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EC number: 245-826-4 | CAS number: 23694-14-6
- 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
Repeated dose toxicity: oral
Administrative data
- Endpoint:
- short-term repeated dose toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- secondary literature
Data source
Reference
- Reference Type:
- review article or handbook
- Title:
- Pharmacotoxicological aspects of levosulpiride.
- Author:
- Rossi F
- Year:
- 1 995
- Bibliographic source:
- Pharmacol Res. 1995 Feb;31(2):81-94.
Materials and methods
Test guideline
- Guideline:
- other: not specified
- GLP compliance:
- not specified
Test material
- Reference substance name:
- N-[[(2S)-1-ethylpyrrolidin-2-yl]methyl]-2-methoxy-5-sulfamoylbenzamide
- Cas Number:
- 23672-07-3
- Molecular formula:
- C15H23N3O4S
- IUPAC Name:
- N-[[(2S)-1-ethylpyrrolidin-2-yl]methyl]-2-methoxy-5-sulfamoylbenzamide
- Test material form:
- not specified
Constituent 1
Results and discussion
Any other information on results incl. tables
Rats, rabbits and dogs were used for subacute toxicity trials. Haematology and blood chemistry analyses have been selected to have an overall picture of the treatment effects on metabolism, on liver and renal functions and on complete blood count. The necropsy was carried out on major organs and apparatuses. This was performed on each animal, while each organ was subjected to histologic examination (See Figure). The subacute oral administration of levosulpiride in rats at 150-300 mg/kg for 12 weeks is well tolerated as shown by the haematology, blood chemistry and urine analysis, and does not significantly differ from controls. There are, however, a slight reduction in body weight and food consumption and some variations in liver function at the highest dosage (300 mg/kg) The subacute administration of levosulpiride by subcutaneous route in rats at 12.5-25 mg/kg/day for 12 weeks is well-tolerated as shown by laboratory analysis. A slight drop in body weight and variations in liver functions were documented with highest dosage (50 mg/kg/day). Similar results were obtained by studying the effects of the subacute oral (125-250 mg/kg/day for 12 weeks) or intramuscular (6.25-12.5 mg/kg/day) administration of levosulpiride in rabbits. In another trial the subacute oral administration of levosulpiride in rats for 13 weeks at 25, 150 and 900 mg/kg/day and racemic sulpiride at 50, 300 and 1800 mg/kg/day, no toxic effect was identified for either compound. However, findings obtained for both tested compounds, notably clinical signs, clinical pathology and mammary gland/vaginal changes are considered to be related to the exaggerated pharmacological action of the compounds. The only toxic effect noted was mortality among females receiving the highest treatment level of racemic sulpiride. In particular, two females receiving the highest dose of racemic sulpiride died during the course of the study. These deaths as a result of treatment cannot be excluded. Clinical signs of somnolence were noted among rats of the highest dose groups of either test substance, but they were predominant among females, particularly those treated with racemic sulpiride. Blood chemistry investigations showed a decrease in creatinine kinase among males receiving racemic sulpiride after 13 weeks of treatment. This decrease was still apparent at the end of the recovery phase, particularly in males receiving the middle and highest dose levels. Indeed, females receiving racemic sulpiride and rats of both sexes receiving levosulpiride were not affected. Several minor differences were noted between control and treated rats in pituitary and adrenal gland weights, vagina/mammary gland hyperplasia and vaginal mucification. It is considered that these changes, which show a marked degree of consistency for both L- and racemic sulpiride, reflect a physiological response to treatment. These changes could be originated from an increase in circulating prolactin concentration. It is known that treatment with dopamine D2 receptor antagonist (such as L- or racemic sulpiride) may cause a blockade of the tubero-infundibular pathway, in which dopamine is believed to act physiologically, via D2-receptors, as an inhibitor of prolactin secretion. The result of this blockade is responsible for an increase in circulating prolactin. It could be considered that an increased circulating level of this hormone could promote the observed vagina/mammary gland hyperplasia and vaginal mucification and may also give rise to the slight changes in pituitary and adrenal gland weights. L- and racemic sulpiride were administered orally (25-200 mg/kg), as capsules, to pure-bred beagle dogs for a period of 13 weeks. The study consisted of six groups, each containing three male and three female or five male and five female dogs. An additional group including five male and five female dogs served as control. Mortality did not occur in any experimental group. Initiation of treatment with L- or racemic sulpiride was associated in most dogs with the following clinical signs: decreased activity, tremor, abnormal gait, stereotyped behaviour, erythema of the mucous membranes of the buccal cavity, and salivation. Treatment with either compound at 200 mg/kg was associated in some dogs with collapse, ptosis, deep respiration and/or bradypnea. Vomiting was also recorded in some dogs treated with either compound; however, in view of the incidence and distribution throughout the groups, no definite association with treatment could be made. In view of the persistence of several of these signs and since animals from all treatment groups were affected, a decision was made to reduce the daily dose of each group by half from day 7. With the exception of salivation, decreased activity and ptosis (L- or racemic sulpiride, 100-200 mg/kg only), the clinical signs described above disappear within 1 or 2 weeks of reducing the dose levels. From the beginning of week 3 slight to moderate mammary development is detected in females receiving either L- or racemic sulpiride. The degree of development is similar for both compounds and shows no relationship to dose. There were also documented: a transient reduction in food consumption during week 1 (levosulpiride or racemic sulpiride, 100 or 200 mg/kg); a slight, transient loss in body weight during week 1 (levosulpiride 200 mg/kg, racemic sulpiride 100-200 mg/kg); increases in plasma cholesterol and phospholipid concentrations during weeks 7 and/or 13, without any relationship to dose. No treatment related change was documented in haematology or urine profiles. A clear reduction in prostate weight is apparent in males treated with L- or racemic sulpiride at all dose. The microscopic study documented hyperplasia and active secretion of the mammary glands of treated females, and atrophy of the prostate glands of treated males.
Applicant's summary and conclusion
- Conclusions:
- Although treatment related effects can be observed after oral sulpiride administration, they do not support the classification as STOT RE in accordance with Regulation (EC) 1272/2008.
- Executive summary:
Rats, rabbits and dogs were used for subacute toxicity trials. Haematology and blood chemistry analyses have been selected to have an overall picture of the treatment effects on metabolism, on liver and renal functions and on complete blood count. The necropsy was carried out on major organs and apparatuses. This was performed on each animal, while each organ was subjected to histologic examination (See Figure). The subacute oral administration of levosulpiride in rats at 150-300 mg/kg for 12 weeks is well tolerated as shown by the haematology, blood chemistry and urine analysis, and does not significantly differ from controls. There are, however, a slight reduction in body weight and food consumption and some variations in liver function at the highest dosage (300 mg/kg) The subacute administration of levosulpiride by subcutaneous route in rats at 12.5-25 mg/kg/day for 12 weeks is well-tolerated as shown by laboratory analysis. A slight drop in body weight and variations in liver functions were documented with highest dosage (50 mg/kg/day). Similar results were obtained by studying the effects of the subacute oral (125-250 mg/kg/day for 12 weeks) or intramuscular (6.25-12.5 mg/kg/day) administration of levosulpiride in rabbits. In another trial the subacute oral administration of levosulpiride in rats for 13 weeks at 25, 150 and 900 mg/kg/day and racemic sulpiride at 50, 300 and 1800 mg/kg/day, no toxic effect was identified for either compound. However, findings obtained for both tested compounds, notably clinical signs, clinical pathology and mammary gland/vaginal changes are considered to be related to the exaggerated pharmacological action of the compounds. The only toxic effect noted was mortality among females receiving the highest treatment level of racemic sulpiride. In particular, two females receiving the highest dose of racemic sulpiride died during the course of the study. These deaths as a result of treatment cannot be excluded. Clinical signs of somnolence were noted among rats of the highest dose groups of either test substance, but they were predominant among females, particularly those treated with racemic sulpiride. Blood chemistry investigations showed a decrease in creatinine kinase among males receiving racemic sulpiride after 13 weeks of treatment. This decrease was still apparent at the end of the recovery phase, particularly in males receiving the middle and highest dose levels. Indeed, females receiving racemic sulpiride and rats of both sexes receiving levosulpiride were not affected. Several minor differences were noted between control and treated rats in pituitary and adrenal gland weights, vagina/mammary gland hyperplasia and vaginal mucification. It is considered that these changes, which show a marked degree of consistency for both L- and racemic sulpiride, reflect a physiological response to treatment. These changes could be originated from an increase in circulating prolactin concentration. It is known that treatment with dopamine D2 receptor antagonist (such as L- or racemic sulpiride) may cause a blockade of the tubero-infundibular pathway, in which dopamine is believed to act physiologically, via D2-receptors, as an inhibitor of prolactin secretion. The result of this blockade is responsible for an increase in circulating prolactin. It could be considered that an increased circulating level of this hormone could promote the observed vagina/mammary gland hyperplasia and vaginal mucification and may also give rise to the slight changes in pituitary and adrenal gland weights. L- and racemic sulpiride were administered orally (25-200 mg/kg), as capsules, to pure-bred beagle dogs for a period of 13 weeks. The study consisted of six groups, each containing three male and three female or five male and five female dogs. An additional group including five male and five female dogs served as control. Mortality did not occur in any experimental group. Initiation of treatment with L- or racemic sulpiride was associated in most dogs with the following clinical signs: decreased activity, tremor, abnormal gait, stereotyped behaviour, erythema of the mucous membranes of the buccal cavity, and salivation. Treatment with either compound at 200 mg/kg was associated in some dogs with collapse, ptosis, deep respiration and/or bradypnea. Vomiting was also recorded in some dogs treated with either compound; however, in view of the incidence and distribution throughout the groups, no definite association with treatment could be made. In view of the persistence of several of these signs and since animals from all treatment groups were affected, a decision was made to reduce the daily dose of each group by half from day 7. With the exception of salivation, decreased activity and ptosis (L- or racemic sulpiride, 100-200 mg/kg only), the clinical signs described above disappear within 1 or 2 weeks of reducing the dose levels. From the beginning of week 3 slight to moderate mammary development is detected in females receiving either L- or racemic sulpiride. The degree of development is similar for both compounds and shows no relationship to dose. There were also documented: a transient reduction in food consumption during week 1 (levosulpiride or racemic sulpiride, 100 or 200 mg/kg); a slight, transient loss in body weight during week 1 (levosulpiride 200 mg/kg, racemic sulpiride 100-200 mg/kg); increases in plasma cholesterol and phospholipid concentrations during weeks 7 and/or 13, without any relationship to dose. No treatment related change was documented in haematology or urine profiles. A clear reduction in prostate weight is apparent in males treated with L- or racemic sulpiride at all dose. The microscopic study documented hyperplasia and active secretion of the mammary glands of treated females, and atrophy of the prostate glands of treated males.
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