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pubmed-article:9350650pubmed:abstractTextThe effect of glycine on hypoxia- and ionomycin-induced increases in calpain activity in rat proximal tubules was determined. Calpain activity was determined both in vitro and in the intact cell using the fluorescent substrate N-succinyl-Leu-Leu-Val-Tyr-7-amido-4-methyl coumarin (N-succinyl-Leu-Leu-Val-Tyr-AMC) and Western blotting for calpain-specific spectrin breakdown products (BDP), respectively. At 7.5 minutes of hypoxia (prelethal injury model) there was a significant (10-fold) increase in in vitro calpain activity that was not inhibited by glycine. At 15 minutes of hypoxia (postlethal injury model) there was a further increase in calpain activity that was inhibited by glycine. Normoxic tubules incubated with the calcium ionophore ionomycin (5 microM) for two minutes and 10 minutes had a significant increase in calpain activity that was not inhibited by glycine. After 15 minutes of hypoxia in the presence of glycine, there was an increase in calpain-specific spectrin breakdown products (BDP) in both Triton X-100 soluble and cytosolic extracts from proximal tubules. Glycine in concentrations up to 10 mM had no direct effect on the in vitro calpain activity of purified calpains. The present study demonstrates that: (1) prelethal increases in calpain activity stimulated by hypoxia and ionomycin treatment are not affected by glycine; (2) calpain-mediated spectrin breakdown during hypoxia occurs in the presence of glycine; (3) glycine does prevent the additional postlethal increase in calpain activity probably by maintaining membrane integrity to calcium influx.lld:pubmed
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pubmed-article:9350650pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:9350650pubmed:articleTitleEffect of glycine on prelethal and postlethal increases in calpain activity in rat renal proximal tubules.lld:pubmed
pubmed-article:9350650pubmed:affiliationDepartment of Medicine, University of Colorado School of Medicine, Denver, USA.lld:pubmed
pubmed-article:9350650pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9350650pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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