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使用一种用于炎症的阿育吠陀多草药配方进行急性和慢性毒性、细胞色素P450酶抑制及人醚-去极化激活的钾离子通道(HERG)阻断研究。

Acute and chronic toxicity, cytochrome p450 enzyme inhibition, and HERG channel blockade studies with a polyherbal, ayurvedic formulation for inflammation.

作者信息

Dey Debendranath, Chaskar Sunetra, Athavale Nitin, Chitre Deepa

机构信息

Bioved Pharmaceuticals Pvt. Ltd., BAIF Bhawan, Z Wing, Warje Malwadi, Pune 411 052, India.

Bioved Pharmaceuticals, Inc., 1929 O'Toole Way, San Jose, CA 95131, USA.

出版信息

Biomed Res Int. 2015;2015:971982. doi: 10.1155/2015/971982. Epub 2015 Mar 17.

Abstract

Ayurvedic plants are known for thousands of years to have anti-inflammatory and antiarthritic effect. We have recently shown that BV-9238, a proprietary formulation of Withania somnifera, Boswellia serrata, Zingiber officinale, and Curcuma longa, inhibits LPS-induced TNF-alpha and nitric oxide production from mouse macrophage and reduces inflammation in different animal models. To evaluate the safety parameters of BV-9238, we conducted a cytotoxicity study in RAW 264.7 cells (0.005-1 mg/mL) by MTT/formazan method, an acute single dose (2-10 g/kg bodyweight) toxicity study and a 180-day chronic study with 1 g and 2 g/kg bodyweight in Sprague Dawley rats. Some sedation, ptosis, and ataxia were observed for first 15-20 min in very high acute doses and hence not used for further chronic studies. At the end of 180 days, gross and histopathology, blood cell counts, liver and renal functions were all at normal levels. Further, a modest attempt was made to assess the effects of BV-9238 (0.5 µg/mL) on six major human cytochrome P450 enzymes and (3)H radioligand binding assay with human hERG receptors. BV-9238 did not show any significant inhibition of these enzymes at the tested dose. All these suggest that BV-9238 has potential as a safe and well tolerated anti-inflammatory formulation for future use.

摘要

数千年来,阿育吠陀植物一直以具有抗炎和抗关节炎作用而闻名。我们最近发现,BV - 9238(一种由睡茄、乳香、姜和姜黄制成的专利配方)可抑制脂多糖诱导的小鼠巨噬细胞产生肿瘤坏死因子 -α和一氧化氮,并减轻不同动物模型中的炎症。为了评估BV - 9238的安全参数,我们通过MTT/甲臜法在RAW 264.7细胞中进行了细胞毒性研究(0.005 - 1 mg/mL),在斯普拉格 - 道利大鼠中进行了急性单剂量(2 - 10 g/kg体重)毒性研究以及180天的慢性研究(1 g/kg体重和2 g/kg体重)。在非常高的急性剂量下,最初15 - 20分钟观察到一些镇静、眼睑下垂和共济失调现象,因此未用于进一步的慢性研究。在180天结束时,大体和组织病理学、血细胞计数、肝功能和肾功能均处于正常水平。此外,还进行了适度尝试,以评估BV - 9238(0.5 µg/mL)对六种主要人类细胞色素P450酶的影响以及用人hERG受体进行的(3)H放射性配体结合试验。在测试剂量下,BV - 9238对这些酶未显示出任何显著抑制作用。所有这些表明,BV - 9238作为一种安全且耐受性良好的抗炎制剂具有未来应用的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d52/4381553/904bb9c0caab/BMRI2015-971982.001.jpg

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