L-citruiline and L-arginine supplementation retards the progression of high-cholesterol-diet-induced atherosclerosis in rabbits

被引:105
作者
Hayashi, T
Juliet, PAR
Matsui-Hirai, H
Miyazaki, A
Fukatsu, A
Funami, J
Iguchi, A
Ignarro, LJ
机构
[1] Nagoya Univ, Grad Sch Med, Dept Geriatr, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
关键词
antioxiclant; nitric oxide; amino acids; endothelial nitric oxide synthase;
D O I
10.1073/pnas.0506595102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The objective of this study was to evaluate the influence of ingested L-arginine, L-Citrulline, and antioxidants (vitamins C and E) on the progression of atherosclerosis in rabbits fed a high-cholesterol diet. The fatty diet caused a marked impairment of endothelium-dependent vasorelaxation in isolated thoracic aorta and blood flow in rabbit ear artery in vivo, the development of atheromatous lesions and increased superoxide anion production in thoracic aorta, and increased oxidation-sensitive gene expression [Elk-1 and phosphorylated cAMP response element-binding protein]. Rabbits were treated orally for 12 weeks with L-arginine, L-Citrulline, and/or antioxiclants. L-arginine Plus L-Citrulline, either alone or in combination with antioxidants, caused a marked improvement in enclothelium-clepenclent vasorelaxation and blood flow, dramatic regression in atheromatous lesions, and decrease in superoxide production and oxidation-sensitive gene expression. These therapeutic effects were associated with concomitant increases in aortic endothelial NO synthase expression and plasma NO2- + NO3- and cGMP levels. These observations indicate that ingestion of certain NO-boosting substances, including L-arginine, L-Citrulline, and antioxiclants, can abrogate the state of oxidative stress and reverse the progression of atherosclerosis. This approach may have clinical utility in the treatment of atherosclerosis in humans.
引用
收藏
页码:13681 / 13686
页数:6
相关论文
共 53 条
[1]  
ALLAIN CC, 1974, CLIN CHEM, V20, P470
[2]   Elevated L-arginine/dimethylarginine ratio contributes to enhanced systemic NO production by dietary L-arginine in hypercholesterolemic rabbits [J].
BodeBoger, SM ;
Boger, RH ;
Kienke, S ;
Junker, W ;
Frolich, JC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 219 (02) :598-603
[3]   L-arginine induces nitric oxide-dependent vasodilation in patients with critical limb ischemia - A randomized, controlled study [J].
BodeBoger, SM ;
Boger, RH ;
Alfke, H ;
Heinzel, D ;
Tsikas, D ;
Creutzig, A ;
Alexander, K ;
Frolich, JC .
CIRCULATION, 1996, 93 (01) :85-90
[4]   Asymmetric dimethylarginine (ADMA):: A novel risk factor for endothelial dysfunction -: Its role in hypercholesterolemia [J].
Böger, RH ;
Bode-Böger, SM ;
Szuba, A ;
Tsao, PS ;
Chan, JR ;
Tangphao, O ;
Blaschke, TF ;
Cooke, JP .
CIRCULATION, 1998, 98 (18) :1842-1847
[5]   Dietary L-arginine decreases myointimal cell proliferation and vascular monocyte accumulation in cholesterol-fed rabbits [J].
Böger, RH ;
Bode-Böger, SM ;
Kienke, S ;
Stan, AC ;
Nafe, R ;
Frölich, JC .
ATHEROSCLEROSIS, 1998, 136 (01) :67-77
[6]  
BOGER RH, 1995, ATHEROSCLEROSIS, V117, P273, DOI 10.1016/0021-9150(95)05582-H
[7]   Asymmetric dimethylarginine, derangements of the endothelial nitric oxide synthase pathway, and cardiovascular diseases [J].
Böger, RH ;
Bode-Böger, SM .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2000, 26 (05) :539-545
[8]   Dietary L-arginine and α-tocopherol reduce vascular oxidative stress and preserve endothelial function in hypercholesterolemic rabbits via different mechanisms [J].
Böger, RH ;
Böde-Boger, SM ;
Phivthong-ngam, L ;
Brandes, RP ;
Schwedhelm, E ;
Mügge, A ;
Böhme, M ;
Tsikas, D ;
Frölich, JC .
ATHEROSCLEROSIS, 1998, 141 (01) :31-43
[9]   Dietary L-arginine reduces the progression of atherosclerosis in cholesterol-fed rabbits - Comparison with lovastatin [J].
Boger, RH ;
BodeBoger, SM ;
Brandes, RP ;
Phivthongngam, L ;
Bohme, M ;
Nafe, R ;
Mugge, A ;
Frolich, JC .
CIRCULATION, 1997, 96 (04) :1282-1290
[10]   The clinical pharmacology of L-arginine [J].
Böger, RH ;
Bode-Böger, SM .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2001, 41 :79-99