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Biomedical subjects

J R Carter

Publications and source records attributed to J R Carter.

At least 109 records · Page 6Linked to original sources
PubMed1975

Cell membrane changes in chronically diabetic rats.

We have examined the effect of chronic diabetes mellitus upon cell membrane composition and turnover in streptozotocin-treated rats and control animals maintained for four to eight weeks. Liver plasma membranes, prepared from diabetic animals, showed enhanced activities of alkaline phosphatase and glucose-6-phosphatase and depressed 5'-nucleotidase when compared with controls. Studies of the nonprotein constituents of liver plasma membranes and red cell "ghosts" showed similar changes in both tissues: sialic acid and cholesterol content were reduced in the membranes of diabetic animals, while phospholipids (total and individual classes) and neutral sugars were unchanged. To look for changes in relative turnover rates of individual membrane proteins, we combined a double-label in-vivo technic using [3H] and [14C] leucine with polyacrylamide gel separation of membrane proteins. No significant differences were observed between control and diabetic animals. In chronically diabetic animals, cell membranes may show significant changes in overall composition with no significant changes in the rate of protein turnover.

Alkaline Phosphatase↗
PubMed1970

Insulin-stimulated glucose uptake by subcellular particles from adipose tissue cells.

Microsomal particles prepared from isolated rat adipose cells take up D-glucose more rapidly than L-glucose. The rate of D-glucose uptake, but not that of L-glucose, is stimulated by incubation of the intact cells with insulin at concentrations as low as 10 microunits per milliliter before disruption and preparation of the microsomes.

Adipose Tissue↗
PubMed1969

Glucose uptake by isolated particles from rat epididymal tissue cells.

A MICROSOMAL FRACTION FROM ISOLATED ADIPOSE TISSUE CELLS HAS BEEN PREPARED WHICH POSSESSES MANY FEATURES INDICATING THE PRESENCE OF A FUNCTIONAL GLUCOSE TRANSPORT SYSTEM: (1) D-glucose is both taken up and released more rapidly than L-glucose at all temperatures, but at 42 degrees L-glucose uptake reaches the level of D-glucose after prolonged incubation; (2) D-glucose uptake is inhibited by a specific inhibitor of glucose transport, phlorizin, while L-glucose uptake is unaffected; (3) Preincubation of the preparation at 42 degrees C has no effect on L-glucose uptake but partially inhibits D-glucose uptake; (4) Equilibrium uptake studies show a linear relationship between the final level of D-glucose taken up and D-glucose concentration in the medium; and (5) Preloading the membrane preparation with unlabeled D-glucose leads to a more rapid uptake of radioactive D-glucose. These findings are interpreted as showing the presence in the microsomal particles of a specific, bidirectionally functioning D-glucose transport system superimposed on uptake of both sugars by passive diffusion or "leaks." The retained D-glucose can be eluted from the membrane preparation and shown to be the unphosphorylated sugar.

Adipose Tissue↗