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001-es BibID:BIBFORM067785
035-os BibID:(scopus)84966269383 (wos)000371109600001
Első szerző:Frecska Ede (pszichiáter)
Cím:The therapeutic potentials of ayahuasca : possible effects against various diseases of civilization / Frecska, E., Bokor, P., Winkelman, M.
Dátum:2016
Megjegyzések:Ayahuasca is an Amazonian psychoactive brew of two main components. Its active agents are ?-carboline and tryptamine derivatives. As a sacrament, ayahuasca is still a central element of many healing ceremonies in the Amazon Basin and its ritual consumption has become common among the mestizo populations of South America. Ayahuasca use amongst the indigenous people of the Amazon is a form of traditional medicine and cultural psychiatry. During the last two decades, the substance has become increasingly known among both scientists and laymen, and currently its use is spreading all over in the Western world. In the present paper we describe the chief characteristics of ayahuasca, discuss important questions raised about its use, and provide an overview of the scientific research supporting its potential therapeutic benefits. A growing number of studies indicate that the psychotherapeutic potential of ayahuasca is based mostly on the strong serotonergic effects, whereas the sigma-1 receptor agonist effect of its active ingredient dimethyltryptamine raises the possibility that the ethnomedical observations on the diversity of treated conditions can be scientifically verified. Moreover, in the right therapeutic or ritual setting with proper preparation and mindset of the user, followed by subsequent integration of the experience, ayahuasca has proven effective in the treatment of substance dependence. This article has two important take-home messages: 1) the therapeutic effects of ayahuasca are best understood from a bio-psycho-socio-spiritual model, and 2) on the biological level ayahuasca may act against chronic low grade inflammation and oxidative stress via the sigma-1 receptor which can explain its widespread therapeutic indications.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
addiktológia
ayahuasca
civilizációs betegségek
dimetiltriptamine
oxidatív stressz
Megjelenés:Frontiers in Pharmacology. - 7 : 35 (2016), p. 1-17. -
További szerzők:Bokor Petra Winkelman, Michael J.
Internet cím:Szerző által megadott URL
DOI
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001-es BibID:BIBFORM105849
035-os BibID:(cikkazonosító)1043275 (WOS)000904989100001 (Scopus)85145269011
Első szerző:Viczján Gábor (kísérletes farmakológus)
Cím:The effect of a long-term treatment with cannabidiol-rich hemp extract oil on the adenosinergic system of the Zucker Diabetic Fatty (ZDF) rat atrium / Viczjan Gabor, Szilagyi Anna, Takacs Barbara, Ovari Ignac, Szekeres Reka, Tarjanyi Vera, Erdei Tamas, Teleki Vanda, Zsuga Judit, Szilvassy Zoltan, Juhasz Bela, Varga Balazs, Gesztelyi Rudolf
Dátum:2022
ISSN:1663-9812
Megjegyzések:Cannabidiol (CBD), the most extensively studied non-intoxicating phytocannabinoid, has been attracting a lot of interest worldwide owing to its numerous beneficial effects. The aim of this study was to explore the effect that CBD exerts on the adenosinergic system of paced left atria isolated from obese type Zucker Diabetic Fatty (ZDF) rats, maintained on diabetogenic rat chow, received 60 mg/kg/day CBD or vehicle via gavage for four weeks. We found that N6-cyclopentyladenosine (CPA), a relatively stable and poorly transported A1 adenosine receptor agonist, elicited a significantly weaker response in the CBD-treated group than in the vehicle-treated one. In contrast, adenosine, a quickly metabolized and transported adenosine receptor agonist, evoked a significantly stronger response in the CBD-treated group than in the vehicle-treated counterpart (excepting its highest concentrations). These results can be explained only with the adenosine transport inhibitory property of CBD (and not with its adenosine receptor agonist activity). If all the effects of CBD are attributed to the interstitial adenosine accumulation caused by CBD in the myocardium, then a significantly increased adenosinergic activation can be assumed during the long-term oral CBD treatment, suggesting a considerably enhanced adenosinergic protection in the heart. Considering that our results may have been influenced by A1 adenosine receptor downregulation due to the chronic interstitial adenosine accumulation, an adenosinergic activation smaller than it seemed cannot be excluded, but it was above the CBD-naïve level in every case. Additionally, this is the first study offering functional evidence about the adenosine transport inhibitory action of CBD in the myocardium.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
cannabidiol
ZDF rat
heart
A1 adenosine receptor
RRM
Megjelenés:Frontiers in Pharmacology. - 13 (2022), p. 1-12. -
További szerzők:Szilágyi Anna Tünde (1981-) Takács Barbara (1992-) (orvos) Óvári Ignác Szekeres Réka (1995-) (orvos) Tarjányi Vera (1993-) (orvos) Erdei Tamás Dániel (1992-) (kísérletes farmakológus) Teleki Vanda Zsuga Judit (1973-) (neurológus, pszichoterapeuta, egészségügyi szakmanager) Szilvássy Zoltán (1957-) (belgyógyász, farmakológus, klinikai farmakológus) Juhász Béla (1978-) (kísérletes farmakológus) Varga Balázs (1984-) (kísérletes farmakológus) Gesztelyi Rudolf (1969-) (kísérletes farmakológus)
Pályázati támogatás:GINOP-2.3.4-15-2020-00008
GINOP
TKP2020-NKA-04
Egyéb
Internet cím:DOI
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