In vitro antibacterial and antioxidant activity of flavonoids from the roots of Tephrosia vogelii: a combined experimental and computational study

被引:2
|
作者
Abera, Bihon [2 ]
Melaku, Yadessa [2 ]
Shenkute, Kebede [2 ]
Degu, Sileshi [1 ]
Abebe, Abiy [1 ]
Gemechu, Worku [1 ]
Endale, Milkyas [1 ]
Woldemariam, Messay [3 ]
Hunsen, Mo [5 ]
Hussein, Ahmed A. [4 ]
Dekebo, Aman [2 ,6 ]
机构
[1] Armauer Hansen Res Inst, Tradit & Modern Med Res & Dev Directorate, POB 1005, Addis Ababa, Ethiopia
[2] Adama Sci & Technol Univ, Sch Appl Nat Sci, Dept Appl Chem, POB 1888, Adama, Ethiopia
[3] Armauer Hansen Res Inst, Pharmaceut Ind Dev, POB 1005, Addis Ababa, Ethiopia
[4] Cape Peninsula Univ Technol, Dept Chem, Bellville Campus, ZA-7535 Bellville, South Africa
[5] Kenyon Coll, Dept Chem, Gambier, OH 43022 USA
[6] Adama Sci & Technol Univ, Inst Pharmaceut Sci, Adama 1888, Ethiopia
关键词
T; vogelii; antibacterial; antioxidant; molecular docking; ADME; binding energy; DRUG; EXTRACTS;
D O I
10.1515/znc-2024-0044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tephrosia vogelii is a traditional medicinal plant used to treat hypertension, diarrhea and urinary disorders. Silica gel chromatographic separation of CH2Cl2/MeOH (1:1) roots extract of T. vogelii afforded seven compounds namely; beta-sitosterol (1a), stigmasterol (1b), 6a, 12a-dehydro-deguelin (2), tephrosin (3), maackiain (4), obovatin (5) and 6-oxo, 6a, 12a-dehydro-deguelin (6). GC-MS analysis of essential oils from the root of T. vogelii displayed a total of 17 compounds of which cis-nerolidol (41.7 %) and cadinol (19.7 %) were the major constituents. CH2Cl2/MeOH (1:1) extract, MeOH extract, maackiain (4) and obovatin (5) showed moderate inhibitory activity against Pseudomonas aeruginosa with MIC value of 0.5, 0.66, 0.83 and 0.83 mg/mL, respectively, compared to ciprofloxacin (MIC of 0.078 mu g/mL). 6a, 12a-dihydro-deguelin (2), and 6-oxo, 6a, 12a-dehydro-deguelin (6) displayed significant activity against S. epidermis with MIC values of 0.66 mg/mL. Tephrosin (3) and maackiain (4) also showed moderate antibacterial activity against Staphylococcus aureus and Proteus mirabilis with MIC values of 0.83 and 0.5 mg/mL, respectively, compared to ciprofloxacin (0.312 mu g/mL). The radical scavenging activity results indicated that tephrosin (3), obovatin (5) and 6-oxo, 6a, 12a-dehydro-deguelin (6) showed potent DPPH scavenging activity with IC50 values of 10.97, 10.43 and 10.73 mu g/mL, respectively, compared to ascorbic acid (IC50 of 5.83 mu g/mL). The docking prediction results revealed that 6a, 12a-dehydro-deguelin (2) displayed the best binding energy of -8.1 kcal/mol towards pyruvate kinase of S. aureus (PDB ID: 3T07) and -7.9 kcal/mol towards P. mirabilis urease (PDB ID: 1E9Y) and DNA gyrase B of Escherichia coli (PDB: 4F86) receptors compared to ciprofloxacin (-7.2 to -8.0 kcal/mol). Maackiain (4) and obovatin (5) displayed the minimum binding energy of -7.9 and -8.2 kcal/mol towards the LasR protein of P. aeruginosa (PDB: ID 2UV) and S. epidermidis FtsZ (PDB: ID 4M8I), respectively. The SwissADME drug-likeness and Pro Tox II toxicity prediction results indicated that compounds (2-6) obeyed Lipinski's rule of five with 0 violations and none of them were found to be hepatotoxic, mutagenic, and cytotoxic, respectively. The in vitro assessment results supported by the in silico analysis revealed that crude extracts and isolated compounds showed promising antibacterial and antioxidant activity, which proves the therapeutic potential of the roots of T. vogelii.
引用
收藏
页码:305 / 327
页数:23
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