首页|暖心康通过"代谢-炎症"网络调控巨噬细胞极化对心肌梗死后小鼠心室重构的影响

暖心康通过"代谢-炎症"网络调控巨噬细胞极化对心肌梗死后小鼠心室重构的影响

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目的 探究暖心康(红参、毛冬青)通过"代谢-炎症"网络调控巨噬细胞极化改善心肌梗死后小鼠心室重构的作用机制.方法 ①将 30 只 C57BL/6J 雄性小鼠随机分为 3 组:假手术组、模型组、暖心康组(1.65 g·kg-1),每组 10 只;采用左前降支冠状动脉结扎术复制心肌梗死小鼠模型;灌胃给药,每日 1 次,连续4 周.采用Masson染色法检测心肌组织胶原沉积情况;超声检测小鼠心功能:左室射血分数(LVEF)、收缩末期左室前壁厚度(LVAWS)及舒张末期左室前壁厚度(LVAWD);流式细胞术检测小鼠心脏巨噬细胞分布情况;qPCR法检测心脏组织乳酸脱氢酶A(LDHA)、肉碱棕榈酰转移酶 1(CPT-1)、葡萄糖转运蛋白 4(GLUT4)、异柠檬酸脱氢酶(IDH)、琥珀酸脱氢酶(SDHa)mRNA表达.②按照 1.15 g·kg-1剂量给予大鼠暖心康混悬液灌胃,每日 2 次,持续 5d,制备暖心康含药血清.采用脂多糖(LPS)诱导RAW 264.7 细胞构建促炎型巨噬细胞模型.细胞分组:空白血清对照组(含 5%空白血清+5%胎牛血清的培养基)、暖心康含药血清组(含 5%暖心康含药血清+5%胎牛血清的培养基)、脂多糖组(含 5%空白血清+5%胎牛血清的培养基+200 μg·mL-1 脂多糖)、暖心康含药血清+脂多糖组(含 5%暖心康含药血清+5%胎牛血清的培养基+200 μg·mL-1 脂多糖),干预 16 h.采用糖酵解压力测试实验检测RAW 264.7 细胞糖酵解水平;qPCR法检测RAW 264.7 细胞线粒体丙酮酸转运载体(MPC1)mRNA表达;MitoSox Red荧光染色法检测RAW 264.7 细胞线粒体氧化应激损伤程度.结果 ①与假手术组比较,模型组小鼠的心脏胶原纤维蓝染面积明显增加,并伴有室壁变薄,左心室腔增大;LVEF、LVAWS、LVAWD等心功能指标水平均显著降低(P<0.01,P<0.001);小鼠心脏组织中LDHA、CPT-1 mRNA表达明显上调(P<0.05),GLUT4、IDH、SDHa mRNA表达显著下调(P<0.05,P<0.01),CD86 染色阳性细胞数量显著增加(P<0.001).与模型组比较,暖心康组小鼠的心脏胶原纤维沉积明显减少,且室壁厚度增加;LVEF、LVAWS、LVAWD 等心功能指标水平均显著升高(P<0.05,P<0.01,P<0.001);小鼠心脏组织中LDHA、CPT-1 mRNA 表达显著下调(P<0.01,P<0.001),GLUT4、SDHa、IDH mRNA 表达显著上调(P<0.01),CD86 阳性细胞数量显著减少(P<0.001).②与空白血清对照组比较,暖心康含药血清组巨噬细胞的糖酵解水平、ROS水平均无明显变化(P>0.05),而脂多糖组巨噬细胞的糖酵解水平、ROS水平均显著升高(P<0.01),MPC1 mRNA表达显著下调(P<0.001).与脂多糖组比较,暖心康含药血清+脂多糖组的巨噬细胞糖酵解水平、ROS水平均显著降低(P<0.05,P<0.01),MPC1 mRNA表达显著上调(P<0.001).结论 暖心康能够减轻小鼠心肌梗死后的心肌纤维化及心室重构,改善心功能,其作用机制可能与下调心脏组织LDHA mRNA表达,上调GLUT4 mRNA表达,改善心肌梗死后心脏葡萄糖摄取能力,抑制促炎型巨噬细胞糖酵解,增加SDHa及IDH的表达以减轻琥珀酸与柠檬酸堆积,减少活性氧(ROS)生成,从而减少促炎型巨噬细胞过度极化有关.
Pharmacological Effect of Nuanxinkang Powder on Ventricular Remodeling in Post-infarction Mice Through"Metabolic-Inflammatory"Network Regulating Macrophage Polarization
Objective To explore the mechanism of Nuanxinkang Powder(aka.NXK,composed of Ginseng Radix et Rhizoma Rubra and Ilex Pubescens Radix)on improving ventricular remodeling in post-infarction mice based on the"metabolic-inflammatory"network regulating macrophage polarization.Methods ①Thirty C57BL/6J male mice were randomly divided into three groups:sham-operation group,model group,and NXK group(1.65 g·kg-1),with 10 mice in each group;the mouse model of myocardial infarction was replicated using left anterior descending coronary artery ligation;and the drug was administered by gavage once a day for 4 consecutive weeks.Masson staining was used to detect collagen deposition in myocardial tissue;ultrasound was used to detect cardiac function in mice:left ventricular ejection fraction(LVEF),left ventricular anterior wall thickness at end-systole(LVAWS)and left ventricular anterior wall thickness at end-diastole(LVAWD);flow cytometry was used to detect distribution of cardiac macrophages in mice;qPCR was used to detect mRNA expressions of lactate dehydrogenase A(LDHA),carnitine palmitoyltransferase 1(CPT-1),glucose transport protein 4(GLUT4),isocitrate dehydrogenase(IDH),and succinate dehydrogenase(SDHa)in heart tissue.②NXK was given 1.15 g·kg-1 NXK suspension to rats by gavage twice a day for 5 consecutive days to prepare NXK-containing serum.Lipopolysaccharide(LPS)-induced RAW 264.7 cells were used to construct a pro-inflammatory macrophage model.The cells were grouped into the following groups:blank serum control group(medium containing 5%blank serum+5%fetal bovine serum),NXK drug-containing serum group(medium containing 5%NXK drug-containing serum+5%fetal bovine serum),lipopolysaccharide group(medium containing 5%blank serum+5%fetal bovine serum+200 μg·mL-1 lipopolysaccharide),NXK drug-containing serum+ lipopolysaccharide group(medium containing 5%NXK drug-containing serum+5%fetal bovine serum+200 μ g·mL-1 lipopolysaccharide),all the groups were intervened for 16 hours.Glycolysis stress test was used to detect the level of glycolysis in RAW 264.7 cells;qPCR was used to detect the mRNA expression of mitochondrial pyruvate carrier(MPC1)in RAW 264.7 cells;and MitoSox Red fluorescent staining was used to detect the level of oxidative stress damage in mitochondria of RAW 264.7 cells.Results ①Compared with the sham-operation group,the blue-stained area of cardiac collagen fibres in mice of the model group was significantly increased,accompanied by thinning of the ventricular wall and enlargement of the left ventricular cavity;cardiac function indexes,such as LVEF,LVAWS,LVAWD,etc.,were all significantly reduced(P<0.01,P<0.001);the mRNA expressions of LDHA and CPT-1 were significantly up-regulated in the cardiac tissues of mice(P<0.05),and the mRNA expressions of GLUT4,IDH and SDHa were significantly down-regulated(P<0.05,P<0.01),and CD86 staining positive cell was significantly increased(P<0.001).Compared with the model group,mice in the NXK group showed a significant decrease in cardiac collagen fiber deposition and an increase in the thickness of the ventricular wall;cardiac function indexes such as LVEF,LVAWS and LVAWD were significantly increased(P<0.05,P<0.01,P<0.001);and the mRNA expressions of LDHA and CPT-1 in the cardiac tissues of the mice were significantly down-regulated(P<0.01,P<0.001),mRNA expressions of GLUT4,SDHa and IDH were significantly up-regulated(P<0.01),and the number of CD86 positive cells was significantly reduced(P<0.001).②Compared with the blank serum control group,the cytosolic glycolysis level and ROS level of macrophages in the NXK serum-containing group did not change significantly(P>0.05),whereas the glycolysis level and ROS level of macrophages in the lipopolysaccharide group were significantly increased(P<0.01),and the mRNA expression of MPC1 was significantly down-regulated(P<0.001).Compared with the lipopolysaccharide group,the macrophage glycolysis level and ROS level were significantly reduced in the NXK serum-containing + lipopolysaccharide group(P<0.05,P<0.01),and mRNA expression of MPC1 was significantly up-regulated(P<0.001).Conclusion NXK can reduce myocardial fibrosis and ventricular remodeling after myocardial infarction and improve cardiac function in mice,and its mechanism may be related to the down-regulation of mRNA expression of LDHA in cardiac tissues,the up-regulation of mRNA expression of GLUT4,the improvement of cardiac glucose uptake after myocardial infarction,the inhibition of pro-inflammatory macrophage glycolysis,the increase in the expressions of SDHa and IDH to alleviate the accumulation of succinate and citrate,and the reduction of reactive oxygen species(ROS)generation,thereby reducing pro-inflammatory macrophage hyperpolarisation.

Nuanxinkangmyocardial infarctionventricular remodellingmyocardial fibrosismacrophage polarisationenergy metabolisminflammatory responseoxidative stressmiceRAW 264.7 cells

林祉均、陈梓欣、江佳林、董鑫、关卓骥、王陵军

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广州中医药大学第一附属医院/中医证候全国重点实验室,广东 广州 510405

暖心康 心肌梗死 心室重构 心肌纤维化 巨噬细胞极化 能量代谢 炎症反应 氧化应激 小鼠 RAW 264.7细胞

国家自然科学基金青年科学基金项目广州市科技计划重点研发计划项目

82004293202206080015

2024

中药新药与临床药理
广州中医药大学

中药新药与临床药理

CSTPCD北大核心
影响因子:0.908
ISSN:1003-9783
年,卷(期):2024.35(2)
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