Cardiolipin Remodeling in the Heart

被引:98
作者
Sparagna, Genevieve C. [1 ]
Lesnefsky, Edward J. [2 ,3 ,4 ,5 ,6 ]
机构
[1] Univ Colorado, Cardiovasc Inst, Dept Integrat Physiol, Boulder, CO 80309 USA
[2] Case Western Reserve Univ, Dept Med, Cleveland, OH 44106 USA
[3] Vet Affairs Med Ctr, Louis Stokes Cleveland Dept Vet, Med Serv, Richmond, VA 23249 USA
[4] Virginia Commonwealth Univ, Dept Med, Richmond, VA 23298 USA
[5] Virginia Commonwealth Univ, Dept Biochem, Richmond, VA USA
[6] Vet Affairs Med Ctr, McGuire Dept, Med Serv, Richmond, VA 23249 USA
基金
美国国家卫生研究院;
关键词
apoptosis; Barth syndrome; congestive heart failure; diabetes; electron transport chain; ischemia; linoleic acid; mitochondria; CYTOCHROME-C-OXIDASE; FATTY-ACID-COMPOSITION; ACYLCARNITINE TRANSLOCASE ACTIVITY; MITOCHONDRIAL COMPLEX-I; RAT-HEART; MYOCARDIAL-ISCHEMIA; PEROXIDASE-ACTIVITY; ELECTRON-TRANSPORT; OXIDATIVE-PHOSPHORYLATION; CARDIAC MITOCHONDRIA;
D O I
10.1097/FJC.0b013e31819b5461
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiolipin (CL) is a mitochondrial phospholipid that fundamentally contributes to the function of many proteins in the inner mitochondrial membrane, where it is actively involved in the integrity and flux of the electron transport chain. In the heart, functional CL is linoleic acid rich, and the loss of linoleic acid content is associated with cardiac disorders including ischemia and reperfusion, heart failure, and diabetes, as well as the X-linked recessive disease, Barth syndrome. To attain its high levels of linoleic acid, newly synthesized CL must initially undergo remodeling. CL modification and depletion by pathological processes may represent a failure of this remodeling pathway or activation of an alternative "pathological remodeling" pathway that causes the substitution of higher molecular weight, polyunsaturated fatty acyl side chains such as arachidonic or docosahexaenoic acid onto CL. This remodeling may occur in response to the alteration of CL by oxidative mechanisms, but the substituted side chains can also provoke further oxidation of CL. It is increasingly thought that cardiac pathology may result, at least partially, due to changes in CL resulting from the pathological remodeling process. Dietary interventions may restore CL to its linoleic acid-rich form and improve cardiac function by redirecting the remodeling process.
引用
收藏
页码:290 / 301
页数:12
相关论文
共 161 条
[91]   AN ESSENTIAL REQUIREMENT OF CARDIOLIPIN FOR MITOCHONDRIAL CARNITINE ACYLCARNITINE TRANSLOCASE ACTIVITY - LIPID REQUIREMENT OF CARNITINE ACYLCARNITINE TRANSLOCASE [J].
NOEL, H ;
PANDE, V .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 155 (01) :99-102
[92]   Cardiolipin synthase of Arabidopsis thaliana [J].
Nowicki, M ;
Müller, F ;
Frentzen, M .
FEBS LETTERS, 2005, 579 (10) :2161-2165
[93]  
OROURKE B, 1992, P SOC EXP BIOL MED, V200, P95
[94]   Cytochrome c release from mitochondria proceeds by a two-step process [J].
Ott, M ;
Robertson, JD ;
Gogvadze, V ;
Zhivotovsky, B ;
Orrenius, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1259-1263
[95]  
PALMER JW, 1977, J BIOL CHEM, V252, P8731
[96]  
PANGBORN MC, 1948, J PAT OFF SOC, P108
[97]   AGE-DEPENDENT DECREASE IN THE CYTOCHROME-C-OXIDASE ACTIVITY AND CHANGES IN PHOSPHOLIPIDS IN RAT-HEART MITOCHONDRIA [J].
PARADIES, G ;
RUGGIERO, FM ;
PETROSILLO, G ;
QUAGLIARIELLO, E .
ARCHIVES OF GERONTOLOGY AND GERIATRICS, 1993, 16 (03) :263-272
[98]   The effect of aging and acetyl-L-carnitine on the pyruvate transport and oxidation in rat heart mitochondria [J].
Paradies, G ;
Petrosillo, G ;
Gadaleta, MN ;
Ruggiero, FM .
FEBS LETTERS, 1999, 454 (03) :207-209
[99]   Alterations in carnitine-acylcarnitine translocase activity and in phospholipid composition in heart mitochondria from hypothyroid rats [J].
Paradies, G ;
Ruggiero, FM ;
Petrosillo, G ;
Quagliariello, E .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1997, 1362 (2-3) :193-200
[100]   Lipid peroxidation and alterations to oxidative metabolism in mitochondria isolated from rat heart subjected to ischemia and reperfusion [J].
Paradies, G ;
Petrosillo, G ;
Pistolese, M ;
Di Venosa, N ;
Serena, D ;
Ruggiero, FM .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (1-2) :42-50