Cargando…

Optimal therapeutic adropin dose intervention in mice and rat animal models: A systematic review

BACKGROUND AND AIM: Adropin is a hormone encoded by the Enho gene, which is associated with energy homeostasis. Preclinical studies using animal models have shown that adropin plays a role in enhancing glucose homeostasis and dyslipidemia. Lately, several studies on animal models have been performed...

Descripción completa

Detalles Bibliográficos
Autores principales: Alzoughool, Foad, Al-Zghoul, Mohammad Borhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Veterinary World 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304445/
https://www.ncbi.nlm.nih.gov/pubmed/34316188
http://dx.doi.org/10.14202/vetworld.2021.1426-1429
_version_ 1783727337235283968
author Alzoughool, Foad
Al-Zghoul, Mohammad Borhan
author_facet Alzoughool, Foad
Al-Zghoul, Mohammad Borhan
author_sort Alzoughool, Foad
collection PubMed
description BACKGROUND AND AIM: Adropin is a hormone encoded by the Enho gene, which is associated with energy homeostasis. Preclinical studies using animal models have shown that adropin plays a role in enhancing glucose homeostasis and dyslipidemia. Lately, several studies on animal models have been performed to examine the therapeutic and pathophysiological effects of adropin in many disorders. The aim of this systematic review was to identify the ideal adropin dose in mice and rat animal models. MATERIALS AND METHODS: We systematically searched PubMed, Science Direct, and Scopus databases from 2008 to 2020. The terms used in the search were “adropin,” “adropin doses in animal models,” “glucose homeostasis related to adropin,” and “adropin therapeutic effects on rats and mice.” Articles that included non-adropin doses, in vitro studies, and factors affecting adropin levels were excluded from the study. RESULTS: Of the total 179 qualified studies, six studies were included. We found that a daily injection of 450 nmol/kg of adropin for 3 days might be considered the optimum dose of effect in mice, whereas injection of 2.1 mg/kg once a day for 10 successive days might be the optimal effective dose in rats. CONCLUSION: Additional investigations are needed to determine the optimum dose of adropin to be used as a therapeutic intervention depending on the animal model.
format Online
Article
Text
id pubmed-8304445
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Veterinary World
record_format MEDLINE/PubMed
spelling pubmed-83044452021-07-26 Optimal therapeutic adropin dose intervention in mice and rat animal models: A systematic review Alzoughool, Foad Al-Zghoul, Mohammad Borhan Vet World Research Article BACKGROUND AND AIM: Adropin is a hormone encoded by the Enho gene, which is associated with energy homeostasis. Preclinical studies using animal models have shown that adropin plays a role in enhancing glucose homeostasis and dyslipidemia. Lately, several studies on animal models have been performed to examine the therapeutic and pathophysiological effects of adropin in many disorders. The aim of this systematic review was to identify the ideal adropin dose in mice and rat animal models. MATERIALS AND METHODS: We systematically searched PubMed, Science Direct, and Scopus databases from 2008 to 2020. The terms used in the search were “adropin,” “adropin doses in animal models,” “glucose homeostasis related to adropin,” and “adropin therapeutic effects on rats and mice.” Articles that included non-adropin doses, in vitro studies, and factors affecting adropin levels were excluded from the study. RESULTS: Of the total 179 qualified studies, six studies were included. We found that a daily injection of 450 nmol/kg of adropin for 3 days might be considered the optimum dose of effect in mice, whereas injection of 2.1 mg/kg once a day for 10 successive days might be the optimal effective dose in rats. CONCLUSION: Additional investigations are needed to determine the optimum dose of adropin to be used as a therapeutic intervention depending on the animal model. Veterinary World 2021-06 2021-06-04 /pmc/articles/PMC8304445/ /pubmed/34316188 http://dx.doi.org/10.14202/vetworld.2021.1426-1429 Text en Copyright: © Alzoughool and Al-Zghoul, et al. https://creativecommons.org/licenses/by/4.0/Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Alzoughool, Foad
Al-Zghoul, Mohammad Borhan
Optimal therapeutic adropin dose intervention in mice and rat animal models: A systematic review
title Optimal therapeutic adropin dose intervention in mice and rat animal models: A systematic review
title_full Optimal therapeutic adropin dose intervention in mice and rat animal models: A systematic review
title_fullStr Optimal therapeutic adropin dose intervention in mice and rat animal models: A systematic review
title_full_unstemmed Optimal therapeutic adropin dose intervention in mice and rat animal models: A systematic review
title_short Optimal therapeutic adropin dose intervention in mice and rat animal models: A systematic review
title_sort optimal therapeutic adropin dose intervention in mice and rat animal models: a systematic review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304445/
https://www.ncbi.nlm.nih.gov/pubmed/34316188
http://dx.doi.org/10.14202/vetworld.2021.1426-1429
work_keys_str_mv AT alzoughoolfoad optimaltherapeuticadropindoseinterventioninmiceandratanimalmodelsasystematicreview
AT alzghoulmohammadborhan optimaltherapeuticadropindoseinterventioninmiceandratanimalmodelsasystematicreview