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Toxicological information

Toxicity to reproduction

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Administrative data

Endpoint:
two-generation reproductive toxicity
Remarks:
based on test type (migrated information)
Type of information:
experimental study
Adequacy of study:
key study
Study period:
March 2008 - August 2009
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: OECD guideline study conducted under GLP. The study was selected as a key study because the information provided for the hazard is sufficient to evaluate the need for classification and labelling and/or risk assessment.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2011
Report Date:
2011

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to
Guideline:
OECD Guideline 416 (Two-Generation Reproduction Toxicity Study)
Qualifier:
according to
Guideline:
EPA OPPTS 870.3800 (Reproduction and Fertility Effects)
GLP compliance:
yes (incl. certificate)
Limit test:
no

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals and environmental conditions:
TEST ANIMALS
- Source: Charles River, Deutschland, Sulzfeld, Germany
- Age at study initiation: (P - 6-7 weeks)
- Weight at study initiation: (P) Males: 173-206 g; Females: 140-175 g; (F1) Males: 36-72 g; Females: 40-75 g
- Housing: macralon cages with wood shavings as bedding and strips of paper for environmental enrichment, during premating animals were housed by sex 4/cage, during mating - 1 male plus 1 female, following mating - females were housed individually and with her litter following delivery
- Diet : ad libitum except during exposure
- Water : ad libitum except during exposure
- Acclimation period: approx 1-2 weeks


ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22±2
- Humidity (%): 40-70
- Air changes (per hr): 10
- Photoperiod (hrs dark / hrs light): 12/12


IN-LIFE DATES: March - November 2008

Administration / exposure

Route of administration:
inhalation
Type of inhalation exposure (if applicable):
other: nose only except during lactation when whole body exposure is used
Vehicle:
other: sham exposed
Details on exposure:
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
nose-only exposure unit
- Exposure apparatus:nose only -cylindrical PVC column with a volume of ca. 70 L, surrounded by a transparent hood.
- Method of holding animals in test chamber:nose only - in plastic animal holders
- humidified compressed air
- System of generating particulates/aerosols: flow of gas will be regulated by volumetric flow meters to achieve the desired concentrations in the exposure apparatus
- Temperature, humidity, : 22 ± 2ºC, 30-77% humidity

whole body exposure unit
- Exposure apparatus: Whole body -2 m3 whole body inhalation chambers made of stainless steel.
- Method of holding animals in test chamber: housed in individual cages
- System of generating atmosphere: flow of gas will be regulated by volumetric flow meters to achieve the desired concentrations in the exposure apparatus
- Temperature, humidity: 22 ± 2ºC, 30-77% humidity

TEST ATMOSPHERE
- Brief description of analytical method used: total carbon content by flame ionization GC
- Samples taken from breathing zone: yes

Details on mating procedure:
- M/F ratio per cage: 1:1
- Length of cohabitation: up to 2 weeks
- Proof of pregnancy:sperm in vaginal smear referred to as day 0 of pregnancy
- After 7 days of unsuccessful pairing replacement of first male by another male with proven fertility.
- After successful mating each pregnant female was caged individually
Analytical verification of doses or concentrations:
yes
Details on analytical verification of doses or concentrations:
total carbon analysis.
Duration of treatment / exposure:
6 hours per day
Frequency of treatment:
F0 generation animals were exposed to the test material in air for 6 hours a day/5 days a week for at least 10 weeks prior to mating and daily during mating. Daily exposure continued for F0 females through gestation day (GD) 19 for 6 hours/day (nose-only). From lactation day 5 - 21, females were exposed daily (6 hours/day) to the test item by whole body exposure.

The F1-generation male and female pups were exposed by whole body exposure(6 hours/day, 5 days/week) from postnatal (PN) day 22 up to ca. 6 weeks of age. Subsequently, the animals were exposed in a similar manner as that described for the F-0 generation.
Details on study schedule:
- Selection of parents from F1 generation when pups were 21 days of age.
- F1 parental animals not mated until 10 weeks after selection from the F1 litters.

