Lack of induced increase in sister chromatid exchanges in human lymphocytes exposed to in vivo therapeutic ultrasound

1991 ◽  
Vol 17 (1) ◽  
pp. 81-83 ◽  
Author(s):  
Morton W. Miller ◽  
Mitra Azadniv ◽  
C. Coxt ◽  
W.Marcus Miller
1984 ◽  
Vol 138 (1) ◽  
pp. 75-85 ◽  
Author(s):  
Mario Stella ◽  
Luisa Trevisan ◽  
Anna Montaldi ◽  
Graziella Zaccaria ◽  
Giovanni Rossi ◽  
...  

1982 ◽  
Vol 1 (4) ◽  
pp. 387-392 ◽  
Author(s):  
G. Kirchner ◽  
U. Bayer

1 Most hair dyes contain the structural isomers ortho-, meta- and para-aminophenol which were investigated concerning their ability to induce sister chromatid exchanges (SCE) in cultured human lymphocytes in vitro and in Chinese hamster bone marrow cells in vivo. 2 In vitro only ortho-aminophenol significantly induced SCE in a dose-dependent manner. 3 In vivo none of the structural isomers increased significantly the SCE frequency. 4 It is concluded that ortho-aminophenol is a weak directly acting compound which is detoxified during its metabolism.


2019 ◽  
Vol 12 (2) ◽  
pp. 160-165 ◽  
Author(s):  
Abeer M. Rababa'h ◽  
Omar F. Khabour ◽  
Karem H. Alzoubi ◽  
Dua'a Al-momani ◽  
Mera Ababneh

Background and Objective: Levosimendan is a positive inotropic and a vasodilator agent with pleotropic characteristics that include antioxidation, anti-inflammation and smooth muscle vasodilation. Methods: In this study, the effects of levosimendan (0, 0.1, 1, 10, and 20 µg/ml) on oxidative DNA damage and sister-chromatid exchanges (SCEs) were evaluated in human cultured lymphocytes. Results: The results showed that levosimendan increased the frequency of SCEs in all examined concentrations (P<0.01) except for 0.1 µg/ml. On the other hand, levosimendan did not induce oxidative DNA damage as measured by the 8-OHdG biomarker (P > 0.05). In addition, neither mitotic arrest nor proliferation index was affected by levosimendan at all examined doses (P > 0.05). Conclusion: In conclusion, levosimendan might be associated with increases in sister-chromatid exchanges in cultured human lymphocytes. In vivo studies are required to confirm the present findings.


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