Recent advances in arginine metabolism

被引:88
作者
Morris, SM [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
关键词
arginase; nitric oxide; ornithine; polyamines; agmatine;
D O I
10.1097/00075197-200401000-00009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Arginine metabolism has been a topic of intense interest over the past 15-20 years, primarily with regard to the role of arginine as the nitrogen donor for nitric oxide synthesis. However, other important aspects of arginine metabolism, such as arginine transport and arginine catabolism via the arginases, arginine decarboxylase or agmatinase, have been less well studied. The purpose of this review is to highlight recent studies on the urea cycle, agmatine metabolism, and the arginases. Recent findings Recent advances include the cloning of complementary DNA encoding agmatinase, N-acetylglutamate synthetase, and proteins involved in mitochondrial arginine transport, as well as initial investigations of their regulation and tissue-specific expression. The most exciting results of studies in this area over the past year or so have indicated new roles for the arginases in health and disease, as a result of their effects on the synthesis of nitric oxide, proline, or polyamines, or on the expression of specific genes by their ability to limit the availability of free arginine. Summary Recent studies have led to refinements in our understanding of the urea cycle. Agmatine metabolism is still largely a mystery, although the isolation of cloned cDNA for agmatinase and possibly also arginine decarboxylase should stimulate much needed investigations in this area. The most exciting findings in the field are coming from studies indicating new roles for the arginases in various diseases.
引用
收藏
页码:45 / 51
页数:7
相关论文
共 46 条
[1]   Nitric oxide synthases: structure, function and inhibition [J].
Alderton, WK ;
Cooper, CE ;
Knowles, RG .
BIOCHEMICAL JOURNAL, 2001, 357 (03) :593-615
[2]   Arginine availability, arginase, and the immune response [J].
Bansal, V ;
Ochoa, JB .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2003, 6 (02) :223-228
[3]   Expression of three mitochondrial solute carriers, citrin, aralarl and ornithine transporter, in relation to urea cycle in mice [J].
Begum, L ;
Jalil, MA ;
Kobayashi, K ;
Iijima, M ;
Li, MX ;
Yasuda, T ;
Horiuchi, M ;
del Arco, A ;
Satrústegui, J ;
Saheki, T .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2002, 1574 (03) :283-292
[4]  
Blantz RC, 2000, ACTA PHYSIOL SCAND, V168, P21
[5]   The clinical pharmacology of L-arginine [J].
Böger, RH ;
Bode-Böger, SM .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2001, 41 :79-99
[6]   IL-4-induced arginase 1 suppresses alloreactive T cells in tumor-bearing mice [J].
Bronte, V ;
Serafini, P ;
De Santo, C ;
Marigo, I ;
Tosello, V ;
Mazzoni, A ;
Segal, DM ;
Staib, C ;
Lowel, M ;
Sutter, G ;
Colombo, MP ;
Zanovello, P .
JOURNAL OF IMMUNOLOGY, 2003, 170 (01) :270-278
[7]   L-arginine metabolism in myeloid cells controls T-lymphocyte functions [J].
Bronte, V ;
Serafini, P ;
Mazzoni, A ;
Segal, DM ;
Zanovello, P .
TRENDS IN IMMUNOLOGY, 2003, 24 (06) :302-306
[8]  
Brusilow S., 2001, The Metabolic Molecular Bases of Inherited Disease, V8th ed., P1909
[9]   Transport and metabolism of agmatine in rat hepatocyte cultures [J].
Cabella, C ;
Gardini, G ;
Corpillo, D ;
Testore, G ;
Bedino, S ;
Solinas, SP ;
Cravanzola, C ;
Vargiu, C ;
Grillo, MA ;
Colombatto, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (04) :940-947
[10]   Arginase I and Polyamines act downstream from cyclic AMP in overcoming inhibition of axonal growth MAG and myelin in vitro [J].
Cai, DM ;
Deng, KW ;
Mellado, W ;
Lee, J ;
Ratan, RR ;
Filbin, MT .
NEURON, 2002, 35 (04) :711-719