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EC number: 233-469-7 | CAS number: 10192-30-0
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
![](https://poisoncentres.echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_toxicological-information.png)
Toxicity to reproduction
Administrative data
- Endpoint:
- three-generation reproductive toxicity
- Type of information:
- read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- not specified
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Remarks:
- Essential details for an assessment are given.
- Justification for type of information:
- see attachment “Read-across concept – Human Health/Environment - Category approach for Inorganic sulfites/thiosulfates/dithionite" in section 13.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- The Toxicity of Sulphite. I. Long-term Feeding and Multigeneration Studies in Rats.
- Author:
- Til, H.P., et al.
- Year:
- 1 972
- Bibliographic source:
- Food and Cosmetics Toxicology, 10: 291-310.
- Reference Type:
- review article or handbook
- Title:
- SIDS Dossier on Sodium Disulphite
- Author:
- Anonymous
- Year:
- 2 001
- Bibliographic source:
- Final Draft for Publication, available on http://www.oecd.org/document/63/0,2340,en_2649_34379_1897983_1_1_1_1,00.html
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- In a three-generation feeding study, groups of 20 male and 20 female Wistar rats received 0, 0.125, 0.25, 0.5, 1.0 and 2.0% sodium metabisulphite, i.e. 49, 108, 220, 460, and 955 mg/kg bw/d as actual dose in a thiamine-containing diet over periods of 2 years.
- GLP compliance:
- not specified
- Limit test:
- no
Test material
- Reference substance name:
- Disodium disulphite
- EC Number:
- 231-673-0
- EC Name:
- Disodium disulphite
- Cas Number:
- 7681-57-4
- Molecular formula:
- Na2S2O5
- IUPAC Name:
- disodium disulphite
- Test material form:
- not specified
- Details on test material:
- - Name of test material (as cited in study report): sodium metabisulfite (obtained from Amsterdamsche Chinine Fabriek (ACF), Amsterdam, Netherlands)
- Molecular formula (if other than submission substance): Na2S2O5
- Analytical purity: between 95 and 99%
Constituent 1
- Specific details on test material used for the study:
- not specified
Test animals
- Species:
- rat
- Strain:
- Wistar
- Details on species / strain selection:
- not specified
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: derived from the Institute's Wistar-derived colony
- Age at study initiation: weanling or young rats
- Housing: housed in groups of 5 in screen-bottomed cages
- Diet (ad libitum): basal diet was Institute's stock diet, with following percentage composition: 35% ground yellow maize, 26 % ground whole wheat, 10% soyabean-oil meal, 8% fish meal, 4% meat scraps, 2.7% dried whey, 3% brewer's yeast, 3.3% vitamin preparations, 1.5% minerals, 0.5% NaCl, 3% soyabean-oil, 3% grass meal.
- Water (ad libitum): tap water
ENVIRONMENTAL CONDITIONS
- Temperature: 24 - 26 °C
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- unchanged (no vehicle)
- Details on exposure:
- DIET PREPARATION
- Rate of preparation of diet (frequency): diets were freshly prepared every 2 weeks.
- Sulphite was added by mechanical mixing of Na2S2O5 at levels varying from 0.125 to 8%.
- In order to compensate for the destruction of thiamine by sulphite, the stock diet was drastically enriched with 50 ppm thiamine.
- Storage temperature of food: diets were stored at -18°C and the rats were provided daily with a fresh portion of previously frozen diet. - Details on mating procedure:
- - All rats of the F0-generation were mated within their diet group at about week 21 (producing F1a) and half of them also at week 34 (producing F1b).
- The rats of the F1a-generation were mated at week 12 and 30 to produce the F2a and F2b litters, respectively.
- Males and females of the F2a litters were selected for producing the next generation by mating them at week 14 and 22.
- Group matings were used throughout and lasted for a period of 2 weeks.
- At day 20 after the beginning of the mating period, the females were caged individually until after the litters had been weaned. - Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- Diets were analysed for SO2 and thiamine.
Results:
- SO2 determinations on the diets showed considerable losses of sulphite.
- proportionally the losses of sulphite decreased with increasing dietary levels of sulphite both immediately after mixing and after storage for 2 wk at - 18 °C and subsequent storage for 24 hr at room temperature.
- thiamine content decreased after storage for 2 wk at -18'C only in the 1 and 2% sulphite diets. Subsequent storage for 24 hr at room temperature showed slight and similar losses at 0, 0.125 and 0.25 %, but at higher sulphite levels there was a definite tendency towards greater losses with an increase of sulphite in the diet.
