Age-Associated Changes in Ca2+-ATPase and Oxidative Damage in Sarcoplasmic Reticulum of Rat Heart

被引：34

作者：

Babusikova, E. ^{[1
]}

Lehotsky, J. ^{[1
]}

Dobrota, D. ^{[1
]}

Racay, P. ^{[1
]}

Kaplan, P. ^{[1
]}

机构：

[1] Comenius Univ, Jessenius Fac Med, Dept Med Biochem, Mala Hora 4, SK-03601 Martin, Slovakia

来源：

PHYSIOLOGICAL RESEARCH | 2012年 / 61卷 / 05期

关键词：

Aging; Ca2+-ATPase; Protein damage; Heart; Oxidative stress; PROTEIN MODIFICATION; DIASTOLIC FUNCTION; GENE-TRANSFER; AGING HEART; IN-VIVO; SERCA2A; STRESS; MODULATION; MOUSE;

D O I：

10.33549/physiolres.932320

中图分类号：

Q4 [生理学];

学科分类号：

071003 [生理学];

摘要：

Altered Ca2+ handling may be responsible for the development of cardiac contractile dysfunctions with advanced age. In the present study, we investigated the roles of oxidative damage to sarcoplasmic reticulum (SR) and expression of Ca2+-ATPase (SERCA 2a) and phospholamban in age-associated dysfunction of cardiac SR. SR vesicles were prepared from hearts of 2-, 6-, 15-, and 26-month-old wistar rats. Although activity of Ca2+-ATPase decreased with advancing age, no differences in relative amounts of SERCA 2a and phospholamban protein were observed. On the other hand, significant accumulation of protein oxidative damage occurred with aging. The results of this study suggest that age-related alteration in Ca2+-ATPase activity in the rat heart is not a consequence of decreased protein levels of SERCA 2a and phospholamban, but could arise from oxidative modifications of SR proteins. Cellular oxidative damage caused by reactive oxygen species could contribute to age-related alternations in myocardial relaxation.

引用

页码：453 / 460

页数：8

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