肺动脉高压心肾阳虚证大鼠模型构建及评价OA
Establishment and evaluation of rat model of pulmonary arterial hypertension with heart-kidney yang deficiency syndrome
目的 本研究通过野百合碱(MCT)联合氢化可的松构建肺动脉高压心肾阳虚证大鼠模型,旨在探索中医证候与肺动脉高压病理进程的关联性,为中医药治疗提供实验依据.方法 将30 只SD 大鼠按随机数字表法分为空白对照组、肺动脉高压组及肺动脉高压心肾阳虚证组,每组 10 只.空白对照组注射同等体积生理盐水,给予正常饮食.肺动脉高压组腹腔注射 MCT 60 mg/kg,每日1 次,连续干预28 d 造模;肺动脉高压心肾阳虚证组在 MCT 干预基础上,于造模第 15 天起皮下注射20 mg/kg 氢化可的松,每日1 次,连续14 d.造模 28 d 后,通过生命体征(肛温),整体外观(体质量、耳廓颜色、爪甲色泽、尾部色泽、目态与色泽、舌色、舌面津液、体毛稀疏、体毛色泽度)及行为学(弓背蜷缩、扎堆)时间对大鼠肾阳虚证候学特征进行评分;酶联免疫吸附测定(ELISA)法检测血液及尿液生物化学指标血尿素氮(BUN)、血肌酐(Scr)、尿蛋白(U-TP)和尿肌酐(Ucr),评估肾功能;ELISA 法检测三碘甲状腺原氨酸(T3)、甲状腺素(T4)、促甲状腺激素(TSH)、促肾上腺皮质激素(ACTH)、皮质酮(CORT)、雌二醇(E2)、睾酮(T)、环磷酸腺苷(cAMP)、环磷酸鸟苷(cGMP)及cAMP/cGMP,评估肾阳虚表现;小动物超声成像系统检测右室前壁厚度(RVWT),主肺动脉内径(MPAD),右心室(RV)前后径、左右径和上下径,肺动脉主干收缩期峰值流速(Vpa),三尖瓣环收缩期峰值流速(s'),三尖瓣环收缩期位移(TAPSE)和三尖瓣反流情况,结合多导生理记录仪检测右心室收缩压(RVSP),评估大鼠心功能;血气生化分析仪检测酸碱度(pH)、二氧化碳分压(PCO2)、氧分压(PO2)、氧饱和度(SaO2)、实际碳酸氢根(HCO-3)、二氧化碳总量(TCO2)、动脉肺泡氧分压(a/A)和乳酸(Lac);ELISA 法检测血管活性标志物内皮素-1(ET-1)及心肌功能标志物氨基末端 B型利钠肽前体(NT-proBNP);脏器系数和右心室肥厚指数(RVHI)评估大鼠心肌损伤程度;HE 染色观察心肌组织及肺动脉的病理学形态,同时测定肺动脉管壁厚度占血管外径百分比(WT)、肺动脉管壁面积占血管总横截面积百分比(WA)定量评估肺动脉病理结构改变;透射电镜评估细胞形态学变化.结果 与空白对照组比较,肺动脉高压心肾阳虚证组大鼠自造模第14 天起肛温下降,耳廓可见清晰血管,舌面津液增加,体质量下降,于第28 天达到中度肾阳虚,肾阳虚证候学特征评分升高(P<0.01).肾功能方面,与空白对照组和肺动脉高压组比较,肺动脉高压心肾阳虚证组 BUN、Scr、U-TP升高,Ucr 降低(P<0.01).肾阳虚相关指标方面,与空白对照组和肺动脉高压组比较,肺动脉高压心肾阳虚证组 T3、T4、TSH、ACTH、CORT、T 及 cGMP 降低,E2、cAMP 及 cAMP/cGMP 比值升高(P<0.01).心功能方面,与空白对照组比较,肺动脉高压组与肺动脉高压心肾阳虚证组 RV 前后径、左右径、上下径及RVWT、MPAD、RVSP、RVHI、ET-1、NT-proBNP 升高,Vpa、s'、TAPSE 降低(P<0.01).血气分析显示,与空白对照组比较,肺动脉高压组与肺动脉高压心肾阳虚证组腹主动脉血 pH、PO2、SaO2降低,Lac 升高;肺动脉高压心肾阳虚证组Lac 较肺动脉高压组进一步升高(P<0.01).脏器系数结果显示,与空白对照组比较,肺动脉高压组与肺动脉高压心肾阳虚证组心脏、肺脏、肾脏脏器系数均升高(P<0.01).HE 染色及透射电镜显示,肺动脉高压组与肺动脉高压心肾阳虚证组均出现心肌组织、肺动脉及肺组织病理损伤、肺动脉重构及线粒体损伤,WT、WA 升高(P<0.01).结论 MCT 联合氢化可的松可改善大鼠肾功能和肾阳虚相关指标,成功构建肺动脉高压心肾阳虚证组病证结合模型,该模型兼具肺动脉高压病理损伤与典型肾阳虚证候特征,为深入阐释心肾阳虚证病理机制及开展中医药干预肺动脉高压的疗效评价提供了稳定可靠的实验载体.
