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Russian Journal |
ISSN 0042-8809 |
| Biomeditsinskaya Khimiya | Biomedical Chemistry |
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Issue:
Volume 54, issue 4
Title: Isatin Causes a Rapid Accumulation of ATP in Synaptosomes: Implication for Stress and regulation of natriuretic peptide receptors
Authors: A.G. Globa1, V. Glover2, A.E. Medvedev3
Address:
1. Vishnevskii Institute of Surgery, Russian Academy of Medical Sciences, Moscow, Russia;
2. Institute of Reproductive and Developmental Biology, Imperial College London, Du Cane Road, London W12 0NN, UK;
3. Orekhovich Institute of Biomedical Chemistry, Russian Academy of Medical Sciences, Pogodinskaya street, 10, Moscow 119121, Russia; e-mail: alexei.medvedev@ibmc.msk.ru.
Abstract:
Isatin is an endogenous indole, which is increased in mammalian brain and
peripheral tissues under conditions of stress. Physiological concentrations of
isatin inhibit natriuretic peptide (NPR) receptor binding and NPR-dependent
signalling. The inhibition of NPR signalling by isatin is attenuated by a
nonhydrolyzable ATP analogue. In this study we have demonstrated that short term
incubation of rat brain synaptosomes with a physiological concentration of
isatin caused a rapid 3-fold accumulation of ATP. The additional increase of ATP
in the presence of tyrphostin, an inhibitor of tyrosine kinase, which uses ATP
for phosphorylation of some proteins, suggests the dependence of this phenomenon
on the activity of ATP-consuming systems.
ATP inhibited binding of [3H]isatin to both
particulate and soluble fractions of the rat brain. These results suggest that
isatin induces accumulation of ATP, which in turn may displace isatin from both
membrane-bound and soluble binding sites. Since natriuretic peptides are known
to decrease stress hormone release this regulatory loop may be involved in the
maintenance of natriuretic peptide signalling under conditions of stress and
thus contribute to the control of stress responses.
Key words: isatin, brain, ATP, natriuretic peptide receptors, stress.
Биомедицинская химия, 2008 том 54, вып. 4, с. 471-476.
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