The intergenerational toxic effects on offspring of medaka fish Oryzias melastigma from parental benzo[a]pyrene exposure via interference of the circadian rhythm. (December 2020)

• Record Type: Journal Article
• Authors: Yin, Xiaohan; Liu, Yong; Zeb, Rabia; Chen, Fangyi; Chen, Huiyun; Wang, Ke-Jian
• Is Part Of: Environmental pollution. Volume 267(2020)
• Publication Date: 2020-12
• Subjects: Oryzias melastigma -- Benzo[a]pyrene (BaP) -- Circadian rhythm -- Intergenerational immunotoxic mechanism -- Hypermethylation; Pollution -- Periodicals; Pollution -- Environmental aspects -- Periodicals; Environmental Pollution -- Periodicals; Pollution -- Périodiques; Pollution -- Aspect de l'environnement -- Périodiques; Pollution -- Effets physiologiques -- Périodiques; Pollution; Pollution -- Environmental aspects; Periodicals; Electronic journals; 363.73
• DOI: 10.1016/j.envpol.2020.115437
• Languages: English
• ISSNs: 0269-7491

Abstract

Abstract: Benzo[a]pyrene (BaP), a widely existed polycyclic aromatic hydrocarbon pollutant in aquatic environment, has toxic effects on marine animals and their generations, but the intergenerational immunotoxic mechanism underlying has not been clearly understood. In the study, the offspring of marine medaka ( oryzias melastigma ) which were exposed to 0.5 μg L −1 BaP suffered from circadian rhythm oscillation disorders and severe DNA damage. Many clock-associated genes like per1 were significantly modulated in offspring, both per1 and p53 were significantly inhibited that altered the progression of cell cycle and inhibited DNA repair, which possibly resulted in the increased mortality of offspring. The hypermethylation of the per1 promotor and abnormal levels of N 6 -methyladenosine (m 6 A) suggested that the underlying mechanism was probably related to the epigenetic modification. Moreover, the offspring from paternal BaP exposure had more severe DNA damage and a higher degree of hypermethylation than those from maternal exposure. F1 larvae from BaP-exposed parents were more sensitive to BaP exposure, showing that the expression of immune and metabolism-related genes were significantly up-regulated. Taken together, the parental toxicity induced by BaP could be passed to F1 generation and the mechanism underlying was probably associated with a characteristic circadian rhythm disorder. Graphical abstract: Image 1 Highlights: Parental BaP exposure induced circadian rhythm disorder in offspring. Parental BaP exposure caused immune disorder in offspring through per1 and p53. The possible mechanism was related to per1 promotor methylation and RNA methylation. The offspring from BaP exposed males suffered more serious effects. F1 larvae from BaP exposed parents were more sensitive to BaP. Abstract : The parental toxicity induced by BaP could be passed to F1 generation and the underlying mechanism was probably associated with circadian rhythm disorder.