In Vivo Genotoxicity Assessment of Sertraline by Using Alkaline Comet Assay and the Cytokinesis‐Block Micronucleus Assay. (25th July 2013)
- Record Type:
- Journal Article
- Title:
- In Vivo Genotoxicity Assessment of Sertraline by Using Alkaline Comet Assay and the Cytokinesis‐Block Micronucleus Assay. (25th July 2013)
- Main Title:
- In Vivo Genotoxicity Assessment of Sertraline by Using Alkaline Comet Assay and the Cytokinesis‐Block Micronucleus Assay
- Authors:
- Battal, Dilek
Aktas, Ayca
Sungur, Mehmet Ali
Kadioglu, Ela
Derici Eker, Ebru
Sahin, Nefise Ozlen
Saygi, Sahan - Abstract:
- <abstract abstract-type="main" id="bcpt12095-abs-0001"> <title>Abstract</title> <p>Sertraline, a leading antidepressant in the selective serotonin reuptake inhibitor (SSRI) group of medicine, is the most frequently prescribed drug. In this study, the alkaline comet assay and the cytokinesis‐block micronucleus (CBMN) assay were used to investigate genotoxicity potential of sertraline in the peripheral blood lymphocytes (PBLs) of acute and chronic sertraline‐treated Wistar albino rats. Male Wistar albino rats (n = 48) were administered low, medium and high doses of sertraline (10, 40, 80 mg/kg) for acute and chronic treatment by employing the gavage method to investigate genotoxicity of the administered drug. The data (tail length, tail intensity and tail moment) were analysed and indicated that there was no statistically significant difference between sertraline‐treated groups and the negative control group with respect to DNA damage (<italic>p </italic>&gt; 0.05). However, it was observed that acute sertraline administration had caused much more DNA damage in comparison with chronic treatment (<italic>p </italic>&lt; 0.05). According to the data obtained from the CBMN test, an increase in the micronucleus (MN) frequency was detected at chronic and high‐dose acute sertraline treatment. Based on the outcome of comet assay, detection of statistically insignificant DNA damage may be due to the fact that sertraline did not cause damage on DNA. Also, increase in frequency of MN in<abstract abstract-type="main" id="bcpt12095-abs-0001"> <title>Abstract</title> <p>Sertraline, a leading antidepressant in the selective serotonin reuptake inhibitor (SSRI) group of medicine, is the most frequently prescribed drug. In this study, the alkaline comet assay and the cytokinesis‐block micronucleus (CBMN) assay were used to investigate genotoxicity potential of sertraline in the peripheral blood lymphocytes (PBLs) of acute and chronic sertraline‐treated Wistar albino rats. Male Wistar albino rats (n = 48) were administered low, medium and high doses of sertraline (10, 40, 80 mg/kg) for acute and chronic treatment by employing the gavage method to investigate genotoxicity of the administered drug. The data (tail length, tail intensity and tail moment) were analysed and indicated that there was no statistically significant difference between sertraline‐treated groups and the negative control group with respect to DNA damage (<italic>p </italic>&gt; 0.05). However, it was observed that acute sertraline administration had caused much more DNA damage in comparison with chronic treatment (<italic>p </italic>&lt; 0.05). According to the data obtained from the CBMN test, an increase in the micronucleus (MN) frequency was detected at chronic and high‐dose acute sertraline treatment. Based on the outcome of comet assay, detection of statistically insignificant DNA damage may be due to the fact that sertraline did not cause damage on DNA. Also, increase in frequency of MN in chronic sertraline treatment suggests that chronic sertraline administration might influence some mechanisms of cell division. Therefore, dose adjustment in depressed patients seems significant as it may help prevent further prognosis of the diseases.</p> </abstract> … (more)
- Is Part Of:
- Basic & clinical pharmacology & toxicology. Volume 113:Number 5(2013)
- Journal:
- Basic & clinical pharmacology & toxicology
- Issue:
- Volume 113:Number 5(2013)
- Issue Display:
- Volume 113, Issue 5 (2013)
- Year:
- 2013
- Volume:
- 113
- Issue:
- 5
- Issue Sort Value:
- 2013-0113-0005-0000
- Page Start:
- 339
- Page End:
- 346
- Publication Date:
- 2013-07-25
- Subjects:
- Pharmacology -- Periodicals
Toxicology -- Periodicals
Pharmacology -- Periodicals
Toxicology -- Periodicals
Pharmacology, Clinical -- Periodicals
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615.1 - Journal URLs:
- http://firstsearch.oclc.org/journal=1742-7835;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1742-7843 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=pto ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bcpt.12095 ↗
- Languages:
- English
- ISSNs:
- 1742-7835
- Deposit Type:
- Legaldeposit
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- Physical Locations:
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