GLP‑1 receptor agonist protects palmitate-induced insulin resistance in skeletal muscle cells by up-regulating sestrin2 to promote autophagy

Abstract In this study, we aimed to determine whether liraglutide could effectively reduce insulin resistance (IR) by regulating Sestrin2 (SESN2) expression in L6 rat skeletal muscle cells by examining its interactions with SESN2, autophagy, and IR. L6 cells were incubated with liraglutide (10–1000 ...

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Main Authors: Xue Tian, Yu Gao, Mowei Kong, Lihua Zhao, Enhong Xing, Qitian Sun, Jianqiu He, Yanan Lu, Zengbin Feng
Format: Article
Language:English
Published: Nature Portfolio 2023-06-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-36602-6
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author Xue Tian
Yu Gao
Mowei Kong
Lihua Zhao
Enhong Xing
Qitian Sun
Jianqiu He
Yanan Lu
Zengbin Feng
author_facet Xue Tian
Yu Gao
Mowei Kong
Lihua Zhao
Enhong Xing
Qitian Sun
Jianqiu He
Yanan Lu
Zengbin Feng
author_sort Xue Tian
collection DOAJ
description Abstract In this study, we aimed to determine whether liraglutide could effectively reduce insulin resistance (IR) by regulating Sestrin2 (SESN2) expression in L6 rat skeletal muscle cells by examining its interactions with SESN2, autophagy, and IR. L6 cells were incubated with liraglutide (10–1000 nM) in the presence of palmitate (PA; 0.6 mM), and cell viability was detected using the cell counting kit-8 (CCK-8) assay. IR-related and autophagy-related proteins were detected using western blotting, and IR and autophagy-related genes were analyzed using quantitative real-time polymerase chain reaction. Silencing SESN2 was used to inhibit the activities of SESN2. A reduction in insulin-stimulated glucose uptake was observed in PA-treated L6 cells, confirming IR. Meanwhile, PA decreased the levels of GLUT4 and phosphorylation of Akt and affected SESN2 expression. Further investigation revealed that autophagic activity decreased following PA treatment, but that liraglutide reversed this PA-induced reduction in autophagic activity. Additionally, silencing SESN2 inhibited the ability of liraglutide to up-regulate the expression of IR-related proteins and activate autophagy signals. In summary, the data showed that liraglutide improved PA-induced IR in L6 myotubes by increasing autophagy mediated by SESN2.
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spelling doaj.art-c9fe457387514cc1a09cf751beecd0da2023-06-11T11:12:43ZengNature PortfolioScientific Reports2045-23222023-06-0113111010.1038/s41598-023-36602-6GLP‑1 receptor agonist protects palmitate-induced insulin resistance in skeletal muscle cells by up-regulating sestrin2 to promote autophagyXue Tian0Yu Gao1Mowei Kong2Lihua Zhao3Enhong Xing4Qitian Sun5Jianqiu He6Yanan Lu7Zengbin Feng8Department of Endocrinology, Affiliated Hospital of Chengde Medical UniversityDepartment of Endocrinology, Affiliated Hospital of Chengde Medical UniversityDepartment of Endocrinology, Affiliated Hospital of Chengde Medical UniversityDepartment of Endocrinology, Affiliated Hospital of Chengde Medical UniversityCentral Laboratory, Affiliated Hospital of Chengde Medical UniversityDepartment of Endocrinology, Affiliated Hospital of Chengde Medical UniversityDepartment of Endocrinology, Affiliated Hospital of Chengde Medical UniversityDepartment of Endocrinology, Affiliated Hospital of Chengde Medical UniversityDepartment of Endocrinology, Affiliated Hospital of Chengde Medical UniversityAbstract In this study, we aimed to determine whether liraglutide could effectively reduce insulin resistance (IR) by regulating Sestrin2 (SESN2) expression in L6 rat skeletal muscle cells by examining its interactions with SESN2, autophagy, and IR. L6 cells were incubated with liraglutide (10–1000 nM) in the presence of palmitate (PA; 0.6 mM), and cell viability was detected using the cell counting kit-8 (CCK-8) assay. IR-related and autophagy-related proteins were detected using western blotting, and IR and autophagy-related genes were analyzed using quantitative real-time polymerase chain reaction. Silencing SESN2 was used to inhibit the activities of SESN2. A reduction in insulin-stimulated glucose uptake was observed in PA-treated L6 cells, confirming IR. Meanwhile, PA decreased the levels of GLUT4 and phosphorylation of Akt and affected SESN2 expression. Further investigation revealed that autophagic activity decreased following PA treatment, but that liraglutide reversed this PA-induced reduction in autophagic activity. Additionally, silencing SESN2 inhibited the ability of liraglutide to up-regulate the expression of IR-related proteins and activate autophagy signals. In summary, the data showed that liraglutide improved PA-induced IR in L6 myotubes by increasing autophagy mediated by SESN2.https://doi.org/10.1038/s41598-023-36602-6
spellingShingle Xue Tian
Yu Gao
Mowei Kong
Lihua Zhao
Enhong Xing
Qitian Sun
Jianqiu He
Yanan Lu
Zengbin Feng
GLP‑1 receptor agonist protects palmitate-induced insulin resistance in skeletal muscle cells by up-regulating sestrin2 to promote autophagy
Scientific Reports
title GLP‑1 receptor agonist protects palmitate-induced insulin resistance in skeletal muscle cells by up-regulating sestrin2 to promote autophagy
title_full GLP‑1 receptor agonist protects palmitate-induced insulin resistance in skeletal muscle cells by up-regulating sestrin2 to promote autophagy
title_fullStr GLP‑1 receptor agonist protects palmitate-induced insulin resistance in skeletal muscle cells by up-regulating sestrin2 to promote autophagy
title_full_unstemmed GLP‑1 receptor agonist protects palmitate-induced insulin resistance in skeletal muscle cells by up-regulating sestrin2 to promote autophagy
title_short GLP‑1 receptor agonist protects palmitate-induced insulin resistance in skeletal muscle cells by up-regulating sestrin2 to promote autophagy
title_sort glp 1 receptor agonist protects palmitate induced insulin resistance in skeletal muscle cells by up regulating sestrin2 to promote autophagy
url https://doi.org/10.1038/s41598-023-36602-6
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