Difference between revisions of "Glutamate-anaplerotic pathway control state"
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:::: In '''human skeletal muscle mitochondria''', [[OXPHOS]] capacity with glutamate alone (G<sub>''P''</sub>) is 50% to 85% of respiration in the [[GM pathway control state]] (GM<sub>''P''</sub>). Accumulation of fumarate inhibits succinate dehydrogenase and glutamate dehydrogenase. | :::: In '''human skeletal muscle mitochondria''', [[OXPHOS]] capacity with glutamate alone (G<sub>''P''</sub>) is 50% to 85% of respiration in the [[GM pathway control state]] (GM<sub>''P''</sub>). Accumulation of fumarate inhibits succinate dehydrogenase and glutamate dehydrogenase. | ||
:::: Glutaminolysis: Glutamate derived from hydrolyzation of glutamine is an important aerobic substrate in cultured cells, supporting anaplerosis. Mitochondrial glutamate dehydrogenase is particularly active in astrocytes, preventing glutamate induced neurotoxicity. Β | :::: Glutaminolysis: Glutamate derived from hydrolyzation of glutamine is an important aerobic substrate in cultured cells, supporting anaplerosis. Mitochondrial glutamate dehydrogenase is particularly active in astrocytes, preventing glutamate-induced neurotoxicity. Β | ||
:::: Anaplerosis from malate: mtNAD-malic enzyme supports an anaplerotic pathway when carbohydrate is limiting. | :::: Anaplerosis from malate: mtNAD-malic enzyme supports an anaplerotic pathway when carbohydrate is limiting. | ||
== [[SUITbrowser]] question: Glutamine/glutamate == | == [[SUITbrowser]] question: Glutamine/glutamate == | ||
:::: The [https://suitbrowser.oroboros.at/ SUITbrowser] can be used to find the best SUIT protocols to analyse glutamine/glutamate metabolism, among other research questions. |
Revision as of 09:07, 3 July 2019
- high-resolution terminology - matching measurements at high-resolution
Glutamate-anaplerotic pathway control state
Description
G: Glutamate is an anaplerotic NADH-linked type 4 substrate (N). When supplied as the sole fuel substrate in the glutamate pathway control state, G is transported by the electroneutral glutamate-/OH- exchanger, and is oxidised via mt-glutamate dehydrogenase in the mitochondrial matrix. The G-pathway plays an important role in glutaminolysis.
Abbreviation: G
Reference: Gnaiger 2014 MitoPathways - Chapter 3.3
MitoPedia concepts:
SUIT state
Communicated by Gnaiger E 2016-01-25, edited 2016-11-29.
G(L)
LEAK state (L) with G alone as substrate can be evaluated in the following SUIT protocol:
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- DL-Protocol for permeabilized cells (pce): SUIT-007 O2 ce-pce D030
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G(P)
OXPHOS state (P) with G alone as substrate can be evaluated in the following SUIT protocol:
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- DL-Protocol for permeabilized cells (pce): SUIT-007 O2 ce-pce D030
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G(E)
ET state (E) with G alone as substrate can be evaluated in the following SUIT protocol:
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- DL-Protocol for permeabilized cells (pce): SUIT-007 O2 ce-pce D030
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Details
- In human skeletal muscle mitochondria, OXPHOS capacity with glutamate alone (GP) is 50% to 85% of respiration in the GM pathway control state (GMP). Accumulation of fumarate inhibits succinate dehydrogenase and glutamate dehydrogenase.
- Glutaminolysis: Glutamate derived from hydrolyzation of glutamine is an important aerobic substrate in cultured cells, supporting anaplerosis. Mitochondrial glutamate dehydrogenase is particularly active in astrocytes, preventing glutamate-induced neurotoxicity.
- Anaplerosis from malate: mtNAD-malic enzyme supports an anaplerotic pathway when carbohydrate is limiting.
SUITbrowser question: Glutamine/glutamate
- The SUITbrowser can be used to find the best SUIT protocols to analyse glutamine/glutamate metabolism, among other research questions.