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치올기 함유 저분자 화합물과의 반응성을 이용하는 간단한 in chemico 피부감작성 시험법의 개발 가능성 평가

A Possible Simple in Chemico Test to Identify Skin Sensitizers and Non-Sensitizers by Using Low Molecular Weight Compounds Containing Thiol Group

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초록

For the initiation of skin sensitization reaction, a sensitizer should react with endogenous proteins. During the haptenization of a sensitizer with proteins, it is also possible for a sensitizer to react with small molecules that contain either amino or thiol group, indicating a possibility to develop a simple skin sensitization test using the reactivity of test compounds with thiol-containing low molecular weight compounds. In the present study, 10 compounds that contain a thiol group were pre-tested to determine whether the reactivity with a thiol-detecting monobromobimane would be in concentration-dependent manners. Subsequently, among thiol compounds, a simple spectrofluorometrical method to identify skin sensitizers in chemico was tested with glutathione, an endogenous substance that contains amino and thiol groups. To flurorometrically quantitate the remaining thiol-containing compounds following a reaction with skin sensitizers, monobromobimane was employed. The conditions optimized included: incubation conditions of thiol compounds including glutathione with monobromobimane, molar ratios of thiol compounds to monobromobimane, optimal concentration and incubation time of monobromobimane, and pH and incubation time with test compounds. With a tentatively optimized conditions, 4 skin sensitizers and 2 non-sensitizers were tested to know whether the method could correctly identify skin sensitizers and non-sensitizers. The results indicated a good possibility. Although further optimization is required, it would be a useful screening tool for determining skin sensitization potential of test compounds, because the present method employs a simple endogenous thiol compound as an acceptor for sensitizers with a spectrofluorometric detection system requiring neither experimental animals nor cell cultures.

Abstract

For the initiation of skin sensitization reaction, a sensitizer should react with endogenous proteins. During the haptenization of a sensitizer with proteins, it is also possible for a sensitizer to react with small molecules that contain either amino or thiol group, indicating a possibility to develop a simple skin sensitization test using the reactivity of test compounds with thiol-containing low molecular weight compounds. In the present study, 10 compounds that contain a thiol group were pre-tested to determine whether the reactivity with a thiol-detecting monobromobimane would be in concentration-dependent manners. Subsequently, among thiol compounds, a simple spectrofluorometrical method to identify skin sensitizers in chemico was tested with glutathione, an endogenous substance that contains amino and thiol groups. To flurorometrically quantitate the remaining thiol-containing compounds following a reaction with skin sensitizers, monobromobimane was employed. The conditions optimized included: incubation conditions of thiol compounds including glutathione with monobromobimane, molar ratios of thiol compounds to monobromobimane, optimal concentration and incubation time of monobromobimane, and pH and incubation time with test compounds. With a tentatively optimized conditions, 4 skin sensitizers and 2 non-sensitizers were tested to know whether the method could correctly identify skin sensitizers and non-sensitizers. The results indicated a good possibility. Although further optimization is required, it would be a useful screening tool for determining skin sensitization potential of test compounds, because the present method employs a simple endogenous thiol compound as an acceptor for sensitizers with a spectrofluorometric detection system requiring neither experimental animals nor cell cultures

참고문헌 (13)

  1. Ahlfors SR, "Reactivity of contact allergenic haptens to amino acid residues in a model carrier peptide, and characterization of formed peptide-hapten adducts", Skin Pharmacology and Physiology, 16, pp.59~68 (2003)
  2. Basketter DA, "Use of the local lymph node assay for the estimation of relative contact allergenic potency", Contact Dermatitis, 42, pp.344~348 (2000)
  3. Basketter DA, "A comparison of statistical approaches to the derivation of EC3 values from local lymph node assay dose responses", Journal of Applied Toxicology, 19, pp.261~266 (1999)
  4. Cockshott A, "The local lymph node assay in practice : a current regulatory perspective", Human & Experimental Toxicology, 25, pp.387~394 (2006)
  5. Ellman OH, "Tissue sulfhydryl group", Archives of Biochemistry et Biophysics, 82, pp.70~77 (1959)
  6. Gerberick GF, "Development of a peptide reactivity assay for screening contact allergens", Toxicological Sciences, 81, pp.332~343 (2004)
  7. Gerberick GF, "Local lymph node assay(LLNA)for detection of sensitization capacity of chemicals", Methods, 41, pp.54~60 (2007)
  8. Gerberick GF, "Quantification of chemical peptide reactivity for screening contact allergens : A classification tree model approach", Toxicological Sciences, 97, pp.417~427 (2007)
  9. Gerberick GF, "Investigation of peptide reactivity of pro-hapten skin sensitizers using a peroxidase-peroxide oxidation system", Toxicological Sciences, 112(1), pp.164~174 (2009)
  10. Kimber I, "The local lymph node assay : past, present and future", Contact Dermatitis, 47, pp.315~328 (2002)
  11. Kimber I, "Assessment of the skin sensitization potential of topical medicaments using the local lymph node assay : An interlaboratory evaluation", Journal of Toxicology and Environmental Health, 53, pp.563~579 (2010)
  12. Nepal MR, "A simple in chemico method for testing skin sensitizing potential of chemicals using small endogenous molecules", Toxicology Letters, 289, pp.75~85 (2018)
  13. Rudyk O, "Biochemical methods for monitoring protein thiol redox states in biological systems", Redox Biology, 2, pp.803~813 (2014)

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