PhD. Capital Medical University - Beijing ChaoYang Hospital - Department of Emergency - Beijing, China.
PhD. Peking University Third Hospital - Department of Critical Care Medicine - Beijing, China.
Acta Cir Bras. 2021 May 28;36(4):e360405. doi: 10.1590/ACB360405. eCollection 2021.
Shen-fu injection (SFI) was used to intervene in the resuscitation of porcine hemorrhagic shock (HS) model to study its protective effects on acute kidney injury.
After 60 min of HS, 28 animals were randomly assigned into four groups. The groups were as follows: hemorrhagic shock group (HS); HS resuscitation with shed-blood group (HSR); HS resuscitation with shed-blood and SFI (1 mL·kg-1) group (HSR-SFI); and the sham operation group (Sham). The bloods were analyzed for serum creatinine (sCr), cystatin C (CysC) and neutrophil gelatinase-associated lipocalin (NGAL). BAX, Bcl-2, and caspase-3 protein expressions by Western blot analysis and immunohistochemical staining. The renal tissues were removed and pathologic changes were observed.
Mean aortic pressure (MAP) in HSR-SFI groups were higher than that in HSR groups after shock. At the 6th hour after shock, the urine volume per hour in the HSR-SFI groups was more than that in the HSR groups. The sCr, NGAL, CysC and cytokine levels of HSR-SFI groups were lower. The Bcl-2 expression was increased in the HSR-SFI groups. The BAX and caspase-3 expressions were reduced. The histopathologic score in the HSR-SFI was lower.
SFI may reduce the risk of acute kidney injury (AKI) following hemorrhagic shock by attenuating systemic inflammatory responses, and regulating the expression of apoptosis-related proteins.
参附注射液(SFI)用于干预猪失血性休克(HS)模型的复苏,以研究其对急性肾损伤的保护作用。
HS 后 60min,将 28 只动物随机分为 4 组。各组如下:失血性休克组(HS);失血复苏组(HSR);失血复苏加 SFI(1mL·kg-1)组(HSR-SFI);假手术组(Sham)。分析血清肌酐(sCr)、胱抑素 C(CysC)和中性粒细胞明胶酶相关脂质运载蛋白(NGAL)。采用 Western blot 分析和免疫组化染色检测 BAX、Bcl-2 和 caspase-3 蛋白的表达。取出肾组织观察病理变化。
HSR-SFI 组的平均主动脉压(MAP)在休克后高于 HSR 组。休克后 6 小时,HSR-SFI 组每小时尿量多于 HSR 组。HSR-SFI 组的 sCr、NGAL、CysC 和细胞因子水平较低。HSR-SFI 组 Bcl-2 表达增加,BAX 和 caspase-3 表达减少,HSR-SFI 组的组织病理学评分较低。
SFI 通过减轻全身炎症反应,调节凋亡相关蛋白的表达,可能降低失血性休克后急性肾损伤(AKI)的风险。