Tetrachloroethylene

Repeated dose toxicity: oral

Administrative data

Endpoint:

repeated dose toxicity: oral

Remarks:

other: Carcinogenicity bioassay

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: Non-GLP, non-guideline study, available as published report, adequate for assessment

Data source

Reference

Reference 1

Reference Type:

study report

Title:

Unnamed

Year:

1977

Reference 2

Reference Type:

publication

Title:

Carcinogencity studies on halogenated hydrocarbons

Author:

Weisburger EK

Year:

1977

Bibliographic source:

Environ Health Perspect. 21; 7-16

Materials and methods

Principles of method if other than guideline:

The bioassay was conducted according to a protocol of the National Cancer Institute

GLP compliance:

not specified

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

Tetrachloroethylene

EC Number:

204-825-9

EC Name:

Tetrachloroethylene

Cas Number:

127-18-4

Molecular formula:

C2Cl4

IUPAC Name:

tetrachloroethene

Details on test material:

- Name of test material (as cited in study report): tetrachloroethylene- Analytical purity: >99%- Source: purchased by Hazleton Laboratories America, Inc., Vienna, Virginia from Aldrich Chemical Company, Milwaukee, Wisconsin.

Test animals

Species:

mouse

Strain:

B6C3F1

Sex:

male/female

Details on test animals or test system and environmental conditions:

TEST ANIMALS- Source: Charles River Breeding Laboratories, Inc., Wilmington, Massachusetts- Age at study initiation: approximately 5 weeks. The vehicle control mice were approximately 2 weeks older than the other rats and were started on test correspondingly earlier.- Housing: by sex in groups of 10 in solid-bottom polypropylene cages equipped with filter tops. - Food: ad libitum - Water: ad libitum- Acclimation period: quarantined for at least 10 daysENVIRONMENTAL CONDITIONS- Temperature (°C): 20-24- Humidity (%): 45-55- Air changes (per hr): 12- Photoperiod (hrs dark / hrs light): 12/12

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

corn oil

Details on oral exposure:

PREPARATION OF DOSING SOLUTIONS:Fresh solutions of tetrachloroethylene and corn oil were prepared weekly, sealed, and stored at 34°F. These tetrachloroethylene solutions were considered generally stable for 10 days under the indicated storage conditions.VEHICLE:- Concentration in vehicle: 6, 8, 9 and 11% tetrachloroethylene in corn oil

Analytical verification of doses or concentrations:

not specified

Details on analytical verification of doses or concentrations:

no data

Duration of treatment / exposure:

78 weeks, followed by a 12-week observation period.

Frequency of treatment:

five consecutive days per week

Doses / concentrations

Doses / concentrations 1

Remarks:

Doses / Concentrations:Males: low dose: 450 mg/kg bw/day (initially) to 550 mg/kg bw/day (maximum low dose); high dose 900 mg/kg bw/day (initially) to 1100 mg/kg bw/day (maximum high dose)Basis:actual ingested

Doses / concentrations 2

Remarks:

Doses / Concentrations:Females: low dose 300 mg/kg bw/day (initially) to 400 mg/kg bw/day (maximum low dose); high dose 600 mg/kg bw/day (initially) to 800 mg/kg bw/day (maximum high dose)Basis:actual ingested

Doses / concentrations 3

Remarks:

Doses / Concentrations:Males: 540 and 1070 mg/kg bw/dayBasis:other: time-weighted average dose

Doses / concentrations 4

Remarks:

Doses / Concentrations:Females: 390 and 770 mg/kg bw/dayBasis:other: time-weighted average dose

No. of animals per sex per dose:

treatment groups: 50 animals per sex/groupcontrol group: 20 animals per sex/group

Control animals:

yes, concurrent no treatment

yes, concurrent vehicle

Details on study design:

Dose selection rationale: subchronic toxicity tests were conducted to establish maximum tolerated dosages. Six groups, each consisting of five males and five females, were utilized and were administered tetrachloroethylene in corn oil at dosages 316, 562, 1000, 1780 and 3160 mg/kg/day; the sixth group served as control (corn oil). The male mice receiving 562 mg/kg/day experienced no reduction in weight gain relative to controls, while male mice receiving 1000 mg/kg/day experienced a 22 percent reduction in weight gain relative to controls. An initial high dose of 900 mg/kg/day was selected for the chronic bioassay of male mice. Female mice receiving 562 mg/kg/day gained 70 percent of the weight gained by controls, while the female mice receiving 1000 mg/kg/day gained 85 percent of the weight gained by controls. An initial high dose of 600 mg/kg/day was selected for the chronic bioassay of female mice.The high and low doses initially utilized for males and females, respectively were 900 and 450 mg/kg/day and 600 and 300 mg/kg/day. After 11 weeks, the animals appeared to be tolerating the chemical, so the high and low doses were, respectively, increased to 1100 and 550 mg/kg/day for male mice and 800 and 400 mg/kg/day for female mice. Treatment continued at this level for the remainder of the 78-week treatment period and was followed by approximately 12 weeks of observation.

