Time-restricted feeding modulates the DNA methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia

Objective: Vascular dementia (VaD) is the second most common cause of dementia worldwide. The increasing contribution of lifestyle-associated risk factors to VaD has pointed towards gene-environment interactions (i.e. epigenetics). This study thus aims to investigate the DNA methylation landscape in...

Full description

Saved in:
Bibliographic Details
Main Authors: Selvaraji, Sharmelee, Efthymios, Motakis, Foo, Roger Sik Yin, Fann, David Y., Lai, Mitchell Kim Peng, Chen, Christopher Li Hsian, Lim, Kah-Leong, Arumugam, Thiruma V.
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2022
Subjects:
Online Access:https://hdl.handle.net/10356/163083
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-163083
record_format dspace
spelling sg-ntu-dr.10356-1630832023-03-05T16:52:10Z Time-restricted feeding modulates the DNA methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia Selvaraji, Sharmelee Efthymios, Motakis Foo, Roger Sik Yin Fann, David Y. Lai, Mitchell Kim Peng Chen, Christopher Li Hsian Lim, Kah-Leong Arumugam, Thiruma V. Lee Kong Chian School of Medicine (LKCMedicine) Science::Medicine Intermittent Fasting DNA Methylation Objective: Vascular dementia (VaD) is the second most common cause of dementia worldwide. The increasing contribution of lifestyle-associated risk factors to VaD has pointed towards gene-environment interactions (i.e. epigenetics). This study thus aims to investigate the DNA methylation landscape in a chronic cerebral hypoperfusion (CCH) mouse model of VaD. As a nexus between the gene-environment interaction, intermittent fasting (IF) was introduced as a prophylactic intervention. Methods: Bilateral common carotid artery stenosis (BCAS) was used to induce CCH by placing micro-coils of 0.18 mm in each common carotid artery of the mice. The coils were left in the mice for 7, 15 and 30 days to study temporal differences. IF was introduced for 16 h daily for 4 months prior to BCAS. Reduced Representation Bisulfite Sequencing (RRBS) was used to study the DNA methylation landscape. Cognitive impairment was measured using Barnes Maze Test. White matter lesions (WML) and neuronal loss were measured using Luxol fast blue staining and cresyl violet staining respectively. Results: IF mice subjected to CCH displayed significantly better cognitive learning ability and memory, improved neuropathological alterations with reduced WMLs and neuronal loss. Modulation of DNA methylation patterns in the cortex of AL CCH mice was re-modelled and signs of reversal was observed in IF CCH mice across all three timepoints. Conclusions: These findings provide an understanding of how IF may protect the brain against damage caused by CCH and show promise in offering potential beneficial effects in mitigating the neuropathology and cognitive deficits in VaD. Ministry of Education (MOE) National Medical Research Council (NMRC) Published version This work was supported by the National Medical Research Council Research Grants (NMRC-CBRG-0102/2016; NMRC/CSA-SI/007/2016 and NMRC/OFIRG/ 0036/2017), Singapore and the Ministry of Education (MOE2017-T3-1-002), Singapore and La Trobe University, Australia. 2022-11-21T02:53:40Z 2022-11-21T02:53:40Z 2022 Journal Article Selvaraji, S., Efthymios, M., Foo, R. S. Y., Fann, D. Y., Lai, M. K. P., Chen, C. L. H., Lim, K. & Arumugam, T. V. (2022). Time-restricted feeding modulates the DNA methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia. Theranostics, 12(7), 3007-3023. https://dx.doi.org/10.7150/thno.71815 1838-7640 https://hdl.handle.net/10356/163083 10.7150/thno.71815 35547760 2-s2.0-85128592658 7 12 3007 3023 en NMRC-CBRG-0102/2016 NMRC/CSA-SI/007/2016 NMRC/OFIRG/ 0036/2017 MOE2017-T3-1-002 Theranostics © The author(s). This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Medicine
Intermittent Fasting
DNA Methylation
spellingShingle Science::Medicine
Intermittent Fasting
DNA Methylation
Selvaraji, Sharmelee
Efthymios, Motakis
Foo, Roger Sik Yin
Fann, David Y.
Lai, Mitchell Kim Peng
Chen, Christopher Li Hsian
Lim, Kah-Leong
Arumugam, Thiruma V.
Time-restricted feeding modulates the DNA methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia
description Objective: Vascular dementia (VaD) is the second most common cause of dementia worldwide. The increasing contribution of lifestyle-associated risk factors to VaD has pointed towards gene-environment interactions (i.e. epigenetics). This study thus aims to investigate the DNA methylation landscape in a chronic cerebral hypoperfusion (CCH) mouse model of VaD. As a nexus between the gene-environment interaction, intermittent fasting (IF) was introduced as a prophylactic intervention. Methods: Bilateral common carotid artery stenosis (BCAS) was used to induce CCH by placing micro-coils of 0.18 mm in each common carotid artery of the mice. The coils were left in the mice for 7, 15 and 30 days to study temporal differences. IF was introduced for 16 h daily for 4 months prior to BCAS. Reduced Representation Bisulfite Sequencing (RRBS) was used to study the DNA methylation landscape. Cognitive impairment was measured using Barnes Maze Test. White matter lesions (WML) and neuronal loss were measured using Luxol fast blue staining and cresyl violet staining respectively. Results: IF mice subjected to CCH displayed significantly better cognitive learning ability and memory, improved neuropathological alterations with reduced WMLs and neuronal loss. Modulation of DNA methylation patterns in the cortex of AL CCH mice was re-modelled and signs of reversal was observed in IF CCH mice across all three timepoints. Conclusions: These findings provide an understanding of how IF may protect the brain against damage caused by CCH and show promise in offering potential beneficial effects in mitigating the neuropathology and cognitive deficits in VaD.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Selvaraji, Sharmelee
Efthymios, Motakis
Foo, Roger Sik Yin
Fann, David Y.
Lai, Mitchell Kim Peng
Chen, Christopher Li Hsian
Lim, Kah-Leong
Arumugam, Thiruma V.
format Article
author Selvaraji, Sharmelee
Efthymios, Motakis
Foo, Roger Sik Yin
Fann, David Y.
Lai, Mitchell Kim Peng
Chen, Christopher Li Hsian
Lim, Kah-Leong
Arumugam, Thiruma V.
author_sort Selvaraji, Sharmelee
title Time-restricted feeding modulates the DNA methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia
title_short Time-restricted feeding modulates the DNA methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia
title_full Time-restricted feeding modulates the DNA methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia
title_fullStr Time-restricted feeding modulates the DNA methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia
title_full_unstemmed Time-restricted feeding modulates the DNA methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia
title_sort time-restricted feeding modulates the dna methylation landscape, attenuates hallmark neuropathology and cognitive impairment in a mouse model of vascular dementia
publishDate 2022
url https://hdl.handle.net/10356/163083
_version_ 1759858386308956160