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Toxicological information

Acute Toxicity: inhalation

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Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1983

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: OECD Guideline 413 (Subchronic Inhalation Toxicity: 90-Day)
Deviations:
yes
Remarks:
yes limited pathology and blood work undertaken
GLP compliance:
no
Test type:
other: 90-d
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Dinitrogen oxide
EC Number:
233-032-0
EC Name:
Dinitrogen oxide
Cas Number:
10024-97-2
Molecular formula:
N2O
IUPAC Name:
nitrogen oxide
Test material form:
gas under pressure: liquefied gas

Test animals

Species:
mouse
Strain:
Swiss Webster
Sex:
male/female

Administration / exposure

Route of administration:
inhalation: gas
Type of inhalation exposure:
whole body
Vehicle:
air
Duration of exposure:
ca. 4 h
Concentrations:
0, 5000, 50000 or 500000 ppm
No. of animals per sex per dose:
15/sex/gp
Control animals:
yes

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 500 000 ppm
Exp. duration:
4 h

Any other information on results incl. tables

OBSERVATIONS:

Clinical signs of toxicity:

All animals survived to the scheduled necropsy.

 

Bodyweight and bodyweight gain:

Treatment related decreases in body weight were observed in high dose group animals, with a depression of 77 and 63% in body weight gain in males and females respectively. This depression in weight gain was statistically significant (p<0.025 and p<0.01, respectively).

 

Haematology & clinical chemistry:

No treatment related changes were observed in any of the parameter measured.

 

Urinalysis:

None undertaken

 

Sacrifice and Gross Pathology:

No treatment related changes were observed in any of the parameter measured.

 

Organ weights: 

No discussion of organ weight data.

Applicant's summary and conclusion

Conclusions:
Swiss Webster mice (15/sex/gp) were exposed to N2Oviawhole body inhalation at concentrations of 0, 5000, 50000 or 500000 ppm [0, 0.5, 5, 50%] for 4/h/d, 5d/wk over 14 wks. At necropsy limited histopathology and haematology / biochemistry parameters were measured. 
 
All animals survived to the scheduled necropsy. The study failed to demonstrate exposure related haematopoietic changes. There was no change in the white blood cell count nor was granulocytopenia or thrombocytopenia observed. The lack of effect suggests that either the strain of mouse was insensitive to N2O, or more likely that continuous exposure is necessary to induce leucocytopenia, as previous demonstrated following continuous exposure to N2O at high concentrations (20-80%). Furthermore, no treatment related changes in organ weights, biochemical or histopathological parameters were observed. 
 
Treatment related decreases in body weight were observed in high dose group animals, with a depression of 77 and 63% in body weight gain in males and females respectively. This depression in weight gain was statistically significant (p<0.025 and p<0.01, respectively).
 
The objective of the study was to demonstrate the maximum tolerated concentration of N2O, which was deemed to be 50% (500000 ppm). In terms of establishing a NOAEL, based on the results of this study and the data presented, 50000 ppm (5%) was deemed to be the NOAEL, based on statistically significant reductions in body weight gains observed at the LOAEL (500000 ppm [50%]).
Executive summary:

Swiss Webster mice (15/sex/gp) were exposed to N2Oviawhole body inhalation at concentrations of 0, 5000, 50000 or 500000 ppm [0, 0.5, 5, 50%] for 4/h/d, 5d/wk over 14 wks. At necropsy limited histopathology and haematology / biochemistry parameters were measured. 

 

All animals survived to the scheduled necropsy. The study failed to demonstrate exposure related haematopoietic changes. There was no change in the white blood cell count nor was granulocytopenia or thrombocytopenia observed. The lack of effect suggests that either the strain of mouse was insensitive to N2O, or more likely that continuous exposure is necessary to induce leucocytopenia, as previous demonstrated following continuous exposure to N2O at high concentrations (20-80%). Furthermore, no treatment related changes in organ weights, biochemical or histopathological parameters were observed. 

 

Treatment related decreases in body weight were observed in high dose group animals, with a depression of 77 and 63% in body weight gain in males and females respectively. This depression in weight gain was statistically significant (p<0.025 and p<0.01, respectively).

 

The objective of the study was to demonstrate the maximum tolerated concentration of N2O, which was deemed to be 50% (500000 ppm). In terms of establishing a NOAEL, based on the results of this study and the data presented, 50000 ppm (5%) was deemed to be the NOAEL, based on statistically significant reductions in body weight gains observed at the LOAEL (500000 ppm [50%]).