» Articles » PMID: 29326137

Expression Changes in Lactate and Glucose Metabolism and Associated Transporters in Basal Ganglia Following Hypoxic-Ischemic Reperfusion Injury in Piglets

Overview
Specialty Neurology
Date 2018 Jan 13
PMID 29326137
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Background And Purpose: The neonatal brain has active energy metabolism, and glucose oxidation is the major energy source of brain tissue. Lactate is produced by astrocytes and released to neurons. In the central nervous system, lactate is transported between neurons and astrocytes via the astrocyte-neuron lactate shuttle. The aim of this study was to investigate the regulatory mechanisms of energy metabolism in neurons and astrocytes in the basal ganglia of a neonatal hypoxic-ischemic brain injury piglet model.

Materials And Methods: A total of 35 healthy piglets (3-5 days of age; 1.0-1.5 kg) were assigned to a control group ( = 5) or a hypoxic-ischemic model group ( = 30). The hypoxic-ischemic model group was further divided into 6 groups according to the H-MR spectroscopy and PET/CT scan times after hypoxia-ischemia (0-2, 2-6, 6-12, 12-24, 24-48, and 48-72 hours; = 5/group). H-MR spectroscopy data were processed with LCModel software. Maximum standard uptake values refer to the maximum standard uptake values for glucose (or FDG). The maximum standard uptake values of the basal ganglia-to-occipital cortex ratio were analyzed. The expression levels of glucose transporters and monocarboxylate transporters were detected by immunohistochemical analysis.

Results: Lactate levels decreased after an initial increase, with the maximal level occurring around 2-6 hours following hypoxia-ischemia. After hypoxia-ischemia, the maximum standard uptake values of the basal ganglia and basal ganglia/occipital cortex initially increased then decreased, with the maximum occurring at approximately 6-12 hours. The lactate and glucose uptake (basal ganglia/occipital cortex maximum standard uptake values) levels were positively correlated. The expression levels of glucose transporter-1 and glucose transporter-3 were positively correlated with the basal ganglia/occipital cortex. The expression levels of monocarboxylic acid transporter-2 and monocarboxylic acid transporter-4 were positively correlated with lactate content.

Conclusions: The results indicate that lactate and glucose transporters have a synergistic effect on the energy metabolism of neurons and astrocytes following hypoxic-ischemic reperfusion brain injury.

Citing Articles

Porcine Astrocytes and Their Relevance for Translational Neurotrauma Research.

Purvis E, Fedorczak N, Prah A, Han D, ODonnell J Biomedicines. 2023; 11(9).

PMID: 37760829 PMC: 10525191. DOI: 10.3390/biomedicines11092388.


Early changes in cerebral metabolism after perinatal hypoxia-ischemia: a study in normothermic and hypothermic piglets.

Andelius T, Bogh N, Pedersen M, Omann C, Andersen M, Andersen H Front Pediatr. 2023; 11:1167396.

PMID: 37325341 PMC: 10264796. DOI: 10.3389/fped.2023.1167396.


Astrocyte-neuron communication mediated by the Notch signaling pathway: focusing on glutamate transport and synaptic plasticity.

Li K, Lu M, Cui M, Wang X, Zheng Y Neural Regen Res. 2023; 18(10):2285-2290.

PMID: 37056149 PMC: 10328266. DOI: 10.4103/1673-5374.369124.


Insight into the Effects of High-Altitude Hypoxic Exposure on Learning and Memory.

Zhang Z, Sun Y, Yuan Z, Wang L, Dong Q, Zhou Y Oxid Med Cell Longev. 2022; 2022:4163188.

PMID: 36160703 PMC: 9492407. DOI: 10.1155/2022/4163188.


Epinephrine vs placebo in neonatal resuscitation: ROSC and brain MRS/MRI in term piglets.

Andersen H, Andersen M, Andelius T, Pedersen M, Lofgren B, Pedersen M Pediatr Res. 2022; 93(3):511-519.

PMID: 35681089 DOI: 10.1038/s41390-022-02126-4.


References
1.
Mehta S, Manhas N, Raghubir R . Molecular targets in cerebral ischemia for developing novel therapeutics. Brain Res Rev. 2007; 54(1):34-66. DOI: 10.1016/j.brainresrev.2006.11.003. View

2.
Ogawa M, Watabe H, Teramoto N, Miyake Y, Hayashi T, Iida H . Understanding of cerebral energy metabolism by dynamic living brain slice imaging system with [18F]FDG. Neurosci Res. 2005; 52(4):357-61. DOI: 10.1016/j.neures.2005.04.007. View

3.
Amaral A, Teixeira A, Martens S, Bernal V, Sousa M, Alves P . Metabolic alterations induced by ischemia in primary cultures of astrocytes: merging 13C NMR spectroscopy and metabolic flux analysis. J Neurochem. 2010; 113(3):735-48. DOI: 10.1111/j.1471-4159.2010.06636.x. View

4.
Chiry O, Fishbein W, Merezhinskaya N, Clarke S, Galuske R, Magistretti P . Distribution of the monocarboxylate transporter MCT2 in human cerebral cortex: an immunohistochemical study. Brain Res. 2008; 1226:61-9. DOI: 10.1016/j.brainres.2008.06.025. View

5.
Kyng K, Skajaa T, Kerrn-Jespersen S, Andreassen C, Bennedsgaard K, Henriksen T . A Piglet Model of Neonatal Hypoxic-Ischemic Encephalopathy. J Vis Exp. 2015; (99):e52454. PMC: 4542803. DOI: 10.3791/52454. View