Description
The P-L control efficiency (P-L flux control efficiency) is defined as jP-L = (P-L)/P = 1-L/P. OXPHOS capacity corrected for LEAK respiration is the P-L net OXPHOS capacity, P-L. The P-L control efficiency is the ratio of net to total OXPHOS capacity, which is equal to the biochemical E-L coupling efficiency, if P=E. jP-L = 1.0 for a fully coupled system (when RCR approaches infinity); jP-L = 0.0 (RCR=1) for a system with zero respiratory phosphorylation capacity (P-L=0) or zero E-L coupling efficiency (E-L=0 when L=P=E). If State 3 is measured at saturating concentrations of ADP and Pi (State 3 = P), then the respiratory acceptor control ratio RCR equals P/L. Under these conditions, the respiratory control ratio and P-L control efficiency are related by a hyperbolic function, jP-L = 1-RCR-1.
» MiPNet article
Abbreviation: jP-L
Reference: Gnaiger 2015 Scand J Med Sci Sports, Gnaiger 2020 BEC MitoPathways
Cell ergometry: OXPHOS-control and ET-coupling efficiency
Gnaiger E (2020) Cell ergometry: OXPHOS-control and ET-coupling efficiency. Mitochondr Physiol Network (2015-01-18) last update 2020-11-12. |
Abstract: The respiratory acceptor control ratio RCR has conceptual limitations that lead to statistical bias, which are resolved by expressing biochemical coupling efficiency in terms of E-L coupling efficiency. The arithmetic mean calculated for RCR values yields a bias of overestimation due to nonsymmetrical variance (Fig. 2). The concept of coupling efficiency is explained in the context of cell ergometry.
• O2k-Network Lab: AT Innsbruck Gnaiger E
From spiroergometry to OXPHOS control efficiency
- Analogous to ergometric measurement of VO2max or VO2peak on a cycle or treadmill (spiroergometry), cell ergometry is based on OXPHOS analysis to determine OXPHOS capacity, JO2P=P [pmol O2·s-1·mg-1], at the cellular and mitochondrial level. VO2peak and JO2P provide reference values for a subject’s or a cell’s aerobic or mitochondrial fitness. Aerobic catabolic flux (1 mL O2·min-1·kg-1 = 0.744 µmol·s-1·kg-1) is multiplied by the corresponding Gibbs force (ΔkFO2 = ∂G/∂kξO2; typically -470 kJ/mol or -0.47 J/µmol O2) to obtain the mass-specific aerobic input power [W·kg-1]. The corresponding mechanical output power Ppeak [W·kg-1] in cycle ergometry results in ergodynamic efficiencies [1] of about 0.25,
εpeak = Ppeak/-(JO2peak·ΔkFO2) = (Ppeak/JO2peak) / -ΔkFO2 (1)
- The apparent E-P excess capacity is available for coupled processes other than phosphorylation P».
- In OXPHOS analysis the output power is mitochondrial ATP production, JP»=P, times the Gibbs force of phosphorylation (ΔpGP» = ∂G/∂pξP»), which is typically 48 to 62 kJ/mol P» [1]. Ergodynamic efficiency is a power ratio, partitioned into a flux ratio (the famous P»/O2 ratio; ATP yield per oxygen consumed, YP»/O2 = JP»/JO2P = (P-L)/P) and force ratio,
εP = (JP»·ΔpFP»)/-(JO2P·ΔkFO2) = P»/P ∙ ΔpGP»/-ΔkFO2 = jP-L ∙ fP-L (2)
- The upper limit of (P-L)/P is the mechanistic P»:O2 ratio or stoichiometric number, νP»/O2. The P-L net OXPHOS capacity is potentially available to drive phosphorylation P» (Figure 1). Quantitatively justified in cases [3] but better adjusted to the protonmotive force pmF, the dissipative LEAK component L in the OXPHOS state can be assessed by respiration L measured in the LEAK state,
νP»/O2 = P-Llimit/P = ~P/(P-L) (3)
- Respiratory acceptor control ratio as a function of OXPHOS P-L control efficiency jP-L. RCR is the State 3/State 4 flux ratio [4], equal to P/L if State 3 is at saturating [ADP] and [Pi]. RCR from 1.0 to infinity is highly non-linear in the typical experimental range of RCR 3 to 10: when jP-L increases from 0.8 to 0.9, RCR doubles from 5 to 10. RCR increases to infinity at the limit of jP-L=1.0. Statistical analyses of RCR±SD require linearization by transformation to jP-L.