Doses / concentrations
Remarks:
Doses / Concentrations:
0, 5000, 15000 and 50000 ppm
Basis:
analytical conc.
No. of animals per sex per dose:
28
Control animals:
yes, sham-exposed
Details on study design:
- Dose selection rationale: high dose same as used for repeated dose toxicity studies. Concentrations higher than 50000 ppm can result in secondary effects due to oxygen deprivation.

Examinations

Parental animals: Observations and examinations:
CAGE SIDE OBSERVATIONS: Yes
- Time schedule: daily
- Cage side observations were included.


DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: daily


BODY WEIGHT: Yes
- Time schedule for examinations: 2 days prior to exposure initiation, day 0, weekly (males, premating females), gestation days 1,7,14,21, lactation days 1,4,7,14, 21
Oestrous cyclicity (parental animals):
vaginal smears daily for 3 weeks prior to mating
Sperm parameters (parental animals):
Parameters examined in all male parental generations:
including testis weight, epididymis weight, daily sperm production, sperm count in testes, sperm count in epididymides, enumeration of cauda epididymal sperm reserve, sperm motility, sperm morphology
Litter observations:
STANDARDISATION OF LITTERS
- Performed on day 4 postpartum: yes
- If yes, maximum of 8 pups/litter (4/sex/litter as nearly as possible)

PARAMETERS EXAMINED
The following parameters were examined in F1 / F2 offspring:
number and sex of pups, stillbirths, live births, postnatal mortality, presence of gross anomalies, weight gain, physical or behavioural abnormalities,


GROSS EXAMINATION OF DEAD PUPS:
yes, for external and internal abnormalities
Postmortem examinations (parental animals):
SACRIFICE
- Male animals: All surviving animals as soon as possible after the last litters in each generation were produced.
- Maternal animals: All surviving animals after the last litter of each generation was weaned.


GROSS NECROPSY
- Gross necropsy consisted of external and internal examinations including the cervical, thoracic, and abdominal viscera.


HISTOPATHOLOGY / ORGAN WEIGHTS
The tissues indicated below were prepared for microscopic examination and weighed, respectively.
- adrenals
- brain
- epididymides *(left cauda which will be used for sperm analysis
- kidneys
- liver
- ovaries including oviduct*
- pituitary gland*
- prostate*
- seminal vesicles and coagulating glands*
- spleen
- testes*(right testis will be preserved in Bouin’s fixative, the left one will be used for
sperm analysis
- thyroid
- uterus* (after counting of the implantation sites) (Salewski 1964)
- vagina*
- organs and tissues showing macroscopic abnormalities
Postmortem examinations (offspring):
SACRIFICE
- The F1 offspring not selected as parental animals and all F2 offspring were sacrificed at [21] days of age.
- These animals were subjected to postmortem examinations (macroscopic a) as follows:


GROSS NECROPSY
- Gross necropsy consisted of external and internal examinations including the cervical, thoracic, and abdominal viscera.


HISTOPATHOLOGY / ORGAN WEIGHTS
The tissues indicated below were prepared for microscopic examination and weighed, respectively.
- brain
- spleen
- thymus
- organs and tissues showing macroscopic abnormalities

