Enhancement of lactate metabolism in the basolateral amygdala by physical and psychological stress: Role of benzodiazepine receptors

Brain Research

Volumn 1065, Issue 1-2, 2005, Pages 86-91

  Uehara, Takashi ^a   Sumiyoshi, Tomiki ^a   Matsuoka, Tadasu ^a   Tanaka, Kodai ^a   Tsunoda, Masahiko ^a   Itoh, Hiroko ^a   Kurachi, Masayoshi ^a  

^a UNIVERSITY OF TOYAMA   (Japan)

Author keywords

Anxiety; Basolateral amygdaloid nucleus; Benzodiazepine receptor; Brain energy metabolism; Footshock stress; Lactate; Panic disorder; Psychological stress

Indexed keywords

BENZODIAZEPINE RECEPTOR; BENZODIAZEPINE RECEPTOR STIMULATING AGENT; DIAZEPAM; LACTIC ACID; N METHYL BETA CARBOLINE 3 CARBOXAMIDE;

AMYGDALOID NUCLEUS; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN FUNCTION; ELECTRIC SHOCK; ENERGY METABOLISM; LACTATE BLOOD LEVEL; MALE; MENTAL STRESS; MICRODIALYSIS; NONHUMAN; PRIORITY JOURNAL; RAT;

AMYGDALA; ANIMALS; CARBOLINES; DIAZEPAM; ELECTROSHOCK; ENERGY METABOLISM; EXTRACELLULAR SPACE; GABA AGONISTS; GABA ANTAGONISTS; GABA MODULATORS; LACTIC ACID; MALE; MICRODIALYSIS; RATS; RATS, WISTAR; RECEPTORS, GABA-A; STRESS; STRESS, PSYCHOLOGICAL;

ANIMALIA;

EID: 28844486973     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2005.10.035     Document Type: Article

References (49)

