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Difference between revisions of "Doeller 2005 Anal Biochem"

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|journal=Analyt. Biochem.
|journal=Analyt. Biochem.
|abstract=The role of nitric oxide (NO) in redox cell signaling is widely accepted. However, the biological role of another candidate small inorganic signaling molecule and the subject of this study, hydrogen sulfide (H<sub>2</sub>S), is much less known. H<sub>2</sub>S as a reductant and nucleophile has numerous potential cellular targets; however, its rapid biological oxidation suggests a fleeting cellular existence. The challenge of accurate real-time measurement of H<sub>2</sub>S at low micromolar or nanomolar concentrations in biological preparations represents a major impediment to H<sub>2</sub>S investigations. We here demonstrate the use of a novel polarographic H<sub>2</sub>S sensor (PHSS) to follow rapid changes in H<sub>2</sub>S concentration in common buffered biological solutions with a detection limit near 10 nM. The PHSS, used in combination with O<sub>2</sub>S and NO sensors in multisensor respirometry, shows stability, a high signal-to-noise ratio, and signal specificity for H<sub>2</sub>S. Preparations of rat vascular tissue exhibit H<sub>2</sub>S production on the addition of sulfhydryl-bearing amino acid substrates and H<sub>2</sub>S consumption when supplied with exogenous H<sub>2</sub>S. Taken together, these findings suggest the existence of dynamic steady-state cellular H<sub>2</sub>S levels. The PHSS should facilitate the investigation of H<sub>2</sub>S biology by providing a previously unattainable continuous record of H<sub>2</sub>S under biologically relevant conditions.
|abstract=The role of nitric oxide (NO) in redox cell signaling is widely accepted. However, the biological role of another candidate small inorganic signaling molecule and the subject of this study, hydrogen sulfide (H<sub>2</sub>S), is much less known. H<sub>2</sub>S as a reductant and nucleophile has numerous potential cellular targets; however, its rapid biological oxidation suggests a fleeting cellular existence. The challenge of accurate real-time measurement of H<sub>2</sub>S at low micromolar or nanomolar concentrations in biological preparations represents a major impediment to H<sub>2</sub>S investigations. We here demonstrate the use of a novel polarographic H<sub>2</sub>S sensor (PHSS) to follow rapid changes in H<sub>2</sub>S concentration in common buffered biological solutions with a detection limit near 10 nM. The PHSS, used in combination with O<sub>2</sub>S and NO sensors in multisensor respirometry, shows stability, a high signal-to-noise ratio, and signal specificity for H<sub>2</sub>S. Preparations of rat vascular tissue exhibit H<sub>2</sub>S production on the addition of sulfhydryl-bearing amino acid substrates and H<sub>2</sub>S consumption when supplied with exogenous H<sub>2</sub>S. Taken together, these findings suggest the existence of dynamic steady-state cellular H<sub>2</sub>S levels. The PHSS should facilitate the investigation of H<sub>2</sub>S biology by providing a previously unattainable continuous record of H<sub>2</sub>S under biologically relevant conditions.
|keywords=Hydrogen sulfide, Sensor, Rat aorta, Organ homogenates, Oxygen, Nitric oxide
|keywords=Hydrogen sulfide, Sensor, Rat aorta, Organ homogenates, Oxygen, Nitric oxide, Instrumental and methodological aspects
|mipnetlab=US AL Birmingham Kraus DW
|mipnetlab=US AL Birmingham Kraus DW
|discipline=Mitochondrial Physiology
|discipline=Mitochondrial Physiology

Revision as of 11:49, 11 November 2011

Publications in the MiPMap
Doeller JE, Isbell TS, Benavides G, Koenitzer J, Patel H, Patel RP, Lancaster JR Jr, Darley-Usmar VM, Kraus DW (2005) Polarographic measurement of hydrogen sulfide production and consumption by mammalian tissues. Anal. Biochem. 341: 40-51.

Β» PMID: 15866526

Doeller JE, Isbell TS, Benavides G, Koenitzer J, Patel H, Patel RP, Lancaster JR Jr, Darley-Usmar VM, Kraus DW (2005) Analyt. Biochem.

Abstract: The role of nitric oxide (NO) in redox cell signaling is widely accepted. However, the biological role of another candidate small inorganic signaling molecule and the subject of this study, hydrogen sulfide (H2S), is much less known. H2S as a reductant and nucleophile has numerous potential cellular targets; however, its rapid biological oxidation suggests a fleeting cellular existence. The challenge of accurate real-time measurement of H2S at low micromolar or nanomolar concentrations in biological preparations represents a major impediment to H2S investigations. We here demonstrate the use of a novel polarographic H2S sensor (PHSS) to follow rapid changes in H2S concentration in common buffered biological solutions with a detection limit near 10 nM. The PHSS, used in combination with O2S and NO sensors in multisensor respirometry, shows stability, a high signal-to-noise ratio, and signal specificity for H2S. Preparations of rat vascular tissue exhibit H2S production on the addition of sulfhydryl-bearing amino acid substrates and H2S consumption when supplied with exogenous H2S. Taken together, these findings suggest the existence of dynamic steady-state cellular H2S levels. The PHSS should facilitate the investigation of H2S biology by providing a previously unattainable continuous record of H2S under biologically relevant conditions. β€’ Keywords: Hydrogen sulfide, Sensor, Rat aorta, Organ homogenates, Oxygen, Nitric oxide, Instrumental and methodological aspects

β€’ O2k-Network Lab: US AL Birmingham Kraus DW


Labels:


Organism: Rat 


Regulation: Respiration; OXPHOS; ETS Capacity"Respiration; OXPHOS; ETS Capacity" 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., Redox State"Redox State" 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, NO