Cyclooxygenase-2 inhibitors modulate skin aging in a catalytic activity-independent manner

Exp Mol Med. 2012 Sep 30;44(9):536-44. doi: 10.3858/emm.2012.44.9.061.

Abstract

It has been proposed that the pro-inflammatory catalytic activity of cyclooxygenase-2 (COX-2) plays a key role in the aging process. However, it remains unclear whether the COX-2 activity is a causal factor for aging and whether COX-2 inhibitors could prevent aging. We here examined the effect of COX-2 inhibitors on aging in the intrinsic skin aging model of hairless mice. We observed that among two selective COX-2 inhibitors and one non-selective COX inhibitor studied, only NS-398 inhibited skin aging, while celecoxib and aspirin accelerated skin aging. In addition, NS-398 reduced the expression of p53 and p16, whereas celecoxib and aspirin enhanced their expression. We also found that the aging-modulating effect of the inhibitors is closely associated with the expression of type I procollagen and caveolin-1. These results suggest that pro-inflammatory catalytic activity of COX-2 is not a causal factor for aging at least in skin and that COX-2 inhibitors might modulate skin aging by regulating the expression of type I procollagen and caveolin-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aspirin / administration & dosage
  • Catalysis
  • Caveolin 1 / genetics
  • Caveolin 1 / metabolism
  • Celecoxib
  • Collagen Type I / genetics
  • Collagen Type I / metabolism
  • Cyclooxygenase 2 Inhibitors / administration & dosage*
  • Cyclooxygenase 2* / metabolism
  • Cyclooxygenase 2* / physiology
  • Gene Expression Regulation
  • Mice
  • Nitrobenzenes / administration & dosage*
  • Pyrazoles / administration & dosage
  • Skin Aging / drug effects*
  • Skin Aging / physiology
  • Sulfonamides / administration & dosage*
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Caveolin 1
  • Collagen Type I
  • Cyclooxygenase 2 Inhibitors
  • Nitrobenzenes
  • Pyrazoles
  • Sulfonamides
  • Tumor Suppressor Protein p53
  • N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide
  • Cyclooxygenase 2
  • Celecoxib
  • Aspirin