Registration Dossier

Toxicological information

Repeated dose toxicity: oral

Currently viewing:

Administrative data

Endpoint:
short-term repeated dose toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2018

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test)
GLP compliance:
yes (incl. certificate)
Limit test:
no

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
liquid
Details on test material:
The test substance is identified as 2-ethylhexyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate. The purity is 100%. The physical state/appearance of material is clear colorless liquid. The expiry date of material is 01 February 2019. The substance can be stored at 4 oC in dark conditions.
Specific details on test material used for the study:
Test item: 2-Ethylhexyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate
Test item identity (including alternative names): MCS-1562
Appearance: Liquid
Storage conditions: In a refrigerator (2 to 8C)
Supplier: Sponsor
Batch number: AH03201
Expiry date: February 2019
Purity: 100%

Test animals

Species:
rat
Strain:
Sprague-Dawley
Details on species / strain selection:
SD rats are proven test subjects for this sort of testing
Sex:
male/female
Details on test animals and environmental conditions:
Animals
Strain/Species Crl:CD(SD) rat.
Supplier Charles River (UK) Ltd.
Number of animals ordered 44 males and 48 females.

Duration of acclimatisation At least 5 days before commencement of estrous cycle evaluation for females or start of treatment for males.
Age of the animals at the start of the study Males 10 to 11 weeks old. Females 12 to 13 weeks old.
Weight range of the animals at the start of the study Males 338 to 400 g. Females 229 to 290 g.

Allocation and Identification
Allocation On arrival and non-selective allocation to cages. On Day 1 of study all animals were weighed and body weights and estrous cycles were reviewed by Study Management before dosing commenced. Body weight of animals did not exceed 20% of the mean for each sex.
Identification of animals Each adult animal was assigned a number and identified uniquely within the study by microchip before Day 1 of treatment. The offspring were numbered individually within each litter on Day 1 of age, using a toe tattoo.
Identification of cages Each cage label was color-coded according to group and was numbered uniquely with cage and study number, as well as the identity of the occupant(s).

Environmental Control

Rodent facility Limited access - to minimise entry of external biological and chemical agents and to minimise the transference of such agents between rooms.
Air supply Filtered fresh air which was passed to atmosphere and not recirculated.
Temperature and relative humidity Monitored and maintained within the range of 20-24ºC and 40-70%. Although conditions were occasionally outside the indicated ranges, these deviations were minor and/or of short duration and were not considered to have influenced the health of the animals and/or the outcome of the study.
Lighting Artificial lighting, 12 hours light: 12 hours dark.
Electricity supply Public supply with automatic stand-by generators.

Animal Accommodation

Cages Cages comprised of a polycarbonate body with a stainless steel mesh lid; changed at appropriate intervals. Solid (polycarbonate) bottom cages were used during the acclimatisation, pre-pairing, gestation, littering and lactation periods. Grid bottomed polypropylene cages were used during pairing. These were suspended above absorbent paper which was changed daily during pairing.
Cage distribution The cages were distributed on the racking to equalise, as far as possible, environmental influences amongst the groups.
Bedding Solid bottom cages contained softwood based bark-free fiber bedding, which was changed at appropriate intervals each week.
Number of animals per cage Pre-pairing: up to five animals of one sex, Pairing: one male and one female , Males after mating: up to five animals, Gestation: one female, Lactation: one female + litter

Environmental Enrichment
Aspen chew block A soft white untreated wood block; provided to each cage throughout the study (except during pairing and lactation), replaced when necessary and returned following removal of offspring.
Plastic shelter Provided to each cage throughout the study (except during pairing and lactation) and replaced at the same time as the cages.

Diet Supply
Diet SDS VRF1 Certified pelleted diet. The diet contained no added antibiotic or other chemotherapeutic or prophylactic agent.
Availability Non-restricted (removed overnight before blood sampling for hematology and blood chemistry investigations).

Water Supply
Supply Potable water from the public supply via polycarbonate bottles with sipper tubes. Bottles were changed at appropriate intervals.
Availability Non-restricted.

Administration / exposure

Route of administration:
oral: gavage
Details on route of administration:
Administration
Dosing was restricted to the F0 generation. Animals of the F1 generation were not dosed directly.

Route Oral gavage using a suitably graduated syringe and a rubber catheter inserted via the mouth. If female was in parturition, dosing was not performed on one day. Treated at Constant doses in mg/kg/day.
Volume dose 5 mL/kg body weight.
Individual dose volume Calculated from the most recently recorded scheduled body weight.
Control (Group 1) Vehicle at the same volume dose as treated groups.
Frequency Once daily at approximately the same time each day.
Formulation A daily record of the usage of formulation was maintained based on weights. This balance was compared with the expected usage
as a check of correct administration.

Formulations were stirred using a magnetic stirrer before and throughout the dosing procedure.
Vehicle:
corn oil
Details on oral exposure:
Rats were gavaged daily with the test article in corn oil.
Analytical verification of doses or concentrations:
yes
Duration of treatment / exposure:
Males were treated for 2 weeks pre-mating, up to 2 weeks of mating and through week 5 of gestation. Females were treated for 2 weeks pre-mating, for up to 2 weeks of mating and then through gestation and to necropsy at lactation day 14.
Frequency of treatment:
Daily
Doses / concentrationsopen allclose all
Dose / conc.:
350 mg/kg bw/day (nominal)
Dose / conc.:
100 mg/kg bw/day (nominal)
Dose / conc.:
30 mg/kg bw/day (nominal)
Dose / conc.:
0 mg/kg bw/day (nominal)
No. of animals per sex per dose:
10
Control animals:
yes, concurrent vehicle

Examinations

Observations and examinations performed and frequency:
Animals were inspected visually at least twice daily for evidence of ill-health or reaction to treatment. Cages were inspected daily for evidence of animal ill-health amongst the occupant(s). Any deviation from normal was recorded at the time in respect of nature and severity, date and time of onset, duration and progress of the observed condition, as appropriate.
During the acclimatisation period, observations of the animals and their cages were recorded at least once per day.
Sacrifice and pathology:
All adult animals were subject to a detailed necropsy. After a review of the history of each animal, a full macroscopic examination of the tissues was performed. All external features and orifices were examined visually. Any abnormality in the appearance or size of any organ and tissue (external and cut surface) was recorded and the required tissue samples preserved in appropriate fixative.
Other examinations:
Hematology, clinical chemistry and an FOB are also conducted.
Statistics:
Statistics are not presented as the system will not allow enough characters to be entered. There is not reason why the space for statistics is limited, and this should be changed.

Results and discussion

Results of examinations

Clinical signs:
no effects observed
Description (incidence and severity):
The distribution of minor signs noted at the detailed physical examination and arena observations showed no test item related effects.
There were no clinical signs associated with dose administration.
Mortality:
mortality observed, treatment-related
Description (incidence):
There were six decedent females; 4 females given 100 mg/kg/day and 2 females given 350 mg/kg/day, all occurring between Days 9 and 13 of lactation.

Female 135, given 350 mg/kg/day, was found dead on Day 13 of lactation with no adverse signs noted previously apart from a firm area on upper ventral surface from Day 20 of gestation, and had macroscopic findings of bedding material present in the oral cavity and a distended stomach. On microscopic examination, most tissues showed changes associated with autolysis. There was slight, multifocal, sub-capsular necrosis seen in the liver and a slight decrease in white pulp cellularity of the spleen.

Female 148, given 350 mg/kg/day was sacrificed due to poor condition including decreased activity, piloerection and cold to touch on Day 9 of lactation and had findings of pale color and pale material in the middle section of the jejunum. Microscopic findings consisted of minimal atrophy of the thymus.

Female 105, given 100 mg/kg/day, was sacrificed due to poor condition including prostate posture and unresponsiveness on Day 9 of lactation. There were no macroscopic findings. Microscopic findings included slight, generalised, decreased cellularity within the mesenteric and axillary lymph nodes, a diffuse cortical hypertrophy within the adrenal glands, and a slight bilateral dilatation of the lateral ventricles of the brain. There was also a minimal, decreased red pulp cellularity within the spleen.

Female 106, given 100 mg/kg/day, was sacrificed due to poor condition including circling behaviour, uncoordinated gait and piloerection on Day 9 of lactation. Macroscopic findings comprised depression of the glandular portion of the stomach which correlated histologically with slight, multifocal erosion in the same area.

Female 107, given 100 mg/kg/day was sacrificed due to poor condition including unresponsiveness, hunched posture, prominent eyes and irregular breathing on Day 11 of lactation. There were no macroscopic findings. Microscopically, there was a slight decrease in cellularity within the mesenteric lymph node and of the red pulp within the spleen. There was also minimal, cortico-medullary mineralisation seen in the kidneys of this female.

Female 141, given 100 mg/kg/day, was found dead on Day 10 of lactation. No prior adverse clinical signs were noted. The only macroscopic finding of pelvic dilatation within both kidneys which was confirmed microscopically. Other microscopic changes included a slight decrease in cellularity within the bone marrow, axillary lymph node and red pulp of the spleen.

No macroscopic or microscopic changes were observed which were considered to have contributed to the poor clinical condition or death of these animals. Factors contributing to poor clinical condition and the cause of death in could not be determined. For all of these decedents, no previous clinical signs had been seen, there were no adverse effects during parturition and no effects on their litters from birth.

Body weight and weight changes:
no effects observed
Description (incidence and severity):
Group mean body weight gain over Weeks 0-5 for males given 350 mg/kg/day was statistically significantly lower than the concurrent control group (0.76x Control).
There were no test item related effects on body weight over Weeks 0-5 in the males given 30 or 100 mg/kg/day.
There were no test item related effects on group mean body weight gain of females over the first 2 weeks of treatment, or during gestation or lactation. Absolute group mean body weight on Day 1 of lactation in females given 100 mg/kg/day and on Days 1, 4 and 13 of lactation in females given 350 mg/kg/day was statistically significantly lower than the concurrent control but was similar to the controls on Gestation Day 20. However, as body weight gain during lactation was similar to the controls this is considered to be of no toxicological significance.
Food efficiency:
not examined
Ophthalmological findings:
not examined
Haematological findings:
no effects observed
Clinical biochemistry findings:
no effects observed
Urinalysis findings:
not examined
Behaviour (functional findings):
no effects observed
Immunological findings:
not examined
Organ weight findings including organ / body weight ratios:
no effects observed
Description (incidence and severity):
Group mean body weight adjusted kidney weights in animals given 350 mg/kg/day were slightly but statistically significantly higher than the concurrent controls (1.14x Control for males and females).
Group mean body weight adjusted liver weights in animals given 100 and 350 mg/kg/day were slightly but (with exception of females given 100 mg/kg/day) statistically significantly higher than the concurrent controls (up to 1.15x Control).
There were considered to be no other effects on the organ weights recorded. Group mean body weight adjusted thymus weight for females given 350 mg/kg/day appeared to be much lower than the control group, but review of the individual data showed intergroup variability and was influenced by 2 high control values and one very low high dose value.
Gross pathological findings:
no effects observed
Neuropathological findings:
no effects observed
Histopathological findings: non-neoplastic:
no effects observed
Description (incidence and severity):
The incidence and distribution of microscopic findings were considered to be unrelated to treatment.
Detailed qualitative examination of the testes was made, taking into account the tubular stages of the spermatogenic cycle. The examination was conducted in order to identify treatment related effects such as missing germ cell layers or types, retained spermatids, multinucleate or apoptotic germ cells and sloughing of spermatogenic cells into the lumen. No stage specific testicular abnormalities were found.
Histopathological findings: neoplastic:
no effects observed

Effect levels

open allclose all
Dose descriptor:
NOAEL
Effect level:
350 mg/kg bw/day (nominal)
Based on:
test mat.
Sex:
male
Basis for effect level:
other: no adverse findings
Dose descriptor:
NOAEL
Effect level:
350 mg/kg bw/day (nominal)
Based on:
test mat.
Sex:
female
Basis for effect level:
other: Reproductive - no adverse findings.
Dose descriptor:
NOAEL
Effect level:
30 mg/kg bw/day (nominal)
Based on:
test mat.
Sex:
female
Basis for effect level:
mortality

Target system / organ toxicity

Critical effects observed:
no

Applicant's summary and conclusion

Executive summary:

The purpose of this study was to assess the general systemic toxicity potential in rats, including a screen for reproductive/developmental effects and assessment of endocrine disruptor relevant endpoints, with administration of 2-ethylhexyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate by oral gavage administration for at least 5 weeks.

Four groups of ten male and ten female rats received 2-ethylhexyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate at doses of 30, 100 or 350 mg/kg/day by oral gavage administration. Males were treated daily for two weeks before pairing, up to necropsy after a minimum of five consecutive weeks. Females were treated daily for two weeks before pairing, throughout pairing, gestation and until Day 13 of lactation. Females were allowed to litter, rear their offspring and were killed on Day 14 of lactation. The F1 generation received no direct administration of the test item; any exposure was in utero or via the milk. A similarly constituted Control group received the vehicle, corn oil, at the same volume dose as treated groups.

