Shobhaben Pratapbhai Patel School of Pharmacy & Technology Management, SVKM's NMIMS, V.L. Mehta Road, Vile Parle (West), Mumbai, 400056, India.
Department of Pharmacy, Birla Institute of Technology and Science Pilani, Pilani Campus, Pilani, 333031, Rajasthan, India.
Chem Biodivers. 2020 Oct;17(10):e2000422. doi: 10.1002/cbdv.202000422. Epub 2020 Sep 21.
Paeonol is a phenolic compound reported for its various pharmacological activities such as antioxidant, anti-inflammatory and antidiabetic activity. There are no systematic scientific reports on the in vivo toxicity of paeonol. So, the present work was designed to study in silico and in vivo toxicity of paeonol. In silico toxicity predictions were carried out using pkCSM, ProTox-II, pre-ADMET server and OSIRIS property explorer. Acute oral toxicity study of paeonol was carried out in female Sprague Dawley rats at a single dose of 300 mg/kg, 2000 mg/kg and 5000 mg/kg. Animals were observed for toxicity signs and mortality for 14 days. Repeated dose oral toxicity study of paeonol was carried out in female and male Sprague Dawley rats at a dose of 50, 100 and 200 mg/kg body weight for 28 days. At the end of the study, hematological, biochemical and urine parameters were assessed. Histopathology of vital organs was also carried out. In silico toxicity study predicted that paeonol is non-toxic. The maximally tolerated dose of paeonol was found to be 5000 mg/kg in acute toxicity study in female rats. Paeonol was found to be safe at a dose of 50, 100 and 200 mg/kg in repeated dose toxicity study in male and female rats.
丹皮酚是一种酚类化合物,具有多种药理活性,如抗氧化、抗炎和抗糖尿病活性。目前尚无关于丹皮酚体内毒性的系统科学报道。因此,本工作旨在研究丹皮酚的体内和体外毒性。采用 pkCSM、ProTox-II、预 ADMET 服务器和 OSIRIS 属性探测器进行了体外毒性预测。在雌性 Sprague Dawley 大鼠中进行了丹皮酚的单次口服毒性研究,剂量分别为 300mg/kg、2000mg/kg 和 5000mg/kg。观察动物 14 天的毒性症状和死亡率。在雌性和雄性 Sprague Dawley 大鼠中进行了丹皮酚的重复剂量口服毒性研究,剂量分别为 50、100 和 200mg/kg 体重,为期 28 天。研究结束时,评估了血液学、生物化学和尿液参数。还进行了重要器官的组织病理学检查。体外毒性研究预测丹皮酚无毒性。在雌性大鼠急性毒性研究中,丹皮酚的最大耐受剂量为 5000mg/kg。在雄性和雌性大鼠的重复剂量毒性研究中,丹皮酚在 50、100 和 200mg/kg 剂量下被发现是安全的。