1998
DOI: 10.1080/15216549800204052
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Dietary fats alter the activity and expression of glucose‐6‐phosphate dehydrogenase in rat lymphoid cells and tissues

Abstract: The effect of diets enriched with fat containing different fatty acids on the activity and expression of the glucose‐6‐phosphate dehydrogenase (EC 1.1.1.49) of mesenteric lymph nodes, lymphocytes and intraperitoneal macrophages was examined. Measurements of the enzyme were also performed using spleen, thymus and liver for comparison. The following fat rich diets containing a variety of fatty acids were used: 1‐standard chow (CC); 2‐medium chain saturated fatty acids (MS)‐cocconut fat‐oil; 3‐long chain saturate… Show more

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Cited by 11 publications
(11 citation statements)
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“…For the enzymatic activities and oxidative lesions in biomolecules cells were pelleted (5 × 10 6 ) and mixed with 1.0 mL of the assayspecific extraction buffer, vortexed briefly and lysed by ultrasonication in a Vibra Cell apparatus (Connecticut, USA) as previously described [25]. A centrifugation step was included (10,000 ×g, 10 min, at 4°C) in order to eliminate debris from the crude homogenate; the supernatant was then used for further analysis.…”
Section: Preparation Of Homogenatesmentioning
confidence: 99%
“…For the enzymatic activities and oxidative lesions in biomolecules cells were pelleted (5 × 10 6 ) and mixed with 1.0 mL of the assayspecific extraction buffer, vortexed briefly and lysed by ultrasonication in a Vibra Cell apparatus (Connecticut, USA) as previously described [25]. A centrifugation step was included (10,000 ×g, 10 min, at 4°C) in order to eliminate debris from the crude homogenate; the supernatant was then used for further analysis.…”
Section: Preparation Of Homogenatesmentioning
confidence: 99%
“…17 A centrifugation step was included (10 000 Âg, 10 min, at 48C) in order to eliminate debris from the crude homogenate; the supernatant was then used for further analysis. The extracts for enzyme assays and oxidative lesions were prepared with a 50 mM phosphate buffer (pH 7.4).…”
Section: Preparation Of Homogenatesmentioning
confidence: 99%
“…Glutathione peroxidase [23] and glutathione reductase [24] activities were measured based on the oxidation of β-NADPH in the presence of tert-butyl hydroperoxide used as substrate. The activity of glucose-6-phosphate dehydrogenase was determined as described in our previous study [25]. …”
Section: Erythrocytes Enzyme Activitiesmentioning
confidence: 99%