Objective A rat model of pulmonary arterial hypertension with heart-kidney yang deficiency syndrome was established using monocrotaline(MCT)plus hydrocortisone.The study aimed to investigate the correlation between traditional Chinese medicine(TCM)syndrome and the pathological progression of pulmonary arterial hypertension to provide experimental evidence for TCM therapeutic research.Methods Thirty Sprague-Dawley rats were randomly divided into the blank control group,pulmonary arterial hypertension group,and pulmonary arterial hypertension with heart-kidney yang deficiency syndrome group using the random number table method,with 10 rats in each group.Rats in the blank control group were injected with equal-volume normal saline.The pulmonary arterial hypertension group received an intraperitoneal injection of 60 mg/kg MCT once daily for 28 consecutive days to induce pulmonary arterial hypertension.On the basis of MCT administration,rats in the pulmonary arterial hypertension with heart-kidney yang deficiency syndrome group were subcutaneously injected with 20 mg/kg hydrocortisone once daily for 14 consecutive days starting from the 15th day of modeling.Twenty-eight days after modeling,the syndromic characteristics of the kidney-yang deficiency of rats were scored based on vital signs(rectal temperature),general appearance(body mass,auricle color,nail color,tail color,ocular state and color,tongue color,tongue fluid,and hair sparsity and hair luster),and behavioral performances(duration of hunching and curling,and duration of huddling).An enzyme-linked immunosorbent assay(ELISA)was used to detect blood and urine biochemical indicators including blood urea nitrogen(BUN),serum creatinine(Scr),urine total protein(U-TP),and urine creatinine(Ucr)for renal function assessment.ELISA was also applied to determine triiodothyronine(T3),thyroxine(T4),thyroid-stimulating hormone(TSH),adrenocorticotropic hormone(ACTH),corticosterone(CORT),estradiol(E2),testosterone(T),cyclic adenosine monophosphate(cAMP),cyclic guanosine monophosphate(cGMP),and cAMP/cGMP ratio to evaluate the manifestations of kidney yang deficiency.A small animal ultrasound imaging system was adopted to measure right ventricular anterior wall thickness(RVWT),main pulmonary artery diamete(MPAD),anteroposterior diameter,left-right diameter and superoinferior diameter of right ventricle(RV),peak systolic velocity of main pulmonary artery(Vpa),tricuspid annular systolic peak velocity(s'),tricuspid annular plane systolic excursion(TAPSE)and tricuspid regurgitation.Combined with right ventricular systolic pressure(RVSP)detected by a multi-channel physiological recorder,cardiac function of rats was assessed.Blood gas analyzer was used to detect potential of hydrogen(pH),partial pressure of carbon dioxide(PCO2),partial pressure of oxyge(PO2),oxygen saturation(SaO2),actual bicarbonate(HCO-3),total carbon dioxide(TCO2),arterial-alveolar oxygen partial pressure ratio(a/A)and lactic acid(Lac).ELISA was performed to detect vasoactive marker endothelin-1(ET-1)and myocardial functional marker N-terminal pro-B-type natriuretic peptide(NT-proBNP).Organ coefficients and right ventricular hypertrophy index(RVHI)were calculated to evaluate the degree of myocardial injury.HE staining was performed to observe the pathological morphology of myocardial and pulmonary arterial tissues.Meanwhile,the percentage of vessel wall thickness to external diameter(WT)and the percentage of vessel wall area to total cross-sectional area(WA)of pulmonary arteries were measured to quantitatively evaluate the pathological structural changes of pulmonary