Maurel Agnès, Hernandez Carole, Kunduzova Oksana, Bompart Guy, Cambon Claudie, Parini Angelo, Francés Bernard
Unité 388, Institut National de la Santé et de la Recherche Médicale, Institut Louis Bugnard, Centre Hospitalier Universitaire Rangueil, 31403 Toulouse cedex 04, France.
Am J Physiol Heart Circ Physiol. 2003 Apr;284(4):H1460-7. doi: 10.1152/ajpheart.00700.2002. Epub 2002 Dec 12.
Oxidative stress is one of the factors involved in age-related impairment of cardiac function. In the present study, we investigated the role of the catecholamine-degrading enzyme monoamine oxidase (MAO) in H(2)O(2) production in the hearts of young, adult, and old rats. MAO-dependent H(2)O(2) production, measured by a chemiluminescence-based assay, increased with age, reaching the maximum in 24-mo-old rats (7.5-fold increase vs. 1-mo-old rats). The following observations indicate that the age-dependent increase in H(2)O(2) generation was fully related to the MAO-A isoform: 1) at all the ages tested, chemiluminescence production was inhibited by the MAO-A inhibitor clorgyline but not by the MAO-B inhibitor RO-19 6327; 2) enzyme assay, Western blot, and semiquantitative RT-PCR analysis showed an age-dependent increase in cardiac MAO-A activity, immunodetection, and mRNA expression, respectively; and 3) the MAO-B isoform was undetectable by enzyme assay and Western blot analysis. These results suggest that MAO-A could be a major source of H(2)O(2) in the aging heart.
氧化应激是与年龄相关的心脏功能损害所涉及的因素之一。在本研究中,我们调查了儿茶酚胺降解酶单胺氧化酶(MAO)在年轻、成年和老年大鼠心脏中过氧化氢(H₂O₂)生成中的作用。通过基于化学发光的测定法测量,依赖MAO的H₂O₂生成随年龄增加,在24月龄大鼠中达到最大值(与1月龄大鼠相比增加了7.5倍)。以下观察结果表明,H₂O₂生成的年龄依赖性增加与MAO-A同工型完全相关:1)在所有测试年龄,化学发光产生均被MAO-A抑制剂氯吉兰抑制,但未被MAO-B抑制剂RO-19 6327抑制;2)酶活性测定、蛋白质印迹和半定量逆转录-聚合酶链反应(RT-PCR)分析分别显示心脏MAO-A活性、免疫检测和mRNA表达随年龄增加;3)通过酶活性测定和蛋白质印迹分析未检测到MAO-B同工型。这些结果表明,MAO-A可能是衰老心脏中H₂O₂的主要来源。