Balietti Marta, Fattoretti Patrizia, Giorgetti Belinda, Casoli Tiziana, Di Stefano Giuseppina, Solazzi Moreno, Platano Daniela, Aicardi Giorgio, Bertoni-Freddari Carlo
Neurobiology of Aging Laboratory, Italian National Research Centers on Aging, Ancona, Italy.
Ann N Y Acad Sci. 2009 Aug;1171:377-84. doi: 10.1111/j.1749-6632.2009.04704.x.
Impairment of energy metabolism and an increase of reactive oxygen species (ROS) production seem to play a major role in age-related apoptotic loss of cardiomyocytes. Succinic dehydrogenase (SDH) is an important marker of the mitochondrial capability to provide an adequate amount of ATP. Moreover, because of its unique redox properties, SDH activity contributes to maintain the reduced state of the ubiquinone pool. Recent reports have shown that ketone body intake improves cardiac metabolic efficiency and exerts a cardioprotective antioxidant action, we therefore performed a cytochemical investigation of SDH activity in cardiomyocytes of late-adult (19-month-old) rats fed for 8 weeks with a medium-chain triglycerides ketogenic diet (MCT-KD). Young, age-matched and old animals fed with a standard chow were used as controls. The overall area of the precipitates (PA) from SDH activity and the area of the SDH-positive mitochondria (MA) were measured. The percent ratios PA/MA and MA/total myocardial tissue area (MA/TA) were the parameters taken into account. We found that PA/MA was significantly higher in young control rats and in MCT-KD-fed rats versus late-adult and old control rats and in young control versus MCT-KD-fed rats. MA/TA of MCT-KD-fed rats was significantly higher versus age-matched and old control rats and tended to be higher versus young control rats; this parameter was significantly higher in young versus old control rats. Thus, MCT-KD intake partially recovers age-related decrease of SDH activity and increases the myocardial area occupied by metabolically active mitochondria. These effects might counteract metabolic alterations leading to apoptosis-induced myocardial atrophy and failure during aging.
能量代谢受损和活性氧(ROS)生成增加似乎在与年龄相关的心肌细胞凋亡性丧失中起主要作用。琥珀酸脱氢酶(SDH)是线粒体产生足够量ATP能力的重要标志物。此外,由于其独特的氧化还原特性,SDH活性有助于维持泛醌池的还原状态。最近的报告表明,酮体摄入可提高心脏代谢效率并发挥心脏保护抗氧化作用,因此我们对喂食中链甘油三酯生酮饮食(MCT-KD)8周的成年晚期(19个月大)大鼠的心肌细胞中SDH活性进行了细胞化学研究。喂食标准饲料的年轻、年龄匹配和老年动物用作对照。测量了SDH活性沉淀物的总面积(PA)和SDH阳性线粒体的面积(MA)。考虑的参数是PA/MA和MA/心肌组织总面积的百分比(MA/TA)。我们发现,与成年晚期和老年对照大鼠相比,年轻对照大鼠和喂食MCT-KD的大鼠的PA/MA显著更高,并且与喂食MCT-KD的大鼠相比,年轻对照大鼠的PA/MA也更高。喂食MCT-KD的大鼠的MA/TA与年龄匹配和老年对照大鼠相比显著更高,与年轻对照大鼠相比有升高趋势;该参数在年轻对照大鼠与老年对照大鼠之间显著更高。因此,摄入MCT-KD可部分恢复与年龄相关的SDH活性下降,并增加代谢活跃线粒体占据的心肌面积。这些作用可能抵消导致衰老过程中凋亡诱导的心肌萎缩和衰竭的代谢改变。