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Difference between revisions of "Dela MiP2010"

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{{Publication
{{Abstract
|title=Kraunsoee R, Boushel R, Hansen CN, Schjerling P, Qvortrup K, Stoecke M, Mikines KJ, Dela F (2010) Mitochondrial respiration in subcutaneous and visceral adipose tissue from patients with morbid obesity. Mitochondr. Physiol. Network 15.6: 50-51.
|title=Kraunsoee R, Boushel RC, Hansen CN, Schjerling P, Qvortrup K, Stoecke M, Mikines KJ, Dela F (2010) Mitochondrial respiration in subcutaneous and visceral adipose tissue from patients with morbid obesity. Mitochondr Physiol Network 15.6:50-1.
|info=[http://www.mitophysiology.org/index.php?mip2010-session2 Abstracts Session 2]
|info=[http://www.mitophysiology.org/index.php?mip2010-session2 Abstracts Session 2]
|authors=Kraunsoee R, Boushel R, Hansen CN, Schjerling P, Qvortrup K, Stoecke M, Mikines KJ, Dela F
|authors=Kraunsoee R, Boushel RC, Hansen CN, Schjerling P, Qvortrup K, Stoecke M, Mikines KJ, Dela F
|year=2010
|year=2010
|journal=Mitochondr. Physiol. Network
|event=MiP2010
|mipnetlab=DK_Copenhagen_ DelaF, DK_Copenhagen_BoushelR
|abstract=Adipose tissue exerts important endocrine and metabolic functions in health and disease. Yet the bioenergetics of this tissue is not characterized in humans and possible regional differences are not elucidated. Using high-resolution respirometry, mitochondrial respiration was quantified in human abdominal subcutaneous and intra-abdominal, visceral (omentum majus) adipose tissue from biopsies obtained in twenty obese patients undergoing bariatric surgery. [[mtDNA]] and gDNA were determined by PCR technique for estimation of mitochondrial density. Adipose tissue samples were permeabilized and respirometric measurements were performed in duplicate at 37 °C. Substrates [glutamate(G) + malate(M) + octanoyl carnitine(Oct) + succinate(S)] were added sequentially to provide electrons to Complexes CI + CII. ADP (D) for [[State 3]] respiration was added after GM. Non-coupled respiration was measured after addition of FCCP. Visceral fat contained more mitochondria per mg tissue than subcutaneous fat, but the cells were smaller. Robust, stable oxygen fluxes were found in both tissues, and coupled State 3 (GMOctSD) and non-coupled respiration were significantly (''P''<0.05) higher in visceral (0.95±0.05 and 1.15±0.06 pmol O2∙s<sup>-1</sup>∙mg<sup>-1</sup>, respectively) compared with subcutaneous (0.76±0.04 and 0.98±0.05 pmol O2∙s<sup>-1</sup>∙mg<sup>-1</sup>, respectively) adipose tissue. Expressed per mtDNA, visceral adipose tissue had significantly (''P''<0.05) lower mitochondrial respiration. Substrate control ratios were higher and uncoupling control ratio lower (''P''<0.05) in visceral compared with subcutaneous adipose tissue.  
|abstract=Adipose tissue exerts important endocrine and metabolic functions in health and disease. Yet the bioenergetics of this tissue is not characterized in humans and possible regional differences are not elucidated. Using high-resolution respirometry, mitochondrial respiration was quantified in human abdominal subcutaneous and intra-abdominal, visceral (omentum majus) adipose tissue from biopsies obtained in twenty obese patients undergoing bariatric surgery. [[mtDNA]] and gDNA were determined by PCR technique for estimation of mitochondrial density. Adipose tissue samples were permeabilized and respirometric measurements were performed in duplicate at 37 °C. Substrates [glutamate(G) + malate(M) + octanoyl carnitine(Oct) + succinate(S)] were added sequentially to provide electrons to Complexes CI + CII. ADP (D) for [[State 3]] respiration was added after GM. Non-coupled respiration was measured after addition of FCCP. Visceral fat contained more mitochondria per mg tissue than subcutaneous fat, but the cells were smaller. Robust, stable oxygen fluxes were found in both tissues, and coupled State 3 (GMOctSD) and non-coupled respiration were significantly (''P''<0.05) higher in visceral (0.95±0.05 and 1.15±0.06 pmol O2∙s<sup>-1</sup>∙mg<sup>-1</sup>, respectively) compared with subcutaneous (0.76±0.04 and 0.98±0.05 pmol O2∙s<sup>-1</sup>∙mg<sup>-1</sup>, respectively) adipose tissue. Expressed per mtDNA, visceral adipose tissue had significantly (''P''<0.05) lower mitochondrial respiration. Substrate control ratios were higher and uncoupling control ratio lower (''P''<0.05) in visceral compared with subcutaneous adipose tissue.  


