Research Article

Metabolomics Study of Resina Draconis on Myocardial Ischemia Rats Using Ultraperformance Liquid Chromatography/Quadrupole Time-of-Flight Mass Spectrometry Combined with Pattern Recognition Methods and Metabolic Pathway Analysis

Table 1

Identified plasma metabolite markers of MI rats.

NoRetention time (min) Exact massIDIdentified resultsMI versus sham*RD versus MI#ID versus MIΔPathway

11.23182.0813181.0739C00082L-tyrosinePhenylalanine, tyrosine, and tryptophan biosynthesis
210.20318.3007317.2930C12144PhytosphingosineSphingolipid metabolism
311.38302.3057301.2981C00836SphinganineSphingolipid metabolism
41.18204.1233203.1158C02571AcetylcarnitineFatty acid transportation
511.45346.3317345.0474C00942Cyclic GMPPurine metabolism
612.64330.3367329.0525C00575Cyclic AMPPurine metabolism
71.17118.0866117.0790C00183L-valineValine, leucine and isoleucine biosynthesis
812.76520.3408519.3325C04230, HMDB10386LPC(18:2)Phospholipids metabolism
913.28518.3227517.3168HMDB10388LPC(18:3)Phospholipids metabolism
1018.99121.0509120.0436HMDB01366PurinePurine metabolism
1114.81482.3243481.3173HMDB11130LPE(18:0)Phospholipids metabolism
1217.91780.5538779.5465C00157PC(18:4)Phospholipids metabolism
132.22166.0866165.0790C00079L-phenylalaninePhenylalanine, tyrosine, and tryptophan biosynthesis
144.16205.0977204.0965C00078L-tryptophanPhenylalanine, tyrosine, and tryptophan biosynthesis
1513.27496.3415495.3325C04230LPC(16:0)Phospholipids metabolism
1614.81504.3063503.3012HMDB11516LPE(20:3)Phospholipids metabolism
171.35203.053180.0634NA C6H12O6Unknown
1810.28274.2747273.2668C13915HexadecasphinganineSphingolipid metabolism
1912.77542.3228541.3168C04230, HMDB10397LPC(20:5)Phospholipids metabolism
201.18150.0584149.0511C00073MethionineAminoacyl-tRNA biosynthesis

↑ or represents the up- or downregulation of the metabolites in MI group compared with the sham group; ↑ or represents the significant up- or downregulation of the metabolites in resina-draconis (RD-) treated group compared with the MI group; ↑ or represents the significant up- or down-regulation of the metabolites in isosorbide dinitrate- (ID, positive control drug) treated group compared with the MI group.