- P»/P divided by P»/(P-L) defines the P-L control efficiency jP-L as a normalized flux ratio, which is a hyperbolic function of RCR (Figure 2) [5],
jP-L = (P-L)/P = 1-L/P = 1-RCR-1 (4)
- The P-L control efficiency in Equation (4) is determined by respirometric OXPHOS analysis. At the limit of maximum jP-L=1.0 the dissipative LEAK processes L are zero. Ergodynamic efficiency ε not only depends on mechanistic coupling but also on the force ratio or force efficiency. At ergodynamic equilibrium, ε=1.0, fluxes vanish to zero when jP-L = fP-L = 1 (Equation 2).
- The OXPHOS state can be established experimentally in cells or tissues by selective permeabilization of plasma membranes, with ADP and Pi at kinetic saturation and CHNO fuel substrate combinations which reconstitute physiological TCA cycle function (Figure 1). The P-L net OXPHOS capacity may be kinetically limited by the phosphorylation system to utilize the pmF. Then ET capacity is in excess of OXPHOS capacity by the E-P control efficiency jE-P=(E-P)/E. Such kinetic limitation diminishes the effective jP-L independent of coupling control. Therefore, the E-L coupling efficiency is defined as jE-L=(E-L)/E (compare Eq. 4) and related to jP-L by taking into account the apparent E-P excess capacity (Figure 1),
jE-L = jP-L∙(1-jE-P) + jE-P (5)
- Flux control efficiencies are derived from principles of thermodynamics rather than being arbitrarily introduced as jargon of a specialized discipline.
References
- Gnaiger E (1993) Efficiency and power strategies under hypoxia. Is low efficiency at high glycolytic ATP production a paradox? In: Surviving hypoxia: mechanisms of control and adaptation. Hochachka PW, Lutz PL, Sick T, Rosenthal M, Van den Thillart G (eds) CRC Press: 77-109. - »Bioblast link«
- Gnaiger E (2020) Mitochondrial pathways and respiratory control. An introduction to OXPHOS analysis. 5th ed. Bioenerg Commun 2020.2. https://doi.org/10.26124/bec:2020-0002
- Gnaiger E (2001) Bioenergetics at low oxygen: dependence of respiration and phosphorylation on oxygen and adenosine diphosphate supply. Respir Physiol 128: 277-97. - »Bioblast link«
- Chance B, Williams GR (1955) Respiratory enzymes in oxidative phosphorylation: III. The steady state. J Biol Chem 217: 409-27. - »Bioblast link«
- Gnaiger 2014 Abstract MiP2014.
Keywords
- Expand Bioblast links to P-L control efficiency
4-compartmental OXPHOS model. (1) ET capacity E of the noncoupled electron transfer system ETS. OXPHOS capacity P is partitioned into (2) the dissipative LEAK component L, and (3) ADP-stimulated P-L net OXPHOS capacity. (4) If P-L is kinetically limited by a low capacity of the phosphorylation system to utilize the protonmotive force pmF, then the apparent E-P excess capacity is available to drive coupled processes other than phosphorylation P» (ADP to ATP) without competing with P».
