In vivo injected mitochondria-targeted plastoquinone antioxidant SkQR1 prevents β-amyloid-induced decay of long-term potentiation in rat hippocampal slices

Biochemistry (Moscow) - Tập 76 - Trang 1367-1370 - 2011
N. A. Kapay1, N. K. Isaev1,2,3, E. V. Stelmashook1,3, O. V. Popova1, D. B. Zorov2,3, V. G. Skrebitsky1, V. P. Skulachev2,3
1Department of Brain Research, Research Center of Neurology, Russian Academy of Medical Sciences, Moscow, Russia
2Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia
3Institute of Mitoengineering, Lomonosov Moscow State University, Moscow, Russia

Tóm tắt

Addition of 200 nM β-amyloid 1–42 (Abeta) to a rat hippocampal slice impairs the induction of a long-term post-tetanic potentiation (LTP) of population spike (PS) in pyramidal neurons of the CA1 field of hippocampus. Intraperitoneal injection into the rat of the mitochondria-targeted plastoquinone derivative SkQR1 (1 μmol/kg of weight given 24 h before the slices were made) abolishes the deleterious effect of Abeta on LTP. These data demonstrate that SkQR1 therapy is able to compensate the Abeta-induced impairments of long-term synaptic plasticity in the hippocampus, which are the main cause of loss of memory and other cognitive functions associated with Alzheimer’s disease.

Tài liệu tham khảo

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