Evidence map›Paper›PMID 36518419›Full record

ArticleToxicology reports2022

Antigenotoxic and antimutagenic effects of lignin derivative BP-C2 against dioxidine and cyclophosphamide in vivo in murine cells.

Aliy K Zhanataev, Sergey E Pigarev, Elena I Fedoros, Andrey V Panchenko, Elena A Anisina, Zlata V Chayka, Andrey D Durnev, Vladimir N Anisimov

Open access · goldAbstract read
In one paragraph

Article in Toxicology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Aliy K ZhanataevFSBI "Zakusov Institute of Pharmacology", 8, Baltijskaya Str., Moscow 125315, Russia.
Sergey E PigarevDepartment of Carcinogenesis and Oncogerontology, FSBI "N.N. Petrov National Medical Research Center of Oncology" of Ministry of Health of the Russia, 68, Leningradskaya Str., Pesochny, Saint Petersburg 197758, Russia.
Elena I FedorosDepartment of Carcinogenesis and Oncogerontology, FSBI "N.N. Petrov National Medical Research Center of Oncology" of Ministry of Health of the Russia, 68, Leningradskaya Str., Pesochny, Saint Petersburg 197758, Russia.
Andrey V PanchenkoDepartment of Carcinogenesis and Oncogerontology, FSBI "N.N. Petrov National Medical Research Center of Oncology" of Ministry of Health of the Russia, 68, Leningradskaya Str., Pesochny, Saint Petersburg 197758, Russia.
Elena A AnisinaFSBI "Zakusov Institute of Pharmacology", 8, Baltijskaya Str., Moscow 125315, Russia.
Zlata V ChaykaFSBI "Zakusov Institute of Pharmacology", 8, Baltijskaya Str., Moscow 125315, Russia.
Andrey D DurnevFSBI "Zakusov Institute of Pharmacology", 8, Baltijskaya Str., Moscow 125315, Russia.
Vladimir N AnisimovDepartment of Carcinogenesis and Oncogerontology, FSBI "N.N. Petrov National Medical Research Center of Oncology" of Ministry of Health of the Russia, 68, Leningradskaya Str., Pesochny, Saint Petersburg 197758, Russia.
Institute of Pharmacology Russian Academy of Medical Sciences · RUMinistry of Health of the Russian Federation · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The study investigated antigenotoxic and antimutagenic activity of novel lignin-derived polyphenolic composition (BP-C2) with ammonium molybdate towards cyclophosphamide and dioxidine in the bone marrow, blood and liver cells of BALB/c mice. BP-C2 was given to mice via gavage at 60, 80 and 120 mg/kg once 1 h before single intraperitoneal injection of a genotoxic agent. 1.5 h and 3 h after dioxidine or cyclophosphamide injection, respectively, cellular suspensions were obtained from mice and assessed with the comet test and cytogenetic analysis of bone marrow cells. It was observed that antigenotoxic activity of BP-C2 against DNA damage induced by dioxidine, a prooxidant genotoxic agent, in the bone marrow, liver and blood cells of mice in vivo was more pronounced at 60 and 80 mg/kg than at 120 mg/kg. When cyclophosphamide was used to induce a DNA damage, the genoprotective effect of BP-C2 was observed in bone marrow, liver and blood cells at 60 mg/kg dose but the effect was not significant at 80 mg/kg. When co-administered with 120 mg/kg BP-C2, cyclophosphamide induced a higher level of DNA damage in liver cells, but its genotoxic effect in bone marrow and blood cells was the same as when it was administered alone. When assessing the effect of BP-C2 on chromosomal aberrations induced by cyclophosphamide and dioxidine in bone marrow cells, it was revealed that all three tested doses of BP-C2 significantly decreased the number of cells with chromosome abnormalities. Thus, BP-C2 has a pronounced antimutagenic and genoprotective effects.

Indexed as

Antimutagenic activityChromosomal aberrationsComet assayGenoprotective activityLigninPolyphenols

Identifiers

PMID36518419
PMCPMC9743438
OpenAlexW4220816156

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.