2,5-xylidine

Repeated dose toxicity: oral

Administrative data

Endpoint:

short-term repeated dose toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

data from handbook or collection of data

Justification for type of information:

Data is from peer reviewed journal

Data source

Reference

Reference 1

Reference Type:

publication

Title:

Repeated oral toxicity study in rats

Author:

G. Magnusson et. al.

Year:

1979

Bibliographic source:

Toxicology,1979

Reference 2

Reference Type:

review article or handbook

Title:

Repeated oral dose toxicity study in rats

Author:

McGraw-Hill

Year:

1999

Bibliographic source:

McGraw-Hill, 1999

Reference 3

Reference Type:

other: Authoritative database

Title:

Repeated dose toxicity study of test chemical in rats

Author:

IFA GESTIS

Year:

2018

Bibliographic source:

IFA GESTIS,2018

Reference 4

Reference Type:

other: authoritative database

Title:

Repeated Dose 28-day Oral Toxicity Study

Author:

J-CHECK Japan Chemicals Collaborative Knowledge database

Year:

2010

Bibliographic source:

J-CHECK Japan Chemicals Collaborative Knowledge database, 2010

Reference 5

Reference Type:

other: Authoritative database

Title:

Repeated dose toxicity study of test chemical in rats

Author:

U.S. National Library of Medicine

Year:

2018

Bibliographic source:

HSDB (Hazardous Substances Data Bank); US national Library of Medicine,2018

Reference 6

Reference Type:

other: Secondary source

Title:

SIDS Initial Assessment Report

Author:

United Nations Environmental Programme (UNEP)

Year:

2012

Bibliographic source:

United Nations Environmental Programme (UNEP),2012

Reference 7

Reference Type:

other: Secondary source

Title:

Repeated oral dose toxicity study : rats

Author:

RTECS

Year:

2018

Bibliographic source:

RTECS,2018

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

other: as mentioned below

Principles of method if other than guideline:

The effect of repeated (4 weeks) oral administration of test chemical at the dose levels of 400 -500 mg/kg/day on the morphology and microsomal drug metabolising enzyme activity of the liver was studied in rats.

GLP compliance:

not specified

Test material

Test material information

Constituent 1

Reference substance name:

2,5-xylidine

EC Number:

202-451-0

EC Name:

2,5-xylidine

Cas Number:

95-78-3

Molecular formula:

C8H11N

IUPAC Name:

2,5-dimethylaniline

Constituent 2

Reference substance name:

2, 5-xylidine

IUPAC Name:

2, 5-xylidine

Details on test material:

- Name of test material: 2, 5-xylidine
- Molecular formula: C8H11N
- Molecular weight: 121.18
- Substance type: Organic
- Physical state: Liquid
- Analytical purity: >=97%

Test animals

Species:

rat

Strain:

Sprague-Dawley

Remarks:

CFY strain

Sex:

male/female

Details on test animals or test system and environmental conditions:

Details on test animal
TEST ANIMALS
- Source: Anglia Laboratory Animals, Alconbury, Huntingdon,
U.K.
- Age at study initiation: 8 weeks old
- Weight at study initiation:
Males: 200g; females: 170 g
- Housing: 5 rats/ polycarbonate cage
- Diet (e.g. ad libitum): The rats were allowed free access to food (Spratt's Laboratory Diet No. 1)
- Water (e.g. ad libitum): The rats were allowed free access to water

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 23-27°C
- Humidity (%):45-55%
- Photoperiod (hrs dark / hrs light): 12 : 12 h.

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

not specified

Details on oral exposure:

No data available

Analytical verification of doses or concentrations:

not specified

Details on analytical verification of doses or concentrations:

No data available

Duration of treatment / exposure:

4 weeks (28 days)

Frequency of treatment:

once daily for 4 weeks

Doses / concentrations

Remarks:

Doses / Concentrations:
dose levels of 400–500 mg/kg/day (Rats were dosed with 400
mg/kg/day during the first week, and thereafter at 500 mg/kg/day.
)
Basis:
no data

No. of animals per sex per dose:

Total:40
10 :male ; 10 :female :400 mg/kg
10 male;10:female:500 mg/kg

Control animals:

yes

Details on study design:

No data available

Positive control:

No data available

Examinations

Observations and examinations performed and frequency:

Observations and examinations performed & frequency

DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule:daily

BODY WEIGHT: Yes
- Time schedule for examinations: once a week


OTHER:
BIOCHEMISTRY:
Microsomal suspensions of the liver were prepared for assay of cytochrome P-450 concentration and activity of aniline hydroxylase and p-nitrophenol glucuronyltransferase.