Skeletal examinations were carried out on F1 pups
Statistics:
Other statistical tests may be performed when considered appropriate. P < 0.05 will be considered as a level of significance.
- Clinical findings will be evaluated by Fisher's exact probability test.
- Body weight, body weight gain, organ weights and food consumption data will be subjected to one-way analysis of variance (ANOVA) followed by Dunnett's multiple comparison tests.
- Fisher's exact probability test will be used to evaluate the number of mated and pregnant females and females with live pups.
- Number of implantation sites, live and dead fetuses or pups will be evaluated by Kruskal-Wallis nonparametric analysis of variance followed by the Mann Whitney U-test.
- Mortality data and data of the pathology of parent females will be evaluated by the Fisher’s exact probability test.
Reproductive indices:
- pre-coital time = time between the start of mating and successful copulation
- duration of gestation = time between gestation day 0 and day of delivery
- mating index= (number of females mated/number of females placed with males) x 100
- male fertility index = (number of males that became sire/number of males
placed with females) x 100
- female fertility index = (number of pregnant females/number of females
placed with males) x 100
- female fecundity index = (number of pregnant females/number of females mated) x
100
- gestation index = (number of females with live pups or pups/number of females
pregnant) x 100
- live birth index = (number of pups born alive/number of pups born) x 100
- viability index day 4-21= (number of pup surviving 21 days/number of liveborn after
culling day 4) x100
- pup mortality day n = (number of dead pups on day n/total number of pups
on day n) x 100
- sex ratio day n = (number of live male fetuses or pups on day n/ number of live
fetuses or pups on day n) x 100
- number of lost implantations = number of implantations sites - number of pups born
alive
- post-implantation loss = [(number of implantation sites - number of pups born
alive)/number of implantation sites] x 100
Offspring viability indices:
- number of pups delivered (live- and stillborn)
- number of live pups at day 1,4,7,14,21
- number of pups lost measured as above
- number of litters lost entirely
- number of male pups at day 1,4,7,14,21
- number of implantation sites
- number of lost implantations
- litter size

Results and discussion

Results: P0 (first parental generation)

General toxicity (P0)

Clinical signs:
no effects observed
Description (incidence and severity):
No statistically significant clinical signs were observed.
Body weight and weight changes:
effects observed, treatment-related
Description (incidence and severity):
see details in section below
Food consumption and compound intake (if feeding study):
effects observed, treatment-related
Description (incidence and severity):
see details in section below
Organ weight findings including organ / body weight ratios:
no effects observed
Histopathological findings: non-neoplastic:
no effects observed
Description (incidence and severity):
No statistically significant changes were observed. A few changes were noted but they were common findings for this strain of rat, were equally distributed amonst the different treatment groups or only occured in one or few animals.
Other effects:
not examined
Description (incidence and severity):
Test substance intake: not relevant for inhalation exposure studies

Reproductive function / performance (P0)

Reproductive function: oestrous cycle:
no effects observed
Description (incidence and severity):
No dose-related changes in the estrus cycles were observed in the test substance exposed animals
Reproductive function: sperm measures:
no effects observed
Description (incidence and severity):
No treatment related effects observed. Epidiymal sperm count was decreased in the F1 mid dose group only. This was not a dose related effect and was not considered to be treatment related.
Reproductive performance:
no effects observed
Description (incidence and severity):
no adverse effects noted in parental animals

Details on results (P0)

CLINICAL SIGNS AND MORTALITY (PARENTAL ANIMALS) The clinical observations observed in the animals of the F0 and F1 parental generation are common findings in rats of this strain and age or occurred as individual fortuitous findings. Furthermore, they were about equally distributed amongst the different treatment groups or occurred in only one or a few animals. Therefore, they were not considered to be related to treatment.

BODY WEIGHT AND FOOD CONSUMPTION (PARENTAL ANIMALS) Statistically significant decreases of body weight, and body weight change and food consumption were observed in the test substance exposed groups during the premating period. In F1-females, there were test substance-related reductions in mean body weights at all doses tested during the first three weeks of the premating period. Mean body weights on approximately post-natal days 28 , 35, and 42 (week 0, 1 and 2 of the F1-generation, respectively) were up to 13, 15, and 14% lower than controls at 5000, 15000, and 50000 ppm, respectively. This period of time corresponded with the initiation of direct exposure. Although test substance-related and toxicologically relevant to the onset of puberty, these reductions were not considered adverse because they were transient and by the end of the premating period, mean body weights for all groups were within 3% of the control mean. Lack of a strong dose-related response, the relative low magnitude of the change, and the fact that the body weight data were consistent with the food consumption data supported that these effects were not considered to be adverse.

