| pubmed-article:1622391 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1622391 | lifeskim:mentions | umls-concept:C0205054 | lld:lifeskim |
| pubmed-article:1622391 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:1622391 | lifeskim:mentions | umls-concept:C0204695 | lld:lifeskim |
| pubmed-article:1622391 | lifeskim:mentions | umls-concept:C2936196 | lld:lifeskim |
| pubmed-article:1622391 | pubmed:dateCreated | 1992-8-4 | lld:pubmed |
| pubmed-article:1622391 | pubmed:abstractText | Previous findings have established a pivotal role for hepatic pyruvate dehydrogenase complex (PDH) in regulating hepatic carbon flux during the starved-to-fed and fed-to-starved nutritional transitions [Holness, McLennan, Palmer & Sugden (1988) Biochem. J. 252, 325-330; Holness & Sugden (1990) Biochem. J. 268, 77-81]. We have therefore examined liver PDH activities during the light and dark phases of the feeding cycle in the adult rat in relation to hepatic glycogenesis, fatty acid synthesis and cholesterogenesis. There was significant synchronous suppression of lipogenesis and glycogenesis during the light phase; rates were restored asynchronously during the dark (feeding) phase. Glycogen concentrations declined during the light phase and increased during the dark phase. Despite quite dramatic changes in rates of glycogen and lipid synthesis and hepatic glycogen concentrations during the light and dark phases, hepatic PDHa (active form) activity remained relatively unchanged. Qualitative and quantitative differences in the pattern of change in rates of synthesis of fatty acid and cholesterol suggested regulation at pathway-specific sites distal to PDH. | lld:pubmed |
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| pubmed-article:1622391 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1622391 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1622391 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:1622391 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1622391 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:1622391 | pubmed:issn | 0264-6021 | lld:pubmed |
| pubmed-article:1622391 | pubmed:author | pubmed-author:SugdenM CMC | lld:pubmed |
| pubmed-article:1622391 | pubmed:author | pubmed-author:HolnessM JMJ | lld:pubmed |
| pubmed-article:1622391 | pubmed:author | pubmed-author:HowardR MRM | lld:pubmed |
| pubmed-article:1622391 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1622391 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:1622391 | pubmed:volume | 284 ( Pt 3) | lld:pubmed |
| pubmed-article:1622391 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1622391 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1622391 | pubmed:pagination | 721-4 | lld:pubmed |
| pubmed-article:1622391 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:1622391 | pubmed:year | 1992 | lld:pubmed |
| pubmed-article:1622391 | pubmed:articleTitle | Variations in hepatic carbon flux during unrestricted feeding. | lld:pubmed |
| pubmed-article:1622391 | pubmed:affiliation | Department of Biochemistry, Queen Mary & Westfield College, London, U.K. | lld:pubmed |
| pubmed-article:1622391 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1622391 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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