新型可逆单胺氧化酶B抑制剂KDS2010在食蟹猴体内的两周剂量范围发现和四周重复剂量口服毒性研究。

IF 1.6 4区 医学 Q4 TOXICOLOGY
Toxicological Research Pub Date : 2023-06-24 eCollection Date: 2023-10-01 DOI:10.1007/s43188-023-00182-4
Kyung-Tai Kim, Doo-Wan Cho, Jae-Woo Cho, Wan-Jung Im, Da-Hee Kim, Jong-Hyun Park, Ki Duk Park, Young-Su Yang, Su-Cheol Han
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引用次数: 0

摘要

一种新的可逆单胺氧化酶B抑制剂KDS2010已被开发为神经退行性疾病的候选治疗药物。这项研究在人类临床试验之前调查了它在非人类灵长类动物中的潜在毒性。食蟹猴(1只动物/性别/组,4只雄性和4只雌性)每天口服KDS2010剂量(25、50或100 mg/kg)2周,以确定剂量范围。100mg/kg/天组中发现一只雄性奄奄一息,一只雌性死亡。50mg/kg/天组中也发现一只雄性死亡。死亡被认为是对两性的不利影响,因为在他们的肾脏中观察到远端小管/集合管扩张和乳头管上皮肥大。基于剂量范围发现结果,口服KDS2010(10、20或40mg/kg/天)4周,给动物2周以恢复。在日常临床观察和宏观和微观检查中,包括体重、食物消耗、血液学、临床化学和器官重量,均未观察到显著变化。在为期2周的研究中,肾脏被视为KDS2010的主要靶器官,但在为期4周的研究中将未观察到不良反应。因此,在食蟹猴的两性中,40 mg/kg/天被认为是未观察到的不良反应水平。补充信息:在线版本包含补充材料,请访问10.1007/s43188-023-00182-4。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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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来源期刊
CiteScore
4.20
自引率
4.30%
发文量
39
期刊介绍: Toxicological Research is the official journal of the Korean Society of Toxicology. The journal covers all areas of Toxicological Research of chemicals, drugs and environmental agents affecting human and animals, which in turn impact public health. The journal’s mission is to disseminate scientific and technical information on diverse areas of toxicological research. Contributions by toxicologists, molecular biologists, geneticists, biochemists, pharmacologists, clinical researchers and epidemiologists with a global view on public health through toxicological research are welcome. Emphasis will be given to articles providing an understanding of the toxicological mechanisms affecting animal, human and public health. In the case of research articles using natural extracts, detailed information with respect to the origin, extraction method, chemical profiles, and characterization of standard compounds to ensure the reproducible pharmacological activity should be provided.
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