1. A. Ableitner, and A. Herz Changes in local cerebral glucose utilization induced by the beta-carbolines FG 7142 and DMCM reveal brain structures involved in the control of anxiety and seizure activity J. Neurosci. 7 1987 1047 1055
2. J. Amat, P. Matus-Amat, L.R. Watkins, and S.F. Maier Escapable and inescapable stress differentially alter extracellular levels of 5-HT in the basolateral amygdala of the rat Brain Res. 812 1998 113 120
3. D.D. Clarke, and L. Sokoloff Circulation and energy metabolism of the brain G. Siegel B.W. Agranoff R.W. Albers S.K. Fisher M.D. Uhler Basic Neurochemistry: Molecular, Cellular and Medical Aspect 6th edition 1999 Lippincott-Raven New York 637 670
4. M. Davis, D. Rainnie, and M. Cassell Neurotransmission in the rat amygdala related to fear and anxiety Trends Neurosci. 17 1994 208 214
5. L.A. De Bruin, E.M. Schasfoort, A.B. Steffens, and J. Korf Effects of stress and exercise on rat hippocampus and striatum extracellular lactate Am. J. Physiol. 259 1990 R773 R779
6. O. Elekes, K. Venema, F. Postema, R. Dringen, B. Hamprecht, and J. Korf Evidence that stress activates glial lactate formation in vivo assessed with rat hippocampus lactography Neurosci. Lett. 208 1996 69 72
7. L.K. Fellows, M.G. Boutelle, and M. Fillenz Physiological stimulation increases nonoxidative glucose metabolism in the brain of the freely moving rat J. Neurochem. 60 1993 1258 1263
8. J.M. Fritschy, and H. Mohler GABAA-receptor heterogeneity in the adult rat brain: differential regional and cellular distribution of seven major subunits J. Comp. Neurol. 359 1995 154 194
9. Y. Hu, and G.S. Wilson A temporary local energy pool coupled to neuronal activity: fluctuations of extracellular lactate levels in rat brain monitored with rapid-response enzyme-based sensor J. Neurochem. 69 1997 1484 1490
10. F.M. Inglis, and B. Moghaddam Dopaminergic innervation of the amygdala is highly responsive to stress J. Neurochem. 72 1999 1088 1094
11. M. Ishikawa, C. Hara, S. Ohdo, and N. Ogawa Plasma corticosterone response of rats with sociopsychological stress in the communication box Physiol. Behav. 52 1992 475 480
12. Y. Izumi, A.M. Benz, H. Katsuki, and C.F. Zorumski Endogenous monocarboxylates sustain hippocampal synaptic function and morphological integrity during energy deprivation J. Neurosci. 17 1997 9448 9457
13. H. Kaneyuki, H. Yokoo, A. Tsuda, M. Yoshida, Y. Mizuki, M. Yamada, and M. Tanaka Psychological stress increases dopamine turnover selectively in mesoprefrontal dopamine neurons of rats: reversal by diazepam Brain Res. 557 1991 154 161
14. H. Kawahara, M. Yoshida, H. Yokoo, M. Nishi, and M. Tanaka Psychological stress increases serotonin release in the rat amygdala and prefrontal cortex assessed by in vivo microdialysis Neurosci. Lett. 162 1993 81 84
15. J. Korf, and J. de Boer Lactography as an approach to monitor glucose metabolism on-line in brain and muscle Int. J. Biochem. 22 1990 1371 1378
16. H.J. Krugers, D. Jaarsma, and J. Korf Rat hippocampal lactate efflux during electroconvulsive shock or stress is differently dependent on entorhinal cortex and adrenal integrity J. Neurochem. 58 1992 826 830
17. W.G. Kuhr, and J. Korf Extracellular lactic acid as an indicator of brain metabolism: continuous on-line measurement in conscious, freely moving rats with intrastriatal dialysis J. Cereb. Blood Flow Metab. 8 1988 130 137
18. W.G. Kuhr, C.J. van den Berg, and J. Korf In vivo identification and quantitative evaluation of carrier-mediated transport of lactate at the cellular level in the striatum of conscious, freely moving rats J. Cereb. Blood Flow Metab. 8 1988 848 856
19. M.G. Larrabee Lactate uptake and release in the presence of glucose by sympathetic ganglia of chicken embryos and by neuronal and nonneuronal cultures prepared from these ganglia J. Neurochem. 40 1983 1237 1250
20. M.G. Larrabee Extracellular intermediates of glucose metabolism: fluxes of endogenous lactate and alanine through extracellular pools in embryonic sympathetic ganglia J. Neurochem. 59 1992 1041 1052
21. M.G. Larrabee Lactate metabolism and its effects on glucose metabolism in an excised neural tissue J. Neurochem. 64 1995 1734 1741
22. J.E. LeDoux, M.E. Thompson, C. Iadecola, L.W. Tucker, and D.J. Reis Local cerebral blood flow increases during auditory and emotional processing in the conscious rat Science 221 1983 576 578
23. J.E. LeDoux, P. Cicchetti, A. Xagoraris, and L.M. Romanski The lateral amygdaloid nucleus: sensory interface of the amygdala in fear conditioning J. Neurosci. 10 1990 1062 1069
24. K. Low, F. Crestani, R. Keist, D. Benke, I. Brunig, J.A. Benson, J.M. Fritschy, T. Rulicke, H. Bluethmann, H. Mohler, and U. Rudolph Molecular and neuronal substrate for the selective attenuation of anxiety Science 290 2000 131 134
