Melatonin modifies SOX2+ cell proliferation in dentate gyrus and modulates SIRT1 and MECP2 in long-term sleep deprivation
Melatonin is a pleiotropic molecule that, after a short-term sleep deprivation, promotes the proliferation of neural stem cells in the adult hippocampus. However, this effect has not been observed in long-term sleep deprivation. The precise mechanism exerted by melatonin on the modulation of neural...
Ausführliche Beschreibung
Autor*in: |
Alan Hinojosa-Godinez [verfasserIn] Luis F Jave-Suarez [verfasserIn] Mario Flores-Soto [verfasserIn] Alma Y Gálvez-Contreras [verfasserIn] Sonia Luquín [verfasserIn] Edith Oregon-Romero [verfasserIn] Oscar González-Pérez [verfasserIn] Rocio E González-Castañeda [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2019 |
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Übergeordnetes Werk: |
In: Neural Regeneration Research - Wolters Kluwer Medknow Publications, 2014, 14(2019), 10, Seite 1787-1795 |
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Übergeordnetes Werk: |
volume:14 ; year:2019 ; number:10 ; pages:1787-1795 |
Links: |
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DOI / URN: |
10.4103/1673-5374.257537 |
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Katalog-ID: |
DOAJ010400931 |
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520 | |a Melatonin is a pleiotropic molecule that, after a short-term sleep deprivation, promotes the proliferation of neural stem cells in the adult hippocampus. However, this effect has not been observed in long-term sleep deprivation. The precise mechanism exerted by melatonin on the modulation of neural stem cells is not entirely elucidated, but evidence indicates that epigenetic regulators may be involved in this process. In this study, we investigated the effect of melatonin treatment during a 96-hour sleep deprivation and analyzed the expression of epigenetic modulators predicted by computational text mining and keyword clusterization. Our results showed that the administration of melatonin under sleep-deprived conditions increased the MECP2 expression and reduced the SIRT1 expression in the dentate gyrus. We observed that let-7b, mir-132, and mir-124 were highly expressed in the dentate gyrus after melatonin administration, but they were not modified by sleep deprivation. In addition, we found more Sox2+/5-bromo-2′-deoxyuridine (BrdU)+ cells in the subgranular zone of the sleep-deprived group treated with melatonin than in the untreated group. These findings may support the notion that melatonin modifies the expression of epigenetic mediators that, in turn, regulate the proliferation of neural progenitor cells in the adult dentate gyrus under long-term sleep-deprived conditions. All procedures performed in this study were approved by the Animal Ethics Committee of the University of Guadalajara, Mexico (approval No. CI-16610) on January 2, 2016. | ||
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10.4103/1673-5374.257537 doi (DE-627)DOAJ010400931 (DE-599)DOAJ5a03fdb3194c4196b2df22c466f755fa DE-627 ger DE-627 rakwb eng RC346-429 Alan Hinojosa-Godinez verfasserin aut Melatonin modifies SOX2+ cell proliferation in dentate gyrus and modulates SIRT1 and MECP2 in long-term sleep deprivation 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Melatonin is a pleiotropic molecule that, after a short-term sleep deprivation, promotes the proliferation of neural stem cells in the adult hippocampus. However, this effect has not been observed in long-term sleep deprivation. The precise mechanism exerted by melatonin on the modulation of neural stem cells is not entirely elucidated, but evidence indicates that epigenetic regulators may be involved in this process. In this study, we investigated the effect of melatonin treatment during a 96-hour sleep deprivation and analyzed the expression of epigenetic modulators predicted by computational text mining and keyword clusterization. Our results showed that the administration of melatonin under sleep-deprived conditions increased the MECP2 expression and reduced the SIRT1 expression in the dentate gyrus. We observed that let-7b, mir-132, and mir-124 were highly expressed in the dentate gyrus after melatonin administration, but they