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
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.