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从 Leucas aspera Linn. 中提取的三萜(C34H68O2)对眼镜蛇蛇毒诱导的毒性的抗蛇毒活性:抗氧化和组织学研究在小鼠中。

Antivenom activity of triterpenoid (C34H68O2) from Leucas aspera Linn. against Naja naja naja venom induced toxicity: antioxidant and histological study in mice.

机构信息

1Aquaculture Biotechnology Division, OIE Reference Laboratory for WTD, Department of Zoology, C. Abdul Hakeem College, Melvisharam, Vellore District, Tamil Nadu, India.

出版信息

Hum Exp Toxicol. 2014 Apr;33(4):336-59. doi: 10.1177/0960327113494901. Epub 2013 Jul 15.

Abstract

The isolated and identified triterpenoid, 1-hydroxytetratriacontane-4-one (C34H68O2), obtained from the methanolic leaf extract of Leucas aspera Linn. was explored for the first time for antisnake venom activity. The plant (L. aspera Linn.) extract significantly antagonized the spectacled cobra (Naja naja naja) venom induced lethal activity in a mouse model. It was compared with commercial antiserum obtained from King Institute of Preventive Medicine (Chennai, Tamil Nadu, India). N. naja naja venom induced a significant decrease in antioxidant superoxide dismutase, glutathione (GSH) peroxidase, catalase, reduced GSH and glutathione-S-transferase activities and increased lipid peroxidase (LPO) activity in different organs such as heart, liver, kidney and lungs. The histological changes following the antivenom treatment were also evaluated in all these organs. There were significant alterations in the histology. Triterpenoid from methanol extract of L. aspera Linn. at a dose level of 75 mg per mouse significantly attenuated (neutralized) the venom-induced antioxidant status and also the LPO activity in different organs.

摘要

从 Leucas aspera Linn. 的甲醇叶提取物中分离并鉴定出的三萜类化合物 1-羟基四廿烷-4-酮(C34H68O2),首次被探索用于抗蛇毒活性。该植物(L. aspera Linn.)提取物在小鼠模型中显著拮抗了眼镜蛇(Naja naja naja)毒液的致死活性。它与来自 King Institute of Preventive Medicine(Chennai,Tamil Nadu,印度)的商业抗血清进行了比较。眼镜蛇毒液诱导不同器官(如心脏、肝脏、肾脏和肺)中的抗氧化超氧化物歧化酶、谷胱甘肽(GSH)过氧化物酶、过氧化氢酶、还原型 GSH 和谷胱甘肽-S-转移酶活性显著降低,脂质过氧化物(LPO)活性增加。还在所有这些器官中评估了抗蛇毒治疗后的组织学变化。组织学有明显的改变。从 L. aspera Linn. 的甲醇提取物中提取的三萜类化合物在 75mg/只小鼠的剂量水平下,显著减弱(中和)了毒液诱导的抗氧化状态和不同器官中的 LPO 活性。

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