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Chemoprevention by Probiotics During 1,2-Dimethylhydrazine-Induced Colon Carcinogenesis in Rats
Background Probiotics are believed to have properties that lower the risk of colon cancer. However, the mechanisms by which they exert their beneficial effects are relatively unknown. Aim To assess the impact of probiotics in preventing induction of colon carcinogenesis in rats. Methods The rats wer...
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Published in: | Digestive diseases and sciences 2018-04, Vol.63 (4), p.900-909 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background
Probiotics are believed to have properties that lower the risk of colon cancer. However, the mechanisms by which they exert their beneficial effects are relatively unknown.
Aim
To assess the impact of probiotics in preventing induction of colon carcinogenesis in rats.
Methods
The rats were divided into six groups viz., normal control,
Lactobacillus plantarum
(AdF10)-treated,
Lactobacillus rhamnosus
GG (LGG)-treated, 1,2-dimethylhydrazine (DMH)-treated,
L
.
plantarum
(AdF10) + DMH-treated and
L
.
rhamnosus
GG (LGG) + DMH-treated. Both the probiotics were supplemented daily at a dose of 2 × 10
10
cells per day. DMH at a dose of 30 mg/kg body weight was administered subcutaneously twice a week for the first 4 weeks and then once every week for a duration of 16 weeks. Glutathione (GSH), superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR), glutathione peroxidase (GPx), glutathione-S-transferase (GST) and catalase as protein expression of genes involved in apoptosis were assessed during DMH-induced colon carcinogenesis in rats.
Results
DMH treatment decreased the activity of GSH, GPx, GST, SOD and catalase. However, AdF10 and LGG supplementation to DMH-treated rats significantly increased the activity of these enzymes. Further, DMH treatment revealed alterations in the protein expressions of various genes involved in the p53-mediated apoptotic pathway such as p53, p21, Bcl-2, Bax, caspase-9 and caspase-3, which, however, were shifted towards normal control levels upon simultaneous supplementation with probiotics.
Conclusion
The present study suggests that probiotics can provide protection against oxidative stress and apoptotic-related protein disregulation during experimentally induced colon carcinogenesis. |
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ISSN: | 0163-2116 1573-2568 |
DOI: | 10.1007/s10620-018-4949-z |