were not modified by sleep deprivation. In addition, we found more Sox2+/5-bromo-2′-deoxyuridine (BrdU)+ cells in the subgranular zone of the sleep-deprived group treated with melatonin than in the untreated group. These findings may support the notion that melatonin modifies the expression of epigenetic mediators that, in turn, regulate the proliferation of neural progenitor cells in the adult dentate gyrus under long-term sleep-deprived conditions. All procedures performed in this study were approved by the Animal Ethics Committee of the University of Guadalajara, Mexico (approval No. CI-16610) on January 2, 2016. sleep-deprivation; melatonin; microRNA; neurogenesis; Sirtuin 1; SIRT1; methyl-CpG-binding protein 2; MECP2; epigenetic; text-mining; mir-9; let-7b Neurology. Diseases of the nervous system Luis F Jave-Suarez verfasserin aut Mario Flores-Soto verfasserin aut Alma Y Gálvez-Contreras verfasserin aut Sonia Luquín verfasserin aut Edith Oregon-Romero verfasserin aut Oscar González-Pérez verfasserin aut Rocio E González-Castañeda verfasserin aut In Neural Regeneration Research Wolters Kluwer Medknow Publications, 2014 14(2019), 10, Seite 1787-1795 (DE-627)545785499 (DE-600)2388460-5 18767958 nnns volume:14 year:2019 number:10 pages:1787-1795 https://doi.org/10.4103/1673-5374.257537 kostenfrei https://doaj.org/article/5a03fdb3194c4196b2df22c466f755fa kostenfrei http://www.nrronline.org/article.asp?issn=1673-5374;year=2019;volume=14;issue=10;spage=1787;epage=1795;aulast=Hinojosa-Godinez kostenfrei https://doaj.org/toc/1673-5374 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_374 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_2700 GBV_ILN_2817 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 14 2019 10 1787-1795 |
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10.4103/1673-5374.257537 doi (DE-627)DOAJ010400931 (DE-599)DOAJ5a03fdb3194c4196b2df22c466f755fa DE-627 ger DE-627 rakwb eng RC346-429 Alan Hinojosa-Godinez verfasserin aut Melatonin modifies SOX2+ cell proliferation in dentate gyrus and modulates SIRT1 and MECP2 in long-term sleep deprivation 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Melatonin is a pleiotropic molecule that, after a short-term sleep deprivation, promotes the proliferation of neural stem cells in the adult hippocampus. However, this effect has not been observed in long-term sleep deprivation. The precise mechanism exerted by melatonin on the modulation of neural stem cells is not entirely elucidated, but evidence indicates that epigenetic regulators may be involved in this process. In this study, we investigated the effect of melatonin treatment during a 96-hour sleep deprivation and analyzed the expression of epigenetic modulators predicted by computational text mining and keyword clusterization. Our results showed that the administration of melatonin under sleep-deprived conditions increased the MECP2 expression and reduced the SIRT1 expression in the dentate gyrus. We observed that let-7b, mir-132, and mir-124 were highly expressed in the dentate gyrus after melatonin administration, but they were not modified by sleep deprivation. In addition, we found more Sox2+/5-bromo-2′-deoxyuridine (BrdU)+ cells in the subgranular zone of the sleep-deprived group treated with melatonin than in the untreated group. These findings may support the notion that melatonin modifies the expression of epigenetic mediators that, in turn, regulate the proliferation of neural progenitor cells in the adult dentate gyrus under long-term sleep-deprived conditions. All procedures performed in this study were approved by the Animal Ethics Committee of the University of Guadalajara, Mexico (approval No. CI-16610) on January 2, 2016. sleep-deprivation; melatonin; microRNA; neurogenesis; Sirtuin 1; SIRT1; methyl-CpG-binding protein 2; MECP2; epigenetic; text-mining; mir-9; let-7b Neurology. Diseases of the nervous system Luis F Jave-Suarez verfasserin aut Mario Flores-Soto verfasserin aut Alma Y Gálvez-Contreras verfasserin aut Sonia Luquín verfasserin aut Edith Oregon-Romero verfasserin aut Oscar González-Pérez verfasserin aut Rocio E González-Castañeda verfasserin aut In Neural Regeneration Research Wolters Kluwer Medknow Publications, 2014 14(2019), 10, Seite 1787-1795 (DE-627)545785499 (DE-600)2388460-5 18767958 nnns volume:14 year:2019 number:10 pages:1787-1795 https://doi.org/10.4103/1673-5374.257537 kostenfrei https://doaj.org/article/5a03fdb3194c4196b2df22c466f755fa kostenfrei http://www.nrronline.org/article.asp?issn=1673-5374;year=2019;volume=14;issue=10;spage=1787;epage=1795;aulast=Hinojosa-Godinez kostenfrei https://doaj.org/toc/1673-5374 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_374 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_2700 GBV_ILN_2817 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 14 2019 10 1787-1795 |
