Hemorrhagic shock induces endothelial cell apoptosis, which is mediated by factors contained in mesenteric lymph

2004 ◽  
Vol 32 (12) ◽  
pp. 2464-2470 ◽  
Author(s):  
Qi Lu ◽  
Da-Zhong Xu ◽  
Marson T. Davidson ◽  
György Haskó ◽  
Edwin A. Deitch
2020 ◽  
Vol 2020 ◽  
pp. 1-12
Author(s):  
Yongjun Liu ◽  
Chuanxi Chen ◽  
Qing Sun ◽  
Huadong Sun ◽  
Ning Liu ◽  
...  

The present study was to investigate the effect of mesenteric lymph duct drainage on lung inflammatory response, histological alteration, and endothelial cell apoptosis in septic rats. Animals were randomly assigned into four groups: control, sham surgery, sepsis, and sepsis plus mesenteric lymph drainage. We used the colon ascendens stent peritonitis (CASP) procedure to induce the septic model in rats, and mesenteric lymph drainage was performed with a polyethylene (PE) catheter inserted into mesenteric lymphatic. The animals were sacrificed at the end of CASP in 6 h. The mRNA expression levels of inflammatory mediators were measured by qPCR, and the histologic damage were evaluated by the pathological score method. It was found that mesenteric lymph drainage significantly reduced the expression of TNF-α, IL-1β, and IL-6 mRNA in the lung. Pulmonary interstitial edema and infiltration of inflammatory cells were alleviated by mesenteric lymph drainage. Moreover, increased mRNA levels of TNF-α, IL-1β, IL-6 mRNA, and apoptotic rate were observed in PMVECs treated with septic lymph. These results indicate that mesenteric lymph duct drainage significantly attenuated lung inflammatory injury by decreasing the expression of pivotal inflammatory mediators and inhibiting endothelial apoptosis to preserve the pulmonary barrier function in septic rats.


Shock ◽  
2003 ◽  
Vol 19 (Supplement) ◽  
pp. 95
Author(s):  
Q. Lu ◽  
D Z. Xu ◽  
M. Davidson ◽  
E A. Deitch

2018 ◽  
Vol 38 (3) ◽  
Author(s):  
Chengfu Song ◽  
Xiangdong Zhao

In patients with cerebral infarction (CI), elevated serum uric acid (UA) level may exacerbate the occurrence and development of carotid atherosclerosis (AS). Our study intended to explore the underlying mechanism. We enrolled 86 patients with CI, and divided them into four groups: Non-AS, AS-mild, AS-moderate, and AS-severe groups; the levels of UA and oxidative stress-related factors in serum were detected. The middle cerebral artery occlusion (MCAO) model was used to stimulate CI in rats, and different doses of UA were administrated. The levels of oxidative stress-related factors in serum were detected. Hematoxylin & eosin (H&E) staining was used to observe the morphological alterations, and the apoptotic cell death detection kit was used to detect apoptotic cells. Increased UA concentration and enhanced oxidative stress were found in AS patients. H&E staining results showed that UA treatment exacerbated morphological damage in rats with MCAO, promoted oxidative stress, and enhanced vascular endothelial cell apoptosis in rats with MCAO.


2021 ◽  
pp. 1-9
Author(s):  
Rima Dardik ◽  
Ophira Salomon

Intracranial hemorrhage (ICH) associated with fetal/neonatal alloimmune thrombocytopenia (FNAIT) is attributed mainly to endothelial damage caused by binding of maternal anti-HPA-1a antibodies to the αvβ3 integrin on endothelial cells (ECs). We examined the effect of anti-HPA-1a antibodies on EC function using 2 EC lines from different vascular beds, HMVEC of dermal origin and hCMEC/D3 of cerebral origin. Anti-HPA-1a sera significantly increased apoptosis in both HMVEC and hCMEC/D3 cells and permeability in hCMEC/D3 cells only. This increase in both apoptosis and permeability was significantly inhibited by a monoclonal anti-β3 antibody (SZ21) binding to the HPA-1a epitope. Our results indicate that (1) maternal anti-HPA-1a antibodies impair EC function by increasing apoptosis and permeability and (2) ECs from different vascular beds vary in their susceptibility to pathological effects elicited by maternal anti-HPA-1a antibodies on EC permeability. Examination of maternal anti-HPA-1a antibodies for their effect on EC permeability may predict potential ICH associated with FNAIT.


2008 ◽  
Vol 283 (43) ◽  
pp. 29447-29460 ◽  
Author(s):  
Ricardo J. Giordano ◽  
Johanna Lahdenranta ◽  
Lijie Zhen ◽  
Ugonma Chukwueke ◽  
Irina Petrache ◽  
...  

2015 ◽  
Vol 13 (1) ◽  
pp. 867-873 ◽  
Author(s):  
MEI-HUA BAO ◽  
JIAN-MING LI ◽  
QI-LIANG ZHOU ◽  
GUANG-YI LI ◽  
JIE ZENG ◽  
...  

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