The combination of berberine and isoliquiritigenin synergistically improved adipose inflammation and obesity‐induced insulin resistance

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Main Authors: Xiao‐Yu Zhang, Lingling Yu, Keke Wang, Mingsu Wang, Ping Li, Zu‐Guo Zheng, Hua Yang
Format: Artículo Open Access
Published: Wiley 2024
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author Xiao‐Yu Zhang
Lingling Yu
Keke Wang
Mingsu Wang
Ping Li
Zu‐Guo Zheng
Hua Yang
author_facet Xiao‐Yu Zhang
Lingling Yu
Keke Wang
Mingsu Wang
Ping Li
Zu‐Guo Zheng
Hua Yang
Xiao‐Yu Zhang
Lingling Yu
Keke Wang
Mingsu Wang
Ping Li
Zu‐Guo Zheng
Hua Yang
collection Wiley Open Access
contents The combination of berberine and isoliquiritigenin synergistically improved adipose inflammation and obesity‐induced insulin resistance Xiao‐Yu Zhang Lingling Yu Keke Wang Mingsu Wang Ping Li Zu‐Guo Zheng Hua Yang Phytotherapy Research AbstractWhite adipose tissue accumulation and inflammation contribute to obesity by inducing insulin resistance. Herein, we aimed to screen the synergistic components of the herbal pair Coptidis Rhizoma‐Glycyrrhizae Radix et Rhizoma for the treatment of insulin resistance and explore the potential synergistic mechanisms. Enzyme‐linked immunosorbent assay and quantitative PCR were used to detect expression levels of inflammatory genes in vitro and in vivo. Western blotting and immunohistochemistry were performed to detect protein levels of the insulin signaling pathway and macrophage markers. The effects on obesity‐induced insulin resistance were verified using a diet‐induced obesity (DIO) mouse model. Interactions between macrophage and adipocyte were assessed using a cellular supernatant transfer assay. Berberine (BBR) and isoliquiritigenin (ISL) alleviated mRNA levels and secretion of inflammatory genes in vitro and in vivo. Furthermore, BBR acted synergistically with ISL to ameliorate obesity and dyslipidemia in DIO mice. Meanwhile, the combination treatment significantly improved glucose intolerance and insulin resistance and decreased M1‐macrophage accumulation and infiltration in the adipose tissue. Mechanistically, co‐treatment with BBR and ISL upregulated the protein expression of the IRS1‐PI3K‐Akt insulin signaling pathway, enhanced glucose uptake in adipocyte, and suppressed the interaction between macrophage and adipocyte. BBR and ISL were identified as the synergistic components of the herbal pair Coptidis Rhizoma‐Glycyrrhizae Radix et Rhizoma for treating insulin resistance. The synergistic combination of BBR with ISL can be a promising and effective strategy for improving obesity‐induced adipose inflammation and insulin resistance. 10.1002/ptr.8233 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1002/ptr.8233
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institution Wiley Open Access
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publishDate 2024
publisher Wiley
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spellingShingle The combination of berberine and isoliquiritigenin synergistically improved adipose inflammation and obesity‐induced insulin resistance
Xiao‐Yu Zhang
Lingling Yu
Keke Wang
Mingsu Wang
Ping Li
Zu‐Guo Zheng
Hua Yang
Phytotherapy Research
The combination of berberine and isoliquiritigenin synergistically improved adipose inflammation and obesity‐induced insulin resistance Xiao‐Yu Zhang Lingling Yu Keke Wang Mingsu Wang Ping Li Zu‐Guo Zheng Hua Yang Phytotherapy Research AbstractWhite adipose tissue accumulation and inflammation contribute to obesity by inducing insulin resistance. Herein, we aimed to screen the synergistic components of the herbal pair Coptidis Rhizoma‐Glycyrrhizae Radix et Rhizoma for the treatment of insulin resistance and explore the potential synergistic mechanisms. Enzyme‐linked immunosorbent assay and quantitative PCR were used to detect expression levels of inflammatory genes in vitro and in vivo. Western blotting and immunohistochemistry were performed to detect protein levels of the insulin signaling pathway and macrophage markers. The effects on obesity‐induced insulin resistance were verified using a diet‐induced obesity (DIO) mouse model. Interactions between macrophage and adipocyte were assessed using a cellular supernatant transfer assay. Berberine (BBR) and isoliquiritigenin (ISL) alleviated mRNA levels and secretion of inflammatory genes in vitro and in vivo. Furthermore, BBR acted synergistically with ISL to ameliorate obesity and dyslipidemia in DIO mice. Meanwhile, the combination treatment significantly improved glucose intolerance and insulin resistance and decreased M1‐macrophage accumulation and infiltration in the adipose tissue. Mechanistically, co‐treatment with BBR and ISL upregulated the protein expression of the IRS1‐PI3K‐Akt insulin signaling pathway, enhanced glucose uptake in adipocyte, and suppressed the interaction between macrophage and adipocyte. BBR and ISL were identified as the synergistic components of the herbal pair Coptidis Rhizoma‐Glycyrrhizae Radix et Rhizoma for treating insulin resistance. The synergistic combination of BBR with ISL can be a promising and effective strategy for improving obesity‐induced adipose inflammation and insulin resistance. 10.1002/ptr.8233 http://onlinelibrary.wiley.com/termsAndConditions#vor
title The combination of berberine and isoliquiritigenin synergistically improved adipose inflammation and obesity‐induced insulin resistance
topic Phytotherapy Research
url https://onlinelibrary.wiley.com/doi/10.1002/ptr.8233