Abstract
In addition to glucose, monocarboxylates including lactate represent a major source of energy for the developing brain and appears to be crucial in the pathogenesis and recovery after brain damage. We hypothesized a role of monocarboxylates transport in the energy supply of neurons of the immature cerebral cortex. The effects of the blockade of monocarboxylates transport in vivo on the cortical development was investigated in neonatal mice using alpha-cyano-4-hydroxycinnamate (CIN) diluted either in DMSO (CD) or in ethanol (CE) administered intraperitoneally over postnatal day (P) P1 to P3. Injection of CIN induced a cytoarchitectonic disorganization in the parietal cortex likely due to a combination of slight disturbance of cortical neuronal migration and an increased neuronal cell death observed in CE (p < 0.05) but not in CD group. An increased number of activated GFAP-positive astroglia was observed in the neocortex in groups treated with CIN (CD and CE) on P10. These data: 1) Provide first evidence of deleterious effects observed in vivo after blockade of monocarboxylates transport in the developing brain; 2) emphasize the role of lactate during neuronal migration as a major source of energy; and 3) suggest the synergistic effect of ethanol-induced hypoglycemia in cortical brain damage induced by CIN.
Similar content being viewed by others
Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
Abbreviations
- CIN:
-
alpha-cyano-4-hydroxycinnamate
- GFAP:
-
glial fibrillary acidic protein
- MAP:
-
microtubule associated protein
- MCT:
-
monocarboxylates transporter
References
Pellerin L, Pellegri G, Martin JL, Magistretti PJ 1998 Expression of monocarboxylate transporter mRNAs in mouse brain: support for a distinct role of lactate as an energy substrate for the neonatal vs. adult brain. Proc Natl Acad Sci USA 95: 3990–3995
Halestrap AP, Price NT 1999 The proton-linked monocarboxylate transporter (MCT) family: structure, function and regulation. Biochem J 343: 281–299
Pellerin L, Magistretti PJ 1994 Glutamate uptake into astrocytes stimulates aerobic glycolysis: a mechanism coupling neuronal activity to glucose utilization. Proc Natl Acad Sci USA 91: 10625–10629
Vannucci RC, Vannucci SJ 2000 Glucose metabolism in the developing brain. Semin Perinatol 24: 107–115
Dringen R, Gebhardt R, Hamprecht B 1993 Glycogen in astrocytes: possible function as lactate supply for neighboring cells. Brain Res 623: 208–214
Izumi Y, Benz AM, Katsuki H, Zorumski CF 1997 Endogenous monocarboxylates sustain hippocampal synaptic function and morphological integrity during energy deprivation. J Neurosci 17: 9448–9457
Schurr A, Miller JJ, Payne RS, Rigor BM 1999 An increase in lactate output by brain tissue serves to meet the energy needs of glutamate-activated neurons. J Neurosci 19: 34–39
Baud O, Fayol L, Gressens P, Pellerin L, Magistretti P, Evrard P, Verney C 2003 Perinatal and early postnatal changes in the expression of monocarboxylate transporters MCT1 and MCT2 in the rat forebrain. J Comp Neurol 465: 445–454
Fayol L, Baud O, Monier A, Pellerin L, Magistretti P, Evrard P, Verney C 2004 Immunocytochemical expression of monocarboxylate transporters in the human visual cortex at midgestation. Brain Res Dev Brain Res 148: 69–76
Schurr A, Payne RS, Miller JJ, Rigor BM 1997 Brain lactate is an obligatory aerobic energy substrate for functional recovery after hypoxia: further in vitro validation. J Neurochem 69: 423–426
Schurr A, Payne RS, Miller JJ, Tseng MT, Rigor BM 2001 Blockade of lactate transport exacerbates delayed neuronal damage in a rat model of cerebral ischemia. Brain Res 895: 268–272
Gadisseux JF, Evrard P 1985 Glial-neuronal relationship in the developing central nervous system. A histochemical-electron microscope study of radial glial cell particulate glycogen in normal and reeler mice and the human fetus. Dev Neurosci 7: 12–32
Gressens P, Lammens M, Picard JJ, Evrard P 1992 Ethanol-induced disturbances of gliogenesis and neuronogenesis in the developing murine brain: an in vitro and in vivo immunohistochemical and ultrastructural study. Alcohol Alcohol 27: 219–226
