1. Decrease of pyruvate dehydrogenase phosphatase activity in patients with congenital lactic acidemia
- Author
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Michinori Ito, A.H.M. Mahbubul Huq, Yasuhiro Kuroda, Etsuo Naito, Takahiko Saijo, Eiji Takeda, and Hideaki Kobashi
- Subjects
Male ,Pyruvate decarboxylation ,Pyruvate dehydrogenase lipoamide kinase isozyme 1 ,Pyruvate dehydrogenase kinase ,Clinical Biochemistry ,Pyruvate dehydrogenase phosphatase ,Biochemistry ,Pregnancy ,Pyruvic Acid ,Humans ,Dihydrolipoyl transacetylase ,Child ,Pyruvates ,Chemistry ,Biochemistry (medical) ,Infant ,General Medicine ,Fibroblasts ,Pyruvate dehydrogenase complex ,Molecular biology ,Mitochondria ,Enzyme Activation ,Pyruvate Dehydrogenase (Lipoamide)-Phosphatase ,Acidosis, Lactic ,Female ,Branched-chain alpha-keto acid dehydrogenase complex ,Oxoglutarate dehydrogenase complex - Abstract
We developed an assay method for pyruvate dehydrogenase phosphatase activity using [1-14C]pyruvate and measured pyruvate dehydrogenase phosphatase activity in cultured skin fibroblasts from three patients with congenital lactic acidemia due to a defect in activation of the pyruvate dehydrogenase complex. The enzyme activity of their fibroblasts was significantly reduced to 50.7%, 64.6% and 63.1% of that of control fibroblasts. These observations suggest that the defect in activation of the pyruvate dehydrogenase complex in these patients might be due to a reduction in pyruvate dehydrogenase phosphatase activity.
- Published
- 1992
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