Role of post-hemorrhagic shock mesenteric lymph in enhancement of vas-cular permeability
10.3969/j.issn.1000-4718.2014.08.030
- VernacularTitle:失血性休克后的肠淋巴液提高血管通透性的作用
- Author:
Gaixia SUN
;
Yaxiong GUO
;
Huibo DU
;
Limin ZHANG
;
Zigang ZHAO
;
Shengjun LIU
;
Chunyu NIU
- Publication Type:Journal Article
- Keywords:
Shock,hemorrhagic;
Mesenteric lymph;
Vascular permeability;
Human umbilical vein endothelialcells;
Drainage
- From:
Chinese Journal of Pathophysiology
2014;(8):1506-1512,1536
- CountryChina
- Language:Chinese
-
Abstract:
AIM: To investigate the role of post-hemorrhagic shock mesenteric lymph (PHSML) in the enhancementof vascular permeability .METHODS: Eighteen Wistar rats were randomized into sham group , shock group,and shock plus mesenteric lymph drainage (shock +drainage) group.The rats in shock group and shock +drainagegroup were routinely subjected to hemorrhagic shock and hypotension [(40 ±2) mmHg] was maintained for 90 min, andthen the fluid resuscitation was performed.Mesenteric lymph was drained in the rats in shock +drainage group from resuscitationfinished to 6 h, for the observation of PHSML drainage on the vascular permeability in multiple tissues of hemorrhagicshock rats.Afterwards, human umbilical vein endothelial cells (HUVECs) were incubated with the PHSML in vitro to observethe effects of PHSML on the morphology and permeability of HUVECs .RESULTS: The degree of blue color and concentrationsof Evens blue in the lung, myocardium, kidney, liver, spleen and small intestine were significantly increased inthe shocked rats than that in sham group, while the ratios of the dry weight to the wet weight were decreased .The mesentericlymph drainage reversed these changes .Meanwhile, 4% and 10% of PHSML at 0 ~3 h and 3 ~6 h after resuscitation,and lipopolysaccharide (10 mg/L) all caused the damage of HUVECs, decreased the viability and trans-endothelial electricalresistance of HUVECs, and increased the permeability of HUVECs to fluorescein isothiocyanate -labeled albumin. CONCLUSION: PHSML is a vital factor in the enhancement of vascular permeability .
