DOI QR코드

DOI QR Code

Effect of Overfeeding on Plasma Parameters and mRNA Expression of Genes Associated with Hepatic Lipogenesis in Geese

  • Han, Chunchun (Key Lab of Animal Genetic Resources, College of Animal Science and Technology Sichuan Agricultural University) ;
  • Wang, Jiwen (Key Lab of Animal Genetic Resources, College of Animal Science and Technology Sichuan Agricultural University) ;
  • Xu, Hengyong (Key Lab of Animal Genetic Resources, College of Animal Science and Technology Sichuan Agricultural University) ;
  • Li, Liang (Key Lab of Animal Genetic Resources, College of Animal Science and Technology Sichuan Agricultural University) ;
  • Ye, Jianqiang (Key Lab of Animal Genetic Resources, College of Animal Science and Technology Sichuan Agricultural University) ;
  • Li, Jiang (Key Lab of Animal Genetic Resources, College of Animal Science and Technology Sichuan Agricultural University) ;
  • Zhuo, Weihua (Key Lab of Animal Genetic Resources, College of Animal Science and Technology Sichuan Agricultural University)
  • Received : 2007.08.22
  • Accepted : 2007.12.02
  • Published : 2008.04.01

Abstract

The aim of our study was to research the effect of overfeeding on plasma parameters and mRNA expression of genes associated with hepatic lipogenesis in the Sichuan white goose and Landes goose. Fifty-four male Landes geese and 57 male Sichuan white geese were hatched on the same day under the same feeding conditions. After overfeeding for 14 days, (1) extrahepatic adipose tissues grew greatly in the Sichuan white geese, while more lipid accumulated in liver tissue in the Landes geese. (2) Sichuan white geese had a higher plasma concentration of triacylglycerols (TG), lipoproteins and insulin than the Landes geese. However, the Landes geese exhibited higher increase of plasma concentrations of TG, lipoproteins and insulin, with greater decrease of the diacylglycerol acyltransferase 2 (DGAT2) activity and DGAT2 mRNA level and a smller decrease of plasma glucose concentration. In addition, the mRNA level of MTP and LPL in liver was down- and up- regulated by overfeeding, respectively. (3) The correlations between the activity of LPL and the proportions of subcutaneous adipose tissue, abdominal adipose tissue, and liver weight, and the plasma concentration of VLDL were different in the two breeds. (4) The proportion of fatty liver weight was positively correlated to plasma concentrations of VLDL and TG in the overfed Sichuan white geese. Such a relationship did not exist in the Landes geese. (5) The activity of DGAT2 and its mRNA abundance in liver had significant negative correlations with the TG content in liver lipid and plasma insulin level in the Landes geese, while in the Sichuan white geese they had negative correlation (p>0.05) with TG concentration in liver lipid and had significant positive correlation with VLDL and TG concentrations in plasma.

Keywords

References

  1. Chen, Z. Y. 1999. Handbook of clinic biochemistry and biochemistry experiment analysis. Beijing: Chinese Medicine Press. (in Chinese).
  2. Davail, S., G. Guy, J. Andre, D. Hermier and R. Hoo-Paris. 2000. Metabolism in two breeds of geese with moderate or large overfeeding induced liver-steatosis. Comparative Biochem. Physiol. A Mol. Integr. Physiol. 126:91-99.
  3. Davail, S., N. Rideau, G. Guy, J. M. Andre and R. Hoo-Paris. 2003a. Pancreatic hormonal and metabolic responses in overfed ducks. Horm. Meta. Res. 35:439-443. https://doi.org/10.1055/s-2003-41626
  4. Davail, S., N. Rideau, G. Guy, J. M. Andre, D. Hermier and R. Hoo-Paris. 2003b. Hormonal and metabolic responses to overfeeding in three genotypes of ducks. Comp. Biochem. Physiol. A Mol. Integr. Physiol. 134:7-15.
  5. Fossati, P. and L. Prencipe. 1982. Serum triglycerides determined colorimetrically with an enzyme that produces hydrogen peroxyde. Clin. Chem. 28:2077-2080.
  6. Fournier, E., R. Peresson, G. Guy and D. Hermier. 1997. Relationships between storage and secretion of hepatic lipids in two breeds of geese with different susceptibility to liver steatosis. Poult. Sci. 76:599-607. https://doi.org/10.1093/ps/76.4.599
  7. Hermier, D., A. Saadoun, M. R. Salichon, N. Sellier and D. Rousselot-Pailley. 1991. Plasma lipoproteins and liver lipids in two breeds of geese with different susceptibility to hepatic steatosis: changes induced by development and force-feeding. Lipids. 26:331-339. https://doi.org/10.1007/BF02537194
  8. Hermier, D. 1997. Lipoprotein metabolism and fattening in poultry. J. Nutr. 127:805S-808S. https://doi.org/10.1093/jn/127.5.805S
  9. Hermier, D., M. R. Salichon, G. Guy and R. Peresson. 1999. Differential channelling of liver lipids in relation to susceptibility to hepatic steatosis in the goose. Poult. Sci. 78:1398-1406. https://doi.org/10.1093/ps/78.10.1398
  10. Hermier, D., G. Guy and S. Guillaumin. 2003. Differential channelling of liver lipids in relation to susceptibility to hepatic steatosis in two species of ducks. Comp. Biochem. Physio. B Biochem. Mol. Biol. 135:663-675. https://doi.org/10.1016/S1096-4959(03)00146-5
  11. Kamisaka, Y., T. Yokochi, T. Nakahara and O. Suzuki. 1993. Characterization of the diacylglycerol acyltransferase activity in the membrane fraction from a fungus. Lipids. 28:583-587. https://doi.org/10.1007/BF02536050
  12. Kamisaka, Y. and T. Nakahara. 1994. Characterization of the diacylglycerol acyltransferase activity in the lipid body fraction from an oleaginous fungus. J. Biochem. 116:1295- 1301. https://doi.org/10.1093/oxfordjournals.jbchem.a124678
  13. Liu, X. Y., R. G. He, C. S. Huang, X. Li, Q. A. Zhou, C. Wang, N. Zhao and S. X. Zhou. 2006. Hepatic lipogenesis associated with biochemical changes in overfed landaise geese and China Xupu geese. Agriculture Science in China 5(5):390-396. https://doi.org/10.1016/S1671-2927(06)60066-7
  14. Molee, W., M. Bouillier-Oudot, A. Auvergne and R. Babile. 2005. Changes in lipid composition of hepatocyte plasma membrane induced by overfeeding in duck. Comp. Biochem. Physio. B Biochem. Mol. Biol. 141:437-444. https://doi.org/10.1016/j.cbpc.2005.05.007
  15. Mourot, J., G. Guy, S. Lagarrigue, P. Peiniau and D. Hermier. 2000. Role of hepatic lipogenesis in the susceptibility to fatty liver in the goose (Anser anser). Comp. Biochem. Physio. B Biochem. Mol. Biol. 126:81-87. https://doi.org/10.1016/S0305-0491(00)00171-1
  16. Pilo, B. and J. C. George. 1983. Diurnal and seasonal variations in liver glycogen and fat in relation to metabolic status of liver and m. pectoralis in the migratory starling, Sturnus roseus, wintering in India. Comp. Biochem. Physiol. A Mol. Integr. Physiol. 74:601-604. https://doi.org/10.1016/0300-9629(83)90554-6
  17. Poujardieu, B., R. Rouvier, D. Rousselot-Pailley, G. Guy, A. Rosinski and S. Wezyk. 1994. Croissance et aptitude augavage de 3 genotypes d'oies. Ann. Zootech. 43:197-211. https://doi.org/10.1051/animres:19940209
  18. Saadoun, A. and B. Leclercq. 1987. In vivo lipogenesis of genetically lean and fat chickens: effects of nutritional state and dietary fat. J. Nutr. 117(3):428-435. https://doi.org/10.1093/jn/117.3.428
  19. SAS. 1999. SAS user's guide: Statistics (Version 8.01 Ed.). SAS Inst. Inc., Cary, N.C. USA.

