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1. 安徽中医药大学中医学院
2. 安徽中医药大学研究生院
3. 安徽中医药大学针灸推拿学院
纸质出版日期:2021
移动端阅览
王炜, 李庆羚, 马强, 等. 艾灸联合贝那普利对慢性心力衰竭大鼠心肌组织白细胞介素-18及磷酸化蛋白激酶B表达水平的影响[J]. 针刺研究, 2021,46(11):935-941.
WANG Wei, LI Qing-ling, MA Qiang, et al. Effect of moxibustion combined with benazepril on expression of IL-18 and phosphorylated protein kinase B in myocardial tissue of rats with chronic heart failure[J]. Acupuncture research, 2021, 46(11): 935-941.
王炜, 李庆羚, 马强, 等. 艾灸联合贝那普利对慢性心力衰竭大鼠心肌组织白细胞介素-18及磷酸化蛋白激酶B表达水平的影响[J]. 针刺研究, 2021,46(11):935-941. DOI: 10.13702/j.1000-0607.201219.
WANG Wei, LI Qing-ling, MA Qiang, et al. Effect of moxibustion combined with benazepril on expression of IL-18 and phosphorylated protein kinase B in myocardial tissue of rats with chronic heart failure[J]. Acupuncture research, 2021, 46(11): 935-941. DOI: 10.13702/j.1000-0607.201219.
目的:观察艾灸联合贝那普利对慢性心力衰竭(CHF)大鼠心功能及心肌组织白细胞介素-18(IL-18)、磷酸化蛋白激酶B(p-Akt)表达水平的影响
探讨艾灸联合贝那普利防治CHF的可能机制。方法:SD大鼠随机分为正常组10只和造模组40只。造模组大鼠采用腹腔隔日注射盐酸多柔比星制备CHF模型。造模成功的存活大鼠随机分为模型组、艾灸组、贝那普利组、艾灸+贝那普利组(艾贝组)
每组各9只。艾灸组予艾条温和灸双侧"肺俞""心俞"
20 min/次;贝那普利组予贝那普利(2 mg/kg)灌胃;艾贝组先予贝那普利灌胃
再行艾灸;均每日1次
连续3周。观察大鼠的一般情况;超声心动图检查大鼠射血分数(EF)、左室内径缩短率(FS)、左室舒张末径(LVIDd)、左室收缩末径(LVIDs)、心率(HR)、室间隔厚度(IVS);酶联免疫吸附法检测血清N末端脑钠素前体(NT-proBNP)含量;蛋白免疫印迹法检测心肌组织IL-18、p-Akt表达水平。结果:与正常组比较
模型组大鼠EF、FS、IVS和心肌组织p-Akt表达水平显著降低(P<0.01)
LVIDd、LVIDs、HR、血清NT-proBNP含量、心肌组织IL-18表达水平显著升高(P<0.01)。与模型组比较
艾灸组、贝那普利组、艾贝组EF、FS、IVS和心肌组织p-Akt表达水平升高(P<0.05
P<0.01)
LVIDd、LVIDs、HR、血清NT-proBNP含量、心肌组织IL-18表达水平降低(P<0.05
P<0.01)。与艾贝组比较
艾灸组、贝那普利组EF、FS、IVS、心肌组织p-Akt表达水平显著降低(P<0.01)
LVIDs、HR、血清NT-proBNP含量、心肌组织IL-18表达水平升高(P<0.05
P<0.01)。结论:艾灸联合贝那普利改善CHF大鼠心功能
其机制可能是通过降低心肌组织中IL-18表达和升高p-Akt
且表达优于单用艾灸和贝那普利。
Objective To observe the effect of moxibustion combined with benazepril on cardiac function and expression levels of myocardial interleukin-18(IL-18)
phosphorylated protein kinase B(p-Akt) in rats with chronic heart failure(CHF)
so as to explore its underlying mechanisms in improvement of CHF. Methods Fifty male rats were randomly divided into normal
model
moxibustion
benazepril and moxibustion+benazepril groups(n=10 rats per group). The CHF model was established by intraperitoneal injection of doxorubicin hydrochloride solution(DOX
2.5 mg/kg) twice a week for 4 weeks. After successful modeling
the rats in the normal and model groups were fed with normal diet
and fixed on a rat plate for 20 min each time without any treatment. Mild moxibustion was applied to bilateral “Feishu”(BL13) and “Xinshu”(BL15) for 20 min each time
for 3 weeks in the moxibustion and moxibustion+benazepril groups. Rats of the benazepril and moxibustion+benazepril groups received gavage of benazepril(2 mg/kg) once daily for 3 weeks. The general behaviors of rats were observed. The ejection fraction(EF)
left ventricular diameter shortening(FS)
left ventricular end-diastolic diameter(LVIDd)
left ventricular end-systolic diameter(LVIDs)
heart rate(HR) and ventricular septal thickness(IVS) were examined by echocardiography. The content of serum N-terminal pro-brain natriuretic peptide(NT-proBNP) was detected by enzyme-linked immunosorbent assay
and expression levels of myocardial IL-18
p-Akt were detected by Western blot. Results Compared with the normal group
the EF
FS
IVS
and myocardial p-Akt expression level were significantly reduced(P<0.01)
and the LVIDd
LVIDs
HR
and serum NT-proBNP content and myocardial IL-18 expression level were significantly increased in the model group(P<0.01). In comparison with the model group
the EF
FS
IVS
and myocardial p-Akt were remarkably up-regulated(P<0.05
P<0.01)
and the LVIDd
LVIDs
HR
serum NT-proBNP content
and myocardial IL-18 expression level were significantly down-regulated(P<0.05
P<0.01) in the moxibustion
benazepril
and moxibustion+benazepril groups. Compared with the moxibustion+benazepr group
the levels of LVIDs
HR
serum NT-proBNP and myocardial IL-18 expression were obviously higher(P<0.05
P<0.01)
while the levels of EF
FS
IVS and p-Akt were significantly lower in the moxibustion and benazepril groups(P<0.01). Conclusion Moxibustion combined with benazepril improves cardiac function in CHF rats
and is superior to simple moxibustion and simple benazepril in reducing IL-18 expression and increasing p-Akt expression in myocardial tissue.
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