Поведенческий фенотипический анализ животных с генетической моделью болезни Альцгеймера
Аннотация
Об авторах
Я. В. ГоринаРоссия
Ю. К. Комлева
Россия
О. Л. Лопатина
Россия
А. И. Черных
Россия
А. Б. Салмина
Россия
Список литературы
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2. Cubinková V., Valachová B., Brezovaková V., Szabó R., Zimová I., Kostecká Z., Jadhav S. Next generation tau models in Alzheimer's disease research - virus based gene delivery systems // Acta Virol. 2017. No. 61(1). doi: 10.4149/av. 2017. 01. 13. [Epub ahead of print].
3. Guillozet A.L., Weintraub S., Mash D.C., Mesulam M.M. Neurofibrillary tangles, amyloid, and memory in aging and mild cognitive impairment // Arch Neurol. 2003. No. 60(5). P. 729-736. doi:10.1001/archneur.60.5.729.
4. Jacobs S.A., Huang F., Tsien J.Z., Wei W. Social Recognition Memory Test in Rodents // Neuroscience. 2016. No. 6(9). doi: https://doi.org/10.21769/bioprotoc.1804.
5. Leal S.L., Landau S.M., Bell R.K., Jagust W.J. Hippocampal activation is associated with longitudinal amyloid accumulation and cognitive decline // Elife. 2017. 6. pii: e22978. doi: 10.7554/eLife.22978. [Epub ahead of print].
6. Leo L.M., Pamplona F. A. Elevated Plus Maze Test to Assess Anxiety-like Behavior in the Mouse // Neuroscience. 2014. No 4(16). doi: https://doi.org/10.21769/bioprotoc.1211.
7. Lugo J.N., Smith G.D., Holley A.J. Trace fear conditioning in mice // J. Vis. Exp. 2014. No. 85. doi: 10.3791/51180.
8. Mak E., Gabel S., Su L., Williams G.B., Arnold R., Passamonti L., Vazquez Rodríguez P., Surendranathan A., Bevan-Jones W.R., Rowe J.B., O'Brien J.T. Multi-modal MRI investigation of volumetric and microstructural changes in the hippocampus and its subfields in mild cognitive impairment, Alzheimer's disease, and dementia with Lewy bodies // Int. Psychogeriatr. 2017. P. 1-11. doi: 10.1017/s1041610216002143. [Epub ahead of print].
9. Martin L, Iceberg E. Quantifying Social Motivation in Mice Using Operant Conditioning // J. Vis. Exp. 2015. No. 102. e53009. doi: 10.3791/53009.
10. Morland R.H., Novejarque A., Spicer C., Pheby T., Rice A.S. Enhanced c-Fosexpression in the central amygdala correlates with increased thigmotaxis inrats with peripheral nerve injury // Eur. J. Pain (Lond. Engl.). 2016. No. 20(7). P.1140-1154. doi: 10.1002/ejp.839.
11. Nesteruk M., Nesteruk T., Styczyńska M., Mandecka M., Barczak A., Barcikowska M. Combined use of biochemical and volumetric biomarkers to assess the risk of conversion of mild cognitive impairment to Alzheimer's disease // Folia Neuropathol. 2016. No. 54(4). P. 369-374. doi: 10.5114/fn.2016.64815.
12. Prieto G.A., Trieu B.H., Dang C.T., Bilousova T., Gylys K.H., Berchtold N.C., Lynch G., Cotman C.W. Pharmacological Rescue of Long-Term Potentiation in Alzheimer Diseased Synapses // J. Neurosci. 2017. No. 37(5). P. 1197-1212. doi: 10.1523/jneurosci.2774-16.2016.
13. Robinson M., Lee B.Y., Hane F.T. Recent Progress in Alzheimer's Disease Research, Part 2: Genetics and Epidemiology // J. Alzheimers Dis. 2017. doi: 10.3233/jad-161149. [Epub ahead of print].
14. Seibenhener M.L., Wooten M.C. Use of the Open Field Maze to Measure Locomotor and Anxiety-like Behavior in Mice // J. Vis. Exp. 2015. No. 96. e52434. doi:10.3791/52434.
15. Takao K., Miyakawa T. Light/dark Transition Test for Mice // J. Vis. Exp. 2006. No. 1. e104. doi:10.3791/104.
16. Thangavel R., Van Hoesen G.W., Zaheer A. Posterior parahippocampal gyrus pathology in Alzheimer’s disease // Neuroscience. 2008. No. 154(2). P. 667-676. doi:10.1016/j.neuroscience.2008.03.077.
17. Gorina YA.V., Komleva YU.K., Lopatina O.L., Volkova V.V., CHernyh A.I., SHabalova A.A., Semenchukov A.A., Olovyannikova R.YA., Salmina A.B. Batareya testov dlya povedencheskogo fenotipirovaniya stareyushchih zhivotnyh v ehksperimente // Uspekhi gerontologii. 2017. T.1. S. 49-56.
