Beta-blocker therapy preserves normal splenic T-lymphocyte numbers reduced in proportion to sepsis severity in a sepsis model

Beta-blocker therapy preserves normal splenic T-lymphocyte numbers reduced in proportion to sepsis severity in a sepsis model
复制标题

β-受体阻滞剂治疗可保留正常的脾 T 淋巴细胞数量,在脓毒症模型中,其数量与脓毒症严重程度成比例减少

DOI:
10.1155/2019/8157482
复制
发表时间:
2019
影响因子:
1.7
通讯作者:
Morisaki H
Morisaki H
中科院分区:
--
文献类型:
--
作者:
Suzuki T;Inoue K;Igarashi T;Kato J;Nagata H;Yamada T;Minamishima S;Morisaki H

文献摘要

相似文献

淋巴细胞死亡有助于脓毒症诱导的免疫抑制,导致预后不良。本研究检查了败血症严重程度和β受体阻滞剂治疗是否会影响败血症小鼠模型中T淋巴细胞死亡的程度。在第一项对照研究中,将20只动物分配至4组:假手术对照组(C组,n= 5)和在3个不同部位进行盲肠结扎和穿刺(CLP)的3个组:盲肠近端、中段和远端(分别为CLP-P、CLP-M和CLP-D组;每组n= 5)。CLP后24 h,在全麻下切除脾脏,流式细胞术检测正常脾T淋巴细胞总数和凋亡T淋巴细胞百分比。在第二项实验研究中,检查了β受体阻滞剂艾司洛尔在CLP-P中的作用(CLP-PE组与CLP-P组;每组n= 5)。每只小鼠正常脾T淋巴细胞总数与CLP严重程度成比例显著降低(C组,18.6 × 106(15 × 106-23.6 × 106); CLP‐D组,9.2 × 106(8.8 × 106-9.8 × 106); CLP‐M,6.7 × 106(6.3 × 106-7.0 × 106); CLP‐P,5.3 × 106(5.1 × 106-6.8 × 106))。β受体阻滞剂治疗恢复了T淋巴细胞数量(CLP-PE组vs. CLP-P组; 6.94 ± 1.52 × 106 vs. 4.18± 1.71 × 106;p= 0.027)而不影响凋亡百分比。β受体阻滞剂治疗可通过正常脾T淋巴细胞保存改善脓毒症诱导的免疫抑制。
Lymphocyte cell death contributes to sepsis‐induced immunosuppression, leading to poor prognosis. This study examined whether sepsis severity and beta‐blocker therapy could affect the degree of T‐lymphocyte cell death in a mouse model of sepsis. In the first control study, 20 animals were allocated to 4 groups: control group with sham operation (group C,n= 5) and 3 groups with cecum ligation and puncture (CLP) performed at 3 different sites: proximal, middle, and distal cecum (groups CLP‐P, CLP‐M, and CLP‐D, respectively;n= 5 in each group). Their spleens were resected under general anesthesia 24 hours after CLP, and the total number of normal splenic T lymphocytes per mouse and the percentage of apoptotic T lymphocytes were evaluated using flow cytometry. In the second experimental study, the effect of the beta‐blocker esmolol was examined in CLP‐P (group CLP‐PE vs. CLP‐P;n= 5 in each group). The total normal splenic T‐lymphocyte numbers per mouse significantly decreased in proportion to CLP severity (group C, 18.6 × 106(15 × 106–23.6 × 106); CLP‐D, 9.2 × 106(8.8 × 106–9.8 × 106); CLP‐M, 6.7 × 106(6.3 × 106–7.0 × 106); and CLP‐P, 5.3 × 106(5.1 × 106–6.8 × 106)). Beta‐blocker therapy restored T‐lymphocyte numbers (group CLP‐PE vs. CLP‐P; 6.94 ± 1.52 × 106vs. 4.18 ± 1.71 × 106;p= 0.027) without affecting apoptosis percentage. Beta‐blocker therapy might improve sepsis‐induced immunosuppression via normal splenic T‐lymphocyte preservation.