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Liver Growth Factor “LGF” as a Therapeutic Agent for Alzheimer’s Disease
Alzheimer’s disease (AD) is a progressive degenerative disorder and the most common cause of dementia in aging populations. Although the pathological hallmarks of AD are well defined, currently no effective therapy exists. Liver growth factor (LGF) is a hepatic albumin–bilirubin complex with activit...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730107/ https://www.ncbi.nlm.nih.gov/pubmed/33276671 http://dx.doi.org/10.3390/ijms21239201 |
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author | Gonzalo-Gobernado, Rafael Perucho, Juan Vallejo-Muñoz, Manuela Casarejos, Maria José Reimers, Diana Jiménez-Escrig, Adriano Gómez, Ana Ulzurrun de Asanza, Gonzalo M. Bazán, Eulalia |
author_facet | Gonzalo-Gobernado, Rafael Perucho, Juan Vallejo-Muñoz, Manuela Casarejos, Maria José Reimers, Diana Jiménez-Escrig, Adriano Gómez, Ana Ulzurrun de Asanza, Gonzalo M. Bazán, Eulalia |
author_sort | Gonzalo-Gobernado, Rafael |
collection | PubMed |
description | Alzheimer’s disease (AD) is a progressive degenerative disorder and the most common cause of dementia in aging populations. Although the pathological hallmarks of AD are well defined, currently no effective therapy exists. Liver growth factor (LGF) is a hepatic albumin–bilirubin complex with activity as a tissue regenerating factor in several neurodegenerative disorders such as Parkinson’s disease and Friedreich’s ataxia. Our aim here was to analyze the potential therapeutic effect of LGF on the APPswe mouse model of AD. Twenty-month-old mice received intraperitoneal (i.p.) injections of 1.6 µg LGF or saline, twice a week during three weeks. Mice were sacrificed one week later, and the hippocampus and dorsal cortex were prepared for immunohistochemical and biochemical studies. LGF treatment reduced amyloid-β (Aβ) content, phospho-Tau/Tau ratio and the number of Aβ plaques with diameter larger than 25 µm. LGF administration also modulated protein ubiquitination and HSP70 protein levels, reduced glial reactivity and inflammation, and the expression of the pro-apoptotic protein Bax. Because the administration of this factor also restored cognitive damage in APPswe mice, we propose LGF as a novel therapeutic tool that may be useful for the treatment of AD. |
format | Online Article Text |
id | pubmed-7730107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77301072020-12-12 Liver Growth Factor “LGF” as a Therapeutic Agent for Alzheimer’s Disease Gonzalo-Gobernado, Rafael Perucho, Juan Vallejo-Muñoz, Manuela Casarejos, Maria José Reimers, Diana Jiménez-Escrig, Adriano Gómez, Ana Ulzurrun de Asanza, Gonzalo M. Bazán, Eulalia Int J Mol Sci Article Alzheimer’s disease (AD) is a progressive degenerative disorder and the most common cause of dementia in aging populations. Although the pathological hallmarks of AD are well defined, currently no effective therapy exists. Liver growth factor (LGF) is a hepatic albumin–bilirubin complex with activity as a tissue regenerating factor in several neurodegenerative disorders such as Parkinson’s disease and Friedreich’s ataxia. Our aim here was to analyze the potential therapeutic effect of LGF on the APPswe mouse model of AD. Twenty-month-old mice received intraperitoneal (i.p.) injections of 1.6 µg LGF or saline, twice a week during three weeks. Mice were sacrificed one week later, and the hippocampus and dorsal cortex were prepared for immunohistochemical and biochemical studies. LGF treatment reduced amyloid-β (Aβ) content, phospho-Tau/Tau ratio and the number of Aβ plaques with diameter larger than 25 µm. LGF administration also modulated protein ubiquitination and HSP70 protein levels, reduced glial reactivity and inflammation, and the expression of the pro-apoptotic protein Bax. Because the administration of this factor also restored cognitive damage in APPswe mice, we propose LGF as a novel therapeutic tool that may be useful for the treatment of AD. MDPI 2020-12-02 /pmc/articles/PMC7730107/ /pubmed/33276671 http://dx.doi.org/10.3390/ijms21239201 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gonzalo-Gobernado, Rafael Perucho, Juan Vallejo-Muñoz, Manuela Casarejos, Maria José Reimers, Diana Jiménez-Escrig, Adriano Gómez, Ana Ulzurrun de Asanza, Gonzalo M. Bazán, Eulalia Liver Growth Factor “LGF” as a Therapeutic Agent for Alzheimer’s Disease |
title | Liver Growth Factor “LGF” as a Therapeutic Agent for Alzheimer’s Disease |
title_full | Liver Growth Factor “LGF” as a Therapeutic Agent for Alzheimer’s Disease |
title_fullStr | Liver Growth Factor “LGF” as a Therapeutic Agent for Alzheimer’s Disease |
title_full_unstemmed | Liver Growth Factor “LGF” as a Therapeutic Agent for Alzheimer’s Disease |
title_short | Liver Growth Factor “LGF” as a Therapeutic Agent for Alzheimer’s Disease |
title_sort | liver growth factor “lgf” as a therapeutic agent for alzheimer’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730107/ https://www.ncbi.nlm.nih.gov/pubmed/33276671 http://dx.doi.org/10.3390/ijms21239201 |
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