Durmaz Selim, Kurtoğlu Tünay, Barbarus Emin, Eliyatkın Nükhet, Yılmaz Mustafa
MD, Aydın Adnan Menderes University, Faculty of Medicine, Department of Cardiovascular Surgery, Aydın, Turkey. Conception and design of the study, acquisition and analysis of data, final approval.
Associate Professor, Aydın Adnan Menderes University, Faculty of Medicine, Department of Cardiovascular Surgery, Aydın, Turkey. Conception and design of the study, acquisition and analysis of data, final approval.
Acta Cir Bras. 2020 Apr 3;35(2):e202000202. doi: 10.1590/s0102-865020200020000002. eCollection 2020.
To investigate the effects of adalimumab pretreatment on the lipopolysaccharide-mediated myocardial injury.
Twenty-eight Wistar rats were randomized into four groups (n=7). Control (C) group animals were injected once a day with intraperitoneal (i.p) 0.9 % saline for two days. In the Adalimumab (Ada) group, adalimumab was injected at a dose of 10 mg/kg/ day (i.p) for two days. Lipopolysaccharide (Lps) group rats were injected with a dose of 5 mg/kg (i.p) lipopolysaccharide. Lipopolysaccharide + Adalimumab (Lps+Ada) group rats received adalimumab before the administration of lipopolysaccharide. The animals were sacrificed 24 h after the last injection and blood samples were obtained for determination of biochemical cardiac injury markers and circulating levels of TNF-α and interleukin-6 (IL-6). Hearts were harvested for histological examination.
Endotoxin exposure resulted in significant increases in serum cardiac injury markers, serum cytokines and histological myocardial injury scores in the Lps group. The levels of circulating cytokines, cardiac injury markers and histological injury scores for myocardial necrosis, perivascular cell infiltration, and inflammation were significantly reduced in Lps+Ada as compared to Lps group (p<0.05).
Adalimumab pretreatment reduces endotoxin-induced myocardial damage in rats. This beneficial effect is thought to be related to the reduction of cytokine release.
研究阿达木单抗预处理对脂多糖介导的心肌损伤的影响。
将28只Wistar大鼠随机分为四组(n = 7)。对照组(C组)动物每天腹腔注射一次0.9%生理盐水,共注射两天。在阿达木单抗(Ada)组中,以10 mg/kg/天的剂量腹腔注射阿达木单抗,共注射两天。脂多糖(Lps)组大鼠注射5 mg/kg剂量的脂多糖(腹腔注射)。脂多糖+阿达木单抗(Lps+Ada)组大鼠在注射脂多糖前接受阿达木单抗治疗。在最后一次注射后24小时处死动物,采集血样以测定心脏生化损伤标志物以及肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)的循环水平。摘取心脏进行组织学检查。
内毒素暴露导致Lps组血清心脏损伤标志物、血清细胞因子和组织学心肌损伤评分显著增加。与Lps组相比,Lps+Ada组循环细胞因子水平、心脏损伤标志物以及心肌坏死、血管周围细胞浸润和炎症的组织学损伤评分均显著降低(p<0.05)。
阿达木单抗预处理可减轻大鼠内毒素诱导的心肌损伤。这种有益作用被认为与细胞因子释放减少有关。