Unresolved questions in the regulation of skeletal muscle insulin action by reactive oxygen species

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

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Unresolved questions in the regulation of skeletal muscle insulin action by reactive oxygen species. / Gallero, Samantha; Persson, Kaspar W.; Henríquez-Olguín, Carlos.

I: FEBS Letters, 2024.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Gallero, S, Persson, KW & Henríquez-Olguín, C 2024, 'Unresolved questions in the regulation of skeletal muscle insulin action by reactive oxygen species', FEBS Letters. https://doi.org/10.1002/1873-3468.14937

APA

Gallero, S., Persson, K. W., & Henríquez-Olguín, C. (Accepteret/In press). Unresolved questions in the regulation of skeletal muscle insulin action by reactive oxygen species. FEBS Letters. https://doi.org/10.1002/1873-3468.14937

Vancouver

Gallero S, Persson KW, Henríquez-Olguín C. Unresolved questions in the regulation of skeletal muscle insulin action by reactive oxygen species. FEBS Letters. 2024. https://doi.org/10.1002/1873-3468.14937

Author

Gallero, Samantha ; Persson, Kaspar W. ; Henríquez-Olguín, Carlos. / Unresolved questions in the regulation of skeletal muscle insulin action by reactive oxygen species. I: FEBS Letters. 2024.

Bibtex

@article{ddbe3064d9ab4b6ca2de42d4c4469969,
title = "Unresolved questions in the regulation of skeletal muscle insulin action by reactive oxygen species",
abstract = "Reactive oxygen species (ROS) are well-established signaling molecules implicated in a wide range of cellular processes, including both oxidative stress and intracellular redox signaling. In the context of insulin action within its target tissues, ROS have been reported to exert both positive and negative regulatory effects. However, the precise molecular mechanisms underlying this duality remain unclear. This Review examines the complex role of ROS in insulin action, with a particular focus on skeletal muscle. We aim to address three critical aspects: (a) the proposed intracellular pro-oxidative redox shift elicited by insulin, (b) the evidence supporting that redox-sensitive cysteine modifications impact insulin signaling and action, and (c) cellular mechanisms underlying how ROS can paradoxically act as both enhancers and inhibitors of insulin action. This Review underscores the urgent need for more systematic research to identify specific reactive species, redox targets, and the physiological significance of redox signaling in maintaining insulin action and metabolic health, with a particular emphasis on human skeletal muscle.",
keywords = "hydrogen peroxide, insulin action, insulin signaling, metabolism, reactive oxygen species, redox signaling, skeletal muscle",
author = "Samantha Gallero and Persson, {Kaspar W.} and Carlos Henr{\'i}quez-Olgu{\'i}n",
note = "Publisher Copyright: {\textcopyright} 2024 The Author(s). FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.",
year = "2024",
doi = "10.1002/1873-3468.14937",
language = "English",
journal = "F E B S Letters",
issn = "0014-5793",
publisher = "JohnWiley & Sons Ltd",

}

RIS

TY - JOUR

T1 - Unresolved questions in the regulation of skeletal muscle insulin action by reactive oxygen species

AU - Gallero, Samantha

AU - Persson, Kaspar W.

AU - Henríquez-Olguín, Carlos

N1 - Publisher Copyright: © 2024 The Author(s). FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.

PY - 2024

Y1 - 2024

N2 - Reactive oxygen species (ROS) are well-established signaling molecules implicated in a wide range of cellular processes, including both oxidative stress and intracellular redox signaling. In the context of insulin action within its target tissues, ROS have been reported to exert both positive and negative regulatory effects. However, the precise molecular mechanisms underlying this duality remain unclear. This Review examines the complex role of ROS in insulin action, with a particular focus on skeletal muscle. We aim to address three critical aspects: (a) the proposed intracellular pro-oxidative redox shift elicited by insulin, (b) the evidence supporting that redox-sensitive cysteine modifications impact insulin signaling and action, and (c) cellular mechanisms underlying how ROS can paradoxically act as both enhancers and inhibitors of insulin action. This Review underscores the urgent need for more systematic research to identify specific reactive species, redox targets, and the physiological significance of redox signaling in maintaining insulin action and metabolic health, with a particular emphasis on human skeletal muscle.

AB - Reactive oxygen species (ROS) are well-established signaling molecules implicated in a wide range of cellular processes, including both oxidative stress and intracellular redox signaling. In the context of insulin action within its target tissues, ROS have been reported to exert both positive and negative regulatory effects. However, the precise molecular mechanisms underlying this duality remain unclear. This Review examines the complex role of ROS in insulin action, with a particular focus on skeletal muscle. We aim to address three critical aspects: (a) the proposed intracellular pro-oxidative redox shift elicited by insulin, (b) the evidence supporting that redox-sensitive cysteine modifications impact insulin signaling and action, and (c) cellular mechanisms underlying how ROS can paradoxically act as both enhancers and inhibitors of insulin action. This Review underscores the urgent need for more systematic research to identify specific reactive species, redox targets, and the physiological significance of redox signaling in maintaining insulin action and metabolic health, with a particular emphasis on human skeletal muscle.

KW - hydrogen peroxide

KW - insulin action

KW - insulin signaling

KW - metabolism

KW - reactive oxygen species

KW - redox signaling

KW - skeletal muscle

U2 - 10.1002/1873-3468.14937

DO - 10.1002/1873-3468.14937

M3 - Review

C2 - 38803005

AN - SCOPUS:85194565971

JO - F E B S Letters

JF - F E B S Letters

SN - 0014-5793

ER -

ID: 395072961