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Neuroprotective Effect of Carnosine on Primary Culture of Rat Cerebellar Cells under Oxidative Stress

A. V. Lopachev1,2*, O. M. Lopacheva1,3, D. A. Abaimov1, O. V. Koroleva2, E. A. Vladychenskaya1,4, A. A. Erukhimovich2, and T. N. Fedorova1

1Research Center of Neurology, 125367 Moscow, Russia; fax: +7 (495) 490-2409; E-mail: lopsasha@yandex.ru

2Bach Institute of Biochemistry, Research Center of Biotechnology, Russian Academy of Sciences, 119071 Moscow, Russia; fax: +7 (495) 954-5283; E-mail: inbi@inbi.ras.ru

3Lomonosov Moscow State University, International Biotechnological Center, 119991 Moscow, Russia; fax: +7 (495) 939-4339; E-mail: olga3511@yandex.ru

4Lomonosov Moscow State University, Faculty of Biology, 119991 Moscow, Russia; fax: +7 (495) 939-1398; E-mail: eavlad@list.ru

* To whom correspondence should be addressed.

Received November 10, 2015
Dipeptide carnosine (β-alanyl-L-histidine) is a natural antioxidant, but its protective effect under oxidative stress induced by neurotoxins is studied insufficiently. In this work, we show the neuroprotective effect of carnosine in primary cultures of rat cerebellar cells under oxidative stress induced by 1 mM 2,2′-azobis(2-amidinopropane)dihydrochloride (AAPH), which directly generates free radicals both in the medium and in the cells, and 20 nM rotenone, which increases the amount of intracellular reactive oxygen species (ROS). In both models, adding 2 mM carnosine to the incubation medium decreased cell death calculated using fluorescence microscopy and enhanced cell viability estimated by the MTT assay. The antioxidant effect of carnosine inside cultured cells was demonstrated using the fluorescence probe dichlorofluorescein. Carnosine reduced by half the increase in the number of ROS in neurons induced by 20 nM rotenone. Using iron-induced chemiluminescence, we showed that preincubation of primary neuronal cultures with 2 mM carnosine prevents the decrease in endogenous antioxidant potential of cells induced by 1 mM AAPH and 20 nM rotenone. Using liquid chromatography-mass spectrometry, we showed that a 10-min incubation of neuronal cultures with 2 mM carnosine leads to a 14.5-fold increase in carnosine content in cell lysates. Thus, carnosine is able to penetrate neurons and exerts an antioxidant effect. Western blot analysis revealed the presence of the peptide transporter PEPT2 in rat cerebellar cells, which suggests the possibility of carnosine transport into the cells. At the same time, Western blot analysis showed no carnosine-induced changes in the level of apoptosis regulating proteins of the Bcl-2 family and in the phosphorylation of MAP kinases, which suggests that carnosine could have minimal or no side effects on proliferation and apoptosis control systems in normal cells.
KEY WORDS: carnosine, AAPH, rotenone, oxidative stress, neuron, antioxidant, neuroprotective effect

DOI: 10.1134/S0006297916050084