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Acetyl‐CoA and acetylcholine metabolism in nerve terminal compartment of thiamine deficient rat brain
Author(s) -
JankowskaKulawy Agnieszka,
Bielarczyk Hanna,
Pawełczyk Tadeusz,
Wróblewska Małgorzata,
Szutowicz Andrzej
Publication year - 2010
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2010.06919.x
Subject(s) - thiamine , acetylcholine , pyruvate dehydrogenase complex , cholinergic , chemistry , acetyl coa , atp citrate lyase , biochemistry , compartment (ship) , mitochondrion , choline acetyltransferase , metabolism , choline , endocrinology , medicine , enzyme , biology , citrate synthase , oceanography , geology
J. Neurochem. (2010) 115 , 333–342. Abstract The decrease of pyruvate and ketoglutarate dehydrogenase complex activities is the main cause of energy and acetyl‐CoA deficits in thiamine deficiency‐evoked cholinergic encephalopathies. However, disturbances in pathways of acetyl‐CoA metabolism leading to appearance of cholinergic deficits remain unknown. Therefore, the aim of this work was to investigate alterations in concentration and distribution of acetyl‐CoA and in acetylcholine metabolism in brain nerve terminals, caused by thiamine deficits. They were induced by the pyrithiamine, a potent inhibitor of thiamine pyrophosphokinase. The thiamine deficit reduced metabolic fluxes through pyruvate and ketoglutarate dehydrogenase steps, yielding deficits of acetyl‐CoA in mitochondrial and cytoplasmic compartments of K‐depolarized nerve terminals. It also inhibited indirect transport of acetyl‐CoA though ATP‐citrate lyase pathway being without effect on its direct Ca‐dependent transport to synaptoplasm. Resulting suppression of synaptoplasmic acetyl‐CoA correlated with inhibition of quantal acetylcholine release ( r = 0.91, p = 0.012). On the other hand, thiamine deficiency activated non‐quantal acetylcholine release that was independent of shifts in intraterminal distribution of acetyl‐CoA. Choline acetyltransferase activity was not changed by these conditions. These data indicate that divergent alterations in the release of non‐quantal and quantal acetylcholine pools from thiamine deficient nerve terminals could be caused by the inhibition of acetyl‐CoA and citrate synthesis in their mitochondria. They in turn, caused inhibition of acetyl‐CoA transport to the synaptoplasmic compartment through ATP‐citrate lyase pathway yielding deficits of cholinergic functions.