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Difference between revisions of "Maarman 2015 Abstract MiPschool Cape Town 2015"

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{{Abstract
{{Abstract
|title=Characterisation of mitochondrial function in a model of pulmonary hypertension-induced right ventricular failure.
|authors=Maarman G, Sliwa K, Lecour S
|year=2015
|year=2015
|event=MiPschool Cape Town 2015
|event=MiPschool Cape Town 2015
|abstract=Pulmonary hypertension (PH) is characterized by increased mean
pulmonary artery pressure causes increased right ventricular (RV)
afterload and failure, which leads to death [1]. PH causes mitochondrial
dysfunction and this impacts the function of the RV [2-4]. Researchers
are now focussing on novel cardioprotective therapies for PH, but the
full extent of mitochondrial dysfunction in PH is not described and this
could influence the efficacy of drugs that target the mitochondrial milieu
[2-4]. Our aim was to characterize RV mitochondrial respiration in model
of PH-induced RV failure. Male Long Evans rats, were injected with
monocrotaline (MCT, 80mg/kg i.p, n=6) and control rats (CON) (n=6)
received saline injections. After 28 days, mitochondria were isolated from
RV sections. Mitochondrial respiration was assessed using an Oroboros Oxygraph-2k, with glutamate+malate or succinate as substrates and rotenone as
inhibitor. When glutamate and malate were used as substrates: MCT
hearts had a 21% lower RV state 2 (''p''< 0.02), 20% lower RV state 3
(''p''< 0.02), a 23% lower RV state 4 (''p''< 0.02) and unchanged RV RCI
compared to controls. When succinate was used as a substrate and
rotenone as inhibitor: MCT hearts had a 52% lower RV state 3 (''p''< 0.002),
a 43% lower RV state 2 (''p''< 0.03), a 33% lower RV state 4 (''p''< 0.04) and
RV RCI was similar between groups. Our data suggest that PH-induced
RV failure is associated with a reduction of mitochondrial respiration
through complexes I and II in both RV and LV sections (data not shown).
This supports the importance of developing cardioprotective therapies
that can correct or augment mitochondrial respiration.
|mipnetlab=ZA Cape Town Smith J
}}
}}
{{Labeling}}
{{Labeling
|area=Respiration, Instruments;methods, Patients, mt-Awareness
|organism=Rat
|tissues=Heart
|preparations=Isolated mitochondria
|diseases=Cardiovascular
|couplingstates=LEAK, OXPHOS
|pathways=N, S, NS
|instruments=Oxygraph-2k
}}
== Affiliations ==
Inst South Africa Newlands, ESSM UCT Dept Human Biol Sports Sc, Univ Cape Town, South Africa.- [email protected]
Β 
== References ==
#Simonneau G, Robbins IM, Beghetti M, Channick RN, Delcroix M, Denton CP, Elliott CG, Gaine SP, Gladwin MT, Jing ZC, Krowka MJ, Langleben D, Nakanishi N, Souza R (2009) Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol 54:43-54.
#Gomez-Arroyo J, Mizuno S, Szczepanek K, Van Tassell B, Natarajan R, dos Remedios CG, Drake JI, Farkas L, Kraskauskas D, Wijesinghe DS, Chalfant CE, Bigbee J, Abbate A, Lesnefsky EJ, Bogaard HJ, Voelkel NF (2013) Metabolic gene remodeling and mitochondrial dysfunction in failing right ventricular hypertrophy secondary to pulmonary arterial hypertension. Circ Heart Fail 6:136-44.
#Tang Z, Iqbal M, Cawthon D, Bottje WG (2002) Heart and breast muscle mitochondrial dysfunction in pulmonary hypertension syndrome in broilers (''Gallus domesticus''). Comp Biochem Physiol A Mol Integr Physiol 132:527-40.
#Vonk-Noordegraaf A, Haddad F, Chin KM, Forfia PR, Kawut SM, Lumens J, Naeije R, Newman J, Oudiz RJ, Provencher S, Torbicki A, Voelkel NF, Hassoun PM (2013) Right heart adaptation to pulmonary arterial hypertension: physiology and pathobiology. J Am Coll Cardiol 62:22-33.

