Patients undergoing long-term continuous ambulatory peritoneal dialysis (CA
PD) sometimes experience ultra-filtration failure. Mesothelial basement mem
brane thickening and the accumulation of submesothelial fibrotic tissue are
common features of the diseased peritoneum, Peritonitis can lead to ultraf
iltration failure, but the precise mechanism is not clear, The key enzymes
in extra-cellular matrix (ECM) remodeling, namely matrix metalloproteinases
(MMPs) and tissue inhibitors of metalloproteinases (TIMPs), are produced b
y human peritoneal mesothelial cells. Using peritoneal effluent from 13 CAP
D patients with peritonitis and 7 noninfected CAPD control individuals, we
examined MMP and TIMP activities by gelatin and reverse zymography. Latent
and activated types of MMP-2 and -9, and TIMP-1 and -2 were identified in p
eritoneal effluent (from all CAPD patients). Levels of latent and activated
type MMP-9, as well as of TIMP-1 activities were higher at the onset of pe
ritonitis than either during the recovery phase of peritonitis and/or in co
ntrol individuals. Activated MMP-9 activity positively correlated with leuk
ocyte numbers and IL-6 levels in peritoneal effluent. Activities of MMP-2 a
nd TIMP-2 in peritoneal effluent did not change between the onset of perito
nitis and recovery. We concluded that increased MMP-9 and TIMP-1 levels mig
ht be associated with peritoneal ECM remodeling during peritonitis. Copyrig
ht (C) 2001 S. Karger AG, Basel.