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Evaluation of general toxicity and genotoxicity of the silkworm extract powder.
Heo, Hyun-Suk; Choi, Jae-Hun; Oh, Jung-Ja; Lee, Woo-Joo; Kim, Seong-Sook; Lee, Do-Hoon; Lee, Hyun-Kul; Song, Si-Whan; Kim, Kap-Ho; Choi, Yang-Kyu; Ryu, Kang-Sun; Kang, Boo-Hyon.
Afiliação
  • Heo HS; Nonclinical Research Center, Chemon Inc., Yongin, Korea ; College of Veterinary Medicine, Konkuk University, Seoul, Korea.
  • Choi JH; Nonclinical Research Center, Chemon Inc., Yongin, Korea.
  • Oh JJ; Nonclinical Research Center, Chemon Inc., Yongin, Korea.
  • Lee WJ; Nonclinical Research Center, Chemon Inc., Yongin, Korea.
  • Kim SS; Nonclinical Research Center, Chemon Inc., Yongin, Korea.
  • Lee DH; Nonclinical Research Center, Chemon Inc., Yongin, Korea.
  • Lee HK; Nonclinical Research Center, Chemon Inc., Yongin, Korea.
  • Song SW; Nonclinical Research Center, Chemon Inc., Yongin, Korea.
  • Kim KH; Nonclinical Research Center, Chemon Inc., Yongin, Korea.
  • Choi YK; College of Veterinary Medicine, Konkuk University, Seoul, Korea.
  • Ryu KS; Department of Agricultural Biology, National Academy of Agricultural Science, Rural Development Administration, Suwon, Korea.
  • Kang BH; Nonclinical Research Center, Chemon Inc., Yongin, Korea.
Toxicol Res ; 29(4): 263-78, 2013 Dec 31.
Article em En | MEDLINE | ID: mdl-24578797
ABSTRACT
The silkworm extract powder contain 1-deoxynojirimycin (DNJ), a potent α-glycosidase inhibitor, has therapeutic potency against diabetes mellitus. Therefore, natural products containing DNJ from mulberry leaves and silkworm are consumed as health functional food. The present study was performed to evaluate the safety of the silkworm extract powder, a health food which containing the DNJ. The repeated toxicity studies and gentic toxicity studies of the silkworm extract powder were performed to obtain the data for new functional food approval in MFDS. The safety was evaluated by a single-dose oral toxicity study and a 90 day repeated-dose oral toxicity study in Sprague-Dawley rats. The silkworm extract powder was also evaluated for its mutagenic potential in a battery of genetic toxicity test in vitro bacterial reverse mutation assay, in vitro chromosomal aberration test, and in vivo mouse bone marrow micronucleus assay. The results of the genetic toxicology assays were negative in all of the assays. The approximate lethal dose in single oral dose toxicity study was considered to be higher than 5000 mg/kg in rats. In the 90 day study, the dose levels were wet at 0, 500, 1000, 2000 mg/kg/day, and 10 animals/sex/dose were treated with oral gavage. The parameters that were monitored were clinical signs, body weights, food and water consumptions, ophthalmic examination, urinalysis, hematology, serum biochemistry, necropsy findings, organ weights, and histopathological examination. No adverse effects were observed after the 90 day administration of the silkworm extract powder. The No-Observed-Adverse-Effect-Level (NOAEL) of silkworm extract powder in the 90 day study was 2000 mg/kg/day in both sexes, and no target organ was identified.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Toxicol Res Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Toxicol Res Ano de publicação: 2013 Tipo de documento: Article
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