Adding New Scientific Evidences on the Pharmaceutical Properties of Pelargonium quercetorum Agnew Extracts by Using In Vitro and In Silico Approaches.
Annalisa ChiavaroliMaria Loreta LiberoSimonetta Cristina Di SimoneAlessandra Acquavivanull NilofarLucia RecinellaSheila LeoneLuigi BrunettiDonatella CiciaAngelo Antonio IzzoGiustino OrlandoMuhammad Imran TousifAbdullahi Ibrahim UbaUgur CakilciogluMuzaffer MukemreOmer ElkiranLuigi MenghiniClaudio FerrantePublished in: Plants (Basel, Switzerland) (2023)
Pelargonium quercetorum is a medicinal plant traditionally used for treating intestinal worms. In the present study, the chemical composition and bio-pharmacological properties of P. quercetorum extracts were investigated. Enzyme inhibition and scavenging/reducing properties of water, methanol, and ethyl acetate extracts were assayed. The extracts were also studied in an ex vivo experimental model of colon inflammation, and in this context the gene expression of cyclooxygenase-2 (COX-2) and tumor necrosis factor α (TNFα) were assayed. Additionally, in colon cancer HCT116 cells, the gene expression of transient receptor potential cation channel subfamily M (melastatin) member 8 (TRPM8), possibly involved in colon carcinogenesis, was conducted as well. The extracts showed a different qualitative and quantitative content of phytochemicals, with water and methanol extracts being richer in total phenols and flavonoids, among which are flavonol glycosides and hydroxycinnamic acids. This could explain, at least in part, the higher antioxidant effects shown by methanol and water extracts, compared with ethyl acetate extract. By contrast, the ethyl acetate was more effective as cytotoxic agent against colon cancer cells, and this could be related, albeit partially, to the content of thymol and to its putative ability to downregulate TRPM8 gene expression. Additionally, the ethyl acetate extract was effective in inhibiting the gene expression of COX-2 and TNFα in isolated colon tissue exposed to LPS. Overall, the present results support future studies for investigating protective effects against gut inflammatory diseases.
Keyphrases
- gene expression
- oxidative stress
- dna methylation
- ionic liquid
- rheumatoid arthritis
- anti inflammatory
- magnetic resonance
- induced apoptosis
- systematic review
- signaling pathway
- inflammatory response
- risk assessment
- high resolution
- climate change
- nitric oxide
- transcription factor
- molecular docking
- single molecule
- blood brain barrier
- drug induced
- high speed
- nitric oxide synthase
- atomic force microscopy
- molecular dynamics simulations