Article Text
Abstract
BACKGROUND The pathogenesis of non-steroidal anti-inflammatory drug (NSAID) enteropathy is complex. It involves uncoupling of mitochondrial oxidative phosphorylation which alters the intercellular junction and increases intestinal permeability with consequent intestinal damage. Metronidazole diminishes the inflammation induced by indomethacin but the mechanisms remain speculative. A direct effect on luminal bacteria has traditionally been thought to account for the protective effect of metronidazole. However, a protective effect of metronidazole on mitochondrial oxidative phosphorylation has never been tested.
AIMS To assess the protective effect of metronidazole on mitochondrial uncoupling induced by indomethacin and also on the increased intestinal permeability and macroscopic damage.
MATERIAL AND METHODS The protective effect of metronidazole was evaluated in rats given indomethacin; a macroscopic score was devised to quantify intestinal lesions, and intestinal permeability was measured by means of 51Cr-ethylenediaminetetraacetic acid. The protective effect of metronidazole against mitochondrial uncoupling induced by indomethacin was assessed using isolated coupled rat liver mitochondria obtained from rats pretreated with metronidazole or saline.
RESULTS Metronidazole significantly reduced the macroscopic intestinal damage and increase in intestinal permeability induced by indomethacin; furthermore, at the mitochondrial level, it significantly reduced the increase in oxygen consumption in state 4 induced by indomethacin and caused less reduction of the respiratory control rate.
CONCLUSION Our study confirmed the beneficial effects of metronidazole on intestinal damage and intestinal permeability, and demonstrated, for the first time, a direct protective effect of metronidazole on uncoupling of mitochondrial oxidative phosphorylation caused by NSAIDs.
- uncoupling agents
- intestinal permeability
- enteropathy
- non-steroidal anti-inflammatory drugs
- metronidazole
- indomethacin
- rats
Abbreviations used in this paper
- NSAIDs
- non-steroidal anti-inflammatory drugs
- DMSO
- dimethyl sulphoxide
- 51Cr-EDTA
- 51Cr-ethylenediaminetetraacetic acid
- EGTA
- ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid
- HEPES
- N-(2-hydroxyethyl)piperazine-N′- (2-ethanesulphonic acid)
- RCR
- respiratory control rate
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- uncoupling agents
- intestinal permeability
- enteropathy
- non-steroidal anti-inflammatory drugs
- metronidazole
- indomethacin
- rats
Abbreviations used in this paper
- NSAIDs
- non-steroidal anti-inflammatory drugs
- DMSO
- dimethyl sulphoxide
- 51Cr-EDTA
- 51Cr-ethylenediaminetetraacetic acid
- EGTA
- ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid
- HEPES
- N-(2-hydroxyethyl)piperazine-N′- (2-ethanesulphonic acid)
- RCR
- respiratory control rate