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Sökning: id:"swepub:oai:DiVA.org:su-225988" > Effects of cylindro...

Effects of cylindrospermopsin, chlorpyrifos and their combination in a SH-SY5Y cell model concerning developmental neurotoxicity

Hinojosa, Maria G. (författare)
Stockholms universitet,Institutionen för biokemi och biofysik,University of Seville, Spain
Johansson, Ylva (författare)
Stockholms universitet,Institutionen för biokemi och biofysik
Jos, A. (författare)
visa fler...
Camean, A. M. (författare)
Forsby, Anna, 1963- (författare)
Stockholms universitet,Institutionen för biokemi och biofysik
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 (creator_code:org_t)
2024
2024
Engelska.
Ingår i: Ecotoxicology and Environmental Safety. - 0147-6513 .- 1090-2414. ; 269
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The cyanotoxin cylindrospermopsin (CYN) has been postulated to cause neurotoxicity, although the studies in this concern are very few. In addition, some studies in vitro indicate its possible effects on development. Furthermore, pesticides can be present in the same environmental samples as cyanotoxins. Therefore, chlor-pyrifos (CPF) has been one of the most common pesticides used worldwide. The aim of this report was to study the effects of CYN, isolated and in combination with CPF, in a developmental neurotoxicity in vitro model. The human neuroblastoma SH-SY5Y cell line was exposed during 6 days of differentiation to both toxics to study their effects on cell viability and neurite outgrowth. To further evaluate effects of both toxicants on cholinergic signaling, their agonistic and antagonistic activities on the alpha 7 homomeric nicotinic acetylcholine receptor (nAChR) were studied upon acute exposure. Moreover, a transcriptomic analysis by qPCR was performed after 6 days of CYN-exposure during differentiation. The results showed a concentration-dependent decrease on both cell viability and neurite outgrowth for both toxics isolated, leading to effective concentration 20 (EC20) values of 0.35 mu M and 0.097 mu M for CYN on cell viability and neurite outgrowth, respectively, and 100 mu M and 58 mu M for CPF, while the combination demonstrated no significant variations. In addition, 95 mu M and 285 mu M CPF demonstrated to act as an antagonist to nicotine on the nAChR, although CYN up to 2.4 mu M had no effect on the efficacy of these receptors. Additionally, the EC20 for CYN (0.097 mu M) on neurite outgrowth downregulated expression of the 5 genes NTNG2 (netrin G2), KCNJ11 (potassium channel), SLC18A3 (vesicular acetylcholine transporter), APOE (apolipoprotein E), and SEMA6B (semaphorin 6B), that are all important for neuronal development. Thus, this study points out the importance of studying the effects of CYN in terms of neurotoxicity and developmental neurotoxicity.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

Cylindrospermopsin
Chlorpyrifos
Developmental neurotoxicity
Neurite outgrowth
NAChRs
Transcriptomics

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