Genetics and Cytology Department, National Research Centre (NRC), 33 El-Bohouth st, Dokki, Cairo, Egypt.
Natural Compounds Department, National Research Centre (NRC), 33 El-Bohouth st, Dokki, Cairo, Egypt.
Environ Sci Pollut Res Int. 2018 Jan;25(2):1621-1636. doi: 10.1007/s11356-017-0601-2. Epub 2017 Nov 3.
The present work was conducted to evaluate the genotoxic effect of carbon tetrachloride (CCl) in mouse bone marrow and male germ cells. The safety and the modulating activity of sage (Salvia officinalis L.) essential oil (SEO) against the possible genotoxic effect of CCl were also evaluated. A combination of in vivo mutagenic endpoints was included: micronucleus (MN), apoptosis using dual acridine orange/ethidium bromide (AO/EB) staining, comet assay, chromosomal aberrations (CAs), and sperm abnormalities. Histological examination of testis tissues was also studied. The extracted SEO was subjected to gas chromatography-mass spectrometry (GC-MS) for identifying its chemical constituents. Safety/genotoxicity of SEO was determined after two consecutive weeks (5 days/week) from oral treatment with different concentrations (0.1, 0.2, and 0.4 mL/kg). For assessing genotoxicity of CCl, both acute (once) and subacute i.p. treatment for 2 weeks (3 days/week) with the concentrations 1.2 mL/kg (for acute) and 0.8 mL/kg (for subacute) were performed. For evaluating the protective role of SEO, simultaneous treatment with SEO plus CCl was examined. In sperm abnormalities, mice were treated with the subject materials for five successive days and the samples were collected after 35 days from the beginning of treatment. Based on GC-MS findings, 22 components were identified in the chromatogram of SEO. The results demonstrated that the three concentrations of SEO were safe and non-genotoxic in all the tested endpoints. Negative results were also observed in bone marrow after acute and subacute treatment with CCl In contrast, CCl induced testicular DNA damage as evidenced by a significant increase of CAs in primary spermatocytes, sperm abnormalities, and histological distortion of testis. A remarkable reduction in these cells was observed in groups treated with SEO plus CCl especially with the two higher concentrations of SEO. In conclusion, SEO is safe and non-genotoxic under the tested conditions and can modulate genetic damage and histological alteration induced by CCl in the testes.
本研究旨在评估四氯化碳(CCl)对小鼠骨髓和雄性生殖细胞的遗传毒性。同时,还评估了鼠尾草(Salvia officinalis L.)精油(SEO)对 CCl 可能遗传毒性的安全性和调节活性。本研究包括体内诱变终点的组合:微核(MN)、双重吖啶橙/溴化乙锭(AO/EB)染色的凋亡、彗星试验、染色体畸变(CAs)和精子异常。还研究了睾丸组织的组织学检查。提取的 SEO 经气相色谱-质谱(GC-MS)进行鉴定,以确定其化学成分。SEO 的安全性/遗传毒性在连续两周(每周 5 天)经口处理不同浓度(0.1、0.2 和 0.4 mL/kg)后进行测定。为评估 CCl 的遗传毒性,采用单次腹腔注射和连续 2 周(每周 3 天)腹腔注射两种方法,浓度分别为 1.2 mL/kg(急性)和 0.8 mL/kg(亚急性)。为评估 SEO 的保护作用,同时进行 SEO 加 CCl 处理。在精子异常中,将受试材料连续处理 5 天,在开始处理后 35 天收集样本。根据 GC-MS 结果,在 SEO 的色谱图中鉴定出 22 种成分。结果表明,在所有测试终点中,SEO 的三个浓度均安全且非遗传毒性。在急性和亚急性 CCl 处理后,骨髓也未出现阳性结果。相反,CCl 诱导睾丸 DNA 损伤,初级精母细胞的 CAs、精子异常和睾丸组织学扭曲显著增加。在 SEO 加 CCl 处理组中,这些细胞显著减少,特别是在 SEO 的两个较高浓度组中。综上所述,在测试条件下,SEO 安全且非遗传毒性,并能调节 CCl 对睾丸引起的遗传损伤和组织学改变。