Silver ions,
delivered to a wound surface appear to decrease excess
surface and matrixs metallo protease (MMPs) activity.
Excess proteinase activity is now considered to be a
major cause of impaired healing by destroying new tissue
and growth factors. There is an increased expression of
MMPs in a burn wound. This response may well be the
mechanism for the clinical observation that pure silver
delivery decreases inflammation and wound surface
exudate. A silver induced decrease in wound Zinc which
is required for MMP activity as well as oxidation of
sulfur bonds, would decrease MMP activity. The decrease
in zinc is likely due to the silver induced increase in
wound metallo thionein, a known binder of zinc.
The control of
inflammation and MMPs is essential as the proteases
not only degrade new tissue but also denature growth
factors. Natural tissue inhibitors of MMPs are
present but often do not increase sufficiently to
counteract an increase in MMPs. The result is
impaired healing.
Silver could be
looked at as a form of tissue proteinase inhibitor. In
addition, silver increases surface calcium ions possibly
via a calmodulin effect. Increased wound calcium
increases the rate of wound epithelial proliferation and
migration.
The
metalloproteinases (MMPs) are a family of proteases
present in wounds for the purpose of breaking down
damaged tissue (gelatin is denatured collagen)
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MMP's
involved in Wounds
-
collagenase
(MMP-1, MMP-8)
-
gelatinases
(MMP-2, MMP-9)
-
elastase
- MMP-13
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Characteristics
of MMP's
-
breakdown
collagen, elastin and matrix
-
should
be in balance with natural inhibitors and
with Growth Factors
-
can
degrade growth factors and also
wound tissue if in excess
-
dependent
on zinc to activate
-
need
sulfhydryl bonds
|
|
Mechanism
of Increased MMP's
-
increase
gene expression for production caused by
the burn
-
production
by neutrophils macrophages and fibroblasts
-
stimulated
production by oxidants released with a
burn
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