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哌醋甲酯在小鼠外周血红细胞中无遗传毒性作用。

Methylphenidate lacks genotoxic effects in mouse peripheral blood erythrocytes.

机构信息

Instituto de Investigación en Odontología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.

出版信息

Drug Chem Toxicol. 2011 Jul;34(3):294-9. doi: 10.3109/01480545.2010.536770.

Abstract

Methylphenidate (MPH; Ritalin®; Novartis Pharmaceuticals, Inc., Basel, Switzerland) has been prescribed to treat attention deficit/hyperactivity disorder (ADHD) since its approval by the U.S. Food and Drug Administration over 50 years ago. Due to concerns that MPH might induce cytogenetic alterations in children, treatment with this drug has been a controversial issue. In the present study, we assessed the frequency of micronucleated erythrocytes (MNEs), micronucleated polychromatic erythrocytes (MNPCEs), and polychromatic erythrocytes (PCEs) in peripheral blood samples from mice treated with three different doses of MPH (30, 60, or 125 mg/kg). We found no evidence of increased MNEs or MNPCEs, nor did PCEs decline. These results add to the accumulating evidence that MPH does not induce genotoxic or cytotoxic damage.

摘要

哌醋甲酯(MPH;利他林®;诺华制药公司,巴塞尔,瑞士)自 50 多年前获得美国食品和药物管理局批准以来,一直被用于治疗注意缺陷/多动障碍(ADHD)。由于担心 MPH 可能会导致儿童细胞遗传学改变,因此对这种药物的治疗一直存在争议。在本研究中,我们评估了用三种不同剂量的 MPH(30、60 或 125mg/kg)处理的小鼠外周血样本中出现微核红细胞(MNEs)、微核多染红细胞(MNPCEs)和多染红细胞(PCEs)的频率。我们没有发现 MNEs 或 MNPCEs 增加的证据,PCEs 也没有减少。这些结果进一步证明 MPH 不会引起遗传毒性或细胞毒性损伤。

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