- Bioblast links: Coupling control - >>>>>>> - Click on [Expand] or [Collapse] - >>>>>>>
1. Mitochondrial and cellular respiratory rates in coupling-control states
Respiratory rate | Defining relations | Icon | |
---|---|---|---|
OXPHOS capacity | P = P´-Rox | ![]() |
mt-preparations |
ROUTINE respiration | R = R´-Rox | ![]() |
living cells |
ET capacity | E = E´-Rox | ![]() |
» Level flow |
» Noncoupled respiration - Uncoupler | |||
LEAK respiration | L = L´-Rox | ![]() |
» Static head |
» LEAK state with ATP | |||
» LEAK state with oligomycin | |||
» LEAK state without adenylates | |||
Residual oxygen consumption Rox | L = L´-Rox | ![]() |
2. Flux control ratios related to coupling in mt-preparations and living cells
FCR | Definition | Icon | |
---|---|---|---|
L/P coupling-control ratio | L/P | ![]() |
» Respiratory acceptor control ratio, RCR = P/L |
L/R coupling-control ratio | L/R | ![]() | |
L/E coupling-control ratio | L/E | ![]() |
» Uncoupling-control ratio, UCR = E/L (ambiguous) |
P/E control ratio | P/E | ![]() | |
R/E control ratio | R/E | ![]() |
» Uncoupling-control ratio, UCR = E/L |
net P/E control ratio | (P-L)/E | ![]() | |
net R/E control ratio | (R-L)/E | ![]() |
3. Net, excess, and reserve capacities of respiration
Respiratory net rate | Definition | Icon |
---|---|---|
P-L net OXPHOS capacity | P-L | ![]() |
R-L net ROUTINE capacity | R-L | ![]() |
E-L net ET capacity | E-L | ![]() |
E-P excess capacity | E-P | ![]() |
E-R reserve capacity | E-R | ![]() |
4. Flux control efficiencies related to coupling-control ratios
Coupling-control efficiency | Definition | Icon | Canonical term | ||
---|---|---|---|---|---|
P-L control efficiency | jP-L | = (P-L)/P | = 1-L/P | ![]() |
P-L OXPHOS-flux control efficiency |
R-L control efficiency | jR-L | = (R-L)/R | = 1-L/R | ![]() |
R-L ROUTINE-flux control efficiency |
E-L coupling efficiency | jE-L | = (E-L)/E | = 1-L/E | ![]() |
E-L ET-coupling efficiency » Biochemical coupling efficiency |
E-P control efficiency | jE-P | = (E-P)/E | = 1-P/E | ![]() |
E-P ET-excess flux control efficiency |
E-R control efficiency | jE-R | = (E-R)/E | = 1-R/E | ![]() |
E-R ET-reserve flux control efficiency |
5. General
- » Basal respiration
- » Cell ergometry
- » Dyscoupled respiration
- » Dyscoupling
- » Electron leak
- » Electron-transfer-pathway state
- » Hyphenation
- » Oxidative phosphorylation
- » Oxygen flow
- » Oxygen flux
- » Permeabilized cells
- » Phosphorylation system
- » Proton leak
- » Proton slip
- » Respiratory state
- » Uncoupling
List of publications
- » OXPHOS and LEAK
Year | Reference | Mammal and model | Tissue and cell | Stress | Diseases | |
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Leduc-Gaudet 2023 Nat Commun | 2023 | Leduc-Gaudet JP, Franco-Romero A, Cefis M, Moamer A, Broering FE, Milan G, Sartori R, Chaffer TJ, Dulac M, Marcangeli V, Mayaki D, Huck L, Shams A, Morais JA, Duchesne E, Lochmuller H, Sandri M, Hussain SNA, Gouspillou G (2023) MYTHO is a novel regulator of skeletal muscle autophagy and integrity. https://doi.org/10.1038/s41467-023-36817-1 | Mouse | Skeletal muscle | ||
Martell 2023 Nat Commun | 2023 | Martell E, Kuzmychova H, Kaul E, Senthil H, Chowdhury SR, Morrison LC, Fresnoza A, Zagozewski J, Venugopal C, Anderson CM, Singh SK, Banerji V, Werbowetski-Ogilvie TE, Sharif T (2023) Metabolism-based targeting of MYC via MPC-SOD2 axis-mediated oxidation promotes cellular differentiation in group 3 medulloblastoma. https://doi.org/10.1038/s41467-023-38049-9 | Human | Nervous system | Cancer | |