Positive control:

no data

Examinations

Observations and examinations performed and frequency:

CAGE SIDE OBSERVATIONS: Yes - Time schedule: cage side observations (appearance, behavior, signs of toxic effects) were recorded at weekly intervals for the first 10 weeks and at monthly intervals thereafter. The incidence, size and location of tissue masses were recorded at weekly intervals for the first 10 weeks and at monthly intervals thereafter and were determined by observation and palpation of each animal. DETAILED CLINICAL OBSERVATIONS: Yes- Time schedule: clinical observations (see above) were recorded at weekly intervals for the first 10 weeks and at monthly intervals thereafter. BODY WEIGHT: Yes - Time schedule for examinations: animals were weighed immediately prior to initiation of the experiment. Body weights were recorded at weekly intervals for the first 10 weeks and at monthly intervals thereafter. FOOD CONSUMPTION: Yes- Food consumption was recorded at weekly intervals for the first 10 weeks and at monthly intervals thereafter.

Sacrifice and pathology:

A necropsy was performed on each animal regardless of whether it died, was killed when moribund, or was sacrificed at the end of the bioassay. the animals were euthanized by exsanguination under sodium pentobarbital anesthesia, and were immediately necropsied. The histopatholic examinationconsisted of gross and microscopic examination of matjor tissues, organs, or gross lesions taken from sacrificed animals and, whenever possible, from animals found dead. Slides were prepared from the following tissues: skin, subcuteaneous tissue, lungs and bronchi, trachea, bone marrow, spleen, lymph nodes, thymus, heart, salivary gland, liver, gallbladder and bile duct, pancreas, esophagus, stomach, small intestine, large intestine, kidney, urinary bladder, pituitary, adrenal, thyroid, parathyroid, pancreatic islets, testis, prostate, brain, uterus, mammary gland, and ovary. A few tissues were not examined for some animals, particularly those that died early. Also, some animals were missing, cannibalized, or judged to be in such an advanced state of autolysis as to preclude histopathologic interpretation.

Statistics:

Several statistical techniques among which: Cochran-Armitage test for linaer trend in proportion, Fisher exact test (Cox, 1970) for the incidence of tumors; product-limit procedure of Kaplan and Meier (1958) for probabilities of survival; method of Cox (1972) for testing two groups for equality and Tarone's (1975) extensions of Cox's methods for testing a dose-related trend for possible dose-related effects on survival.

Results and discussion

Results of examinations

Clinical signs:

effects observed, treatment-related

Mortality:

mortality observed, treatment-related

Body weight and weight changes:

effects observed, treatment-related

Food consumption and compound intake (if feeding study):

not specified

Food efficiency:

not specified

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

not specified

Ophthalmological findings:

not specified

Haematological findings:

not specified

Clinical biochemistry findings:

not specified

Urinalysis findings:

not specified

Behaviour (functional findings):

not specified

Organ weight findings including organ / body weight ratios:

not specified

Gross pathological findings:

effects observed, treatment-related

Histopathological findings: non-neoplastic:

effects observed, treatment-related

Histopathological findings: neoplastic:

effects observed, treatment-related

Details on results:

CLINICAL SIGNS AND MORTALITYAppearance and behavior were generally similar for control and treated mice during the first 26 weeks of the study. Signs often observed in group-housed laboratory mice were noted with a slightly greater frequency in the treated mice of both sexes than in the respective control animals during the remainder of the first year. These signs included body sores, anal or penile irritation, rough or stained rfur, and generalized or localize alopecia. A number of treated mice of both sexed showed a hunched appearance from week 42 through 62. Furthermore, low incidence of bloating or abdominal distension and palpable nodules were observed in treated animals. Survival was markedly lower in both high dose groups and in the female low dose group, compared with the control groups, from about week 40. At least 50% of each of the four control groups survived to the end of the study at 90 weeks, compared with median survivals in the groups treated with tetrachloroethylene of 78 weeks for males and 62 weeks for females at the low dose, and respectively 43 and 50 weeks at the high dose.BODY WEIGHT AND WEIGHT GAINDosed male mice did gain less weight than vehicle control males after the first three months, and dosed female mice did gain less than vehicle control females during the second year of the bioassay. HISTOPATHOLOGY: NON-NEOPLASTICToxic nephropathy (degenerative changes in the proximal convoluted tubules, with cloudy swelling, fatty degeneration and necrosis of the epithelium) similar to that apparent in the rat NCI cancer bioassay, was seen in the majority of males (low dose 40/49; high dose 45/48) and females (low dose 46/48; high dose 48/48) receiving tetrachloroethylene, but was not found in controls.HISTOPATHOLOGY: NEOPLASTICIncidence of hepatocellular carcinomas exhibited a significant positive dose-related trend in mice of both sexes. Hepatocellular carcinomas appeared early in dosed mice. The first hepatocellular carcinoma observed at necropsy occurred in a male low dose mouse that died during week 27. No hepatocellular carcinomas were observed in control mice dying before week 90. A small number o hepatocellular carcinomas in treated mice of both sexes metastasized to the lung, while a single hepatocellular carcinoma in an untreated control male metastasized to the kidney.

Effect levels

1

Dose descriptor:

LOAEL

Effect level:

390 mg/kg bw/day (actual dose received)

Sex:

female

Basis for effect level:

other: kidney lesions (degeneration of the proximal convoluted tubules with cloudy swelling, fatty degeneration and necrosis)

2

Dose descriptor:

LOAEL

Effect level:

540 mg/kg bw/day (actual dose received)

Sex:

male

Basis for effect level:

other: kidney lesions (degeneration of the proximal convoluted tubules with cloudy swelling, fatty degeneration and necrosis)

Target system / organ toxicity

Critical effects observed:

not specified