Evidence map›Paper›PMID 26336585›Full record

ArticleBiomolecules & therapeutics2015

A Dunnione Compound MB12662 Improves Cisplatin-Induced Tissue Injury and Emesis.

Dongsun Park, In Geun Jo, Ja Young Jang, Tae Hwan Kwak, Sang Ku Yoo, Jeong Hee Jeon, Ehn-Kyoung Choi, Seong Soo Joo, Okjin Kim, Yun-Bae Kim

Abstract read
In one paragraph

Article in Biomolecules & therapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

10 authors at 5 institutions in 1 country.

Dongsun ParkCollege of Veterinary Medicine, Chungbuk National University, Cheongju 362-763 ; Department of Physiology, Ajou University School of Medicine, Suwon 443-749, Republic of Korea.
In Geun JoCollege of Pharmacy, Advanced Science, Dankook University, Cheonan 330-714.
Ja Young JangCollege of Veterinary Medicine, Chungbuk National University, Cheongju 362-763.
Tae Hwan KwakKT&G Life Science Corporation R&D Center, Suwon 443-702.
Sang Ku YooErum Biotechnologies Incorporation, Suwon 443-380.
Jeong Hee JeonCollege of Veterinary Medicine, Chungbuk National University, Cheongju 362-763.
Ehn-Kyoung ChoiCollege of Veterinary Medicine, Chungbuk National University, Cheongju 362-763.
Seong Soo JooDepartment of Marine Molecular Biotechnology, College of Life Science, Gangneung-Wonju National University, Gangneung 210-702.
Okjin KimCollege of Natural Resources, Wonkwang University, Iksan 570-749.
Yun-Bae KimCollege of Veterinary Medicine, Chungbuk National University, Cheongju 362-763.
Chungbuk National University · KRDankook University · KRErum Biotechnologies (South Korea) · KRGangneung–Wonju National University · KRWonkwang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study was aimed to investigate the effects of MB12662, a synthetic dunnione compound, on cisplatin-induced vomiting reflexes and intestinal, renal, immune system, and hematopoietic toxicities in ferrets and mice, respectively. Male ICR mice were orally administered MB12662 (5, 10, 25 or 50 mg/kg) for 10 days, during which intraperitoneally challenged with cisplatin (3.5 mg/kg) from day 4 to 7, and sacrificed on day 10 for the pathological examination. Male ferrets were orally administered MB12662 (25, 50 or 100 mg/kg) for 7 days, subcutaneously challenged with cisplatin (5 mg/kg), and monitored for vomiting reflexes and survival of the animals. Four-day injection of cisplatin (3.5 mg/kg) to mice caused body weight loss and degeneration and atrophy of intestinal villi, reducing villi/crypt ratio to a half level of control animals. Cisplatin also induced renal and hepatic toxicities, and depletion of splenocytes and bone marrow progenitor cells. The systemic toxicities including decreased villi/crypt ratio, immune system atrophy, splenocyte depletion, and decreased cellularity in bone marrow were improved by MB12662. Cisplatin (5 mg/kg) induced retching and emetic responses of ferrets, which were remarkably attenuated by MB12662 in a dose-dependent manner. All the ferrets pretreated with MB12662 survived the challenge of cisplatin, in comparison with 40% mortality in vehicle-treated animals, and blood parameters of nephrotoxicity and hepatotoxicity were markedly recovered. It is expected that MB12662 could be a candidate for the body protection against burden, including emesis, of chemotherapeutic agents.

Indexed as

CisplatinDunnioneEmesisIntestinal injuryMB12662Nephrotoxicity

Identifiers

PMID26336585
PMCPMC4556205
OpenAlexW2400647057

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.