We examined the route of uptake of 2-aminoethylphosphonate (NEthPo) and of phenylphosphonate (PhePo; 10 mM each) in perfused liver by 31 P-NMR. Uptake of NEthPo was concentrative. The rate of uptake was reduced to 21 AE 2% (n = 3; all percentages refer to control rates) by substituting choline for N
Ph and compartmentation of isolated perfused rat liver studied by 31p and 19f nmr
✍ Scribed by William J. Thoma; Kǎmil Uurbil
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 615 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0952-3480
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✦ Synopsis
The phosphorus N M R spectra of isolated perfused rat liver displays a prominent inorganic phosphate peak at 2.76 f 0.05 ppm relative to liver glycerolphosphocholine at 0.49 ppm. From titration curves of phosphoruscontaining compounds this corresponds to a pH of 7.4. The spectra also display a shoulder on the prominent inorganic phosphate peak at 2.22 f 0.55 ppm corresponding to a pH of 7.0. Fructose is phosphorylated in the C1 position by the liver and the resulting fructose-1-phosphate is located in the cytosol. From the titration curves, this compound was at pH 7.0. When inorganic phosphate was added to the perfusate, 13 of 25 livers showed two inorganic phosphate peaks resolved in the difference spectra, one originating from the perfusate, the other at pH 7.0. When large (50 mM) fructose doses were administered to the liver, the prominent peak decreased allowing two peaks to be resolved. FCCP treatment of the liver caused the two peaks to coalesce with the final pH of both the fructose-1-phosphate and inorganic phosphate being the same. 'v N M R of difluoromethylalanine gave an intracellular pH of 7.4 for the isolated perfused liver. The data presented do not lend themselves to satisfactory interpretation, and call into question the correctness of the traditional assignment of liver inorganic phosphate being cytosolic in origin.
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We evaluated phosphonates (Po) as markers of the extra-and intracellular space in perfused rat liver. (i) In-and outwash behaviour of phenylphosphonate (PhePo), 3-amino-propylphosphonate (NProPo) and methyl phosphonate (MePo) was compared with that of creatine phosphate (CrP), a marker of the extrac
## Abstract This spectroscopic study compares the mechanisms of the hepatic uptake of manganese chloride (MnCl~2~) and manganese dipyridoxyl diphosphate (MnDPDP). Alterations of the phosphorus‐31 (^31^P)‐NMR spectrum of the intracellular adenosine 5′‐triphosphate (ATP) are used to monitor the inter