Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Difference between revisions of "Thomas 2011 Mitochondrion"

From Bioblast
Line 1: Line 1:
{{Publication
{{Publication
|title=Thomas RR, Khan SM, Portell FR, Smigrodzki RM, Bennett JP Jr (2011) Recombinant human mitochondrial transcription factor A stimulates mitochondrial biogenesis and ATP synthesis, improves motor function after MPTP, reduces oxidative stress and increases survival after endotoxin. Mitochondrion 11: 108-118.
|title=Thomas RR, Khan SM, Portell FR, Smigrodzki RM, Bennett JP Jr (2011) Recombinant human mitochondrial transcription factor A stimulates mitochondrial biogenesis and ATP synthesis, improves motor function after MPTP, reduces oxidative stress and increases survival after endotoxin. Mitochondrion 11:108-118.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/20727424 PMID:20727424 ]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/20727424 PMID:20727424 ]
|authors=Thomas RR, Khan SM, Portell FR, Smigrodzki RM, Bennett JP
|authors=Thomas RR, Khan SM, Portell FR, Smigrodzki RM, Bennett JP
Line 13: Line 13:
|tissues=Heart, Skeletal muscle, Nervous system
|tissues=Heart, Skeletal muscle, Nervous system
|model cell lines=Fibroblast
|model cell lines=Fibroblast
|preparations=Homogenate, Isolated Mitochondria
|preparations=Homogenate, Isolated mitochondria
|injuries=RONS; Oxidative Stress
|injuries=Oxidative stress;RONS
|topics=ATP; ADP; AMP; PCr
|topics=ATP; ADP; AMP; PCr
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
}}
}}

Revision as of 14:39, 13 February 2015

Publications in the MiPMap
Thomas RR, Khan SM, Portell FR, Smigrodzki RM, Bennett JP Jr (2011) Recombinant human mitochondrial transcription factor A stimulates mitochondrial biogenesis and ATP synthesis, improves motor function after MPTP, reduces oxidative stress and increases survival after endotoxin. Mitochondrion 11:108-118.

Β» PMID:20727424

Thomas RR, Khan SM, Portell FR, Smigrodzki RM, Bennett JP (2011) Mitochondrion

Abstract: Recombinant human mitochondrial transcription factor A protein (rhTFAM) was evaluated for its acute effects on cultured cells and chronic effects in mice. Fibroblasts incubated with rhTFAM acutely increased respiration in a chloramphenicol-sensitive manner. SH-SY5Y cells showed rhTFAM concentration-dependent reduction of methylpyridinium (MPP+)-induced oxidative stress and increases in lowered ATP levels and viability. Mice treated with weekly i.v. rhTFAM showed increased mitochondrial gene copy number, Complex I protein levels and ATP production rates; oxidative damage to proteins was decreased ~50%. rhTFAM treatment improved motor recovery rate after treatment with MPTP and dose-dependently improved survival in the lipopolysaccharide model of endotoxin sepsis. β€’ Keywords: recombinant TFAM, mitochondrial biogenesis, ATP synthesis, MPTP, sepsis

β€’ O2k-Network Lab: US_VA Richmond_Bennett JP, US VA Richmond Iyer S


Labels:

Stress:Oxidative stress;RONS  Organism: Human, Mouse  Tissue;cell: Heart, Skeletal muscle, Nervous system  Preparation: Homogenate, Isolated mitochondria 

Regulation: ATP; ADP; AMP; PCr"ATP; ADP; AMP; PCr" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property. 


HRR: Oxygraph-2k