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10.4103/1673-5374.257537 doi (DE-627)DOAJ010400931 (DE-599)DOAJ5a03fdb3194c4196b2df22c466f755fa DE-627 ger DE-627 rakwb eng RC346-429 Alan Hinojosa-Godinez verfasserin aut Melatonin modifies SOX2+ cell proliferation in dentate gyrus and modulates SIRT1 and MECP2 in long-term sleep deprivation 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Melatonin is a pleiotropic molecule that, after a short-term sleep deprivation, promotes the proliferation of neural stem cells in the adult hippocampus. However, this effect has not been observed in long-term sleep deprivation. The precise mechanism exerted by melatonin on the modulation of neural stem cells is not entirely elucidated, but evidence indicates that epigenetic regulators may be involved in this process. In this study, we investigated the effect of melatonin treatment during a 96-hour sleep deprivation and analyzed the expression of epigenetic modulators predicted by computational text mining and keyword clusterization. Our results showed that the administration of melatonin under sleep-deprived conditions increased the MECP2 expression and reduced the SIRT1 expression in the dentate gyrus. We observed that let-7b, mir-132, and mir-124 were highly expressed in the dentate gyrus after melatonin administration, but they were not modified by sleep deprivation. In addition, we found more Sox2+/5-bromo-2′-deoxyuridine (BrdU)+ cells in the subgranular zone of the sleep-deprived group treated with melatonin than in the untreated group. These findings may support the notion that melatonin modifies the expression of epigenetic mediators that, in turn, regulate the proliferation of neural progenitor cells in the adult dentate gyrus under long-term sleep-deprived conditions. All procedures performed in this study were approved by the Animal Ethics Committee of the University of Guadalajara, Mexico (approval No. CI-16610) on January 2, 2016. sleep-deprivation; melatonin; microRNA; neurogenesis; Sirtuin 1; SIRT1; methyl-CpG-binding protein 2; MECP2; epigenetic; text-mining; mir-9; let-7b Neurology. Diseases of the nervous system Luis F Jave-Suarez verfasserin aut Mario Flores-Soto verfasserin aut Alma Y Gálvez-Contreras verfasserin aut Sonia Luquín verfasserin aut Edith Oregon-Romero verfasserin aut Oscar González-Pérez verfasserin aut Rocio E González-Castañeda verfasserin aut In Neural Regeneration Research Wolters Kluwer Medknow Publications, 2014 14(2019), 10, Seite 1787-1795 (DE-627)545785499 (DE-600)2388460-5 18767958 nnns volume:14 year:2019 number:10 pages:1787-1795 https://doi.org/10.4103/1673-5374.257537 kostenfrei https://doaj.org/article/5a03fdb3194c4196b2df22c466f755fa kostenfrei http://www.nrronline.org/article.asp?issn=1673-5374;year=2019;volume=14;issue=10;spage=1787;epage=1795;aulast=Hinojosa-Godinez kostenfrei https://doaj.org/toc/1673-5374 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_374 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_2700 GBV_ILN_2817 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 14 2019 10 1787-1795 |
allfieldsGer |
