Department of Burnand Plastic Surgery, Affiliated Hospital of Chengde Medical College, Chengde, Hebei 067000, China.
J Healthc Eng. 2022 Mar 3;2022:2129629. doi: 10.1155/2022/2129629. eCollection 2022.
The aim of this study was to investigate the effects of thymosin 4 on myocardial apoptosis following burns. Fifty healthy Sprague Dawley (SD) rats were randomly divided into the normal control group, resuscitation group the low-dose T4 (thymosin 4) group (2g), the medium-dose T4 group (6g), and the high-dose T4 group (18g). The rats were immersed in 95°C hot water for 18 seconds, and then the model of 30% body surface area (TBSA) III° scald was established. The resuscated rats were injected with lactate Ringer's solution for antishock rehydration, while the T4 treatment group was injected with lactate Ringer's solution for antishock rehydration, and the animals were sacrificed 6 h after scald. The degree of histopathological damage was observed by HE (hematoxylin and eosin) staining. Western blot was used to detect STAT1 and STAT3 protein expression levels. Real-time PCR was used to detect mRNA expressions of STAT1 and STAT3. The results showed that the apoptosis rate of the resuscitation group was significantly higher than that of the control group ( < 0.01). Compared with the resuscitation group, the apoptosis rate of thymosin 4 in the treatment group was significantly reduced ( < 0.01). Compared with the normal control group, the expression of STAT1 protein was increased and the expression of STAT3 protein was decreased in model group rats after ischemia and reperfusion. Compared with the model group, the expression of STAT1 protein decreased and the expression of STAT3 protein increased after ischemia-reperfusion in the thymosin 4 treatment group. Thymosin 4 may protect the myocardium by downregulating STAT1 and upregulating STAT3 expression and inhibiting myocardial apoptosis induced by ischemia and reperfusion after severe scald injury.
本研究旨在探讨胸腺肽 4 对烧伤后心肌细胞凋亡的影响。将 50 只健康的 SD 大鼠随机分为正常对照组、复苏组、低剂量 T4 组(2g)、中剂量 T4 组(6g)和高剂量 T4 组(18g)。将大鼠浸入 95°C 的热水中 18 秒,然后建立 30%体表面积(TBSA)Ⅲ°烫伤模型。复苏组大鼠给予乳酸林格液抗休克补液,T4 治疗组给予乳酸林格液抗休克补液,烫伤后 6h 处死动物。HE 染色观察组织病理学损伤程度,Western blot 检测 STAT1 和 STAT3 蛋白表达水平,实时 PCR 检测 STAT1 和 STAT3mRNA 表达水平。结果显示,复苏组的细胞凋亡率明显高于对照组(<0.01)。与复苏组相比,T4 治疗组的细胞凋亡率明显降低(<0.01)。与正常对照组相比,模型组大鼠缺血再灌注后 STAT1 蛋白表达增加,STAT3 蛋白表达减少。与模型组相比,T4 治疗组缺血再灌注后 STAT1 蛋白表达减少,STAT3 蛋白表达增加。胸腺肽 4 可能通过下调 STAT1 和上调 STAT3 的表达,抑制严重烫伤后缺血再灌注引起的心肌细胞凋亡,从而起到心肌保护作用。