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. 1989 May 1;259(3):651–657. doi: 10.1042/bj2590651

Changes in the lipogenic response to feeding of liver, white adipose tissue and brown adipose tissue during the development of obesity in the gold-thioglucose-injected mouse.

G J Cooney 1, M A Vanner 1, J L Nicks 1, P F Williams 1, I D Caterson 1
PMCID: PMC1138568  PMID: 2499313

Abstract

Lipogenic response to feeding was measured in vivo in liver, epididymal white adipose tissue (WAT) and interscapular brown adipose tissue (BAT), during the development of obesity in gold-thioglucose (GTG)-injected mice. The fatty acid synthesis after a meal was higher in all tissues of GTG-treated mice on a total-tissue basis, but the magnitude of this increase varied, depending on the tissue and the time after the initiation of obesity. Lipogenesis in BAT from GTG mice was double that of control mice for the first 2 weeks, but subsequently decreased to near control values. In WAT, lipogenesis after feeding was highest 2-4 weeks after GTG injection, and in liver, lipid synthesis in fed obese mice was greatest at 7-12 weeks after the induction of obesity. The post-prandial insulin concentration was increased after 2 weeks of obesity, and serum glucose concentration was higher in fed obese mice after 4 weeks. These results indicate that increased lipogenesis in GTG-injected mice may be due to an increase in insulin concentration after feeding and that insulin resistance (assessed by lipogenic response to insulin release) is apparent in BAT before WAT and liver.

