School of Pharmacy, Second Military Medical University, Shanghai 200433, China.
School of Pharmacy, Second Military Medical University, Shanghai 200433, China; School of Pharmacy, Fourth Military Medical University, Xi'an 710032, China.
J Ethnopharmacol. 2015 Jan 15;159:262-73. doi: 10.1016/j.jep.2014.11.033. Epub 2014 Nov 27.
Hypothyroidism is known to be closely associated with lipid metabolism. Although our previous serum and urine metabonomics studies have provided some clues about the molecular mechanism of hypothyroidism at the metabolic level, the precise mechanism underlying the pathogenesis of hypothyroidism remains elusive, especially from the aspect of lipid metabolism. In the present study, we applied an ultra high performance liquid chromatography/time-of-flight mass spectrometry (UHPLC/TOF-MS)-based lipidomics method to analyze the global lipid profiles of hypothyroidism in rat cerebellum. Using unsupervised analysis and multivariate statistical analysis, we separated the Sham and hypothyroid groups clearly and screened out 23 potential lipid biomarkers related to hypothyroidism that were primarily involved in sphingolipid metabolism, glycerophospholipid metabolism and β-oxidation of fatty acid. Subsequently, we conducted computational analysis to build and simulate the lipid network of hypothyroidism, knowing that it would be useful to elucidate the pathological mechanism of hypothyroidism. Based on the selected 23 lipid biomarkers, we systematically evaluated the therapeutic effects of Sini decoction (SND) and the positive drug T4. The results showed that both SND and T4 can to some extent convert the pathological status of hypothyroidism through different pathways. Overall, this investigation illustrates that lipidomic profiling approach is powerful in giving a complementary view to the pathophysiology of hypothyroidism and offers a valuable tool for systematic study of the therapeutic effects of SND on hypothyroidism at lipid level.
甲状腺功能减退症与脂质代谢密切相关。虽然我们之前的血清和尿液代谢组学研究已经为甲状腺功能减退症的代谢水平的分子机制提供了一些线索,但甲状腺功能减退症发病机制的确切机制仍不清楚,特别是在脂质代谢方面。在本研究中,我们应用超高效液相色谱/飞行时间质谱(UHPLC/TOF-MS)-基于脂质组学的方法分析大鼠小脑甲状腺功能减退症的全局脂质谱。通过无监督分析和多变量统计分析,我们清楚地分离了 Sham 和甲状腺功能减退症组,并筛选出 23 种与甲状腺功能减退症相关的潜在脂质生物标志物,这些生物标志物主要涉及鞘脂代谢、甘油磷脂代谢和脂肪酸的β氧化。随后,我们进行了计算分析以构建和模拟甲状腺功能减退症的脂质网络,我们知道这将有助于阐明甲状腺功能减退症的病理机制。基于选定的 23 种脂质生物标志物,我们系统地评估了四逆汤(SND)和阳性药物 T4 的治疗效果。结果表明,SND 和 T4 均可通过不同途径在一定程度上改变甲状腺功能减退症的病理状态。总的来说,这项研究表明,脂质组学分析方法在补充甲状腺功能减退症的病理生理学方面具有强大的作用,并为系统研究 SND 对甲状腺功能减退症的治疗效果提供了有价值的工具。