HUMAN SCIATIC-NERVE PHOSPHOLIPID PROFILES FROM NON-DIABETES MELLITUS,NON-INSULIN-DEPENDENT DIABETES-MELLITUS AND INSULIN-DEPENDENT DIABETES-MELLITUS INDIVIDUALS - A P-31 NMR-SPECTROSCOPY STUDY

Citation
D. Driscoll et al., HUMAN SCIATIC-NERVE PHOSPHOLIPID PROFILES FROM NON-DIABETES MELLITUS,NON-INSULIN-DEPENDENT DIABETES-MELLITUS AND INSULIN-DEPENDENT DIABETES-MELLITUS INDIVIDUALS - A P-31 NMR-SPECTROSCOPY STUDY, International Journal of Biochemistry, 26(6), 1994, pp. 759-767
Citations number
48
Categorie Soggetti
Biology
ISSN journal
0020711X
Volume
26
Issue
6
Year of publication
1994
Pages
759 - 767
Database
ISI
SICI code
0020-711X(1994)26:6<759:HSPPFN>2.0.ZU;2-T
Abstract
1.Human sciatic nerve phospholipids obtained from non-diabetes mellitu s (NDM), non-insulin-dependent diabetes mellitus (NIDDM), and insulin- dependent diabetes mellitus (IDDM) patients, after lower extremity amp utation, were studied by P-31 NMR spectrometry. 2. Nine phospholipids resonances in NDM and NIDDM groups were identified as followed: Ethano lamine plasmalogen (Eplas, Chemical shift = 0.07 delta); phosphatidyle thanolamine (PE, 0.03 delta); phosphatidylserine (PS, -0.05 delta); sp hingomyelin (SM, -0.09 delta); lysophosphatidylcholine (LPC, -0.28 del ta); phosphatidylinositol (PI, -0.30 delta); alkylacylphosphorylcholin e (A1.PC, -0.78 delta); phosphatidylcholine (PC -0.84 delta), and an u nknown resonance (U, 0.13 delta). 3. In the IDDM group a resonance of lysophosphatidylinositol (LPI, 0.01 delta) was detected in addition to the nine phospholipids listed above. 4. IDDM showed that PI and A1.PC were elevated and U was lower when compared with NDM; also, Eplas was lower when compared with NIDDM. PC was elevated and PS was lower when compared with both NDM and NIDDM. 5.Indices calculated from this data , showed that the choline ratio and choline/ ethanolamine ratio were e levated; while ethanolamine ratio, and myelin ratio were lower in IDDM group, when compared with both NDM and NIDDM groups. 6. Inactivation of the cholineacethyltransferase enzyme (ChAT) and enhancement of the phospholipidmethyltransferase enzyme (PLMT), secondary to an insulin d eficiency, are proposed as an interpretation of these findings.