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1.
Neuropsychologia ; 35(1): 25-35, 1997 Jan.
Article in English | MEDLINE | ID: mdl-8981374

ABSTRACT

This study examined whether the frequently reported word-stem completion priming deficit of Alzheimer's disease (AD) patients could be characterized as either a semantic encoding deficit or a conceptual priming deficit. AD patients and normal elderly control subjects studied words in two conditions: (1) reading visually presented words aloud, which maximizes perceptual encoding of seen words, and (2) generating words aloud from definitions, which maximizes conceptual encoding of words not seen but retrieved on the basis of semantic context. Recognition accuracy was greater for words that were generated at study, and word-stem completion priming was greater for words that were read at study. For the AD patients, recognition accuracy was impaired and word-stem completion priming was intact for words encoded in both conditions. The findings are discussed in terms of discrepant results about word-stem completion priming in AD.


Subject(s)
Alzheimer Disease/psychology , Memory/physiology , Perception/physiology , Aged , Cognition/physiology , Cues , Humans , Memory, Short-Term/physiology , Mental Recall/physiology , Verbal Learning
2.
Lipids ; 27(3): 169-76, 1992 Mar.
Article in English | MEDLINE | ID: mdl-1522760

ABSTRACT

Adult male marmoset monkeys were fed eicosapentaenoic acid (20:5n-3) as the ethyl ester in diets containing either 32% (reference diet, no added cholesterol) or 7% (atherogenic diet with 0.2% added cholesterol) linoleic acid (18:2n-6) for 30 wk. No changes were seen in the level of phosphatidylcholine (PC) or phosphatidylethanolamine (PE) but minor changes were observed in both the sphingomyelin (SPM) and phosphatidylinositol plus phosphatidylserine (PI+PS) fractions of erythrocyte lipids. The extent of total n-3 fatty acid incorporation into membrane lipids was higher in atherogenic diets (polyunsaturated/monounsaturated/saturated (P/M/S) ratio 0.2:0.6:1.0) than reference diets (P/M/S ratio 1:1:1) and this was true for both PE (33.4 +/- 1.0% vs 24.3 +/- 1.1%) and PC (9.3 +/- 0.5% vs 4.9 +/- 0.3%). Although suitable controls for cholesterol effects were not included in the study, earlier results obtained with marmosets lead us to believe such effects were probably small. Regardless of basic diet (atherogenic, reference), 20:5n-3 was preferentially incorporated into PE (10.8 +/- 0.2%, 6.0 +/- 0.02%) while smaller amounts were incorporated into PC (6.9 +/- 0.4%, 3.2 +/- 0.2%). The major n-3 polyunsaturated fatty acid found in PE in response to dietary 20:5n-3 was the elongation metabolite 22:5n-3 in both the atherogenic (17.7 +/- 0.7%) and reference (14.3 +/- 1.0%) dietary groups; 22:6n-3 levels were less affected by diet (4.7 +/- 0.3% and 3.9 +/- 0.2%, respectively).(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Dietary Fats/pharmacology , Eicosapentaenoic Acid/pharmacology , Erythrocytes/metabolism , Fatty Acids/blood , Phospholipids/blood , Animals , Callithrix , Cholesterol, Dietary/pharmacology , Diet, Atherogenic , Erythrocytes/drug effects , Fatty Acids/isolation & purification , Linoleic Acid , Linoleic Acids/pharmacology , Male , Phosphatidylcholines/blood , Phosphatidylethanolamines/blood , Phospholipids/isolation & purification , Reference Values , Sphingomyelins/blood
3.
Biochim Biophys Acta ; 1045(2): 164-73, 1990 Jul 16.
Article in English | MEDLINE | ID: mdl-2378908

ABSTRACT

The effect of dietary eicosapentaenoic acid (EPA, 20:5(n-3), as the ethyl ester) on plasma lipid levels and the incorporation of EPA into erythrocyte and plasma lipids were investigated in the marmoset monkey. Marmosets were fed high mixed-fat diets (14.5% total fat) supplemented with or without 0.8% EPA for 30 weeks. Markedly elevated plasma cholesterol (16.4 mmol/l) was induced by an atherogenic-type diet but with EPA supplementation, plasma cholesterol increased to only 6.6 mmol/l. Plasma triacylglycerol levels were not elevated with an atherogenic type diet. Substantial EPA incorporation was evident for plasma phospholipid, triacylglycerol and cholesterol ester fractions. The proportion of docosapentaenoic acid (22:5(n-3)) but not docosahexaenoic acid (22:6(n-3)) was also elevated in these plasma lipid fractions. Greatest incorporation of EPA occurred when it was administered with an atherogenic type diet having a P:M:S (polyunsaturated:monounsaturated:saturated) fatty acid ratio of about 0.2:0.6:1.0 in comparison to the control diet of 1.0:1.0:1.0. Incorporation of EPA and 22:5(n-3)) into erythrocyte phospholipids was also apparent and this was at the expense of linoleic acid (18:2(n-6)). These results in the marmoset highlight both the cholesterol-lowering properties of EPA and the extent of its incorporation into plasma lipids and erythrocyte membrane phospholipids with far greater incorporation occurring when the level of dietary linoleic acid was reduced.


Subject(s)
Dietary Fats/pharmacology , Eicosapentaenoic Acid/blood , Erythrocytes/metabolism , Linoleic Acids/administration & dosage , Lipids/blood , Animals , Callithrix , Cholesterol/blood , Diet, Atherogenic , Dietary Fats/administration & dosage , Eicosapentaenoic Acid/pharmacology , Fatty Acids/blood , Male , Phospholipids/blood , Triglycerides/blood
4.
Biochem Biophys Res Commun ; 162(2): 686-93, 1989 Jul 31.
Article in English | MEDLINE | ID: mdl-2547370

ABSTRACT

Eicosapentaenoic acid (EPA; 20:5 n-3; ethyl ester) in combination with atherogenic or non-atherogenic high fat diets was fed to young adult male marmoset monkeys for a period of 30 weeks. EPA markedly reduced the raised plasma cholesterol level evident when feeding an atherogenic diet but did not influence the cardiac membrane cholesterol-to-phospholipid ratio. EPA and its elongation product 22:5 n-3 was incorporated into cardiac membrane phospholipids at the expense of linoleic and arachidonic acids. Dietary EPA increased cardiac beta-AR affinity and reversed the decreased beta-AR affinity evident when feeding an atherogenic diet.


Subject(s)
Dietary Fats/pharmacology , Eicosapentaenoic Acid/pharmacology , Myocardium/metabolism , Receptors, Adrenergic, beta/metabolism , Animals , Callithrix , Cell Membrane/metabolism , Cholesterol/blood , Cholesterol/metabolism , Eicosapentaenoic Acid/administration & dosage , Eicosapentaenoic Acid/metabolism , Iodocyanopindolol , Male , Membrane Lipids/metabolism , Microsomes/metabolism , Myocardium/ultrastructure , Phospholipids/metabolism , Pindolol/analogs & derivatives , Pindolol/metabolism , Propranolol/pharmacology , Receptors, Adrenergic, beta/drug effects
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