Kankuri 2023 Exp Mol Med | 2023 | Kankuri E, Finckenberg P, Leinonen J, Tarkia M, Björk S, Purhonen J, Kallijärvi J, Kankainen M, Soliymani R, Lalowski M, Mervaala E (2023) Altered acylcarnitine metabolism and inflexible mitochondrial fuel utilization characterize the loss of neonatal myocardial regeneration capacity. https://doi.org/10.1038/s12276-023-00967-5 | Mouse | Heart | Cardiovascular | |
Wu 2023 Int Immunopharmacol | 2023 | Wu F, Zhang YT, Teng F, Li HH, Guo SB (2023) S100a8/a9 contributes to sepsis-induced cardiomyopathy by activating ERK1/2-Drp1-mediated mitochondrial fission and respiratory dysfunction. https://doi.org/10.1016/j.intimp.2023.109716 | Mouse | Heart | Cardiovascular Myopathy Sepsis | |
Calabria 2023 Biomedicines | 2023 | Calabria E, Muollo V, Cavedon V, Capovin T, Saccenti L, Passarotti F, Ghiotto L, Milanese C, Gelati M, Rudi D, Salvagno GL, Lippi G, Tam E, Schena F, Pogliaghi S (2023) Type 2 diabetes related mitochondrial defects in peripheral mononucleated blood cells from overweight postmenopausal women. https://doi.org/10.3390/biomedicines11010121 | Human | Blood cells | Diabetes | |
Mioc 2023 Molecules | 2023 | Mioc M, Mioc A, Racoviceanu R, Ghiulai R, Prodea A, Milan A, Barbu Tudoran L, Oprean C, Ivan V, Șoica C (2023) The antimelanoma biological assessment of triterpenic acid functionalized gold nanoparticles. https://doi.org/10.3390/molecules28010421 | Human | Endothelial;epithelial;mesothelial cell | Cancer | |
Gautam 2023 Neurobiol Dis | 2023 | Gautam M, Genç B, Helmold B, Ahrens A, Kuka J, Makrecka-Kuka M, Günay A, Koçak N, Aguilar-Wickings IR, Keefe D, Zheng G, Swaminathan S, Redmon M, Zariwala HA, Özdinler PH (2023) SBT-272 improves TDP-43 pathology in ALS upper motor neurons by modulating mitochondrial integrity, motility, and function. https://doi.org/10.1016/j.nbd.2023.106022 | Rat | Heart Nervous system | Neurodegenerative | |
Pacheco-Fuentes 2023 Oecologia | 2023 | Pacheco-Fuentes H, Ton R, Griffith SC (2023) Short- and long-term consequences of heat exposure on mitochondrial metabolism in zebra finches (Taeniopygia castanotis). https://doi.org/10.1007/s00442-023-05344-7 | Birds | Blood cells | ||
Devaux 2023 J Comp Physiol B | 2023 | Devaux JBL, Hedges CP, Birch N, Herbert N, Renshaw GMC, Hickey AJR (2023) Electron transfer and ROS production in brain mitochondria of intertidal and subtidal triplefin fish (Tripterygiidae). https://doi.org/10.1007/s00360-023-01495-4 | Fishes | Nervous system | Oxidative stress;RONS | |
Kyriazis 2023 Res Sq | 2023 | Kyriazis G, Serrano J, Boyd J, Mason C, Smith K, Karolyi K, Kondo S, Brown I, Maurya S, Meshram N, Serna V, Gilger J, Branch D, Gardell S, Baskin K, Ayala J, Pratley R, Goodpaster B, Coen P (2023) The TAS1R2 sweet taste receptor regulates skeletal muscle mass and fitness. https://doi.org/10.21203/rs.3.rs-2475555/v1 | Mouse | Skeletal muscle | Aging;senescence Obesity | |
Thoral 2023 J Exp Biol | 2023 | Thoral E, Roussel D, Gasset E, Dutto G, Queiros Q, McKenzie DJ, Bourdeix JH, Metral L, Saraux C, Teulier L (2023) Temperature-dependent metabolic consequences of food deprivation in the European sardine. https://doi.org/10.1242/jeb.244984 | Fishes | Skeletal muscle | ||
Bellissimo 2023 BEC | 2023 | Bellissimo CA, Soendergaard S, Hughes MC, Ramos SV, Larsen S, Perry CGR (2022) The influence of adenylate cycling on mitochondrial calcium-induced permeability transition in permeabilized skeletal muscle fibers. Bioenerg Commun 2023.1. https://doi.org/10.26124/bec:2023-0001 | Mouse | Skeletal muscle | Permeability transition | |
