[U-13C] aspartate metabolism in cultured cortical astrocytes and cerebellar granule neurons studied by NMR spectroscopy
- PMID: 9633811
- DOI: 10.1002/(sici)1098-1136(199807)23:3<271::aid-glia9>3.0.co;2-7
[U-13C] aspartate metabolism in cultured cortical astrocytes and cerebellar granule neurons studied by NMR spectroscopy
Abstract
The metabolism of [U-13C]aspartate was studied in cultured cortical astrocytes and cerebellar granule neurons in the presence of glucose and during inhibition of glycolysis. Redissolved, lyophilized cell extracts and incubation media were analyzed by 13C nuclear magnetic resonance spectroscopy for the determination of metabolites labeled from aspartate. Uniformly labeled lactate was prominent in control media of astrocytes and cerebellar granule neurons. In both cell types, aspartate entered the tricarboxylic acid (TCA) cycle, as shown by labeling patterns in glutamate and, in astrocytes, in glutamine. From the complex labeling patterns in aspartate in astrocytic perchloric acid extracts it was clear that acetylcoenzyme A (acetyl-CoA) derived from aspartate via oxaloacetate and pyruvate could enter the TCA cycle. Such "recycling," however, could not be detected in cerebellar granule neurons. Inhibition of glycolysis reduced aspartate uptake and metabolism in both cell types. Most notably, lactate derived from aspartate showed a large reduction, and in astrocytes, incorporation of labeled acetyl-CoA into the TCA cycle was significantly reduced. Thus, astrocytes and cerebellar granule neurons differ in their handling of aspartate. Furthermore, inhibition of glycolysis clearly affected aspartate metabolism by such cells.
Similar articles
-
Comparison of lactate and glucose metabolism in cultured neocortical neurons and astrocytes using 13C-NMR spectroscopy.Dev Neurosci. 1998;20(4-5):310-20. doi: 10.1159/000017326. Dev Neurosci. 1998. PMID: 9778567
-
[U-13C]glutamate metabolism in astrocytes during hypoglycemia and hypoxia.J Neurosci Res. 1998 Mar 1;51(5):636-45. doi: 10.1002/(SICI)1097-4547(19980301)51:5<636::AID-JNR11>3.0.CO;2-0. J Neurosci Res. 1998. PMID: 9512008
-
Lactate formation from [U-13C]aspartate in cultured astrocytes: compartmentation of pyruvate metabolism.Neurosci Lett. 1997 Nov 21;237(2-3):117-20. doi: 10.1016/s0304-3940(97)00834-3. Neurosci Lett. 1997. PMID: 9453229
-
Regulation of glial metabolism studied by 13C-NMR.NMR Biomed. 2003 Oct-Nov;16(6-7):370-99. doi: 10.1002/nbm.850. NMR Biomed. 2003. PMID: 14679501 Review.
-
Metabolic trafficking between neurons and astrocytes: the glutamate/glutamine cycle revisited.Dev Neurosci. 1995;17(4):203-11. doi: 10.1159/000111288. Dev Neurosci. 1995. PMID: 8575339 Review.
Cited by
-
Astrocytic amino acid metabolism under control conditions and during oxygen and/or glucose deprivation.Neurochem Res. 2003 Feb;28(2):243-58. doi: 10.1023/a:1022377100379. Neurochem Res. 2003. PMID: 12608698
-
Glucose and lactate metabolism in the awake and stimulated rat: a (13)C-NMR study.Front Neuroenergetics. 2013 May 31;5:5. doi: 10.3389/fnene.2013.00005. eCollection 2013. Front Neuroenergetics. 2013. PMID: 23755012 Free PMC article.
-
Metabolism of [U-(13)C]aspartate by astroglial cultures: nuclear magnetic resonance analysis of the culture media.Neurochem Res. 2010 Dec;35(12):2053-61. doi: 10.1007/s11064-010-0326-9. Epub 2010 Nov 25. Neurochem Res. 2010. PMID: 21107687
-
Effects of adrenergic agents on intracellular Ca2+ homeostasis and metabolism of glucose in astrocytes with an emphasis on pyruvate carboxylation, oxidative decarboxylation and recycling: implications for glutamate neurotransmission and excitotoxicity.Neurotox Res. 2012 May;21(4):405-17. doi: 10.1007/s12640-011-9296-1. Epub 2011 Dec 23. Neurotox Res. 2012. PMID: 22194159
-
Exogenous Substrates Prevent the Decline in the Cellular ATP Content of Primary Rat Astrocytes During Glucose Deprivation.Neurochem Res. 2024 May;49(5):1188-1199. doi: 10.1007/s11064-024-04104-0. Epub 2024 Feb 11. Neurochem Res. 2024. PMID: 38341839 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources