Oral Administration of Vitamin C, Cimetidine and Famotidine on Micronuclei Induced by Low Dose Radiation in Mouse Bone Marrow Cells

Background: In many studies, chemicals and natural materials were tested to reduce the harmful effects of radiation. It is known that Famotidine and vitamin C reduce DNA damage. Objective: The aim of this study was to evaluate the radioprotective effect of vitamin C, Cimetidine and Famotidine on gam...

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Main Authors: Naeeji A., Mozdarani H., Shabestani Monfared A., Faeghi F., Ahmadi A. A., Gholami M., Behzadi R., Momtaz M. R.
Format: Article
Language:English
Published: Shiraz University of Medical Sciences 2017-06-01
Series:Journal of Biomedical Physics and Engineering
Subjects:
Online Access:http://www.jbpe.org/Journal_OJS/JBPE/index.php/jbpe/article/view/380/291
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spelling doaj-7963d3eabb0e4d4da65d9b74cdd8036d2020-11-24T21:02:17ZengShiraz University of Medical SciencesJournal of Biomedical Physics and Engineering2251-72002251-72002017-06-0172117126Oral Administration of Vitamin C, Cimetidine and Famotidine on Micronuclei Induced by Low Dose Radiation in Mouse Bone Marrow CellsNaeeji A.0 Mozdarani H.1 Shabestani Monfared A.2Faeghi F.3 Ahmadi A. A.4 Gholami M.5Behzadi R.6Momtaz M. R.7Radiology Technology Department, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran Cellular & Molecular Biology Research Center, Medical Physics Department, Babol University of Medical Sciences, Babol, Iran Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran North Research Center, Pasteur Institute of Iran, Amol, IranObesity and Eating Habits Research Center, Endocrinology and Metabolism Molecular -Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran | Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, IranNorth Research Center, Pasteur Institute of Iran, Amol, Iran North Research Center, Pasteur Institute of Iran, Amol, Iran Background: In many studies, chemicals and natural materials were tested to reduce the harmful effects of radiation. It is known that Famotidine and vitamin C reduce DNA damage. Objective: The aim of this study was to evaluate the radioprotective effect of vitamin C, Cimetidine and Famotidine on gamma-radiation-induced damage on mouse bone marrow. Methods: Six-to-seven week male NMRI mice (28 g ±3) were randomly divided into fourteen groups: control, 2Gy irradiation, six group drugs without irradition (Famotidine, Cimetidine, vitaminC, Fam-Cim, Fam-Vit, Cim-Vit), six groups received drugs and 2Gy radiation with a 60Co |γ|-ray source at room temperature 22 ± 2 °C. The mice were killed 48 hours after irradiation by cervical dislocation. Slides were prepared from bone marrow cells and stained in May-Granwald and Giemsa. Finally, the cells were counted with microscope, frequencies of polychromatic erythrocyte (PCE), normochoromatic erythrocyte (NCE) and their micronuclated cell were recorded. PCE / PCE + NCE were calculated. Results: There were significant differences of MNPCE/1000PCE, MNNCE/1000NCE and PCE/PCE+NCE among different groups with similar radiation doses (p≤0.01). Moreover, there were significant differences of MNPCE/1000PCE and PCE/PCE+NCE among different doses of radiation (p≤0.01). While considering MNNCE/1000NCE, there were no significant differences among silimar groups with radiation dose (p˃0.05). Conclusion: Oral administration of Famotidine, vitamin C and Cimetidine demonstrate reliable and similar radioprotective effects. Additionally, the protective effect of single use of these drugs was similar to the combination form. Thus, the oral use of combination, 48 hours after irradiation cannot induce more radioprotective effect. http://www.jbpe.org/Journal_OJS/JBPE/index.php/jbpe/article/view/380/291MicronucleiRadiationRadioprotectionCimetidineVitamin CFamotidine
collection DOAJ
language English
format Article
sources DOAJ
author Naeeji A.
Mozdarani H.
