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Oryeong-san 的安全性评估:亚急性毒性研究以及对细胞色素 P450s 和 UDP-葡糖醛酸基转移酶的影响。

Safety assessment of Oryeong-san, a traditional herbal formula: Study of subacute toxicity and influence of cytochrome P450s and UDP-glucuronosyltransferases.

机构信息

Clinical Medicine Division, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Daejeon, 34054, Republic of Korea.

Herbal Medicine Research Division, Korea Institute of Oriental Medicine, 1672 Yuseong-daero, Yuseong-gu, Daejeon, 34054, Republic of Korea.

出版信息

Regul Toxicol Pharmacol. 2018 Oct;98:88-97. doi: 10.1016/j.yrtph.2018.07.010. Epub 2018 Jul 17.

Abstract

Oryeong-san is a traditional herbal formula that is used for the treatment of common genitourinary diseases in Korea and other Asian countries. However, little is known about its safety and influence on drug metabolism. In the present study, we investigated the subacute toxicity of an Oryeong-san water extract (OSWE) in rats and its effects on activities of drug-metabolizing enzymes. Subacute toxicity was modeled in animals exposed to treatment with the extract at multiple doses. Rats were given OSWE by oral gavage at 0, 1000, 2000 and 5000 mg/kg/day for 4 weeks. We checked general observations and investigated any changes of body/organ weight, food consumption, hematology, serum biochemistry, and urinalysis in vivo; and the activities of human microsomal cytochrome P450s (CYP450s) and UDP-glucuronosyltransferase (UGT) isozymes in vitro. We found that OSWE caused no significant toxicological changes at the doses tested. Therefore, the no observed adverse effect level of OSWE was more than 5000 mg/kg/day for male and female rats. OSWE inhibited the activities of CYP2C19 (IC: 737.69 μg/mL) and CYP2E1 (IC: 177.77 μg/mL). These results indicate that OSWE may be safe with no drug-related toxicity for up to 4 weeks and provide useful information concerning its potential to interact with conventional drugs or other herbal medicines.

摘要

奥良散是一种传统的草药配方,用于治疗韩国和其他亚洲国家常见的泌尿生殖系统疾病。然而,关于其安全性和对药物代谢的影响知之甚少。在本研究中,我们研究了奥良散水提取物(OSWE)在大鼠中的亚急性毒性及其对药物代谢酶活性的影响。通过给予动物多个剂量的提取物来建立亚急性毒性模型。大鼠通过口服灌胃给予 OSWE,剂量分别为 0、1000、2000 和 5000mg/kg/天,持续 4 周。我们检查了一般观察结果,并研究了体内体重/器官重量、食物消耗、血液学、血清生物化学和尿液分析的任何变化;以及体外人微粒体细胞色素 P450(CYP450)和 UDP-葡萄糖醛酸转移酶(UGT)同工酶的活性。我们发现,在测试的剂量下,OSWE 没有引起明显的毒性变化。因此,OSWE 的未观察到不良效应水平(NOAEL)对于雄性和雌性大鼠超过 5000mg/kg/天。OSWE 抑制 CYP2C19(IC:737.69μg/mL)和 CYP2E1(IC:177.77μg/mL)的活性。这些结果表明,OSWE 在长达 4 周的时间内可能是安全的,没有与药物相关的毒性,并且为其与传统药物或其他草药相互作用的潜力提供了有用的信息。

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