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Rosiglitazone promotes glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway

The study aimed to explore the effects of rosiglitazone on glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway. The experiment was divided into five groups: normal starch group (32%, LC), high starch group (53%, HC), high starch +rosiglitazone group 1 (10 mg/kg, R1), high star...

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Autores principales: Guan, Dong‐Yan, Sun, Hui‐Wen, Wang, Ji‐Ting, Wang, Zhen, Li, Yang, Han, Hao‐Jun, Li, Xiang, Fang, Ting‐Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923568/
https://www.ncbi.nlm.nih.gov/pubmed/33650786
http://dx.doi.org/10.14814/phy2.14765
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author Guan, Dong‐Yan
Sun, Hui‐Wen
Wang, Ji‐Ting
Wang, Zhen
Li, Yang
Han, Hao‐Jun
Li, Xiang
Fang, Ting‐Ting
author_facet Guan, Dong‐Yan
Sun, Hui‐Wen
Wang, Ji‐Ting
Wang, Zhen
Li, Yang
Han, Hao‐Jun
Li, Xiang
Fang, Ting‐Ting
author_sort Guan, Dong‐Yan
collection PubMed
description The study aimed to explore the effects of rosiglitazone on glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway. The experiment was divided into five groups: normal starch group (32%, LC), high starch group (53%, HC), high starch +rosiglitazone group 1 (10 mg/kg, R1), high starch + rosiglitazone group 2 (20 mg/kg, R2), and high starch + rosiglitazone group 3 (30 mg/kg, R3). The results showed that a high starch diet supplemented with 10–20 mg/kg rosiglitazone had a better specific growth rate and protein efficiency that was beneficial for the growth of the tilapia. Rosiglitazone had no significant effect on the contents of crude lipid, crude protein, crude ash, and moisture of the whole fish body (p > 0.05). The contents of triglycerides and total cholesterol in the R1, R2, and R3 groups were lower than those in the HC group. The levels of glutamic oxaloacetic transaminase (GOT) and glutamic pyruvic transaminase (GPT) in R1 and R2 groups were significantly lower than those in the HC groups (p < 0.05). However, the GOT and GPT levels in the R3 groups were significantly higher than those in the R1 and R2 groups (p < 0.05). With an increase in the rosiglitazone concentration, the contents of serum glucose, insulin, and hepatic glycogen in the R1, R2, and R3 groups decreased gradually. Meanwhile, the muscle glycogen content in the R1, R2, and R3 groups increased gradually. The mRNA expression of the IRS‐1, PI3K, GLUT‐4, and Akt proteins in the R1, R2, and R3 groups was significantly higher than that in the HC group (p < 0.05). Compared with the HC group, the expression of the GSK‐3 mRNA in the R1, R2, and R3 groups was significantly reduced (p < 0.05). The protein expression of p‐Akt in the R1 and R2 groups was higher than that in the HC group (p > 0.05). The protein expression of p‐GSK‐3β in the R1 and R2 groups was significantly higher than that in the HC group (p < 0.05). In conclusion, a high starch diet supplemented with rosiglitazone can improve growth, enhance the serum biochemical indices, and increase the muscle glycogen content in the GIFT tilapia. It benefits in upregulating the IRS‐1, PI3K, and GLUT‐4 mRNA levels in the skeletal muscle and promotes glucose uptake. Meanwhile, the phosphorylation of Akt and GSK‐3β increased significantly and resulted in the inactivation of GSK‐3β and alleviation of insulin resistance.
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spelling pubmed-79235682021-03-12 Rosiglitazone promotes glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway Guan, Dong‐Yan Sun, Hui‐Wen Wang, Ji‐Ting Wang, Zhen Li, Yang Han, Hao‐Jun Li, Xiang Fang, Ting‐Ting Physiol Rep Original Articles The study aimed to explore the effects of rosiglitazone on glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway. The experiment was divided into five groups: normal starch group (32%, LC), high starch group (53%, HC), high starch +rosiglitazone group 1 (10 mg/kg, R1), high starch + rosiglitazone group 2 (20 mg/kg, R2), and high starch + rosiglitazone group 3 (30 mg/kg, R3). The results showed that a high starch diet supplemented with 10–20 mg/kg rosiglitazone had a better specific growth rate and protein efficiency that was beneficial for the growth of the tilapia. Rosiglitazone had no significant effect on the contents of crude lipid, crude protein, crude ash, and moisture of the whole fish body (p > 0.05). The contents of triglycerides and total cholesterol in the R1, R2, and R3 groups were lower than those in the HC group. The levels of glutamic oxaloacetic transaminase (GOT) and glutamic pyruvic transaminase (GPT) in R1 and R2 groups were significantly lower than those in the HC groups (p < 0.05). However, the GOT and GPT levels in the R3 groups were significantly higher than those in the R1 and R2 groups (p < 0.05). With an increase in the rosiglitazone concentration, the contents of serum glucose, insulin, and hepatic glycogen in the R1, R2, and R3 groups decreased gradually. Meanwhile, the muscle glycogen content in the R1, R2, and R3 groups increased gradually. The mRNA expression of the IRS‐1, PI3K, GLUT‐4, and Akt proteins in the R1, R2, and R3 groups was significantly higher than that in the HC group (p < 0.05). Compared with the HC group, the expression of the GSK‐3 mRNA in the R1, R2, and R3 groups was significantly reduced (p < 0.05). The protein expression of p‐Akt in the R1 and R2 groups was higher than that in the HC group (p > 0.05). The protein expression of p‐GSK‐3β in the R1 and R2 groups was significantly higher than that in the HC group (p < 0.05). In conclusion, a high starch diet supplemented with rosiglitazone can improve growth, enhance the serum biochemical indices, and increase the muscle glycogen content in the GIFT tilapia. It benefits in upregulating the IRS‐1, PI3K, and GLUT‐4 mRNA levels in the skeletal muscle and promotes glucose uptake. Meanwhile, the phosphorylation of Akt and GSK‐3β increased significantly and resulted in the inactivation of GSK‐3β and alleviation of insulin resistance. John Wiley and Sons Inc. 2021-03-02 /pmc/articles/PMC7923568/ /pubmed/33650786 http://dx.doi.org/10.14814/phy2.14765 Text en © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Guan, Dong‐Yan
Sun, Hui‐Wen
Wang, Ji‐Ting
Wang, Zhen
Li, Yang
Han, Hao‐Jun
Li, Xiang
Fang, Ting‐Ting
Rosiglitazone promotes glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway
title Rosiglitazone promotes glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway
title_full Rosiglitazone promotes glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway
title_fullStr Rosiglitazone promotes glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway
title_full_unstemmed Rosiglitazone promotes glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway
title_short Rosiglitazone promotes glucose metabolism of GIFT tilapia based on the PI3K/Akt signaling pathway
title_sort rosiglitazone promotes glucose metabolism of gift tilapia based on the pi3k/akt signaling pathway
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923568/
https://www.ncbi.nlm.nih.gov/pubmed/33650786
http://dx.doi.org/10.14814/phy2.14765
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