Temelie 2023 Int J Mol Sci | 2023 | Temelie M, Talpur R, Dominguez-Prieto M, Dantas Silva A, Cenusa C, Craciun L, Savu DI, Moisoi N (2023) Impaired integrated stress response and mitochondrial integrity modulate genotoxic stress impact and lower the threshold for immune signalling. https://doi.org/10.3390/ijms24065891 | Mouse | Fibroblast | ||
Scandalis 2023 JAMA Cardiol | 2023 | Scandalis L, Kitzman DW, Nicklas BJ, Lyles M, Brubaker P, Nelson MB, Gordon M, Stone J, Bergstrom J, Neufer PD, Gnaiger E, Molina AJA (2023) Skeletal muscle mitochondrial respiration and exercise intolerance in patients with heart failure with preserved ejection fraction. https://doi.org/10.1001/jamacardio.2023.0957 | Human | Skeletal muscle | Cardiovascular | |
Kim 2023 bioRxiv | 2023 | Kim Y, Li C, Gu C, Tycksen E, Puri A, Pietka TA, Sivapackiam J, Fang Y, Kidd K, Park SJ, Johnson BG, Kmoch S, Duffield JS, Bleyer AJ, Jackrel ME, Urano F, Sharma V, Lindahl M, Chen YM (2023) MANF stimulates autophagy and restores mitochondrial homeostasis to treat toxic proteinopathy. https://doi.org/10.1101/2023.01.10.523171 | Mouse | Endothelial;epithelial;mesothelial cell | Other | |
Pharaoh 2023 bioRxiv | 2023 | Pharaoh G, Kamat V, Kannan S, Stuppard RS, Whitson J, Martin-Perez M, Qian WJ, MacCoss MJ, Villen J, Rabinovitch P, Campbell MD, Sweet IR, Marcinek DJ (2023) Elamipretide improves ADP sensitivity in aged mitochondria by increasing uptake through the adenine nucleotide translocator (ANT). https://doi.org/10.1101/2023.02.01.525989 | Mouse | Skeletal muscle | Aging;senescence | |
Moellering 2023 Arthritis Res Ther | 2023 | Moellering DR, Smith-Johnston K, Kelley C, Sammy MJ, Benedict J, Brock G, Johnson J, Baskin KK, Jarjour WN, Belury MA, Reiser PJ, Nagareddy PR, Hanaoka BY (2023) Association between skeletal muscle mitochondrial dysfunction and insulin resistance in patients with rheumatoid arthritis: a case-control study. https://doi.org/10.1186/s13075-023-03065-z | Human | Skeletal muscle | Other | |
Robertson 2023 J Cell Sci | 2023 | Robertson GL, Riffle S, Patel M, Bodnya C, Marshall A, Beasley HK, Garza-Lopez E, Shao J, Vue Z, Hinton A, Stoll MS, de Wet S, Theart RP, Chakrabarty RP, Loos B, Chandel NS, Mears JA, Gama V (2023) DRP1 mutations associated with EMPF1 encephalopathy alter mitochondrial membrane potential and metabolic programs. https://doi.org/10.1242/jcs.260370 | Human | Fibroblast | Neurodegenerative | |
Gong 2023 Biomed Pharmacother | 2023 | Gong DF, Sun SC, Wang RR, Dawuti A, Kong DW, Liu RQ, Du LD, Wang SB, Lu Y, Yuan TY, Du GH, Fang LH (2023) Salvianolic acid A improve mitochondrial respiration and cardiac function via inhibiting apoptosis pathway through CRYAB in diabetic cardiomyopathy. https://doi.org/10.1016/j.biopha.2023.114382 | Rat | Heart | Cardiovascular Diabetes | |
Shirakawa 2023 Sci Rep | 2023 | Shirakawa R, Nakajima T, Yoshimura A, Kawahara Y, Orito C, Yamane M, Handa H, Takada S, Furihata T, Fukushima A, Ishimori N, Nakagawa M, Yokota I, Sabe H, Hashino S, Kinugawa S, Yokota T (2023) Enhanced mitochondrial oxidative metabolism in peripheral blood mononuclear cells is associated with fatty liver in obese young adults. https://doi.org/10.1038/s41598-023-32549-w | Human | Blood cells | Obesity | |
