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绿茶提取物对乙酰氨基酚诱导的小鼠肝毒性的代谢组学评价。

Metabolomics evaluation of the effects of green tea extract on acetaminophen-induced hepatotoxicity in mice.

机构信息

Division of Systems Biology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR 72079, USA.

出版信息

Food Chem Toxicol. 2013 Dec;62:707-21. doi: 10.1016/j.fct.2013.09.025. Epub 2013 Sep 27.

Abstract

Green tea has been purported to have beneficial health effects including protective effects against oxidative stress. Acetaminophen (APAP) is a widely used analgesic drug that can cause acute liver injury in overdose situations. These studies explored the effects of green tea extract (GTE) on APAP-induced hepatotoxicity in liver tissue extracts using ultra performance liquid chromatography/quadrupole time-of-flight mass spectrometry and nuclear magnetic resonance spectroscopy. Mice were orally administered GTE, APAP or GTE and APAP under three scenarios. APAP alone caused a high degree of hepatocyte necrosis associated with increases in serum transaminases and alterations in multiple metabolic pathways. The time of GTE oral administration relative to APAP either protected against or potentiated the APAP-induced hepatotoxicity. Dose dependent decreases in histopathology scores and serum transaminases were noted when GTE was administered prior to APAP; whereas, the opposite occurred when GTE was administered after APAP. Similarly, metabolites altered by APAP alone were less changed when GTE was given prior to APAP. Significantly altered pathways included fatty acid metabolism, glycerophospholipid metabolism, glutathione metabolism, and energy pathways. These studies demonstrate the complex interaction between GTE and APAP and the need to employ novel analytical strategies to understand the effects of dietary supplements on pharmaceutical compounds.

摘要

绿茶据称具有有益的健康作用,包括对氧化应激的保护作用。对乙酰氨基酚(APAP)是一种广泛使用的镇痛药,过量使用会导致急性肝损伤。这些研究使用超高效液相色谱/四极杆飞行时间质谱和核磁共振波谱法,探索了绿茶提取物(GTE)对肝组织提取物中 APAP 诱导的肝毒性的影响。将 GTE、APAP 或 GTE 和 APAP 以三种情况经口给予小鼠。APAP 单独使用会导致高度的肝细胞坏死,伴随着血清转氨酶的升高和多种代谢途径的改变。GTE 相对于 APAP 的口服时间要么对 APAP 诱导的肝毒性具有保护作用,要么增强其毒性。当 GTE 在 APAP 之前给予时,组织病理学评分和血清转氨酶的剂量依赖性降低;而当 GTE 在 APAP 之后给予时,则相反。同样,当 GTE 在 APAP 之前给予时,APAP 单独改变的代谢物变化较小。发生显著改变的途径包括脂肪酸代谢、甘油磷脂代谢、谷胱甘肽代谢和能量途径。这些研究表明 GTE 和 APAP 之间存在复杂的相互作用,需要采用新的分析策略来了解膳食补充剂对药物化合物的影响。

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