the 28th day,cardiac function was assessed using echocardiography,including left ventricular ejection fraction(LVEF),left ventricular fractional shortening(LVFS),left ventricular end-systolic volume(LVESV),and left ventricular end-diastolic volume(LVEDV).Histopathological changes in myocardial tissue were evaluated using hematoxylin-eosin(HE)and Masson stainings.Serum contents of cardiac troponin I(cTnI),tumor necrosis factor-α(TNF-α),and interleukin-6(IL-6)were measured using an enzyme-linked immunosorbent assay.The macroscopic manifestations of TCM syndromes in the mice were observed weekly for 4 weeks.On the Thursdays of each week(i.e.,the 4th,11th,18th,and 25th days),general condition was recorded;forelimb grip strength was assessed using a grip strength test,the open field experiment was used to measure the movement distance of the mice within 5 min,and the rectal temperature was measured.On the Fridays of each week(i.e.,the 5th,12th,19th,and 26th days),the exhaustive swimming test was conducted,and the paw temperature,as well as red-green-blue(RGB)values of the tongue surface and both lower limbs were measured.Results Compared with the control group,mice in the model group showed decreased LVEF and LVFS and increased LVESV and LVEDV(P<0.05);serum contents of cTnI,TNF-α,and IL-6 were elevated(P<0.05);and HE and Masson stainings revealed disorganized myocardial architecture,prominent immune cell infiltration,and marked fibrosis in the model group.Compared with the control group,mice in the model group exhibited slightly dull and yellowish fur,reduced vigor,decreased activity,and poor claw appearance in weeks 3 and 4;exhaustive swimming time and forelimb grip strength were reduced,whereas rectal temperature was increased(P<0.05).Compared with the control group,mice in the model group exhibited decreased locomotion distance within 5 min of the open field test in week 4(P<0.05).Compared with week 1,mice in the model group showed an increased r value and a decreased g value of the tongue surface in week 4(P<0.05),with no significant change in the b value.Conclusion Based on the comprehensive detection results of macroscopic manifestations and microscopic indicators,the TCM syndromes of ICIM model mice exhibited a dynamic evolution,evolving from the qi deficiency syndrome in week 3 to the qi-yin deficiency syndrome in week 4.

关键词

免疫检查点抑制剂相关心肌炎/病证结合/气阴两虚证/小鼠

Key words

immune checkpoint inhibitor-associated myocarditis/disease-syndrome combination/qi-yin deficiency syndrome/mice

分类

医药卫生

引用本文复制引用

刘恒,郭抒娟,王勇,葛菲,李伟利,张亚雯,吴云霞,张虞钦,李一琳,凌观静,卫岩..免疫检查点抑制剂相关心肌炎小鼠模型的中医证候研究[J].北京中医药大学学报,2026,49(2):157-167,11.

基金项目

国家自然科学基金项目(No.82374420,No.82174364) (No.82374420,No.82174364)

非传染性慢性病国家科技重大专项(No.2023ZD0502605) (No.2023ZD0502605)

京津冀基础研究合作项目(No.J230033) (No.J230033)

北京中医药大学科技处项目(No.2022-JYB-JBZR-001,No.BZY-BZX-2022-08) (No.2022-JYB-JBZR-001,No.BZY-BZX-2022-08)

中国中科医学创新基金中医药理论传承与创新项目(No.KYG-202403) National Natural Science Foundation of China(Nos.82374420 and 82174364) (No.KYG-202403)

北京中医药大学学报

1006-2157

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