Abstract
It has been described that dietary cysteine reverses many of the beneficial changes induced by methionine restriction in aging rodents. In this investigation male Wistar rats were subjected to diets low in methionine, supplemented with cysteine, or simultaneously low in methionine and supplemented with cysteine. The results obtained in liver showed that cysteine supplementation reverses the decrease in mitochondrial ROS generation induced by methionine restriction at complex I. Methionine restriction also decreased various markers of oxidative and non-oxidative stress on mitochondrial proteins which were not reversed by cysteine. Instead, cysteine supplementation also lowered protein damage in association with decreases in mTOR activation. The results of the present study add the decrease in mitochondrial ROS production to the various beneficial changes induced by methionine restriction that are reversed by cysteine dietary supplementation.
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Abbreviations
- AIF:
-
Apoptosis-inducing factor
- CEL:
-
Carboxyethyl-lysine
- CML:
-
Carboxymethyl-lysine
- CMC:
-
S-(carboxymethyl)-cysteine
- ERK:
-
Extracellular-signal regulated kinase
- GSA:
-
Glutamic semialdehyde
- MDA:
-
Malondialdehyde-lysine
- MetR:
-
Methionine restriction
- mitROSp:
-
Mitochondrial ROS production
- mTOR:
-
Mammalian target of rapamycin
- ROS:
-
Reactive oxygen species
- SC:
-
Succinyl-cysteine
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Acknowledgments
This investigation was supported by grants from the Spanish Ministry of Economy and Competitiveness (BFU2009-118/79BFI, RD12/0043/0018, PI1300584, and PI1400328), and the Autonomous Government of Catalonia (2014SGR168) to R. Pamplona; and from the Spanish Ministry of Economy and Competitiveness (BFU 2011-23888) to G. Barja. A. Gomez received a pre-doctoral fellowship from the Spanish Government.
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Gomez, A., Gomez, J., Torres, M.L. et al. Cysteine dietary supplementation reverses the decrease in mitochondrial ROS production at complex I induced by methionine restriction. J Bioenerg Biomembr 47, 199–208 (2015). https://doi.org/10.1007/s10863-015-9608-x
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DOI: https://doi.org/10.1007/s10863-015-9608-x