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Abstract W MP88: Worsening Of Stroke Outcome With Age Is Associated With Increased Intestinal Permeability And Peripheral Inflammation

Authors :
Joshua Crapser
Rodney Ritzel
Sarah Doran
Edward Koellhoffer
Anita Patel
Brett Friedler
Rajkumar Verma
Louise McCullough
Source :
Stroke. 46
Publication Year :
2015
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2015.

Abstract

Introduction: Aging remains the biggest risk factor for ischemic stroke. Initial observations into the role of aging on stroke outcome revealed that while aged mice had significantly smaller infarcts compared to young mice, they had greater long-term deficits in behavioral recovery. This study aimed to elucidate the role of systemic factors, such as intestinal stress, underlying the poor outcomes of aging mice after stroke. Methods: Young (8-12 wks) and aged (18-20 mos) wildtype mice were subjected to 90min of right middle cerebral artery occlusion (MCAO) followed by reperfusion. Intestinal permeability was measured with 4kDa FITC-dextran gavage. Mesenteric lymph node (MLNs) homogenates were plated on blood agar to measure bacterial growth. Bacterial endotoxin was measured using a LAL assay. Flow cytometry was used to assess immune cells. Plasma IL-6 was measured by ELISA. Results: Baseline gut permeability increased with age as evidenced by increased FITC-dextran extravasation across the intestinal lumina. Bacterial burden in MLNs and serum bacterial endotoxin levels were also elevated with age (p Conclusion: Our data suggest that the high mortality in aged mice after stroke is secondary to exacerbation of intestinal permeability, increased bacterial translocation, and subsequent induction of sepsis. This data points to gut-targeted interventions as a means to reduce the severity of peripheral inflammation and improve prognosis in aged stroke victims.

Details

ISSN :
15244628 and 00392499
Volume :
46
Database :
OpenAIRE
Journal :
Stroke
Accession number :
edsair.doi...........3564d8d317451c4e9cb2808d9acca31b
Full Text :
https://doi.org/10.1161/str.46.suppl_1.wmp88