Visceral fat is bioenergetically more active and more sensitive to mitochondrial substrate supply than subcutaneous fat. [[OXPHOS]] has a higher relative activity in visceral compared with subcutaneous adipose tissue.
Visceral fat is bioenergetically more active and more sensitive to mitochondrial substrate supply than subcutaneous fat. [[OXPHOS]] has a higher relative activity in visceral compared with subcutaneous adipose tissue.
|mipnetlab=SE Stockholm Boushel RC, DK Copenhagen Dela F, CA Vancouver Boushel RC, DK Copenhagen Larsen S
|journal=Mitochondr. Physiol. Network
|discipline=Mitochondrial Physiology
|articletype=MiPNet-online Publication, MiPsociety-Publication
}}
}}
{{Labeling
{{Labeling
|discipline=Mitochondrial Physiology
|organism=Human
|organism=Human
|preparations=Permeabilized Cell or Tissue; Homogenate
|preparations=Permeabilized tissue
|topics=Respiration; OXPHOS; ETS Capacity, Coupling; Membrane Potential, Substrate; Glucose; TCA Cycle, Fatty Acid
|topics=Substrate, Fatty acid
|couplingstates=OXPHOS
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|additional=Adipose tissue, mtDNA
|journal=Mitochondr. Physiol. Network
|discipline=Mitochondrial Physiology
|articletype=MiPNet-online Publication, MiPsociety-Publication
|articletype=MiPNet-online Publication, MiPsociety-Publication
|additional=Adipose tissue, mtDNA
}}
}}
==New reference==
==New reference==


* [[Kraunsoee_2010_JPhysiol|Kraunsoee R, Boushel R, Hansen CN, Schjerling P, Qvortrup K, Stoeckel M, Mikines KJ, Dela F (2010) Mitochondrial respiration in subcutaneous and visceral adipose tissue from patients with morbid obesity. J. Physiol. 588: 2023-2032.]]
* [[Kraunsoee_2010_J_Physiol|Kraunsoee R, Boushel R, Hansen CN, Schjerling P, Qvortrup K, Stoeckel M, Mikines KJ, Dela F (2010) Mitochondrial respiration in subcutaneous and visceral adipose tissue from patients with morbid obesity. J. Physiol. 588: 2023-2032.]]

Latest revision as of 15:40, 5 March 2019

Kraunsoee R, Boushel RC, Hansen CN, Schjerling P, Qvortrup K, Stoecke M, Mikines KJ, Dela F (2010) Mitochondrial respiration in subcutaneous and visceral adipose tissue from patients with morbid obesity. Mitochondr Physiol Network 15.6:50-1.

Link: Abstracts Session 2

Kraunsoee R, Boushel RC, Hansen CN, Schjerling P, Qvortrup K, Stoecke M, Mikines KJ, Dela F (2010)

Event: MiP2010

Adipose tissue exerts important endocrine and metabolic functions in health and disease. Yet the bioenergetics of this tissue is not characterized in humans and possible regional differences are not elucidated. Using high-resolution respirometry, mitochondrial respiration was quantified in human abdominal subcutaneous and intra-abdominal, visceral (omentum majus) adipose tissue from biopsies obtained in twenty obese patients undergoing bariatric surgery. mtDNA and gDNA were determined by PCR technique for estimation of mitochondrial density. Adipose tissue samples were permeabilized and respirometric measurements were performed in duplicate at 37 °C. Substrates [glutamate(G) + malate(M) + octanoyl carnitine(Oct) + succinate(S)] were added sequentially to provide electrons to Complexes CI + CII. ADP (D) for State 3 respiration was added after GM. Non-coupled respiration was measured after addition of FCCP. Visceral fat contained more mitochondria per mg tissue than subcutaneous fat, but the cells were smaller. Robust, stable oxygen fluxes were found in both tissues, and coupled State 3 (GMOctSD) and non-coupled respiration were significantly (P<0.05) higher in visceral (0.95±0.05 and 1.15±0.06 pmol O2∙s-1∙mg-1, respectively) compared with subcutaneous (0.76±0.04 and 0.98±0.05 pmol O2∙s-1∙mg-1, respectively) adipose tissue. Expressed per mtDNA, visceral adipose tissue had significantly (P<0.05) lower mitochondrial respiration. Substrate control ratios were higher and uncoupling control ratio lower (P<0.05) in visceral compared with subcutaneous adipose tissue.

Visceral fat is bioenergetically more active and more sensitive to mitochondrial substrate supply than subcutaneous fat. OXPHOS has a higher relative activity in visceral compared with subcutaneous adipose tissue.


O2k-Network Lab: SE Stockholm Boushel RC, DK Copenhagen Dela F, CA Vancouver Boushel RC, DK Copenhagen Larsen S


Labels:


Organism: Human 

Preparation: Permeabilized tissue 

Regulation: Substrate, Fatty acid  Coupling state: OXPHOS 

HRR: Oxygraph-2k 

Adipose tissue, mtDNA 

New reference