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Akt: A Potential Drug Target for Metabolic Syndrome

The serine/threonine kinase Akt, also known as protein kinase B (PKB), is one of the key factors regulating glucose and lipid energy metabolism, and is the core focus of current research on diabetes and metabolic diseases. Akt is mostly expressed in key metabolism-related organs and it is activated...

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Autores principales: Miao, Runyu, Fang, Xinyi, Wei, Jiahua, Wu, Haoran, Wang, Xinmiao, Tian, Jiaxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940245/
https://www.ncbi.nlm.nih.gov/pubmed/35330934
http://dx.doi.org/10.3389/fphys.2022.822333
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author Miao, Runyu
Fang, Xinyi
Wei, Jiahua
Wu, Haoran
Wang, Xinmiao
Tian, Jiaxing
author_facet Miao, Runyu
Fang, Xinyi
Wei, Jiahua
Wu, Haoran
Wang, Xinmiao
Tian, Jiaxing
author_sort Miao, Runyu
collection PubMed
description The serine/threonine kinase Akt, also known as protein kinase B (PKB), is one of the key factors regulating glucose and lipid energy metabolism, and is the core focus of current research on diabetes and metabolic diseases. Akt is mostly expressed in key metabolism-related organs and it is activated in response to various stimuli, including cell stress, cell movement, and various hormones and drugs that affect cell metabolism. Genetic and pharmacological studies have shown that Akt is necessary to maintain the steady state of glucose and lipid metabolism and a variety of cellular responses. Existing evidence shows that metabolic syndrome is related to insulin resistance and lipid metabolism disorders. Based on a large number of studies on Akt-related pathways and reactions, we believe that Akt can be used as a potential drug target to effectively treat metabolic syndrome.
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spelling pubmed-89402452022-03-23 Akt: A Potential Drug Target for Metabolic Syndrome Miao, Runyu Fang, Xinyi Wei, Jiahua Wu, Haoran Wang, Xinmiao Tian, Jiaxing Front Physiol Physiology The serine/threonine kinase Akt, also known as protein kinase B (PKB), is one of the key factors regulating glucose and lipid energy metabolism, and is the core focus of current research on diabetes and metabolic diseases. Akt is mostly expressed in key metabolism-related organs and it is activated in response to various stimuli, including cell stress, cell movement, and various hormones and drugs that affect cell metabolism. Genetic and pharmacological studies have shown that Akt is necessary to maintain the steady state of glucose and lipid metabolism and a variety of cellular responses. Existing evidence shows that metabolic syndrome is related to insulin resistance and lipid metabolism disorders. Based on a large number of studies on Akt-related pathways and reactions, we believe that Akt can be used as a potential drug target to effectively treat metabolic syndrome. Frontiers Media S.A. 2022-03-07 /pmc/articles/PMC8940245/ /pubmed/35330934 http://dx.doi.org/10.3389/fphys.2022.822333 Text en Copyright © 2022 Miao, Fang, Wei, Wu, Wang and Tian. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Miao, Runyu
Fang, Xinyi
Wei, Jiahua
Wu, Haoran
Wang, Xinmiao
Tian, Jiaxing
Akt: A Potential Drug Target for Metabolic Syndrome
title Akt: A Potential Drug Target for Metabolic Syndrome
title_full Akt: A Potential Drug Target for Metabolic Syndrome
title_fullStr Akt: A Potential Drug Target for Metabolic Syndrome
title_full_unstemmed Akt: A Potential Drug Target for Metabolic Syndrome
title_short Akt: A Potential Drug Target for Metabolic Syndrome
title_sort akt: a potential drug target for metabolic syndrome
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940245/
https://www.ncbi.nlm.nih.gov/pubmed/35330934
http://dx.doi.org/10.3389/fphys.2022.822333
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