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Acta Physiologica Congress

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Acta Physiologica 2008; Volume 193, Supplement 664
Scandinavian Physiological Society’s Annual Meeting 2008
8/15/2008-8/17/2008
Oulu, Finland


TAURINE REDUCES ETHANOL-INDUCED CASPASE-3 ACTIVATION IN THE DEVELOPING CEREBELLUM
Abstract number: P54

TARANUKHIN1,2 A, TARANUKHINA1 E, SARANSAARI1 P, DJATCHKOVA1 I, PELTO-HUIKKO1,3 M, OJA1 SS

1Medical School, University of Tampere, Finland
2Laboratory of Comparative Somnology and Neuroendocrinology, Sechenov Institute of Evolutionary Physiology and Biochemistry, St.Petersburg, Russia
3Department of Pathology, University of Tampere, Finland

Taurine is a sulphur-containing amino acid with multiple functions, including cell protection. In the present work we studied the possible neuroprotective effect of taurine on ethanol-induced apoptosis in 7-day-old male mice whose cerebella are extremely sensitive to ethanol during synaptogenesis. The degree of apoptosis was estimated with immunostaining for activated caspase-3 in mid-sagittal paraffin-embedded sections containing lobules II-X of the cerebellum. Eight hours after ethanol administration (total dose 5 g/kg) the number of activated caspase-3-immunoreactive neurons was increased in the external and internal granular layers of all cerebellar lobules, indicating ethanol-triggered apoptotic neurodegeneration. Taurine treatment (two injections per 1 g/kg each) significantly decreased the number of activated caspase-3-immunoreactive cells in both external and internal granular layers after ethanol administration but its effect varied in different lobules. We conclude that taurine protects immature cerebellar neurons, reducing markedly ethanol-induced caspase-3 activation but does not abolish it completely. This study was supported by the Center for International Mobility (grants EH-04-2615 and MK-05-3550), the competitive research funding of Pirkanmaa Hospital District (grants 9F070, 9G051, 9G203) and the Finnish Cultural Foundation (2007).

To cite this abstract, please use the following information:
Acta Physiologica 2008; Volume 193, Supplement 664 :P54

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