USE OF STABLE ISOTOPES TO STUDY FATTY-ACID AND LIPOPROTEIN METABOLISMIN MAN

Authors
Citation
Jt. Brenna, USE OF STABLE ISOTOPES TO STUDY FATTY-ACID AND LIPOPROTEIN METABOLISMIN MAN, Prostaglandins, leukotrienes and essential fatty acids, 57(4-5), 1997, pp. 467-472
Citations number
28
Categorie Soggetti
Endocrynology & Metabolism",Biology
ISSN journal
09523278
Volume
57
Issue
4-5
Year of publication
1997
Pages
467 - 472
Database
ISI
SICI code
0952-3278(1997)57:4-5<467:UOSITS>2.0.ZU;2-J
Abstract
Tracer studies have long been an important tool for lipid metabolism r esearch. Recent advances and availability of high performance mass spe ctrometers (MS) and improved stable isotopically labeled tracers contr ibute to an increase in stable isotope tracer studies in humans. We br iefly review recent studies and discuss advances in high sensitivity m ethods and applications. GC/MS analysis. Tracer studies with gas chrom atography/mass spectrometry (GC/MS) usually rely on D labeling, where labeling with more that three D atoms shifts the analyte mass above th at of the natural abundance envelope, and the MS monitors selected mas ses representing the isotopimers of interest. Recent examples are the work of Emken and coworkers, who investigated the desaturation of 18:0 and 16:0, and 18:2n-6 and 18:3n-3 elongation/desaturation, in adults, with oral doses of about 3 g of d(2,4,6) fatty acids. They showed mod est levels of 18:0 and 16:0 desaturation over 2 days and an influence of dietary 18:2n-6 on elongation. In premature infants, Salem, Uauy an d coworkers recently have used d(5)-18:2n-6 and d(5)-18:3n-3 doses of 50-100 mg/kg body weight to show that infants as small as 1980 g and 3 2 weeks gestation elongate and desaturate both precursors within 24 h. Most fatty acid metabolites including 20:4n-6, 20:5n-3, and 22:6n-3 w ere easily detected in serum. High precision isotope ratio MS (IRMS). In 1992, we introduced a high sensitivity fatty acid tracer method bas ed on [U-C-13] tracers and GC-combustion-IRMS (GCC-IRMS). The combusti on interface facilitates carbon-by-carbon tracer detection; with U-C-1 3 tracers all GC peaks are detected with highest precision. Rhee et al have quantified the desaturation of 18:0 and 16:0 in lipoproteins of adults using 30 mg oral doses (0.5 mg/kg). In the first 12 h, conversi on of 18.0 to 18.1 was 7% in chylomicrons and 17% in VLDL, showing tha t both intestine and liver desaturate 18:0. Plasma conversion of 18.0 over 144 h was 14%, while that for 16.0 was 2%, showing that combined intestine and liver desaturation is minor compared with normal fluctua tions in dietary levels. Carnielli applied GCC-IRMS to 8:0 elongation in very-low-birth-weight infants. Significant conversion products of 8 :0 were 14:0 (5%), 16:0 (8%) but not 10:0 or 12:0.