Review Article

Effects of Metal Oxide Nanoparticles in Zebrafish

Table 4

Impact of ZnO NPs on zebrafish.

StageNPs diameterTreatment timeTested concentrationsGeneral toxicity responseSpecific ROS responsesReference

Embryos20 nm96 h0.1, 0.5, 1, 5, 10, and 50 mg/LSignificant decrease of survival rate; delay in hatching rate dose-dependent; 96 h LC50 = 1.793 mg/L; and several abnormalities (body accusation and pericardial edema).[34]
Embryos20 nm96 hpf0.1, 0.5, 1, 5, 10, 50, and 100 mg/LDecrease of survival rate; delay in hatching rate; and incidence of pericardial edema dose-dependent.Increase in ROS production; low levels of Gstp2 and Nqo1 expressions; and downfall in counteracting the ROS by oxidative stress responses.[138]
Embryos<100 nm144 hpf1, 5, 10, 20, 50, and 100 mg/LNo effect bin the survival rate; important decrease in the hatching rate; and different malformations (spinal curvature and hyperemia).Important elevation in the SOD activity and MDA levels in a dose-dependent way; decrease in CAT activity; high levels of ROS; DNA damage only at the highest concentration tested; and important downregulation in Bcl-2, Nqo1, and Gstp2 transcriptions and upregulation in Ucp-2 level.[18]
Embryos30 nm96 hpf1, 5, 10, 25, 50, and 100 mg/LDecrease in survival rate and increase in hatching rate dose-dependent; severe decrease in body length.[18]
Embryos<100 nm96 hpf1, 5, 10, 20, 50, and 100 mg/LIncrease in the lipid peroxidation and SOD activity; upregulation in the expression of the ppaα and sod1; downregulation of cat; altered expression of antiapoptotic genes (bcl-2) and proapoptotic (bax, puma, and apaf-1; upregulation of p53 gene, with overexpression of its protein; and increase in the activity of caspase-3 and caspase-9.[116]
Embryos9.4 nm96 hpf0.2, 1, and 5 mg/L/Dramatic delay in hatching.Upregulation of the cat and Cu/Zn-sod transcripts in embryos and downregulation in eleuthero; important upregulation of Mt2<; different expression of mRNA of IL-1β, TNFα, and proinflammatory cytokines in eleuthero-embryos in comparison to embryos; alteration in the jun proto-oncogene (c-jun) embryos treated with high concentration; and perturbation in antiviral and immune-related gene Myxovirus resistance A.[131]
Embryos50–70 nm144 hpf0.1, 0.5, 1, 5, and 10 mg/LSignificant delay in hatching for ZnO NPs and Zn ions; no significant difference in cotreatment with ZnO NPs and NAC; and increased rates of delay in hatching in cotreatment with BSO.ROS generation; cotreatment with BSO: lower production of GSH.[132]
EmbryosNanospheres: 27 nm; nanosticks: 32×81 nmM; and SMPs: 202 nm120 hpf2, 4, 8, 16, and 32 mg Zn/LLC50 for Zn2+ =7.9 mg Zn/L, LC50 ZnO SMPs =10.0 mg Zn/L
LC50 nanosticks =7.1 Zn/L
LC50 nanospheres =11.9 mg Zn/L, respectively; higher toxicity of Zn ions in comparison to the different shaped NPs; and decrease of hatching rate dose-dependent in the embryos treated with all the different kind of nanoparticles and sulfate, strongest delay in samples exposed to nanosticks. Decrease dose-dependent of swimming activity; nanosticks more toxic than the other NPs.
[133]
Embryos5, 10, 15, 26, 34, 62, and 70 nm120 hpf0.016 to 250 mg/LSignificant mortality at 24 hpf for all the coated NPs; no alteration in mortality with bare nanoparticles.[134]
