Potential of NRF2 Pathway in Preventing Developmental and Reproductive Toxicity of Fine Particles

Air pollution is associated with significant adverse health effects. Recent studies support the idea that inhalation of fine particles can instigate extrapulmonary effects on the cardiovascular system through several pathways. The systemic transfer of ultrafine particles (UFPs) or soluble particle c...

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Main Authors: Ying-Ji Li, Ken Takeda, Masayuki Yamamoto, Tomoyuki Kawada
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Toxicology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/ftox.2021.710225/full
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spelling doaj-44f61105e0e14d589025a6c2088188f02021-09-13T05:50:32ZengFrontiers Media S.A.Frontiers in Toxicology2673-30802021-09-01310.3389/ftox.2021.710225710225Potential of NRF2 Pathway in Preventing Developmental and Reproductive Toxicity of Fine ParticlesYing-Ji Li0Ken Takeda1Masayuki Yamamoto2Tomoyuki Kawada3Department of Hygiene and Public Health, Nippon Medical School, Tokyo, JapanFaculty of Pharmaceutical Sciences, Sanyo-onoda City University, Sanyo-Onoda, JapanMedical Biochemistry, Tohoku University Graduate School of Medicine, Sendai, JapanDepartment of Hygiene and Public Health, Nippon Medical School, Tokyo, JapanAir pollution is associated with significant adverse health effects. Recent studies support the idea that inhalation of fine particles can instigate extrapulmonary effects on the cardiovascular system through several pathways. The systemic transfer of ultrafine particles (UFPs) or soluble particle components (organic compounds and metals) is of particular concern. An integral role of reactive oxygen species (ROS)-dependent pathways has been suggested in systemic inflammatory responses and vascular dysfunction at the molecular level. Accumulating lines of evidence suggest that fine particles affect fetal development, giving rise to low birth weight and a reduction in fetal growth, and also affect the immune, cardiovascular, and central nervous systems. Oxidative stress plays an important role in fine particles toxicity; pre-treatment with antioxidants partially suppresses the developmental toxicity of fine particles. On the other hand, Nuclear factor erythroid-derived 2-like 2 (Nfe2l2), also known as NRF2, is a transcription factor essential for inducible and/or constitutive expression of phase II and antioxidant enzymes. Studies using Nrf2-knockout mice revealed that NRF2 dysfunction is intimately involved in the pathogenesis of various human diseases. Multiple single nucleotide polymorphisms (SNPs) have been detected in human NRF2 locus. An NRF2 gene SNP (−617C > A; rs6721961), located in the upstream promoter region, affects the transcriptional level of NRF2 and thereby the protein level and downstream gene expression. It has been reported that the SNP-617 is associated with various diseases. The onset and exacerbation of the diseases are regulated by genetic predisposition and environmental factors; some people live in the air-polluted environment but are not affected and remain healthy, suggesting the presence of individual differences in the susceptibility to air pollutants. NRF2 polymorphisms may also be associated with the fetal effects of fine particles exposure. Screening high-risk pregnant women genetically susceptible to oxidative stress and prevention by antioxidant interventions to protect fetal development in air-polluted areas should be considered. This article reviews the recent advances in our understanding of the fetal health effects of fine particles and describes potential chemoprevention via the NRF2 pathway to prevent the developmental and reproductive toxicity of fine particles.https://www.frontiersin.org/articles/10.3389/ftox.2021.710225/fullultrafine and nano-sized particlesoxidative stressantioxidantsfetal developmentNRF2 SNP
collection DOAJ
language English
format Article
sources DOAJ
author Ying-Ji Li
Ken Takeda
Masayuki Yamamoto
Tomoyuki Kawada
spellingShingle Ying-Ji Li
Ken Takeda
Masayuki Yamamoto
Tomoyuki Kawada
Potential of NRF2 Pathway in Preventing Developmental and Reproductive Toxicity of Fine Particles
Frontiers in Toxicology
ultrafine and nano-sized particles
oxidative stress
antioxidants
fetal development
NRF2 SNP
author_facet Ying-Ji Li
Ken Takeda
Masayuki Yamamoto
Tomoyuki Kawada
author_sort Ying-Ji Li
title Potential of NRF2 Pathway in Preventing Developmental and Reproductive Toxicity of Fine Particles
title_short Potential of NRF2 Pathway in Preventing Developmental and Reproductive Toxicity of Fine Particles
title_full Potential of NRF2 Pathway in Preventing Developmental and Reproductive Toxicity of Fine Particles
title_fullStr Potential of NRF2 Pathway in Preventing Developmental and Reproductive Toxicity of Fine Particles
title_full_unstemmed Potential of NRF2 Pathway in Preventing Developmental and Reproductive Toxicity of Fine Particles
title_sort potential of nrf2 pathway in preventing developmental and reproductive toxicity of fine particles
publisher Frontiers Media S.A.
series Frontiers in Toxicology
issn 2673-3080
publishDate 2021-09-01
description Air pollution is associated with significant adverse health effects. Recent studies support the idea that inhalation of fine particles can instigate extrapulmonary effects on the cardiovascular system through several pathways. The systemic transfer of ultrafine particles (UFPs) or soluble particle components (organic compounds and metals) is of particular concern. An integral role of reactive oxygen species (ROS)-dependent pathways has been suggested in systemic inflammatory responses and vascular dysfunction at the molecular level. Accumulating lines of evidence suggest that fine particles affect fetal development, giving rise to low birth weight and a reduction in fetal growth, and also affect the immune, cardiovascular, and central nervous systems. Oxidative stress plays an important role in fine particles toxicity; pre-treatment with antioxidants partially suppresses the developmental toxicity of fine particles. On the other hand, Nuclear factor erythroid-derived 2-like 2 (Nfe2l2), also known as NRF2, is a transcription factor essential for inducible and/or constitutive expression of phase II and antioxidant enzymes. Studies using Nrf2-knockout mice revealed that NRF2 dysfunction is intimately involved in the pathogenesis of various human diseases. Multiple single nucleotide polymorphisms (SNPs) have been detected in human NRF2 locus. An NRF2 gene SNP (−617C > A; rs6721961), located in the upstream promoter region, affects the transcriptional level of NRF2 and thereby the protein level and downstream gene expression. It has been reported that the SNP-617 is associated with various diseases. The onset and exacerbation of the diseases are regulated by genetic predisposition and environmental factors; some people live in the air-polluted environment but are not affected and remain healthy, suggesting the presence of individual differences in the susceptibility to air pollutants. NRF2 polymorphisms may also be associated with the fetal effects of fine particles exposure. Screening high-risk pregnant women genetically susceptible to oxidative stress and prevention by antioxidant interventions to protect fetal development in air-polluted areas should be considered. This article reviews the recent advances in our understanding of the fetal health effects of fine particles and describes potential chemoprevention via the NRF2 pathway to prevent the developmental and reproductive toxicity of fine particles.
topic ultrafine and nano-sized particles
oxidative stress
antioxidants
fetal development
NRF2 SNP
url https://www.frontiersin.org/articles/10.3389/ftox.2021.710225/full
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