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

Authors :
Aliy K. Zhanataev
Sergey E. Pigarev
Elena I. Fedoros
Andrey V. Panchenko
Elena A. Anisina
Zlata V. Chayka
Andrey D. Durnev
Vladimir N. Anisimov
Source :
Toxicology Reports, Vol 9, Iss , Pp 743-749 (2022)
Publication Year :
2022
Publisher :
Elsevier, 2022.

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.

Details

Language :
English
ISSN :
22147500
Volume :
9
Issue :
743-749
Database :
Directory of Open Access Journals
Journal :
Toxicology Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.3c6cf83a06824b30a6c9b6de5b00575f
Document Type :
article
Full Text :
https://doi.org/10.1016/j.toxrep.2022.03.041