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Table 6 Inhibitory effects of quercetin, riboflavin, resveratrol, pterostilbene, morin hydrate and nicotinic acid with or without δ-tocotrienol on the secretion of TNF-α and production of nitric oxide by LPS-induced peritoneal macrophages from C57BL/6 mice 1

From: Inhibition of nitric oxide and inflammatory cytokines in LPS-stimulated murine macrophages by resveratrol, a potent proteasome inhibitor

NO

Assay mixture

Concentration

Serum concentration

Serum concentration

in μM

of TNF-α (pg/mL)

of nitric oxide (μM)

1

Medium + Cells = A

 

0

0

2

A + LPS (10 ng/well) = B

 

1098.87

28.89

3

B + 0.2 % DMSO2 = C

 

1056.23 (100)3

28.54 (100)3

4

C + δ-Tocotrienol = D

5.0

674.56 (64)

18.98 (67)

5

C + Quercetin

40.0

589.98 (56)

20.43 (72)

6

C + Riboflavin

40.0

502.87 (58)

22.54 (79)

7

C + Resveratrol

40.0

542.76 (51)

17.56 (61)

8

C + Pterostilbene

40.0

567.34 (54)

16.87 (59)

9

C + Morin hydrate

40.0

597.42 (57)

19.65 (69)

10

C + Nicotinic acid

40.0

727.71 (69)

23.89 (84)

11

B + 0.2 % DMSO = C

 

1062.45 (100)

27.98 (100)

12

D + Quercetin

40.0

432.87 (41)

14.76 (53)

13

D + Riboflavin

40.0

465.21 (44)

17.43 (62)

14

D + Resveratrol

40.0

346.76 (33)

12.67 (45)

15

D + Pterostilbene

40.0

412.45 (39)

13.25 (47)

16

D + Morin hydrate

40.0

432.67 (41)

15.32 (55)

17

D + Nicotinic acid

40.0

588.56 (55)

18.96 (68)

  1. 1Thioglycolate-elicited peritoneal macrophages from 8-week-old C57BL/6 mice were pre treated with quercetin, riboflavin, resveratrol, pterostilbene, morin hydrate, or nicotinic acid (40 μM) with or without δ-tocotrienol (5 μM) for 1 h, followed by treatment with LPS (10 ng/well). After 4 h (TNF-α) or 36 h (NO) of LPS challenge, supernatants were collected and assayed for TNF-α and NO, respectively. Cell viability was >95% in all the treatments.
  2. 2DMSO = dimethyl sulfuoxide.
  3. 3Percentages based on actual values of TNF-α (pg/mL) and NO (μM), compared to controls, are in parentheses.