Literature DB >> 3449192

In vitro inhibition of calcium binding by alloxan and of calcium transport by isolated vascular smooth muscle microsomes.

C Y Kwan1, J S Beazley.   

Abstract

The primary purpose of this study was to investigate the possible direct toxic effect of alloxan on the Ca2+ handling by microsomal membranes isolated from rat mesenteric arteries. It was found that preincubation of the vascular muscle microsomal membranes with alloxan had a suppressive effect on both binding of Ca2+ (in the absence of ATP) and ATP-supported Ca2+ transport. Such an inhibition was time, dose, pH, and temperature dependent. ATP-supported Ca2+ transport was more susceptible to the inhibitory action of alloxan than Ca2+ binding. Unlike alloxan, another commonly used diabetogenic drug, streptozotocin, was not effective in causing such an in vitro inhibition of Ca2+ handling.

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Year:  1987        PMID: 3449192     DOI: 10.1139/y87-371

Source DB:  PubMed          Journal:  Can J Physiol Pharmacol        ISSN: 0008-4212            Impact factor:   2.273


  2 in total

1.  The plasma-membrane component is the primary site of action of alloxan on ATP-driven Ca2+ transport in vascular-muscle microsomal fractions.

Authors:  C Y Kwan
Journal:  Biochem J       Date:  1988-08-15       Impact factor: 3.857

2.  Alloxan inhibits ligand binding to adrenoceptors of vascular smooth muscle microsomes.

Authors:  C Y Kwan; S Sipos; V Gaspar
Journal:  Biochem J       Date:  1990-08-15       Impact factor: 3.857

  2 in total

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