Effect of paternal exposure to gamma rays on juvenile rat forebrain

Abstract We studied the transgenerational effect of the sublethal dose of gamma radiation on the proliferative activity of cells in the rostral migratory stream (RMS) in the brain of neonatal and young progeny of male rats exposed to the dose of 3 Gy 25 days before conception with intact control fem...

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Published in:Neurotoxicology and teratology Vol. 29; no. 4; pp. 521 - 526
Main Authors: BHLENTOVA, Sofia, RACEKOVA, Eniko, MISUROA, Eva
Format: Journal Article
Language:English
Published: New York, NY Elsevier Inc 01-07-2007
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Abstract Abstract We studied the transgenerational effect of the sublethal dose of gamma radiation on the proliferative activity of cells in the rostral migratory stream (RMS) in the brain of neonatal and young progeny of male rats exposed to the dose of 3 Gy 25 days before conception with intact control females. To label proliferating cells, the progeny received bromodeoxyuridine (BrdU) injection before sacrifice. The number of BrdU-positive cells was counted in three parts of the forebrain RMS, i.e. in the vertical arm, elbow and horizontal arm, at the 3rd, 7th, 14th, 21st and 28th postnatal days (P3–P28). In the RMS of control rats' progeny, the number of BrdU+ cells transiently decreased at the 7th–14th postnatal days. In the progeny of irradiated rats, the dynamics of the changes was similar to that in the corresponding control groups, however, the number of BrdU-positive cells was significantly higher along the whole RMS at all intervals of investigation. These results suggest that paternal exposure to ionizing radiation induced the genome instability, which manifested itself in the progeny by alteration in proliferative activity or slackening of cell migration in the RMS.
AbstractList We studied the transgenerational effect of the sublethal dose of gamma radiation on the proliferative activity of cells in the rostral migratory stream (RMS) in the brain of neonatal and young progeny of male rats exposed to the dose of 3 Gy 25 days before conception with intact control females. To label proliferating cells, the progeny received bromodeoxyuridine (BrdU) injection before sacrifice. The number of BrdU-positive cells was counted in three parts of the forebrain RMS, i.e. in the vertical arm, elbow and horizontal arm, at the 3rd, 7th, 14th, 21st and 28th postnatal days (P3–P28). In the RMS of control rats' progeny, the number of BrdU + cells transiently decreased at the 7th–14th postnatal days. In the progeny of irradiated rats, the dynamics of the changes was similar to that in the corresponding control groups, however, the number of BrdU-positive cells was significantly higher along the whole RMS at all intervals of investigation. These results suggest that paternal exposure to ionizing radiation induced the genome instability, which manifested itself in the progeny by alteration in proliferative activity or slackening of cell migration in the RMS.
We studied the transgenerational effect of the sublethal dose of gamma radiation on the proliferative activity of cells in the rostral migratory stream (RMS) in the brain of neonatal and young progeny of male rats exposed to the dose of 3 Gy 25 days before conception with intact control females. To label proliferating cells, the progeny received bromodeoxyuridine (BrdU) injection before sacrifice. The number of BrdU-positive cells was counted in three parts of the forebrain RMS, i.e. in the vertical arm, elbow and horizontal arm, at the 3rd, 7th, 14th, 21st and 28th postnatal days (P3-P28). In the RMS of control rats' progeny, the number of BrdU super(+) cells transiently decreased at the 7th-14th postnatal days. In the progeny of irradiated rats, the dynamics of the changes was similar to that in the corresponding control groups, however, the number of BrdU-positive cells was significantly higher along the whole RMS at all intervals of investigation. These results suggest that paternal exposure to ionizing radiation induced the genome instability, which manifested itself in the progeny by alteration in proliferative activity or slackening of cell migration in the RMS.
We studied the transgenerational effect of the sublethal dose of gamma radiation on the proliferative activity of cells in the rostral migratory stream (RMS) in the brain of neonatal and young progeny of male rats exposed to the dose of 3 Gy 25 days before conception with intact control females. To label proliferating cells, the progeny received bromodeoxyuridine (BrdU) injection before sacrifice. The number of BrdU-positive cells was counted in three parts of the forebrain RMS, i.e. in the vertical arm, elbow and horizontal arm, at the 3rd, 7th, 14th, 21st and 28th postnatal days (P3-P28). In the RMS of control rats' progeny, the number of BrdU(+) cells transiently decreased at the 7th-14th postnatal days. In the progeny of irradiated rats, the dynamics of the changes was similar to that in the corresponding control groups, however, the number of BrdU-positive cells was significantly higher along the whole RMS at all intervals of investigation. These results suggest that paternal exposure to ionizing radiation induced the genome instability, which manifested itself in the progeny by alteration in proliferative activity or slackening of cell migration in the RMS.
Abstract We studied the transgenerational effect of the sublethal dose of gamma radiation on the proliferative activity of cells in the rostral migratory stream (RMS) in the brain of neonatal and young progeny of male rats exposed to the dose of 3 Gy 25 days before conception with intact control females. To label proliferating cells, the progeny received bromodeoxyuridine (BrdU) injection before sacrifice. The number of BrdU-positive cells was counted in three parts of the forebrain RMS, i.e. in the vertical arm, elbow and horizontal arm, at the 3rd, 7th, 14th, 21st and 28th postnatal days (P3–P28). In the RMS of control rats' progeny, the number of BrdU+ cells transiently decreased at the 7th–14th postnatal days. In the progeny of irradiated rats, the dynamics of the changes was similar to that in the corresponding control groups, however, the number of BrdU-positive cells was significantly higher along the whole RMS at all intervals of investigation. These results suggest that paternal exposure to ionizing radiation induced the genome instability, which manifested itself in the progeny by alteration in proliferative activity or slackening of cell migration in the RMS.
Author Bálentová, Soňa
Račeková, Enikő
Mišúrová, Eva
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  fullname: MISUROA, Eva
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Issue 4
Keywords Neural cell proliferation
Rat progeny
Ionizing radiation
Genomic instability
Cell proliferation
Rat
Genomics
Rodentia
Nervous system
Exposure
Young animal
Progeny
Vertebrata
Gamma irradiation
Mammalia
Instability
Genome
Father
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PublicationTitle Neurotoxicology and teratology
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Snippet Abstract We studied the transgenerational effect of the sublethal dose of gamma radiation on the proliferative activity of cells in the rostral migratory...
We studied the transgenerational effect of the sublethal dose of gamma radiation on the proliferative activity of cells in the rostral migratory stream (RMS)...
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SubjectTerms Age Factors
Animals
Animals, Newborn
Behavior, Animal - radiation effects
Biological and medical sciences
Bromodeoxyuridine - metabolism
Cell Count
Cell Proliferation - radiation effects
Emergency
Female
Gamma Rays - adverse effects
Genomic instability
Ionizing radiation
Male
Medical Education
Medical sciences
Neural cell proliferation
Neurons - radiation effects
Paternal Exposure
Pregnancy
Prosencephalon - pathology
Prosencephalon - radiation effects
Radiation Injuries, Experimental - pathology
Rat progeny
Rats
Rats, Wistar
Sex Factors
Toxicology
Whole-Body Irradiation - methods
Title Effect of paternal exposure to gamma rays on juvenile rat forebrain
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https://dx.doi.org/10.1016/j.ntt.2007.03.063
https://www.ncbi.nlm.nih.gov/pubmed/17478076
https://search.proquest.com/docview/19673872
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