Latest revision as of 12:15, 23 January 2019

Characterisation of mitochondrial function in a model of pulmonary hypertension-induced right ventricular failure.

Link:

Maarman G, Sliwa K, Lecour S (2015)

Event: MiPschool Cape Town 2015

Pulmonary hypertension (PH) is characterized by increased mean pulmonary artery pressure causes increased right ventricular (RV) afterload and failure, which leads to death [1]. PH causes mitochondrial dysfunction and this impacts the function of the RV [2-4]. Researchers are now focussing on novel cardioprotective therapies for PH, but the full extent of mitochondrial dysfunction in PH is not described and this could influence the efficacy of drugs that target the mitochondrial milieu [2-4]. Our aim was to characterize RV mitochondrial respiration in model of PH-induced RV failure. Male Long Evans rats, were injected with monocrotaline (MCT, 80mg/kg i.p, n=6) and control rats (CON) (n=6) received saline injections. After 28 days, mitochondria were isolated from RV sections. Mitochondrial respiration was assessed using an Oroboros Oxygraph-2k, with glutamate+malate or succinate as substrates and rotenone as inhibitor. When glutamate and malate were used as substrates: MCT hearts had a 21% lower RV state 2 (p< 0.02), 20% lower RV state 3 (p< 0.02), a 23% lower RV state 4 (p< 0.02) and unchanged RV RCI compared to controls. When succinate was used as a substrate and rotenone as inhibitor: MCT hearts had a 52% lower RV state 3 (p< 0.002), a 43% lower RV state 2 (p< 0.03), a 33% lower RV state 4 (p< 0.04) and RV RCI was similar between groups. Our data suggest that PH-induced RV failure is associated with a reduction of mitochondrial respiration through complexes I and II in both RV and LV sections (data not shown). This supports the importance of developing cardioprotective therapies that can correct or augment mitochondrial respiration.


β€’ O2k-Network Lab: ZA Cape Town Smith J


Labels: MiParea: Respiration, Instruments;methods, Patients, mt-Awareness  Pathology: Cardiovascular 

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


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


Affiliations

Inst South Africa Newlands, ESSM UCT Dept Human Biol Sports Sc, Univ Cape Town, South Africa.- [email protected]

References

  1. Simonneau G, Robbins IM, Beghetti M, Channick RN, Delcroix M, Denton CP, Elliott CG, Gaine SP, Gladwin MT, Jing ZC, Krowka MJ, Langleben D, Nakanishi N, Souza R (2009) Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol 54:43-54.
  2. Gomez-Arroyo J, Mizuno S, Szczepanek K, Van Tassell B, Natarajan R, dos Remedios CG, Drake JI, Farkas L, Kraskauskas D, Wijesinghe DS, Chalfant CE, Bigbee J, Abbate A, Lesnefsky EJ, Bogaard HJ, Voelkel NF (2013) Metabolic gene remodeling and mitochondrial dysfunction in failing right ventricular hypertrophy secondary to pulmonary arterial hypertension. Circ Heart Fail 6:136-44.
  3. Tang Z, Iqbal M, Cawthon D, Bottje WG (2002) Heart and breast muscle mitochondrial dysfunction in pulmonary hypertension syndrome in broilers (Gallus domesticus). Comp Biochem Physiol A Mol Integr Physiol 132:527-40.
  4. Vonk-Noordegraaf A, Haddad F, Chin KM, Forfia PR, Kawut SM, Lumens J, Naeije R, Newman J, Oudiz RJ, Provencher S, Torbicki A, Voelkel NF, Hassoun PM (2013) Right heart adaptation to pulmonary arterial hypertension: physiology and pathobiology. J Am Coll Cardiol 62:22-33.