Marine Drugs (May 2023)

<i>Tisochrysis lutea</i> F&M-M36 Mitigates Risk Factors of Metabolic Syndrome and Promotes Visceral Fat Browning through β3-Adrenergic Receptor/UCP1 Signaling

  • Mario D’Ambrosio,
  • Elisabetta Bigagli,
  • Lorenzo Cinci,
  • Manuela Gencarelli,
  • Sofia Chioccioli,
  • Natascia Biondi,
  • Liliana Rodolfi,
  • Alberto Niccolai,
  • Francesca Zambelli,
  • Annunziatina Laurino,
  • Laura Raimondi,
  • Mario R. Tredici,
  • Cristina Luceri

DOI
https://doi.org/10.3390/md21050303
Journal volume & issue
Vol. 21, no. 5
p. 303

Abstract

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Pre-metabolic syndrome (pre-MetS) may represent the best transition phase to start treatments aimed at reducing cardiometabolic risk factors of MetS. In this study, we investigated the effects of the marine microalga Tisochrysis lutea F&M-M36 (T. lutea) on cardiometabolic components of pre-MetS and its underlying mechanisms. Rats were fed a standard (5% fat) or a high-fat diet (20% fat) supplemented or not with 5% of T. lutea or fenofibrate (100 mg/Kg) for 3 months. Like fenofibrate, T. lutea decreased blood triglycerides (p p p p T. lutea did not increase liver weight and steatosis, reduced renal fat (p p p T. lutea, but not fenofibrate, increased the β3-adrenergic receptor (β3ADR) (p p p p T. lutea up-regulated energy-metabolism-related genes and down-regulated inflammatory and autophagy pathways. The multitarget activity of T. lutea suggests that this microalga could be useful in mitigating risk factors of MetS.

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