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

Difference between revisions of "Reverse electron flow from CII to CI"

From Bioblast
Β 
(6 intermediate revisions by 3 users not shown)
Line 2: Line 2:
|abbr=RET
|abbr=RET


|description=Reverse electron flow from CII to CI stimulates production of [[ROS]] when mitochondria are incubated with succinate without rotenone in the LEAK state. Depolarisation of mitochondrial membrane potential (e.g. after ADP addition to stimulate OXPHOS) leads to inhibition of RET and therefore, decrease of RET-initiated ROS production. RET can be also measured when mitochondria are respiring on [[Glycerophosphate |Gp]] without rotenone in the [[LEAK]] state. Addition of I<sub>Q</sub>-side inhibitors (ubiquinone-binding side of CI) of [[Complex I |CI]] usually block RET. Β 
|description=Reverse electron flow from CII to CI stimulates production of [[ROS]] when mitochondria are incubated with succinate without rotenone in the LEAK state at a high [[mt-membrane potential]]. Depolarisation of the mt-membrane potential (''e.g.'' after ADP addition to stimulate OXPHOS) leads to inhibition of RET and therefore, decrease of RET-initiated ROS production. RET can be also measured when mitochondria are respiring using [[Glycerophosphate |Gp]] without rotenone in the [[LEAK respiration|LEAK]] state. Addition of I<sub>Q</sub>-side inhibitors (ubiquinone-binding side of CI) of [[Complex I |CI]] usually block RET. The following SUIT protocols allow you to measure RET-initiated H<sub>2</sub>O<sub>2</sub> flux in [[mitochondrial preparations]]: [[SUIT-009]] and [[SUIT-026]].
|info=
|info=


* <div>[http://www.oroboros.at/?Gnaiger_2012_MitoPathways Gnaiger 2012 MitoPathways]</div>
* <div>[https://wiki.oroboros.at/index.php/Gnaiger_2012_MitoPathways Gnaiger 2012 MitoPathways]</div>
* [https://wiki.oroboros.at/index.php/Komlodi_2018_J_Bioenerg_Biomembr Komlodi_2018_J_Bioenerg_Biomembr]
* [https://wiki.oroboros.at/index.php/Komlodi_2018_J_Bioenerg_Biomembr Komlodi_2018_J_Bioenerg_Biomembr]
* [https://wiki.oroboros.at/index.php/Makrecka-Kuka_2015_Biomolecules Makrecka-Kuka_2015_Biomolecules]
* [https://wiki.oroboros.at/index.php/Tretter_2012_Free_Radic_Biol_Med Tretter_2012_Free_Radic_Biol_Med]
* [https://wiki.oroboros.at/index.php/Tretter_2012_Free_Radic_Biol_Med Tretter_2012_Free_Radic_Biol_Med]
* [https://onlinelibrary.wiley.com/doi/full/10.1111/j.1471-4159.2006.04223.x Tretter_2006_J_Neurochem]
* [https://onlinelibrary.wiley.com/doi/full/10.1111/j.1471-4159.2006.04223.x Tretter_2006_J_Neurochem]


* [[SUIT-026]]
* [[Amplex UltraRed]]
Β 
Β 


* [[SUIT-009]]
|type=Respiration
|type=Respiration
}}
}}

Latest revision as of 12:20, 25 November 2020


high-resolution terminology - matching measurements at high-resolution


Reverse electron flow from CII to CI

Description

Reverse electron flow from CII to CI stimulates production of ROS when mitochondria are incubated with succinate without rotenone in the LEAK state at a high mt-membrane potential. Depolarisation of the mt-membrane potential (e.g. after ADP addition to stimulate OXPHOS) leads to inhibition of RET and therefore, decrease of RET-initiated ROS production. RET can be also measured when mitochondria are respiring using Gp without rotenone in the LEAK state. Addition of IQ-side inhibitors (ubiquinone-binding side of CI) of CI usually block RET. The following SUIT protocols allow you to measure RET-initiated H2O2 flux in mitochondrial preparations: SUIT-009 and SUIT-026.

Abbreviation: RET

Reference:






MitoPedia topics: Enzyme