REPRODUCTIVE FUNCTION: ESTROUS CYCLE (PARENTAL ANIMALS) although a statistically significant increase of the mean cycle length was observed in the females of the mid-concentration group when compared to the control group and the length of the longest cycle was statistically significantly decreased in the females of the low- and midconcentration groups of the F0-generation, this effect was not considered to be a test substance related effect as no effect was observed in the high-concentration group of the F0-generation and no effect on estrus cycle was observed in the test substance-exposed groups of the F1-generation (see attached tables).

REPRODUCTIVE FUNCTION: SPERM MEASURES (PARENTAL ANIMALS)- Sperm analysis did not reveal a treatment-related effect

REPRODUCTIVE PERFORMANCE (PARENTAL ANIMALS)Duration of the gestation period was slightly increased in the test substance-exposed groups and was statistically significant in the low and high dose group of the F0 generation and the mid- and high concentration groups of the F1 generation. The gestation period did not exceeded the 22 days, which is a normal duration of gestation period for this strain of rats, in the control or treatment related dams. Therefore, this effect on mean gestation length is not considered as an adverse effect.

ORGAN WEIGHTS (PARENTAL ANIMALS) - although some statistically significant changes were observed, they were not related to dose. The decrease in organ weights and the decrease and increase in relative organ weights was related to the reducted body weights of the exposed groups and was not considered adverse.

GROSS PATHOLOGY (PARENTAL ANIMALS) - macroscopic examination at necropsy did not reveal treatment related gross changes

HISTOPATHOLOGY (PARENTAL ANIMALS)- There were no statistically significant changes observed

Effect levels (P0)

Dose descriptor:
NOAEC
Effect level:
50 000 ppm
Based on:
test mat.
Sex:
male/female
Basis for effect level:
other: no adverse effects noted at any dose including the highest dose tested

Results: F1 generation

General toxicity (F1)

Clinical signs:
no effects observed
Mortality / viability:
no mortality observed
Description (incidence and severity):
not considered to be an adverse event. See details below.
Body weight and weight changes:
no effects observed
Description (incidence and severity):
pup body weights and body weight changes were considered not to be affected by exposure to the test substance
Sexual maturation:
effects observed, treatment-related
Description (incidence and severity):
see details below
Organ weight findings including organ / body weight ratios:
no effects observed
Gross pathological findings:
no effects observed
Histopathological findings:
no effects observed

Details on results (F1)

VIABILITY (OFFSPRING) - The statistically significant increase of pup mortality (8.5%) as observed in the high-concentration group of the F1-generation on PN 4 was within the historical range (0-20.7%) and therefore not considered to be an adverse effect.

BODY WEIGHT (OFFSPRING)pup body weights and body weight changes were considered not to be affected by exposure to the test substance. In F1-females, there were test substance-related reductions in mean body weights at all doses tested during the first three weeks of the premating period for this generation. Mean body weights on post-natal days 28, 35, and 42 were up to 13, 15, and 14% lower than controls at 5000, 15000, and 50000 ppm, respectively. This period of time corresponded with the initiation of direct exposure. Although test substance-related and toxicologically relevant to the onset of puberty, these reductions were not considered adverse because they were transient and by the end of the premating period, mean body weights for all groups were within 3% of the control mean. In addition, and similar to the effects seen in males, there was not a strong dose-related response and the data was consistent with food consumption data for these females.

SEXUAL MATURATION (OFFSPRING) - In F1-females, there was an apparent delay in the onset of puberty evident as a delay in days to achievement of vaginal opening. These apparent delays were not considered to reflect a direct effect on this endpoint but rather, were considered secondary to previously described test substance-related reductions in body weight and food consumption parameters that were evident during the first three weeks of exposures and concurrent with the onset of vaginal patency. The relationship between onset of puberty in rats and body weight and food consumption data was described in a published feed restriction study in which it was demonstrated that pubertal delays of up to 6 days were produced in rats with weight gain reductions that were induced by feed restriction (Carney et al., 2004 - article attached).

