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SIRT1 Interacts with Prepro-Orexin in the Hypothalamus in SOD1G93A Mice

The participation of silent mating type information regulation 2 homolog 1 (SIRT1) in amyotrophic lateral sclerosis (ALS) has been reported in many studies. However, the role of the expression and function of SIRT1 in the hypothalamus in ALS remains unknown. In the current study, we performed wester...

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Autores principales: Zhang, Gan, Liu, Rong, Sheng, Zhaofu, Zhang, Yonghe, Fan, Dongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031500/
https://www.ncbi.nlm.nih.gov/pubmed/35448021
http://dx.doi.org/10.3390/brainsci12040490
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author Zhang, Gan
Liu, Rong
Sheng, Zhaofu
Zhang, Yonghe
Fan, Dongsheng
author_facet Zhang, Gan
Liu, Rong
Sheng, Zhaofu
Zhang, Yonghe
Fan, Dongsheng
author_sort Zhang, Gan
collection PubMed
description The participation of silent mating type information regulation 2 homolog 1 (SIRT1) in amyotrophic lateral sclerosis (ALS) has been reported in many studies. However, the role of the expression and function of SIRT1 in the hypothalamus in ALS remains unknown. In the current study, we performed western blot, co-immunoprecipitation and immunofluorescence analyses to determine the expression and in-depth mechanism of SIRT1 in the hypothalamus in SOD1G93A transgenic mice. We found that SIRT1 was overexpressed in the hypothalamus after motor symptom onset. In addition, SIRT1 interacted with prepro-orexin, a molecule involved in energy balance and the sleep/wake cycle, in both preclinical and clinical ALS regardless of whether SIRT1 levels were elevated. These findings indicate that SIRT1 might participate in sleep and metabolic changes in ALS, suggesting that SIRT1 is a new target for ALS treatment.
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spelling pubmed-90315002022-04-23 SIRT1 Interacts with Prepro-Orexin in the Hypothalamus in SOD1G93A Mice Zhang, Gan Liu, Rong Sheng, Zhaofu Zhang, Yonghe Fan, Dongsheng Brain Sci Brief Report The participation of silent mating type information regulation 2 homolog 1 (SIRT1) in amyotrophic lateral sclerosis (ALS) has been reported in many studies. However, the role of the expression and function of SIRT1 in the hypothalamus in ALS remains unknown. In the current study, we performed western blot, co-immunoprecipitation and immunofluorescence analyses to determine the expression and in-depth mechanism of SIRT1 in the hypothalamus in SOD1G93A transgenic mice. We found that SIRT1 was overexpressed in the hypothalamus after motor symptom onset. In addition, SIRT1 interacted with prepro-orexin, a molecule involved in energy balance and the sleep/wake cycle, in both preclinical and clinical ALS regardless of whether SIRT1 levels were elevated. These findings indicate that SIRT1 might participate in sleep and metabolic changes in ALS, suggesting that SIRT1 is a new target for ALS treatment. MDPI 2022-04-11 /pmc/articles/PMC9031500/ /pubmed/35448021 http://dx.doi.org/10.3390/brainsci12040490 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Zhang, Gan
Liu, Rong
Sheng, Zhaofu
Zhang, Yonghe
Fan, Dongsheng
SIRT1 Interacts with Prepro-Orexin in the Hypothalamus in SOD1G93A Mice
title SIRT1 Interacts with Prepro-Orexin in the Hypothalamus in SOD1G93A Mice
title_full SIRT1 Interacts with Prepro-Orexin in the Hypothalamus in SOD1G93A Mice
title_fullStr SIRT1 Interacts with Prepro-Orexin in the Hypothalamus in SOD1G93A Mice
title_full_unstemmed SIRT1 Interacts with Prepro-Orexin in the Hypothalamus in SOD1G93A Mice
title_short SIRT1 Interacts with Prepro-Orexin in the Hypothalamus in SOD1G93A Mice
title_sort sirt1 interacts with prepro-orexin in the hypothalamus in sod1g93a mice
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031500/
https://www.ncbi.nlm.nih.gov/pubmed/35448021
http://dx.doi.org/10.3390/brainsci12040490
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