• Am J Emerg Med · Apr 2019

    The value of endoplasmic reticulum stress markers (GRP78 and CHOP) in the diagnosis of acute mesenteric ischemia.

    • Senol Ardic, Aysegul Gumrukcu, Ozgen Gonenc Cekic, Mehmet Erdem, Goksen Derya Reis Kose, Selim Demir, Bestami Kose, Esin Yulug, Ahmet Mentese, and Suleyman Turedi.
    • University of Health Science, Faculty of Medicine, Department of Emergency Medicine, Trabzon, Turkey.
    • Am J Emerg Med. 2019 Apr 1; 37 (4): 596-602.

    AimTo evaluate levels of the endoplasmic reticulum (ER) stress markers GRP78 and CHOP in acute mesenteric ischemia (AMI) and to examine relations with degrees of AMI-related intestinal injury.Materials And MethodsTwenty-four rats were divided into four groups. Group I and Group III represented the control groups, from which blood and tissue specimens were collected 2 and 6 h after laparotomy without superior mesenteric artery (SMA) ligation. Group II and Group IV constituted the ischemia groups, from which blood and tissue specimens were collected 2 and 6 h after SMA ligation. The ER stress markers GRP78 and CHOP, total oxidant status (TOS), total antioxidant status (TAS), and the oxidative stress index (OSI) were investigated in each group. Ileum specimens were assessed in terms of ischemic injury, and appropriate comparisons were performed.ResultsSignificantly higher GRP78, CHOP, TOS, and TAS values were determined in the ischemia groups (groups II and IV) compared to the control groups (groups I and III). This elevation was greater in the 6 h ischemia group, the group exposed to the greatest ischemic injury (Group IV). Significant and powerful correlation was present between histopathological damage and levels of the ER stress markers and oxidative markers.ConclusionAccording to our results, ER stress markers (GRP78 and CHOP) increase significantly following ischemic injury. This elevation has the potential to be used diagnostically and also in prognostic terms due to the powerful correlation it exhibits with AMI-related ischemic injury.Copyright © 2018 Elsevier Inc. All rights reserved.

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