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Effects of oxidative alcohol metabolism on the mitochondrial permeability transition pore and necrosis in a mouse model of alcoholic pancreatitis.
- Source :
-
Gastroenterology [Gastroenterology] 2013 Feb; Vol. 144 (2), pp. 437-446.e6. Date of Electronic Publication: 2012 Oct 24. - Publication Year :
- 2013
-
Abstract
- Background & Aims: Opening of the mitochondrial permeability transition pore (MPTP) causes loss of the mitochondrial membrane potential (ΔΨm) and, ultimately, adenosine triphosphate depletion and necrosis. Cells deficient in cyclophilin D (CypD), a component of the MPTP, are resistant to MPTP opening, loss of ΔΨm, and necrosis. Alcohol abuse is a major risk factor for pancreatitis and is believed to sensitize the pancreas to stressors, by poorly understood mechanisms. We investigated the effects of ethanol on the pancreatic MPTP, the mechanisms of these effects, and their role in pancreatitis.<br />Methods: We measured ΔΨm in mouse pancreatic acinar cells incubated with ethanol alone and in combination with physiologic and pathologic concentrations of cholecystokinin-8 (CCK). To examine the role of MPTP, we used ex vivo and in vivo models of pancreatitis, induced in wild-type and CypD(-/-) mice by a combination of ethanol and CCK.<br />Results: Ethanol reduced basal ΔΨm and converted a transient depolarization, induced by physiologic concentrations of CCK, into a sustained decrease in ΔΨm, resulting in reduced cellular adenosine triphosphate and increased necrosis. The effects of ethanol and CCK were mediated by MPTP because they were not observed in CypD(-/-) acinar cells. Ethanol and CCK activated MPTP through different mechanisms-ethanol by reducing the ratio of oxidized nicotinamide adenine dinucleotide to reduced nicotinamide adenine dinucleotide, as a result of oxidative metabolism, and CCK by increasing cytosolic Ca(2+). CypD(-/-) mice developed a less-severe form of pancreatitis after administration of ethanol and CCK.<br />Conclusions: Oxidative metabolism of ethanol sensitizes pancreatic mitochondria to activate MPTP, leading to mitochondrial failure; this makes the pancreas susceptible to necrotizing pancreatitis.<br /> (Copyright © 2013 AGA Institute. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Acinar Cells drug effects
Acinar Cells metabolism
Acinar Cells pathology
Animals
Disease Models, Animal
Ethanol toxicity
Membrane Potential, Mitochondrial drug effects
Mice
Mitochondria drug effects
Mitochondria pathology
Mitochondrial Permeability Transition Pore
Pancreas drug effects
Pancreas metabolism
Pancreas pathology
Pancreatitis, Acute Necrotizing etiology
Pancreatitis, Acute Necrotizing pathology
Pancreatitis, Alcoholic complications
Pancreatitis, Alcoholic pathology
Ethanol pharmacokinetics
Mitochondria metabolism
Mitochondrial Membrane Transport Proteins metabolism
Oxidative Stress
Pancreatitis, Acute Necrotizing metabolism
Pancreatitis, Alcoholic metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1528-0012
- Volume :
- 144
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Gastroenterology
- Publication Type :
- Academic Journal
- Accession number :
- 23103769
- Full Text :
- https://doi.org/10.1053/j.gastro.2012.10.037