Gemmink 2023 Mol Metab | 2023 | Gemmink A, Daemen S, Wefers J, Hansen J, van Moorsel D, Astuti P, Jorgensen JA, Kornips E, Schaart G, Hoeks J, Schrauwen P, Hesselink MKC (2023) Twenty-four hour rhythmicity in mitochondrial network connectivity and mitochondrial respiration; a study in human skeletal muscle biopsies of young lean and older individuals with obesity. https://doi.org/10.1016/j.molmet.2023.101727 | Human | Skeletal muscle | ||
Vamesu 2023 JCI Insight | 2023 | Vamesu BM, Nicola T, Li R, Hazra S, Matalon S, Kaminski N, Ambalavanan N, Kandasamy J (2023) Thyroid hormone modulates hyperoxic neonatal lung injury and mitochondrial function. https://doi.org/10.1172/jci.insight.160697 | Mouse | Lung;gill | Other | |
Horcas-Nieto 2023 Biochim Biophys Acta Mol Basis Dis | 2023 | Horcas-Nieto JM, Versloot CJ, Langelaar-Makkinje M, Gerding A, Blokzijl T, Koster MH, Baanstra M, Martini IA, Coppes RP, Bourdon C, van Ijzendoorn SCD, Kim P, Bandsma RHJ, Bakker BM (2023) Organoids as a model to study intestinal and liver dysfunction in severe malnutrition. https://doi.org/10.1016/j.bbadis.2022.166635 | Mouse | Liver Other cell lines | Other | |
Szulik 2023 Basic Res Cardiol | 2023 | Szulik MW, Valdez S, Walsh M, Davis K, Bia R, Horiuchi E, O'Very S, Laxman AK, Sandaklie-Nicolova L, Eberhardt DR, Durrant JR, Sheikh H, Hickenlooper S, Creed M, Brady C, Miller M, Wang L, Garcia-Llana J, Tracy C, Drakos SG, Funai K, Chaudhuri D, Boudina S, Franklin S (2023) SMYD1a protects the heart from ischemic injury by regulating OPA1-mediated cristae remodeling and supercomplex formation. https://doi.org/10.1007/s00395-023-00991-6 | Mouse | Heart | Cardiovascular | |
Airik 2023 Antioxidants (Basel) | 2023 | Airik M, Arbore H, Childs E, Huynh AB, Phua YL, Chen CW, Aird K, Bharathi S, Zhang B, Conlon P, Kmoch S, Kidd K, Bleyer AJ, Vockley J, Goetzman E, Wipf P, Airik R (2023) Mitochondrial ROS triggers KIN pathogenesis in FAN1-deficient kidneys. https://doi.org/10.3390/antiox12040900 | Human | Kidney | Oxidative stress;RONS | Inherited |
Sathiaseelan 2023 J Gerontol A Biol Sci Med Sci | 2023 | Sathiaseelan R, Ahn B, Stout MB, Logan S, Wanagat J, Van M Nguyen H, Hord NG, Vandiver AR, Selvarani R, Ranjit R, Yarbrough H, Masingale A, Miller BF, Wolf RF, Austad SN, Richardson A (2023) A genetically heterogeneous rat model with divergent mitochondrial genomes. https://doi.org/10.1093/gerona/glad056 | Rat | Skeletal muscle | ||
Koizumi 2023 Front Cardiovasc Med | 2023 | Koizumi T, Watanabe M, Yokota T, Tsuda M, Handa H, Koya J, Nishino K, Tatsuta D, Natsui H, Kadosaka T, Koya T, Nakao M, Hagiwara H, Kamada R, Temma T, Tanaka S, Anzai T (2023) Empagliflozin suppresses mitochondrial reactive oxygen species generation and mitigates the inducibility of atrial fibrillation in diabetic rats. Front Cardiovasc Med 10: 1005408. | Rat | Heart | Cardiovascular Diabetes | |
Hoogstraten 2023 Arch Toxicol | 2023 | Hoogstraten CA, Jacobs MME, de Boer G, van de Wal MAE, Koopman WJH, Smeitink JAM, Russel FGM, Schirris TJJ (2023) Metabolic impact of genetic and chemical ADP/ATP carrier inhibition in renal proximal tubule epithelial cells. https://doi.org/10.1007/s00204-023-03510-7 | Human | Kidney | ||
Dominguez-Lopez 2023 Neuropharmacology | 2023 | Dominguez-Lopez S, Ahn B, Sataranatarajan K, Ranjit R, Premkumar P, Van Remmen H, Beckstead MJ (2023) Long-term methamphetamine self-administration increases mesolimbic mitochondrial oxygen consumption and decreases striatal glutathione. https://doi.org/10.1016/j.neuropharm.2023.109436 | Mouse | Nervous system | ||
