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Effects of continuous light and melatonin treatment on energy metabolism of the rat

Abstract

Melatonin affects food intake, body mass and adiposity of several mammals, but the effects of melatonin on energy metabolism remain largely unknown. This study investigated subacute effects of persistent melatonin treatment and continuous light on carbohydrate and fat metabolism of rat liver and kidney. The male and female rats (no.=40) were maintained either in 12L:12D photoperiod or in constant light. Half the rats in both lighting conditions were treated with continuousrelease melatonin implants. Liver lipid concentrations, liver and kidney glucose-6-phosphatase, glycogen phosphorylase and lipase esterase activities, glycogen contents as well as plasma T4, T3, insulin, glucose and melatonin concentrations were determined. There was clear sexual dimorphism in the responses to exogenous melatonin and constant light. Continuous light stimulated carbohydrate metabolism of rat liver. Exogenous melatonin enhanced utilization of liver carbohydrates but suppressed hepatic lipolysis. Changes in normal circulating melatonin concentrations led to enhanced utilization of kidney carbohydrates supporting a role for melatonin in renal function. Both exogenous melatonin and constant light seem to have a strong regulatory effect on rat energy metabolism.

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References

  1. Arendt J. Melatonin and the mammalian pineal gland. Chapman & Hall, Cambridge, 1995, p. 72.

    Google Scholar 

  2. Reiter R.J. Pineal melatonin: cell biology of its synthesis and of its physiological interactions. Endocr. Rev. 1991, 12: 151–180.

    PubMed  Article  CAS  Google Scholar 

  3. Reiter R.J., Klein D.C. Observations on the pineal gland, the Harderian glands, the retina, and the reproductive organs of adult female rats exposed to continuous light. J. Endocrinol. 1971, 51: 117–125.

    PubMed  Article  CAS  Google Scholar 

  4. Tamarkin L., Baird C.J., Almeida O.F.X. Melatonin: a coordinating signal for mammalian reproduction? Science 1985, 227: 714–720.

    PubMed  Article  CAS  Google Scholar 

  5. Saarela S., Reiter R.J. Function of melatonin in thermoregulatory processes. Life Sci. 1994, 54: 295–311.

    PubMed  Article  CAS  Google Scholar 

  6. Allain D., Rougeot J. Induction of autumn moult in mink (Mustela vison Peale and Beauvois) with melatonin. Reprod. Nutr. Dev. 1980, 20: 197–201.

    PubMed  Article  CAS  Google Scholar 

  7. Martin M.T., Azpiroz F., Malagelada J.R. Melatonin and the gastrointestinal tract. Thérapie 1998, 53: 453–458.

    PubMed  CAS  Google Scholar 

  8. Acuña-Castroviejo D., Reiter R.J., Menéndez-Peláez A., Pablos M.I., Burgos A. Characterization of high-affinity melatonin binding sites in purified cell nuclei of rat liver. J. Pineal Res. 1994, 16: 100–112.

    PubMed  Article  Google Scholar 

  9. Song Y., Tam P.C., Poon A.M.S., Brown G.M., Pang S.F. 2-[125I]Iodomelatonin-binding sites in the human kidney and the effect of guanosine 5′-O-(3-thiotriphosphate). J. Clin. Endocrinol. Metab. 1995, 80: 1560–1565.

    PubMed  CAS  Google Scholar 

  10. Williams L.M., Hannah L.T., Adam C.L., Bourke D.A. Melatonin receptors in red deer fetuses (Cervus elaphus). J. Reprod. Fert. 1997, 110: 145–151.

    Article  CAS  Google Scholar 

  11. Wade G.N., Bartness T.J. Seasonal obesity in Syrian hamsters: effects of age, diet, photoperiod, and melatonin. Am. J. Physiol. 1984, 247: R328–R334.

    PubMed  CAS  Google Scholar 

  12. Valtonen M., Vakkuri O., Blomstedt L. Autumnal timing of photoperiodic manipulation critical via melatonin to winter pelage development in mink. Anim. Sci. 1995, 61: 589–596.

