Paniagua-Pérez Rogelio, Madrigal-Bujaidar Eduardo, Molina-Jasso Dolores, Reyes-Cadena Susana, Alvarez-González Isela, Sánchez-Chapul Laura, Pérez-Gallaga Javier
Laboratory of Muscular Biochemistry, National Institute of Reahabilitation, National School of Biological Sciences, I.P.N., Carpio y Plan de Ayala s/n, Sto. Tomás, D.F., Mexico.
Basic Clin Pharmacol Toxicol. 2009 Mar;104(3):222-7. doi: 10.1111/j.1742-7843.2008.00366.x. Epub 2009 Jan 20.
Pteropodine is a heterohimbine-type oxindole alkaloid specifically isolated from 'Cat's claw' (Uncaria tomentosa), a plant that has shown cytostatic, anti-inflammatory and antimutagenic properties and is used in traditional medicine to cure a number of diseases. In this report, we studied the ability of pteropodine to decrease the rate of sister-chromatid exchanges and micronucleated polychromatic erythrocytes in mice administered doxorubicin. We also determined its capacity to induce lymphocyte production in mice as well as its free radical scavenging potential by applying the DPPH assay. We found pteropodine (100-600 mg/kg) to significantly decrease the frequency of sister-chromatid exchanges and micronucleated polychromatic erythrocytes in mice administered with 10 mg/kg of doxorubicin. Furthermore, we determined that pteropodine partially corrected bone marrow cytotoxicity induced by doxorubicin, as it showed an improvement in the rate of polychromatic erythrocytes. Besides, 600 mg/kg of pteropodine increased 25.8% of the production of lymphocytes over the control value along a 96-hr assay, and it exhibited a strong capacity to trap the DPPH-free radical (98.26% with 250 microg/ml). Our results establish that pteropodine is an effective antimutagen in the model used, and suggest that pteropodine deserves further research in the area of cell protective potential and its mechanism of action.
翼籽辛是一种异胡豆碱型氧化吲哚生物碱,从“猫爪藤”(钩藤)中特别分离得到。这种植物具有细胞抑制、抗炎和抗诱变特性,在传统医学中用于治疗多种疾病。在本报告中,我们研究了翼籽辛对给予阿霉素的小鼠姐妹染色单体交换率和微核多染性红细胞率的降低能力。我们还通过应用DPPH测定法确定了其在小鼠中诱导淋巴细胞产生的能力及其自由基清除潜力。我们发现翼籽辛(100 - 600毫克/千克)能显著降低给予10毫克/千克阿霉素的小鼠的姐妹染色单体交换频率和微核多染性红细胞频率。此外,我们确定翼籽辛部分纠正了阿霉素诱导的骨髓细胞毒性,因为它显示出多染性红细胞率有所改善。此外,在96小时的试验中,600毫克/千克的翼籽辛使淋巴细胞产生量比对照值增加了25.8%,并且它表现出强大的捕获DPPH自由基的能力(250微克/毫升时为98.26%)。我们的结果表明,在所用模型中翼籽辛是一种有效的抗诱变剂,并表明翼籽辛在细胞保护潜力及其作用机制方面值得进一步研究。