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Apoptotic effects of imidazo[1,2-a]pyrazine derivatives in the human Dami cell line

Authors :
Alain Michel
Claude Chevillard
Marie-Noëlle Mathieu
Leila Gannoun-Zaki
Pierre-Antoine Bonnet
Katja Zurbonsen
gannoun, laila
Physiopathologie cellulaire et moléculaire
Institut National de la Santé et de la Recherche Médicale (INSERM)
Université Montpellier 1 (UM1)
Source :
European Journal of Pharmacology, European Journal of Pharmacology, Elsevier, 1997, 320 (2-3), pp.215-21. ⟨10.1016/s0014-2999(96)00890-4⟩
Publication Year :
1997
Publisher :
HAL CCSD, 1997.

Abstract

International audience; cAMP-elevating agents like phosphodiesterase inhibitors and purines have been shown to induce apoptosis. In the present work we have studied the effects of imidazo[1,2-a]pyrazine derivatives with a purine-like structure: PAB13 (6-bromo-8-(methylamino)imidazo[1,2-a] pyrazine), PAB15 (6-bromo-8-(ethylamino)imidazo[1,2-a]pyrazine), PAB23 (3-bromo-8-(methylamino)imidazo[1,2-a]pyrazine) on the growth of the Dami cell line in comparison to that of adenosine. The growth effect of PAB13, PAB15 and PAB23 was investigated in relation to their phosphodiesterase-inhibitory action and their activity on purinoceptors. Inhibition in cell growth was up to 71.0%, 76.3% and 89.7% for PAB23, PAB13 and PAB15, respectively and 100% for adenosine. Cell viability was affected in a concentration-dependent manner by PAB13, PAB15 and adenosine, with a correlation between growth inhibition and cytotoxicity. These effects of imidazo[1,2-a]pyrazine derivatives were found to be unrelated to an action on purinoceptors, but rather appear quantitatively linked to their ability in inducing apoptosis through their cAMP-increasing and phosphodiesterase-inhibitory potency.

Details

Language :
English
ISSN :
00142999
Database :
OpenAIRE
Journal :
European Journal of Pharmacology, European Journal of Pharmacology, Elsevier, 1997, 320 (2-3), pp.215-21. ⟨10.1016/s0014-2999(96)00890-4⟩
Accession number :
edsair.doi.dedup.....c071bfc933e59038c6994d0b471e5c33
Full Text :
https://doi.org/10.1016/s0014-2999(96)00890-4