    Article  Google Scholar 

  13. Le Gouic S., Delagrange P., Atgié C., et al. Effects of both a melatonin agonist and antagonist on seasonal changes in body mass and energy intake in the garden dormouse. Int. J. Obes. Relat. Metab. Disord. 1996, 20: 661–667.

    PubMed  Google Scholar 

  14. Milcu S.M., Milcu I. Über ein hypoglykämisch wirkendes Hormon in der Zirbeldrüse. Die Medizinische 1958, 17: 711–715.

    Google Scholar 

  15. de Vlaming V.L., Sage M., Charlton C.B., Tiegs B. The effects of melatonin on lipid deposition in Cyprinodontid fishes and on pituitary prolactin activity in Fundulus similis. J. Comp. Physiol. 1974, 94: 309–319.

    Article  Google Scholar 

  16. Harris R.A. Carbohydrate metabolism I: major metabolic pathways and their control. In: Devlin T.M. (Ed.), Textbook of biochemistry with clinical correlations, 2nd ed. John Wiley & Sons, Singapore, 1986, p. 261.

    Google Scholar 

  17. Richardson B.A., Studier E.H., Stallone J.N., Kennedy C.M. Effects of melatonin on water metabolism and renal function in male Syrian hamsters (Mesocricetus auratus). J. Pineal Res. 1992, 13: 49–59.

    PubMed  Article  CAS  Google Scholar 

  18. Kawashima K., Miwa Y., Fujimoto K., Oohata H., Nishino H., Koike H. Antihypertensive action of melatonin in the spontaneously hypertensive rat. Clin. Exp. Hypertens. 1987, A9: 1121–1131.

    Article  CAS  Google Scholar 

  19. Tsuda T., Ide M., Iigo M. Influences of season and of temperature, photoperiod, and subcutaneous melatonin infusion on the glomerular filtration rate of ewes. J. Pineal Res. 1995, 19: 166–172.

    PubMed  Article  CAS  Google Scholar 

  20. O’Callaghan D., Karsch F.J., Boland M.P., Roche J.F. What photoperiodic signal is provided by a continuous-release melatonin implant? Biol. Reprod. 1991, 45: 927–933.

    PubMed  Article  Google Scholar 

  21. Hers H.G., van Hoof F. Enzymes of glycogen degradation in biopsy material. In: Colowick S., Kaplan N.O. (Eds.), Methods in enzymology. Academic Press, NY, 1966, p. 525.

    Google Scholar 

  22. Seligman A.M., Nachlas M.M. Lipase. In: Bermayer H.U. (Ed.), Methoden der Enzymatischen Analyse. Verlag Chemie GmbH, Weinheim, Germany, 1962, p. 776.

    Google Scholar 

  23. Lo S., Russell J.C., Taylor A.W. Determination of glycogen in small tissue samples. J. Appl. Physiol. 1970, 28: 234–236.

    PubMed  CAS  Google Scholar 

  24. Folch J., Lees M., Sloane Stanley G.H. A simple method for the isolation and purification of total lipides from animal tissues J. Biol. Chem. 1957, 226: 497–509.

    PubMed  CAS  Google Scholar 

  25. Dark J., Rayha L.L., Clark-Lane I., Kimler V. Melatonin and lighting condition: absence of long-term effects on food intake and body weight regulation in the albino rat. Physiol. Behav. 1980, 25: 855–857.

    PubMed  Article  CAS  Google Scholar 

  26. Kaminsky Y.G., Kosenko E.A., Kondrashova M.N. Analysis of the circadian rhythm in energy metabolism of rat liver. Int. J. Biochem. 1984, 16: 629–639.

    PubMed  Article  CAS  Google Scholar 

  27. Chesworth M.J., Cassone V.M., Armstrong S.M. Effects of daily melatonin injections on activity rhythms of rats in constant light. Am. J. Physiol. 1987, 253: R101–R107.

