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Difference between revisions of "Oliveira MF 2013 Abstract MiP2013"

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|year=2013
|event=MiP2013
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|abstract=Text
|abstract=Hematophagy poses a challenge to blood-feeding organisms since products of blood digestion can exert cellular deleterious effects. Mitochondria perform multiple roles in cell biology acting as the site of aerobic energy transducing pathways, and also an important source of reactive oxygen species (ROS), modulating redox metabolism. Our research group is currently investigating basic aspects of mitochondrial physiology in some hematophagous organisms that cause or transmit tropical diseases. The models currently investigated include the blood fluke Schistosoma mansoni, the mosquito Aedes aegypti and the kissing bug Rhodnius prolixus. In Aedes flight muscle mitochondria, we observed that blood intake caused a transient reduction in both oxygen consumption and hydrogen peroxide generation, which were parallel to blood digestion process, regardless the mitochondrial metabolic state. In the kissing bug Rhodnius, a transient reduction on flight muscle oxygen consumption was observed along the blood digestion cycle, without affecting hydrogen peroxide generation. Interestingly in Rhodnius, both parameters were profoundly affected by aging, causing a 75% inhibition of respiration and hydrogen peroxide production during state 3 in old insects. Maximum hydrogen peroxide production was also specifically affected by blood intake but not plasma. Sexual differences in oxygen consumption in Aedes flight muscle were also identified, being significantly higher in females than in males, regardless the substrate utilized. In this model, pyruvate and proline were the preferential substrates utilized to sustain oxygen consumption. Finally, in the blood fluke Schistosoma, where adult female worms digest ten times more blood than males, sexual differences in terms of respiratory capacity were also reported, where male worms exhibit higher mitochondrial oxygen consumption rates than females, regardless the substrates utilized. Curiously, in female worms, hydrogen peroxide production was higher than in males, whereas females were more resistant to oxidative challenge promoted by menadione than males. Concluding, the blood-feeding habit promotes functional and structural remodeling in mitochondria from hematophagous organisms, which may represent an important adaptation to this exquisite dietary source.
|mipnetlab=BR Rio de Janeiro Oliveira MF
}}
{{Labeling
|instruments=Oxygraph-2k
|injuries=RONS; Oxidative Stress, Aging; Senescence
|taxonomic group=Hexapods, Platyhelminthes
|tissues=Skeletal muscle
|couplingstates=OXPHOS
|substratestates=CI
}}
}}
{{Labeling}}
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__TOC__




== Affiliations and author contributions ==
== Affiliations and author contributions ==
1 - Institute of Medical Biochemistry, Federal University of Rio de Janeiro, Brazil.
Institute of Medical Biochemistry, Federal University of Rio de Janeiro, Brazil.


Email: maroli@bioqmed.ufrj.br
Email: maroli@bioqmed.ufrj.br
Financial support: CNPq, FAPERJ

Revision as of 06:56, 9 July 2013

Oliveira MF(2013) Comparative mitochondrial physiology in blood feeding insect vectors and parasites. Mitochondr Physiol Network 18.08.

Link:

Oliveira MF (2013)

Event: MiP2013

Hematophagy poses a challenge to blood-feeding organisms since products of blood digestion can exert cellular deleterious effects. Mitochondria perform multiple roles in cell biology acting as the site of aerobic energy transducing pathways, and also an important source of reactive oxygen species (ROS), modulating redox metabolism. Our research group is currently investigating basic aspects of mitochondrial physiology in some hematophagous organisms that cause or transmit tropical diseases. The models currently investigated include the blood fluke Schistosoma mansoni, the mosquito Aedes aegypti and the kissing bug Rhodnius prolixus. In Aedes flight muscle mitochondria, we observed that blood intake caused a transient reduction in both oxygen consumption and hydrogen peroxide generation, which were parallel to blood digestion process, regardless the mitochondrial metabolic state. In the kissing bug Rhodnius, a transient reduction on flight muscle oxygen consumption was observed along the blood digestion cycle, without affecting hydrogen peroxide generation. Interestingly in Rhodnius, both parameters were profoundly affected by aging, causing a 75% inhibition of respiration and hydrogen peroxide production during state 3 in old insects. Maximum hydrogen peroxide production was also specifically affected by blood intake but not plasma. Sexual differences in oxygen consumption in Aedes flight muscle were also identified, being significantly higher in females than in males, regardless the substrate utilized. In this model, pyruvate and proline were the preferential substrates utilized to sustain oxygen consumption. Finally, in the blood fluke Schistosoma, where adult female worms digest ten times more blood than males, sexual differences in terms of respiratory capacity were also reported, where male worms exhibit higher mitochondrial oxygen consumption rates than females, regardless the substrates utilized. Curiously, in female worms, hydrogen peroxide production was higher than in males, whereas females were more resistant to oxidative challenge promoted by menadione than males. Concluding, the blood-feeding habit promotes functional and structural remodeling in mitochondria from hematophagous organisms, which may represent an important adaptation to this exquisite dietary source.


β€’ O2k-Network Lab: BR Rio de Janeiro Oliveira MF


Labels:

Stress:RONS; Oxidative Stress"RONS; Oxidative Stress" is not in the list (Cell death, Cryopreservation, Ischemia-reperfusion, Permeability transition, Oxidative stress;RONS, Temperature, Hypoxia, Mitochondrial disease) of allowed values for the "Stress" property., Aging; Senescence"Aging; Senescence" is not in the list (Cell death, Cryopreservation, Ischemia-reperfusion, Permeability transition, Oxidative stress;RONS, Temperature, Hypoxia, Mitochondrial disease) of allowed values for the "Stress" property. 

Tissue;cell: Skeletal muscle 


Coupling state: OXPHOS 

HRR: Oxygraph-2k 



Affiliations and author contributions

Institute of Medical Biochemistry, Federal University of Rio de Janeiro, Brazil.

Email: maroli@bioqmed.ufrj.br

Financial support: CNPq, FAPERJ