- during the experimental period, the rats consumed food that was stored on average for 1 week at -18°C and subsequently kept in the feeders for 12 hr at 24°C. The losses amounted to 22, 14, 12, 8 and 4.5 % Na2S20s and 2.7, 1.7, 8.3, 14.5 and 15.4% thiamine in the diets supplemented with 0.125, 0.25, 0.5, 1 and 2 % sulphite, respectively. - Duration of treatment / exposure:
- F0-Generation: 104 weeks (21 weeks or 34 weeks before mating and up to a total of 104 weeks)
F1a-Generation: 104 weeks (12 weeks or 30 weeks before mating and up to a total of 104 weeks)
F2a-Generation: ca. 30 weeks (14 weeks or 22 weeks before mating and up to a total of about 30 weeks) - Frequency of treatment:
- continuously
- Details on study schedule:
- not specified
Doses / concentrationsopen allclose all
- Dose / conc.:
- 0.125 other: %
- Remarks:
- ca. 50 mg/kg bw (nominal in diet)
- Dose / conc.:
- 0.25 other: %
- Remarks:
- ca. 110 mg/kg bw (nominal in diet)
- Dose / conc.:
- 0.5 other: %
- Remarks:
- ca. 220 mg/kg bw (nominal in diet)
- Dose / conc.:
- 1 other: %
- Remarks:
- ca. 460 mg/kg bw (nominal in diet)
- Dose / conc.:
- 2 other: %
- Remarks:
- ca. 960 mg/kg bw (nominal in diet)
- No. of animals per sex per dose:
- F0 - Generation: 20 males / 20 females
F1a - Generation: 10 males / 10 females
F2a - Generation: 10 males / 15 females - Control animals:
- yes, plain diet
- Details on study design:
- not specified
- Positive control:
- not specified
Examinations
- Parental animals: Observations and examinations:
- CAGE SIDE OBSERVATIONS: Yes
- Cage side observations checked: clinical signs and mortality
At week 32, 64 and 100 all rats of the F0- and F1a-Generations and at week 28 those of the F2a-Generation were examined for occult blood in the faeces.
DETAILED CLINICAL OBSERVATIONS: Not specified
BODY WEIGHT: Yes
- Time schedule for examinations: weekly for the first 12 weeks and once every four week thereafter.
FOOD CONSUMPTION AND COMPOUND INTAKE:
- Time schedule for examinations of food consumption: at intervals during 1-week periods.
HAEMATOLOGY: Yes
- Time schedule for collection of blood:
F0-Generation: week 52, 78, and 100
F1a-Generation: week 52, and 102
F2a-Generation: week 20
- Anaesthetic used for blood collection: Not specified
- Animals fasted: Not specified
- How many animals: 6 – 10 animals of each sex from the control, 1 and 2 % groups
- Parameters checked: haemoglobin concentration, haematocrit value, numbers of erythrocytes, total and individual types of leukocytes
CLINICAL CHEMISTRY: Yes (F0-Generation only)
- Time schedule for collection of blood: week 52 and 104.
- Animals fasted: Not specified
- How many animals: not specified
- Parameters checked: glutamic-oxalacetic transaminases and glutamic-pyruvic transaminases.
URINALYSIS: Yes
- Time schedule for collection of urine:
F0-Generation: week13, 28, 52, 78, and 101
F1a-Generation: week 28, 52, and 100
F2a-Generation: week 28
- Metabolism cages used for collection of urine: Not specified
- Animals fasted: Not specified
- How many animals: 5 - 11 rats of each sex, usually from the controls and the 1 and 2 % groups
- Parameters checked: phenol-red excretion. glutamic-oxalacetic transaminases, specific gravity, appearance, pH, glucose, albumin, occult blood, ketones, and microscopy of the sediment.
FURTHER EXAMINATIONS
- Thiamine was determined in the pooled urine samples of 5-10 male and 5 - 10 female rats of each group in the three generations at several stages and also in pooled liver samples of five F0-Generation rats of each sex at week 52 and 104. - Oestrous cyclicity (parental animals):
- not specified
- Sperm parameters (parental animals):
- Parameters examined in [all/P/F1/F2] male parental generations: testis weight
- Litter observations:
- STANDARDISATION OF LITTERS
- Performed: yes, on the first day, the litters containing more than eight pups were randomly reduced to that number in order to equalize the stress of lactation among the dams.
