The Neuroprotective Effect of N-Docosahexaenoyldopamine on Degenerating Dopaminergic Neurons of the Mesencephalon

This study was aimed at evaluating the neuroprotective effect of N -docosahexaenoyldopamine (DHA-DA), an endogenous bioactive lipid of the neurolipin family, on mesencephalic dopaminergic neurons of mouse fetuses in a cell culture under exposure to 1-methyl-4-phenylpyridinium + (MPP + ), a specific...

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Veröffentlicht in:Biology bulletin of the Russian Academy of Sciences 2020-09, Vol.47 (5), p.466-473
Hauptverfasser: Surkov, S. A., Mingazov, E. R., Blokhin, V. E., Sturova, A. I., Gretskaya, N. M., Zinchenko, G. N., Bezuglov, V. V., Ugrumov, M. V.
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Sprache:eng
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Zusammenfassung:This study was aimed at evaluating the neuroprotective effect of N -docosahexaenoyldopamine (DHA-DA), an endogenous bioactive lipid of the neurolipin family, on mesencephalic dopaminergic neurons of mouse fetuses in a cell culture under exposure to 1-methyl-4-phenylpyridinium + (MPP + ), a specific neurotoxin for catecholaminergic neurons. The state of neurons in the experiment (MPP + ) and in the control (0.9% NaCl) was estimated according to three parameters: the number of surviving dopaminergic neurons, the length of the neurites, and the total content of dopamine in the neurons. DHA-DA was shown to have a dose-dependent neuroprotective effect on degenerating dopaminergic neurons under the influence of MPP + . DHA-DA at concentrations of 0.5 μM or lower does not have a neuroprotective effect. However, at higher concentrations it has a neuroprotective effect, preventing the death of dopaminergic neurons and the degradation of neuritis. At a concentration of 1 μM, DHA-DA protects the neuron cell bodies from degradation to a higher extent than their processes, whereas at a concentration 2 μM it protects and/or stimulates to a greater extent the growth of processes of the surviving neurons. In addition, DHA-DA reduces significantly the loss of dopamine in neurons under exposure to MPP + . Thus, it is shown that DHA-DA has a dose-dependent neuroprotective effect on degenerating dopaminergic neurons.
ISSN:1062-3590
1608-3059
DOI:10.1134/S1062359020050106