• Corpus ID: 34031610

Modification of cyclophosphamide-induced clastogenesis and apoptosis in rats by alpha-lipoic acid.

@article{Selvakumar2006ModificationOC,
  title={Modification of cyclophosphamide-induced clastogenesis and apoptosis in rats by alpha-lipoic acid.},
  author={Elangovan Selvakumar and Chidambaram Prahalathan and P. Varalakshmi and P. Kumarasamy and Revathy Saravanan},
  journal={Mutation research},
  year={2006},
  volume={606 1-2},
  pages={
          85-91
        }
}

• E. Selvakumar, C. Prahalathan, +2 authors R. Saravanan
• Published 2006
• Biology
• Mutation research

The aim of the present study was to investigate the protective efficacy of alpha-lipoic acid (LA) on the cyclophosphamide (CP)-induced chromosomal aberrations (CA) and apoptosis in the bone marrow of rats. Male Wistar rats of 140+/-20 g were categorized into eight groups. Five groups were administered CP (40 mg/kg body weight, intraperitoneally) to induce toxicity; four of these groups received a single intraperitoneal injection of LA at a dose of either 100 or 200 mg/kg body weight, and either 30 or 60 min prior to CP administration. A vehicle-treated control group and LA control groups were also included. Twenty-four hours after CP treatment, the frequency of CA in bone marrow cells were significantly increased in comparison with the controls. The CP-induced CA were associated with significant increase in DNA damage in the bone marrow as evidenced by increased single strand breaks, whereas in rats treated with LA and CP, the frequency of CA and single strand breaks were significantly decreased in comparison to those given CP alone. CP administration distinctly triggered the apoptotic and necrotic cell death, and LA pretreatment affected cell death by decreasing the number of apoptotic and necrotic cells. The protective effect of LA was found to be stronger at a dose of 200 mg/kg body weight than 100 mg/kg body weight dosage, indicating the dose dependent protective effect of LA. However, the protection by LA was not dependent on the time intervals between LA and CP administration. The results of this study illustrate the protective effect of LA on the CA and apoptosis induced by CP in the erythropoietic system of rats.