Sacrifice and pathology:

GROSS PATHOLOGY: Yes ;At the termination of the study (24 h after the final dose of xylidine) the rats were sacrificed by cervical dislocation. Post-mortem examination was performed on all rats, including those dying during the study.

HISTOPATHOLOGY: Yes
Tissue samples of the liver were fixed in 10% neutral formalin solution,paraffin-embedded, sectioned and stained with haematoxylin and eosin and with Feulgen reaction. Fresh frozen sections were stained with haemalum and Oil Red O for detection of fat, with PAS for glycogen, and according to Wachstein and Meisel for glucose-6-phosphatase activity. For electron microscopical examination, small pieces of the livers were fixed in 4% glutaraldehyde in 0.05 M cacodylate buffer pH 7.3 for 2 h at +4°C and then post-fixed with 1% osmium tetroxide in 0.05 M cacodylate buffer pH 7.3 for 2 h at +4°C. The samples were dehydrated and embedded in epoxy resin. Survey sections were cut at 1 #m and stained with toluidine blue. Centrilobular areas in these sections were selected for ultrastructural examination.Silver-gold thin sections were then cut, picked up on uncoated grids,stained with lead citrate and examined electron microscopically.A Quantimet 720 Image analysing computer {Cambridge Instruments, Melbourn, Hertfordshire) was used to detect the Feulgen stained nuclei of the hepatocytes in the relevant centri- and perilobular regions. The nuclei count in a given area enabled the size of the hepatocytes to be calculated. The glucose-6-phosphatase activity was also measured on a Quantimet 720 using the densitometer module.

Other examinations:

Biochemistry:
The liver samples were placed in ice-cold 0.05 M Tris buffer (pH 7.4) containing 0.25 M sucrose and homogenised individually in 4 volumes of 0.05 M Tris buffer: 0.25 M sucrose solution (pH 7.4). The homogenates were centrifuged at 10 000 g for 20 min at 4°C, and the supernatant decanted. Microsomal fractions were prepared by centrifugation of this supernatant at 105 000 g for 1 h at 4°C. The microsomal pellet was suspended in 0.05 M Tris buffer: 0.25 M sucrose (pH 7.4) so that 1 ml of the suspension was approximately equivalent to 330 mg liver (wet wt). The microsomal suspension was kept at 4°C until used, within 2 h, for enzyme assays and cytochrome P-450 estimations. Concentrations of cytochrome P-450 in microsomal suspensions were assayed by the method of Omura and Sato and calculated from the molar extinction coefficient of 91 mM-1 cm-1.The activities of aniline hydroxylase and p-nitrophenol glucuronyltransferase were assayed in the microsomes at 37°C according to Wills and Pogell and Krisman .The protein concentration of the microsomal suspensions was determined by the method of Lowry et al. using bovine serum albumin as a standard.

Statistics:

Statistical significance between the values was calculated by Bartlett's t-test.

Results and discussion

Results of examinations

Clinical signs:

not specified

Description (incidence and severity):

not specified

Mortality:

mortality observed, non-treatment-related

Description (incidence):

During the study there were a few mortalities but none of them were due to the compounds administered.

Body weight and weight changes:

effects observed, non-treatment-related

Description (incidence and severity):

A reduction in body weight gain was observed in all treated rats

Food consumption and compound intake (if feeding study):

no effects observed

Description (incidence and severity):

There was no essential difference in food consumption between the control and treated groups.

Food efficiency:

not specified

Description (incidence and severity):

not specified

Water consumption and compound intake (if drinking water study):

not specified

Description (incidence and severity):

not specified

Ophthalmological findings:

not specified

Description (incidence and severity):

not specified

Haematological findings:

not specified

Description (incidence and severity):

not specified

Clinical biochemistry findings:

effects observed, treatment-related

Description (incidence and severity):

Glucose-6-phosphatase activity was evenly distributed in the control animals.

