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. 2021 Jun 15;26(12):3652. doi: 10.3390/molecules26123652

Table 5.

Effect of R. albiflorum essential oils and component compounds on agonist-induced functional responses in human neutrophils and microglial cells.

Essential Oil or Pure Compound FPR1- HL60 a FPR2- HL60 b C20 Cells a Neutro-phils a Neutrophils c
Ca2+ Influx Chemotaxis
IC50 (µg/mL)
REOLv 12.3 ± 2.5 7.6 ± 2.3 8.0 ± 0.1 2.7 ± 0.6 3.3 ± 0.5
REOFl N.A. N.A. N.A. N.A. N.A.
Composition (%)
REOLv REOFl IC50 (µM)
β-Phellandrene 0 8.9 N.A. N.A. N.A. N.A. N.A.
Viridiflorol 22.0 1.2 19.5 ± 4.7 10.7 ± 3.8 22.6 ± 3.1 7.8 ± 2.3 18.3 ± 4.1
Spathulenol 14.4 0.3 32.2 ± 6.4 31.6 ± 5.3 9.8 ± 3.4 36.2 ± 8.2 4.9 ± 0.8
Curzerene 17.8 2.2 21.8 ± 6.1 16.7 ± 5.5 30.7 ± 4.4 11.0 ± 3.8 37.9 ± 2.2
Germacrone 3.3 0 27.7 ± 2.9 25.0 ± 7.2 10.7 ± 2.3 27.9 ± 8.9 8.5 ± 0.6

a Ca2+ influx was induced by 5 nM fMLF in HL60-FPR1 cells and primary human neutrophils or 10 μM fMLF in human C20 microglial cells. b Ca2+ influx was induced by 5 nM WKYMVM in HL60-FPR2 cells. c Neutrophil chemotaxis was induced by 1 nM fMLF. N.A. indicates the samples had essentially no activity (IC50 > 50 µM or > 50 µg/mL). The data are presented as the mean ± SD of three independent experiments.