Evidence map›Paper›PMID 37779583›Full record

ArticleToxicological research2023

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.

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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In one paragraph

Article in Toxicological research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Kyung-Tai Kim *Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.
Doo-Wan Cho *Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.
Jae-Woo ChoDepartment of Advanced Toxicology Research, Korea Institute of Toxicology (KIT), 141 Gajeong-Ro, Yuseong-Gu, Daejeon, Republic of Korea.
Wan-Jung ImDepartment of Advanced Toxicology Research, Korea Institute of Toxicology (KIT), 141 Gajeong-Ro, Yuseong-Gu, Daejeon, Republic of Korea.
Da-Hee KimJeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.
Jong-Hyun ParkConvergence Research Center for Diagnosis, Treatment and Care System of Dementia, Korea Institute of Science and Technology (KIST), Seoul, 02792 Republic of Korea.
Ki Duk ParkConvergence Research Center for Diagnosis, Treatment and Care System of Dementia, Korea Institute of Science and Technology (KIST), Seoul, 02792 Republic of Korea.
Young-Su YangJeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.ORCID 0000-0002-6633-8958
Su-Cheol HanJeonbuk Branch Institute, Korea Institute of Toxicology, Jeonbuk, 56212 Republic of Korea.
Jeonbuk State Institute · KRConvergence Research Center for Diagnosis Treatment and Care System of Dementia · KRKorea Institute of Toxicology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Acute oral toxicity testKDS2010Non-human primateNo-observed-adverse-effect levelNovel selective monoamine oxidase B inhibitor

Identifiers

PMID37779583
PMCPMC10541392
OpenAlexW4381890790

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.