18. Cubinková V., Valachová B., Brezovaková V., Szabó R., Zimová I., Kostecká Z., Jadhav S. Next generation tau models in Alzheimer's disease research - virus based gene delivery systems // Acta Virol. 2017. No. 61(1). doi: 10.4149/av. 2017. 01. 13. [Epub ahead of print].
19. Guillozet A.L., Weintraub S., Mash D.C., Mesulam M.M. Neurofibrillary tangles, amyloid, and memory in aging and mild cognitive impairment // Arch Neurol. 2003. No. 60(5). P. 729-736. doi:10.1001/archneur.60.5.729.
20. Jacobs S.A., Huang F., Tsien J.Z., Wei W. Social Recognition Memory Test in Rodents // Neuroscience. 2016. No. 6(9). doi: https://doi.org/10.21769/bioprotoc.1804.
21. Leal S.L., Landau S.M., Bell R.K., Jagust W.J. Hippocampal activation is associated with longitudinal amyloid accumulation and cognitive decline // Elife. 2017. 6. pii: e22978. doi: 10.7554/eLife.22978. [Epub ahead of print].
22. Leo L.M., Pamplona F. A. Elevated Plus Maze Test to Assess Anxiety-like Behavior in the Mouse // Neuroscience. 2014. No 4(16). doi: https://doi.org/10.21769/bioprotoc.1211.
23. Lugo J.N., Smith G.D., Holley A.J. Trace fear conditioning in mice // J. Vis. Exp. 2014. No. 85. doi: 10.3791/51180.
24. Mak E., Gabel S., Su L., Williams G.B., Arnold R., Passamonti L., Vazquez Rodríguez P., Surendranathan A., Bevan-Jones W.R., Rowe J.B., O'Brien J.T. Multi-modal MRI investigation of volumetric and microstructural changes in the hippocampus and its subfields in mild cognitive impairment, Alzheimer's disease, and dementia with Lewy bodies // Int. Psychogeriatr. 2017. P. 1-11. doi: 10.1017/s1041610216002143. [Epub ahead of print].
25. Martin L, Iceberg E. Quantifying Social Motivation in Mice Using Operant Conditioning // J. Vis. Exp. 2015. No. 102. e53009. doi: 10.3791/53009.
26. Morland R.H., Novejarque A., Spicer C., Pheby T., Rice A.S. Enhanced c-Fosexpression in the central amygdala correlates with increased thigmotaxis inrats with peripheral nerve injury // Eur. J. Pain (Lond. Engl.). 2016. No. 20(7). P.1140-1154. doi: 10.1002/ejp.839.
27. Nesteruk M., Nesteruk T., Styczyńska M., Mandecka M., Barczak A., Barcikowska M. Combined use of biochemical and volumetric biomarkers to assess the risk of conversion of mild cognitive impairment to Alzheimer's disease // Folia Neuropathol. 2016. No. 54(4). P. 369-374. doi: 10.5114/fn.2016.64815.
28. Prieto G.A., Trieu B.H., Dang C.T., Bilousova T., Gylys K.H., Berchtold N.C., Lynch G., Cotman C.W. Pharmacological Rescue of Long-Term Potentiation in Alzheimer Diseased Synapses // J. Neurosci. 2017. No. 37(5). P. 1197-1212. doi: 10.1523/jneurosci.2774-16.2016.
29. Robinson M., Lee B.Y., Hane F.T. Recent Progress in Alzheimer's Disease Research, Part 2: Genetics and Epidemiology // J. Alzheimers Dis. 2017. doi: 10.3233/jad-161149. [Epub ahead of print].
30. Seibenhener M.L., Wooten M.C. Use of the Open Field Maze to Measure Locomotor and Anxiety-like Behavior in Mice // J. Vis. Exp. 2015. No. 96. e52434. doi:10.3791/52434.
31. Takao K., Miyakawa T. Light/dark Transition Test for Mice // J. Vis. Exp. 2006. No. 1. e104. doi:10.3791/104.
32. Thangavel R., Van Hoesen G.W., Zaheer A. Posterior parahippocampal gyrus pathology in Alzheimer’s disease // Neuroscience. 2008. No. 154(2). P. 667-676. doi:10.1016/j.neuroscience.2008.03.077.
Рецензия
Для цитирования:
Горина Я.В., Комлева Ю.К., Лопатина О.Л., Черных А.И., Салмина А.Б. Поведенческий фенотипический анализ животных с генетической моделью болезни Альцгеймера. БИОМЕДИЦИНА. 2017;(3):47-59.
For citation:
Gorina Y.V., Komleva Yu.K., Lopatina O.L., Chernykh A.I., Salmina A.B. Behavioral phenotypic analysis of animals with a genetic model of Alzheimer's disease. Journal Biomed. 2017;(3):47-59. (In Russ.)