PARAMETERS EXAMINED
The following parameters were examined in F1 / F2 / F3 offspring:
- number of pups in each litter
- total weight of the litter at days 1, 8 and 21. - Postmortem examinations (parental animals):
- SACRIFICE: Yes
- After 52 weeks, 5 males and 5 females of each diet group in the F0 generation were killed for interim organ weights analysis and gross pathology.
- At week 104 all survivors of the F0 and F1-generations were killed.
- At about week 30 all survivors of the F2 generation were killed.
GROSS PATHOLOGY: Yes,
- At week 104 all survivors in the F0 and F1 generations and at about 30 weeks those of the F2 generation were killed and autopsied.
- Rats that died or killed when moribund were also autopsied, but tissue samples were preserved only if autolysis was not too advanced.
- The heart, kidneys, liver, spleen, brain, testes, ovaries, pituitary, thyroid and adrenals were weighed.
HISTOPATHOLOGY: Yes
- Tissue samples were fixed in 10% buffered formalin, embedded in paraffin, sectioned at 5 µm and stained with haematoxylin and eosin.
- The following tissues were examined: heart, kidneys, liver, spleen, brain (three levels), testes, ovaries, pituitary, thyroids, parathyroids, adrenals, thymus, lungs, trachea, salivary glands, gastro-intestinal tract (six levels), pancreas, urinary bladder, skeletal muscle, spinal cord, femoral nerve, skin, bone marrow (sternum), axillary and mesenteric lymph nodes, exorbital lachrymal gland, aorta, mammary glands, uterus, prostate, seminal vesicle and coagulating gland. - Postmortem examinations (offspring):
- not specified
- Statistics:
- not specified
- Reproductive indices:
- not specified
- Offspring viability indices:
- not specified
Results and discussion
Results: P0 (first parental generation)
General toxicity (P0)
- Clinical signs:
- effects observed, treatment-related
- Description (incidence and severity):
- - All rats in the highest dose group showed indications of occult blood in the faeces, while this effect occurred in only 21-60% of the animals on diets containing 1 % sulphite.
- In 10 % of the females given 0.25 % and in 10 % of the males given 0.5 % sulphite slight indications of intestinal blood loss were observed at wk 32 only. - Dermal irritation (if dermal study):
- not specified
- Mortality:
- mortality observed, non-treatment-related
- Body weight and weight changes:
- no effects observed
- Food consumption and compound intake (if feeding study):
- no effects observed
- Food efficiency:
- not specified
- Water consumption and compound intake (if drinking water study):
- not specified
- Ophthalmological findings:
- not specified
- Haematological findings:
- no effects observed
- Clinical biochemistry findings:
- no effects observed
- Urinalysis findings:
- no effects observed
- Behaviour (functional findings):
- not specified
- Immunological findings:
- not specified
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Histopathological findings: non-neoplastic:
- effects observed, treatment-related
- Description (incidence and severity):
- - Hyperplastic changes were seen in both the forestomach and glandular stomach at the 1.0 and 2.0% sulphite level. They were either present only at the 1 and 2 % dosage levels or their incidence was distinctly increased at these levels.
- Histopathological findings: neoplastic:
- no effects observed
- Other effects:
- no effects observed
Reproductive function / performance (P0)
- Reproductive function: oestrous cycle:
- not specified
- Reproductive function: sperm measures:
- not specified
- Reproductive performance:
- no effects observed
Details on results (P0)
- General conditions of the rats remained good during the first 72 weeks.
- After this time, aging symptoms developed in many rats and mortality increased rapidly.
- The survival in the sulphite groups was generally higher than in the controls.
BODY WEIGHT AND WEIGHT GAIN
- Body weights were comparable irrespective of treatment.
FOOD CONSUMPTION AND COMPOUND INTAKE
- There were no distinct differences in food consumption.
HAEMATOLOGY
- Haemoglobin, haematocrit values and erythrocyte counts were marginally reduced at 2% sulphite at week 52, 78, and 100.
CLINICAL CHEMISTRY
- Significant (P < 0.05) decreases in serum glutamic-pyruvic-transaminase values occured at wk 104 in male rats receiving 0.125 % sulfite.
- Otherwise, there were no differences between the test and control animals in transaminase activities either at week 52 or at week 104.
URINALYSIS
- Kidney function: phenol-red excretion, specific gravity and glutamic-oxalacetic-transaminase activity in the urine were not adversely affected.
- Urine analysis values were essentially normal.
ORGAN WEIGHTS
- Interim results obtained after 1 year did not indicate any effect of sulphite on organ to body weight ratios.
