Clinical Pharmaceutical Research Institute, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China.
J Pharm Biomed Anal. 2012 Nov;70:534-8. doi: 10.1016/j.jpba.2012.04.032. Epub 2012 May 10.
Depression is frequently comorbid with cardiovascular diseases (CVDs), but a full understanding of the mechanisms is still on its way. Chronic unpredictable mild stress (CUMS) model is a commonly used model to mimic clinical depression, here we present a GC/MS-based metabolic profiling approach to investigate myocardial metabolic changes of CUMS SD rats. Principal Component Analysis (PCA) and Partial Least Squares-Discriminant Analysis (PLS-DA) were utilized to reveal differences between the model and control group. This study found that molecules proved cardioprotective involving glutamine (P=0.019) and inosine (P=0.013), fatty acid (9,12-octadecadienoic acid, P=0.002; hexadecanoic acid, P=0.006; octadecanoic acid, P=0.030) which serve as the major energy source of heart and collagen molecule precursor proline (P=0.036) had down-regulated in CUMS model group.
抑郁症常与心血管疾病(CVDs)共存,但对其机制的全面理解仍在进行中。慢性不可预测轻度应激(CUMS)模型是一种常用于模拟临床抑郁症的模型,在这里我们提出了一种基于 GC/MS 的代谢组学方法来研究 CUMS SD 大鼠的心肌代谢变化。主成分分析(PCA)和偏最小二乘判别分析(PLS-DA)用于揭示模型组和对照组之间的差异。这项研究发现,涉及谷氨酰胺(P=0.019)和肌苷(P=0.013)的分子被证明具有心脏保护作用,脂肪酸(9,12-十八碳二烯酸,P=0.002;十六烷酸,P=0.006;十八烷酸,P=0.030)是心脏的主要能量来源,胶原蛋白分子前体脯氨酸(P=0.036)在 CUMS 模型组中下调。