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A Commonly Used Biocide 2-N-octyl-4-isothiazolin-3-oneInduces Blood-Brain Barrier Dysfunction via Cellular Thiol Modification and Mitochondrial Damageopen access

Authors
Kim, DonghyunKim, Eun-HyeChoi, SungbinLim, Kyung-MinTie, LuMajid, ArshadBae, Ok-Nam
Issue Date
Mar-2021
Publisher
MDPI
Keywords
isothiazolinone (IT) biocide; 2-n-Octyl-4-isothiazolin-3-one (OIT); blood– brain barrier (BBB) model; protein S-nitrosylation (SNO); mitochondrial dysfunction; oxidative stress
Citation
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.22, no.5, pp 1 - 17
Pages
17
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume
22
Number
5
Start Page
1
End Page
17
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/438
DOI
10.3390/ijms22052563
ISSN
1661-6596
1422-0067
Abstract
Isothiazolinone (IT) biocides are potent antibacterial substances commonly used as preservatives or disinfectants, and 2-n-Octyl-4-isothiazolin-3-one (OIT; octhilinone) is a common IT biocide that is present in leather products, glue, paints, and cleaning products. Although humans are exposed to OIT through personal and industrial use, the potentially deleterious effects of OIT on human health are still unknown. To investigate the effects of OIT on the vascular system, which is continuously exposed to xenobiotics through systemic circulation, we treated brain endothelial cells with OIT. OIT treatment significantly activated caspase-3-mediated apoptosis and reduced the bioenergetic function of mitochondria in a bEnd.3 cell-based in vitro blood-brain barrier (BBB) model. Interestingly, OIT significantly altered the thiol redox status, as evidenced by reduced glutathione levels and protein S-nitrosylation. The endothelial barrier function of bEnd.3 cells was significantly impaired by OIT treatment. OIT affected mitochondrial dynamics through mitophagy and altered mitochondrial morphology in bEnd.3 cells. N-acetyl cysteine significantly reversed the effects of OIT on the metabolic capacity and endothelial function of bEnd.3 cells. Taken together, we demonstrated that the alteration of the thiol redox status and mitochondrial damage contributed to OIT-induced BBB dysfunction, and we hope that our findings will improve our understanding of the potential hazardous health effects of IT biocides.
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