Antioxidants (Nov 2020)

Nicotinamide Prevents Apolipoprotein B-Containing Lipoprotein Oxidation, Inflammation and Atherosclerosis in Apolipoprotein E-Deficient Mice

  • Karen Alejandra Méndez-Lara,
  • Nicole Letelier,
  • Núria Farré,
  • Elena M. G. Diarte-Añazco,
  • Núria Nieto-Nicolau,
  • Elisabeth Rodríguez-Millán,
  • David Santos,
  • Victor Pallarès,
  • Joan Carles Escolà-Gil,
  • Tania Vázquez del Olmo,
  • Enrique Lerma,
  • Mercedes Camacho,
  • Ricardo P Casaroli-Marano,
  • Annabel F. Valledor,
  • Francisco Blanco-Vaca,
  • Josep Julve

DOI
https://doi.org/10.3390/antiox9111162
Journal volume & issue
Vol. 9, no. 11
p. 1162

Abstract

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The potential of nicotinamide (NAM) to prevent atherosclerosis has not yet been examined. This study investigated the effect of NAM supplementation on the development of atherosclerosis in a mouse model of the disease. The development of aortic atherosclerosis was significantly reduced (NAM low dose: 45%; NAM high dose: 55%) in NAM-treated, apolipoprotein (Apo)E-deficient mice challenged with a Western diet for 4 weeks. NAM administration significantly increased (1.8-fold) the plasma concentration of proatherogenic ApoB-containing lipoproteins in NAM high-dose (HD)-treated mice compared with untreated mice. However, isolated ApoB-containing lipoproteins from NAM HD mice were less prone to oxidation than those of untreated mice. This result was consistent with the decreased (1.5-fold) concentration of oxidized low-density lipoproteins in this group. Immunohistochemical staining of aortas from NAM-treated mice showed significantly increased levels of IL-10 (NAM low-dose (LD): 1.3-fold; NAM HD: 1.2-fold), concomitant with a significant decrease in the relative expression of TNFα (NAM LD: −44%; NAM HD: −57%). An improved anti-inflammatory pattern was reproduced in macrophages cultured in the presence of NAM. Thus, dietary NAM supplementation in ApoE-deficient mice prevented the development of atherosclerosis and improved protection against ApoB-containing lipoprotein oxidation and aortic inflammation.

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