Yao Bo, Wang Fu-Hua, Han Xiao-Ning, Yang Jun, Xue Ping, Qi Qi, Wei Guang-Yao, Xing Jin-Yan
The Department of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Wutaishan Road 1677, Qingdao, 26600, China.
Intensive Care Med Exp. 2024 Mar 4;12(1):22. doi: 10.1186/s40635-023-00589-1.
Disorders of the gut microbiome could be responsible for the progression of multiple organ dysfunction syndrome. In this study, we examined the effect of esmolol on the gut microbiome in a rat model of sepsis induced by cecal ligation and puncture (CLP).
The animals (n = 32) were randomly divided into 3 groups: Sham group (sham operation + normal saline treatment, n = 8), CLP group (cecal ligation and puncture + normal saline treatment, n = 12), and CLP + ESM group (cecal ligation and puncture + esmolol treatment, n = 12). After 24 h, feces in the colon were collected for 16S rRNA gene sequencing and nitric oxide analysis. In addition, colon was removed for immunohistochemical staining of inducible nitric oxide synthase (iNOS).
Four rats in the CLP group and two rats in the CLP + ESM group died. The abundance of Lactobacillus in the CLP + ESM group was higher than CLP group (P = 0.048). In the linear discriminant analysis effect size analysis, Norank f Muribaculaceae, Escherichia-Shigella and Lactobacillus were the predominant bacteria in the Sham group, CLP group and CLP + ESM group, respectively. The iNOS expression in colonocytes stained by brown in the CLP group were much more than Sham group (P = 0.001). Compared to CLP group, the iNOS expression in colonocytes reduced after esmolol treatment (P = 0.013). The concentration of nitric oxide in colon feces was different in Sham group, CLP group and CLP + ESM group (1.31 ± 0.15μmmol/l vs. 1.98 ± 0.27μmmol/l vs. 1.51 ± 0.14μmmol/l, P = 0.001). In addition, the concentration of nitric oxide in CLP group was higher than Sham group (P = 0.001) or CLP + ESM group (P = 0.001).
Esmolol increased the fecal abundance of Lactobacillus in a rat model of sepsis. Moreover, esmolol reduced the iNOS expression of colonocytes and the nitric oxide concentration of colon feces.
肠道微生物群紊乱可能是多器官功能障碍综合征进展的原因。在本研究中,我们在盲肠结扎穿刺(CLP)诱导的脓毒症大鼠模型中研究了艾司洛尔对肠道微生物群的影响。
将动物(n = 32)随机分为3组:假手术组(假手术+生理盐水治疗,n = 8)、CLP组(盲肠结扎穿刺+生理盐水治疗,n = 12)和CLP + ESM组(盲肠结扎穿刺+艾司洛尔治疗,n = 12)。24小时后,收集结肠粪便进行16S rRNA基因测序和一氧化氮分析。此外,取出结肠进行诱导型一氧化氮合酶(iNOS)的免疫组织化学染色。
CLP组4只大鼠和CLP + ESM组2只大鼠死亡。CLP + ESM组中乳酸杆菌的丰度高于CLP组(P = 0.048)。在线性判别分析效应大小分析中,无分类的Muribaculaceae、埃希氏菌属-志贺氏菌属和乳酸杆菌分别是假手术组、CLP组和CLP + ESM组中的优势菌。CLP组结肠细胞中iNOS表达经棕色染色的比假手术组多得多(P = 0.001)。与CLP组相比,艾司洛尔治疗后结肠细胞中iNOS表达降低(P = 0.013)。假手术组、CLP组和CLP + ESM组结肠粪便中一氧化氮浓度不同(1.31±0.15μmmol/l对1.98±0.27μmmol/l对1.51±0.14μmmol/l,P = )。此外,CLP组中一氧化氮浓度高于假手术组(P = 0.001)或CLP + ESM组(P = 0.001)。
艾司洛尔增加了脓毒症大鼠模型粪便中乳酸杆菌的丰度。此外,艾司洛尔降低了结肠细胞的iNOS表达和结肠粪便中的一氧化氮浓度。