Abstract

Pretreatment of Chang liver cells with N- ethylmaleimide (0.5 or 1 mM) stimulated Na +-independent uptake of leucine at low concentrations (⩽1 mM). The stimulatory effect of N- ethylmaleimide on the uptake of leucine measured in Na +-replete medium was completely blocked by the addition of b-2- aminobicyclo[2,2,1] heptane-2- carboxylate (5 mM), which shows that the L system participates in the stimulation. The Na +-dependent uptake of glycine was depressed by N- ethylmaleimide pretreatment. The stimulation of the Na +-independent component of leucine uptake continued for at least 30 min after N- ethylmaleimide treatment, while the inhibition of glycine uptake was progressive with time and the Na +-dependent uptake of leucine became depressed later, after the treatment. It has been demonstrated that treatment of cells with N- ethylmaleimide is capable of increasing the Na +-independent influx of leucine and at the same time slightly decreasing the efflux of it. These results suggest that N- ethylmaleimide attacks the Na +-independent system of amino acid transport at the reactive SH groups(s) of relevant protein(s) in favor of specific activation of that system in this cell.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.