Excessive matrix metalloproteinase activity in diabetes: inhibition by tetracycline analogues with zinc reactivity

Curr Med Chem. 2001 Feb;8(3):305-16. doi: 10.2174/0929867013373598.


Diabetes mellitus in rats is characterized by excessive activity of several matrix metalloproteinases (MMPs), notably collagenase(s) and gelatinase(s), in skin, gingiva, and other tissues. A number of tetracyclines (TCs), both antimicrobial compounds as well as chemically modified non-antimicrobial TC analogues (CMTs) are known to possess potent inhibitory activity against these enzymes. Three conventional antimicrobial TCs and six CMTs were used in this study. In vitro, doxycycline was shown to possess higher inhibitory capacity (i.e. lower IC(max)) against diabetic rat skin collagenase than either minocycline or tetracycline HCl. Addition of excess zinc partially reversed the proteinase inhibition by TCs. In vivo, using rats made diabetic with streptozotocin (STZ), oral administration of various TCs led to decreased weight loss and substantial reductions in the activity of both skin collagenase and skin gelatinase (primarily MMP-9, 92 kDa) without affecting blood glucose. Using an in vitro spectrophotometric technique, the Zn(++) reactivity of several CMTs was assessed and found to be positively related to the potency of these compounds as MMP inhibitors. One particular CMT (CMT-5, pyrazole analogue), which is neither antimicrobial nor capable of binding metal cations, did not inhibit the MMPs. TCs have potential utility in management of diabetic complications mediated by excessive activity of MMPs.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Collagen / metabolism
  • Collagenases / metabolism
  • Diabetes Mellitus, Experimental / enzymology*
  • Gelatinases / metabolism
  • Gingiva / enzymology
  • Male
  • Matrix Metalloproteinase Inhibitors
  • Matrix Metalloproteinases / metabolism*
  • Molecular Structure
  • Rats
  • Rats, Sprague-Dawley
  • Skin / enzymology
  • Structure-Activity Relationship
  • Tetracycline / pharmacology
  • Tetracyclines / chemistry
  • Tetracyclines / pharmacology*


  • Matrix Metalloproteinase Inhibitors
  • Tetracyclines
  • tetracycline CMT-3
  • tetracycline CMT-7
  • tetracycline CMT-8
  • 4-des-dimethylaminotetracycline
  • Collagen
  • Collagenases
  • Gelatinases
  • Matrix Metalloproteinases
  • Tetracycline