Department of Zoology, Cell and Molecular Biology Laboratory, University of North Bengal, Raja Rammohunpur, Darjeeling, West Bengal, 734013, India.
Chemical Science and Technology Division, Pharmacology Lab, Natural Products Chemistry Group, CSIR-North East Institute of Science and Technology (CSIR-NEIST), Jorhat, Assam, 785006, India.
BMC Complement Med Ther. 2024 Aug 30;24(1):324. doi: 10.1186/s12906-024-04606-y.
Equisetum diffusum D. Don commonly known as 'Himalayan horsetail', has been traditionally used in the treatment of back pain, bone fracture and dislocation, and arthritis by various tribal communities of India. Our previous study confirmed the anti-inflammatory efficacy of the plant through in silico, in vitro, and in vivo model studies. Therefore, the current research is focused on safety dose evaluation for the first-time of the whole-plant methanol extract (EDME) of E. diffusum through appropriate in silico, in vitro, and in vivo approaches.
The whole plant, along with its rhizomes, was collected, and the methanol extract was prepared. The in silico ADMET study was performed to predict the pharmacokinetics profile and toxicity of all the identified phyto-compounds of EDME previously screened by GC-MS study. In vitro cytotoxicity study of EDME was performed using two cell lines: kidney (HEK293) and liver (Huh7) cell lines. The in vivo toxicity study of EDME was validated by the acute toxicity (OECD 423, 2002) and sub-acute toxicity assays (OECD 407, 2008) in the Wistar Albino rat model.
The in silico ADMET study of all 47 bioactives predicted good pharmacokinetic and low toxicity profiles. In vitro cytotoxicity showed higher IC values of EDME viz., 672 ± 15.7 μg/mL and 1698 ± 6.54 μg/mL for both kidney (HEK293) and liver (Huh7) cell lines, respectively, which were considered as low-toxic. Based on acute oral toxicity, the LD value of the extract was considered "non-toxic" up to a feeding range of 2000 mg/kg of body weight. The regular consumption of the extract for an extended period (28 days) was also qualified as safe based on the body and organ weight, hematological, biochemical, and histoarchitecture results in the sub-acute toxicity assay.
The detailed in silico, in vitro, in vivo (acute and sub-acute oral toxicity) studies gave us a new insight to the safety dose evaluation of Equisetum diffusum, which may serve as a reliable documentation for undertaking the experimental validation of the ethnobotanical uses of the plant which would help in the field of drug development for the treatment of inflammation related complications.
贯众,俗称“喜马拉雅马尾草”,在印度的各种部落社区中,传统上用于治疗背痛、骨折和脱位以及关节炎。我们之前的研究通过计算机模拟、体外和体内模型研究证实了该植物的抗炎功效。因此,目前的研究首次集中在通过适当的计算机模拟、体外和体内方法评估贯众全株甲醇提取物(EDME)的安全剂量。
采集全株及其根茎,制备甲醇提取物。通过 GC-MS 研究先前筛选出的 EDME 中的所有植物化合物的计算机模拟 ADMET 研究,预测其药代动力学特征和毒性。采用两种细胞系:肾(HEK293)和肝(Huh7)细胞系,进行 EDME 的体外细胞毒性研究。通过急性毒性(OECD 423,2002)和亚急性毒性试验(OECD 407,2008)在 Wistar 白化大鼠模型中验证 EDME 的体内毒性。
对所有 47 种生物活性成分的计算机模拟 ADMET 研究预测其具有良好的药代动力学和低毒性特征。体外细胞毒性显示 EDME 的 IC 值较高,分别为 672±15.7μg/ml 和 1698±6.54μg/ml,用于肾(HEK293)和肝(Huh7)细胞系,这被认为是低毒性的。根据急性口服毒性,提取物的 LD 值被认为在 2000mg/kg 体重的摄食范围内是“无毒”的。在亚急性毒性试验中,根据体重和器官重量、血液学、生化学和组织学结构结果,延长时间(28 天)的常规提取物消耗也被认为是安全的。
详细的计算机模拟、体外、体内(急性和亚急性口服毒性)研究使我们对贯众的安全剂量评估有了新的认识,这可能为该植物的民族植物学用途的实验验证提供可靠的依据,从而有助于炎症相关并发症治疗的药物开发领域。