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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Genetic toxicity: in vivo

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Administrative data

Endpoint:
in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
Remarks:
Type of genotoxicity: chromosome aberration
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable publication which meets basic scientific principles

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1982

Materials and methods

Principles of method if other than guideline:
see details in remarks on material and methods.
GLP compliance:
not specified
Type of assay:
micronucleus assay

Test material

Constituent 1
Reference substance name:
nickel nitrate hexahydrate
IUPAC Name:
nickel nitrate hexahydrate
Details on test material:
- Name of test material (as cited in study report): nickel nitrate hexahydrate

Test animals

Species:
mouse
Strain:
Balb/c
Sex:
male
Details on test animals or test system and environmental conditions:



ENVIRONMENTAL CONDITIONS
- Temperature (°C):
- Humidity (%):
- Air changes (per hr):
- Photoperiod (hrs dark / hrs light):


IN-LIFE DATES: From: To:

Administration / exposure

Route of administration:
intraperitoneal
Duration of treatment / exposure:
5 weeks
Frequency of treatment:
single application
Post exposure period:
5 weeks
Doses / concentrations
Remarks:
Doses / Concentrations:
28; 56; 112; 224 mg/kg bw
Basis:
nominal conc.
No. of animals per sex per dose:
5 (males only)
Control animals:
other: physiological salt solution
Positive control(s):
200 mg/kg bw cyclophosphamide

Results and discussion

Test results
Sex:
male
Genotoxicity:
negative
Toxicity:
yes
Remarks:
from 56 mg/kg bw onwards
Vehicle controls validity:
not specified
Negative controls validity:
valid
Positive controls validity:
valid

Any other information on results incl. tables

Doses of 112 and 224 mg/kg bw Ni(N03)2*6H20 were highly toxic, all animals dying immediately or a few hours after treatment. Two mice injected with 56 mg Ni(N03)2*6H20 died after 1 week and these doses, corresponding roughly to 12 mg/kg bw nickel, were used for subsequent experiments.

The yield of micronuclei (per 1000) in the nickel nitrate group was 3.20 + 0.58 compared to 2.60 + 0.24 in the control group. The positive control group (200 mg/kg cyclophospamide) showed a yield of 46.60 + 6.08. No figures are given for the NCE/PCE ratio.Ni(N03)2*6H20 did not increase the number of polychromatic erythrocytes with micronuclei above the control level whereas many polychromatic erythrocytes carrying micronuclei were observed in the animals treated with the positive control cyclophosphamide.

Applicant's summary and conclusion