During the study, clinical condition, detailed physical examination and arena observations, sensory reactivity, grip strength, motor activity, body weight, food consumption, hematology (peripheral blood), blood chemistry, thyroid hormone analysis, estrous cycles, pre-coital interval, mating performance, fertility, gestation length, organ weight and macroscopic pathology and histopathology investigations were undertaken.

The clinical condition, litter size and survival, sex ratio, body weight, ano-genital distance, nipple counts (male only) and macropathology for all offspring were also assessed. 

Results

F0 responses


Four females given 100 mg/kg/day and two females given 350 mg/kg/day died or were sacrificed due to poor clinical condition including decreased activity, unresponsiveness, prostate posture, uncoordinated gait, circling behaviour or hunched posture between lactation Days 9 and 13. There were no pathological findings that elucidated the cause of demise.

There were no clinical signs seen during the weekly detailed physical examinations that were considered to be test item related and no clinical signs were recorded in association with dose administration. Sensory reactivity, grip strength and motor activity were unaffected by treatment.

Body weight gain of males given 350 mg/kg/day was statistically significantly lower than controls (0.76x) and food consumption of females given 100 or 350 mg/kg/day was lower (up to 0.88x) than controls, occasionally attaining statistical significance.

Estrous cyclicity, pre-coital interval, gestation length, mating performance and fertility were unaffected by treatment.

 

 

Haematology and blood chemistry investigations revealed no effect of treatment and there was no effect upon circulating levels of thyroxine (T4) in adult males.

 

After five weeks of treatment for males and on Day 14 of lactation for females, liver weights were higher in males and females given 100 and 350 mg/kg/day and kidney weights were higher in males and females given 350 mg/kg/day. There were no test item related macropathological or micropathological findings in the full list of tissues examined.

 

F1 responses


Body weight gain of male and female offspring from the 100 and 350 mg/kg/day groups were statistically significantly lower (0.75X to 0.82x) than the Controls.

The clinical condition, litter size, sex ratio and survival indices of offspring were unaffected by parental treatment.

 

There was no effect of parental treatment upon circulating levels of thyroxine (T4) in offspring on Day 13 of age.

 

The ano-genital distances of offspring were unaffected by paternal treatment and no nipples were seen on any male offspring on Day 13 of age.

 

No macroscopic findings in the offspring were considered to be related to paternal treatment.

Conclusion

It was concluded that the oral administration of 2-ethylhexyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate to parental Sprague Dawley male rats at dose levels of 30, 100 or 350 mg/kg/day for two weeks before pairing, during pairing and then up to termination after five weeks of treatment was associated with statistically significantly lower bodyweight gain (0.76x). Oral administration of the same dose levels to female rats for two weeks before pairing, during pairing and during gestation and lactation up to termination on Day 14 of lactation was associated with 4 decedent females during lactation at 100 mg/kg/day and 2 decedent females during lactation at 350 mg/kg/day. There were no pathological changes noted and the cause of the demise was not established. Food consumption was slightly and occasionally statistically significantly reduced in females given 100 (up to 0.88x, gestation and lactation only) or 350 mg/kg/day (up to 0.89x) and considered non adverse.

Growth of offspring from parental doses of 100 or 350 mg/kg/day was slightly and statistically significantly lower (up to0.75x), but considered non adverse. There were no other effects on reproductive performance, fertility, litter size or offspring survival.

In the context of this study,2-ethylhexyl 7-oxabicyclo[4.1.0]heptane-3-carboxylateshowed no evidence of being an endocrine disruptor, as assessed by measurement of thyroxine (T4) in adult males and offspring, organ weights, ano-genital distance and external examination of offspring, and nipple counts in male offspring,

The no-observed-adverse-effect level (NOAEL) of2-ethylhexyl 7-oxabicyclo[4.1.0]heptane-3-carboxylatefor systemic toxicity of males was considered to be 350 mg/kg/day.

The no-observed-adverse-effect level (NOAEL) of2-ethylhexyl 7-oxabicyclo[4.1.0]heptane-3-carboxylatefor systemic toxicity of females was considered to be 30 mg/kg/day, based on mortaliy.

The no-observed-adverse-effect level (NOAEL) of2-ethylhexyl 7-oxabicyclo[4.1.0]heptane-3-carboxylatefor reproductive/developmental toxicity was considered to be 350 mg/kg/day.