Hyperlipidemic plasma molecules bind and inhibit adiponectin activity
Autor: | Yan‐Qing Zhang, Sen Fan, Wen‐Qing Wang, Wayne Bond Lau, Jian‐Li Dai, Hai‐Feng Zhang, Xiao‐Ming Wang, Xiao‐Gang Liu, Rong Li |
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Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: | |
Zdroj: | Journal of Diabetes Investigation, Vol 13, Iss 6, Pp 947-954 (2022) |
Druh dokumentu: | article |
ISSN: | 2040-1124 2040-1116 |
DOI: | 10.1111/jdi.13746 |
Popis: | Abstract Introduction Adiponectin is a potent vascular protective molecule. Recent findings have suggested adiponectin resistance during early diabetes. However, the molecular mechanisms responsible remain unidentified. Here, we took an unbiased approach to identify whether hyperlipidemic plasma molecules exist that bind and inhibit adiponectin function, contributing to adiponectin resistance and diabetic vascular injury. Methods Adult rats were randomly assigned to receive either a normal or a high‐fat diet for 8 weeks. Plasma was co‐immunoprecipitated with anti‐APN antibody and analyzed by mass spectrometry. The APN binding molecules and their effect upon APN biological activity were determined. Results As expected, the high‐fat‐diet increased plasma triglyceride, total cholesterol, and low‐density lipoprotein. Importantly, the circulating APN level was significantly increased at this time point. Mass spectrometry identified 18 proteins with increased APN binding in hyperlipidemic plasma, among which four proteins critical in lipid metabolism, including apolipoprotein A1 (APOA1), APOA4, APOC1, and paraoxonase 1, were further investigated. Incubating recombinant APN with APOA1 markedly (P |
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