Shabestani Monfared A.
Faeghi F.
Ahmadi A. A.
Gholami M.
Behzadi R.
Momtaz M. R.
spellingShingle Naeeji A.
Mozdarani H.
Shabestani Monfared A.
Faeghi F.
Ahmadi A. A.
Gholami M.
Behzadi R.
Momtaz M. R.
Oral Administration of Vitamin C, Cimetidine and Famotidine on Micronuclei Induced by Low Dose Radiation in Mouse Bone Marrow Cells
Journal of Biomedical Physics and Engineering
Micronuclei
Radiation
Radioprotection
Cimetidine
Vitamin C
Famotidine
author_facet Naeeji A.
Mozdarani H.
Shabestani Monfared A.
Faeghi F.
Ahmadi A. A.
Gholami M.
Behzadi R.
Momtaz M. R.
author_sort Naeeji A.
title Oral Administration of Vitamin C, Cimetidine and Famotidine on Micronuclei Induced by Low Dose Radiation in Mouse Bone Marrow Cells
title_short Oral Administration of Vitamin C, Cimetidine and Famotidine on Micronuclei Induced by Low Dose Radiation in Mouse Bone Marrow Cells
title_full Oral Administration of Vitamin C, Cimetidine and Famotidine on Micronuclei Induced by Low Dose Radiation in Mouse Bone Marrow Cells
title_fullStr Oral Administration of Vitamin C, Cimetidine and Famotidine on Micronuclei Induced by Low Dose Radiation in Mouse Bone Marrow Cells
title_full_unstemmed Oral Administration of Vitamin C, Cimetidine and Famotidine on Micronuclei Induced by Low Dose Radiation in Mouse Bone Marrow Cells
title_sort oral administration of vitamin c, cimetidine and famotidine on micronuclei induced by low dose radiation in mouse bone marrow cells
publisher Shiraz University of Medical Sciences
series Journal of Biomedical Physics and Engineering
issn 2251-7200
2251-7200
publishDate 2017-06-01
description Background: In many studies, chemicals and natural materials were tested to reduce the harmful effects of radiation. It is known that Famotidine and vitamin C reduce DNA damage. Objective: The aim of this study was to evaluate the radioprotective effect of vitamin C, Cimetidine and Famotidine on gamma-radiation-induced damage on mouse bone marrow. Methods: Six-to-seven week male NMRI mice (28 g ±3) were randomly divided into fourteen groups: control, 2Gy irradiation, six group drugs without irradition (Famotidine, Cimetidine, vitaminC, Fam-Cim, Fam-Vit, Cim-Vit), six groups received drugs and 2Gy radiation with a 60Co |γ|-ray source at room temperature 22 ± 2 °C. The mice were killed 48 hours after irradiation by cervical dislocation. Slides were prepared from bone marrow cells and stained in May-Granwald and Giemsa. Finally, the cells were counted with microscope, frequencies of polychromatic erythrocyte (PCE), normochoromatic erythrocyte (NCE) and their micronuclated cell were recorded. PCE / PCE + NCE were calculated. Results: There were significant differences of MNPCE/1000PCE, MNNCE/1000NCE and PCE/PCE+NCE among different groups with similar radiation doses (p≤0.01). Moreover, there were significant differences of MNPCE/1000PCE and PCE/PCE+NCE among different doses of radiation (p≤0.01). While considering MNNCE/1000NCE, there were no significant differences among silimar groups with radiation dose (p˃0.05). Conclusion: Oral administration of Famotidine, vitamin C and Cimetidine demonstrate reliable and similar radioprotective effects. Additionally, the protective effect of single use of these drugs was similar to the combination form. Thus, the oral use of combination, 48 hours after irradiation cannot induce more radioprotective effect.
topic Micronuclei
Radiation
Radioprotection
Cimetidine
Vitamin C
Famotidine
url http://www.jbpe.org/Journal_OJS/JBPE/index.php/jbpe/article/view/380/291
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