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xanthium commune/glutatioon

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Male rats (10 rats/group) were treated with phenobarbital (PB), phenylbutazone (PBZ), stanozolol (3 inducers of cytochrome P450-dependent enzymes), piperonyl butoxide (PBO; a P450 inhibitor), cobaltous chloride (CoCl2; an inhibitor of hemoprotein synthesis), 5,6-benzoflavone (BNF; an inducer of

Effect of glutathione and alloxan on the photoperiodic response of Xanthium.

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Hepatotoxicity of kaurene glycosides from Xanthium strumarium L. fruits in mice.

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The fruit of Xanthium strumarium L. (Cang-Er-Zi) is a traditional Chinese medicine that is used in curing nasal diseases and headache according to the Chinese Pharmacopoeia. However, clinical utilization of Xanthium strumarium is relatively limited because of its toxicity. The present investigation
1β-hydroxyl-5α-chloro-8-epi-xanthatin (XTT), a sesquiterpene lactone isolated from Xanthium sibiricum, possessed potent cytotoxicity on cancer cells in vitro. The objective of this study was to investigate the anti-tumor effect and underlying mechanisms of XTT on human hepatocellular carcinoma

Effects of glycyrrhizic acid on cocklebur-induced hepatotoxicity in rat and human hepatocytes.

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Herbal medicines are gradually being accepted for their low toxicity and high efficacy, but their hepatotoxicity still needs to be recognized. For the multiple compounds in herbs, hepatocytes in vitro would be a useful tool for the evaluation of herbal hepatotoxicity. This study aimed at

MSMA resistance studies.

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Monosodium methanearsonate (MSMA)-resistant and -susceptible common cocklebur (Xanthium strumarium L.) and cotton (Gossypium hirsutum L.) were treated with MSMA. Plant parameters analyzed were: glutathione synthetase activity, selected amino acid (arginine, glutamic acid, alanine, citrulline,
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