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新型可逆性单胺氧化酶B抑制剂KDS2010在食蟹猴中的两周剂量范围查找及四周重复剂量口服毒性研究。

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.

作者信息

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

机构信息

Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.

Department of Advanced Toxicology Research, Korea Institute of Toxicology (KIT), 141 Gajeong-Ro, Yuseong-Gu, Daejeon, Republic of Korea.

出版信息

Toxicol Res. 2023 Jun 24;39(4):693-709. doi: 10.1007/s43188-023-00182-4. eCollection 2023 Oct.

Abstract

UNLABELLED

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.

摘要

未标记

一种新型可逆单胺氧化酶B抑制剂KDS2010已被开发作为神经退行性疾病的治疗候选药物。本研究在人体临床试验前调查了其在非人类灵长类动物中的潜在毒性。将KDS2010每日剂量(25、50或100mg/kg)口服给予食蟹猴(每组1只动物/性别,4只雄性和4只雌性),持续2周以确定剂量范围。在100mg/kg/天组中,1只雄性濒死,1只雌性死亡。在50mg/kg/天组中也发现1只雄性死亡。由于在它们的肾脏中观察到远端小管/集合管扩张以及乳头管上皮肥大,因此认为该死亡对两性均为不良反应。根据剂量范围确定结果,口服给予KDS2010(10、20或40mg/kg/天)4周,并给予动物2周恢复时间。在每日临床观察以及宏观和微观检查(包括体重、食物消耗、血液学、临床化学和器官重量)期间未观察到显著变化。并且,在2周的研究中肾脏被视为KDS2010的主要靶器官,但在4周的研究中未观察到不良反应。因此,40mg/kg/天被认为是食蟹猴两性的未观察到不良反应水平。

补充信息

在线版本包含可在10.1007/s43188-023-00182-4获取的补充材料。

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