Evidence map›Paper›PMID 33731220›Full record

ArticleBMC pharmacology & toxicology2021

Preliminary study of the toxicity and radioprotective effects of zymosan in vitro and in vivo.

Yue-Zhi Zhang, Shu-Jing Ge, Qing-Zhen Leng, Jian-Jun Ma, Han-Chen Liu

Open access · goldAbstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2021. 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 53% 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. Review
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

5 authors at 3 institutions in 1 country.

Yue-Zhi Zhang *Laboratory of Biochemistry and Molecular Biology, Binzhou Medical University, Yantai, 264000, China.
Shu-Jing Ge *Nursing Department, 970 Hospital of Chinese People's Liberation Army, Yantai, 264002, China.
Qing-Zhen LengCancer Non-Invasive Diagnosis and Treatment Center, 970 Hospital of Chinese People's Liberation Army, No. 7, ZhiChu South Road, Yantai, 264002, China.
Jian-Jun MaCancer Non-Invasive Diagnosis and Treatment Center, 970 Hospital of Chinese People's Liberation Army, No. 7, ZhiChu South Road, Yantai, 264002, China.
Han-Chen LiuCancer Non-Invasive Diagnosis and Treatment Center, 970 Hospital of Chinese People's Liberation Army, No. 7, ZhiChu South Road, Yantai, 264002, China. fnd789@163.com.ORCID 0000-0002-3647-2072
Chinese People 's Liberation Army No. 85 Hospital · CNBinzhou Medical University · CNChinese People's Liberation Army · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to confirm the cytotoxicity of zymosan in vitro and in vivo and determine the appropriate treatment time and the dose of zymosan.

methodsAHH-1 cells and HIECs were administered by 0, 20, 40, 80 or 160 μg/mL zymosan. The CCK-8 assay and flow cytometry were used to evaluate the cell viability and apoptosis 24 h, 48 h, and 72 h after administration. Furthermore, 12 h before irradiation, the cells were treated with 0, 5, 10, or 20 μg/mL zymosan and then irradiated with 4 Gy X-rays. Cell viability and apoptosis were measured by the CCK-8 assay and flow cytometry at 24 h. In addition, the protective effect of zymosan against radiation in vitro was compared to that of 20 μg/mL LPS. In vivo, weight, the spleen index, and the thymus index were measured to evaluate the toxicity of 0, 5, 10, 20, and 10 mg/kg zymosan. In addition, rats were treated with 0, 2, 4, 8, or 10 mg/kg zymosan and then irradiated with 7 Gy X-rays. The survival rate, organ index were evaluated. The protective effect of zymosan against radiation in vivo was compared to that of 10 mg/kg LPS a positive control.

resultsThe viability and apoptosis of cells treated with different doses and treatment times of zymosan were not different from those of control cells (p < 0.05). Furthermore, cell viability and apoptosis were clearly improved after zymosan preadministration (p < 0.05). The radioprotective effect of zymosan was dose-dependent. In addition, the viability of cells pretreated with zymosan was higher than that of cells pretreated with LPS, and the apoptosis rate of zymosan-treated cells was lower than that of cells pretreated with LPS (p < 0.05). In vivo, weight, the spleen index and the thymus index were significantly decreased by zymosan at a concentration of 20 mg/kg (p < 0.05). Further experiments showed that the concentration at which zymosan exerted radioprotective effects was 10 mg/kg. The survival curves in the irradiated rats were barely separated between the LPS treatment and zymosan treatment.

conclusionZymosan administration before radiation exposure significantly increased cell viability and the survival rates of rats.

Indexed as

AnimalsApoptosisCell LineCell SurvivalHumansLipopolysaccharidesMaleRadiation-Protective AgentsRatsRats, Sprague-DawleyX-RaysZymosanLipopolysaccharidesRadiation-Protective AgentsZymosanApoptosisCytotoxicityRadioprotectionSurvival rateZymosan

Identifiers

PMID33731220
PMCPMC7968253
OpenAlexW3120736064

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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.