SUIT-004 O2 pfi D010: Difference between revisions

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::: '''[[Mark names in DatLab]]:''' SUIT_NS(PM)01
::: '''[[Mark names in DatLab]]:''' SUIT_NS(PM)01
::: '''[[DatLab-Excel templates |DatLab-Excel template]]:''' ''in prep.'' SUIT_NS(PM)01.xlsx
::: '''[[DatLab-Analysis templates |DatLab-Analysis template]]:''' ''in prep.'' SUIT_NS(PM)01.xlsx
::::* Linked to [[SUIT_FNSGp(PGM)01]] - SUIT RP1, specifically for human skeletal muscle mitochondria.
::::* Linked to [[SUIT_FNSGp(PGM)01]] - SUIT RP1, specifically for human skeletal muscle mitochondria.
::::* Harmonized with [[SUIT_FNS(PM)01]].
::::* Harmonized with [[SUIT_FNS(PM)01]].

Revision as of 16:25, 20 September 2016


high-resolution terminology - matching measurements at high-resolution


SUIT-004 O2 pfi D010

Description

SUIT NS(PM)01.jpg

Abbreviation: NS_1PM,2D,3U,4S,5Rot-

Reference: A linked to SUIT_FNSGp(PGM)01 - SUIT RP1 (human skeletal muscle)


MitoPedia concepts: SUIT protocol, SUIT A 






SUIT-catg: NS(PM)
SUIT protocol pattern: orthogonal
Mark names in DatLab: SUIT_NS(PM)01
DatLab-Analysis template: in prep. SUIT_NS(PM)01.xlsx

SUIT_NS(PM)01_D(c)

File:SUIT NS(PM)01 D(c).jpg

NS_1PM,2D(c),3U,4S,5Rot-

Link to RP1

The SUIT_NS(PM)01 protocol is linked to SUIT_FNSGp(PGM)01 for healthy human skeletal muscle mitochondria on the basis of the following rationale.
RP1
  1. The first coupling control steps (1-4) are identical.
  2. RP1-5G is skipped, since PM and PGM yield nearly identical OXPHOS capacity. However, PM<PGM is a potential diagnostic for a defect in the PM-linked pathway upstream of CI.
  3. RP1-7Oct is skipped, since octanoylcarnitine exerts practically no stimulatory effect on OXPHOS capacity in state PMS or PGMS, but in conjunction with prolonged exposure may even yield a slight decline of respiration.
  4. RP1-9Gp is skipped, since glycerolphosphate exerts only a minor stimulatory effect on OXPHOS capacity in state SRot.
  5. Omission of the three steps described above shortens the SUIT protocol, thus reducing the risk of diminishing respiratory capacity over time, reducing the number of necessary reoxygenations, and providing more time for detailed evaluation of steady-states. The loss of diagnostic information may be minor relative to the benefits of simplification of the protocol, particularly in studies of exercise in healthy humans.
  6. RP1-10Ama may be skipped, since correction of the initial states by ROX measured in RP1-10 Ama may represent an over-correction, and inhibition takes a very long time in several cases (Pesta 2012 Methods Mol Biol).
  7. RP1-11Tm and RP1-12Azd are skipped, if a prolonged protocol is not practical due to limination of time.
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