Research Article

Study on the Mechanism of Qing-Fei-Shen-Shi Decoction on Asthma Based on Integrated 16S rRNA Sequencing and Untargeted Metabolomics

Table 3

Differential metabolites in asthmatic mice after the treatment of QFSS.

No.FormulaRT (min)m/zMetabolitesVIPFCTrendPathway
M vs. CQ vs. MM vs. CQ vs. MM vs. CQ vs. M

1C11H20O212.77183.14Methyl 10-undecenoate1.341.341.510.60##
2C26H52NO7P15.01520.341-Oleoyl-Sn-glycero-3-phosphocholine2.301.010.501.46##e
3C13H14N2O48.29263.102-(Acetylamino)-3-[4-(acetylamino)phenyl]acrylic acid1.981.500.501.96#
4C9H12N2O51.61227.072-Deoxyuridine1.331.010.632.37##d
5C11H18N2O28.96211.143-(2-Methylpropyl)-octahydropyrrolo[1,2-a]pyrazine-1,4-dione2.511.400.411.89##
6C6H13NO21.37132.103-Amino-4-methylpentanoic acid2.141.660.561.82##
7C13H14O510.02251.094-(3,4-Dihydro-2H-1,5-benzodioxepin-7-yl)-4-oxobutanoic acid1.751.670.463.03#
8C5H11N3O21.41146.094-Guanidinobutyric acid2.451.670.243.40##a
9C27H44O214.05401.347-Ketocholesterol1.471.231.440.69#
10C9H17NO41.42204.12Acetyl-L-carnitine1.301.351.280.72#
11C13H14O510.02233.08Citrinin1.751.660.453.12#
12C6H12N2O31.40161.09D-Ala-D-Ala2.331.210.371.89#
13C6H13O9P1.20259.02D-Glucose6-phosphate1.281.086.050.34#c
14C18H32O161.44503.16D-Raffinose1.951.100.166.36##
15C9H7N10.55130.06Isoquinoline1.541.690.502.63#
16C6H12O51.40165.08L-Fucose1.731.379.140.26##
17C5H11NO3S1.32166.05L-Methionine sulfoxide1.692.080.681.84##
18C5H12N2O21.33131.08L-Ornithine1.811.828.100.53##a, b
19C23H46NO7P14.32480.31LysoPC (15 : 1)1.091.730.791.61#e
20C24H48NO7P14.50492.31LysoPC (16 : 1)2.051.540.561.76#e
21C26H48NO7P14.40516.31LysoPC (18 : 3)1.861.450.591.76#e
22C26H46NO7P14.06516.31LysoPC (18 : 4)1.521.830.622.30#e
23C28H56NO7P15.53608.39LysoPC (20 : 1)1.871.000.731.23#e
24C28H54NO7P15.26606.38LysoPC (20 : 2)2.321.250.621.40##e
25C24H48NO9P14.82524.30LysoPS (18 : 0)1.871.590.442.50#
26C11H11NO210.55190.09Methyl indole-3-acetate1.501.560.522.45#
27C20H40NO412.97358.29O-acylcarnitine1.581.671.670.51#
28C32H64NO7P16.56606.45PC (14 : 1e/10 : 0)1.192.040.761.73##
29C43H76NO8P16.57764.53PE (18 : 1/20 : 4)1.711.342.110.40##e
30C11H16N2O29.34209.13Pilocarpine2.801.340.451.66##
31C5H9NO21.39116.07Proline1.321.851.750.49#a
32C4H4N2O21.54113.03Uracil1.951.360.562.06##d
33C9H12N2O61.62243.06Uridine1.841.090.532.02##d
34C8H16N2O41.40205.12Val-ser1.751.590.581.97#
35C10H14N2O61.40259.092′-O-Methyluridine1.941.450.292.15#
36C19H20O31.56297.14Cryptotanshinone1.971.250.521.74#
37C24H50NO7P14.47496.34PC (14 : 0e/2 : 0)1.461.4421.810.16#
38C11H15N5O41.40282.121-Methyladenosine1.571.580.651.59
39C8H7NO4S6.56212.003-Indoxyl sulphate1.781.820.483.00
40C18H34O414.35315.259,10-Dihome2.001.671.900.48
41C22H28N2O12.33342.26Fentanyl-d51.341.721.840.43
42C22H46NO7P14.35526.31LysoPC (14 : 0)1.441.550.741.60e
43C10H14O412.15181.09Modiolide G1.201.240.651.91

Control, model, and HD-QFSS groups (n = 6 per group). RT, retention time; VIP, variable importance of projection; FC, fold change; ↑: content increased; ↓: content decreased; vs., versus; C, control group; M, model group; Q, HD-QFSS group; PC, phosphatidylcholine; PE, phosphatidylethanolamine; PS, phosphatidylserine. # compared with the control group. ## compared with the control group; compared with the model group; compared with the model group. a, arginine and proline metabolism; b, arginine biosynthesis; c, starch and sucrose metabolism; d, pyrimidine metabolism; e, glycerophospholipid metabolism. The bold text in “pathway” column indicates the pathway which the metabolite related with. a: arginine and proline metabolism; b: arginine biosynthesis; c: starch and sucrose metabolism; d: pyrimidine metabolism; e: glycerophospholipid metabolism.