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Iranian Journal of Toxicology، جلد ۱۸، شماره ۲، صفحات ۶۸-۷۷

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عنوان انگلیسی Extract of Actaea racemosa Protects Mice Ovarian Follicles Against Doxorubicin-induced Toxicity
چکیده انگلیسی مقاله Background: Given the cytotoxicity of chemotherapy drugs used in cancer treatment, there is a need to develop alternative agents to protect female fertility. This study investigated the effect of Actaea racemosa (A. racemosa) extract on mice ovarian cells and the damage caused by doxorubicin (DOX) to the mice ovaries.
Methods: We evaluated the effects of A. racemosa extract on mice ovaries (n=42) after DOX treatment. The mice were pre-treated with saline solution (controls) or with 0.5 or 5 mg/kg A. Racemosa extract. Afterward, during a period of 10 days, they were treated daily with one of the six protocols: (i) saline solution (control), (ii) 10 mg/kg DOX, (iii) 0.5 mg/kg A. racemosa extract, (iv) both DOX and 5 mg/kg A. racemosa extract, (v) A. racemosa extract (5 mg/kg), and (vi) both DOX and 0.5 mg/kg A. racemosa extract. At the end of these treatments, the ovaries were fixed for histopathological examinations. Ovarian follicular morphology, stromal cell density, collagen fibers, and TNF-α expression were evaluated. Some ovaries were fixed for transmission electron microscopy or stored at -80oC to study the mRNA expression for Caspase-3 and TNF-α.
Results: The Mice treated with A. racemosa extract had reduced follicular degeneration and cell death after exposure to DOX. Ovaries of mice treated with 0.5 mg/kg A. racemosa extract had granulosa cells and oocytes with preserved ultrastructure, decreased immunostaining for TNF-α, and reduced Caspase-3 mRNA.
Conclusion: The A. racemosa extract supported follicular survival and protected the ovarian follicles and stromal cells against DOX-induced cytotoxicity.
کلیدواژه‌های انگلیسی مقاله Cancer, Cytotoxicity, Folliculogenesis, Gene expression, Ovaries

نویسندگان مقاله | Miguel Fernandes de Lima Neto
Laboratory of Biotechnology and Physiology of Reproduction–LABIREP, Federal University of Ceara, Sobral, CE, Brazil


| Ernando Igo Teixeira de Assis
Laboratory of Biotechnology and Physiology of Reproduction–LABIREP, Federal University of Ceara, Sobral, CE, Brazil


| Antônia Venância Nunes Azevedo
Laboratory of Biotechnology and Physiology of Reproduction–LABIREP, Federal University of Ceara, Sobral, CE, Brazil


| Laís Raiane Feitosa Melo Paulino
Laboratory of Biotechnology and Physiology of Reproduction–LABIREP, Federal University of Ceara, Sobral, CE, Brazil


| Mariana Aragão Matos Donato
Laboratory of Ultrastructure, CNPqAM/FIOCRUZ, Federal University of Pernambuco Recife, PE, Brazil


| Christina Alves Peixoto
Laboratory of Ultrastructure, CNPqAM/FIOCRUZ, Federal University of Pernambuco Recife, PE, Brazil


| Alane Pains Oliveira do Monte
Nucleus of Biotechnology Applied to Ovarian Follicle Development, Federal University of São Francisco Valley, Petrolina, PE, Brazil


| Maria Helena Tavares de Matos
Nucleus of Biotechnology Applied to Ovarian Follicle Development, Federal University of São Francisco Valley, Petrolina, PE, Brazil


| Alana Nogueira Godinho
Nucleus of Research in Animal Experimentation–NUPEX, Federal University of Ceara, Sobral, CE, Brazil


| Jordânia Marques de Oliveira Freire
Nucleus of Research in Animal Experimentation–NUPEX, Federal University of Ceara, Sobral, CE, Brazil


| Ricássio de Sousa Barberino
Nucleus of Biotechnology Applied to Ovarian Follicle Development, Federal University of São Francisco Valley, Petrolina, PE, Brazil


| Anderson Weiny Barbalho Silva
Laboratory of Biotechnology and Physiology of Reproduction–LABIREP, Federal University of Ceara, Sobral, CE, Brazil


| José Roberto Viana Silva
Laboratory of Biotechnology and Physiology of Reproduction–LABIREP, Federal University of Ceara, Sobral, CE, Brazil



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