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Vol. 294, Issue 3, 1083-1087, September 2000
Department of Pharmacology and Toxicology, University of Arkansas
for Medical Sciences, Little Rock, Arkansas (J.F.H., S.W.-W., R.G.S.);
and School of Chemistry and Biochemistry, Georgia Institute of
Technology, Atlanta, Georgia (D.-L.C., J.C.P.)
Inhibitors of calpains, calcium-activated neutral proteases, protect
against cell death produced by anoxia and a variety of toxicants both
in vitro and in vivo. The problems with known calpain inhibitors are a
lack of specificity, low membrane permeability, and/or low potency. The
goal of this study was to determine the effects of seven novel
dipeptide and tripeptide calpain inhibitors on calpain activity and
antimycin A-induced cell death in rabbit renal proximal tubule (RPT)
suspensions. We chose the compounds based on their inhibitory constants
for µ- versus m-calpain, specificity of the inhibitors for calpain,
and membrane permeability. Only three of the compounds inhibited
calpain in RPT and were cytoprotective (Z-Leu-Phe-COOH,
Z-Leu-Abu-CONH-CH2-CH(OH)-Ph, and Z-Leu-Phe-CONH-Et). Interestingly, Z-Leu-Phe-COOEt,
Z-Leu-Abu-CONH-CH2-CH(OH)-C6F5, and
Z-Leu-Abu-CONH-CH2-2-quinolinyl were greater than 60%
cytoprotective but did not inhibit calpain in RPT.
Z-Leu-Abu-CONH(CH2)3-morpholine was neither
cytoprotective nor inhibited calpain. Although these results suggest
that six of the seven peptide calpain inhibitors are cell permeable,
only three of them inhibited calpain activity in RPT and were
cytoprotective. Their ability to inhibit calpain or produce
cytoprotection did not correlate with their ability to selectively
inhibit purified µ- or m-calpain. Thus it remains to be determined
whether they inhibit µ-calpain, m-calpain, or both in RPT. These
results also suggest that inhibition of other protease(s) in addition
to calpains may be responsible for the cytoprotective actions of some compounds.
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