Biochemistry investigation:
The hepatic microsomal protein content in male and female rats treated with test chemical. A slight increase was evident in males dosed with test chemical, but not in female rats.

The hepatic microsomal cytochrome P-450 content was increased in males and females dosed with test chemical.

Total aniline hydroxylase activity was increased in all treated Rats.

Glucuronyltranferase activity (using p-nitrophenol as substrate) was increased in male and female rats dosed with test chemical and which was evident when results were expressed both in term of the total liver and per unit liver weight.

Urinalysis findings:

not specified

Description (incidence and severity):

not specified

Behaviour (functional findings):

not specified

Description (incidence and severity):

not specified

Immunological findings:

not specified

Description (incidence and severity):

not specified

Organ weight findings including organ / body weight ratios:

effects observed, treatment-related

Description (incidence and severity):

Livers were enlarged, but had a normal gross appearance. Relative liver weight was significantly increased compared to controls in both male and female rats (p<0.05 and p<0.01, respectively).

Gross pathological findings:

not specified

Description (incidence and severity):

not specified

Neuropathological findings:

not specified

Description (incidence and severity):

not specified

Histopathological findings: non-neoplastic:

effects observed, treatment-related

Description (incidence and severity):

Microscopic examination revealed a minimal fine droplet fatty change of the livers of comparable degree in both control and treated groups. Furthermore, there was an apparent enlargement of the hepatocytes, which was significant in the centrilobular region (p<0.01) for both males and females.

Staining with PAS demonstrated a centrilobular decrease in liver glycogen. This decrease was greater in males than in females.

Histopathological findings: neoplastic:

not specified

Description (incidence and severity):

not specified

Other effects:

not specified

Description (incidence and severity):

not specified

Details on results:

not specified

Effect levels

Dose descriptor:

LOAEL

Effect level:

475 mg/kg bw/day (nominal)

Based on:

test mat.

Sex:

male/female

Basis for effect level:

body weight and weight gain

clinical biochemistry

histopathology: non-neoplastic

organ weights and organ / body weight ratios

Target system / organ toxicity

Critical effects observed:

not specified

System:

other: not specified

Any other information on results incl. tables

Table:BODY AND LIVER WEIGHTS IN RATS TREATED WITH 400-500 mg/kg/day OF XYLIDINE ISOMERS FOR 4 WEEKS

GROUP	MALE				FEAMLE
	No. of animals	Final body weight(g)^a	Liver weight (g)	Liver wt. in % of final body wt	No. of animals	Final body weight(g)^a	Liver weight (g)	Liver wt. in % of final body wt
Control	5	400 ± 5	14.88 ± 0.60	3.72 ± 0.09	3	270 ± 16	9.86 + 1.07	3.62 ± 0.17
Test chemical	4	373 ± 11	20.56 ± 0.60^c	5.52 ± 0.13^d	4	238±12	10.99±0.54	4.62±0.18^b

^aInitial mean body weights of males and females were 192 ± 3 g and 172 ± 2 g respectively.

Symbols for statistical significance (compared with the control group)^bP < 0.05 ; cP < 0.01 ;^dP< 0.001.

 

Table:QUANTIFICATION OF THE MEAN HEPATOCYTE SIZE IN RATS TREATED WITH 400-500 mg/kg/day OF XYLIDINE ISOMERS FOR 4 WEEKS

GROUP	MALE			FEAMLE
	No. of animals	Mean hepatocyte area (μm^2)		No. of animals	Mean hepatocyte area (μm^2)
		Periportal region	Centrilobular region		Periportal region	Centrilobular region
Control	5	524	531	3	428	416
Test chemical	4	623^a	676^b	4	487^a	510^b

Symbols for statistical significance (compared with the control group):^aP <: 0.05;^bP <: 0.01.

 

Table:DENSITOMETRIC ESTIMATION OF MEAN GLUCOSE:6-PHOSPHATASE ACTIVITY IN THE LIVERS OF RATS TREATED WITH 400-500 mg/kg/day OF XYLIDINE ISOMERS FOR 4 WEEKS

GROUP	MALES		FEMALES
	Number of animals	Average density	Number of animals	Average density
CONTROL	5	51	3	45
TEST CHEMICAL	4	44^a	4	45

Symbols for statistical significance (compared with the control group):^aP < 0.05;^bP < 0.01.

