Reduction of Alamar Blue, a novel redox indicator, is dependent on both the glycolytic and oxidative metabolism of glucose in rat cultured neurons

被引:26
作者
Abe, T [1 ]
Takahashi, S
Fukuuchi, Y
机构
[1] Keio Univ, Sch Med, Dept Neurol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, Japan
[2] Saitama Municipal Hosp, Dept Neurol, Saitama 3368522, Japan
关键词
astrocyte; brain energy metabolism; glycolysis; lactate; pyruvate; tricarboxylic acid cycle;
D O I
10.1016/S0304-3940(02)00347-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recently, it has been hypothesized that neurons mainly utilize lactate produced by astrocytes to generate energy (i.e. ATP). Regardless of numerous studies, whether lactate rather than glucose fuels neurons in vivo remains a matter of controversy. In the present study we have examined the substrate-preference of the reduction of Alamar Blue, a novel redox indicator, by cultured rat astroglia and neurons. Alamar Blue reduction is dependent on cellular reducing equivalents. Therefore, the substrate-preference of Alamar Blue reduction could reflect that for cellular energy production. Rates of Alamar Blue reduction by 2 mM glucose were two-fold higher in astroglia than those in neurons. Alamar Blue reduction induced by 2 mM lactate was 78% of that by 2 mM glucose in neurons while only 20% in astroglia. Nevertheless, glucose elicited larger Alamar Blue reduction than lactate both in astroglia and neurons. These results indicate that neuronal energy production in vivo depends on both the glycolytic and oxidative metabolism of glucose even though astroglia rely on glycolysis as has been reported. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:179 / 182
页数:4
相关论文
共 21 条
[1]  
ABE T, 2001, SOC NEUR ABSTR, V27
[2]   Selective distribution of lactate dehydrogenase isoenzymes in neurons and astrocytes of human brain [J].
Bittar, PG ;
Charnay, Y ;
Pellerin, L ;
Bouras, C ;
Magistretti, PJ .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (06) :1079-1089
[3]   Do active cerebral neurons really use lactate rather than glucose? [J].
Chih, CP ;
Lipton, P ;
Roberts, EL .
TRENDS IN NEUROSCIENCES, 2001, 24 (10) :573-578
[4]  
Clarke Donald D., 1999, P637
[5]  
Coles Jonathan A., 1995, P793
[6]   NONOXIDATIVE GLUCOSE CONSUMPTION DURING FOCAL PHYSIOLOGIC NEURAL ACTIVITY [J].
FOX, PT ;
RAICHLE, ME ;
MINTUN, MA ;
DENCE, C .
SCIENCE, 1988, 241 (4864) :462-464
[7]   FOCAL PHYSIOLOGICAL UNCOUPLING OF CEREBRAL BLOOD-FLOW AND OXIDATIVE-METABOLISM DURING SOMATOSENSORY STIMULATION IN HUMAN-SUBJECTS [J].
FOX, PT ;
RAICHLE, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (04) :1140-1144
[8]   Glycolysis in neurons, not astrocytes, delays oxidative metabolism of human visual cortex during sustained checkerboard stimulation in vivo [J].
Gjedde, A ;
Marrett, S .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2001, 21 (12) :1384-1392
[9]   Evaluation of hepatic subcellular fractions for Alamar blue and MTT reductase activity [J].
Gonzalez, RJ ;
Tarloff, JB .
TOXICOLOGY IN VITRO, 2001, 15 (03) :257-259
[10]   Mechanism of cellular 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reduction [J].
Liu, YB ;
Peterson, DA ;
Kimura, H ;
Schubert, D .
JOURNAL OF NEUROCHEMISTRY, 1997, 69 (02) :581-593