ORGAN WEIGHTS (OFFSPRING)the decrease in absolute and relative thymus weight (F1-pups, F0-generation) and in relative thymus weight (F2- pups, F1-generation) of the low-concentration group were considered not to be treatment-related as no relation with concentration was observed. In addition, no histopathology findings were noted.

GROSS PATHOLOGY (OFFSPRING) - Two dams of the high-concentration group gave birth to 3 pups with malformations. One pup showed acauda and anal atresia and another pup of the same dam showed polypodia of the right hind limb. A pup of another dam showed acauda. As no malformations were observed in the prenatal developmental toxicity study with the test substance, this finding was not considered to be a treatment-related effect

HISTOPATHOLOGY (OFFSPRING) Microscopic observation of the thymus of the control and high-concentration groups of the F1-generation, F2-pups, did not reveal any treatment-related effects. For that reason the decrease detected in absolute and relative thymus weight of the F2-pups, F1-generation, of the high-concentration group was not considered to be a relevant effect. No statistically significant findings were observed. The changes observed were common findings in rats of this strain and age or occured as indicifual fortiutous findings. They were also equally distributed amongst different treatment groups of in only one or few animals and were not considered to be treatment related.

No skeletal abnormalities, such as wavy ribs (observed in the rat developmental toxicity study) were noted in the F1 pups

Effect levels (F1)

open allclose all
Dose descriptor:
NOAEC
Generation:
F1
Effect level:
50 000 ppm
Based on:
test mat.
Sex:
female
Basis for effect level:
other: see 'Remark'
Dose descriptor:
NOAEC
Generation:
F1
Effect level:
50 000 ppm
Based on:
test mat.
Sex:
male
Basis for effect level:
other: No treatment related adverse effects observed in male pups even at the highest dose tested

Overall reproductive toxicity

Reproductive effects observed:
not specified

Applicant's summary and conclusion

Conclusions:
Based on the data of this two-generation reproduction toxicity study in rats, the high-concentration group (50000 ppm) is considered to be NOAEL (No Observed Adverse Effect Level) for systemic toxicity and reproductive toxicity.
Executive summary:

No reproductive or systemic toxicity directly attributed to the test material were noted. While in the F1-generation females a delay in the onset of puberty was seen in the high exposure level group, this was attributed to a reduction of body weight gain seen in these animals early in exposure. It is well-established that the onset of puberty in rats is a body weight-dependent event. In feed restriction studies designed to examine the relationship between body weight and the onset of puberty evident as vaginal patency and preputial separation, it has been demonstrated that lower body weights and weights gains can delay the onset of puberty in rats by up to 6 days (Carney et al., 2004). In the current study, vaginal patency onset generally occurred during the third week of exposures for the F1-generation females (first week of exposure was designated week 0, see report Table 9). At the end of the second and third weeks of exposures (weeks 1 and 2, Table 9), mean body weights in treated F1-generation females were up to 14% lower than controls. On the basis of these data and considering the lack of any other corroborative evidence of either developmental or reproductive toxicity, these apparent delays in vaginal patency are considered secondary to lower body weights. There were no effects on mating, fertility, or other structural or functional indicators of reproductive performance in either generation. In compliance with the testing guidelines for this study, measurement of anogenital distance in F2-generation offspring was triggered by the observed apparent delays in the F1-generation females and no test substance-related changes were observed for this endpoint. Therefore, the apparent delay in onset of puberty in F1-generation females is not considered indicative of specific developmental or reproductive toxicity but rather is considered a consequence of test substance-related reductions in body weights. Considering this conclusion and taking into consideration the lack of any other evidence of test substance-related effect on either the structure or function of the reproductive system or on the offspring exposed in utero and via milk intake during lactation, the NOAEC for reproductive and systemic toxicity for the current study is considered 50000 ppm (233000 mg/m3), the highest exposure concentration tested.