10.4103/1673-5374.257537 doi (DE-627)DOAJ010400931 (DE-599)DOAJ5a03fdb3194c4196b2df22c466f755fa DE-627 ger DE-627 rakwb eng RC346-429 Alan Hinojosa-Godinez verfasserin aut Melatonin modifies SOX2+ cell proliferation in dentate gyrus and modulates SIRT1 and MECP2 in long-term sleep deprivation 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Melatonin is a pleiotropic molecule that, after a short-term sleep deprivation, promotes the proliferation of neural stem cells in the adult hippocampus. However, this effect has not been observed in long-term sleep deprivation. The precise mechanism exerted by melatonin on the modulation of neural stem cells is not entirely elucidated, but evidence indicates that epigenetic regulators may be involved in this process. In this study, we investigated the effect of melatonin treatment during a 96-hour sleep deprivation and analyzed the expression of epigenetic modulators predicted by computational text mining and keyword clusterization. Our results showed that the administration of melatonin under sleep-deprived conditions increased the MECP2 expression and reduced the SIRT1 expression in the dentate gyrus. We observed that let-7b, mir-132, and mir-124 were highly expressed in the dentate gyrus after melatonin administration, but they were not modified by sleep deprivation. In addition, we found more Sox2+/5-bromo-2′-deoxyuridine (BrdU)+ cells in the subgranular zone of the sleep-deprived group treated with melatonin than in the untreated group. These findings may support the notion that melatonin modifies the expression of epigenetic mediators that, in turn, regulate the proliferation of neural progenitor cells in the adult dentate gyrus under long-term sleep-deprived conditions. All procedures performed in this study were approved by the Animal Ethics Committee of the University of Guadalajara, Mexico (approval No. CI-16610) on January 2, 2016. sleep-deprivation; melatonin; microRNA; neurogenesis; Sirtuin 1; SIRT1; methyl-CpG-binding protein 2; MECP2; epigenetic; text-mining; mir-9; let-7b Neurology. Diseases of the nervous system Luis F Jave-Suarez verfasserin aut Mario Flores-Soto verfasserin aut Alma Y Gálvez-Contreras verfasserin aut Sonia Luquín verfasserin aut Edith Oregon-Romero verfasserin aut Oscar González-Pérez verfasserin aut Rocio E González-Castañeda verfasserin aut In Neural Regeneration Research Wolters Kluwer Medknow Publications, 2014 14(2019), 10, Seite 1787-1795 (DE-627)545785499 (DE-600)2388460-5 18767958 nnns volume:14 year:2019 number:10 pages:1787-1795 https://doi.org/10.4103/1673-5374.257537 kostenfrei https://doaj.org/article/5a03fdb3194c4196b2df22c466f755fa kostenfrei http://www.nrronline.org/article.asp?issn=1673-5374;year=2019;volume=14;issue=10;spage=1787;epage=1795;aulast=Hinojosa-Godinez kostenfrei https://doaj.org/toc/1673-5374 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_374 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_2700 GBV_ILN_2817 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 14 2019 10 1787-1795 |
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Melatonin modifies SOX2+ cell proliferation in dentate gyrus and modulates SIRT1 and MECP2 in long-term sleep deprivation |
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Melatonin is a pleiotropic molecule that, after a short-term sleep deprivation, promotes the proliferation of neural stem cells in the adult hippocampus. However, this effect has not been observed in long-term sleep deprivation. The precise mechanism exerted by melatonin on the modulation of neural stem cells is not entirely elucidated, but evidence indicates that epigenetic regulators may be involved in this process. In this study, we investigated the effect of melatonin treatment during a 96-hour sleep deprivation and analyzed the expression of epigenetic modulators predicted by computational text mining and keyword clusterization. Our results showed that the administration of melatonin under sleep-deprived conditions increased the MECP2 expression and reduced the SIRT1 expression in the dentate gyrus. We observed that let-7b, mir-132, and mir-124 were highly expressed in the dentate gyrus after melatonin administration, but they were not modified by sleep deprivation. In addition, we found more Sox2+/5-bromo-2′-deoxyuridine (BrdU)+ cells in the subgranular zone of the sleep-deprived group treated with melatonin than in the untreated group. These findings may support the notion that melatonin modifies the expression of epigenetic mediators that, in turn, regulate the proliferation of neural progenitor cells in the adult dentate gyrus under long-term sleep-deprived conditions. All procedures performed in this study were approved by the Animal Ethics Committee of the University of Guadalajara, Mexico (approval No. CI-16610) on January 2, 2016. |
