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Pregled bibliografske jedinice broj: 495936

Molecular regulations induced by acrolein in neuroblastoma SK-N-SH cells : Relevance to Alzheimer’s disease


Nam, Dang Thanh; Arseneault, Madeleine; Žarković, Neven; Waeg, Georg; Ramassamy, Charles
Molecular regulations induced by acrolein in neuroblastoma SK-N-SH cells : Relevance to Alzheimer’s disease // Journal of alzheimers disease, 21 (2010), 4; 1197-1216 doi:10.3233/JAD-2010-100417 (međunarodna recenzija, članak, znanstveni)


Naslov
Molecular regulations induced by acrolein in neuroblastoma SK-N-SH cells : Relevance to Alzheimer’s disease

Autori
Nam, Dang Thanh ; Arseneault, Madeleine ; Žarković, Neven ; Waeg, Georg ; Ramassamy, Charles

Izvornik
Journal of alzheimers disease (1387-2877) 21 (2010), 4; 1197-1216

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Acrolein ; lipid peroxidation ; neuroblastoma ; Alzheimers disease

Sažetak
Acrolein is the most reactive aldehyde among the by-products of lipid peroxidation. Growing evidence indicates that acrolein may play an important role in the pathogenesis of Alzheimer’s disease (AD). In AD, levels of acrolein are significantly higher in hippocampus and temporal cortex regions of the brain. However, little is known about its toxicity in neuronal cells. Using the neuroblastoma cell line SK-N-SH, our results show that acrolein is toxic from 10 µM, but its toxicity does not induce the activation of caspase-3 and DNA fragmentation. Protein carbonylation and 4-hydroxy-nonenal levels were increased after 0.5 h and 1 h of treatment, respectively. Furthermore acrolein induced a biphasic effect on glutathione levels with a rapid depletion followed by a progressive increase. We have further investigated the regulation of different redox signaling pathways. A treatment with 10 µM of acrolein for 30 min activated NFκB while this activation was suppressed after a 24 h of treatment. In contrast, Nrf2 was activated only after 24 h of acrolein exposure. Consequently, the expression of heme oxygenase-1 and γ-glutamyl-cysteine-synthase were elevated after 24 h of acrolein treatment. Sirt-1 was also upregulated after 24 h of acrolein treatment. The p66Shc and ERK1/2 proteins are known to be involved in oxidative stress. Acrolein, at 10 µM, induced the phosphorylation of p66Shc and ERK1/2 only after a short period of treatment. Collectively, these data strengthen the contribution of acrolein in the induction of oxidative stress as observed in mild cognitive impairment and in AD brain.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Projekt / tema
098-0982464-2519 - Lipidi, slobodni radikali i njihovi glasnici u integrativnoj onkologiji (Neven Žarković, )
108-0000000-0028 - Oksidacijski stres i tumori središnjeg živčanog sustava (Kamelija Žarković, )

Ustanove
Institut "Ruđer Bošković", Zagreb,
Medicinski fakultet, Zagreb

Autor s matičnim brojem:
Neven Žarković, (126952)

Časopis indeksira:


  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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