Table:HEPATIC DRUG-METABOLISING ENZYME ACTIVITY/rag MICROSOMAL PROTEIN IN RATS TREATED WITH 400-500 mg/kg/day OF XYLIDINE ISOMERS FOR 4 WEEKS

The values are expressed as meant S.E.M.

 

GROUP	MALES				FEMALES
	Number of animals	Cytochrome P-450 (nmol/mg protein)	Aniline hydroxylase (μg product/h/mg protein)	Glucuronyl-tranferase (μg conjugate/h/mg protein)	Number of animals	Cytochrome P-450 (nmol/mg protein)	Aniline hydroxylase (μg product/h/mg protein)	Glucuronyl-tranferase (μg conjugate/h/mg protein)
CONTROL	5	0.252±0.011	1.78±0.18	3.83± 1.22	3	0.176±0.005	0.88±0.14	2.49 ±1.06
TEST CHEMICAL	4	0.342±0.038^a	2.10±0.30	10.76±1.36^b	4	0.246±0.008^b	1.17±0.19	11.33±1.64^c

Symbols for statistical significance (compared with control group):^aP < 0.05;^bP < 0.01;^cP < 0.001.

 

Table:HEPATIC DRUG-METABOLISING ENZYME ACTIVITY/g LIVER TISSUE IN RATS TREATED WITH 400--500 mg/kg/day OF XYLIDINE ISOMERS FOR 4 WEEKS

The values are expressed as mean + S.E.M.

GROUP	MALES
	Number of animals	Microsomal protein (mg/g liver)	Cytochrome P-450 (nmol/g liver)	Aniline hydroxylase (μg product/h/g liver)	Glucuronyl-tranferase (μg conjugate/h/g liver)
CONTROL	5	22.23 ± 1.82	5.53 ± 0.26	38.5 ± 2.4	78.2 ±18.6
TEST CHEMICAL	4	23.91 ± 1.41	8.23 ± 1.06^b	50.3 ± 1.1	258.0 ± 38.6^b
	FEMALES
CONTROL	3	23.02 ± 1.76	4.03 ± 0.26	20.1 ± 3.1	58.7± 26.9
TEST CHEMICAL	4	23.42 ± 3.16	5.38 ± 0.97	26.0 ± 2.0	257.9 ± 33.8 b

  Symbols for statistical significance (compared with control group):^aP < 0.05;^bP < 0.01;

^cP < 0.001.

Applicant's summary and conclusion

Conclusions:

The low-observed-adverse-effect-level (LOAEL) was considered to be 475 mg/kg/day when Sprague-Dawley derived rats (CFY strain) male and female rats were treated with test chemical via gavage for 28 days.

Executive summary:

The effect of repeated (4 weeks) oral administration of test chemical at the dose levels of 400 - 500 mg/kg/day on the morphology and microsomal drug metabolising enzyme activity of the liver was studied in Sprague-Dawley derived rats (CFY strain). No mortalities due to test substance administration occurred during the study. A reduction in body weight gain was observed in all treated rats, especially the males, but this was not significant. There was no difference in food consumption between control and treated groups. Livers were enlarged, but had a normal gross appearance. Relative liver weight was significantly increased compared to controls in both male and female rats (p<0.05 and p<0.01, respectively). Microscopic examination revealed a minimal fine droplet fatty change of the livers of comparable degree in both control and treated groups. Furthermore, there was an apparent enlargement of the hepatocytes, which was significant in the centrilobular region (p<0.01) for both males and females. Staining with PAS demonstrated a centrilobular decrease in liver glycogen. This decrease was greater in males than in females. Glucose-6-phosphatase activity was evenly distributed in control animals but in treated animals there was a centrilobular decrease in enzyme activity. The hepatic microsomal protein content was increased in males, but not in females. The hepatic microsomal cytochrome P-450 content was increased in males and females. Total aniline hydroxylase activity was not increased.Glucuronyltransferase activity was increased, but not significantly, over controls.Therefore, The low-observed-adverse-effect-level (LOAEL) was considered to be 475 mg/kg/day when Sprague-Dawley derived rats (CFY strain) male and female rats were treated with test chemical via gavage for 28 days.