Effect of a short-term fast on hepatic microsomal glutathione-insulin transhydrogenase. 1985

J S Striffler

The effect of nutritional state on the hepatic insulin degrading enzyme glutathione-insulin transhydrogenase (GIT) was assessed by comparing the distribution of GIT activity between its nonlatent and latent forms in fractionated liver microsomes from ad lib fed (n = 11) and overnight fasted (n = 11) rats. In fed state microsomes, treatment with the membrane disrupting agent phospholipase-A2 (PLA2) over a range of PLA2 concentrations (less than or equal to 2.0 micrograms/ml) caused biphasic release of GIT with a peak activity of 651 +/- 58 U/mg microsomal protein (n = 11) occurring at PLA2 = 1.0 microgram/ml. In total liver microsomes from fasted animals, GIT release in response to PLA2 was sigmoidal over the entire range of PLA2 concentrations, with a plateau of activities (450 U/mg microsomal protein) occurring at PLA2 greater than or equal to 0.75 microgram/ml. Peak activities (478 +/- 88 U/mg prot., n = 11, PLA2 = 1.0 microgram/ml) were 30% lower as compared to the fed state (p less than .05). In untreated (intact) microsomes from fed rat liver nonlatent activity was 126 +/- 8 U/mg protein, representing 19.9 +/- 1.2% of the total GIT activity. In contrast, nonlatent activity measurable in suspensions of intact microsomes from fasted rat liver (110 +/- 6 U/mg) expressed as a % of total activity was significantly increased (p less than .05) being 23.3 +/- 1.1%. Similar fasting-induced changes were also apparent in isolated smooth microsomes but not in rough membrane preparations.(ABSTRACT TRUNCATED AT 250 WORDS)

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D008297 Male Males
D008862 Microsomes, Liver Closed vesicles of fragmented endoplasmic reticulum created when liver cells or tissue are disrupted by homogenization. They may be smooth or rough. Liver Microsomes,Liver Microsome,Microsome, Liver
D010088 Oxidoreductases The class of all enzymes catalyzing oxidoreduction reactions. The substrate that is oxidized is regarded as a hydrogen donor. The systematic name is based on donor:acceptor oxidoreductase. The recommended name will be dehydrogenase, wherever this is possible; as an alternative, reductase can be used. Oxidase is only used in cases where O2 is the acceptor. (Enzyme Nomenclature, 1992, p9) Dehydrogenases,Oxidases,Oxidoreductase,Reductases,Dehydrogenase,Oxidase,Reductase
D010741 Phospholipases A Phospholipases that hydrolyze one of the acyl groups of phosphoglycerides or glycerophosphatidates.
D011490 Protein Disulfide Reductase (Glutathione) An enzyme that catalyzes the reduction of a protein-disulfide in the presence of glutathione, forming a protein-dithiol. Insulin is one of its substrates. EC 1.8.4.2. Glutathione Insulin Transhydrogenase,Glutathione Protein Disulfide Oxidoreductase,Thiol-Disulfide Oxidoreductase,Thiol-Protein Disulfide Oxidoreductase,Disulfide Oxidoreductase, Thiol-Protein,Insulin Transhydrogenase, Glutathione,Oxidoreductase, Thiol-Disulfide,Oxidoreductase, Thiol-Protein Disulfide,Thiol Disulfide Oxidoreductase,Thiol Protein Disulfide Oxidoreductase,Transhydrogenase, Glutathione Insulin
D011919 Rats, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations or by parent x offspring matings carried out with certain restrictions. This also includes animals with a long history of closed colony breeding. August Rats,Inbred Rat Strains,Inbred Strain of Rat,Inbred Strain of Rats,Inbred Strains of Rats,Rat, Inbred Strain,August Rat,Inbred Rat Strain,Inbred Strain Rat,Inbred Strain Rats,Inbred Strains Rat,Inbred Strains Rats,Rat Inbred Strain,Rat Inbred Strains,Rat Strain, Inbred,Rat Strains, Inbred,Rat, August,Rat, Inbred Strains,Rats Inbred Strain,Rats Inbred Strains,Rats, August,Rats, Inbred Strain,Strain Rat, Inbred,Strain Rats, Inbred,Strain, Inbred Rat,Strains, Inbred Rat
D002458 Cell Fractionation Techniques to partition various components of the cell into SUBCELLULAR FRACTIONS. Cell Fractionations,Fractionation, Cell,Fractionations, Cell
D004435 Eating The consumption of edible substances. Dietary Intake,Feed Intake,Food Intake,Macronutrient Intake,Micronutrient Intake,Nutrient Intake,Nutritional Intake,Ingestion,Dietary Intakes,Feed Intakes,Intake, Dietary,Intake, Feed,Intake, Food,Intake, Macronutrient,Intake, Micronutrient,Intake, Nutrient,Intake, Nutritional,Macronutrient Intakes,Micronutrient Intakes,Nutrient Intakes,Nutritional Intakes
D005215 Fasting Abstaining from FOOD. Hunger Strike,Hunger Strikes,Strike, Hunger,Strikes, Hunger

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