Ikonomidou C, Bittigau P, Ishimaru MJ, Wozniak DF, Koch C, Genz K, Price MT, Stefovska V, Horster F, Tenkova T, Dikranian K, Olney JW 2000 Ethanol-induced apoptotic neurodegeneration and fetal alcohol syndrome. Science 287: 1056–1060
Olney JW, Tenkova T, Dikranian K, Muglia LJ, Jermakowicz WJ, D'Sa C, Roth KA 2002 Ethanol-induced caspase-3 activation in the in vivo developing mouse brain. Neurobiol Dis 9: 205–219
De Vivo DC, DiMauro S 1990 Mitochondrial defects of brain and muscle. Biol Neonate 58: 54–69
Baud O, Verney C, Evrard P, Gressens P 2005 Injectable dexamethasone administration enhances cortical GABAergic neuronal differentiation in a novel model of postnatal steroid therapy in mice. Pediatr Res 57: 149–156
Paxinos G, Watson C 1998 The rat brain in stereotaxic coordinates, fourth edition. Academic press, San Diego, pp 32–39
Adle-Biassette H, Levy Y, Colombel M, Poron F, Natchev S, Keohane C, Gray F 1995 Neuronal apoptosis in HIV infection in adults. Neuropathol Appl Neurobiol 21: 218–227
Melena J, Safa R, Graham M, Casson RJ, Osborne NN 2003 The monocarboxylate transport inhibitor, alpha-cyano-4-hydroxycinnamate, has no effect on retinal ischemia. Brain Res 989: 128–134
Verney C, Takahashi T, Bhide PG, Nowakowski RS, Caviness VS Jr 2000 Independent controls for neocortical neuron production and histogenetic cell death. Dev Neurosci 22: 125–138
Nehlig A 1996 Respective roles of glucose and ketone bodies as substrates for cerebral energy metabolism in the suckling rat. Dev Neurosci 18: 426–433
Baud O, Fayol L, Evrard P, Verney C 2002 Movements of energy substrates in the mammalian brain, with special emphasis on transporters during normal and pathological development. Neuroembryology 1: 161–168
Rafiki A, Boulland JL, Halestrap AP, Ottersen OP, Bergersen L 2003 Highly differential expression of the monocarboxylate transporters MCT2 and MCT4 in the developing rat brain. Neuroscience 122: 677–688
Kadhim HJ, Gadisseux JF, Evrard P 1988 Topographical and cytological evolution of the glial phase during prenatal development of the human brain: histochemical and electron microscopic study. J Neuropathol Exp Neurol 47: 166–188
Auer RN, Kalimo H, Olsson Y, Siesjo BK 1985 The temporal evolution of hypoglycemic brain damage. I.Light- and electron-microscopic findings in the rat cerebral cortex. Acta Neuropathol (Berl) 67: 13–24
Olney JW, Wozniak DF, Jevtovic-Todorovic V, Farber NB, Bittigau P, Ikonomidou C 2002 Glutamate and GABA receptor dysfunction in the fetal alcohol syndrome. Neurotox Res 4: 315–325
Bhave SV, Ghoda L, Hoffman PL 1999 Brain-derived neurotrophic factor mediates the anti-apoptotic effect of NMDA in cerebellar granule neurons: signal transduction cascades and site of ethanol action. J Neurosci 19: 3277–3286
Thibault C, Lai C, Wilke N, Duong B, Olive MF, Rahman S, Dong H, Hodge CW, Lockhart DJ, Miles MF 2000 Expression profiling of neural cells reveals specific patterns of ethanol-responsive gene expression. Mol Pharmacol 58: 1593–1600
Almeida A, Moncada S, Bolanos JP 2004 Nitric oxide switches on glycolysis through the AMP protein kinase and 6-phosphofructo-2-kinase pathway. Nat Cell Biol 6: 45–51
Author information
Authors and Affiliations
Corresponding authors
Additional information
Supported by: INSERM, Fondation Grace de Monaco and the Association des Juniors en Pédiatrie. H.A.-B. and P.O. contributed equally to this work.
Rights and permissions
About this article
Cite this article
Adle-Biassette, H., Olivier, P., Verney, C. et al. Cortical Consequences of In Vivo Blockade of Monocarboxylate Transport During Brain Development in Mice. Pediatr Res 61, 54–60 (2007). https://doi.org/10.1203/01.pdr.0000250040.61888.61
Received:
Accepted:
Issue date:
DOI: https://doi.org/10.1203/01.pdr.0000250040.61888.61
This article is cited by
-
Molecular biology of the blood-brain and the blood-cerebrospinal fluid barriers: similarities and differences
Fluids and Barriers of the CNS (2011)