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Selected References

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  1. Ashwell M., Holt S., Jennings G., Stirling D. M., Trayhurn P., York D. A. Measurement by radioimmunoassay of the mitochondrial uncoupling protein from brown adipose tissue of obese (ob/ob) mice and Zucker (fa/fa) rats at different ages. FEBS Lett. 1985 Jan 7;179(2):233–237. doi: 10.1016/0014-5793(85)80525-1. [DOI] [PubMed] [Google Scholar]
  2. Caterson I. D., Astbury L. D., Williams P. F., Vanner M. A., Cooney G. J., Turtle J. R. The activity of the pyruvate dehydrogenase complex in heart and liver from mice during the development of obesity and insulin resistance. Biochem J. 1987 Apr 15;243(2):549–553. doi: 10.1042/bj2430549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Clark M. G., Rattigan S., Clark D. G. Obesity with insulin resistance: experimental insights. Lancet. 1983 Nov 26;2(8361):1236–1240. doi: 10.1016/s0140-6736(83)91280-1. [DOI] [PubMed] [Google Scholar]
  4. Cooney G. J., Astbury L. D., Williams P. F., Caterson I. D. Insulin response in individual tissues of control and gold thioglucose-obese mice in vivo with [1-14C]2-deoxyglucose. Diabetes. 1987 Feb;36(2):152–158. doi: 10.2337/diab.36.2.152. [DOI] [PubMed] [Google Scholar]
  5. Ferré P., Burnol A. F., Leturque A., Terretaz J., Penicaud L., Jeanrenaud B., Girard J. Glucose utilization in vivo and insulin-sensitivity of rat brown adipose tissue in various physiological and pathological conditions. Biochem J. 1986 Jan 1;233(1):249–252. doi: 10.1042/bj2330249. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Godbole V., York D. A. Lipogenesis in situ in the genetically obese Zucker fatty rat (fa/fa): role of hyperphagia and hyperinsulinaemia. Diabetologia. 1978 Mar;14(3):191–197. doi: 10.1007/BF00429780. [DOI] [PubMed] [Google Scholar]
  7. Goodbody A. E., Trayhurn P. GDP binding to brown-adipose-tissue mitochondria of diabetic--obese (db/db) mice. Decreased binding in both the obese and pre-obese states. Biochem J. 1981 Mar 15;194(3):1019–1022. doi: 10.1042/bj1941019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hems D. A., Rath E. A., Verrinder T. R. Fatty acid synthesis in liver and adipose tissue of normal and genetically obese (ob/ob) mice during the 24-hour cycle. Biochem J. 1975 Aug;150(2):167–173. doi: 10.1042/bj1500167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Himms-Hagen J. Thermogenesis in brown adipose tissue as an energy buffer. Implications for obesity. N Engl J Med. 1984 Dec 13;311(24):1549–1558. doi: 10.1056/NEJM198412133112407. [DOI] [PubMed] [Google Scholar]
  10. Lavau M., Bazin R., Karaoghlanian Z., Guichard C. Evidence for a high fatty acid synthesis activity in interscapular brown adipose tissue of genetically obese Zucker rats. Biochem J. 1982 May 15;204(2):503–507. doi: 10.1042/bj2040503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Le Marchand Y., Freychet P., Jeanrenaud B. Longitudinal study on the establishment of insulin resistance in hypothalamic obese mice. Endocrinology. 1978 Jan;102(1):74–85. doi: 10.1210/endo-102-1-74. [DOI] [PubMed] [Google Scholar]
  12. MARSHALL N. B., BARRNETT R. J., MAYER J. Hypothalamic lesions in goldthioglucose injected mice. Proc Soc Exp Biol Med. 1955 Oct;90(1):240–244. doi: 10.3181/00379727-90-21995. [DOI] [PubMed] [Google Scholar]
  13. Mercer S. W., Trayhurn P. Developmental changes in fatty acid synthesis in interscapular brown adipose tissue of lean and genetically obese (ob/ob) mice. Biochem J. 1983 May 15;212(2):393–398. doi: 10.1042/bj2120393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Pénicaud L., Ferré P., Terretaz J., Kinebanyan M. F., Leturque A., Doré E., Girard J., Jeanrenaud B., Picon L. Development of obesity in Zucker rats. Early insulin resistance in muscles but normal sensitivity in white adipose tissue. Diabetes. 1987 May;36(5):626–631. doi: 10.2337/diab.36.5.626. [DOI] [PubMed] [Google Scholar]
  15. Ravussin E., Lillioja S., Knowler W. C., Christin L., Freymond D., Abbott W. G., Boyce V., Howard B. V., Bogardus C. Reduced rate of energy expenditure as a risk factor for body-weight gain. N Engl J Med. 1988 Feb 25;318(8):467–472. doi: 10.1056/NEJM198802253180802. [DOI] [PubMed] [Google Scholar]
  16. Rothwell N. J., Stock M. J. The development of obesity in animals: the role of dietary factors. Clin Endocrinol Metab. 1984 Nov;13(3):437–449. doi: 10.1016/s0300-595x(84)80032-8. [DOI] [PubMed] [Google Scholar]
  17. Saito M., Shimazu T. Decreased rate of fatty acid synthesis in brown adipose tissue of hypothalamic obese rats. FEBS Lett. 1984 Jan 23;166(1):151–154. doi: 10.1016/0014-5793(84)80062-9. [DOI] [PubMed] [Google Scholar]
  18. Shimazu T., Takahashi A. Stimulation of hypothalamic nuclei has differential effects on lipid synthesis in brown and white adipose tissue. Nature. 1980 Mar 6;284(5751):62–63. doi: 10.1038/284062a0. [DOI] [PubMed] [Google Scholar]
  19. Stansbie D., Brownsey R. W., Crettaz M., Denton R. M. Acute effects in vivo of anti-insulin serum on rates of fatty acid synthesis and activities of acetyl-coenzyme A carboxylase and pyruvate dehydrogenase in liver and epididymal adipose tissue of fed rats. Biochem J. 1976 Nov 15;160(2):413–416. doi: 10.1042/bj1600413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Trayhurn P. Fatty acid synthesis in mouse brown adipose tissue. The influence of environmental temperature on the proportion of whole-body fatty acid synthesis in brown adipose tissue and the liver. Biochim Biophys Acta. 1981 Jun 23;664(3):549–560. doi: 10.1016/0005-2760(81)90132-6. [DOI] [PubMed] [Google Scholar]
  21. Trayhurn P. Fatty acid synthesis in vivo in brown adipose tissue, liver and white adipose tissue of the cold-acclimated rat. FEBS Lett. 1979 Aug 1;104(1):13–16. doi: 10.1016/0014-5793(79)81075-3. [DOI] [PubMed] [Google Scholar]

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