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Quercetin improves the adipose inflammatory response and insulin signaling to reduce “real-world” particulate matter-induced insulin resistance

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Abstract

Numerous epidemiological data and experimental studies support a strong link between fine particulate matter (less than 2.5 mm in aerodynamic diameter, PM2.5) exposure and the development of insulin resistance/type 2 diabetes mellitus (T2DM). Quercetin (Que), a flavonoid compound with anti-inflammatory effects, has been confirmed to improve glucose metabolic disorders in rodents and humans. In this study, we investigated the underlying mechanisms of particulate matter (PM)-induced glucose metabolic disorder and subsequently examined the protective effect and mechanism of quercetin supplementation. Male C57BL/6 mice in the control group and PM group were exposed to ambient filtered air (FA) or PM (6 h/day, 7 days/week) for 18 weeks. Mice in the Que group were exposed to PM for 18 weeks and administered Que (50 or 100 mg/kg bw). Glucose tolerance, insulin sensitivity, and systemic and visceral white adipose tissue (vWAT) inflammatory responses were measured. The expression of proteins involved in insulin signal transduction in vWAT was assessed. Chronic PM exposure caused systemic and vWAT inflammation characterized by an increase in serum IL-6 and TNF-α levels and increased vWAT macrophage filtration, triggering NLRP3 inflammasome activation, impairing the classic glucose metabolism signal in vWAT, and inducing whole-body insulin resistance. Moreover, Que administration significantly alleviated systemic and vWAT inflammation, abolished NLRP3 inflammasome activation, and improved signaling abnormalities characteristic of insulin resistance in vWAT and adipocytes. Based on these findings, chronic PM exposure activated the NLRP3 inflammasome and subsequently caused systemic and WAT inflammation and impaired insulin signaling in vWAT and adipocytes. Most importantly, Que administration inhibited NLRP3 inflammasome-mediated inflammation and insulin signaling in vWAT to improve these adverse effects.

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Availability of data and materials

All data generated or analyzed during this study are included in this published article and its supplementary information files.

Abbreviations

Que:

quercetin

FA:

filtered air

PM:

ambient particulate matter

PM2.5 :

PM with aerodynamic diameter less than 2.5 μm

WAT:

white adipose tissue

vWAT:

visceral white adipose tissue

sWAT:

subcutaneous white adipose tissue

HOMA-IR:

insulin resistance index

IPGTT:

intraperitoneal glucose tolerance test

AUC:

area under the curve

TNF-α:

tumor necrosis factor-α

IL-6:

interleukin-6

IRS-1:

insulin receptor substrate

GLUT4:

glucose transporter 4

NLRP3:

nucleotide-binding domain and leucine-rich repeat protein 3

ASC:

apoptosis-associated speck-like protein containing a caspase activation recruitment domain

IL-1β:

interleukin-1β

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Acknowledgements

Professor Wu Weidong is acknowledged for providing the “real-world” PM exposure system.

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Authors and Affiliations

Authors

Contributions

All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by Shibin Ding, Jinjin Jiang, and Guofu Zhang. The experiments were completed by Shibin Ding, Yang Zheng, and Jinxia Sun. The first draft of the manuscript was written by Jinjin Jiang, Min Yu, and Juan Gu. All authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Shibin Ding.

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The animal protocols were approved by the Committee on Use and Care of Animals of Xinxiang Medical University (No. XXMU-2016-0007).

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Not applicable.

Competing interests

The authors declare no competing interests.

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Responsible Editor: Mohamed M. Abdel-Daim

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Jiang, J., Zhang, G., Yu, M. et al. Quercetin improves the adipose inflammatory response and insulin signaling to reduce “real-world” particulate matter-induced insulin resistance. Environ Sci Pollut Res 29, 2146–2157 (2022). https://doi.org/10.1007/s11356-021-15829-8

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  • DOI: https://doi.org/10.1007/s11356-021-15829-8

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