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Table 2 Collagen formation in 3T3-Swiss fibroblasts (n = 3, ± SD). Cells were incubated for 48 hr with bovine serum albumin alone as control or bovine serum albumin-soap loaded fatty acids (25 μM). The wound was then created and the medium was then replaced with fresh fatty acid enriched medium containing 50 μM ascorbic acid and 5 μCi of 3H-proline with or without lipopolysaccharide (LPS, 10 μg/ml) and NG-nitro-L-arginine methyl ester (L-NAME, 100 nM). A duplicate set of plates was made without wounding. Cells were harvested at 24 hr post wounding and assayed for collagen, total protein and DNA. The amount of collagen is expressed as DPM from 3H-proline per μg of DNA. Mean values within rows having different superscripts are significantly different (P < 0.05) by 1-way ANOVA and Tukey test. EPA, eicosapentaenoic acid; AA, arachidonic acid; LPS, lipopolysaccharide; L-NAME, NG-nitro-L-arginine methyl ester.

From: Inducible nitric oxide synthase links NF-κB to PGE2 in polyunsaturated fatty acid altered fibroblast in-vitro wound healing

Treatments

Collagen production (CP) (DPM/μg DNA amount)

Collagen as a percentage of total protein (C-PTP) (%)

Control

2419.6 ± 318.1a

18.7 ± 1.6a

Wound

3044.8 ± 269.2b

21.8 ± 1.5b

LPS

3953.3 ± 57.3c

26.5 ± 0.8c

L-NAME

1225.6 ± 270.7d

11.4 ± 2.7d

LPS + Wound

2650.3 ± 146.9ab

19.0 ± 1.8ab

LPS + L-NAME

5393.7 ± 583.4e

37.5 ± 3.3e

LPS + L-NAME + EPA

6580.2 ± 418.3e

42.4 ± 5.6e

LPS + L-NAME + AA

3511.3 ± 561.4c

26.7 ± 4.0c