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Journal of Lipid Research
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    • Research Article
      Open Access

      Adaptations of the 3T3-L1 adipocyte lipidome to defective ether lipid catabolism upon Agmo knockdown

      Journal of Lipid Research
      Vol. 63Issue 6100222Published online: May 7, 2022
      • Sabrina Sailer
      • Katharina Lackner
      • Mia L. Pras-Raves
      • Eric J.M. Wever
      • Jan B. van Klinken
      • Adriaan D. Dane
      • and others
      Cited in Scopus: 0
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        Little is known about the physiological role of alkylglycerol monooxygenase (AGMO), the only enzyme capable of cleaving the 1-O-alkyl ether bond of ether lipids. Expression and enzymatic activity of this enzyme can be detected in a variety of tissues including adipose tissue. This labile lipolytic membrane-bound protein uses tetrahydrobiopterin as a cofactor, and mice with reduced tetrahydrobiopterin levels have alterations in body fat distribution and blood lipid concentrations. In addition, manipulation of AGMO in macrophages led to significant changes in the cellular lipidome, and alkylglycerolipids, the preferred substrates of AGMO, were shown to accumulate in mature adipocytes.
        Adaptations of the 3T3-L1 adipocyte lipidome to defective ether lipid catabolism upon Agmo knockdown
      • Research Article
        Open Access

        PEGylated AdipoRon derivatives improve glucose and lipid metabolism under insulinopenic and high-fat diet conditions

        Journal of Lipid Research
        Vol. 62100095Published online: June 29, 2021
        • Toshiharu Onodera
        • Ebrahim Ghazvini Zadeh
        • Peng Xu
        • Ruth Gordillo
        • Zheng Guo
        • Nolwenn Joffin
        • and others
        Cited in Scopus: 0
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          The pleiotropic actions of adiponectin in improving cell survival and metabolism have motivated the development of small-molecule therapeutic agents for treating diabetes and lipotoxicity. AdipoRon is a synthetic agonist of the adiponectin receptors, yet is limited by its poor solubility and bioavailability. In this work, we expand on the protective effects of AdipoRon in pancreatic β-cells and examine how structural modifications could affect the activity, pharmacokinetics, and bioavailability of this small molecule.
          PEGylated AdipoRon derivatives improve glucose and lipid metabolism under insulinopenic and high-fat diet conditions
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