- Terminally the relative weights of the livers were lower in all the test groups than in the controls, but there was no evidence of a dose-related response.
HISTOPATHOLOGY: NON-NEOPLASTIC
- The type and incidence of the other non-neoplastic lesions observed were comparable in test and control groups.
HISTOPATHOLOGY: NEOPLASTIC
- The number of lymphoreticular pulmonary tumours in males decreased with increasing levels of sulphite in the diet.
- The incidence of thyroid and pituitary tumours in the control group of the males was exceptionally low, whereas those noted in the various test groups represented numbers normally found in the strain used.
- All other neoplasms occurred in a random manner with no apparent relationsship between number, location of tumours and treatment.
REPRODUCTIVE PERFORMANCE (PARENTAL ANIMALS)
- The results of the matings in successive generations showed no consistent differences between groups for fertility and the number of pups/litter.
OTHER FINDINGS
- There was a dose-related decrease in the thiamine content of the urine at sulphite levels of 0.125 % and above and in the liver at levels above 0.25 %
- The group given 2 % sulphite showed no distinct changes in the thiamine status when compared with control rats on the stock diet without extra thiamine.
Effect levels (P0)
open allclose all
- Key result
- Dose descriptor:
- NOAEL
- Remarks:
- local toxicity
- Effect level:
- 108 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: see 'Remark'
- Dose descriptor:
- NOAEL
- Remarks:
- fertility
- Effect level:
- > 955 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: see 'Remark'
Target system / organ toxicity (P0)
- Critical effects observed:
- not specified
Results: P1 (second parental generation)
General toxicity (P1)
- Clinical signs:
- effects observed, treatment-related
- Description (incidence and severity):
- - All rats in the highest dose group showed indications of occult blood in the faeces, while this effect occurred in only 13-40% of the animals on diets containing 1 % sulphite.
- Dermal irritation (if dermal study):
- not specified
- Mortality:
- mortality observed, non-treatment-related
- Body weight and weight changes:
- no effects observed
- Food consumption and compound intake (if feeding study):
- no effects observed
- Food efficiency:
- not specified
- Water consumption and compound intake (if drinking water study):
- not specified
- Ophthalmological findings:
- not specified
- Haematological findings:
- no effects observed
- Clinical biochemistry findings:
- not specified
- Urinalysis findings:
- no effects observed
- Behaviour (functional findings):
- not specified
- Immunological findings:
- not specified
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Gross pathological findings:
- effects observed, treatment-related
- Description (incidence and severity):
- - Pathological changes attributable to the feeding of sulphite were observed only in the stomach.
- A distinctly raised and thickened limiting ridge and small amounts of a reddish-brown flocky material in the mucus layer of the glandular stomach were seen grossly in the groups given the two highest sulphite levels. - Neuropathological findings:
- not specified
- Histopathological findings: non-neoplastic:
- effects observed, treatment-related
- Description (incidence and severity):
- - lesions occurred in both the fore- and glandular stomach and were mainly characterized by either hyperplasia or inflanunation. They were either present only at the 1 and 2 % dosage levels or their incidence was distinctly increased at these levels.
- Histopathological findings: neoplastic:
- no effects observed
- Other effects:
- no effects observed
- Details on results:
- CLINICAL SIGNS AND MORTALITY
- General conditions of the rats remained good during the first 72 weeks.
- After this time, aging symptoms developed in many rats and mortality increased rapidly.
- The survival in the sulphite groups was generally higher than in the controls, except in the case of males of the F1-Genertion given 2 % sulphite. However, no deaths occurred in the females of the same group.
BODY WEIGHT AND WEIGHT GAIN
- There was a marginal reduction in body-weight gain in both sexes of the F1- Generation rats given 2 % sulphite. This occurred also in females given 0.125, 0.25 and 0.5% sulphite in the F1-generation, but there was no dose-relationship and, moreover, the differences could partly be explained by the higher initial body weights of the controls.
FOOD CONSUMPTION AND COMPOUND INTAKE
- There were no distinct differences in food consumption.
HAEMATOLOGY
- Males at 2 % showed an increase in leucocyte count at wk 102.
- Otherwise, all haematological values for test and control animals were within normal ranges at all stages.
URINALYSIS
- Kidney function: phenol-red excretion, specific gravity and glutamic-oxalacetic-transaminase activity in the urine were not adversely affected.
- Urine analysis values were essentially normal.
ORGAN WEIGHTS
- The interim results obtained after 1 yr did not indicate any effect of sulphite on organ-to-body weight ratios.
