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A toxicological assessment of spermidine trihydrochloride produced using an engineered strain of Saccharomyces cerevisiae.
Chrysostomou, Paola P; Freeman, Elaine L; Murphy, Mary M; Pereira, Rui; Esdaile, David J; Keohane, Patrick.
Afiliação
  • Chrysostomou PP; Exponent Inc., Center for Chemical Regulation and Food Safety, 1150 Connecticut Ave, NW, Suite 1100, Washington, DC, 20036, USA. Electronic address: pchrysostomou@exponent.com.
  • Freeman EL; Exponent Inc., Center for Chemical Regulation and Food Safety, 1150 Connecticut Ave, NW, Suite 1100, Washington, DC, 20036, USA.
  • Murphy MM; Exponent Inc., Center for Chemical Regulation and Food Safety, 1150 Connecticut Ave, NW, Suite 1100, Washington, DC, 20036, USA.
  • Pereira R; Chrysea Labs Lda, Parque Tecnológico de Cantanhede Nucleo 4 Lote 2, 3060-197, Cantanhede, Portugal.
  • Esdaile DJ; Charles River Laboratories Hungary, Kft. H-8200 Veszprém, Szabadságpuszta, Hrsz. 028/1., Hungary.
  • Keohane P; Chrysea Labs Lda, Parque Tecnológico de Cantanhede Nucleo 4 Lote 2, 3060-197, Cantanhede, Portugal.
Food Chem Toxicol ; 184: 114428, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38163454
ABSTRACT
Spermidine is a polyamine consumed in the diet, endogenously biosynthesized in most cells, and produced by the intestinal microbiome. A variety of foods contribute to intake of spermidine along with other polyamines. Spermidine trihydrochloride (spermidine-3HCl) of high purity can be produced using an engineered strain of Saccharomyces cerevisiae. Spermidine has a demonstrated history of safe use in the diet; however, limited information is available in the public literature to assess the potential toxicity of spermidine-3HCl. To support a safety assessment for this spermidine-3HCl as a dietary source of spermidine, authoritative guideline and good laboratory practice (GLP) compliant in vitro genotoxicity assays (bacterial reverse mutation and mammalian micronucleus assays) and a 90-day oral (dietary) toxicity study in rats were conducted with spermidine-3HCl. Spermidine-3HCl was non-genotoxic in the in vitro assays, and no adverse effects were reported in the 90-day oral toxicity study up to the highest dose tested, 12500 ppm, equivalent to 728 mg/kg bw/day for males and 829 mg/kg bw/day for females. The subchronic no observed adverse effect level (NOAEL) is 728 mg/kg bw/day.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Espermidina Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Espermidina Idioma: En Ano de publicação: 2024 Tipo de documento: Article