the General Program of National Natural Science Foundation of China(81871313);the Major Basic Science Research Project of Guizhou Province(黔科合J重大字〔2015〕2003);the Major Special Funds of Guizhou Province(黔科合重大专项字〔2014〕6008)
Pingping REN, Liping SHU, Yihui WANG, et al. Developmental toxicity of embryonic 1-naphthol exposure in zebrafish[J]. Journal of Third Military Medical University, 2019, 41(14): 1321-1327.
DOI:
Pingping REN, Liping SHU, Yihui WANG, et al. Developmental toxicity of embryonic 1-naphthol exposure in zebrafish[J]. Journal of Third Military Medical University, 2019, 41(14): 1321-1327. DOI: 10.16016/j.1000-5404.201901133.
Developmental toxicity of embryonic 1-naphthol exposure in zebrafish
To investigate the toxic effects of embryonic exposure to 1-naphthol (1-NAP) on zebrafish development and explore the possible mechanism.
Methods
2
Fertilized zebrafish eggs were exposed to 1-NAP at the concentrations of 40
80
160 and 200 μmol/L on 24 h post fertilization (hpf). The numbers of zebrafish malformations and deaths were recorded at 120 hpf
and the deformity rate
hatching rate and the median lethal concentration (IC
50
) of 1-NAP were calculated. The hatched zebrafish with or without embryonic exposure to 50 μmol/L 1-NAP and pretreatment with N-acetylcysteine (NAC) were examined for levels of reactive oxygen species (ROS)
malondialdehyde (MDA)
reduced glutathione (GSH)
total sulfhydryl
and activities of superoxide dismutase (SOD) and catalase (CAT); Western blotting was performed to detect the expression of Caspase-3 and Bax.
Results
2
The IC
50
of 1-NAP in zebrafish embryos was 111.31 μmol/L
and the zebrafish embryos exposed to high-concentration (
>
80 μmol/L) 1-NAP exhibited obviously increased mortality and deformity rates with a significantly reduced hatch
ing rate
demonstrating significant developmental toxicity of 1-NAP. Embryonic exposure to 50 μmol/L 1-NAP significantly increased the levels of ROS and MDA
lowered the levels of GSH and total sulfhydryl
suppressed the activities of antioxidant enzymes CAT and SOD (
P
<
0.001)
and decreased the expression levels of Caspase-3 and Bax in the hatched zebrafish. The zebrafish embryos pretreated with 0.5 mmol/L NAC prior to 1-NAP exposure showed a significantly decreased abnormality rate with obviously lowered ROS and MDA levels
restoration of GSH and total sulfhydryl content and SOD and CAT activities
and obviously reduced expression levels of Caspase-3 and Bax.
Conclusion
2
The developmental toxicity of 1-NAP in zebrafish embryos is probably associated with enhanced oxidative stress induced by 1-NAP.
关键词
Keywords
references
YAN X L, HU X Y, CHEN T, et al . Adsorptive removal of 1-naphthol from water with Zeolitic imidazolate framework-67[J ] . J Phys Chem Solid, 2017, 107: 50-54. DOI:10.1016/j.jpcs.2017.03.024.
YANG X Z, ZHANG Y Z, WANG L P, et al . Preparation of a thermally modified diatomite and a removal mechanism for 1-naphthol from solution[J ] . Water, 2017, 9(9): 651. DOI: 10.3390/w9090651.
HU W Y, MIN X B, LI X Y, et al . Enhanced degradation of 1-naphthol in landfill leachate using Arthrobacter sp[J ] . Environ Technol, 2019, 40(7): 835-842. DOI:10. 1080/09593330.2017.1408695.
QIANG Y, WANG W F, DHODARY B, et al . Zeolitic imidazolate framework 8 (ZIF-8) reinforced macroporous resin D101 for selective solid-phase extraction of 1-naphthol and 2-naphthol from phenol compounds[J ] . Electrophoresis, 2017, 38(13/14): 1685-1692. DOI: 10.1002/elps.201600569.
ZHENG H L, GAO Y, ZHU K R, et al . Investigation of the adsorption mechanisms of Pb(Ⅱ) and 1-naphthol by β-cyclodextrin modified graphene oxide nanosheets from aqueous solution[J ] . J Colloid Interface Sci, 2018, 530: 154-162. DO I: 10.1016/j.jcis. 2018.06.083.
MOLINA-ESPEJA P, CAÑELLAS M, PLOU F J, et al . Synthesis of 1-naphthol by a natural peroxygenase engineered by directed evolution[J ] . Chembiochem, 2016, 17(4): 341-349. DOI: 10.1002/cbic.201500493.
WANG C, YANG X, ZHENG Q, et al . Halobenzoquinone-induced developmental toxicity, oxidative stress, and apoptosis in zebrafish embryos[J ] . Environ Sci Technol, 2018, 52(18): 10590-10598. DOI: 10.1021/ acs.est.8b02831.
MU X Y, SHEN G M, HUANG Y, et al . The enantioselective toxicity and oxidative stress of beta-cypermethrin on zebrafish[J ] . Environ Pollut, 2017, 229: 312-320. DOI: 10.1016/j.envpol.2017.05.088.