- Terminally the relative weights of the livers were lower in all the test groups than in the controls, but there was no evidence of a dose-related response.
- sulphite feeding had no apparent effect on the relative weights of any other organs.
GROSS PATHOLOGY
- Pathological changes attributable to the feeding of sulphite were observed only in the stomach.
- A distinctly raised and thickened limiting ridge and small amounts of a reddish-brown flocky material in the mucus layer of the glandular stomach were seen grossly in the groups given the two highest sulphite levels.
HISTOPATHOLOGY: NON-NEOPLASTIC
- The type and incidence of the other non-neoplastic lesions observed were comparable in test and control groups.
HISTOPATHOLOGY: NEOPLASTIC
- The number of Iymphoreticular pulmonary tumours in males decreased with increasing levels of sulphite in the diet.
- The incidence of thyroid and pituitary tumours in the control group of the male rats was exceptionally low, whereas those noted in the various test groups represented numbers normally found in the strain of rats used.
- All other neoplasms occurred in a random manner with no apparent relationship between number, location or type of tumours and the treatment.
OTHER FINDINGS
- There was a dose-related decrease in the thiamine content of the urine at sulphite levels of 0.125 % and above
- However, the group given 2 % sulphite showed no distinct changes in the thiamine status when compared with control rats on the stock diet without extra thiamine.
Reproductive function / performance (P1)
- Reproductive function: oestrous cycle:
- not specified
- Reproductive function: sperm measures:
- not specified
- Reproductive performance:
- no effects observed
Details on results (P1)
- The results of the matings showed no consistent differences between groups in female fertility
Effect levels (P1)
open allclose all
- Key result
- Dose descriptor:
- NOAEL
- Remarks:
- local toxicity (P1-Generation)
- Effect level:
- 108 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: see "Remarks"
- Key result
- Dose descriptor:
- NOAEL
- Remarks:
- fertility (P1-Generation)
- Effect level:
- > 955 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: see "Remarks"
- Key result
- Dose descriptor:
- NOAEL
- Remarks:
- local toxicity (P2-Generation)
- Effect level:
- 108 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: see "Remarks"
- Key result
- Dose descriptor:
- NOAEL
- Remarks:
- fertility (P2-Generation)
- Effect level:
- > 955 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: see "Remarks"
Target system / organ toxicity (P1)
- Critical effects observed:
- not specified
Results: F1 generation
General toxicity (F1)
- Clinical signs:
- no effects observed
- Dermal irritation (if dermal study):
- not specified
- Mortality / viability:
- mortality observed, non-treatment-related
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- - during the lactation period the body weights of the young in the 2 % group were generally lower than those of the controls and the lower sulphite groups.
- 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
- Sexual maturation:
- not specified
- Organ weight findings including organ / body weight ratios:
- not specified
- Gross pathological findings:
- not specified
- Histopathological findings:
- not specified
- Other effects:
- not specified
Developmental neurotoxicity (F1)
- Behaviour (functional findings):
- not specified
Developmental immunotoxicity (F1)
- Developmental immunotoxicity:
- not specified
Details on results (F1)
Effect levels (F1)
- Remarks on result:
- other: there was a slight growth retardation during lactation in offspring of the 2% group.
Target system / organ toxicity (F1)
- Critical effects observed:
- not specified
Results: F2 generation
General toxicity (F2)
- Clinical signs:
- not specified
- Dermal irritation (if dermal study):
- not specified
- Mortality / viability:
- mortality observed, non-treatment-related
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- - during the lactation period the body weights of the young in the 2 % group were generally lower than those of the controls and the lower sulphite groups.
- 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
- Sexual maturation:
- not specified
- Organ weight findings including organ / body weight ratios:
- not specified
- Gross pathological findings:
- not specified
- Histopathological findings:
- not specified
- Other effects:
- not specified
Developmental neurotoxicity (F2)
- Behaviour (functional findings):
- not specified
Developmental immunotoxicity (F2)
- Developmental immunotoxicity:
- not specified
Details on results (F2)
- dietary levels of 1 % or below were sometimes associated with significantly decreased body weights at days 8 and 21, but there was no distinct dose-related response.
Effect levels (F2)
- Remarks on result:
- other: here was a slight growth retardation during lactation in offspring of the 2% group.
Target system / organ toxicity (F2)
- Critical effects observed:
- not specified
Overall reproductive toxicity
- Reproductive effects observed:
- not specified
Any other information on results incl. tables
Calculation of the dose level in mg/kg bw/d was done by converting % diet into ppm and by assuming an average body weight for older rats of 400 g and a daily feed intake of 20 g as follows:
0.215 % = 2150 ppm x 0.05 = 108 mg/kg bw/d Na2S2O5, equivalent to 72 mg/kg bw/d SO2
1.91% = 19100 ppm x 0.05 = 955 mg/kg bw/dNa2S2O5, equivalent to 640 mg/kg bw/d SO2
P2 (third parental generation)
CLINICAL SIGNS AND MORTALITY
- General conditions of the rats remained good during the first 72 weeks.
- After this time, aging symptoms developed in many rats and mortality increased rapidly.
- The survival in the sulphite groups was generally higher than in the controls.
- All rats in the highest dose group showed indications of occult blood in the faeces, while this effect occurred in only 20-30% of the animals on diets containing 1 % sulphite.
BODY WEIGHT AND WEIGHT CHANGES
- There was a marginal reduction in body-weight gain in both sexes of the F2-generation rats given 2 % sulphite.. This occurred also in females given 0·25 and 0·5 % in the F2-generation, but there was no dose-relationship and, moreover, the differences could partly be explained by the higher initial body weights of the controls.
FOOD CONSUMPTION AND COMPOUND INTAKE
- There were no distinct differences in food consumption, but a slight reduction was observed in the 2 % group of the F2-Generation during the first 2 wk of the experiment.
HAEMATOLOGY
- all haematological values for test and control animals were within normal ranges at all stages.
URINALYSIS
- Kidney function: phenol-red excretion, specific gravity and glutamic-oxalacetic-transaminase activity in the urine were not adversely affected.
- Urine analysis values were essentially normal.
ORGAN WEIGHTS
- The interim results obtained after 1 yr did not indicate any effect of sulphite on organ-to-body weight ratios.
- No distinct decrease in liver weight was observed.
- The relative weight of the kidneys was slightly, but significantly (P < 0·05), increased in the 2 % females.
- Sulphite feeding had no apparent effect on the relative weights of any other organs in any of the successive generations.
GROSS PATHOLOGY
- Pathological changes attributable to the feeding of sulphite were observed only in the stomach.
- A distinctly raised and thickened limiting ridge and small amounts of a reddish-brown flocky material in the mucus layer of the glandular stomach were seen grossly in the groups given the two highest sulphite levels.
HISTOPATHOLOGY: NON-NEOPLASTIC
- lesions occurred in both the fore- and glandular stomach and were mainly characterized by either hyperplasia or inflanunation. They were either present only at the 1 and 2 % dosage levels or their incidence was distinctly increased at these levels.
- The type and incidence of the other non-neoplastic lesions observed were comparable in test and control groups.
REPRODUCTIVE PERFORMANCE
- The results of the matings showed no consistent differences between groups in female fertility
OTHER FINDINGS
- There was a dose-related decrease in the thiamine content of the urine at sulphite levels of 0.125 % and above.
- However, the group given 2 % sulphite showed no distinct changes in the thiamine status when compared with control rats on the stock diet without extra thiamine.
F3 generation
- No consistent differences between groups were observed for the number of pups/litter, birth weight or mortality of the offspring.
- A significant reduction in the number of young was observed with 0·5, 1 and 2 % sulphite. However, there was no tendency towards a decrease with increasing dietary levels and moreover this reduction didnot occur in the second litters.
- during the lactation period the body weights of the young in the 2 % group were generally lower than those of the controls and the lower sulphite groups.
- dietary levels of 1 % or below were sometimes associated with significantly decreased body weights at days 8 and 21, but there was no distinct dose-related response.
Applicant's summary and conclusion
- Conclusions:
- The most sensitive parameters of chronic treatment of rats wit Na2S2O5 was the occurrence of occult blood in the faeces and changes in gastric morphology at dose levels of 0.5% or more. Thus, the NOAEL for local effects is represented by the dose of 0.25% metabisulphite (or 0.215% accounting for the los/s of metabisulphite). The corrected dose level corresponds to a dose of 108 mg/kg bw/d Na2S2O5 or an equivalent dose of 72 mg SO2/kg bw/day.
Based on the results of this study, no evidence of a treatment-related effect on reproduction and fertility was seen. Thus, the NOAEL for fertility can be expected above a dose level of 2% metabisulfite, corresponding to a dose of 955 mg/kg bw/d Na2S2O5 or 640 mg SO2/kg bw/day. However, there was a slight growth retardation during lactation in offspring of the 2% group.
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