Propionic acidemia is caused by lack of propionyl-CoA carboxylase activity. It is biochemically characterized by accumulation of propionic (PA) and 3-hydroxypropionic (3OHPA) acids and clinically by severe encephalopathy and cardiomyopathy. High urinary excretion of maleic acid (MA) and 2-methylcitric acid (2MCA) is also found in the affected patients. Considering that the underlying mechanisms of cardiac disease in propionic acidemia are practically unknown, we investigated the effects of PA, 3OHPA, MA and 2MCA (0.05–5 mM) on important mitochondrial functions in isolated rat heart mitochondria, as well as in crude heart homogenates and cultured cardiomyocytes. MA markedly inhibited state 3 (ADP-stimulated), state 4 (non-phosphorylating) an...
Patients with long-chain 3-hydroxy-acyl-CoA dehydrogenase (LCHAD) deficiency commonly present liver ...
Propionic aciduria (PA) is caused by deficiency of the mitochondrial enzyme propionyl-CoA carboxylas...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do...
Mitochondrial dysfunction during acute metabolic crises is considered an important pathomechanism in...
Propionate is a naturally-occurring monocarboxylate short-chain fatty acid in humans derived from th...
Propionic acidemia (PA) is a rare metabolic disease associated with mutations in genes encoding the ...
Maleic acid (MA), which has been reported to be highly excreted in propionic acidemia (PAcidemia), w...
Maleic acid (MA), which has been reported to be highly excreted in propionic acidemia (PAcidemia), w...
Barth syndrome (BTHS) and dilated cardiomyopathy with ataxia syndrome (DCMA) are biochemically chara...
AbstractCardiovascular changes of still obscure origin are sometimes correlated with co-existing liv...
Phytanic acid (Phyt) accumulates in tissues and biological fluids of patients affected by Refsum dis...
Aim: Calcium ions play a pivotal role in matching energy supply and demand in cardiac muscle. Mitoch...
Clinical observations and experimental studies have determined that systemic acid-base disturbances ...
It has been demonstrated previously that the mammalian heart cannot sustain physiologic levels of pr...
AbstractThe formation of malonyl-CoA in rat heart is catalyzed by cytosolic acetyl-CoA carboxylase. ...
Patients with long-chain 3-hydroxy-acyl-CoA dehydrogenase (LCHAD) deficiency commonly present liver ...
Propionic aciduria (PA) is caused by deficiency of the mitochondrial enzyme propionyl-CoA carboxylas...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do...
Mitochondrial dysfunction during acute metabolic crises is considered an important pathomechanism in...
Propionate is a naturally-occurring monocarboxylate short-chain fatty acid in humans derived from th...
Propionic acidemia (PA) is a rare metabolic disease associated with mutations in genes encoding the ...
Maleic acid (MA), which has been reported to be highly excreted in propionic acidemia (PAcidemia), w...
Maleic acid (MA), which has been reported to be highly excreted in propionic acidemia (PAcidemia), w...
Barth syndrome (BTHS) and dilated cardiomyopathy with ataxia syndrome (DCMA) are biochemically chara...
AbstractCardiovascular changes of still obscure origin are sometimes correlated with co-existing liv...
Phytanic acid (Phyt) accumulates in tissues and biological fluids of patients affected by Refsum dis...
Aim: Calcium ions play a pivotal role in matching energy supply and demand in cardiac muscle. Mitoch...
Clinical observations and experimental studies have determined that systemic acid-base disturbances ...
It has been demonstrated previously that the mammalian heart cannot sustain physiologic levels of pr...
AbstractThe formation of malonyl-CoA in rat heart is catalyzed by cytosolic acetyl-CoA carboxylase. ...
Patients with long-chain 3-hydroxy-acyl-CoA dehydrogenase (LCHAD) deficiency commonly present liver ...
Propionic aciduria (PA) is caused by deficiency of the mitochondrial enzyme propionyl-CoA carboxylas...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do...