School of Chemistry and Chemical Engineering, Guangxi University for Nationalities, Nanning 530006, China.
Collaborative Innovation Center of Zhuang and Yao Ethnic Medicine, Guangxi Key Laboratory of Zhuang and Yao Ethnic Medicine, Guangxi University of Chinese Medicine, Nanning 530200, China.
Molecules. 2022 Apr 11;27(8):2465. doi: 10.3390/molecules27082465.
Fever is caused by an increase in the heat production process when the body is under the action of a heat source or the dysfunction of the temperature center. Ellagic acid (EA) is a polyphenol dilactone that has anti-inflammatory, anti-tumor, and antioxidant activities. Male Sprague-Dawley rats were injected yeast to reproduce an experimental fever model (150 ± 20 g), and the rectal temperature and its change values were subsequently taken 19 h later; the excessive production of interleukin-1β (IL-1β) and prostaglandin2 (PGE2) induced by yeast was regulated to normal by EA administration. Rat brain metabolomics investigation of pyrexia and the antipyretic anti-inflammatory effect of EA was performed using Ultra-High-Performance Liquid Chromatography-Mass spectrometry (UPLC-MS). Twenty-six metabolites, as potential biomarkers, significantly altered metabolites that were found in pyretic rats, and eleven metabolites, as biomarkers of the antipyretic mechanism of EA, were significantly adjusted by EA to help relieve pyrexia, which was involved in glycerophospholipid metabolism and sphingolipid metabolism, etc. In conclusion, potential metabolic biomarkers in the brain shed light on the mechanism of EA's antipyretic effects, mainly involving metabolic pathways, which may contribute to a further understanding of the therapeutic mechanisms of fever and therapeutic mechanism of EA.
发热是机体在热源作用下或体温调节中枢功能障碍时产热过程增加引起的。鞣花酸(EA)是一种多酚二内酯,具有抗炎、抗肿瘤和抗氧化活性。雄性 Sprague-Dawley 大鼠注射酵母,复制实验性发热模型(150±20g),19 小时后测量直肠温度及其变化值;通过 EA 给药调节酵母诱导的白细胞介素-1β(IL-1β)和前列腺素 2(PGE2)的过度产生,使其恢复正常。采用超高效液相色谱-质谱联用技术(UPLC-MS)对发热大鼠的脑代谢组学和 EA 的解热抗炎作用进行研究。发现 26 种代谢物作为潜在生物标志物,明显改变了发热大鼠的代谢物,11 种代谢物作为 EA 解热机制的生物标志物,通过 EA 显著调节,有助于缓解发热,涉及甘油磷脂代谢和鞘脂代谢等。总之,脑内潜在的代谢生物标志物揭示了 EA 解热作用的机制,主要涉及代谢途径,这可能有助于进一步了解发热的治疗机制和 EA 的治疗机制。