HU R Y, SUN C J, JIN L, et al . Vinblastine enhances the expression of tumor resistance gene abcb4 in zebrafish[J ] . Basic Clin Med, 2017, 37(6): 758-762. DOI: 10.16352/j.issn.1001-6325.2017.06.003.
MUGONI V, CAMPOREALE A, SANTORO M M. Analysis of oxidative stress in zebrafish embryos[J]. J Vis Exp, 2014 (89). DOI: 10. 3791/51328.
FÉLIX L M, VIDAL A M, SERAFIM C, et al . Ketamine induction of p53-dependent apoptosis and oxidative stress in zebrafish (Danio rerio) embryos[J ] . Chemosphere, 2018, 201: 730-739. DOI: 10.1016/j. chemosphere.2018.03.049.
WANG Z K, LI G Y, WU Q, et al . Microcystin-LR exposure induced nephrotoxicity by triggering apoptosis in female zebrafish[J ] . Chemosphere, 2019, 214: 598-605. DOI: 10.1016/j.chemosphere. 2018.09.103.
ALDERMAN S L, LEISHMAN E M, FUZZEN M L M, et al . Corticotropin-releasing factor regulates caspase-3 and may protect developing zebrafish from stress-induced apoptosis[J ] . Gen Comp Endocrinol, 2018, 265: 207-213. DOI: 10.1016/j.ygcen. 2018.05.025.
ZENG C, SUN H, XIE P, et al . The role of apoptosis in MCLR-induced developmental toxicity in zebrafish embryos[J ] . Aquat Toxicol, 2014, 149: 25-32. DOI: 10.1016/j. aquatox.2014.01.021.
KHAYYAT A, TOBWALA S, HART M, et al . N-acetylcysteine amide, a promising antidote for acetaminophen toxicity[J ] . Toxicol L ett, 2016, 241: 133-142. DOI: 10.1016/j.toxlet. 2015.11.008.
ZHAO S J, LIU Y, WANG F, et al . N-acetylcysteine protects against microcystin-LR-induced endoplasmic reticulum stress and germ cell apoptosis in zebrafish testes[J ] . Chemo- sphere, 2018, 204: 463-473. DOI: 10.1016/j.chemosphere.2018.04.020.
ZOU Y, ZHANG Y, HAN L W, et al . Oxidative stress-mediated developmental toxicity induced by isoniazide in zebrafish embryos and larvae[J ] . J Appl Toxicol, 2017, 37(7):842-852. DOI: 10.1002/jat.3432.
USENKO C Y, ABEL E L, KUDELA M, et al . Comparison of PBDE congeners as inducers of oxidative stress in zebrafish[J ] . Environ Toxicol Chem, 2015, 34(5): 1154-1160. DOI: 10.1002/etc.2922.
LIU H, GOONERATNE R, HUANG X, et al . A rapid in vivo zebrafish model to elucidate oxidative stress-mediated PCB126-induced apoptosis and developmental toxicity[J ] . Free Radic Biol Med, 2015, 84: 91-102. DOI: 10.1016/j.freeradbiomed.2015.03.002..
NI H, PENG L, GAO X G, et al . Effects of maduramicin on adult zebrafish (Danio rerio): Acute toxicit y, tissue damage and oxidative stress[J ] . Ecotoxicol Environ Saf, 2019, 168: 249-259. DOI: 10.1016/j.ecoenv.2018.10.040.
KRAMER A C, WEBER J, ZHANG Y, et al . TP53 modulates oxidative stress in gata1+ erythroid cells[J ] . Stem Cell Reports, 2017, 8(2): 360-372. DOI: 10.1016/j.stemcr.2016. 12.025.
PATRINOSTRO X, CARTER M L, KRAMER A C, et al . A model of glucose-6-phosphate dehydrogenase deficiency in the zebrafish[J ] . Exp Hematol, 2013, 41(8): 697-710.e2. DOI: 10.1016/j.exphem.2013.04.002.
Role and mechanism of SIRT3 in oxidative stress and mitochondrial biogenesis in alveolar type II cells
p300 promotes hepatic lipid accumulation in dyslipidemia by regulating SREBP-1c acetylation
Protein phosphatase 2A promotes mitophagy to alleviate fructose-induced mitochondrial oxidative damage in M2-type macrophages
Regulation and mechanism of Gm49394 on islet-β cell apoptosis
Asiaticoside alleviates ferroptosis in myelodysplastic syndrome by activating SMAD7
Related Author
ZHOU Jun
LIU Yaojun
LIU Jing
GAO Ruobing
LI Changhong
FENG Xifeng
SHEN Hao
HUANG Hong
Related Institution
Department of Human Anatomy, Anhui Medical University
Laboratory of Stem Cell and Tissue Engineering, Chongqing Medical University
Institute of Field Surgery, Daping Hospital, Army Medical University
Department of Geriatrics and Special Service Medicine, First Affiliated Hospital(Southwest Hospital), Army Medical University (Third Military Medical University)