Paper
Uncoupling effect of the general anesthetic 2,6-diisopropylphenol in isolated rat liver mitochondria.
Published Nov 1, 1991 · D. Branca, M. Roberti, E. Vincenti
Archives of biochemistry and biophysics
Q1 SJR score
53
Citations
1
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
2,6-diisopropylphenol reduces ATP synthetase activity in isolated rat liver mitochondria without affecting ATP production, acting as a mild protonophore.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
Influence of the anesthetic 2,6-diisopropylphenol on the oxidative phosphorylation of isolated rat liver mitochondria.
2,6-diisopropylphenol decreases the transmembrane electrical potential in rat liver mitochondria, increasing electron transfer or ATP hydrolysis rates, while maintaining the coupling between electron flow and ATP synthesis.
1991·64citations·D. Branca et al.·Biochemical pharmacology
Biochemical pharmacology
Quantitative analysis of uncoupling activity of substituted phenols with a physicochemical substituent and molecular parameters.
Substituted phenols' uncoupling potency is influenced by factors such as incorporation, balance between neutral and ionized forms, and steric shielding effects on the negatively charged center of ionized form.
1990·33citations·H. Miyoshi et al.·Biochimica et biophysica acta
Biochimica et biophysica acta
Unique relationships between the rates of oxidation and phosphorylation and the protonmotive force in rat-liver mitochondria.
There is a unique relationship between ATP synthesis and the protonmotive force in rat-liver mitochondria, and TPMP+ accumulation in mitochondria is influenced by factors like TBP and uncouplers.
1988·13citations·H. Woelders et al.·Biochimica et biophysica acta
Biochimica et biophysica acta
Uncoupling of oxidative phosphorylation. 1. Protonophoric effects account only partially for uncoupling.
Protonophoric effects account only partially for uncoupling of oxidative phosphorylation, with increased membrane conductance causing a depression of the transmembrane proton electrochemical potential gradient and a stimulation of ATP hydrolysis.
1987·90citations·S. Luvisetto et al.·Biochemistry
Biochemistry
Quantitative relationship between protonophoric and uncoupling activities of substituted phenols.
Substituted phenols' protonophoric and uncoupling activities are influenced by two factors: the partition coefficient between liposome and aqueous buffer phases and the acid dissociation constant.
1987·55citations·H. Miyoshi et al.·Biochimica et biophysica acta
Biochimica et biophysica acta
Propofol combined with nitrous oxide‐oxygen for induction and maintenance of anaesthesia
Propofol infusion combined with nitrous oxide-oxygen can be safely used for anesthesia during ear surgery, with minimal cardiovascular changes and recovery of cortisol levels within one hour.
1987·61citations·L. Herregods et al.·Anaesthesia
Anaesthesia
L-carnitine effect on halothane-treated mitochondria.
L-carnitine effectively reduces the negative effects of halothane on mitochondrial energy-linked processes, potentially involving long-chain acyl CoA.
1986·15citations·A. Toninello et al.·Biochemical pharmacology
Biochemical pharmacology
Energy-storage capacity of the mitochondrial proton-motive force.
The mitochondrial proton-motive force has a total energy storage capacity of 3.3 nmol ATP/mg protein or about 130 J/mg protein, with three protons per molecule ATP.
1986·18citations·L. Wojtczak et al.·Biochimica et biophysica acta
Biochimica et biophysica acta
Citations
Overdose with the anesthetic propofol causes hematological cytotoxicity and immune cell alteration in an experimental ex vivo whole blood culture model.
Propofol overdose causes hematological cytotoxicity and immune cell alteration in an ex vivo model, particularly affecting neutrophils and granulocytes.
2023·1citation·C. Hsing et al.·Toxicology in vitro : an international journal published in association with BIBRA
Toxicology in vitro : an international journal published in association with BIBRA
A Commentary on the Effect of Targeted Temperature Management in Patients Resuscitated from Cardiac Arrest.
Induced hypothermia treatment is beneficial for comatose patients after cardiac arrest, but recent trials may not show a significant improvement in neurologic outcome due to multiple factors.
2022·2citations·M. Holzer et al.·Therapeutic hypothermia and temperature management
Therapeutic hypothermia and temperature management
L-Carnitine and Acylcarnitines: Mitochondrial Biomarkers for Precision Medicine
L-carnitine and acylcarnitines are useful clinical biomarkers for identifying and prognosticating diseases and adverse drug reactions in various disorders, with potential for future therapeutic decisions and new pharmacologic targets.
2021·178citations·M. R. McCann et al.·Metabolites
Metabolites
Lipid emulsion, but not propofol, induces skeletal muscle damage and lipid peroxidation
Lipofundin causes muscle damage through lipid peroxidation, while propofol (Maruishi) suppresses it through antioxidant effects.
2019·6citations·Tomohiro Chaki et al.·Journal of Anesthesia
Journal of Anesthesia
Kinetic characteristics of propofol-induced inhibition of electron-transfer chain and fatty acid oxidation in human and rodent skeletal and cardiac muscles
Propofol-induced inhibition of bioenergetic pathways in human skeletal and cardiac muscles is more marked than in rodent tissues, with a potential link to Propofol Infusion Syndrome.
2019·6citations·T. Urban et al.·PLoS ONE
PLoS ONE
The Basic Study of the Mechanism of Propofol-Related Infusion Syndrome Using a Murine Skeletal Muscle Injury Model
Propofol-related infusion syndrome (PRIS) is caused by dose-dependent cell damage to the mitochondrial electron transport chain and metabolic disorders, providing a potential experimental model for further investigations.
2019·3citations·Yuryo Murakami et al.·Anesthesiology and Pain Medicine
Anesthesiology and Pain Medicine
Propofol infusion syndrome: a structured literature review and analysis of published case reports
Propofol infusion syndrome is a rare, potentially fatal condition with different clinical features in children and adults, and should be considered in cases of unexplained metabolic acidosis, ECG changes, and rhabdomyolysis.
2019·206citations·S. Hemphill et al.·BJA: British Journal of Anaesthesia
BJA: British Journal of Anaesthesia