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Dubouchaud 2018 MiPschool Tromso

From Bioblast
Dubouchaud Herve
AMPK deficiency elicits changes in OXPHOS in heart mitochondria.

Link: MitoEAGLE

Isola R, Dubouchaud H, Viollet B, Tokarska-Schlattner M, Schlattner U (2018)

Event: MiPschool Tromso-Bergen 2018


AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme, which is a sensor and regulator of the energetic state of the cell. Its activation results, among others, in increase of glucose uptake, mitochondrial fatty acid oxidation and mitochondria biogenesis. The role of AMPK for mitochondrial function in cardiac tissue has not been deeply investigated. The purpose of this study was to assess whether the loss of AMPK in heart induces any alterations in mitochondrial physiology and whether potential changes are gender specific. Heart-specific double (ฮฑ1 and ฮฑ2 subunits) AMPK deletion was obtained in a model of a conditional tamoxifen-inducible KO mouse. Experiments were carried out with heart mitochondria, isolated from control and KO mice, both male and female. Mitochondrial respiration was measured with a Clark-type electrode, with substrates for Complex I (glutamate, malate), II (succinate), IV (TMPD), as well as with palmitoyl carnitine and DNP as uncoupling agent. Enzymatic activities of complex I and carnitine palmitoyl transferase 1 and 2 were assessed by a spectrophotometric assay. In addition, markers of mitochondrial density, such as citrate synthase activity have been analyzed. Our results show that AMPK-deficiency results in defects in OXPHOS and altered mitochondrial mass, and that some of these changes are gender-specific. The data indicate that loss of cardiac AMPK has some consequences already observed for skeletal muscle, but also additional effects. In particular, they reveal sex-specific responses possibly related to gender-specific metabolic differences in the heart.

โ€ข Bioblast editor: Plangger M โ€ข O2k-Network Lab: FR Grenoble Schlattner U

Labels: MiParea: Respiration, mt-Biogenesis;mt-density, Genetic knockout;overexpression, Gender 

Organism: Mouse  Tissue;cell: Heart  Preparation: Isolated mitochondria 

Pathway: N, CIV, NS  HRR: Oxygraph-2k 


Isola R(1), Dubouchaud H(2), Viollet B(3), Tokarska-Schlattner M(2), Schlattner U(2)

  1. Dept Biological Sciences, Univ Cagliari, Italy
  2. Lab Fundamental and Applied Bioenergetics (LBFA), Univ Grenoble Alpes
  3. Inst Cochin, Univ Paris Descartes, Sorbonne Paris Citรฉ, Paris, France. โ€“


Short Scientific Mission (STSM) within the European Union Framework Programme Horizon 2020 COST Action CA15203 MitoEAGLE.