𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Phospholipid profile of the human brain: 31P NMR spectroscopic study

✍ Scribed by Ingrid L. Kwee; Tsutomu Nakada


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
238 KB
Volume
6
Category
Article
ISSN
0740-3194

No coin nor oath required. For personal study only.

✦ Synopsis


Phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, phosphatidylinositol, sphingomyelin, and ethanolamine plasmalogen represent the six most abundant phospholipids of brain cell membrane. The ratio of the phospholipid contents (phospholipid profile) of the brain is remarkably consistent under various metabolic conditions and alteration of the phospholipid profile is believed to reflect changes in the membrane system. We describe here a simple but sensitive method to analyze the phospholipid profile of the human brain utilizing the acidified chloroform-methanol lipid extraction method of Folch et al. and 31P nuclear magnetic resonance (NMR) spectroscopy. Unique regional phospholipid profiles were consistently obtained. Although the large chemical-shift anisotropy of the 31P confined to rigid structures such as the cell membrane precludes direct observation of phospholipid profiles in living tissue, a reflection of the membrane phospholipid profiles can nevertheless be obtained by studying "NMR visible" water soluble intermediate metabolites of membrane phospholipids in vivo.


πŸ“œ SIMILAR VOLUMES


31P NMR detection of mobile dog brain ph
✍ S. Cerdan; V. Harihara Subramanian; M. Hilberman; J. Cone; J. Egan; B. Chance; J πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 395 KB

The in vivo dog brain "P NMR spectrum has a large peak in the phosphodiester region accounting for more than 35% of the total observable phosphorus metabolites. It is possible to reduce the intensity of this peak by off-resonance saturation. To characterize the nature of this peak, extracts of dog b

Phospholipid composition of postmortem s
✍ John M. Pearce; Richard A. Komoroski; Robert E. Mrak πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 165 KB

## Abstract Cell membrane abnormalities due to changes in phospholipid (PL) composition and metabolism have been implicated in schizophrenia pathogenesis. That work has generally assessed membrane phospholipids from nonneural tissues such as erythrocytes and platelets. High‐resolution ^31^P NMR spe

31P NMR spectroscopy of phospholipid met
✍ Richard A. Komoroski; John M. Pearce; Robert E. Mrak πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 102 KB

## Abstract Evidence has been accumulating that schizophrenia involves abnormalities in the composition and metabolism of cell membrane phospholipids (PLs) in the brain. In vivo ^31^P MRS has been used to measure the metabolic precursors and degradation products of PL metabolism in schizophrenia. B

Spin echo 31P spectroscopic imaging in t
✍ A. A. Maudsley; D. B. Twieg; D. Sappey-Marinier; B. Hubesch; J. W. Hugg; G. B. M πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 448 KB

## Abstract Spectroscopic imaging of phosphorus metabolites in the human brain has been carried out with two data acquisition methods: by observation of the free induction decay (FID) signal and by a short spin echo sequence. The resultant spectral images and spatially resolved spectra are compared

Analysis of phospholipid molecular speci
✍ John M. Pearce; Richard A. Komoroski πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 173 KB πŸ‘ 2 views

Techniques are described for the (31)P NMR analysis of glycerophospholipid (PL) headgroup and molecular species in brain. The (31)P NMR spectrum of PLs from human temporal cortex, solubilized in aqueous Na cholate, typically showed 3 major resonances, assigned to phosphatidylcholine (PC) molecular s