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A Carruthers

Publications and source records attributed to A Carruthers.

102 records · Page 6Linked to original sources

3-O-methylglucose transport in internally dialysed giant axons of Loligo.

1. The transport of the non-metabolized sugar, 3-O-methylglucose, has been studied in the squid axon under conditions where the intracellular environment of the axon is controlled by internal dialysis. 2. Sugar transport is passive, shows saturation kinetics and is asymmetric. At 15 degrees C, the Michaelis and velocity constants for exit are approximately four times those for uptake. The asymmetry of transport is increased by raising the temperature. 3. Sugar uptake is not affected by intracellular sugar levels as high as 100 mM. Sugar exit is, however, reduced by external sugars although the apparent Km for exit is unaffected. 4. The kinetics of sugar exit under exchange conditions are determined by the kinetics of sugar uptake. These results can be accounted for by the asymmetric mobile-carrier and simultaneous-carrier models for transport. 5. Both sugar uptake and exit are reduced in the absence of ATPi. Kinetic analysis of transport under these conditions show that the capacity of the system to transport sugar is unchanged but that the affinity of the system for sugar is reduced. Internal cyclic AMP, AMP, ADP or GTP (2 mM) do not mimic this action of ATP. The hydrolysable analogue of ATP, alpha, beta-methylene-5-ATP (2 mM), (but not the nonhydrolysable analogue beta, gamma-methylene-5-ATP, 2 mM) has an ATP-like action on sugar transport. 6. Transport is unaffected by internal Ca2+ concentrations in the range 4 X 10(-8)--9 X 10(-7) M.

3-O-Methylglucose↗

Insulin stimulates sugar transport in giant muscle fibres of the barnacle.

Insulin stimulates sugar transport in vertebrate skeletal muscle but the mechanism of insulin action is unknown. It has been reported that Na transport in giant muscle fibers of the barnacle (Balanus nubilis) is sensitive to insulin but no one has examined the sensitivity of sugar tansport to insulin in this preparation. We show here that insulin does, indeed, stimulate sugar transport in barnacle muscle. The great advantage of barnacle muscle over all other muscles used so far for investigating the mechanism of insulin action is its large size, which facilitates measurements on single cells and permits the experimenter to control the intracellular environment of the muscle fibre by the technique of internal dialysis. Using single muscle fibres it is possible to show that acceleration of sugar transport by insulin is associated with a fall in ionized Ca, a fall in cyclic AMP and a rise in cyclic GMP. Working with internally dialysed muscle fibres we find that insulin only increases sugar transport when the dialysis solution contains ATP. In the absence of insulin, sugar transport is dialysed muscle is increased by a rise in ionized Ca, a fall in cyclic AMP and, when the internal Ca is elevated, by a rise in cyclic GMP.

Adenosine Triphosphate↗