Son Tae Gen, Zou Yani, Yu Byung Pal, Lee Jaewon, Chung Hae Young
Department of Pharmacy, College of Pharmacy, Aging Tissue Bank, Longevity Life Science and Technology Institutes, Pusan National University, Gumjung-gu, Busan 609-735, South Korea.
Free Radic Res. 2005 Mar;39(3):283-9. doi: 10.1080/10715760500053461.
Myeloperoxidase (MPO), a heme protein existing in neutrophil and monocyte, is implicated in various stages of inflammatory conditions with the production of a variety of potent oxidants. To investigate the extent of the involvement of MPO in aging, we measured MPO activities in kidney of rats at different ages maintained with an ad libitum (AL) or a calorie restriction (CR) dietary regimen. Results showed that the MPO activities increased during aging in AL rats, but were significantly attenuated by CR. This result was consistent with altered protein level of MPO during aging. In addition, we were able to detect dityrosine that is a stable end MPO-oxidation product. The amount of dityrosine increased in old AL, but not in old CR rats. To examine the source responsible for increased MPO activity during aging for leukocyte recruitment and infiltration, the levels of vascular cell adhesion molecule (VCAM-1) protein were measured. The level of VCAM-1 showed age-dependent increase in AL rats, which was correlated with higher activity of MPO in old AL rats. Furthermore, we have found that LPS-induced inflammation increased the activity and protein levels of MPO, and VCAM-1 expression in young rat kidneys. These findings suggest that increased MPO activity with aging may related to increased recruitment of inflammatory cells, contributing to protein oxidation accumulation in the aging process. We propose that age-related alterations of MPO, dityrosine, and VCAM were modulated by CR through its anti-inflammatory action.
髓过氧化物酶(MPO)是一种存在于中性粒细胞和单核细胞中的血红素蛋白,通过产生多种强效氧化剂参与炎症反应的各个阶段。为了研究MPO在衰老过程中的参与程度,我们测量了自由摄食(AL)或热量限制(CR)饮食方案喂养的不同年龄大鼠肾脏中的MPO活性。结果表明,AL组大鼠在衰老过程中MPO活性增加,但CR组显著降低。这一结果与衰老过程中MPO蛋白水平的变化一致。此外,我们能够检测到作为MPO氧化稳定终产物的二酪氨酸。二酪氨酸的量在老年AL组大鼠中增加,但在老年CR组大鼠中未增加。为了研究衰老过程中MPO活性增加导致白细胞募集和浸润的来源,我们测量了血管细胞粘附分子(VCAM-1)蛋白的水平。VCAM-1的水平在AL组大鼠中随年龄增长而增加,这与老年AL组大鼠中较高的MPO活性相关。此外,我们发现脂多糖诱导的炎症增加了年轻大鼠肾脏中MPO的活性和蛋白水平以及VCAM-1的表达。这些发现表明,衰老过程中MPO活性增加可能与炎症细胞募集增加有关,导致衰老过程中蛋白质氧化积累。我们认为,CR通过其抗炎作用调节了与年龄相关的MPO、二酪氨酸和VCAM的变化。