arteries.Transmission electron microscope was used to assess cellular morphological changes.Results Compared with the blank control group,rats in the pulmonary arterial hypertension with heart-kidney yang deficiency syndrome group exhibited decreased rectal temperature,visible distinct auricular blood vessels,increased tongue fluid,and reduced body weight starting from day 14 after modeling,and developed moderate heart-kidney yang deficiency on day 28.The score of the syndromic characteristics of the kidney-yang deficiency increased(P<0.01).In terms of renal function,compared with the blank control group and pulmonary arterial hypertension group,BUN,Scr,and U-TP were elevated,whereas Ucr was reduced in the pulmonary arterial hypertension with heart-kidney yang deficiency syndrome group(P<0.01).For kidney yang deficiency related indicators,compared with the blank control group and pulmonary arterial hypertension group,the levels of T3,T4,TSH,ACTH,CORT,T,and cGMP were decreased,while E2,cAMP,and cAMP/cGMP ratio were elevated in the pulmonary arterial hypertension with heart-kidney yang deficiency syndrome group(P<0.01).In terms of cardiac function,both in the pulmonary arterial hypertension group and pulmonary arterial hypertension with heart-kidney yang deficiency syndrome group,the anteroposterior,left-right,and superior-inferior diameters of the RV,together with RVWT,MPAD,RVSP,RVHI,ET-1,and NT-proBNP levels,were higher,while Vpa,s',and TAPSE were lower than those in the blank control group(P<0.01).Blood gas analysis showed that,compared with the blank control group,the pH value,PO2,and SaO2 in abdominal aortic blood decreased in both model groups,while Lac increased.Additionally,Lac was further higher in the pulmonary arterial hypertension with heart-kidney yang deficiency syndrome group than that in the pulmonary arterial hypertension group(P<0.01).Organ coefficients revealed that the cardiac,pulmonary,and renal coefficients of the two model groups were increased compared with the blank control group(P<0.01).HE staining and transmission electron microscopy results revealed that pathological damage of myocardium,pulmonary arteries and lung tissues,pulmonary arterial remodeling as well as mitochondrial damage were observed in both model groups.Besides,both WT and WA levels were increased(P<0.01).Conclusion Combined administration of MCT and hydrocortisone can alter renal function and kidney-yang deficiency-related phenotypic indicators in rats,successfully establishing a disease-syndrome combined model of pulmonary arterial hypertension complicated with heart-kidney yang deficiency syndrome.This model simultaneously presents pathological injuries of pulmonary arterial hypertension and typical manifestations of kidney-yang deficiency,which provides a stable and reliable experimental platform for further exploring the pathological mechanism of heart-kidney yang deficiency syndrome and evaluating the efficacy of TCM against pulmonary arterial hypertension.
杜红枝;侯红平;魏晓露;王连嵋;刘艳;陈韡亚;陈腾飞;高云航;宋玲;张广平
中国中医科学院中药研究所 北京 100700||山西省儿童医院(山西省妇幼保健院)中国中医科学院中药研究所 北京 100700中国中医科学院中药研究所 北京 100700中国中医科学院中药研究所 北京 100700中国中医科学院中药研究所 北京 100700中国中医科学院中药研究所 北京 100700中国中医科学院中药研究所 北京 100700中国中医科学院中药研究所 北京 100700中国中医科学院中药研究所 北京 100700中国中医科学院中药研究所 北京 100700
医药卫生
肺动脉高压心肾阳虚证中医证候动物模型大鼠
pulmonary arterial hypertensionheart-kidney yang deficiency syndrometraditional Chinese medicine syndromeanimal modelrat
《北京中医药大学学报》 2026 (8)
1058-1070,13
国家自然科学基金项目(No.82104502)中国中医科学院科技创新工程项目(No.CI2023E002-Y-43) National Natural Science Foundation of China(No.82104502)
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