Amelioration of rotenone-induced alterations in energy/redox system, stress response and cytoskeleton proteins by octanoic acid in zebrafish: A proteomic study

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Küçük Resim

Tarih

2022

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Wiley

Erişim Hakkı

info:eu-repo/semantics/embargoedAccess

Özet

Rotenone is used to generate Parkinson's disease (PD)-like symptoms in experimental animals. Octanoic acid (C8), is the principal fatty acid of medium-chain triglycerides in ketogenic diets. Beneficial effects of ketogenic diets were shown in PD. We applied proteomic methods to reveal the effects of octanoic acid in rotenone toxicity in zebrafish to gain information on the use of ketogenic diets in PD. Zebrafish were exposed to 5 mu g/ml rotenone and octanoic acid (20 and 60 mg/ml) for 30 days. LC-MS/MS analysis was performed. Raw files were analyzed by Proteome Discoverer 2.4 software, peptide lists were searched against Danio rerio proteins. STRING database was used for protein annotations or interactions. 2317 unique proteins were quantified, 302 proteins were differentially expressed. Proteins involved in cell organization, biogenesis, transport, response to stimulus were most frequently expressed. Our study is first to report that the alterations in the expressions of proteins related to energy and redox system, stress response, and cytoskeleton proteins caused by rotenone exposure were normalized by octanoic acid treatment in zebrafish.

Açıklama

Anahtar Kelimeler

Mass Spectrometry, Octanoic Acid, Parallel Reaction Monitoring, Proteomics, Rotenone, Zebrafish

Kaynak

Journal of Biochemical and Molecular Toxicology

WoS Q Değeri

Q2

Scopus Q Değeri

Q2

Cilt

36

Sayı

5

Künye

Sürmen, M. G., Sürmen, S., Cansız, D., Ünal, İ., Üstündağ, Ü. V., Alturfan, A. A. ... Emekli Alturfan, E. (2022). Amelioration of rotenone-induced alterations in energy/redox system, stress response and cytoskeleton proteins by octanoic acid in zebrafish: A proteomic study. Journal of Biochemical and Molecular Toxicology, 36(5). https://doi.org/10.1002/jbt.23024