Stimulation of cytosolic and mitochondrial calcium mobilization by indomethacin in Caco-2 cells: Modulation by the polyphenols quercetin,resveratrol and rutin |
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Authors: | Catalina Carrasco-Pozo Edgar Pastene Carola Vergara Moises Zapata Cristian Sandoval Martin Gotteland |
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Affiliation: | 1. Laboratory of Microbiology and Probiotics, Institute of Nutrition and Food Technology (INTA), University of Chile, Av. Macul 5540, Santiago, P.O. Box 138-11, Chile;2. Department of Nutrition, Faculty of Medicine, University of Chile, Independencia 1027, P.O. Box 13898, Chile;3. Laboratory of Pharmacognosy, Department of Pharmacy, Faculty of Pharmacy, University of Concepción, Concepción, P.O. Box 237, Chile;4. Laboratory of Antioxidants, Institute of Nutrition and Food Technology, University of Chile, Av. Macul 5540, Santiago, P.O. Box 138-11, Chile;5. Laboratory of Chromatography, Department of Instrumental Analysis, Faculty of Pharmacy, University of Concepción, Concepción, P.O. Box 237, Chile |
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Abstract: | BackgroundThe effect of indomethacin (INDO) on Ca2 + mobilization, cytotoxicity, apoptosis and caspase activation and the potential protective effect of quercetin (QUE), resveratrol (RES) and rutin (RUT) were determined in Caco-2 cells.MethodsCaco-2 cells were incubated with INDO in the presence or absence of QUE, RES or RUT. The concentrations of Ca2 + in the cytosol (Fluo-3 AM) and mitochondria (Rhod-2 AM) were determined as well as the cytotoxicity (MTT reduction and LDH leakage), apoptosis (TUNEL) and caspase-3 and 9 activities.ResultsINDO promoted Ca2 + efflux from the endoplasmic reticulum (ER), resulting in an early, but transient, increment of cytosolic Ca2 + at 3.5 min, followed by a subsequent increment of intra-mitochondrial Ca2 + at 24 min. INDO also induced cytotoxicity, apoptosis, and increased caspase activities and cytochrome c release. All these alterations were prevented by the inhibitors of the IP3R and RyR receptors, 2-Aminoethoxydiphenyl borate (2-APB) and dantrolene. QUE was the most efficient polyphenol in preventing Ca2 + mobilization induced by INDO and all of its consequences including cytotoxicity and apoptosis.ConclusionsIn Caco-2 cells, INDO stimulates ER Ca2 + mobilization, probably through the activation of IP3R and RyR receptors, and the subsequent entry of Ca2 + into the mitochondria. Polyphenols protected the cells against the Ca2 + mobilization induced by INDO and its consequences on cytotoxicity and apoptosis.General significanceThese results confirm the possibility of using polyphenols and particularly QUE for the protection of the gastroduodenal mucosa in subjects consuming NSAIDs. |
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Keywords: | 2-APB, 2-Aminoethoxydiphenyl borate QUE, quercetin RES, resveratrol RUT, rutin PPs, polyphenols IP3R, inositol trisphosphate receptors RyR, ryanodine receptors EGTA, ethylene glycol tetraacetic acid GI, gastrointestinal INDO, indomethacin MMP, mitochondrial membrane potential NSAID, nonsteroidal anti-inflammatory drug RFU, relative fluorescence unit mPTP, mitochondrial permeability transition pore ER, endoplasmic reticulum DMSO, dimethylsulphoxide SOCI, store-operated Ca2 + influx SOCC, Store-Operated Ca2 + Channel SERCA, Sarcoplasmic reticulum Ca2 + ATPase |
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