Wrońska Agata, Kieżun Jacek, Kmieć Zbigniew
Department of Histology, Faculty of Medicine, Medical University of Gdańsk, 80-210 Gdańsk, Poland.
Department of Anatomy and Histology, School of Medicine, University of Warmia and Mazury in Olsztyn, 10-082 Olsztyn, Poland.
Int J Mol Sci. 2025 Aug 20;26(16):8038. doi: 10.3390/ijms26168038.
Fenofibrate (FF), a lipid-lowering drug, may decrease the risk of cardiovascular diseases in some pathological settings, yet data on its cardiac effects in physiological aging is scarce. To determine FF and age effects on the heart's morphology and expression of metabolism-related genes, we treated young and old male rats for 30 days with 0.1% or 0.5% FF. FF did not affect serum activities of LDH and creatine kinase in both age groups. Upon FF treatment the structure of the heart muscle did not change in young rats; however, 0.5% FF increased the abundance of collagen fibers in old rats, and lipid accumulation in cardiomyocytes in young and old animals. FF increased immunoreactivity of the hypertrophy marker NPPA that was more pronounced in old than in young rats, while VEGFB immunoreactivity did not change. FF upregulated phospho-AMPK and PGC1α protein levels only in the cardiac muscle of old rats, while in both age groups it mildly increased the expression of selected fatty acid oxidation genes. We conclude that the cardiac muscle response to FF is dose-dependent and influenced by age. The observed negative impact of high-dose FF in the hearts of aged rats underscores the importance of dose optimization in the elderly.
非诺贝特(FF)是一种降脂药物,在某些病理情况下可能会降低心血管疾病的风险,但关于其在生理衰老过程中心脏效应的数据却很少。为了确定FF和年龄对心脏形态及代谢相关基因表达的影响,我们用0.1%或0.5%的FF对年轻和老年雄性大鼠进行了30天的治疗。FF对两个年龄组的血清乳酸脱氢酶(LDH)和肌酸激酶活性均无影响。经FF治疗后,年轻大鼠的心肌结构未发生变化;然而,0.5%的FF增加了老年大鼠心肌中胶原纤维的丰度,以及年轻和老年动物心肌细胞中的脂质积累。FF增加了肥大标志物NPPA的免疫反应性,老年大鼠比年轻大鼠更明显,而血管内皮生长因子B(VEGFB)的免疫反应性没有变化。FF仅在老年大鼠的心肌中上调了磷酸化腺苷酸活化蛋白激酶(phospho-AMPK)和过氧化物酶体增殖物激活受体γ共激活因子1α(PGC1α)的蛋白水平,而在两个年龄组中,它都轻度增加了所选脂肪酸氧化基因的表达。我们得出结论,心肌对FF的反应是剂量依赖性的,并且受年龄影响。在老年大鼠心脏中观察到的高剂量FF的负面影响强调了老年人剂量优化的重要性。