Accumulation of medium chain Acyl-CoAs during beta-oxidation of long chainfatty acid by isolated peroxisomes from rat liver

Citation
F. Hashimoto et al., Accumulation of medium chain Acyl-CoAs during beta-oxidation of long chainfatty acid by isolated peroxisomes from rat liver, BIOL PHAR B, 24(6), 2001, pp. 600-606
Citations number
44
Categorie Soggetti
Pharmacology & Toxicology
Journal title
BIOLOGICAL & PHARMACEUTICAL BULLETIN
ISSN journal
09186158 → ACNP
Volume
24
Issue
6
Year of publication
2001
Pages
600 - 606
Database
ISI
SICI code
0918-6158(200106)24:6<600:AOMCAD>2.0.ZU;2-X
Abstract
We have reported fatty alcohol synthesis accompanied by chain elongation in liver peroxisomes (Biochim. Biophys. Acta, 1346, 38 (1997)). In the presen t experiment, we studied what kind of acyl-CoA(s) destined to be utilized a s primer for fatty alcohol synthesis accumulate(s) during peroxisomal beta -oxidation. Peroxisomes were prepared from rat liver treated with clofibrat e, a peroxisome proliferator, and incubated with [U-C-14]palmitate, in orde r to investigate acyl-CoAs after beta -oxidation. At 1 mM concentration, Mg ATP activated beta -oxidation, but inhibited beta -oxidation at concentrati ons higher than 1 mM. After incubation of peroxisomes with palmitate, vario us acyl-CoAs were formed. Among medium-chain labelled acyl-CoAs, octanoyl-C oA was mainly detected. These results suggest that octanoyl-CoA accumulates during beta -oxidation of palmitate. When peroxisomes were incubated with [9,10-H-3]palmitate and [9,10-H-3]stearate, among medium-chain acyl-CoAs, o ctanoyl-CoA and decanoyl-CoA were primarily detected, respectively, suggest ing the occurrence of at least 1 cycles of beta -oxidation of both fatty ac ids by peroxisomes.