New isolate from Salvinia molesta with antioxidant and urease inhibitory activity.
Nadra NaheedSaima MaherFarooq SaleemAjmal KhanAbdul WadoodSaima RasheedM Iqbal ChoudharyMatheus FroeyenIskandar AbdullahMuhammad Usman MirzaJohn F TrantSarfraz AhmadPublished in: Drug development research (2021)
Urease plays a significant role in the pathogenesis of urolithiasis pyelonephritis, urinary catheter encrustation, hepatic coma, hepatic encephalopathy, and peptic acid duodenal ulcers. Salvinia molesta was explored to identify new bioactive compounds with particular emphasis on urease inhibitors. The aqueous methanol extract was fractionated using solvents of increasing polarity. A series of column chromatography and later HPLC were performed on butanol extract. The structures of the resulting pure compounds were resolved using NMR (1D and 2D), infrared, and mass spectroscopy. The novel isolate was evaluated for antioxidant activity (using DPPH, superoxide anion radical scavenging, oxidative burst, and Fe+2 chelation assays), anti-glycation behavior, anticancer activity, carbonic anhydrase inhibition, phosphodiesterase inhibition, and urease inhibition. One new glucopyranose derivative 6'-O-(3,4-dihydroxybenzoyl)-4'-O-(4-hydroxybenzoyl)-α/β-D-glucopyranoside (1) and four known glycosides were identified. Glycoside 1 demonstrated promising antioxidant potential with IC50 values of 48.2 ± 0.3, 60.3 ± 0.6, and 42.1 ± 1.8 μM against DPPH, superoxide radical, and oxidative burst, respectively. Its IC50 in the Jack bean urease inhibition assay was 99.1 ± 0.8 μM. The mechanism-based kinetic studies presented that compound 1 is a mixed-type inhibitor of urease with a Ki value of 91.8 ± 0.1 μM. Finally, molecular dynamic simulations exploring the binding mode of compound 1 with urease provided quantitative agreement between estimated binding free energies and the experimental results. The studies corroborate the use of compound 1 as a lead for QSAR studies as an antioxidant and urease inhibitor. Moreover, it needs to be further evaluated through the animal model, that is, in vivo or tissue culture-based ex-vivo studies, to establish their therapeutic potential against oxidative stress phosphodiesterase-II and urease-induced pathologies.
Keyphrases
- oxidative stress
- high resolution
- anti inflammatory
- diabetic rats
- case control
- magnetic resonance
- ms ms
- hydrogen peroxide
- mass spectrometry
- high frequency
- molecular dynamics
- squamous cell carcinoma
- high throughput
- small cell lung cancer
- dna damage
- liquid chromatography
- ultrasound guided
- lymph node
- endothelial cells
- simultaneous determination
- solid state
- early onset
- endoplasmic reticulum stress
- risk assessment
- high speed
- single cell
- solid phase extraction
- high glucose
- ischemia reperfusion injury
- drug induced
- carbon dioxide
- urinary tract infection