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Sulforaphane reprograms the metabolomic landscape of chronic kidney disease: insights from NMR-based metabolomics

Ribeiro M, Cardozo LFMF, Borges NA, Manhães L, Pereira AD, Sforça ML, Rodrigues da Silva GH, Mafra D

Food & function · 0 citas

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Quién lo pagó

Financiación
Financiación independiente
Gobierno
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Gobierno
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Gobierno
Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Según 3 financiadores declarados.

Publicación

Publicado
2026-01-01 · Food Funct · vol. 17 · número 12 · págs. 5538–5547
Editorial
Royal Society of Chemistry
Citado
1 cita · más que el 86% de estudios similares · 1.9× el promedio de su campo
Referencias
49 trabajos
Acceso
De pago
Áreas de investigación
Genomics, phytochemicals, and oxidative stress · Metabolomics and Mass Spectrometry Studies · Dialysis and Renal Disease Management
Palabras clave
sulforaphane, chronic kidney disease, metabolomics, oxidative stress, inflammation, heme oxygenase-1, Nrf2, amino acid metabolism, insulin resistance, mitochondrial function, lipid metabolism, nutraceuticals, dietary supplementation, glycerol, methanol
MeSH
humans, isothiocyanates, sulfoxides, magnetic resonance spectroscopy, oxidative stress, aged, middle aged, female, male, nf-e2-related factor 2, renal insufficiency, chronic, metabolomics

8 autores

  • Marcia Maria Ribeiro🇧🇷Universidade Federal do Rio de Janeiro; Instituto de Biofísica Carlos Chagas Filho
  • L. Cardozo🇧🇷Universidade Federal Fluminense
  • Natália Alvarenga Borges🇧🇷Universidade do Estado do Rio de Janeiro
  • Larissa Ribeiro Manhães🇧🇷Universidade do Estado do Rio de Janeiro
  • Aline D. Pereira🇧🇷Universidade do Estado do Rio de Janeiro
  • Mauricio Luis Sforça🇧🇷Brazilian Center for Research in Energy and Materials; Brazilian Biosciences National Laboratory
  • Gustavo H. Rodrigues da Silva🇧🇷Brazilian Center for Research in Energy and Materials; Brazilian Biosciences National Laboratory
  • Denise Mafra🇧🇷 · autor de correspondenciaUniversidade Federal do Rio de Janeiro; Universidade Federal Fluminense; Instituto de Biofísica Carlos Chagas Filho

Resumen

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

Chronic kidney disease (CKD) is characterized by systemic metabolic disturbances and oxidative stress. Nutritional interventions using bioactive compounds such as sulforaphane (SFN) may represent a promising adjuvant strategy to attenuate these alterations. This study evaluated the effects of SFN supplementation on the untargeted metabolomic profile of non-dialysis CKD patients. A randomized, placebo-controlled clinical trial was conducted in 14 patients with CKD stages 3-5 who received either 400 µg per day of SFN or placebo for 30 days. Serum samples were analyzed using proton nuclear magnetic resonance (1H NMR) spectroscopy to identify metabolomic alterations and their correlations with markers of oxidative stress, inflammation, and gene expression. SFN supplementation tended to reduce 2-hydroxyisovalerate and glycerol levels, metabolites associated with insulin resistance and oxidative stress, and attenuated methanol elevation. Correlations were identified between heme oxygenase-1 (HO-1) and several amino acids, and between NRF2 and glycerol, suggesting an interplay between amino acid metabolism and antioxidant defense. Overall, SFN modulated the metabolomic profile of CKD patients, particularly metabolites related to mitochondrial function, lipid metabolism, and oxidative balance. These findings demonstrate that NMR-based metabolomics is a powerful non-invasive approach for elucidating the molecular effects of nutritional therapies in CKD and support SFN as a potential nutraceutical strategy in renal care.

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