张明亮, 赵旭, 李伟霞, 王晓艳, 陈毓龙, 孔德鑫, 吴承钊, 陈小菲, 柏兆方, 牛明, 王伽伯, 赵艳玲, 肖小河, 唐进法. 补骨脂“大燥伤肝”的客观性及生物学机制研究J. 药学学报, 2023, 58(4): 1014-1023. DOI: 10.16438/j.0513-4870.2022-1222
引用本文: 张明亮, 赵旭, 李伟霞, 王晓艳, 陈毓龙, 孔德鑫, 吴承钊, 陈小菲, 柏兆方, 牛明, 王伽伯, 赵艳玲, 肖小河, 唐进法. 补骨脂“大燥伤肝”的客观性及生物学机制研究J. 药学学报, 2023, 58(4): 1014-1023. DOI: 10.16438/j.0513-4870.2022-1222
ZHANG Ming-liang, ZHAO Xu, LI Wei-xia, WANG Xiao-yan, CHEN Yu-long, KONG De-xin, WU Cheng-zhao, CHEN Xiao-fei, BAI Zhao-fang, NIU Ming, WANG Jia-bo, ZHAO Yan-ling, XIAO Xiao-he, TANG Jin-fa. Study on the objectivity and biological mechanism of Psoralea corylifolia Linn.'s 'Great dryness damages the liver'J. Acta Pharmaceutica Sinica, 2023, 58(4): 1014-1023. DOI: 10.16438/j.0513-4870.2022-1222
Citation: ZHANG Ming-liang, ZHAO Xu, LI Wei-xia, WANG Xiao-yan, CHEN Yu-long, KONG De-xin, WU Cheng-zhao, CHEN Xiao-fei, BAI Zhao-fang, NIU Ming, WANG Jia-bo, ZHAO Yan-ling, XIAO Xiao-he, TANG Jin-fa. Study on the objectivity and biological mechanism of Psoralea corylifolia Linn.'s 'Great dryness damages the liver'J. Acta Pharmaceutica Sinica, 2023, 58(4): 1014-1023. DOI: 10.16438/j.0513-4870.2022-1222

补骨脂“大燥伤肝”的客观性及生物学机制研究

Study on the objectivity and biological mechanism of Psoralea corylifolia Linn.'s 'Great dryness damages the liver'

  • 摘要: 依据补骨脂“性本大燥”的药性理论, 寻找补骨脂致肝损伤的易感证候及生物标志物。分别构建肾阴虚证、肾阳虚大鼠模型, 所有动物实验操作和福利均遵循河南中医药大学第一附属实验动物伦理与动物福利委员会的规定(批号YFYDW2020017)。结果发现补骨脂可显著降低肾阴虚证大鼠体质量、饮水量、尿量, 并增加其肝、睾丸、肾上腺、脾脏脏器指数及谷丙转氨酶(alanine aminotransferase, ALT) 表达; 同时, 补骨脂还显著增加了肾阳虚证大鼠尿量, 并降低ALT、天冬氨酸氨基转移酶(aspartate aminotransferase, AST) 表达; 苏木素-伊红(hematoxylin and eosin, HE) 染色显示补骨脂明显加剧肾阴虚证大鼠肝细胞炎症浸润, 并减轻肾阳虚证大鼠肝损伤。超高效液相色谱-质谱(ultra-performance liquid chromatography-tandem mass spectrometry, UPLC-MS) 检测血浆后共鉴定出17个补骨脂共同调控肾阴/阳虚证大鼠的具有显著差异的内源性代谢标志物。其中, 谷氨酰胺、喹啉酸、胆绿素、乳糖基酰基鞘氨醇等8个代谢物呈相反变化趋势, 主要涉及半胱氨酸和蛋氨酸代谢、酪氨酸代谢、色氨酸代谢、嘌呤代谢、鞘脂代谢、甘油磷脂代谢、谷氨酰胺代谢等通路。因此, 本研究推测肾阴虚证与肾阳虚证可能分别是补骨脂发挥肝损害与肝保护的易感证候, 这可能与其调控体内相关氨基酸代谢和鞘脂代谢等有关, 可为中医临床补骨脂的安全精准使用提供一定的实验数据支撑。

     

    Abstract: According to the theory of 'Xingben Dazao' of Psoralea corylifolia Linn. (BL), the susceptible syndromes and biomarkers of liver injury caused by BL were searched. Rat models of kidney-yin deficiency syndrome (M_yin) and kidney-yang deficiency syndrome (M_yang) were established, and all animal experimental operations and welfare following the provisions of the First Affiliated Experimental Animal Ethics and Animal Welfare Committee of Henan University of Traditional Chinese Medicine (No. YFYDW2020017). The results showed that BL significantly decreased the body weight, water intake, and urine weight of M_yin rats and increase the organ indexes of the liver, testis, adrenal gland, and spleen and the expression of alanine aminotransferase (ALT). Meantime, BL significantly increased the urine weight of M_yang rats and decreased the expression of ALT and aspartate aminotransferase (AST). Hematoxylin and eosin (HE) staining showed that BL could aggravate inflammatory infiltration of hepatocytes in rats with M_yin and alleviate liver injury in rats with M_yang. Metabolomics identified 17 BL co-regulated significant differential metabolic markers in M_yin and M_yang rats. Among them, 8 metabolites such as glutamine, quinolinate, biliverdin, and lactosylceramide showed opposite trends, mainly involving cysteine and methionine metabolism, tyrosine metabolism, tryptophan metabolism, purine metabolism, sphingolipid metabolism, glycerol phospholipid metabolism, glutamine metabolism, and other pathways. M_yin/M_yang may be the susceptible constitution of BL for liver damage or protection, which may be related to the regulation of amino acid metabolism and sphingolipid metabolism. The study can provide some experimental data support for the safe and accurate use of BL in the clinical practice of traditional Chinese medicine.

     

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