Phytochemical Profile, Antioxidant Potential and Toxicity Evaluation of the Essential Oils from Duguetia and Xylopia Species (Annonaceae) from the Brazilian Amazon

• Published in: Antioxidants Vol. 11; no. 9; p. 1709
• Main Authors: Cascaes, Márcia Moraes, De Moraes, Ângelo Antônio Barbosa, Cruz, Jorddy Neves, Franco, Celeste de Jesus Pereira, E Silva, Renan Campos, Nascimento, Lidiane Diniz do, Ferreira, Oberdan Oliveira, Anjos, Tainá Oliveira dos, de Oliveira, Mozaniel Santana, Guilhon, Giselle Maria Skelding Pinheiro, Andrade, Eloisa Helena de Aguiar
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 30.08.2022; MDPI
• Subjects: Acetylcholinesterase; Amazon; Annonaceae; Antioxidants; Artemia salina; bioactive compounds; Biological activity; Caryophyllene; Caryophyllene oxide; Chemical composition; Cosmetics; Cytotoxicity; Duguetia; Essential oils; Free radicals; Humulene; medicinal plant; Metabolism; Multivariate analysis; natural products; Oils & fats; Phytochemicals; Sabinene; Software; Spathulenol; Species; Statistical analysis; Terpinolene; Toxicity; volatile compounds; Xylopia; α-Pinene; Brazil; United States > US; Amazon Basin
• ISSN: 2076-3921; 2076-3921
• DOI: 10.3390/antiox11091709

The essential oils (EOs) of Duguetia echinophora, D. riparia, Xylopia emarginata and X. frutescens (Annonaceae) were obtained by hydrodistillation and the chemical composition was analyzed by GC-MS. An antioxidant assay using the ABTS and DPPH radicals scavenging method and cytotoxic assays against Artemia salina were also performed. We evaluated the interaction of the major compounds of the most toxic EO (X. emarginata) with the binding pocket of the enzyme Acetylcholinesterase, a molecular target related to toxicity in models of Artemia salina. The chemical composition of the EO of D. echinophora was characterized by β-phellandrene (39.12%), sabinene (17.08%) and terpinolene (11.17%). Spathulenol (22.22%), caryophyllene oxide (12.21%), humulene epoxide II (11.86%) and allo-aromadendrene epoxide (10.20%) were the major constituents of the EO from D. riparia. Spathulenol (5.65%) and caryophyllene oxide (5.63%) were the major compounds of the EO from X. emarginata. The EO of X. frutescens was characterized by α-pinene (20.84%) and byciclogermacrene (7.85%). The results of the radical scavenger DPPH assays ranged from 15.87 to 69.38% and the highest percentage of inhibition was observed for the EO of X. emarginata, while for ABTS radical scavenging, the antioxidant capacity of EOs varied from 14.61 to 63.67%, and the highest percentage of inhibition was observed for the EO of X. frutescens. The EOs obtained from D. echinophora, X. emarginata and X. frutescens showed high toxicity, while the EO of D. riparia was non-toxic. Because the EO of X. emarginata is the most toxic, we evaluated how its major constituents were able to interact with the Acetylcholinesterase enzyme. The docking results show that the compounds are able to bind to the binding pocket through non-covalent interactions with the residues of the binding pocket. The species X. emarginata and X. frutescens are the most promising sources of antioxidant compounds; in addition, the results obtained for preliminary cytotoxicity of the EOs of these species may also indicate a potential biological activity.