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Remote ischemic conditioning counteracts the intestinal damage of necrotizing enterocolitis by improving intestinal microcirculation

Authors :
Niloofar Ganji
Alan Daneman
Bo Li
Agostino Pierro
Yuhki Koike
Carlos Zozaya
Zhen Zhang
Masaya Yamoto
Maarten Janssen Lok
Ethan Lau
Paul Delgado-Olguin
Sinobol Chusilp
Simon Eaton
Carol Lee
Masato Kusunoki
Mikihiro Inoue
Hiromu Miyake
Yong Chen
Keiichi Uchida
Luc Mertens
Richard Y. Wu
Philip M. Sherman
Haitao Zhu
Dorothy Lee
Source :
Nature Communications, Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
Publication Year :
2020
Publisher :
Springer Science and Business Media LLC, 2020.

Abstract

Necrotizing enterocolitis (NEC) is a devastating disease of premature infants with high mortality rate, indicating the need for precision treatment. NEC is characterized by intestinal inflammation and ischemia, as well derangements in intestinal microcirculation. Remote ischemic conditioning (RIC) has emerged as a promising tool in protecting distant organs against ischemia-induced damage. However, the effectiveness of RIC against NEC is unknown. To address this gap, we aimed to determine the efficacy and mechanism of action of RIC in experimental NEC. NEC was induced in mouse pups between postnatal day (P) 5 and 9. RIC was applied through intermittent occlusion of hind limb blood flow. RIC, when administered in the early stages of disease progression, decreases intestinal injury and prolongs survival. The mechanism of action of RIC involves increasing intestinal perfusion through vasodilation mediated by nitric oxide and hydrogen sulfide. RIC is a viable and non-invasive treatment strategy for NEC.<br />Necrotizing enterocolitis (NEC) is one of the most lethal gastrointestinal emergencies in neonates needing precision treatment. Here the authors show that remote ischemic conditioning is a non-invasive therapeutic method that enhances blood flow in the intestine, reduces damage, and improves NEC outcome.

Details

ISSN :
20411723
Volume :
11
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....b351396c8fce32a57fa9bd30db3ce4db