Synergistic differential DNA demethylation activity of danshensu (Salvia miltiorrhiza) associated with different probiotics in nonalcoholic fatty liver disease

  • Amr Hassan
  • , Patrícia Rijo
  • , Tamer M.M. Abuamara
  • , Lashin Saad Ali Lashin
  • , Sherif A. Kamar
  • , Gabrielle Bangay
  • , Majid Mohammed Al-Sawahli
  • , Marina K. Fouad
  • , Mohammad A. Zoair
  • , Tamer I. Abdalrhman
  • , Dalia Elebeedy
  • , Ibrahim A. Ibrahim
  • , Aly F. Mohamed
  • , Ahmed I. Abd El Maksoud

Resultado de pesquisarevisão de pares

12 Citações (Scopus)

Resumo

Nonalcoholic fatty liver disease (NAFLD) is a major hepatic disorder occurring in non-alcohol-drinking individuals. Salvianic acid A or Danshensu (DSS, 3-(3, 4-dihydroxyphenyl)-(2R)-lactic acid), derived from the root of Danshen (Salvia miltiorrhiza), has demonstrated heart and liver protective properties. In this work, we investigated the antioxidant activity and hepatoprotective activity of Danshensu alone and in combination with different agents, such as probiotic bacteria (Lactobacillus casei and Lactobacillus acidophilus), against several assays. The inhibition mechanism of the methylation gene biomarkers, such as DNMT-1, MS, STAT-3, and TET-1, against DSS was evaluated by molecular docking and RT-PCR techniques. The physicochemical and pharmacokinetic ADMET properties of DSS were determined by SwissADME and pkCSM. The results indicated that all lipid blood test profiles, including cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C), were reduced after the oral administration of Danshensu combined with probiotics (L. casei and L. acidophilus) that demonstrated good, efficient free radical scavenging activity, measured using anti-oxidant assays. ADMET and drug-likeness properties certify that the DSS could be utilized as a feasible drug since DSS showed satisfactory physicochemical and pharmacokinetic ADMET properties.

Idioma originalInglês
Número do artigo279
RevistaBiomedicines
Volume12
Número de emissão2
DOIs
Estado da publicaçãoPublicadas - 25 jan. 2024

Nota bibliográfica

Publisher Copyright:
© 2024 by the authors.

Financiamento

Financiadoras/-esNúmero do financiador
Fundação para a Ciência e TecnologiaUIDP/04567/2020

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