Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1988 Sep 15;254(3):661–665. doi: 10.1042/bj2540661

Changes in the sensitivity to glucagon of lipolysis in adipocytes from pregnant and lactating rats.

V A Zammit 1
PMCID: PMC1135136  PMID: 3058115

Abstract

1. Rates of lipolysis were measured at different concentrations of glucagon in adipocytes prepared from parametrial adipose tissue of fed or starved rats in different reproductive states. All experiments were performed in the presence of a high concentration of adenosine deaminase (1 unit/ml). 2. Maximal rates of lipolysis (elicited by 25 nM-glucagon in each instance) were higher in adipocytes from peak-lactating rats than those from pregnant animals in both the fed and starved states. 3. Of adipocytes from fed animals, those from peak-lactating rats were the most sensitive to glucagon, whereas those from late-pregnant and early-lactating rats were 1-2 orders of magnitude less sensitive. 4. Adipocytes from 24 h-starved rats showed a much smaller stimulation of lipolysis by glucagon, making the assessment of sensitivity difficult. Therefore, rates of lipolysis were also measured in the presence of a maximally anti-lipolytic dose of insulin. The presence of insulin did not alter the relative sensitivities to glucagon of adipocytes from fed animals in different reproductive states, although all dose-response curves were shifted to the right. When lipolysis in adipocytes from starved animals was measured in the presence of insulin, it became evident that starvation for 24 h markedly increased the sensitivity of adipocytes from late-pregnant rats to glucagon, but did not affect that of cells from animals in the other reproductive states. 5. It is concluded that the large changes in sensitivity to glucagon that occurred during the reproductive cycle may enable the modulation of adipose-tissue lipolysis in vivo to satisfy the different metabolic requirements of the animal in the transition from pregnancy to peak lactation.

