摘要
目的观察中药心康方对大鼠心力衰竭模型心肌胶原代谢的影响。方法阿霉素腹腔注射法建立大鼠心力衰竭模型,随机分为对照组(10只)、模型组(9只)、心康方组(9只)和卡托普利组(9只)。Masson染色观察心肌胶原变化,Western blot检测心肌Ⅰ型、Ⅲ型胶原、转化生长因子β1(TGF-β1)、核因子κB的抑制蛋白(IκB)和p56的表达,Western blot和RT-q PCR分别检测心肌基质金属蛋白酶(MMP)-2、MMP-9、基质金属蛋白酶组织抑制因子(TIMP)-1和TIMP-2的蛋白和mRNA表达水平。结果与对照组比较,模型组大鼠心肌Ⅰ型和Ⅲ型胶原表达显著增加,胶原容积分数显著升高(均为P<0.01);TGF-β1和p56表达显著增加,IκB显著降低(均为P<0.05);MMP-2、MMP-9、TIMP-1和TIMP-2的蛋白和mRNA表达水平显著升高(P<0.01或P<0.05)。与模型组比较,心康方组和卡托普利组大鼠的心肌Ⅰ型和Ⅲ型胶原表达显著减少,胶原容积分数显著降低(均为P<0.01);TGF-β1和p56显著降低,IκB显著升高(均为P<0.05);MMP-2、MMP-9、TIMP-1和TIMP-2的蛋白和mRNA表达水平显著降低(P<0.01或P<0.05)。结论中药心康方可减轻心力衰竭大鼠的心肌胶原沉积,其机制可能与抑制核因子κB介导的TGF-β1上调有关。
Objective To investigate the effects of Xinkang recipe on myocardial collagen metabolism in rats with doxorubicin-induced heart failure. Methods The heart failure rat model was induced by intraperitoneal injection of doxorubicin. Male SD rats were randomly divided into the control group (n =10),the model group( n = 9) , the Xinkang group( n = 9 ) and the captopril group( n =10). Masson's trichrome staining was used to observe myocardial fibrosis. Western blotting was used to detect of expression of collagen I ,collagen Ⅲ, TGF-p1, IkB and p56 in myocardium. Myocardial protein and mRNA levels of matrix metalloproteinase-2 ( MMP-2 ) , MMP-9, tissue inhibitor of matrix metalloproteinase-1 (TIMP-1 ) and TIMP-2 were detected by Western blotting and RT-qPCR, respectively. Results Compared with control group,expression of type I and type Ⅲ collagen protein significantly increased, and the collagen volume fraction( CVF) significantly increased in the model group(all P 〈0. 0 1 ) . TGF-p1 and p56 protein expression significantly increased,while IkB protein expression significantly decreased in the model group (a l l P 〈 0. 05) . The myocardial protein and mRNA levels of MMP-2, MMP-9, TIMP-1 and TIMP-2 were significantly higher in the model group( P 〈0. 01 or P 〈0. 05) . Compared with the model group, expression of collagen I and collagen Ⅲ protein significantly decreased,and the CVF significantly reduced in Xinkang group and captopril group(both P 〈 0. 01). The TGF-β1 and p56 protein expression significantly decreased, and the IkB protein expression significantly increased in Xinkang group and captopril group (all P 〈 0 . 0 5 ) . The levels of protein and mRNA of MMP-2, MMP-9, TIMP-1 and TIMP-2 were significantly lower in Xinkang group and captopril group ( P 〈0. 01 or P 〈0. 05 ) . Conclusions Xinkang recipe can reduce collagen deposition in myocardium in rats with doxorubicin-induced heart failure. Down-regulating of TGF-β1 protein expression through the inhibition of NF-kB signal transduction pathway might be a potential mechanism underlying effects of Xinkang recipe.
出处
《中国心血管杂志》
2018年第1期56-62,共7页
Chinese Journal of Cardiovascular Medicine
基金
广东省中医药局科研项目(20151118)~~
关键词
心康方
心力衰竭
心肌胶原
核因子ΚB
转化生长因子Β1
Xinkang recipe
Heart failure
Myocardium collagen
Nuclear factor kappa B
Transforming growth factor beta 1