The effect of amino acid depletion or supplementation and the effect of glucagon and insulin on the amino acid transport mediated by s stem A were acid (AIB) or N-methyl 2-amino [l-'4C]isobutyric acid (MeAIB) in rat hepatocytes, freshly isolated at different stages of pre-and postnatal development.
Effects of polyamines on cyclic AMP-mediated stimulation of amino acid transport in isolated rat hepatocytes
✍ Scribed by Patrick Auberger; Michel Samson; Ginette Le Cam; Alphonse Le Cam
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 858 KB
- Volume
- 117
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
The effects of natural polyamines on cyclic AMP-mediated stimulation of amino acid transport in isolated rat hepatocytes were analyzed. Despite the fact that polyamines could directly compete with alpha-aminoisobutyric acid (AIB) for uptake, preincubation of hepatocytes with polyamines did not significantly alter basal AIB transport. The stimulatory effect of glucagon or cyclic AMP analogs was differently affected by polyamines, since it was reduced in the presence of spermine and, inversely, potentiated by spermidine, putrescine, and cadaverine. Dose-dependence analysis showed that half maximal and maximal effects occurred with 2-3 and 6-10 mM external concentrations, respectively. None of the polyamine effects could be ascribed to transstimulation or transinhibition of amino acid uptake. The inhibitory effect exerted by spermine correlated its capacity to inhibit [3H]-leucine incorporation into proteins partially. The potentiating effect of the other polyamines did not result from stabilization of newly synthesized carrier proteins. Instead, the increase in Vmax of the high affinity transport component suggested that more carriers became available, presumably because polyamines facilitated their synthesis by interacting directly with one or several steps controlled by cyclic AMP. Polyamines appear to represent a new class of factors capable of modulating the cyclic AMP-mediated stimulation of amino acid transport, in hepatocytes.
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