Cited by

  1. The role of LXRα in goose primary hepatocyte lipogenesis vol.322, pp.1-2, 2009, https://doi.org/10.1007/s11010-008-9937-8
  2. Identification of differentially expressed genes between hepatocytes of Landes geese (Anser anser) and Sichuan White geese (Anser cygnoides) vol.37, pp.8, 2010, https://doi.org/10.1007/s11033-010-0065-7
  3. Cloning and expression of stearoyl-CoA desaturase 1 (SCD-1) in the liver of the Sichuan white goose and landes goose responding to overfeeding vol.38, pp.5, 2011, https://doi.org/10.1007/s11033-010-0451-1
  4. Effect of cholesterol on lipogenesis and VLDL–TG assembly and secretion in goose primary hepatocytes vol.374, pp.1-2, 2013, https://doi.org/10.1007/s11010-012-1516-3
  5. Response of the Hepatic Transcriptome to Aflatoxin B1 in Domestic Turkey (Meleagris gallopavo) vol.9, pp.6, 2014, https://doi.org/10.1371/journal.pone.0100930
  6. The Regulation of Lipid Deposition by Insulin in Goose Liver Cells Is Mediated by the PI3K-AKT-mTOR Signaling Pathway vol.10, pp.5, 2015, https://doi.org/10.1371/journal.pone.0098759
  7. CHANGE OF THE MTOR PATHWAY IN TISSUES OF OVERFED GEESE vol.17, pp.3, 2015, https://doi.org/10.1590/1516-635x1703293-300
  8. Inhibition of PI3K-Akt-mTOR signal pathway dismissed the stimulation of glucose on goose liver cell growth vol.101, pp.5, 2016, https://doi.org/10.1111/jpn.12574
  9. Increased fat synthesis and limited apolipoprotein B cause lipid accumulation in the liver of broiler chickens exposed to chronic heat stress pp.1525-3171, 2019, https://doi.org/10.3382/ps/pez056
  10. The role of insulin and glucose in goose primary hepatocyte triglyceride accumulation vol.212, pp.10, 2008, https://doi.org/10.1242/jeb.022210
  11. Tissue Distribution of Lipoprotein Lipase (LPL) and Regulation of LPL Gene Expression Induced by Insulin and Glucose in Goose Primary Hepatocytes vol.47, pp.2, 2010, https://doi.org/10.2141/jpsa.009106
  12. Effects of linoleate on cell viability and lipid metabolic homeostasis in goose primary hepatocytes vol.159, pp.2, 2008, https://doi.org/10.1016/j.cbpa.2011.01.019
  13. Effect of liver X receptor activation on the very low density lipoprotein secretion and messenger ribonucleic acid level of related genes in goose primary hepatocytes vol.90, pp.2, 2011, https://doi.org/10.3382/ps.2010-00995
  14. Research progress into the physiological changes in metabolic pathways in waterfowl with hepatic steatosis vol.62, pp.1, 2008, https://doi.org/10.1080/00071668.2020.1812527