Therapeutic use of citrulline in cardiovascular disease

被引:167
作者
Romero, Maritza J.
Platt, Daniel H.
Caldwell, Ruth B.
Caldwell, R. William
机构
[1] Med Coll Georgia, Dept Pharmacol & Toxicol, Augusta, GA 30912 USA
[2] Med Coll Georgia, Dept Cell Biol & Anat, Augusta, GA 30912 USA
[3] Med Coll Georgia, Vasc Biol Ctr, Augusta, GA 30912 USA
来源
CARDIOVASCULAR DRUG REVIEWS | 2006年 / 24卷 / 3-4期
关键词
arginase; arginine; citrulline; nitric oxide synthase; NO; oxidative stress; vascular endothelial dysfunction;
D O I
10.1111/j.1527-3466.2006.00275.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
L-citrulline is the natural precursor of L-arginine, substrate for nitric oxide synthase (NOS) in the production of NO. Supplemental administration L-arginine has been shown to be effective in improving NO production and cardiovascular function in cardiovascular diseases associated with endothelial dysfunction, such as hypertension, heart failure, atherosclerosis, diabetic vascular disease and ischemia-reperfusion injury, but the beneficial actions do not endure with chronic therapy. Substantial intestinal and hepatic metabolism of L-arginine to ornithine and urea by arginase makes oral delivery very ineffective. Additionally, all of these disease states as well as supplemental L-arginine enhance arginase expression and activity, thus reducing the effectiveness of L-arginine therapy. In contrast, L-citrulline is not metabolized in the intestine or liver and does not induce tissue arginase, but rather inhibits its activity. L-citrulline entering the kidney, vascular endothelium and other tissues can be readily converted to L-arginine, thus raising plasma and tissue levels of L-arginine and enhancing NO production. Supplemental L-citrulline has promise as a therapeutic adjunct in disease states associated with L-arginine deficiencies.
引用
收藏
页码:275 / 290
页数:16
相关论文
共 107 条
  • [1] Roles of superoxide, peroxynitrite, and protein kinase C in the development of tolerance to nitroglycerin
    Abou-Mohamed, G
    Johnson, JA
    Jin, L
    El-Remessy, AB
    Do, K
    Kaesemeyer, WH
    Caldwell, RB
    Caldwell, RW
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 308 (01) : 289 - 299
  • [2] Protein deimination in the rat brain after kainate administration: citrulline-containing proteins as a novel marker of neurodegeneration
    Asaga, H
    Ishigami, A
    [J]. NEUROSCIENCE LETTERS, 2001, 299 (1-2) : 5 - 8
  • [3] DISCRIMINATION BETWEEN CITRULLINE AND ARGININE TRANSPORT IN ACTIVATED MURINE MACROPHAGES - INEFFICIENT SYNTHESIS OF NO FROM RECYCLING OF CITRULLINE TO ARGININE
    BAYDOUN, AR
    BOGLE, RG
    PEARSON, JD
    MANN, GE
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1994, 112 (02) : 487 - 492
  • [4] Arginase reciprocally regulates nitric oxide synthase activity and contributes to endothelial dysfunction in aging blood vessels
    Berkowitz, DE
    White, R
    Li, DC
    Minhas, KM
    Cernetich, A
    Kim, S
    Burke, S
    Shoukas, AA
    Nyhan, D
    Champion, HC
    Hare, JM
    [J]. CIRCULATION, 2003, 108 (16) : 2000 - 2006
  • [5] Increased expression of arginase II in human diabetic corpus cavernosum: In diabetic-associated erectile dysfunction
    Bivalacqua, TJ
    Hellstrom, WJG
    Kadowitz, PJ
    Champion, HC
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 283 (04) : 923 - 927
  • [6] Intestinal renal metabolism of L-citrulline and L-arginine following enteral or parenteral infusion of L-alanyl-L-[2,15N] glutamine or L-[2,15N] glutamine in mice
    Boelens, PG
    van Leeuwen, PAM
    Dejong, CHC
    Deutz, NEP
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2005, 289 (04): : G679 - G685
  • [7] Interorgan amino acid transport and its regulation
    Brosnan, JT
    [J]. JOURNAL OF NUTRITION, 2003, 133 (06) : 2068S - 2072S
  • [8] Renal arginine metabolism
    Brosnan, ME
    Brosnan, JT
    [J]. JOURNAL OF NUTRITION, 2004, 134 (10) : 2791S - 2795S
  • [9] L-ARGININE ABROGATES SALT-SENSITIVE HYPERTENSION IN DAHL RAPP RATS
    CHEN, PY
    SANDERS, PW
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (05) : 1559 - 1567
  • [10] Arginase inhibition increases nitric oxide production in bovine pulmonary arterial endothelial cells
    Chicoine, LG
    Paffett, ML
    Young, TL
    Nelin, LD
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2004, 287 (01) : L60 - L68