abstractGer |
Melatonin is a pleiotropic molecule that, after a short-term sleep deprivation, promotes the proliferation of neural stem cells in the adult hippocampus. However, this effect has not been observed in long-term sleep deprivation. The precise mechanism exerted by melatonin on the modulation of neural stem cells is not entirely elucidated, but evidence indicates that epigenetic regulators may be involved in this process. In this study, we investigated the effect of melatonin treatment during a 96-hour sleep deprivation and analyzed the expression of epigenetic modulators predicted by computational text mining and keyword clusterization. Our results showed that the administration of melatonin under sleep-deprived conditions increased the MECP2 expression and reduced the SIRT1 expression in the dentate gyrus. We observed that let-7b, mir-132, and mir-124 were highly expressed in the dentate gyrus after melatonin administration, but they were not modified by sleep deprivation. In addition, we found more Sox2+/5-bromo-2′-deoxyuridine (BrdU)+ cells in the subgranular zone of the sleep-deprived group treated with melatonin than in the untreated group. These findings may support the notion that melatonin modifies the expression of epigenetic mediators that, in turn, regulate the proliferation of neural progenitor cells in the adult dentate gyrus under long-term sleep-deprived conditions. All procedures performed in this study were approved by the Animal Ethics Committee of the University of Guadalajara, Mexico (approval No. CI-16610) on January 2, 2016. |
abstract_unstemmed |
Melatonin is a pleiotropic molecule that, after a short-term sleep deprivation, promotes the proliferation of neural stem cells in the adult hippocampus. However, this effect has not been observed in long-term sleep deprivation. The precise mechanism exerted by melatonin on the modulation of neural stem cells is not entirely elucidated, but evidence indicates that epigenetic regulators may be involved in this process. In this study, we investigated the effect of melatonin treatment during a 96-hour sleep deprivation and analyzed the expression of epigenetic modulators predicted by computational text mining and keyword clusterization. Our results showed that the administration of melatonin under sleep-deprived conditions increased the MECP2 expression and reduced the SIRT1 expression in the dentate gyrus. We observed that let-7b, mir-132, and mir-124 were highly expressed in the dentate gyrus after melatonin administration, but they were not modified by sleep deprivation. In addition, we found more Sox2+/5-bromo-2′-deoxyuridine (BrdU)+ cells in the subgranular zone of the sleep-deprived group treated with melatonin than in the untreated group. These findings may support the notion that melatonin modifies the expression of epigenetic mediators that, in turn, regulate the proliferation of neural progenitor cells in the adult dentate gyrus under long-term sleep-deprived conditions. All procedures performed in this study were approved by the Animal Ethics Committee of the University of Guadalajara, Mexico (approval No. CI-16610) on January 2, 2016. |
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container_issue |
10 |
title_short |
Melatonin modifies SOX2+ cell proliferation in dentate gyrus and modulates SIRT1 and MECP2 in long-term sleep deprivation |
url |
https://doi.org/10.4103/1673-5374.257537 https://doaj.org/article/5a03fdb3194c4196b2df22c466f755fa http://www.nrronline.org/article.asp?issn=1673-5374;year=2019;volume=14;issue=10;spage=1787;epage=1795;aulast=Hinojosa-Godinez https://doaj.org/toc/1673-5374 |
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author2 |
Luis F Jave-Suarez Mario Flores-Soto Alma Y Gálvez-Contreras Sonia Luquín Edith Oregon-Romero Oscar González-Pérez Rocio E González-Castañeda |
author2Str |
Luis F Jave-Suarez Mario Flores-Soto Alma Y Gálvez-Contreras Sonia Luquín Edith Oregon-Romero Oscar González-Pérez Rocio E González-Castañeda |
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doi_str |
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up_date |
2024-07-03T14:37:22.248Z |
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