Literature DB >> 23468207

The flavonoid chrysin attenuates colorectal pathological remodeling reducing the number and severity of pre-neoplastic lesions in rats exposed to the carcinogen 1,2-dimethylhydrazine.

Priscila L Sequetto1, Tânia T Oliveira, Italo A C Soares, Izabel R S C Maldonado, Vanessa J Mello, Virginia R Pizziolo, Márcia R Almeida, Rômulo D Novaes.   

Abstract

Phenolic compounds are naturally occurring, bioactive substances with marked antioxidant and anti-inflammatory potential. The flavonoid chrysin, found in high levels in honey bee propolis, inhibits the activity of enzymes involved in carcinogenesis. We have investigated the effect of chrysin on pre-neoplastic colorectal lesions (ACF, aberrant crypt foci) in a rat model of chemical carcinogenesis induced by 1,2-dimethylhydrazine (DMH). Female Wistar rats weighing 137.2 ± 24.3 g received weekly one subcutaneous injection of DMH (20 mg/kg) for 10 weeks. The animals were divided into five groups each with seven animals: Group 1, 0.9% saline; Group 2, DMH+0.9% saline; Group 3, DMH+chrysin (10 mg/kg); Group 4, DMH+chrysin (100 mg/kg); Group 5, DMH+chrysin (200 mg/kg). Groups 2 and 3 showed a significant increase in ACF number, nucleolus organizer regions per enterocyte nucleus and nitrite/nitrate serum levels compared with Group 1. Groups 4 and 5 presented a significant reduction in all these parameters compared with Group 2. The levels of antioxidant minerals (copper, magnesium, selenium, zinc) and the number of enteroendocrine and mucin-producing cells were significantly reduced in Groups 2 and 3 but were similar in Groups 4 and 5 compared with Group 1. Chrysin, at 100 mg/kg and 200 mg/kg, was effective in attenuating pathological colorectal remodeling, reducing the number of pre-neoplastic lesions in rats exposed to DMH. Some of these effects might be attributable to the recovery of antioxidant mineral levels, a reduction in systemic nitrosative stress and an inhibition of the cellular proliferation induced by this flavonoid.

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Year:  2013        PMID: 23468207     DOI: 10.1007/s00441-013-1562-5

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  7 in total

1.  Chrysin and its emerging antineoplastic effects.

Authors:  E R Kasala; L N Bodduluru; C C Barua
Journal:  Cancer Gene Ther       Date:  2016-01       Impact factor: 5.987

2.  Protective effects of the flavonoid chrysin against methylmercury-induced genotoxicity and alterations of antioxidant status, in vivo.

Authors:  Eduardo Scandinari Manzolli; Juliana Mara Serpeloni; Denise Grotto; Jairo Kennup Bastos; Lusânia Maria Greggi Antunes; Fernando Barbosa Junior; Gustavo Rafael Mazzaron Barcelos
Journal:  Oxid Med Cell Longev       Date:  2015-02-24       Impact factor: 6.543

3.  Differential Susceptibility of Germ and Leydig Cells to Cadmium-Mediated Toxicity: Impact on Testis Structure, Adiponectin Levels, and Steroidogenesis.

Authors:  Marli C Cupertino; Rômulo D Novaes; Eliziária C Santos; Ana C Neves; Edson Silva; Juraci A Oliveira; Sérgio L P Matta
Journal:  Oxid Med Cell Longev       Date:  2017-12-20       Impact factor: 6.543

Review 4.  Protective Effects of Chrysin Against Drugs and Toxic Agents.

Authors:  Saeed Samarghandian; Tahereh Farkhondeh; Mohsen Azimi-Nezhad
Journal:  Dose Response       Date:  2017-06-23       Impact factor: 2.658

Review 5.  Emerging cellular and molecular mechanisms underlying anticancer indications of chrysin.

Authors:  Marjan Talebi; Mohsen Talebi; Tahereh Farkhondeh; Jesus Simal-Gandara; Dalia M Kopustinskiene; Jurga Bernatoniene; Saeed Samarghandian
Journal:  Cancer Cell Int       Date:  2021-04-15       Impact factor: 5.722

Review 6.  An Association Map on the Effect of Flavonoids on the Signaling Pathways in Colorectal Cancer.

Authors:  Sanaz Koosha; Mohammed A Alshawsh; Chung Yeng Looi; Atefehalsadat Seyedan; Zahurin Mohamed
Journal:  Int J Med Sci       Date:  2016-04-29       Impact factor: 3.738

7.  Hydroethanolic Extract of Strychnos pseudoquina Accelerates Skin Wound Healing by Modulating the Oxidative Status and Microstructural Reorganization of Scar Tissue in Experimental Type I Diabetes.

Authors:  Mariáurea M Sarandy; Rômulo D Novaes; Antônio A Xavier; Camilo E Vital; João P V Leite; Fabiana C S A Melo; Reggiani V Gonçalves
Journal:  Biomed Res Int       Date:  2017-09-13       Impact factor: 3.411

  7 in total

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