Antimutagenic Effects of Selenium-Enriched Polysaccharides from Pyracantha Fortuneana Through Suppression of Cytochrome P450 1A Subfamily in the Mouse Liver

Overview

Journal Molecules

Publisher MDPI

Specialty Biology

Date 2016 Dec 22

PMID 27999293

Citations 9

Authors

Fan Peng

Xin Guo

Zhihong Li

Changzheng Li

Changdong Wang

Weiran Lv

Junjie Wang

Fangxiang Xiao

Mohammad Amjad Kamal

Chengfu Yuan

Affiliations

Soon will be listed here.

Abstract

Both selenium (Se) and polysaccharides from (Maxim.) Li (PFPs) () have been reported to possess antioxidative and immuno-protective activities. Whether or not Se-containing polysaccharides (Se-PFPs) have synergistic effect of Se and polysaccharides on enhancing the antioxidant and immune activities remains to be determined. We previously reported that polysaccharides isolated from Se-enriched (Se-PFPs) possessed hepatoprotective effects. However, it is not clear whether or not they have anti-mutagenic effects. In the present study, we compared and evaluated anti-mutagenic effects of Se-PFPs at three concentrations (1.35, 2.7 and 5.4 g/kg body weight) with those of PFPs, Se alone or Se + PFPs in mice using micronucleus assay in bone marrow and peripheral blood as well as mitomycin C-induced chromosomal aberrations in mouse testicular cells. We also elucidated the underlying mechanism. Our results demonstrated that Se-PFPs inhibited cyclophosphamide (CP)-induced micronucleus formation in both bone marrow and peripheral blood, enhanced the activities of superoxide dismutase (SOD) and glutathione peroxidase (GPx) in mouse liver, and reduced the activity and expression of cytochrome P450 1A (CYP4501A) in mouse liver in a dose-dependent manner. In addition, we found that the anti-mutagenic potential of Se-PFPs was higher than those of PFPs, Se alone or Se + PFPs at the same level. These results suggest that the anti-mutagenic potential of Se-PFPs may be mediated through the inhibition of the activity and expression of CYP4501A. This study indicates that application of Se-PFPs may provide an alternative strategy for cancer therapy by targeting CYP1A family.

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