Clarithromycin Genotoxicity in Mice
Aziza A. E. Ibrahim, Kawser M. El‐Sherbeny
Abstract
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Aziza A. E. Ibrahim, Kawser M. El‐Sherbeny
Abstract
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The effect of clarithromycin on the induction of chromosome aberrations in mice bone-marrow, splenocyte cells and spermatocyte cells was investigated. Male Swiss mice were orally treated by gavage once with doses 50, 100, 200 and 300 mg kg−1 b.wt. A repeated daily dose of 50 mg kg−1 b.wt. was given for successive days. Clarithromycin induced chromosome aberrations in both bone-marrow and splenocyte cells. The percentage of chromosome aberrations was found to be statistically significant after single and repeated treatments.The percentage of chromosome aberrations in diakinesis–metaphase I spermatocytes increased in a dose dependent manner and was found to be statistically significant after 2 higher and repeated doses.The high doses of the antibiotic caused a significant increase in the frequency of sister chromatid exchanges in mice bone-marrow. Its highest values were 9.99±0.48/cell after treatment with high dose (300 mg kg−1 b.wt.) compared with 4.24±0.44/cell in the non treated mice.
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The effect of clarithromycin on the induction of chromosome aberrations in mice bone-marrow, splenocyte cells and spermatocyte cells was investigated. Male Swiss mice were orally treated by gavage once with doses 50, 100, 200 and 300 mg kg−1 b.wt. A repeated daily dose of 50 mg kg−1 b.wt. was given for successive days. Clarithromycin induced chromosome aberrations in both bone-marrow and splenocyte cells. The percentage of chromosome aberrations was found to be statistically significant after single and repeated treatments.The percentage of chromosome aberrations in diakinesis–metaphase I spermatocytes increased in a dose dependent manner and was found to be statistically significant after 2 higher and repeated doses.The high doses of the antibiotic caused a significant increase in the frequency of sister chromatid exchanges in mice bone-marrow. Its highest values were 9.99±0.48/cell after treatment with high dose (300 mg kg−1 b.wt.) compared with 4.24±0.44/cell in the non treated mice.
Key concepts: Biology, Bone marrow, Clarithromycin, Andrology, Metaphase, Genotoxicity, Chromosome, Splenocyte