Full text

PDF
661

Selected References

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

  1. Aitchison R. E., Clegg R. A., Vernon R. G. Lipolysis in rat adipocytes during pregnancy and lactation. The response to noradrenaline. Biochem J. 1982 Jan 15;202(1):243–247. doi: 10.1042/bj2020243. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Burnol A. F., Guerre-Millo M., Lavau M., Girard J. Effect of lactation on insulin sensitivity of glucose metabolism in rat adipocytes. FEBS Lett. 1986 Jan 6;194(2):292–296. doi: 10.1016/0014-5793(86)80103-x. [DOI] [PubMed] [Google Scholar]
  3. Burnol A. F., Leturque A., Ferré P., Girard J. Glucose metabolism during lactation in the rat: quantitative and regulatory aspects. Am J Physiol. 1983 Oct;245(4):E351–E358. doi: 10.1152/ajpendo.1983.245.4.E351. [DOI] [PubMed] [Google Scholar]
  4. Chohan P., Carpenter C., Saggerson E. D. Changes in the anti-lipolytic action and binding to plasma membranes of N6-L-phenylisopropyladenosine in adipocytes from starved and hypothyroid rats. Biochem J. 1984 Oct 1;223(1):53–59. doi: 10.1042/bj2230053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Flint D. J., Sinnett-Smith P. A., Clegg R. A., Vernon R. G. Role of insulin receptors in the changing metabolism of adipose tissue during pregnancy and lactation in the rat. Biochem J. 1979 Aug 15;182(2):421–427. doi: 10.1042/bj1820421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Girard J. R., Cuendet G. S., Marliss E. B., Kervran A., Rieutort M., Assan R. Fuels, hormones, and liver metabolism at term and during the early postnatal period in the rat. J Clin Invest. 1973 Dec;52(12):3190–3200. doi: 10.1172/JCI107519. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Honnor R. C., Dhillon G. S., Londos C. cAMP-dependent protein kinase and lipolysis in rat adipocytes. I. Cell preparation, manipulation, and predictability in behavior. J Biol Chem. 1985 Dec 5;260(28):15122–15129. [PubMed] [Google Scholar]
  8. Honnor R. C., Dhillon G. S., Londos C. cAMP-dependent protein kinase and lipolysis in rat adipocytes. II. Definition of steady-state relationship with lipolytic and antilipolytic modulators. J Biol Chem. 1985 Dec 5;260(28):15130–15138. [PubMed] [Google Scholar]
  9. Honnor R. C., Saggerson E. D. Altered lipolytic response to glucagon and adenosine deaminase in adipocytes from starved rats. Biochem J. 1980 Jun 15;188(3):757–761. doi: 10.1042/bj1880757. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Jones R. G., Ilic V., Williamson D. H. Regulation of lactating-rat mammary-gland lipogenesis by insulin and glucagon in vivo. The role and site of action of insulin in the transition to the starved state. Biochem J. 1984 Oct 15;223(2):345–351. doi: 10.1042/bj2230345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kilgour E., Vernon R. G. Defect in signal transduction at the level of the plasma membrane accounts for inability of insulin to activate pyruvate dehydrogenase in white adipocytes of lactating rats. Biochem J. 1988 Jun 15;252(3):667–672. doi: 10.1042/bj2520667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Kilgour E., Vernon R. G. Tissue-specific changes in the ability of insulin and noradrenaline to activate pyruvate dehydrogenase in vivo during lactation in the rat. Biochem J. 1987 Apr 1;243(1):69–74. doi: 10.1042/bj2430069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Labarca C., Paigen K. A simple, rapid, and sensitive DNA assay procedure. Anal Biochem. 1980 Mar 1;102(2):344–352. doi: 10.1016/0003-2697(80)90165-7. [DOI] [PubMed] [Google Scholar]
  14. Robinson A. M., Girard J. R., Williamson D. H. Evidence for a role of insulin in the regulation of lipogenesis in lactating rat mammary gland. Measurements of lipogenesis in vivo and plasma hormone concentrations in response to starvation and refeeding. Biochem J. 1978 Oct 15;176(1):343–346. doi: 10.1042/bj1760343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Robson N. A., Clegg R. A., Zammit V. A. Regulation of peripheral lipogenesis by glucagon. Inability of the hormone to inhibit lipogenesis in rat mammary acini in vitro in the presence or absence of agents which alter its effects on adipocytes. Biochem J. 1984 Feb 1;217(3):743–749. doi: 10.1042/bj2170743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Saggerson E. D. Sensitivity of adipocyte lipolysis to stimulatory and inhibitory agonists in hypothyroidism and starvation. Biochem J. 1986 Sep 1;238(2):387–394. doi: 10.1042/bj2380387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Saudek C. D., Finkowski M., Knopp R. H. Plasma glucagon and insulin in rat pregnancy. Roles in glucose homeostasis. J Clin Invest. 1975 Jan;55(1):180–187. doi: 10.1172/JCI107909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Vega F. V., Kono T. Sugar transport in fat cells: effects of mechanical agitation, cell-bound insulin, and temperature. Arch Biochem Biophys. 1979 Jan;192(1):120–127. doi: 10.1016/0003-9861(79)90077-8. [DOI] [PubMed] [Google Scholar]
  19. Vernon R. G., Finley E., Taylor E. Adenosine and the control of lipolysis in rat adipocytes during pregnancy and lactation. Biochem J. 1983 Oct 15;216(1):121–128. doi: 10.1042/bj2160121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Zammit V. A., Corstorphine C. G. Changes in the proportion of acetyl-CoA carboxylase in the active form in rat liver. Effect of starvation, lactation and weaning. Biochem J. 1982 Jun 15;204(3):757–764. doi: 10.1042/bj2040757. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Zammit V. A., Corstorphine C. G. Inhibition of acetyl-CoA carboxylase activity in isolated rat adipocytes incubated with glucagon. Interactions with the effects of insulin, adrenaline and adenosine deaminase. Biochem J. 1982 Dec 15;208(3):783–788. doi: 10.1042/bj2080783. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Zammit V. A. Regulation of hepatic fatty acid metabolism. The activities of mitochondrial and microsomal acyl-CoA:sn-glycerol 3-phosphate O-acyltransferase and the concentrations of malonyl-CoA, non-esterified and esterified carnitine, glycerol 3-phosphate, ketone bodies and long-chain acyl-CoA esters in livers of fed or starved pregnant, lactating and weaned rats. Biochem J. 1981 Jul 15;198(1):75–83. doi: 10.1042/bj1980075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Zammit V. A. Regulation of lipogenesis in rat tissues during pregnancy and lactation. Biochem Soc Trans. 1985 Oct;13(5):831–833. doi: 10.1042/bst0130831. [DOI] [PubMed] [Google Scholar]
  24. Zammit V. A. The effect of glucagon treatment and starvation of virgin and lactating rats on the rates of oxidation of octanoyl-L-carnitine and octanoate by isolated liver mitochondria. Biochem J. 1980 Aug 15;190(2):293–300. doi: 10.1042/bj1900293. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES