Di-san junyi daxue xuebao (Oct 2020)

Protective effect of pericytes against vascular leakage in rats with hemorrhagic shock

  • HE Shuangshuang,
  • ZHU Yu,
  • ZHOU Henan,
  • WANG Hongchen,
  • LI Tao,
  • LIU Liangming

DOI
https://doi.org/10.16016/j.1000-5404.202004227
Journal volume & issue
Vol. 42, no. 19
pp. 1882 – 1889

Abstract

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Objective To investigate the protective effect of pericytes (PCs) against vascular leakage in rats with hemorrhagic shock. Methods Sixty-four 12- to 24-week-old SD rats weighing 200~220 g were randomized equally into sham-operated group, hemorrhagic shock group (HS group), Ringer's lactate solution treatment group (LR group), and PC treatment group (PC group). In the latter 3 groups, rat models of hemorrhagic shock were established by lowering the blood pressure to 30 mmHg, which was maintained for 3 h. Tissue samples were collected 12 h after corresponding treatment for determination of the number of pericytes, vascular permeability of the pulmonary vessels and the mesenteric microvessels, and expressions of zonula occludens 1 (ZO-1) and VE-cadherin. Results The vascular permeability was increased (P < 0.05) and the number of pericytes and expressions of ZO-1 and VE-cadherin were decreased significantly (P < 0.05) in rats with hemorrhagic shock compared with the sham-operated rats. At 12 h after LR treatment, the vascular permeability was slightly reduced, the tight junction between the endothelial cells was moderately improved and the expression levels of ZO-1 and VE-cadherin were mildly increased in rats with hemorrhagic shock. At 12 h after PC treatment, the number of pericytes in the pulmonary vein was increased, the cell morphology and tight junction between the endothelial cells were restored, and the expressions of ZO-1 and VE-cadherin were increased significantly to nearly the normal levels in rats with hemorrhagic shock (P < 0.05); the mesenteric microvascular permeability and vascular leakage were improved significantly after treatment with PCs. Conclusion PC infusion produces significantly protective effect against vascular leakage in rats with hemorrhagic shock.

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