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春黄菊(L.)雷氏精油对小鼠精原细胞的抗原毒性作用及其体外抗氧化能力的测定。

Antigenotoxic effect of Chamomilla recutita (L.) Rauschert essential oil in mouse spermatogonial cells, and determination of its antioxidant capacity in vitro.

机构信息

Laboratorio de Toxicología, Instituto de Ciencias de la Salud, UAEH, Ex-Hacienda de la Concepción. Tilcuautla. Pachuca de Soto, Hgo. Cp 42080, Mexico; E-Mails:

出版信息

Int J Mol Sci. 2010 Sep 30;11(10):3793-802. doi: 10.3390/ijms11103793.

Abstract

Chamomilla recutita (L.) Rauschert (Asteraceae), popularly known as chamomile, is a plant used in traditional medicine for various therapeutic purposes. Chamomile essential oil (CEO) is particularly known to inhibit the genotoxic damage produced by mutagens in mice somatic cells. The aim of this research was to determine the inhibitory potential of CEO on the genotoxic damage produced by daunorubicin (DAU) in mice germ cells. We evaluated the effect of 5, 50, and 500 mg/kg of essential oil on the rate of sister chromatid exchange (SCE) induced in spermatogonia by 10 mg/kg of the mutagen. We found no genotoxicity of CEO, but detected an inhibition of SCE after the damage induced by DAU; from the lowest to the highest dose of CEO we found an inhibition of 47.5%, 61.9%, and 93.5%, respectively. As a possible mechanism of action, the antioxidant capacity of CEO was determined using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging method and ferric thiocyanate assays. In the first test we observed a moderate scavenging potential of the oil; nevertheless, the second assay showed an antioxidant capacity similar to that observed with vitamin E. In conclusion, we found that CEO is an efficient chemoprotective agent against the damage induced by DAU in the precursor cells of the germinal line of mice, and that its antioxidant capacity may induce this effect.

摘要

春黄菊(L.)Rauschert(菊科),俗称甘菊,是一种用于传统医学的植物,具有多种治疗用途。特别是,洋甘菊精油(CEO)被认为可以抑制突变剂在小鼠体细胞中产生的遗传毒性损伤。本研究旨在确定 CEO 对 DAU 在小鼠生殖细胞中产生的遗传毒性损伤的抑制潜力。我们评估了 5、50 和 500mg/kg 精油对 10mg/kg 诱变剂诱导的精原细胞姐妹染色单体交换(SCE)率的影响。我们没有发现 CEO 的遗传毒性,但检测到 DAU 诱导的损伤后 SCE 受到抑制;从最低到最高剂量的 CEO,我们发现分别抑制了 47.5%、61.9%和 93.5%。作为一种可能的作用机制,我们使用 1,1-二苯基-2-苦基肼(DPPH)自由基清除法和铁硫氰酸盐测定法测定了 CEO 的抗氧化能力。在第一个测试中,我们观察到油具有中等的清除潜力;然而,第二个测定显示出与维生素 E 观察到的相似的抗氧化能力。总之,我们发现 CEO 是一种有效的化学保护剂,可以防止 DAU 在小鼠生殖细胞前体细胞中诱导的损伤,其抗氧化能力可能诱导这种作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf46/2996809/bdac52a60fd5/ijms-11-03793f1.jpg

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