Modulatory Effect of Fermented Papaya Extracts on Mammary Gland Hyperplasia Induced by Estrogen and Progestin in Female Rats

Fermented papaya extracts (FPEs) are obtained by fermentation of papaya by Aspergillus oryzae and yeasts. In this study, we investigated the protective effects of FPEs on mammary gland hyperplasia induced by estrogen and progestogen. Rats were randomly divided into 6 groups, including a control grou...

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Veröffentlicht in:Oxidative medicine and cellular longevity 2017-01, Vol.2017 (2017), p.1-11
Hauptverfasser: Song, Yisheng, Xuan, Yaoxian, Zheng, Gaoli, Xin, Yanfei, Li, Lili, Liu, Fang, Chen, Hao, Zhang, Sheng, Chen, Zhiqin, Xie, Feng, Sun, Junying, You, Zhenqiang, Chen, Guocan
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container_issue 2017
container_start_page 1
container_title Oxidative medicine and cellular longevity
container_volume 2017
creator Song, Yisheng
Xuan, Yaoxian
Zheng, Gaoli
Xin, Yanfei
Li, Lili
Liu, Fang
Chen, Hao
Zhang, Sheng
Chen, Zhiqin
Xie, Feng
Sun, Junying
You, Zhenqiang
Chen, Guocan
description Fermented papaya extracts (FPEs) are obtained by fermentation of papaya by Aspergillus oryzae and yeasts. In this study, we investigated the protective effects of FPEs on mammary gland hyperplasia induced by estrogen and progestogen. Rats were randomly divided into 6 groups, including a control group, an FPE-alone group, a model group, and three FPE treatment groups (each receiving 30, 15, or 5 ml/kg FPEs). Severe mammary gland hyperplasia was induced upon estradiol benzoate and progestin administration. FPEs could improve the pathological features of the animal model and reduce estrogen levels in the serum. Analysis of oxidant indices revealed that FPEs could increase superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities, decrease malondialdehyde (MDA) level in the mammary glands and serum of the animal models, and decrease the proportion of cells positive for the oxidative DNA damage marker 8-oxo-dG in the mammary glands. Additionally, estradiol benzoate and progestin altered the levels of serum biochemical compounds such as aspartate transaminase (AST), total bilirubin (TBIL), and alanine transaminase (ALT), as well as hepatic oxidant indices such as SOD, GSH-Px, MDA, and 8-oxo-2′-deoxyguanosine (8-oxo-dG). These indices reverted to normal levels upon oral administration of a high dose of FPEs. Taken together, our results indicate that FPEs can protect the mammary glands and other visceral organs from oxidative damage.
doi_str_mv 10.1155/2017/8235069
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In this study, we investigated the protective effects of FPEs on mammary gland hyperplasia induced by estrogen and progestogen. Rats were randomly divided into 6 groups, including a control group, an FPE-alone group, a model group, and three FPE treatment groups (each receiving 30, 15, or 5 ml/kg FPEs). Severe mammary gland hyperplasia was induced upon estradiol benzoate and progestin administration. FPEs could improve the pathological features of the animal model and reduce estrogen levels in the serum. Analysis of oxidant indices revealed that FPEs could increase superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities, decrease malondialdehyde (MDA) level in the mammary glands and serum of the animal models, and decrease the proportion of cells positive for the oxidative DNA damage marker 8-oxo-dG in the mammary glands. Additionally, estradiol benzoate and progestin altered the levels of serum biochemical compounds such as aspartate transaminase (AST), total bilirubin (TBIL), and alanine transaminase (ALT), as well as hepatic oxidant indices such as SOD, GSH-Px, MDA, and 8-oxo-2′-deoxyguanosine (8-oxo-dG). These indices reverted to normal levels upon oral administration of a high dose of FPEs. 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In this study, we investigated the protective effects of FPEs on mammary gland hyperplasia induced by estrogen and progestogen. Rats were randomly divided into 6 groups, including a control group, an FPE-alone group, a model group, and three FPE treatment groups (each receiving 30, 15, or 5 ml/kg FPEs). Severe mammary gland hyperplasia was induced upon estradiol benzoate and progestin administration. FPEs could improve the pathological features of the animal model and reduce estrogen levels in the serum. Analysis of oxidant indices revealed that FPEs could increase superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities, decrease malondialdehyde (MDA) level in the mammary glands and serum of the animal models, and decrease the proportion of cells positive for the oxidative DNA damage marker 8-oxo-dG in the mammary glands. 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subjects Animals
Antioxidants
Bilirubin
Breast cancer
Cancer therapies
Carica - chemistry
Deoxyribonucleic acid
DNA
Drug dosages
Estradiol
Estrogens - toxicity
Female
Fermentation
Functional foods & nutraceuticals
Hyperplasia
Hyperplasia - chemically induced
Hyperplasia - drug therapy
Laboratory animals
Mammary Glands, Animal - drug effects
Mammary Glands, Animal - pathology
Medical research
Pharmaceuticals
Phenols
Plant Extracts - pharmacology
Progestins - toxicity
Protective Agents - pharmacology
Rats
Rats, Sprague-Dawley
Rodents
Superoxide
Tumorigenesis
Wound healing
title Modulatory Effect of Fermented Papaya Extracts on Mammary Gland Hyperplasia Induced by Estrogen and Progestin in Female Rats
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