    PubMed  CAS  Google Scholar 

  28. Mazepa R.C., Cuevas M.J., Collado P.S., Gonzáles-Gallego J. Melatonin increases muscle and liver glycogen content in nonexercised and exercised rats. Life Sci. 2000, 66: 153–160.

    PubMed  Article  CAS  Google Scholar 

  29. Nieminen P., Käkelä R., Mustonen A-M., Hyvärinen H., Asikainen J. Exogenous melatonin affects lipids and enzyme activities in mink (Mustela vison) liver. Comp. Biochem. Physiol. 2001, 128C: 203–211.

    CAS  Google Scholar 

  30. Osei P., Robbins K.R., Shirley H.V. Effects of exogenous melatonin on growth and energy metabolism of chickens. Nutr. Res. 1989, 9: 69–81.

    Article  CAS  Google Scholar 

  31. Esquifino A., Agrasal C., Velázquez E., Villanúa M.A., Cardinali D.P. Effect of melatonin on serum cholesterol and phospholipid levels, and on prolactin, thyroid-stimulating hormone and thyroid hormone levels, in hyperprolactinemic rats. Life Sci. 1997, 61: 1051–1058.

    PubMed  Article  CAS  Google Scholar 

  32. Hoyos M., Guerrero J.M., Perez-Cano R., et al. Serum cholesterol and lipid peroxidation are decreased by melatonin in diet-induced hypercholesterolemic rats. J. Pineal Res. 2000, 28: 150–155.

    PubMed  Article  CAS  Google Scholar 

  33. Vance D.E. Biosynthesis of membrane lipids. In: Zubay G.L. (Ed.), Biochemistry, 4th ed. Wm. C. Brown Publishers, Dubuq-ue, 1998, p. 507.

    Google Scholar 

  34. Gorray K.C., Quay W.B., Ewart R.B.L. Effects of pinealectomy and pineal incubation medium and sonicates on insulin release by isolated pancreatic islets in vitro. Horm. Metab. Res. 1979, 11: 432–436.

    PubMed  Article  CAS  Google Scholar 

  35. Aoyama H., Mori W., Mori N. Anti-glucocorticoid effects of melatonin in young rats. Acta Pathol. Jpn. 1986, 36: 423–428.

    PubMed  CAS  Google Scholar 

  36. Vriend J., Richardson B.A., Vaughan M.K., Johnson L.Y., Reiter R.J. Effects of melatonin on thyroid physiology of female hamsters. Neuroendocrinology 1982, 35: 79–85.

    PubMed  Article  CAS  Google Scholar 

  37. John T.M., Viswanathan M., George J.C., Scanes C.G. Influence of chronic melatonin implantation on circulating levels of catecholamines, growth hormone, thyroid hormones, glucose, and free fatty acids in the pigeon. Gen. Comp. Endocrinol. 1990, 79: 226–232.

    PubMed  Article  CAS  Google Scholar 

  38. Randall D., Burggren W., French K. Ionic and osmotic balance. In: Eckert animal physiology, mechanisms and adaptations, 4th ed. W.H. Freeman and Company, NY, 1997, p. 571.

    Google Scholar 

  39. Campbell C.S., Schwartz N.B. The impact of constant light on the estrous cycle of the rat. Endocrinology 1980, 106: 1230–1238.

    PubMed  Article  CAS  Google Scholar 

  40. Rocha D.C.M., Debeljuk L., Franca L.R. Exposure to constant light during testis development increases daily sperm production in adult Wistar rats. Tissue Cell 1999, 31: 372–379.

    PubMed  Article  CAS  Google Scholar 

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Correspondence to A-. M. Mustonen.

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Mustonen, A..M., Nieminen, P. & Hyvärinen, H. Effects of continuous light and melatonin treatment on energy metabolism of the rat. J Endocrinol Invest 25, 716–723 (2002). https://doi.org/10.1007/BF03345106

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  • DOI: https://doi.org/10.1007/BF03345106

Key-words

  • Glucose-6-phosphatase
  • glycogen
  • glycogen phosphorylase
  • lipase esterase
  • lipids
  • melatonin
  • rat
  • T4
  • T3