Embryos20-30 nm96 hpf0.01, 0.1, 1, and 10 mg/LHigher mortality rate by ZnO NPs than ZnSO4; LC25 for ZnO NPs =2.64 mg/L; LC25 for ZnSO4 = 7.75 mg/L; and significant embryonic malformations after both treatments (tail malformation, pericardial edema, and yolk sac edema).Downregulation of ogfrl2 and intl2 transcripts; upregulation of cyb5d1.[17]
Embryos<100 nm48 h10, 30, 60, 90, or 120 mg/LDelay in hatching, increased heart rate, pericardial edema, hyperemia, yolk sac edema, spinal curvature, tail deformities, and swim bladder abnormalities.SOD increased activity; sod1 upregulation; CAT downregulation; increased MDA levels; and increased production of ROS.[116]
Embryos40 nm96 hpf12.5, 25, 50 mg/L; PFOS (0, 0.4, 0.8, and 1.6 mg/L); and PFOS plus ZnO-NPs (0.4 + 12.5, 0.8 + 25, and 1.6 +50 mg/LSignificant increase of SOD activity as well as the activity of glutathione peroxidase; decrease dose-dependent of CAT activity: excess of ROD; increase of MDA level; upregulation of Bax; downregulation of Bcl-2; and no changes in the activities of the caspase-3 and caspase-9 (apart at 50 mg/L).[124]
Embryos300 nm72 h, 96 h10-100 ppmMitigate effects on the toxicity of ZnO NPs induced organic matter.[4]
Embryos, adultsPEG =2588 nm
PVA =58 nm
PVP =60
Bare =69 nm
Embryos: 72 h
Adults: 96 h
Embryos: 0.001-100 mg/LEmbryos: morphological defects (yolk sac edema, notochord bending, and egg coagulation) for bare and the capped NPs; rates of toxicity after treatment with 10 mg/L were 38.67%, 28.49%, 95.46%, and 89.32% for PEG-, PVA-, and PVP-capped and bare ZnO NPs, respectively; toxicity of bulk ZnO < ZnO-PVA < ZnO-PEG < ZnO NPs < ZnO-PVP.
Adults: LC50 of bulk ZnO =3239 mg/L; LC50 ZnO-PEG =6.44 mg/L; LC50 ZnO-PVA =9.40 mg/L; LC50 ZnO-PVP =3.77 mg/L; LC50 ZnO NPs =20.72 mg/L; and different morphological alterations; severe damages to the gill tissues (secondary lamellar structure alterations, necrosis, desquamation, acute cellular swelling, aneurysm, and lamellar disorganization).
[16]
Adults30 nm96 h2, 5, 10, 30, and 50 mg/LToxicity dose-dependent; 100% of mortality at 30 mg/mL of ZnO NPs and bulk ZnO; and LC50 = 4.92 mg/L and 3.31 mg/L, for the ZnO NPs and bulk ZnO, respectively.Increase of SOD activity SOD in the gut; reduction of CAT activity in the liver; increase of CAT activity in gut and gills (only slightly); decrease of GSH in the liver; MDA levels higher in the case of liver; and injuries in the gill tissues with shrinkage of the cells, loss of the cytoplasm, and abnormalities in the nuclei shapes.[9]

Abbreviations: Bax: BCL2-associated X, apoptosis regulator; bcl2: B-cell lymphoma 2; BSO: buthionine sulfoximine; CAT: catalase; cyb5d1: cytochrome b5 domain containing 1; GSH: glutathione; Gstp2: glutathione S-transferase P 2; hpf: hours post fertilization; IL-1β: interleukin-1β; intl2: Intelectin 2; LC50: 50% of lethal concentration; MDA: malondialdehyde; Mt2: metalloprotein 2; NAC: N-acetyl cysteine; Nqo1: NAD(P)H:quinone oxidoreductase; ogfrl2: opioid growth factor receptor-like; PEG: polyethylene glycol; PVA: polyvinyl alcohol; PVP: polyvinylpyrrolidone; PFOS: perfluoro octane sulfonate; ROS: reactive oxygen species; SMPs: submicron particles; TNFα: tumor necrosis factor-α; Ucp-2: uncoupling protein 2.