Department of Cellular Assay, R&D Centre, Natural Remedies Pvt Ltd, Bangalore 560 100, Karnataka, India.
Toxicol In Vitro. 2010 Apr;24(3):885-97. doi: 10.1016/j.tiv.2009.11.021. Epub 2009 Dec 1.
Indigenous plants are used as a traditional source of raw materials for the manufacture of medicines. Modernizing the ancient art of herbal medicine bequeathed from generations entails addressing two interrelated issues i.e. efficacy, and safety prior to their acceptance and use worldwide. The present study was designed to investigate three of our veterinary poly-herbal formulations - Phytocee an antistressor; Zigbir(R) a hepatoprotectant; and Zist(R) as an immunomodulator in the pertinent in vitro cell assay models in order to validate their therapeutic potential. Cellular antioxidant potential of Phytocee was demonstrated against AAPH induced oxidative stress using HepG2 cells. Zigbir(R) was confirmed as a hepatoprotectant against tert-butylhydroperoxide induced cytotoxicity in HepG2 cells. Immunomodulatory activity of Zist(R) was established by its ability to inhibit the proliferation of mitogen stimulated murine splenocytes in vitro. On treatment with Zist(R), a trend of decline in IL-6, and IL-12 levels was observed following stimulation with Con A, and LPS respectively in murine splenocytes. Further, all the three poly-herbal formulations were subjected to Ames II assay for ensuring their safety profile. Results epitomize that all the three poly-herbal formulations were devoid of significant mutagenic effect in TA98, and TAMix strains of Salmonella typhimurium under our experimental conditions.
本土植物被用作制造药物的传统原料。在将世代相传的古老草药医学现代化的过程中,需要解决两个相互关联的问题,即在被全球接受和使用之前,要解决疗效和安全性的问题。本研究旨在调查我们的三种兽医复方草药制剂 - Phytocee(抗应激)、Zigbir(R)(肝保护剂)和 Zist(R)(免疫调节剂),以在相关的体外细胞测定模型中验证其治疗潜力。使用 HepG2 细胞,Phytocee 的细胞抗氧化能力针对 AAPH 诱导的氧化应激进行了证明。Zigbir(R) 被确认为 HepG2 细胞中叔丁基过氧化物诱导的细胞毒性的肝保护剂。Zist(R) 的免疫调节活性通过其抑制有丝分裂原刺激的鼠脾细胞在体外增殖的能力来建立。在用 Zist(R)治疗后,在用 Con A 和 LPS 分别刺激后,观察到 IL-6 和 IL-12 水平呈下降趋势。此外,还对所有三种复方草药制剂进行了 Ames II 测定,以确保其安全性。结果表明,在我们的实验条件下,所有三种复方草药制剂在鼠伤寒沙门氏菌 TA98 和 TAMix 菌株中均无明显的致突变作用。