ZFIN ID: ZDB-PUB-141012-2
Embryonic exposure to carbendazim induces the transcription of genes related to apoptosis, immunotoxicity and endocrine disruption in zebrafish (Danio rerio)
Jiang, J., Wu, S., Wu, C., An, X., Cai, L., Zhao, X.
Date: 2014
Source: Fish & shellfish immunology   41(2): 493-500 (Journal)
Registered Authors:
Keywords: apoptosis, carbendazim, endocrine disruption, immunotoxicity, zebrafish
MeSH Terms:
  • Analysis of Variance
  • Animals
  • Apoptosis/drug effects*
  • Apoptosis/genetics
  • Benzimidazoles/pharmacology*
  • Carbamates/pharmacology*
  • DNA Primers/genetics
  • Electrophoresis, Agar Gel
  • Endocrine Disruptors/pharmacology*
  • Gene Expression Regulation, Developmental/drug effects*
  • Gene Expression Regulation, Developmental/immunology
  • Gonadal Steroid Hormones/biosynthesis
  • Gonadal Steroid Hormones/metabolism
  • Immunity, Innate/drug effects*
  • Immunotoxins/pharmacology*
  • RNA, Messenger/immunology
  • RNA, Messenger/metabolism
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Spectrophotometry, Ultraviolet
  • Thyroid Hormones/biosynthesis
  • Thyroid Hormones/metabolism
  • Zebrafish/embryology
  • Zebrafish/genetics*
  • Zebrafish/immunology
PubMed: 25304545 Full text @ Fish Shellfish Immunol.
ABSTRACT
Carbendazim is one of the most widespread environmental contaminant that can cause major concern to human and animal reproductive system. To date, very few studies have been conducted on the toxic effect of carbendazim in the non-target organism zebrafish (Danio rerio). The study presented here aimed to assess how carbendazim triggers apoptosis, immunotoxicity and endocrine disruption pathways in zebrafish during its embryo development. Our results demonstrated that the expression patterns of many key genes involved in cell apoptosis pathway (e.g. P53, Mdm2, Bbc3 and Cas8) were significantly up-regulated upon the exposure to carbendazim at the concentration of 500 μg/L, while the Bcl2 and Cas3 were down-regulated at the same concentration, interestingly, the expression level of Ogg1 decreased at all the exposure concentrations. It was also observed that the mRNA levels of CXCL-C1C, CCL1, IL-1b and TNFα which were closely related to the innate immune system, were affected in newly hatched zebrafish after exposed to different concentrations of carbendazim. Moreover, the expression of genes that are involved in the hypothalamic-pituitary-gonadal/thyroid (HPG/HPT) axis including VTG, ERα, ERβ2, Dio1, Dio2, Thraa and Thrb were all down-regulated significantly after the exposure to carbendazim. The expression levels of two cytochrome P450 aromatases CYP19a and CYP19b were increased significantly after 20 and 100 μg/L carbendazim exposure, respectively. Taken together, our results indicated that carbendazim had the potential to induce cell apoptosis and cause immune toxicity as well as endocrine disruption in zebrafish during the embryo developmental stage. The information presented here also help to elucidate the environmental risks caused by the carbendazim-induced toxicity in aquatic organisms.
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