AI Article Synopsis

  • The study investigated how different dietary fats affect mitochondrial membrane lipids during calorie restriction (CR) in mice.
  • Mice on CR showed changes in reactive oxygen species (ROS) production and proton leak based on the type of dietary fat consumed, specifically with fish oil showing lower ROS and increased proton leak compared to other fats.
  • The findings suggest that the fatty acid composition from dietary sources influences mitochondrial function and enzyme activities during CR, with notable differences among the types of fats tested.

Article Abstract

To investigate the role mitochondrial membrane lipids play in the actions of CR (calorie restriction), C57BL/6 mice were assigned to four groups (control and three 40% CR groups) and the CR groups were fed diets containing soya bean oil (also in the control diet), fish oil or lard. The fatty acid composition of the major mitochondrial phospholipid classes, proton leak and H(2)O(2) production were measured in liver mitochondria following 1 month of CR. The results indicate that mitochondrial phospholipid fatty acids reflect the PUFA (polyunsaturated fatty acid) profile of the dietary lipid sources. CR significantly decreased the capacity of ROS (reactive oxygen species) production by Complex III but did not markedly alter proton leak and ETC (electron transport chain) enzyme activities. Within the CR regimens, the CR-fish group had decreased ROS production by both Complexes I and III, and increased proton leak when compared with the other CR groups. The CR-lard group showed the lowest proton leak compared with the other CR groups. The ETC enzyme activity measurements in the CR regimens showed that Complex I activity was decreased in both the CR-fish and CR-lard groups. Moreover, the CR-fish group also had lower Complex II activity compared with the other CR groups. These results indicate that dietary lipid composition does influence liver mitochondrial phospholipid composition, ROS production, proton leak and ETC enzyme activities in CR animals.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522480PMC
http://dx.doi.org/10.1042/BSR20120060DOI Listing

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