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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >MITRAGYNA SPECIOSA-INDUCED HEPATOTOXICITY-TREATED EFFECTIVELY BY PIPER BETLE: SCOPE AS A FUTURE ANTIDOTE
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MITRAGYNA SPECIOSA-INDUCED HEPATOTOXICITY-TREATED EFFECTIVELY BY PIPER BETLE: SCOPE AS A FUTURE ANTIDOTE

机译:猪甲虫有效地减轻了由米特拉木霉引起的肝毒性:将其作为未来的解毒药

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摘要

Objective: Consumption of Mitragyna speciosa (MS) leads to various toxicities including hepatotoxicity. Piper betle (PB) is a herb that possesses various therapeutic properties. The aim of the present study was to examine the protective effect of PB methanol extract (PBME) on MS-induced hepatotoxicity which could pave the way for any future antidote. Methods: Twenty-four male Sprague–Dawley rats were randomized into control and experimental groups. The control group was further divided into the negative (G-T80) and positive (G-PB) control groups. The G-T80 group (n=6) received oral gavage of the vehicle, 15% Tween 80. The G-PB group (n=6) received PBME 200 mg/kg/day, orally. The experimental group was divided into two groups, i.e., The G-MS and G-MS (PB) groups. The G-MS group (n=6) received only MS methanol extract (MSME) 500 mg/kg/day, while the G-MS (PB) group (n=6) received MSME with concomitant treatment with PBME. Results: Histopathology examination of the G-T80 and G-PB groups showed normal histology of the liver. The G-MS group showed liver injury features such as microvesicular steatosis, ballooning degeneration, acidophilic bodies, scattered focal necrosis, fibrous portal expansion, bridging fibrosis, sinusoidal congestion, and dilatation. These features were fewer in the G-MS (PB) group which received concomitant treatment with PBME. Conclusion: Administration of PBME exerted a protective effect against MS-induced hepatotoxicity. Future clinical trials using PB as an antidote may help in combating MS-induced hepatoxicity.
机译:目的:食用Mitragyna speciosa(MS)会导致各种毒性,包括肝毒性。吹牛(PB)是一种具有多种治疗特性的草药。本研究的目的是研究PB甲醇提取物(PBME)对MS诱导的肝毒性的保护作用,这可能为将来的解毒剂铺平道路。方法:将24只雄性Sprague-Dawley大鼠随机分为对照组和实验组。对照组进一步分为阴性(G-T80)和阳性(G-PB)对照组。 G-T80组(n = 6)接受了15%Tween 80的媒介物的口服管饲。G-PB组(n = 6)口服了200 mg / kg /天的PBME。实验组分为两组,即G-MS和G-MS(PB)组。 G-MS组(n = 6)仅接受500 mg / kg /天的MS甲醇提取物(MSME),而G-MS(PB)组(n = 6)则接受PBME伴随治疗的MSME。结果:G-T80和G-PB组的组织病理学检查显示肝脏组织学正常。 G-MS组表现出肝损伤特征,例如微囊性脂肪变性,球囊变性,嗜酸性小体,局灶性坏死散布,纤维门脉扩张,桥接纤维化,正弦充血和扩张。在接受PBME伴随治疗的G-MS(PB)组中,这些特征较少。结论:PBME的给药对MS诱导的肝毒性具有保护作用。将来使用PB作为解毒剂的临床试验可能有助于对抗MS诱导的肝毒性。

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