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Preliminary chemical profile and in vitro pharmacological evaluation of the hallucinogenic plant Diplopterys cabrerana

dc.contributor.authorGarcia, Maria Rita
dc.contributor.authorDutka, Mykhaylo
dc.contributor.authorGuimarães, Sofia
dc.contributor.authorAndrade, Paula B.
dc.contributor.authorSeabra, Vítor
dc.contributor.authorDiana Dias da Silva
dc.contributor.authorGomes, Nelson G. M.
dc.contributor.authorDias da Silva, Diana Cristina
dc.date.accessioned2025-10-28T14:45:57Z
dc.date.available2025-10-28T14:45:57Z
dc.date.issued2024-05-01
dc.description.abstractFor the last few years, Ayahuasca ceremonies have been gaining popularity in recreational settings in Europe and North America [1]. Similar to Psychotria viridis, Diplopterys cabreranais also suggested to contain the psychoactive compound N,N-dimethyltryptamine, and is therefore used in Aya-huasca rituals for its ability to induce hallucinations, euphoria and entheogenic effects [1-3]. However, while information on the toxic profile of D. cabreranaremains very limited, its acquisition is easily ac-complished by consumers. We aimed to characterize the aqueous extracts of D. cabreranaleaves, mimicking those typically consumed, to identify bioactives that underlie the psychoactive or toxic effects, and evaluate their impact on neuronal function, neurotransmission and radical stress. Chemical characterization was attained by HPLC-DAD. Impact upon neuronal viability was assessed by the MTT assay (up to 1000 μg/mL) in SH-SY5Y neuroblastoma cells. Impact on neuromodulation and neuroinflammation was evaluated through acetylcholinesterase and 5-lipoxygenase inhibition, while an-tiradical properties were assessed by evaluating nitric oxide (•NO) and xanthine oxidase (XO) activity. Inhibition of the α-glucosidase enzyme was also evaluated. Statistical comparisons among groups per-formed by one-way ANOVA followed by Dunnett post hoc test. Preliminary characterization results revealed the presence of several catechin derivates, alongside two apigenin derivates and one tryp-tamine derivate. Cytotoxicity was not verified up to the highest concentration tested. Acetylcholinesterase inhibition was recorded starting at 250 μg/mL, and a concentration-dependent inhibition of 5-lipoxygen-ase was found (IC50=79.77 μg/mL). Concentration-dependent scavenging effects upon •NO and XO inhi-bition were verified at concentrations higher than 1.953 μg/mL and 31.25 μg/mL, respectively. At last, inhibition of α-glucosidase occurred with concentration-dependency and an IC50of 4.78 μg/mL. Conclu-sions:Although antiradical, anti-inflammatory and antidiabetic properties were verified, with no in vitrocytotoxicity being detected, further research is needed to elucidate the underlying mechanisms that might be involved in our preliminary results.por
dc.description.sponsorshipUIDB/50006/2020 REQUIMTE/LAQV.
dc.identifier.citationGarcia, M. R., Dutka, M., Guimarães, S., Andrade, P. B., Seabra, V., & Dias-da-Silva, D. (2024). Preliminary chemical profile and in vitro pharmacological evaluation of the hallucinogenic plant Diplopterys cabrerana. Scientific Letters, 1(Sup 1). https://doi.org/10.48797/sl.2024.221
dc.identifier.doi10.48797/sl.2024.221
dc.identifier.issn2795-5117
dc.identifier.urihttp://hdl.handle.net/10400.22/30693
dc.language.isoeng
dc.peerreviewedyes
dc.publisherIUCS-CESPU Publishing
dc.relation.hasversionhttps://publicacoes.cespu.pt/index.php/sl/article/view/221
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectNew psychoactive substances
dc.subjectAyahuasca
dc.subjectHallucinogenic plants
dc.subjectRecreational setting
dc.subjectNeuro-toxicity
dc.titlePreliminary chemical profile and in vitro pharmacological evaluation of the hallucinogenic plant Diplopterys cabreranapor
dc.typeconference poster
dspace.entity.typePublication
oaire.citation.conferenceDate2024-05
oaire.citation.conferencePlacePorto
oaire.citation.issuesup1
oaire.citation.titleScientific Letters - III TOXRUN International Congress
oaire.citation.volume1
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85
person.familyNameDias da Silva
person.givenNameDiana Cristina
person.identifier.ciencia-id7715-CF06-F0B5
person.identifier.orcid0000-0002-7331-9157
relation.isAuthorOfPublication1f32faf1-efa5-4ea0-982d-a755e1940abf
relation.isAuthorOfPublication.latestForDiscovery1f32faf1-efa5-4ea0-982d-a755e1940abf

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