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Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats.
Lira, Antonio Cascajosa; Prieto, Ana Isabel; Baños, Alberto; Guillamón, Enrique; Moyano, Rosario; Jos, Angeles; Cameán, Ana M.
Afiliação
  • Lira AC; Area of Toxicology, Faculty of Pharmacy, University of Sevilla, Sevilla, Spain.
  • Prieto AI; Area of Toxicology, Faculty of Pharmacy, University of Sevilla, Sevilla, Spain.
  • Baños A; DMC Research Center SLU, Camino de Jayena s/n, Alhedin, 18620, Granada, Spain.
  • Guillamón E; DMC Research Center SLU, Camino de Jayena s/n, Alhedin, 18620, Granada, Spain.
  • Moyano R; Department of Pharmacology, Toxicology and Legal and Forensic Medicine, University of Cordoba, Campus de Rabanales Carretera Madrid-Cadiz s/n, Spain.
  • Jos A; Area of Toxicology, Faculty of Pharmacy, University of Sevilla, Sevilla, Spain. Electronic address: angelesjos@us.es.
  • Cameán AM; Area of Toxicology, Faculty of Pharmacy, University of Sevilla, Sevilla, Spain.
Food Chem Toxicol ; 144: 111612, 2020 Oct.
Article em En | MEDLINE | ID: mdl-32738370
Propyl-propane-thiosulfonate (PTSO) is one of the main organosulfur compounds present in Allium essentials oil. Different applications in the food sector have been proposed for PTSO, such as food and feed additive and as active packaging. However, the authorization of its use depends on its toxicity profile. Thus, as a part of its safety assessment, in this work a repeated dose 90-day oral toxicity study has been conducted for the first time in rats following the OECD guideline 408. PTSO was administered to groups of 10 male and 10 female rats at dose levels of 0, 14, 28, and 55 mg/kg/day. No clinical signs or mortality and no changes in body weight, food consumption and feed conversion efficiency were detected through the study. Moreover, no treatment-related changes in hematological and biochemical parameters were observed, for either sex or dose groups. The histopathology study performed revealed no differences in organ weights, and no morphological and histopathological changes were observed. Based on these results, the no-observed-adverse-effect level (NOAEL) of PTSO was judged to be ≥ 55 mg/kg/day for both sexes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes de Toxicidade Subcrônica Tipo de estudo: Guideline Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes de Toxicidade Subcrônica Tipo de estudo: Guideline Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article