Folic acid supplementation modifies β-adrenoceptor-mediated in vitro lipolysis of obese/diabetic (+db/+db) mice

Tsz Yan Lam, Sai Wang Seto, Alice Lai Shan Au, Christina Chui Wa Poon, Rachel Wai Sum Li, Ho Yeung Lam, Wing Sze Lau, Shun Wan Chan, Sai Ming Ngai, George Pak Heng Leung, Simon Ming Yuen Lee, Stephen Kwok Wing Tsui, Yiu Wa Kwan

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The effects of folic acid (5.7 and 71 µg/kg, 4 weeks) consumption on the β-adrenoceptors (β-ARs)-elicited lipolysis in vitro of the abdominal adipocytes of lean/control (+m/+db) and obese/diabetic (+db/+db) mice (female) were investigated. β-AR agonists (salbutamol, a β₂-AR agonist; BRL 37344 and CGP 12177, β₃-AR agonists; adrenaline, a β-AR agonist)-mediated lipolysis, β₂-, and β₃-ARs protein expression of the adipose tissues after folic acid consumption were evaluated. Our results demonstrate that a smaller magnitude of the basal (spontaneous) and the β-AR agonists-triggered lipolysis was observed in +db/+db mice, and folic acid supplementation (71 μg/kg) resulted in an improvement of both the baseline and the β-ARs-mediated lipolysis. In controls, a lower β₂- and β₃-ARs protein expression of the adipose tissues was detected in +db/+db mice, compared to +m/+db mice. In both strains fed with folic acid (71 μg/kg), a reduction of β-AR protein expression was observed compared to the respective controls. In +db/+db mice, folic acid (5.7 and 71 μg/kg) consumption caused a dose-dependent increase of β₃-AR protein expression compared to controls. We demonstrate that lipolysis elicited by β-AR (β₂- and β₃-ARs) agonists was blunted in +db/+db mice. Folic acid consumption has significant modulatory effects on β-ARs protein expression and lipolysis.
    Original languageEnglish
    Pages (from-to)1047-1055
    Number of pages9
    JournalExperimental Biology and Medicine
    Volume234
    Issue number9
    DOIs
    Publication statusPublished - 2009

    Keywords

    • fat cells
    • folic acid
    • lipolysis
    • mice
    • receptors

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