Synergistic Differential DNA Demethylation Activity of Danshensu (Salvia miltiorrhiza) Associated with Different Probiotics in Nonalcoholic Fatty Liver Disease

Author:

Hassan Amr1ORCID,Rijo Patrícia23ORCID,Abuamara Tamer M. M.45,Ali Lashin Lashin Saad46,Kamar Sherif A.47ORCID,Bangay Gabrielle28ORCID,Al-Sawahli Majid Mohammed910ORCID,Fouad Marina K.11,Zoair Mohammad A.12,Abdalrhman Tamer I.13ORCID,Elebeedy Dalia11,Ibrahim Ibrahim A.14,Mohamed Aly F.15,Abd El Maksoud Ahmed I.1116ORCID

Affiliation:

1. Department of Bioinformatics, Genetic Engineering and Biotechnology Research Institute (GEBRI), University of Sadat City, Sadat 32897, Egypt

2. CBIOS—Lusófona University’s Research Center for Biosciences and Health Technologies, 1749-024 Lisbon, Portugal

3. Instituto de Investigação do Medicamento (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, 1649-003 Lisbon, Portugal

4. Department of Basic Medical Science, Faculty of Dentistry, Al-Ahliyya Amman University, Amman 19111, Jordan

5. Department of Histology, Faculty of Medicine, Al-Azhar University, Cairo 11884, Egypt

6. Department of Medical Physiology, Faculty of Medicine, Mansoura University, Mansoura 35516, Egypt

7. Department of Anatomy and Embryology, Faculty of Medicine, Ain Shams University, Cairo 11566, Egypt

8. Universidad de Alcalá de Henares. Facultad de Farmacia, Departamento de Ciencias Biomédicas (Área de Farmacología; Nuevos agentes antitumorales, Acción tóxica sobre células leucémicas), Ctra. Madrid-Barcelona km. 33,600, 28805 Alcalá de Henares, Madrid, España

9. Department of Pharmaceutics, College of Pharmacy, The Islamic University, Najaf 54001, Iraq

10. Department of Pharmaceutical Technology, Faculty of Pharmacy, Kafr Elsheikh University, Kafr Elsheikh 33516, Egypt

11. College of Biotechnology, Misr University of Science and Technology, Giza 12573, Egypt

12. Department of Physiology, Faculty of Medicine, Al-Azhar University, Cairo 11884, Egypt

13. Department of Histology, Faculty of Medicine, Al-Azhar University, Assiut 71524, Egypt

14. Department of Plant Biotechnology, Genetic Engineering and Biotechnology Research Institute (GEBRI), University of Sadat City, Sadat 32897, Egypt

15. Holding Company for Vaccine and Sera Production (VACSERA), Giza 22311, Egypt

16. Department of Industrial Biotechnology, Genetic Engineering and Biotechnology Research Institute (GEBRI), University of Sadat City, Sadat 32897, Egypt

Abstract

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.

Funder

FCT—Fundação para a Ciência e a Tecnologia

Publisher

MDPI AG

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