Difference between revisions of "Hroudova 2013 Mitochondrion"
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|tissues=Blood cells, Platelet | |tissues=Blood cells, Platelet | ||
|preparations=Intact cells, Permeabilized cells | |preparations=Intact cells, Permeabilized cells | ||
|couplingstates=LEAK, ROUTINE, OXPHOS, | |couplingstates=LEAK, ROUTINE, OXPHOS, ET | ||
|pathways=N, S, NS, ROX | |pathways=N, S, NS, ROX | ||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
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Revision as of 14:40, 13 November 2017
Hroudová J, Fišar Z, Kitzlerová E, Zvěřová M, Raboch J (2013) Mitochondrial respiration in blood platelets of depressive patients. Mitochondrion 13:795-800. |
Hroudova J, Fisar Z, Kitzlerova E, Zverova M, Raboch J (2013) Mitochondrion
Abstract: Recent evidences include mitochondrial dysfunctions in pathophysiology of mood disorders. We examined association between depressive disorders and mitochondrial respiration using both intact and permeabilized blood platelets. In intact platelets, physiological respiration, maximal capacity of electron transport system and respiratory rate after Complex I inhibition were decreased in depressive patients, who reached partial remission, compared to healthy controls. Respiratory rates were unchanged in several respiratory states in permeabilized platelets. Results indicate that changes in respiratory rate in intact platelets can be used as biological marker of depressive disorder. Hypothesis was supported that decreased mitochondrial respiratory rate participate in pathophysiology of depression. • Keywords: Blood platelet, Depressive disorder, Mitochondrion, Respiratory rate
• O2k-Network Lab: CZ Prague Fisar Z
Labels: MiParea: Respiration, mt-Medicine
Stress:Mitochondrial disease Organism: Human Tissue;cell: Blood cells, Platelet Preparation: Intact cells, Permeabilized cells
Coupling state: LEAK, ROUTINE, OXPHOS, ET
Pathway: N, S, NS, ROX
HRR: Oxygraph-2k