Hind Limb Ischemia-Reperfusion in the Leptin Receptor Deficient (db/db) Mouse

Background Diabetic patients have high incidence of peripheral vascular disease and limb loss after acute extremity injury. Experiments were designed to test the hypothesis that acute tissue injury in leptin receptor deficient (Db) diabetic (type2) mice would be more severe than in non-diabetic mice...

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Veröffentlicht in:The Journal of surgical research 2007-05, Vol.139 (1), p.97-105
Hauptverfasser: Entabi, Fateh, M.D, Albadawi, Hassan, M.D, Stone, David H., M.D, Sroufe, Rameses, A.B, Conrad, Mark F., M.D, Watkins, Michael T., M.D
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Sprache:eng
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Zusammenfassung:Background Diabetic patients have high incidence of peripheral vascular disease and limb loss after acute extremity injury. Experiments were designed to test the hypothesis that acute tissue injury in leptin receptor deficient (Db) diabetic (type2) mice would be more severe than in non-diabetic mice. Methods Db and wild type (Wt) mice were subjected to 3 h of ischemia followed by either 4 or 24 h of reperfusion (3/4 IR, 3/24 IR). Muscle analyzed for tissue viability (mitochondrial activity), cytokines (KC-murine equivalent of human IL-8, TNFα, IL-6), growth factor, and histological evaluation (neutrophils/uninjured muscle fibers). Tissue perfusion was detected during basal and reperfusion conditions using laser Doppler imaging. Results Mitochondrial activity and histological evaluation for tissue injury did not differ in the Db versus Wt mice at the time intervals studied. When compared with their respective sham animals, both Db and Wt mice had similarly increased levels of KC, IL-6, and VEGF after 3/24 IR. TNFα levels increased in Db but not Wt mice after IR. Although absolute increases in TNFα and KC were higher in Db mice, VEGF levels were actually lower in the Db mice. Conclusion The patterns of tissue perfusion, cytokines, and growth factors were different in Db versus Wt mice. At the acute time intervals studied, these differences did not correlate with an expected greater degree of acute muscle injury in Db mice.
ISSN:0022-4804
1095-8673
DOI:10.1016/j.jss.2006.08.008