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pubmed-article:8145069pubmed:abstractTextFemale SENCAR mice were pre-fed a control or 40% energy-restricted (ER) diet with energy removed from fat and carbohydrate, or a control, balanced high fat (BHF, with similar energy from fat and carbohydrate), 35% energy restricted from fat (HCR) or 35% energy restricted from carbohydrate (HFR) diet. Epidermal cells were isolated by trypsin digestion for measurement of protein kinase C (PKC) activity, lipid composition or lipid metabolism. Dietary restriction of fat or carbohydrate energy (HFR or HCR group) reduced particulate PKC activity in epidermal cells compared with cells from control mice. The ratio of soluble particulate PKC activity was higher in epidermal cells from mice fed the HCR diet compared with those fed the HFR diet. Diet did not affect soluble PKC activity. Inositol accumulation was measured in the water- or lipid-soluble fractions of prelabeled ([3H]inositol) epidermal cells following a 1-h incubation in media with LiCl. Phosphatidylinositol, inositol biphosphate and inositol triphosphate fractions were more heavily labeled in cells from mice fed the ER diet. Energy restriction did not modify epidermal total lipid or phospholipid composition, but 1,2-diacylglycerol levels were elevated in relation to cell number in epidermal cells from mice fed the ER diet. These data suggest that dietary energy restriction modified PKC activity through a pathway other than alteration in membrane lipid composition or inositol lipid metabolism.lld:pubmed
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pubmed-article:8145069pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:8145069pubmed:articleTitleProtein kinase C activity is reduced in epidermal cells from energy-restricted SENCAR mice.lld:pubmed
pubmed-article:8145069pubmed:affiliationEppley Institute for Research in Cancer, University of Nebraska Medical Center, Omaha 68198-6805.lld:pubmed
pubmed-article:8145069pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8145069pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:8145069pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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