Qingfei Zhisou oral liquid alleviates fever-induced inflammation by regulating arachidonic acid and lysophospholipids metabolism and inhibiting hypothalamus transient receptor potential ion channels expression.

Gao Jiaming, Zhang Yehao, Chen Yuanyuan, Jin Long, Zhao Jianfeng, Guo Hao, F U Jianhua
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Abstract

Objective: To explore how Qingfei Zhisou oral liquid (, QFZS) adjusts body temperature bias and the interaction of inflammatory factors levels and metabolomic differences.

Methods: Dry yeast was subcutaneously injected at 10 mL/kg to establish the pyrexia model. We randomly divided 60 Sprague-Dawley rats into five groups: control, model, positive, low dose of QFZS and high dose of QFZS. Inflammatory proteins were evaluated by Western blotting and immunohistochemistry. For the examination of the endogenous metabolites, enzyme linked immunosorbent assay and ultra-high-performance liquid chromatography high-resolution mass spectrometry were employed.

Results: QFZS significantly reduced rats' body temperature within 6 h after dry yeast injection and reduced the secretion of the arginine vasopressin, cyclic adenosine monophosphate, prostaglandin E-2, tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-1β in serum. Meanwhile, we identified 41 metabolites between the model and QFZS groups, including arachidonic acid and lysophospholipids. QFZS restored normal arachidonic acid levels. Based on the differential metabolite enrichment analysis, QFZS's anti-inflammatory and anti-pyrexia effects might be related to the inflammatory pathway regulated by transient receptor potential. Additionally, QFZS treatment reduced transient receptor potential melastatin 2 ion channel expression and affected TNF-α, heat shock protein 70, and cyclooxygenase-2 expression in the hypothalamus.

Conclusion: QFZS exerts its regulatory effects on fever by regulating the metabolism of lysophospholipids and arachidonic acid and the regulation of inflammation via transient receptor potential ion channels channels.

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清热解毒口服液通过调节花生四烯酸和溶血磷脂代谢,抑制下丘脑瞬时受体电位离子通道的表达,缓解发热引起的炎症。
目的探讨清热解毒口服液(QFZS)如何调节体温偏差以及炎症因子水平和代谢组差异的相互作用:方法:以 10 mL/kg 的剂量皮下注射干酵母,建立热病模型。我们将 60 只 Sprague-Dawley 大鼠随机分为五组:对照组、模型组、阳性组、低剂量 QFZS 组和高浓度 QFZS 组。用 Western 印迹法和免疫组化法评估炎症蛋白。在检测内源性代谢物时,采用了酶联免疫吸附测定法和超高效液相色谱-高分辨质谱法:结果:干酵母注射后6 h内,QFZS能明显降低大鼠体温,减少血清中精氨酸加压素、环磷酸腺苷、前列腺素E-2、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-1β的分泌。同时,我们在模型组和 QFZS 组之间发现了 41 种代谢物,包括花生四烯酸和溶血磷脂。QFZS恢复了正常的花生四烯酸水平。根据差异代谢物富集分析,QFZS的抗炎和抗厌食作用可能与瞬时受体电位调控的炎症通路有关。此外,QFZS还能降低瞬时受体电位美拉塔素2离子通道的表达,并影响下丘脑中TNF-α、热休克蛋白70和环氧合酶-2的表达:结论:QFZS通过调节溶血磷脂和花生四烯酸的代谢,并通过瞬态受体电位离子通道调节炎症,从而对发热产生调节作用。
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