» Articles » PMID: 19062182

Preferential Transport and Metabolism of Glucose in Bergmann Glia over Purkinje Cells: a Multiphoton Study of Cerebellar Slices

Overview
Journal Glia
Specialty Neurology
Date 2008 Dec 9
PMID 19062182
Citations 46
Authors
Affiliations
Soon will be listed here.
Abstract

Knowing how different cell types handle glucose should help to decipher how energy supply is adjusted to energy demand in the brain. Previously, the uptake of glucose by cultured brain cells was studied in real-time using fluorescent tracers and confocal microscopy. Here, we have adapted this technique to acute slices prepared from the rat cerebellum by means of multiphoton microscopy. The transport of the fluorescent glucose analogs 2NBDG and 6NBDG was several-fold faster in the molecular layer of the cerebellar cortex than in Purkinje cell somata and granule cells. After washout of free tracer, it became apparent that most phosphorylated tracer was located in Bergmann glia, which was confirmed by counterstaining with the glial marker sulforhodamine 101. The effective recovery of fluorescence after photobleaching showed that 2NBDG-P can diffuse horizontally across the molecular layer, presumably through gap junctions between Bergmann glial cells. Our main conclusion is that in acute cerebellar slices, the glucose transport capacity and glycolytic rate of Bergmann glia are several-fold higher than those of Purkinje cells. Given that the cerebellum is largely fueled by glucose and Purkinje neurons are estimated to spend more energy than Bergmann glial cells, these results suggest substantial shuttling of an energy-rich metabolite like lactate between glial cells and neurons.

Citing Articles

Modulation of brain energy metabolism in hepatic encephalopathy: impact of glucose metabolic dysfunction.

Prasad S, Acharjee A, Singh V, Trigun S, Acharjee P Metab Brain Dis. 2024; 39(8):1649-1665.

PMID: 39120853 DOI: 10.1007/s11011-024-01407-7.


Lactate Metabolism, Signaling, and Function in Brain Development, Synaptic Plasticity, Angiogenesis, and Neurodegenerative Diseases.

Wu A, Lee D, Xiong W Int J Mol Sci. 2023; 24(17).

PMID: 37686202 PMC: 10487923. DOI: 10.3390/ijms241713398.


Ataxia in Neurometabolic Disorders.

Kaminiow K, Rygula I, Paprocka J Metabolites. 2023; 13(1).

PMID: 36676973 PMC: 9866741. DOI: 10.3390/metabo13010047.


Fluoxetine increases astrocytic glucose uptake and glycolysis in corticosterone-induced depression through restricting GR-TXNIP-GLUT1 Pathway.

Pan S, Zhou Y, Zuo N, Jiao R, Kong L, Pan Y Front Pharmacol. 2022; 13:872375.

PMID: 36105196 PMC: 9465171. DOI: 10.3389/fphar.2022.872375.


The potential mechanisms of lactate in mediating exercise-enhanced cognitive function: a dual role as an energy supply substrate and a signaling molecule.

Xue X, Liu B, Hu J, Bian X, Lou S Nutr Metab (Lond). 2022; 19(1):52.

PMID: 35907984 PMC: 9338682. DOI: 10.1186/s12986-022-00687-z.