S.K. Patel College of Pharmaceutical Education and Research, Ganpat University, Mehsana, India.
Drug Chem Toxicol. 2013 Jan;36(1):35-41. doi: 10.3109/01480545.2011.648328. Epub 2012 Jan 21.
The present study investigated the protective effects of Foeniculum vulgare (fennel) essential oil (FEO) against genotoxicity induced by cyclophosphamide (CP). Mice bone marrow chromosomal aberration (CA), micronucleus, and sperm abnormality assays were employed to measure genotoxicity and cytotoxicity, respectively. The activities of superoxide dismutase (SOD), glutathione (GSH), catalase (CAT), and malondialdehyde (MDA) content in the liver were also investigated spectrophotometrically. Animals were administered two different doses of FEO (1 and 2 mL/kg) continuously for 3 days at intervals of 24 hours by the oral route before tissue sampling. The results showed that CP produced a significant increase in the average percentage of aberrant metaphases and CAs, excluding gap and micronuclei formation in polychromatic erythrocytes (PCEs), produced cytotoxicity in mouse bone marrow cells, and induced abnormal sperms in the male germ line. CP also markedly inhibited the activities of SOD, CAT, and GSH and increased MDA content. Pretreatments with FEO significantly inhibited the frequencies of aberrant metaphases, CAs, micronuclei formation, and cytotoxicity in mouse bone marrow cells induced by CP and also produced a significant reduction of abnormal sperm and antagonized the reduction of CP-induced SOD, CAT, and GSH activities and inhibited increased MDA content in the liver. FEO inhibits genotoxicity and oxidative stress induced by CP.
本研究调查了茴香精油(FEO)对环磷酰胺(CP)诱导的遗传毒性的保护作用。采用小鼠骨髓染色体畸变(CA)、微核和精子畸形检测分别测量遗传毒性和细胞毒性。还通过分光光度法研究了肝脏中超氧化物歧化酶(SOD)、谷胱甘肽(GSH)、过氧化氢酶(CAT)和丙二醛(MDA)含量的活性。动物在组织取样前通过口服途径连续 3 天每隔 24 小时给予两种不同剂量的 FEO(1 和 2 mL/kg)。结果表明,CP 导致多染红细胞(PCE)中异常有丝分裂体和 CA 的平均百分比显著增加,不包括间隙和微核形成,导致小鼠骨髓细胞的细胞毒性,并诱导雄性生殖系中的异常精子。CP 还显著抑制 SOD、CAT 和 GSH 的活性,增加 MDA 含量。FEO 预处理显著抑制 CP 诱导的异常有丝分裂体、CA、微核形成和小鼠骨髓细胞的细胞毒性,还显著降低异常精子的发生率,并拮抗 CP 诱导的 SOD、CAT 和 GSH 活性降低,抑制肝脏 MDA 含量增加。FEO 抑制 CP 诱导的遗传毒性和氧化应激。