Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1985 Feb 15;226(1):275–282. doi: 10.1042/bj2260275

Reversible inactivation by noradrenaline of long-chain fatty acyl-CoA synthetase in rat adipocytes.

M Hall, E D Saggerson
PMCID: PMC1144702  PMID: 3883997

Abstract

Incubation of rat adipocytes with the same range of noradrenaline concentrations that stimulate lipolysis caused a rapid and stable decrease in the activity of fatty acyl-CoA synthetase. Corticotropin, glucagon and dibutyryl cyclic AMP also decreased the activity of the enzyme. The effect of noradrenaline was apparent over a wide range of concentrations for the three substrates of the enzyme. A novel fluorescence assay of fatty acyl-CoA synthetase using (1,N6-etheno)-CoA is described. The effect of noradrenaline was not abolished by inclusion of albumin in homogenization buffers, persisted through subcellular fractionation and isolation of microsomes (microsomal fractions) and even survived treatment of microsomes with Triton X-100. The effect of noradrenaline was rapidly reversed within cells by the subsequent addition of insulin or propranolol. The inclusion of fluoride in homogenization buffers did not alter the observed effect of noradrenaline. Additions of cyclic AMP-dependent protein kinase to adipocyte microsomes caused considerable phosphorylation of microsomal protein by [gamma-32P]ATP, but did not affect the activity of fatty acyl-CoA synthetase.

Full text

PDF
275

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Brostrom M. A., Reimann E. M., Walsh D. A., Krebs E. G. A cyclic 3',5'-amp-stimulated protein kinase from cardiac muscle. Adv Enzyme Regul. 1970;8:191–203. doi: 10.1016/0065-2571(70)90017-8. [DOI] [PubMed] [Google Scholar]
  2. Cheng C. H., Saggerson E. D. Rapid antagonistic actions of noradrealine and insulin on rat adipocyte phosphatidate phosphohydrolase activity. FEBS Lett. 1978 Sep 1;93(1):120–124. doi: 10.1016/0014-5793(78)80818-7. [DOI] [PubMed] [Google Scholar]
  3. Cheng C. H., Saggerson E. D. Rapid effects of noradrenaline on Mg2+-dependent phosphatidate phosphohydrolase activity in rat adipocytes. FEBS Lett. 1978 Mar 1;87(1):65–68. doi: 10.1016/0014-5793(78)80134-3. [DOI] [PubMed] [Google Scholar]
  4. Cheng C. H., Saggerson E. D. The inactivation of rat adipocyte Mg2+-dependent phosphatidate phosphohydrolase by noradrenaline. Biochem J. 1980 Sep 15;190(3):659–662. doi: 10.1042/bj1900659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Evans G. L., Denton R. M. Regulation of fatty acid synthesis and esterification in rat epididymal adipose tissue: effects of insulin, palmitate and 2-bromopalmitate [proceedings]. Biochem Soc Trans. 1977;5(5):1288–1291. doi: 10.1042/bst0051288. [DOI] [PubMed] [Google Scholar]
  6. GARLAND P. B., RANDLE P. J. A rapid enzymatic assay for glycerol. Nature. 1962 Dec 8;196:987–988. doi: 10.1038/196987a0. [DOI] [PubMed] [Google Scholar]
  7. Jason C. J., Polokoff M. A., Bell R. M. Triacylglycerol synthesis in isolated fat cells. An effect of insulin on microsomal fatty acid coenzyme A ligase activity. J Biol Chem. 1976 Mar 10;251(5):1488–1492. [PubMed] [Google Scholar]
  8. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  9. Lawson N., Pollard A. D., Jennings R. J., Gurr M. I., Brindley D. N. The activities of lipoprotein lipase and of enzymes involved in triacylglycerol synthesis in rat adipose tissue. Effects of starvation, dietary modification and of corticotropin injection. Biochem J. 1981 Nov 15;200(2):285–294. doi: 10.1042/bj2000285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Martin B. R., Denton R. M. The intracellular localization of enzymes in white-adipose-tissue fat-cells and permeability properties of fat-cell mitochondria. Transfer of acetyl units and reducing power between mitochondria and cytoplasm. Biochem J. 1970 May;117(5):861–877. doi: 10.1042/bj1170861. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Nimmo H. G., Houston B. Rat adipose-tissue glycerol phosphate acyltransferase can be inactivated by cyclic AMP-dependent protein kinase. Biochem J. 1978 Nov 15;176(2):607–610. doi: 10.1042/bj1760607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. RODBELL M. METABOLISM OF ISOLATED FAT CELLS. I. EFFECTS OF HORMONES ON GLUCOSE METABOLISM AND LIPOLYSIS. J Biol Chem. 1964 Feb;239:375–380. [PubMed] [Google Scholar]
  13. Reimann E. M., Walsh D. A., Krebs E. G. Purification and properties of rabbit skeletal muscle adenosine 3',5'-monophosphate-dependent protein kinases. J Biol Chem. 1971 Apr 10;246(7):1986–1995. [PubMed] [Google Scholar]
  14. Rider M. H., Saggerson E. D. Regulation by noradrenaline of the mitochondrial and microsomal forms of glycerol phosphate acyltransferase in rat adipocytes. Biochem J. 1983 Jul 15;214(1):235–246. doi: 10.1042/bj2140235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Saggerson E. D., Carpenter C. A., Cheng C. H., Sooranna S. R. Subcellular distribution and some properties of N-ethylmaleimide-sensitive and-insensitive forms of glycerol phosphate acyltransferase in rat adipocytes. Biochem J. 1980 Jul 15;190(1):183–189. doi: 10.1042/bj1900183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Sooranna S. R., Saggerson E. D. A stable decrease in long chain fatty acyl CoA synthetase activity after treatment of rat adipocytes with adrenaline. FEBS Lett. 1978 Aug 15;92(2):241–244. doi: 10.1016/0014-5793(78)80762-5. [DOI] [PubMed] [Google Scholar]
  17. Sooranna S. R., Saggerson E. D. Interactions of insulin and adrenaline with glycerol phosphate acylation processes in fat-cells from rat. FEBS Lett. 1976 Apr 15;64(1):36–39. doi: 10.1016/0014-5793(76)80242-6. [DOI] [PubMed] [Google Scholar]
  18. Tanaka T., Hosaka K., Hoshimaru M., Numa S. Purification and properties of long-chain acyl-coenzyme-A synthetase from rat liver. Eur J Biochem. 1979 Jul;98(1):165–172. doi: 10.1111/j.1432-1033.1979.tb13173.x. [DOI] [PubMed] [Google Scholar]
  19. Walsh D. A., Perkins J. P., Brosom C. O., Ho E. S., Kreb E. G. Catlysis of the phosphrylaseinase actition reaction. J Biol Chem. 1971 Apr 10;246(7):1968–1976. [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES