AGE-DEPENDENT DIFFERENCES OF LPS-INDUCED BDNF AND iNOS IN RAT SUBSTANTIA NIGRA

Ye. S. Zakoliukina , V. M. Chuchkov , T. N. Sergeyeva , O. A. Vezheyeva , V. G. Sergeyev

Morphology ›› 2018, Vol. 153 ›› Issue (2) : 7 -13.

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Morphology ›› 2018, Vol. 153 ›› Issue (2) : 7 -13. DOI: 10.17816/morph.398217
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AGE-DEPENDENT DIFFERENCES OF LPS-INDUCED BDNF AND iNOS IN RAT SUBSTANTIA NIGRA

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Abstract

Objective - to study the intensity of Brain-Derived Neurotrophic Factor (BDNF) and inducible NO-synthase (iNOS) expression by substantia nigra glial cells in rats of different ages in norm and in neuroinflammation. Materials and methods. Experiments were performed on 36 male Wistar rats:18 young animals with the body weight of 250- 300 g and 18 old animals weighing 380-420 g. Using immunohistochemical method, these markers were detected in frozen sections in substantia nigra astro - and microgliocytes 8 weeks after stereotaxic unilateral injection of lipopolysaccharide (LPS). into this region. Results: Number of GFAP- and CD11β-positive cells (astro-and microgliocytes respectively) was significantly increased in the substantia nigra of old animals. 8 weeks after endotoxin administration, age-related differences in LPS-induced production of BDNF and iNOS were found. The injection of LPS intensified the production of BDNF in astrocytes in young but not old animals, while at the same time microglial cells of older animals expressed iNOS much more intensively. Conclusions: The balance of trophic and damaging factors synthesized by glial cells of the substance nigra in response to endotoxin stimulation depends on age. The glial response to endotoxin stimulation in young animals has a protective character, whereas in older animals it increases the risk of oxidative damage of neurons.

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BDNF / iNOS / BDNF / iNOS / microglia / astroglia / neuroinflammation

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Ye. S. Zakoliukina, V. M. Chuchkov, T. N. Sergeyeva, O. A. Vezheyeva, V. G. Sergeyev. AGE-DEPENDENT DIFFERENCES OF LPS-INDUCED BDNF AND iNOS IN RAT SUBSTANTIA NIGRA. Morphology, 2018, 153(2): 7-13 DOI:10.17816/morph.398217

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References

[1]

Заколюкина Е. С., Тукмачева К. А., Сергеев В. Г. Дозозависимый эффект ЛПС-индуцированной экспрессии BDNF в черной субстанции мозга крыс // Вестн. Удмуртск. ун-та. Сер. Биология. Науки о Земле. 2017. Т. 27, вып. 1. С. 80-86.

[2]

Сергеева Т. Н., Сергеев В. Г., Чучков В. М. Клеточные механизмы хронического нейровоспаления // Морфологические ведомости. 2014. № 4. С. 31-36.

[3]

Cardile V., Pavone A., Gulino R. et al. Expression of brain-derived neurotrophic factor (BDNF) and inducible nitric oxide synthase (iNOS) in rat astrocyte cultures treated with Levetiracetam // Brain Res. 2003. Vol. 976, № 2. P. 227-233.

[4]

Kettenmann H., Hanisch U. K., Noda M., Verkhratsky A. Physiology of microglia // Physiol. Rev. 2011. Vol. 91, № 2. P. 461-553.

[5]

Liberatore G. T., Jackson-Lewis V., Vukosavic S. et al. Inducible nitric oxide synthase stimulates dopaminergic neurodegeneration in the MPTP model of Parkinson disease // Nature Med. 1999. Vol. 5, № 12. P. 1403-1409.

[6]

Madinier A., Bertrand N., Mossiat C. et al. Microglial involvement in neuroplastic changes following focal brain ischemia in rats // PLoS One. 2010. Vol. 4, № 12. P. 1-12.

[7]

Murer M. G., Yan Q. Raisman-Vozari R. Brainderived neurotrophic factor in the control human brain, and in Alzheimer’s disease and Parkinson’s disease // Progr. Neurobiol. 2001. Vol. 3. P. 71-124.

[8]

Murphy S. Production of nitric oxide by glial cells: regulation and potential roles in the CNS // Glia. 2000. Vol. 29, № 1. P. 1-13.

[9]

Porritt M. J., Batchelor P., Howells D. Inhibiting BDNF ex pres sion by antisense oligonucleotide infusion causes loss of nigral dopaminergic neurons // Exp. Neurol. 2005. Vol. 192. P. 226-234.

[10]

Przedborski S., Ischiropoulos H. Reactive oxygen and nitrogen species: weapons of neuronal destruction in models of Parkinson’s disease // Antioxid. Redox. Signal. 2005. Vol. 7. P. 685-693.

[11]

Sastre M., Richardson J. C., Gentleman S. M., Brooks D. J. In flammatory risk factors and pathologies associated with Alzheimer’s disease // Curr. Alzheimer Res. 2011. Vol. 8, № 2. P. 132-141.

[12]

Takano K., Yamasaki H., Kawabe K., Moriyama M., Nakamura Y. Imipramine induces brain-derived neurotrophic factor mRNA expression in cultured astrocytes // J. Pharmacol. Sci. 2012. Vol. 120, № 3. P. 176-186.

[13]

Takemoto T., Ishihara Y., Ishida A., Yamazaki T. Neuroprotection elicited by nerve growth factor and brain-derived neurotrophic factor released from astrocytes in response to methylmercury // Environ. Toxicol. Pharmacol. 2015. Vol. 40, № 1. P. 199-205.

[14]

Tansey M. G., Goldberg M. S. Neuroinflammation in Parkinson’s disease: its role in neuronal death and implications for therapeutic intervention // Neurobiol Dis. 2010. Vol. 37, № 3. P. 510-518.

[15]

Wu D. C., Teismann P., Tieu K. et al. NADPH oxidase mediates oxidative stress in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson’s disease // PNAS. 2003. Vol. 100, № 10. P. 6145-6150.

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