25. C.K. McIntyre, L.K. Marriott, and P.E. Gold Cooperation between memory systems: acetylcholine release in the amygdala correlates positively with performance on a hippocampus-dependent task Behav. Neurosci. 117 2003 320 326
26. J. Nagy, K. Zambo, and L. Decsi Anti-anxiety action of diazepam after intra-amygdaloid application in the rat Neuropharmacology 18 1979 573 576
27. T. Narahashi Chemicals as tools in the study of excitable membranes Physiol. Rev. 54 1974 813 889
28. D.L. Niehoff, and M.J. Kuhar Benzodiazepine receptors: localization in rat amygdala J. Neurosci. 3 1983 2091 2097
29. G. Paxinos, and C. Watson The Rat Brain in Stereotaxic Coordinates 1998 Academic Press Sydney
30. L. Pellerin Lactate as a pivotal element in neuron-glia metabolic cooperation Neurochem. Int. 43 2003 331 338
31. L. Pellerin, and P.J. Magistretti Glutamate uptake into astrocytes stimulates aerobic glycolysis: a mechanism coupling neuronal activity to glucose utilization Proc. Natl. Acad. Sci. U. S. A. 91 1994 10625 10629
32. L. Pellerin, G. Pellegri, P.G. Bittar, Y. Charnay, C. Bouras, J.L. Martin, N. Stella, and P.J. Magistretti Evidence supporting the existence of an activity-dependent astrocyte-neuron lactate shuttle Dev. Neurosci. 20 1998 291 299
33. J. Prichard, D. Rothman, E. Novotny, O. Petroff, T. Kuwabara, M. Avison, A. Howseman, C. Hanstock, and R. Shulman Lactate rise detected by 1H NMR in human visual cortex during physiologic stimulation Proc. Natl. Acad. Sci. U. S. A. 88 1991 5829 5831
34. G.L. Quirarte, R. Galvez, B. Roozendaal, and J.L. McGaugh Norepinephrine release in the amygdala in response to footshock and opioid peptidergic drugs Brain Res. 808 1998 134 140
35. U. Rudolph, F. Crestani, and H. Mohler GABA(A) receptor subtypes: dissecting their pharmacological functions Trends Pharmacol. Sci. 22 2001 188 194
36. Y. Sakurai-Yamashita, K. Yamashita, M. Niwa, and K. Taniyama Involvement of 5-hydroxytryptamine4 receptor in the exacerbation of neuronal loss by psychological stress in the hippocampus of SHRSP with a transient ischemia Brain Res. 973 2003 92 98
37. E.M. Schasfoort, L.A. De Bruin, and J. Korf Mild stress stimulates rat hippocampal glucose utilization transiently via NMDA receptors, as assessed by lactography Brain Res. 475 1988 58 63
38. A. Schurr, C.A. West, and B.M. Rigor Lactate-supported synaptic function in the rat hippocampal slice preparation Science 240 1988 1326 1328
39. A. Schurr, R.S. Payne, J.J. Miller, and B.M. Rigor Brain lactate, not glucose, fuels the recovery of synaptic function from hypoxia upon reoxygenation: an in vitro study Brain Res. 744 1997 105 111
40. M. Takita, M. Mikuni, and K. Takahashi Habituation of lactate release responding to stressful stimuli in rat prefrontal cortex in vivo Am. J. Physiol. 263 1992 R722 R727
41. T. Tanaka, H. Yokoo, K. Mizoguchi, M. Yoshida, A. Tsuda, and M. Tanaka Noradrenaline release in the rat amygdala is increased by stress: studies with intracerebral microdialysis Brain Res. 544 1991 174 176
42. M. Tanaka, M. Yoshida, H. Emoto, and H. Ishii Noradrenaline systems in the hypothalamus, amygdala and locus coeruleus are involved in the provocation of anxiety: basic studies Eur. J. Pharmacol. 405 2000 397 406
43. D. Treit, C. Pesold, and S. Rotzinger Dissociating the anti-fear effects of septal and amygdaloid lesions using two pharmacologically validated models of rat anxiety Behav. Neurosci. 107 1993 770 785
44. M. Tsacopoulos, and P.J. Magistretti Metabolic coupling between glia and neurons J. Neurosci. 16 1996 877 885
45. T. Uehara, K. Kurata, T. Sumiyoshi, and M. Kurachi Immobilization stress-induced increment of lactate metabolism in the basolateral amygdaloid nucleus is attenuated by diazepam in the rat Eur. J. Pharmacol. 459 2003 211 215
46. T. Uehara, T. Sumiyoshi, H. Itoh, and M. Kurachi Modulation of stress-induced dopamine release by excitotoxic damage of the entorhinal cortex in the rat Brain Res. 989 2003 112 116
47. C.L. Williams, D. Men, and E.C. Clayton The effects of noradrenergic activation of the nucleus tractus solitarius on memory and in potentiating norepinephrine release in the amygdala Behav. Neurosci. 114 2000 1131 1144
48. Y.L. Wu, M. Yoshida, H. Emoto, and M. Tanaka Psychological stress selectively increases extracellular dopamine in the 'shell', but not in the 'core' of the rat nucleus accumbens: a novel dual-needle probe simultaneous microdialysis study Neurosci. Lett. 275 1999 69 72
49. A.M. Young, and K.R. Rees Dopamine release in the amygdaloid complex of the rat, studied by brain microdialysis Neurosci. Lett. 249 1998 49 52