dc.contributorETT Spa
dc.contributorInstitute of Biophysics
dc.contributorUniversity of Eastern Piedmont
dc.contributorUniversity of Genova
dc.contributorItalian National Police
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2020-12-12T01:30:22Z
dc.date.accessioned2022-12-19T20:48:34Z
dc.date.available2020-12-12T01:30:22Z
dc.date.available2022-12-19T20:48:34Z
dc.date.created2020-12-12T01:30:22Z
dc.date.issued2020-01-01
dc.identifierDrug and Chemical Toxicology.
dc.identifier1525-6014
dc.identifier0148-0545
dc.identifierhttp://hdl.handle.net/11449/199084
dc.identifier10.1080/01480545.2020.1788057
dc.identifier2-s2.0-85087653699
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5379718
dc.description.abstractZornia latifolia is a plant suspected to possess psychoactive properties and marketed as a marijuana substitute under the name ‘maconha brava’. In this study, the effects of fractions obtained from a 2-propanol extract of aerial portions of the plant were determined by multielectrode array (MEA) analyses on cultured networks of rat cortical neurons. Lipophilic (ZL_lipo, mainly containing flavonoid aglycones), and hydrophilic (ZL_hydro, mainly containing flavonoid glycosides) fractions were initially obtained from the raw extract. ZL_lipo significantly inhibited mean firing rate (MFR) and mean bursting rate (MBR) of MEA recordings, while ZL_hydro induced no inhibition. Column chromatography separation of ZL_lipo yielded five fractions (ZL1-ZL5), among which ZL1 induced the strongest MFR and MBR inhibition. NMR and HPLC-MS analyses of ZL1 revealed the prevalence of the common flavonoids genistein (1) and apigenin (2) (in about a 1:1 ratio), and the presence of the rare flavone syzalterin (6,8-dimethylapigenin) (3) as a minor compound. Exposures of MEA to apigenin and genistein standards did not induce the MFR and MBR inhibition observed with ZL1, whereas exposure to syzalterin standard or to a 1:9 mixture syzalterin-genistein induced effects similar to ZL1. These inhibitory effects were comparable to that observed with high-THC hashish, possibly accounting for the plant psychoactive properties. Data indicate that Z. latifolia, currently marketed as a free herbal product, should be subjected to measures of control. In addition, syzalterin showed distinctive pharmacological properties, opening the way to its possible exploitation as a neuroactive drug.
dc.languageeng
dc.relationDrug and Chemical Toxicology
dc.sourceScopus
dc.subjectFlavonoids
dc.subjecthashish
dc.subjectmultielectrode array
dc.subjectpsychoactive metabolites
dc.subjectsmart drugs
dc.titleCannabis-like activity of Zornia latifolia Sm. detected in vitro on rat cortical neurons: major role of the flavone syzalterin
dc.typeArtículos de revistas


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