Zhao Linjing, Zhao Aihua, Chen Tianlu, Chen Wenlian, Liu Jiajian, Wei Runmin, Su Jing, Tang Xuelan, Liu Keyi, Zhang Ran, Xie Guoxiang, Panee Jun, Qiu Mingfeng, Jia Wei
College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science , Shanghai 201620, China.
Metabolomics Shared Resource, University of Hawaii Cancer Center , Honolulu, Hawaii 96813, United States.
J Proteome Res. 2016 Jul 1;15(7):2327-36. doi: 10.1021/acs.jproteome.6b00409. Epub 2016 Jun 20.
Glucocorticoids are commonly used in anti-inflammatory and immunomodulatory therapies, but glucocorticoid withdrawal can result in life-threatening risk of adrenal insufficiency. Chinese patented pharmaceutical product Jinkui Shenqi pill (JKSQ) has potent efficacy on clinical adrenal insufficiency resulting from glucocorticoid withdrawal. However, the underlying molecular mechanism remains unclear. We used an animal model to study JKSQ-induced metabolic changes under adrenal insufficiency and healthy conditions. Sprague-Dawley rats were treated with hydrocortisone for 7 days with or without 15 days of JKSQ pretreatment. Sera were collected after 72 h hydrocortisone withdrawal and used for global and free fatty acids (FFAs)-targeted metabolomics analyses using gas chromatography/time-of-flight mass spectrometry and ultraperformance liquid chromatography/quadruple time-of-flight mass spectrometry. Rats without hydrocortisone treatment were used as controls. JKSQ pretreatment normalized the significant changes of 13 serum metabolites in hydrocortisone-withdrawal rats, involving carbohydrates, lipids, and amino acids. The most prominent effect of JKSQ was on the changes of FFAs and some [product FFA]/[precursor FFA] ratios, which represent estimated desaturase and elongase activities. The opposite metabolic responses of JKSQ in adrenal insufficiency rats and normal rats highlighted the "Bian Zheng Lun Zhi" (treatment based on ZHENG differentiation) guideline of TCM and suggested that altered fatty acid metabolism was associated with adrenal insufficiency after glucocorticoid withdrawal and the protective effects of JKSQ.
糖皮质激素常用于抗炎和免疫调节治疗,但停用糖皮质激素会导致危及生命的肾上腺功能不全风险。中国专利药品金匮肾气丸(JKSQ)对糖皮质激素撤药所致临床肾上腺功能不全具有显著疗效。然而,其潜在分子机制仍不清楚。我们使用动物模型研究了JKSQ在肾上腺功能不全和健康状态下诱导的代谢变化。将Sprague-Dawley大鼠用氢化可的松治疗7天,同时或不同时进行15天的JKSQ预处理。在停用氢化可的松72小时后收集血清,并使用气相色谱/飞行时间质谱和超高效液相色谱/四极杆飞行时间质谱进行全代谢组和游离脂肪酸(FFA)靶向代谢组学分析。未用氢化可的松治疗的大鼠用作对照。JKSQ预处理使氢化可的松撤药大鼠血清中13种代谢物的显著变化恢复正常,这些代谢物涉及碳水化合物、脂质和氨基酸。JKSQ最显著的作用是对FFA以及一些代表估计的去饱和酶和延长酶活性的[产物FFA]/[前体FFA]比值的变化。JKSQ在肾上腺功能不全大鼠和正常大鼠中相反的代谢反应突出了中医“辨证论治”的原则,并表明脂肪酸代谢改变与糖皮质激素撤药后肾上腺功能不全及JKSQ的保护作用有关。