Key result
In senescent mouse hearts, postconditioning significantly reduced reperfusion dysfunction (P<0.05) and was associated with a reduction in heart superoxide anion staining.
Why the study?
Does postconditioning improve cardiac output recovery and reduce oxidative stress in a senescent mouse model subjected to ischemia-reperfusion?
Does postconditioning improve cardiac output recovery and reduce oxidative stress in a senescent mouse model subjected to ischemia-reperfusion?
p-value: p=<0.05
Postconditioning reduces reperfusion dysfunction and oxidative stress in senescent mouse hearts, suggesting potential cardioprotective strategies for older donor hearts.
May inform aged donor heart preservation; extends postconditioning to senescence but leaves clinical translation open.
BACKGROUND: There is at present a tragic lack of organs available for transplantation. This has led to the harvesting of hearts from older donors. Unfortunately, hearts from such donors are much more sensitive to ischemic insult. Models such as "Senescence Accelerated Mouse" Prone 8 (SAM-P8) can help understand this sensitivity. New cardioprotective techniques such as postconditioning (PostC) could be of interest in this context. We studied (1) senescence in vessels and hearts and (2) the ability of the senescent heart to adapt to an ischemia-reperfusion (I/R) sequence in the context of PostC. METHODS: Isolated working mouse hearts (8 months) were subjected to total ischemia, followed by 36 min of reperfusion; PostC was performed in the first minutes of reperfusion as three 10-sec sequences of I/R. Superoxide anion (O2.-) production was evaluated on heart and aorta cryosections with the dihydroethidium staining method. The collagen content in aortas was quantified. RESULTS: The aortas of SAM-P8 mice showed a higher production of O2.- and a higher collagen content than did those of SAM-R1 mice (P<0.05). During reperfusion, SAM-P8 hearts showed the worst recovery of cardiac output. PostC significantly reduced reperfusion dysfunction (P<0.05) and was associated with a reduction in heart O2.- staining. CONCLUSIONS: These results indicate that SAM-P8 presents a high degree of cardiovascular oxidative stress and a higher susceptibility to I/R injury, which confirms the senescence of the cardiovascular system in these animals. However, they remain sensitive to cardioprotection afforded by in vitro PostC.
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Lauzier et al. (2008) studied Ischemia-reperfusion injury in senescent hearts. Postconditioning (PostC) vs. Ischemia-reperfusion without PostC was evaluated on Reperfusion dysfunction (recovery of cardiac output) and superoxide anion production (p=<0.05). In senescent mouse hearts, postconditioning significantly reduced reperfusion dysfunction (P<0.05) and was associated with a reduction in heart superoxide anion staining.
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