Literature DB >> 24655666

Hind limb ischemia-reperfusion injury in diet-induced obese mice.

Hassan Albadawi1, Rahmi Oklu2, Nicholas R Cormier3, Ryan M O'Keefe3, James T Heaton4, James B Kobler4, William G Austen5, Michael T Watkins6.   

Abstract

BACKGROUND: Obesity is a major risk factor for the development of diabetes. Limb ischemia-reperfusion injury (IR) is a common clinical problem in diabetics who have compromised lower extremity perfusion. This study compared the histologic, metabolic, and functional outcomes after hind limb IR in diet-induced obese (DIO) and non-diabetic (ND) mice during the acute and the regenerative phases of IR.
METHODS: DIO and ND mice were subjected to 1.5 h unilateral hind limb ischemia followed by 1- or 28-d IR. Muscle morphology, metabolic, and genomic stress were evaluated at days 1 and 28 IR; Acute inflammation and thrombosis were only measured at day-1 IR. At day 28, IR, skeletal muscle contractility, and maturation were also assessed.
RESULTS: At day-1 IR, similar levels of acute muscle fiber necrosis were seen in both groups. DIO mice demonstrated substantially greater inflammatory, prothrombotic, and genomic stress responses, which were also associated with a greater reduction in energy substrates and Akt phosphorylation. At 28d, there was no difference in the peak forces generated in the hind limbs for the two groups. DIO mice had reduced fatigue resistance compared with ND and larger areas of fat accumulation although there was no significant difference in muscle fiber maturation.
CONCLUSIONS: DIO mice had an exacerbated acute response to IR with enhanced metabolic deficit, fat accumulation, and defective functional recovery during the regenerative phase of IR. These changes in fatigue resistance reflect compromised functional recovery after IR injury and have relevance for the functional recovery of patients with metabolic syndrome and insulin resistance.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Diabetes; Diet-induced obesity; Inflammation; Insulin resistance; Limb ischemia; Metabolism; Muscle contraction; Muscle regeneration; Phosphoinositide-3-kinase–protein kinase B/Akt pathway; Reperfusion injury

Mesh:

Substances:

Year:  2014        PMID: 24655666      PMCID: PMC4096585          DOI: 10.1016/j.jss.2014.01.020

Source DB:  PubMed          Journal:  J Surg Res        ISSN: 0022-4804            Impact factor:   2.192


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