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Giovarelli 2023 Mol Med | 2023 | Giovarelli M, Serati A, Zecchini S, Guelfi F, Clementi E, Mandò C (2023) Cryopreserved placental biopsies maintain mitochondrial activity for high-resolution respirometry. https://doi.org/10.1186/s10020-023-00645-2 | Human | Genital | Cryopreservation | |
Vilas-Boas 2023 J Biol Chem | 2023 | Vilas-Boas EA, Cabral-Costa JV, Ramos VM, Caldeira da Silva CC, Kowaltowski AJ (2023) Goldilocks calcium concentrations and the regulation of oxidative phosphorylation: too much, too little, or just right. https://doi.org/10.1016/j.jbc.2023.102904 | Mouse | Liver | ||
Salmon 2023 Geroscience | 2023 | Salmón P, Millet C, Selman C, Monaghan P, Dawson NJ (2023) Tissue-specific reductions in mitochondrial efficiency and increased ROS release rates during ageing in zebra finches, Taeniopygia guttata. https://doi.org/10.1007/s11357-022-00624-1 | Birds | Skeletal muscle Liver | Oxidative stress;RONS | Aging;senescence |
Marin 2023 Exp Gerontol | 2023 | Marin CT, de Souza Lino AD, Avelar IDS, Barbosa MR, Scarlato GCG, Cavalini DF, Tamanini F, Alexandrino AV, Vercesi AE, Shiguemoto GE (2023) Resistance training prevents dynamics and mitochondrial respiratory dysfunction in vastus lateralis muscle of ovariectomized rats. https://doi.org/10.1016/j.exger.2023.112081 | Rat | Skeletal muscle | ||
Horvath 2023 Antioxidants (Basel) | 2023 | Horváth T, Sándor L, Baráth B, Donka T, Baráth B, Mohácsi Á, Jász KD, Hartmann P, Boros M (2023) Methane admixture protects liver mitochondria and improves graft function after static cold storage and reperfusion. Antioxidants (Basel) 12:271. https://doi.org/10.3390/antiox12020271 | Rat | Liver | Ischemia-reperfusion | |
Risiglione 2022 Life (Basel) | 2022 | Risiglione P, Cubisino SAM, Lipari CLR, De Pinto V, Messina A, Magrì A (2022) α-Synuclein A53T promotes mitochondrial proton gradient dissipation and depletion of the organelle respiratory reserve in a neuroblastoma cell line. https://doi.org/10.3390/life12060894 | Human | Neuroblastoma | Parkinson's | |
Galambo 2022 Curr Res Physiol | 2022 | Galambo D, Bergdahl A (2022) Physiological levels of cardiolipin acutely affect mitochondrial respiration in vascular smooth muscle cells. https://doi.org/10.1016/j.crphys.2022.100097 | Mouse | Other cell lines | ||
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Spagnuolo 2022 Mol Neurobiol | 2022 | Spagnuolo MS, Mazzoli A, Nazzaro M, Troise AD, Gatto C, Tonini C, Colardo M, Segatto M, Scaloni A, Pallottini V, Iossa S, Cigliano L (2022) Long-lasting Impact of sugar intake on neurotrophins and neurotransmitters from adolescence to young adulthood in rat frontal cortex. https://doi.org/10.1007/s12035-022-03115-8 | Rat | Nervous system | ||
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Wu 2020 Chemosphere | 2020 | Wu F, Sokolov EP, Dellwig O, Sokolova IM (2020) Season-dependent effects of ZnO nanoparticles and elevated temperature on bioenergetics of the blue mussel Mytilus edulis. Chemosphere 263:127780. | Molluscs | Other cell lines | Temperature | |
Hraoui 2020 J Exp Biol | 2020 | Hraoui G, Bettinazzi S, Gendron AD, Boisclair D, Breton S (2020) Mitochondrial thermo-sensitivity in invasive and native freshwater mussels. J Exp Biol 223:jeb215921. | Molluscs | Lung;gill | Temperature | |
... further results |
Labels:
Regulation: Coupling efficiency;uncoupling
Coupling state: LEAK, OXPHOS
HRR: Theory
MitoPedia concepts:
Respiratory control ratio,
Ergodynamics
MitoPedia methods:
Respirometry