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Palmitate incorporation into lipids pools of contracting red and white muscles

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Abstract

We compared the incorporation of the blood-borne [14C]-palmitate into selected lipid and phospholipid pools in rat muscles (soleus, red and white gastrocnemius), at rest and during contractions (15 and 60 tetani/min) in one leg (5 min) while the contralateral leg served as a control. [1-14C]-palmitate (20 µCi/rat) was administered into the carotid artery (t = 1 min). [14C]-palmitate deposition was greatest in soleus (100%) and lower in red (82%) and white gastrocnemius muscles (63%), respectively (p < 0.05). [14C] was deposited primarily into the tri-acylglycerol (∼50%) and phospholipid pools (∼30%) of soleus and red gastrocnemius muscles, and into the di-acylglycerol (∼30%), tri-acylglycerol (∼30%) and phospholipid pools (∼30%) in white gastrocnemius muscle. During contraction the concentrations of tri-acylglycerol were not changed. But, contraction increased [14C]-palmitate incorporation into soleus and red gastrocnemius muscles (600-700%) and into white gastrocnemius muscles (200%). Slightly more [14C] was directed from the phospholipids into the tri-acylglycerol pool during contraction. [14C]-palmitate deposition was also increased in the subclasses of phospholipids during contraction in red and white gastrocnemius. In conclusion, the deposition of [14C]palmitate into different lipid and phospholipid pools is quite rapid, and is dependent on contraction and the muscle fiber type. (Mol Cell Biochem 166: 73-83, 1997)

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References

  1. Baldwin KM, Klinkerfuss GH, Teljung RL, Molé PA, Holloszy JO: Respiratory capacity of white, red and intermediate muscle: adaptive response to exercise. Am J Physiol 222: 373–378, 1972

    Google Scholar 

  2. Gorski J: Muscle triglyceride metabolism during exercise. Can J Physiol Pharmacol 70: 123–131, 1992

    Google Scholar 

  3. Gorski J, Krawczuk I, Gorska M, Rutkiewicz J: Inhibition of glycogenesis in rat muscles partially depleted of glycogen. Am J Physiol (Cell Physiol) 261: C305-C309, 1991

    Google Scholar 

  4. Denton RM, Randle PJ: Concentrations of glycerides and phospholipids in rat heart and gastrocnemius muscles. Biochem J 104: 416–422, 1967

    Google Scholar 

  5. Jato-Rodriguez JJ, Hudson AJ, Strickland KP: Triglyceride metabolism in skeletal muscles from normal and dystrophic mice. Biochim Biophsy Acta 348: 1–13, 1974

    Google Scholar 

  6. Linder C, Chernick SS, Gleck TR, Scow RO: Lipoprotein lipase and uptake of chylomicron triglyceride by skeletal muscle of rats. Am J Physiol 231: 860–864, 1976

    Google Scholar 

  7. Neptune Jr EM, Sudduth HC, Foreman DR: Phospholipid and triglyceride metabolism of excised rat diaphragm and the role of these lipids in fatty acid uptake and oxidation. J Lipid Res 1: 229–235, 1960

    Google Scholar 

  8. Okano G, Matsuzaka H, Shimojo T: A comparative study of the lipid composition of white, intermediate, red and heart muscle in rats. Biochim Biophys Acta 619: 168–175, 1980

    Google Scholar 

  9. Tan MH, Sata T, Havel RJ: The significance of lipoprotein lipase in rat skeletal muscles. J Lipid Res 18: 363–370, 1977

    Google Scholar 

  10. Armstrong RB, Saubert IV CW, Sembrowich WL, Shepherd RE, Gollnick PD: Glycogen depletion in rat skeletal muscle fibers at different intensities and durations of exercise. Pflugers Arch 352: 243–256, 1974

    Google Scholar 

  11. Bonen A, McDermott JC, Hutber AC: Carbohydrate metabolism in skeletal muscle: an update. Int J Sports Med 10: 385–401, 1989

    Google Scholar 

  12. Hagenfeldt L: Metabolism of free fatty acids and ketone bodies during exercise in normal and diabetic man. Diabetes 28(Suppl 1): 68–70, 1979

    Google Scholar 

  13. Hargreaves M, Kiens B, Richter EA: Effect of increased plasma free fatty acid concentrations on muscle metabolism in exercising men. J Appl Physiol 70: 194–201, 1991

    Google Scholar 

  14. Turcote LP, Richter EA, Kiens B: Increased Plasma FFA uptake and oxidation during prolonged exercise in trained vs untrained humans. Am J Physiol 262: E791-E799, 1992

    Google Scholar 

  15. Hopp JF, Palmer WK: Electrical stimulation alters fatty acid metabolism in isolated skeletal muscle. J Appl Physiol 68: 2473–2481, 1990

    Google Scholar 

  16. Mackie B, Terjung RL: Blood flow to different skeletal muscle fiber types during contraction. Am J Physiol (Heart Circ Physiol) 245: H265-H275, 1983

