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The cholecystokinin receptor agonist, CCK‐8, induces adiponectin production in rat white adipose tissue
Author(s) -
Plaza Adrián,
Merino Beatriz,
Del Olmo Nuria,
RuizGayo Mariano
Publication year - 2019
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/bph.14690
Subject(s) - medicine , endocrinology , cholecystokinin , adiponectin , cholecystokinin receptor , white adipose tissue , adipokine , chemistry , agonist , receptor , adipose tissue , insulin , biology , insulin resistance
Background and Purpose A cholecystokinin (CCK) system has been identified in white adipose tissue (WAT). Nevertheless, the endocrine actions of CCK on WAT remain unknown. Our goal was to investigate the role of CCK in regulating the production of adiponectin, an adipokine expressed in WAT, which is pivotal in preserving energy homeostasis. Experimental Approach The effect of the bioactive CCK fragment CCK‐8 on adiponectin production was studied both in vivo and in vitro. CCK‐8 effects were characterized in rats treated with selective CCK 1 and CCK 2 receptor antagonists as well as in pre‐adipocytes carrying the selective silencing of either CCK 1 or CCK 2 receptors. The influence of insulin on CCK‐8 responses was also analysed. Key Results In WAT, CCK‐8 increased plasma adiponectin levels and the expression of the adiponectin gene ( Adipoq ). In pre‐adipocytes, CCK‐8 up‐regulated adiponectin production. CCK‐8 effects were abolished by L‐365,260, a selective CCK 2 receptor antagonist. CCK 2 receptor knockdown also abolished the effects of CCK‐8 in pre‐adipocytes. Moreover, in vitro CCK‐8 effects were blocked by triciribine, a specific inhibitor of protein kinase B (Akt) and by the PPARγ antagonist T0070907. Silencing the expression of the insulin receptor inhibited CCK‐8‐induced Adipoq expression in pre‐adipocytes. Furthermore, insulin potentiated the effect of CCK‐8. Conclusion and Implications CCK‐8 stimulates adiponectin production in WAT by acting on CCK 2 receptors, through a mechanism involving both Akt and PPARγ. Moreover, CCK‐8 actions are only observed in the presence of insulin. Our results could have translational value in the design of new insulin‐sensitizing therapies.