Determination of the flux control coefficient of nitric oxide synthase for nitric oxide synthesis in discrete brain regions in vivo

被引:5
作者
Salter, M
机构
[1] Lead Discovery Unit, Glaxo Wellcome Res. and Development, Medicines Research Centre, Stevenage, Hertfordshire SG1 2NY, Gunnels Wood Road
[2] Wellcome Research Laboratories, Beckenham, Kent BR3 3BS, Langley Court
关键词
D O I
10.1006/jtbi.1996.0185
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The flux control coefficient of nitric oxide synthase (NOS), for the in vivo synthesis of the key biological mediator nitric oxide (NO), was determined in four rat brain regions with varying NOS activities (cerebral cortex, hippocampus, amygdala and cerebellum) using metabolic control theory. Flux control coefficients were calculated from the ratio of the initial slopes of the fractional effect of the NOS inhibitor N-omega-nitro-L-arginine (L-NA) on NO pathway flux and NOS activity. Under conditions of normal behaviour in the rat, NOS had a flux control coefficient not significantly different from one in all regions examined. These data demonstrate that the large majority of flux control for the synthesis of NO in the brain resides in NOS itself and not in the transport of its amino acid precursor, L-arginine, across the blood-brain or neuronal cell membranes. This paper describes the first example in which the control of metabolic flux has been quantified in a mammalian system in vivo and demonstrates the power of metabolic control theory to elucidate the distribution of control within a metabolic pathway in vivo. (C) 1996 Academic Press Limited.
引用
收藏
页码:449 / 452
页数:4
相关论文
共 27 条
[11]  
Kacser H, 1973, Symp Soc Exp Biol, V27, P65
[12]   NITRIC-OXIDE SYNTHASES IN MAMMALS [J].
KNOWLES, RG ;
MONCADA, S .
BIOCHEMICAL JOURNAL, 1994, 298 :249-258
[13]   BLOCKADE OF TOLERANCE TO MORPHINE BUT NOT TO KAPPA-OPIOIDS BY A NITRIC-OXIDE SYNTHASE INHIBITOR [J].
KOLESNIKOV, YA ;
PICK, CG ;
CISZEWSKA, G ;
PASTERNAK, GW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :5162-5166
[14]   LONG-TERM SYNAPTIC DEPRESSION IN THE MAMMALIAN BRAIN [J].
LINDEN, DJ .
NEURON, 1994, 12 (03) :457-472
[15]   A QUANTITATIVE-ANALYSIS OF THE CONTROL OF GLUTAMINE CATABOLISM IN RAT-LIVER CELLS - USE OF SELECTIVE INHIBITORS [J].
LOW, SY ;
SALTER, M ;
KNOWLES, RG ;
POGSON, CI ;
RENNIE, MJ .
BIOCHEMICAL JOURNAL, 1993, 295 :617-624
[16]   NITRIC-OXIDE (NO) AND NOCICEPTIVE PROCESSING IN THE SPINAL-CORD [J].
MELLER, ST ;
GEBHART, GF .
PAIN, 1993, 52 (02) :127-136
[17]  
MIDDLETON RJ, 1983, GENETICS, V105, P633
[18]  
MONCADA S, 1993, NEW ENGL J MED, V329, P2002
[19]   NITRIC-OXIDE MEDIATES NEURONAL DEATH AFTER FOCAL CEREBRAL-ISCHEMIA IN THE MOUSE [J].
NOWICKI, JP ;
DUVAL, D ;
POIGNET, H ;
SCATTON, B .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1991, 204 (03) :339-340
[20]   DETERMINATION OF BRAIN NITRIC-OXIDE SYNTHASE INHIBITION IN-VIVO - EX-VIVO ASSAYS OF NITRIC-OXIDE SYNTHASE CAN GIVE INCORRECT RESULTS [J].
SALTER, M ;
DUFFY, C ;
HAZELWOOD, R .
NEUROPHARMACOLOGY, 1995, 34 (03) :327-334