Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Difference between revisions of "Horvath 2012 Abstract Bioblast"

From Bioblast
Line 16: Line 16:
# [[Pesta 2012 Methods Mol Biol|Pesta D, Gnaiger E (2012) High-resolution respirometry. OXPHOS protocols for human cells and permeabilized fibres from small biopisies of human muscle. Methods Mol Biol 810: 25-58.]]
# [[Pesta 2012 Methods Mol Biol|Pesta D, Gnaiger E (2012) High-resolution respirometry. OXPHOS protocols for human cells and permeabilized fibres from small biopisies of human muscle. Methods Mol Biol 810: 25-58.]]
|keywords=Mitochondrial membrane potential, Cardiac muscle
|keywords=Mitochondrial membrane potential, Cardiac muscle
|mipnetlab=HU Budapest Tretter L, AT Innsbruck OROBOROS,
|mipnetlab=HU Budapest Tretter L, AT Innsbruck Oroboros ,
|journal=Mitochondr Physiol Network
|journal=Mitochondr Physiol Network
|articletype=Abstract
|articletype=Abstract

Revision as of 10:45, 23 January 2019

Horvath G, Eigentler A, Gnaiger E, Tretter L (2012) Respiratory substrate effects on mitochondrial membrane potential - experiments with mouse cardiac muscle homogenate. Mitochondr Physiol Network 17.12.

Link: MiPNet17.12 Bioblast 2012 - Open Access

Horvath G, Eigentler A, Gnaiger E, Tretter L (2012)

Event: Bioblast 2012

Gergรถ Horvath

Mitochondria play a key role in the pathogenesis of different diseases including the pathologies of the heart. According to the World Health Organization, chronic diseases are responsible for 63% of all deaths in the world, with cardiovascular disease as the leading cause of death. New findings of the cardiac muscle mitochondria functions can be further used to develop new therapeutic strategies.

The most important parameters of heart mitochondrial activity are oxidative phosphorylation capacity and mitochondrial membrane potential. With these two properties of mitochondria we can determine the coupling state of respiration and the impact of the mitochondrial substrate on the membrane potential [1]. The Fluorescence module for the Oxygraph-2k (Oroboros Instruments, Innsbruck) combines optical measurement with high-resolution respirometry and with this new technology it is possible to detect changes in both parameters simultaneously.

The experiments were carried out in mouse heart homogenate. The measurements were performed using the O2k. We detect the oxygen-consumption with a Clark-electrode and the membrane potential changes with safranin fluorescence dye at 480 nm. The experiments were carried out following SUIT protocols, with minor modifications [2]. We investigated Complex I and II and a combination of I+II in different coupling control levels.

  1. Brand MD, Nicholls DG (2011) Assessing mitochondrial dysfunction in cells (2011) 435: 297โ€“312. Open Access
  2. Pesta D, Gnaiger E (2012) High-resolution respirometry. OXPHOS protocols for human cells and permeabilized fibres from small biopisies of human muscle. Methods Mol Biol 810: 25-58.

โ€ข Keywords: Mitochondrial membrane potential, Cardiac muscle

โ€ข O2k-Network Lab: HU Budapest Tretter L, AT Innsbruck Oroboros


Labels: MiParea: Respiration 


Organism: Mouse  Tissue;cell: Heart  Preparation: Homogenate 


Coupling state: LEAK, OXPHOS, ET  Pathway: N, S, NS  HRR: Oxygraph-2k, O2k-Fluorometer 




Affiliations and author contributions

Horvath Gergoe (1), Eigentler Andrea (2), Gnaiger Erich (2,3), Tretter Laszlo (1)

(1) Department of Medical Biochemistry, Semmelweis University, Budapest, Hungary; Email: [email protected]

(2) Medical University of Innsbruck, Department of Visceral, Transplant and Thoracic Surgery, D. Swarovski Research Laboratory, Innsbruck, Austria

(3) Oroboros Instruments Corp, High Resolution Respirometry, Innsbruck, Austria


Help