    Google Scholar 

  17. Bonen A, Megeney LA, McCarthy SC, McDermott JC, Tan MH: Epinephrine administration stimulates GLUT4 translocation but reduces glucose trancport in muscle. Biochem Biophys Res Comm 187: 685–691, 1992

    Google Scholar 

  18. Megeney LA, Neufer PD, Dohm GL, Tan MH, Blewett CA, Elder GCB, Bonen A: Effects of muscle activity and fiber composition on glucose transport and GLUT-4. Am J Physiol 264 (Endocrinol Metab): E583-E593, 1993

    Google Scholar 

  19. Bligh EG, Dyer WJ: A rapid method of total lipid extraction and purification. Can J Biochem Physiol 37: 911–917, 1959

    Google Scholar 

  20. Mahadevappa VG, Holub BJ: Chromatographic analysis of phosphoinositides and their breakdown products in activated blood platelets/neutrophils. Amsterdam: Elsevier, A. Kuksis (ed.) Chromatography of lipids in biomedical research and clinical diagnosis.; vol Chromatography Library. (Vol 37), 1987

    Google Scholar 

  21. Marsh JB, Weinstein DB: Simple charring method for determination of lipids. J Lipid Res 7: 574–576, 1966

    Google Scholar 

  22. Bartlett GR: Phosphorus assay in column chromatography. J Biol Chem 234: 466–468, 1959

    Google Scholar 

  23. Bonen A, Clark MG, Henriksen EJ: Experimental approaches to the study of skeletal muscle metabolism: a comparison of hindlimb perfusion and isolated muscle incubations. Am J Physiol 266 (Endocrinol Metab): E1-E16, 1994

    Google Scholar 

  24. Dyck DJ, Peters SJ, Liu S, Kiens B, Richter EA, Gorski J, van der Vusse G, Keizer HA, Glatz J, Spriet L: Endogenous and exogenous lipid metabolism in resting skeletal muscle. FASEB J 10: A3851, 1996

    Google Scholar 

  25. Hopp JF, Palmer WK: Effect of electrical stimulation on intracellular triacyglycerol in isolated skeletal muscle. J Appl Physiol 68: 348–354, 1990

    Google Scholar 

  26. Schaffer JE, Lodish HF: Expression cloning and characterization of a novel adipocyte long chain fatty acid transport protein. Cell 79: 427–436, 1994

    Google Scholar 

  27. McCullagh KJA, Poole RC, Halestrap AP, O'Brien M, Bonen A: The role of the lactate transporter (MCT1) in skeletal muscles. Am J Physiol (Endocrinol Metab) in press, 1996

  28. Liu S, Dyck DJ, Peters SJ, McCullagh KJA, Kiens B, Richter EA, Gorski J, van der Vusse G, Keizer HA, Glatz J: Palmitate transport in skeletal muscle giant sarcolemmal vesicles. FASEB J. 10: A3853, 1996

    Google Scholar 

  29. Glatz JFC, van der Vusse GJ: Intracellular transport of lipids. Mol Cell Biochem 88: 37–44, 1989

    Google Scholar 

  30. Wilschut J, Scholma J, Eastman SJ, Hope MJ, Cullis PR: Ca2+-induced fusion of phospholipids vesicles containing free fatty acids: Modulation by transmembrane pH gradients. Biochemistry 31: 2030–2036, 1992

    Google Scholar 

  31. Terjung RL, Budohoski L, Nazar K, Kobryn A, Kaciuba-Ucilko H: Chylomicron triglyceride metabolism in resting and exercising fed dogs. J Appl Physiol 52: 815–820, 1982

    Google Scholar 

  32. Zierler KL: Fatty acids as substrates for heart and skeletal muscle. Circ Res 38: 459–463, 1976

    Google Scholar 

  33. Simon G, Rouser G: Species variations in phospholipid class distribution of organs: IL Heart and skeletal muscle. Lipids. 4: 607–614, 1969

    Google Scholar 

  34. Voelker DR: Lipid transport pathways in mammalian cells. Experientia 46: 569–578, 1990

    Google Scholar 

  35. Morgan TE, Short FA, Cobb LA: Effect of long-term exercise on skeletal muscle lipid composition. Am J Physiol 216: 82–86, 1969

    Google Scholar 

  36. Froberg SO, Mossfeldt F: Effect of prolonged strenuous exercise on the concentration of triglycerides, phospholipids and glycogen in muscle of man. Acta Physiol Scand 82: 167–171, 1971

    Google Scholar 

  37. Froberg SO: Effect of acute exercise on tissue lipids in rats. Metabolism 20: 714–720, 1971

    Google Scholar 

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Gorski, J., Bonen, A. Palmitate incorporation into lipids pools of contracting red and white muscles. Mol Cell Biochem 166, 73–83 (1997). https://doi.org/10.1023/A:1006882515938

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