Pregled bibliografske jedinice broj: 1165600
Cytotoxic, genotoxic, and oxidative stress-related effects of lysergic acid diethylamide (LSD) and phencyclidine (PCP) in the human neuroblastoma SH- SY5Y cell line
Cytotoxic, genotoxic, and oxidative stress-related effects of lysergic acid diethylamide (LSD) and phencyclidine (PCP) in the human neuroblastoma SH- SY5Y cell line // Arhiv za higijenu rada i toksikologiju, 72 (2021), 4; 333-342 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1165600 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Cytotoxic, genotoxic, and oxidative stress-related
effects of lysergic acid diethylamide (LSD) and
phencyclidine (PCP) in the human neuroblastoma SH-
SY5Y cell line
Autori
Jurič, Andreja ; Zandona, Antonio ; Tariba Lovaković, Blanka ; Rašić, Dubravka ; Pizent, Alica ; Kozina, Goran ; Katalinić, Maja ; Lucić Vrdoljak, Ana ; Brčić Karačonji, Irena
Izvornik
Arhiv za higijenu rada i toksikologiju (0004-1254) 72
(2021), 4;
333-342
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
antioxidant enzymes ; cell viability ; DNA damage ; GSH ; hallucinogenic drugs ; psychoactive substances ; ROS ; toxicity
Sažetak
Lysergic acid diethylamide (LSD) is a classic hallucinogen, widely abused for decades, while phencyclidine (PCP) has increased in popularity in recent years, especially among the adolescents. Very little is known about the general toxicity of these compounds, especially about their possible neurotoxic effects at the cell level. The aim of this study was to address these gaps by assessing the toxic effects of 24-hour exposure to LSD and PCP in the concentration range of 0.39–100 µmol/L in the human neuroblastoma SH-SY5Y cell line. After cell viability was established, cells treated with concentrations that reduced their viability up to 30 % were further subjected to the alkaline comet assay and biochemical assays that enable estimation of oxidative stress-related effects. Treatment with LSD at 6.25 µmol/L and with PCP at 3.13 µmol/L resulted with 88.06±2.05 and 84.17±3.19 % of viable cells, respectively, and led to a significant increase in primary DNA damage compared to negative control. LSD also caused a significant increase in malondialdehyde level, reactive oxygen species (ROS) production, and glutathione (GSH) level, PCP significantly increased ROS but lowered GSH compared to control. Treatment with LSD significantly increased the activities of all antioxidant enzymes, while PCP treatment significantly increased superoxide dismutase (SOD) and glutathione peroxidase (GPx) but decreased catalase (CAT) activity compared to control. Our findings suggest that LSD has a greater DNA damaging potential and stronger oxidative activity than PCP in SH-SY5Y cells.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
UIP-2017-05-7260 - MOLEKULARNI MEHANIZMI TOKSIČNOSTI PROTUOTROVA I POTENCIJALNIH LIJEKOVA (CellToxTargets) (Katalinić, Maja, HRZZ - 2017-05) ( CroRIS)
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb,
Sveučilište Sjever, Koprivnica,
Fakultet zdravstvenih studija u Rijeci
Profili:
Maja Katalinić
(autor)
Antonio Zandona
(autor)
Ana Lucić Vrdoljak
(autor)
Dubravka Rašić
(autor)
Blanka Tariba
(autor)
Goran Kozina
(autor)
Alica Pizent
(autor)
Irena Brčić Karačonji
(autor)
Andreja Jurič
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE