3-methylthiazolidine-2-thione

Genetic toxicity: in vitro

Administrative data

Endpoint:

in vitro cytogenicity / micronucleus study

Type of information:

experimental study

Adequacy of study:

key study

Study period:

2015-03-11 - 2015-04-30

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: Well-documented GLP OECD Guideline study without deviations on the registered substance itself

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2015

Report date:

2015

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

other: OECD 487 “In vitro Mammalian Cell Micronucleus Test”, adopted 26 September 2014

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Remarks:

Hess. Ministerium für Umwelt, Energie, Landwirtschaft und Verbraucherschutz, Mainzer Str. 80, D65189 Wiesbaden, Germany

Type of assay:

in vitro mammalian cell micronucleus test

Test material

Test material information

Constituent 1

Reference substance name:

3-methylthiazolidine-2-thione

EC Number:

217-614-1

EC Name:

3-methylthiazolidine-2-thione

Cas Number:

1908-87-8

Molecular formula:

C4H7NS2

IUPAC Name:

3-methyl-1,3-thiazolidine-2-thione

Test material form:

solid: pellets

Details on test material:

- Name of test material (as cited in study report): 3-Methyl-thiazolidin-2-thion
- Substance type: pure substance
- Storage condition of test material: At room temperature

Method

Target gene:

not applicable

Species / strain

Species / strain / cell type:

lymphocytes: human

Details on mammalian cell type (if applicable):

Blood samples were drawn from healthy non-smoking donors not receiving medication. For this study, blood was collected from a female donor (32 years old) for Experiment I and for Experiment II. The lymphocytes of the respective donor have been shown to respond well to stimulation of proliferation with PHA and to positive control substances. All donors had a previously established low incidence of micronuclei in their peripheral blood lymphocytes.
Human lymphocytes were stimulated for proliferation by the addition of the mitogen PHA to the culture medium for a period of 48 hours. The cell harvest time point was approximately 2 – 2.5 x AGT (average generation time). Any specific cell cycle time delay induced by the test item was not accounted for directly.

Metabolic activation:

with and without

Metabolic activation system:

Mammalian Microsomal Fraction S9 Mix

Test concentrations with justification for top dose:

8.65, 15.14, 26.50, 46.37, 81.15, 142.02, 248.54, 434.94, 761.14, 1332.00 µg/ml

Vehicle / solvent:

- Vehicle(s)/solvent(s) used: DMSO (test item), deionised water (MMC, Demecolcin), saline (CPA)

Controls

Untreated negative controls:

yes

Remarks:

solvent control

Negative solvent / vehicle controls:

yes

Remarks:

DMSO

Positive controls:

yes

Positive control substance:

cyclophosphamide

mitomycin C

other: Demecolcin

Details on test system and experimental conditions:

METHOD OF APPLICATION: in medium

DURATION
- Exposure duration: 4 or 20 hours
- Expression time (cells in growth medium): 16h or none plus 20 hours with Cytochalasin B
- Fixation time (start of exposure up to fixation or harvest of cells): 40 hours

SPINDLE INHIBITOR (cytogenetic assays): Cytochalasin B
STAIN (for cytogenetic assays): Giemsa

NUMBER OF REPLICATIONS: duplicates

NUMBER OF CELLS EVALUATED: At least 1000 binucleate cells per culture

DETERMINATION OF CYTOTOXICITY
- Method: other: % cytostasis

Evaluation criteria:

The criteria for the evaluation of micronuclei are described in the publication of Countryman and Heddle (1976) (COUNTRYMAN P.I. and HEDDLE J.A. (1976) The production on micronuclei from chromosome aberrations in irradiated cultures of human lymphocytes. Mutation Research, 41, 321-332.). The micronuclei have to be stained in the same way as the main nucleus. The area of the micronucleus should not extend the third part of the area of the main nucleus.

Statistics:

Chi square test (α < 0.05), using the validated R Script CHI2.Rnw

Results and discussion

Test results

Species / strain:

lymphocytes: human

Metabolic activation:

with and without

Genotoxicity:

negative

Cytotoxicity / choice of top concentrations:

no cytotoxicity nor precipitates, but tested up to recommended limit concentrations

Remarks:

10 mM

Vehicle controls validity:

valid

Untreated negative controls validity:

valid

Positive controls validity:

valid

Additional information on results:

TEST-SPECIFIC CONFOUNDING FACTORS
- Effects of pH: No relevant influence on pH value was observed
- Effects of osmolality: No relevant influence on osmolarity value was observed
- Precipitation: none noted

COMPARISON WITH HISTORICAL CONTROL DATA:
The micronucleus rates of the cells after treatment with the test item (0.45 – 0.90 % micronucleated cells) did not exceed the range of the solvent control values (0.60 – 1.05 % micronucleated cells) and were within the range of the laboratory historical control data.

ADDITIONAL INFORMATION ON CYTOTOXICITY:
No relevant cytotoxicity, indicated by reduced CBPI and described as cytostasis could be observed up to the highest applied concentration.

Remarks on result:

other: all strains/cell types tested

Remarks:

Migrated from field 'Test system'.

Any other information on results incl. tables

The test item 3-Methyl-thiazolidin-2-thion, dissolved in DMSO, was assessed for its potential to induce micronuclei in human lymphocytes in vitro in the absence and presence of metabolic activation by S9 mix. Two independent experiments were performed. In Experiment I, the exposure period was 4 hours with and without S9 mix. In Experiment II, the exposure period was 20 hours without S9 mix. The cells were prepared 40 hours after start of treatment with the test item. In each experimental group two parallel cultures were analysed. 1000 binucleate cells per culture were scored for cytogenetic damage on coded slides. To determine a cytotoxic effect the CBPI was determined in 500 cells per culture and cytotoxicity is described as % cytostasis. The highest treatment concentration in this study, 1332.00 μg/mL (approx. 10 mM) was chosen with regard to the molecular weight of the test item and with respect to the OECD Guideline 487 for the in vitro mammalian cell micronucleus test. No relevant influence on osmolarity or pH value was observed. No relevant cytotoxicity, indicated by reduced CBPI and described as cytostasis could be observed up to the highest applied concentration. In both experiments, in the absence and presence of S9 mix, no biologically relevant increase in the number of cells carrying micronuclei was observed. The micronucleus rates of the cells after treatment with the test item (0.45 – 0.90 % micronucleated cells) did not exceed the range of the solvent control values (0.60 – 1.05 % micronucleated cells) and were within the range of the laboratory historical control data. In both experiments, either Demecolcin (75.0 µg/mL), MMC (2.0 μg/mL) or CPA (17.5 μg/mL) were used as positive controls and showed distinct increases in cells with micronuclei. See attachment for tables

Applicant's summary and conclusion

Conclusions:

The study was conducted under GLP according to OECD guideline 487 on the registered substance itself. The method is to be considered scientifically reasonable with no deficiencies in documentation. Positive and negative controls gave the appropriate response. Hence, the results can be considered as reliable to assess the potential of 3-Methyl-thiazolidin-2-thion to induce micronuclei in mammalian cells. Under the experimental conditions reported, the test item did not induce micronuclei as determined by the in vitro micronucleus test in human lymphocytes. Therefore, 3-Methyl-thiazolidin-2-thion is considered to be non-mutagenic in this in vitro micronucleus test, when tested up to the highest required concentration.

Executive summary:

In a mammalian cell cytogenetics assay, an in vitro micronucleus test (OECD 487), human primary lymphocyte cultures were exposed to 3-Methyl-thiazolidin-2-thion in DMSO at concentrations of 0, 8.65, 15.14, 26.50, 46.37, 81.15, 142.02, 248.54, 434.94, 761.14, and 1332.00 µg/ml with and without metabolic activation (induced rat liver S9). In two independent experiments, cells were either exposed to the test item over 4h (±S9) or 20h (-S9).

In each experimental group two parallel cultures were analysed. Per culture 1000 binucleated cells were evaluated for cytogenetic damage. The highest applied concentration in this study (1332.0 µg/mL of the test item, approx. 10 mM) was chosen with regard to the molecular weight of the test item and with respect to the current OECD Guideline 487.

In Experiment I and II in the absence and presence of S9 mix, no cytotoxicity was observed up to the highest evaluated concentration.

In both independent experiments, neither a statistically significant nor a biologically relevant increase in the number of micronucleated cells was observed after treatment with the test item. 3-Methyl-thiazolidin-2-thion is considered to be non-mutagenic in this in vitro micronucleus test, when tested up to the highest required concentration.

Appropriate mutagens (Demecolcin (75.0 ng/mL), MMC (2.0 μg/mL) or CPA (17.5 μg/mL)) were used as positive controls. They induced statistically significant increases in cells with micronuclei.

This study is classified as acceptable. This study satisfies the requirement for an in vitro micronucleus test (OECD 487) for in vitro cytogenetic mutagenicity data.