{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,19]],"date-time":"2026-02-19T07:39:24Z","timestamp":1771486764933,"version":"3.50.1"},"reference-count":67,"publisher":"American Physiological Society","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American Journal of Physiology-Heart and Circulatory Physiology"],"published-print":{"date-parts":[[2008,7]]},"abstract":"<jats:p>Calpain activation is linked to the cleavage of several cytoskeletal proteins and could be an important contributor to the loss of cardiomyocytes and contractile dysfunction during cardiac pressure overload (PO). Using a feline right ventricular (RV) PO model, we analyzed calpain activation during the early compensatory period of cardiac hypertrophy. Calpain enrichment and its increased activity with a reduced calpastatin level were observed in 24- to 48-h-PO myocardium, and these changes returned to basal level by 1 wk of PO. Histochemical studies in 24-h-PO myocardium revealed the presence of TdT-mediated dUTP nick-end label (TUNEL)-positive cardiomyocytes, which exhibited enrichment of calpain and gelsolin. Biochemical studies showed an increase in histone H2B phosphorylation and cytoskeletal binding and cleavage of gelsolin, which indicate programmed cardiomyocyte cell death. To test whether calpain inhibition could prevent these changes, we administered calpeptin (0.6 mg\/kg iv) by bolus injections twice, 15 min before and 6 h after induction of 24-h PO. Calpeptin blocked the following PO-induced changes: calpain enrichment and activation, decreased calpastatin level, caspase-3 activation, enrichment and cleavage of gelsolin, TUNEL staining, and histone H2B phosphorylation. Although similar administration of a caspase inhibitor, N-benzoylcarbonyl-Val-Ala-Asp-fluoromethylketone (Z-VD-fmk), blocked caspase-3 activation, it did not alleviate other aforementioned changes. These results indicate that biochemical markers of cardiomyocyte cell death, such as sarcomeric disarray, gelsolin cleavage, and TUNEL-positive nuclei, are mediated, at least in part, by calpain and that calpeptin may serve as a potential therapeutic agent to prevent cardiomyocyte loss and preserve myocardial structure and function during cardiac hypertrophy.<\/jats:p>","DOI":"10.1152\/ajpheart.00085.2008","type":"journal-article","created":{"date-parts":[[2008,5,17]],"date-time":"2008-05-17T01:09:25Z","timestamp":1210986565000},"page":"H314-H326","source":"Crossref","is-referenced-by-count":48,"title":["In vivo administration of calpeptin attenuates calpain activation and cardiomyocyte loss in pressure-overloaded feline myocardium"],"prefix":"10.1152","volume":"295","author":[{"given":"Santhosh K.","family":"Mani","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hirokazu","family":"Shiraishi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sundaravadivel","family":"Balasubramanian","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kentaro","family":"Yamane","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Meenakshi","family":"Chellaiah","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"George","family":"Cooper","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Naren","family":"Banik","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael R.","family":"Zile","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dhandapani","family":"Kuppuswamy","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"24","reference":[{"key":"R1","doi-asserted-by":"publisher","DOI":"10.1038\/sj.jcbfm.9600043"},{"key":"R2","doi-asserted-by":"publisher","DOI":"10.1007\/s10741-007-9072-8"},{"key":"R3","doi-asserted-by":"publisher","DOI":"10.1074\/jbc.275.6.3761"},{"key":"R4","doi-asserted-by":"publisher","DOI":"10.1007\/BF00964996"},{"key":"R5","doi-asserted-by":"publisher","DOI":"10.1016\/S0006-8993(96)01302-9"},{"key":"R6","doi-asserted-by":"publisher","DOI":"10.1016\/S0167-4889(97)00068-2"},{"key":"R7","doi-asserted-by":"publisher","DOI":"10.1002\/jcp.20058"},{"key":"R8","doi-asserted-by":"publisher","DOI":"10.1038\/sj.emboj.7600280"},{"key":"R9","doi-asserted-by":"publisher","DOI":"10.1083\/jcb.147.3.619"},{"key":"R10","doi-asserted-by":"publisher","DOI":"10.1161\/01.RES.0000069364.24820.8B"},{"key":"R11","doi-asserted-by":"publisher","DOI":"10.1074\/jbc.M204951200"},{"key":"R12","doi-asserted-by":"publisher","DOI":"10.1016\/S0092-8674(03)00355-6"},{"key":"R13","doi-asserted-by":"publisher","DOI":"10.1002\/pmic.200401127"},{"key":"R14","doi-asserted-by":"publisher","DOI":"10.1016\/j.cardiores.2005.07.016"},{"key":"R16","doi-asserted-by":"publisher","DOI":"10.1161\/01.CIR.99.23.3071"},{"key":"R17","doi-asserted-by":"publisher","DOI":"10.1146\/annurev.med.48.1.13"},{"key":"R18","doi-asserted-by":"publisher","DOI":"10.1161\/01.RES.33.2.213"},{"key":"R19","doi-asserted-by":"publisher","DOI":"10.4161\/cc.6.2.3759"},{"key":"R20","doi-asserted-by":"publisher","DOI":"10.1016\/S0014-5793(00)01613-6"},{"key":"R21","doi-asserted-by":"crossref","unstructured":"Fox JE, Lipfert L, Clark EA, Reynolds CC, Austin CD, Brugge JS.On the role of the platelet membrane skeleton in mediating signal transduction. 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