Yang Zhijun, Cheng Feng, Yan Guosheng, Xiong Lang, Liu Huizhang
Department of Anesthesiology, Ezhou Central Hospital, Ezhou, Hubei 436000, P.R. China.
Department of Clinical Laboratory, Ezhou Central Hospital, Ezhou, Hubei 436000, P.R. China.
Exp Ther Med. 2018 Feb;15(2):2032-2036. doi: 10.3892/etm.2017.5605. Epub 2017 Dec 7.
This study investigated whether propofol protects against endotoxin-induced myocardial injury by inhibiting NF-κB-mediated inflammation. Thirty clean male SD rats were randomly divided into a control (n=10), a model (n=10) and a propofol group (n=10). The model and propofol groups were injected with lipopolysaccharide (LPS) via the caudal vein to establish animal models of myocardial injury. At the same time, the control group was injected with normal saline via the caudal vein. At 30 min after the injections, the propofol group was treated with a continuous intravenous infusion of propofol, the control and model groups were injected with normal saline, and the three groups were treated continuously for 4 h. The changes in levels of interleukin-1 (IL-1), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) in serum were detected via enzyme-linked immunosorbent assay (ELISA). The mRNA expression level of nuclear factor-κB (NF-κB) in myocardial tissues was detected via quantitative real-time polymerase chain reaction (qRT-PCR). The protein expression levels of NF-κB, Bax and Bcl-2 in atrial muscles in each group were measured via Western blotting. The damage of myocardial tissues was detected via hematoxylin eosin (H&E) staining of tissues. Our results showed that compared with those in control group, the levels of IL-1, IL-6 and TNF-α in serum in the model and propofol groups were significantly higher; however, the levels in the model group, were significantly higher than those in the propofol group (P<0.01). The mRNA and protein expression levels of NF-κB in the propofol group were significantly lower than those in the model group (P<0.01). Likewise, the protein expression levels of Bax were significantly lower, while those of Bcl-2 were significantly increased. H&E staining showed that the myocardial tissues in the model group were damaged significantly, but the damage in the propofol group was significantly less severe. Based on our findings, it seems propofol can indeed protect against endotoxin-induced myocardial injury through its inhibition of the NF-κB-mediated inflammatory pathway.
本研究调查了丙泊酚是否通过抑制核因子-κB(NF-κB)介导的炎症反应来预防内毒素诱导的心肌损伤。30只清洁级雄性SD大鼠被随机分为对照组(n = 10)、模型组(n = 10)和丙泊酚组(n = 10)。模型组和丙泊酚组通过尾静脉注射脂多糖(LPS)以建立心肌损伤动物模型。同时,对照组通过尾静脉注射生理盐水。注射后30分钟,丙泊酚组持续静脉输注丙泊酚,对照组和模型组注射生理盐水,三组持续处理4小时。通过酶联免疫吸附测定(ELISA)检测血清中白细胞介素-1(IL-1)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)水平的变化。通过定量实时聚合酶链反应(qRT-PCR)检测心肌组织中核因子-κB(NF-κB)的mRNA表达水平。通过蛋白质免疫印迹法检测每组心房肌中NF-κB、Bax和Bcl-2的蛋白质表达水平。通过苏木精-伊红(H&E)染色检测心肌组织的损伤情况。我们的结果显示,与对照组相比,模型组和丙泊酚组血清中IL-1、IL-6和TNF-α水平显著升高;然而,模型组的水平显著高于丙泊酚组(P<0.01)。丙泊酚组中NF-κB的mRNA和蛋白质表达水平显著低于模型组(P<0.01)。同样,Bax的蛋白质表达水平显著降低,而Bcl-2的蛋白质表达水平显著升高。H&E染色显示,模型组心肌组织损伤显著,但丙泊酚组的损伤明显较轻。基于我们的研究结果,丙泊酚似乎确实可以通过抑制NF-κB介导的炎症途径来预防内毒素诱导的心肌损伤。