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Blueberry Metabolites Attenuate Lipotoxicity-Induced Endothelial Dysfunction

Bharat D, Cavalcanti RRM, Petersen C, Begaye N, Cutler BR, Costa MMA, Ramos RKLG, Ferreira MR, Li Y, Bharath LP, Toolson E, Sebahar P, Looper RE, Jalili T, Rajasekaran NS, Jia Z, Symons JD, Anandh Babu PV

Molecular nutrition & food research · 60 citas

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Cómo se estudió

Diseño
Estudio in vitro o de mecanismos (clasificado por nuestro filtro de IA)
Estudiado en
Células o muestras de laboratorio
Resultado principal
Solo mecanismos

Quién lo pagó

Financiación
Financiación independiente
Organización sin fines de lucro
American Heart Association
Universidad u hospital
University of Utah
Gobierno
National Institutes of Health
Gobierno
National Institute on Aging
Gobierno
National Heart, Lung, and Blood Institute
Gobierno
NIA NIH HHS
Gobierno
NHLBI NIH HHS
Subvenciones
National Institute on Aging (R03AG042860); National Heart, Lung, and Blood Institute (R01HL118067); National Heart, Lung, and Blood Institute (R01HL141540); American Heart Association ((AHA:16GRNT31050004)); National Institute on Aging (R03 AG052848); National Institutes of Health (RO3AGO52848); National Institutes of Health (AG042860); National Institutes of Health (HL118067)

Según 7 financiadores declarados.

Publicación

Publicado
2017-10-12 · Mol Nutr Food Res · vol. 62 · número 2
Editorial
Wiley
Citado
78 citas · más que el 94% de estudios similares · 3.4× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
47 trabajos
Acceso
Acceso abierto (copia en repositorio)
Áreas de investigación
Phytochemicals and Antioxidant Activities · Plant Gene Expression Analysis · Biological and pharmacological studies of plants
Palabras clave
Chemistry, Lipotoxicity, Endothelial dysfunction, Nitric oxide, Reactive oxygen species, Biochemistry, Endothelium, Pharmacology, Vanillic acid, Food science, Endocrinology, Medicine, Diabetes mellitus
MeSH
aorta, endothelium, vascular, cells, cultured, endothelial cells, animals, mice, inbred c57bl, humans, nitric oxide, reactive oxygen species, anthocyanins, insulin, palmitic acid, gene expression regulation, male, blueberry plants

18 autores

  • Divya Bharat🇺🇸University of Utah
  • Rafaela Ramos Mororo Cavalcanti🇺🇸University of Utah
  • Chrissa Petersen🇺🇸University of Utah
  • Nathan Begaye🇺🇸University of Utah
  • Brett Ronald Cutler🇺🇸University of Utah
  • Marcella Melo Assis Costa🇺🇸University of Utah
  • Renata Kelly Luna Gomes Ramos🇺🇸University of Utah
  • Marina Ramos Ferreira🇺🇸University of Utah
  • Youyou Li🇺🇸University of Utah
  • Leena P. Bharath🇺🇸University of Utah
  • Emma Toolson🇺🇸University of Utah
  • Paul R. Sebahar🇺🇸University of Utah
  • Ryan Looper🇺🇸University of Utah
  • Thunder Jalili🇺🇸University of Utah
  • Namakkal Soorappan Rajasekaran🇺🇸University of Alabama at Birmingham
  • Zhenquan Jia🇺🇸University of North Carolina at Greensboro
  • J. David Symons🇺🇸University of Utah
  • Pon Velayutham Anandh Babu🇺🇸 · autor de correspondenciaUniversity of Utah

Resumen

El texto original del estudio, en el idioma en que se publicó.

Scope

Lipotoxicity-induced endothelial dysfunction is an important vascular complication associated with diabetes. Clinical studies support the vascular benefits of blueberry anthocyanins, but the underlying mechanism is unclear. The hypothesis that metabolites of blueberry anthocyanins attenuate lipotoxicity-induced endothelial dysfunction was tested.

Methods and results

Human aortic endothelial cells (HAECs) were treated for 6 h with either: (i) the parent anthocyanins (malvidin-3-glucoside and cyanidin-3-glucoside); or (ii) the blueberry metabolites (hydroxyhippuric acid, hippuric acid, benzoic acid-4-sulfate, isovanillic acid-3-sulfate, and vanillic acid-4-sulfate), at concentrations known to circulate in humans following blueberry consumption. For the last 5 h HAECs were treated with palmitate or vehicle. HAECs treated with palmitate displayed elevated reactive oxygen species generation, increased mRNA expression of NOX4, chemokines, adhesion molecules, and IκBα, exaggerated monocyte binding, and suppressed nitric oxide production. Of note, the damaging effects of palmitate were ameliorated in HAECs treated with blueberry metabolites but not parent anthocyanins. Further, important translational relevance of these results was provided by our observation that palmitate-induced endothelial dysfunction was lessened in arterial segments that incubated concurrently with blueberry metabolites.

Conclusion

The presented findings indicate that the vascular benefits of blueberry anthocyanins are mediated by their metabolites. Blueberries might complement existing therapies to lessen vascular complications.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial.

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