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Two weeks dose range-finding and four weeks repeated dose oral toxicity study of a novel reversible monoamine oxidase B inhibitor KDS2010 in cynomolgus monkeys.
Kim, Kyung-Tai; Cho, Doo-Wan; Cho, Jae-Woo; Im, Wan-Jung; Kim, Da-Hee; Park, Jong-Hyun; Park, Ki Duk; Yang, Young-Su; Han, Su-Cheol.
Afiliação
  • Kim KT; Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.
  • Cho DW; Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.
  • Cho JW; Department of Advanced Toxicology Research, Korea Institute of Toxicology (KIT), 141 Gajeong-Ro, Yuseong-Gu, Daejeon, Republic of Korea.
  • Im WJ; Department of Advanced Toxicology Research, Korea Institute of Toxicology (KIT), 141 Gajeong-Ro, Yuseong-Gu, Daejeon, Republic of Korea.
  • Kim DH; Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.
  • Park JH; Convergence Research Center for Diagnosis, Treatment and Care System of Dementia, Korea Institute of Science and Technology (KIST), Seoul, 02792 Republic of Korea.
  • Park KD; Convergence Research Center for Diagnosis, Treatment and Care System of Dementia, Korea Institute of Science and Technology (KIST), Seoul, 02792 Republic of Korea.
  • Yang YS; Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.
  • Han SC; Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.
Toxicol Res ; 39(4): 693-709, 2023 Oct.
Article em En | MEDLINE | ID: mdl-37779583
ABSTRACT
A novel reversible monoamine oxidase B inhibitor, KDS2010, has been developed as a therapeutic candidate for neurodegenerative diseases. This study investigated its potential toxicity in non-human primates before human clinical trials. Daily KDS2010 doses (25, 50, or 100 mg/kg) were orally administered to cynomolgus monkeys (1 animal/sex/group, 4 males and 4 females) for 2 weeks to determine the dose range. One male was moribund, and one female was found dead in the 100 mg/kg/day group. One male was also found dead in the 50 mg/kg/day group. The death was considered an adverse effect in both sexes since distal tubules/collecting duct dilation and hypertrophy in the epithelium of the papillary duct were observed in their kidneys. Based on dose range finding results, KDS2010 (10, 20, or 40 mg/kg/day) was administered orally for 4 weeks, and animals were given 2 weeks for recovery. No significant changes were observed during daily clinical observations and macro-and microscopic examinations, including body weight, food consumption, hematology, clinical chemistry, and organ weight. And, the kidney was seen as the primary target organ of KDS2010 in the 2 weeks study, but no adverse effect was observed in the 4 weeks study. Therefore, 40 mg/kg/day is considered the no-observed-adverse-effect level in both sexes of cynomolgus monkeys. Supplementary Information The online version contains supplementary material available at 10.1007/s43188-023-00182-4.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Toxicol Res Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Toxicol Res Ano de publicação: 2023 Tipo de documento: Article