Effect of melatonin supplementation on food and water intake in streptozotocin-diabetic and non-diabetic male Wistar rats

Nutricion Hospitalaria

Volumn 25, Issue 6, 2010, Pages 931-938

  Montano, M E ^b   Molpeceres, V ^a   Mauriz, J L ^a   Garzo, E ^a   Cruz, I B M ^c   Gonzalez P ^a   Barrio, J P ^a  

^a UNIVERSITY OF LEÓN   (Spain)

^b Universidade Do Noroeste Do Estado de Santa Catarina   (Brazil)

^c FEDERAL UNIVERSITY OF SANTA MARIA   (Brazil)

Author keywords

Diabetes; Feeding behavior; Feeding pattern; Melatonin; Rat

Indexed keywords

ANIMALIA; RATTUS; RATTUS NORVEGICUS;

ANTIOXIDANT; MELATONIN;

ANIMAL; ARTICLE; DIET SUPPLEMENTATION; DRINKING; DRUG EFFECT; EATING; EXPERIMENTAL DIABETES MELLITUS; FEEDING BEHAVIOR; GLUCOSE BLOOD LEVEL; LIVER; MALE; METABOLISM; PATHOLOGY; PSYCHOLOGICAL ASPECT; RAT; WISTAR RAT;

ANIMALS; ANTIOXIDANTS; BLOOD GLUCOSE; DIABETES MELLITUS, EXPERIMENTAL; DIETARY SUPPLEMENTS; DRINKING; EATING; FEEDING BEHAVIOR; LIVER; MALE; MELATONIN; RATS; RATS, WISTAR;

EID: 78649623947     PISSN: 02121611     EISSN: 16995198     Source Type: Journal    
DOI: 10.3305/nh.2010.25.6.4803     Document Type: Article

References (49)

1. Teff K. Nutritional implications of the cephalic-phase reflexes: Endocrine responses. Appetite 2000; 34: 206-13.
2. Sahu A. A hypothalamic role in energy balance with special emphasis on leptin. Endocrinology 2004; 145: 2613-20.
3. Konturek SJ, Konturek PC, Brzozowska I, Pawlik M, Sliwowski Z, Czesnikiewicz-Guzik M et al. Localization and biological activities of melatonin in intact and diseased gastrointestinal tract (GIT). J Physiol Pharmacol 2007; 58: 381-405.
4. Bubenik GA. Gastrointestinal Melatonin. Localization, Function, and Clinical Relevance. Dig Dis Sci 2002; 42: 2336-48.
5. Thor PJ, Krolczyk G, Gil K, Zurowski D, Nowak L. Melatonin and serotonin effects on gastrointestinal motility. J Physiol Pharmacol 2007; 58: 97-103.
6. Kasimay O, Cakir B, Devseren E, Yegen BC. Exogenous melatonin delays gastric emptying rate in rats: role of CCK2 and 5-HT3 receptors. J Physiol Pharmacol 2005; 56: 543-53.
7. Cardinali DP, Vacas MI, Keller-Sarmiento MI, Etchegoyen GS, Pereyra EN, Chuluyan HE. Neuroendocrine integrative mechanisms in mammalian pineal gland: effects of steroid and adenohypophisial hormones on melatonin synthesis in vitro. J Steroid Biochem 1984; 83-107.
8. Nakagawa H, Nagai K, Kida K, Nishio T. Control mechanisms of circadian rhythms of feeding behavior and metabolism influenced by food intake. In: Suda H, Hayaishi O, Nakagawa H, editors. Biological rhythms and their central mechanisms. Amsterdam:Elsevier-North Holland Press; 1979, pp. 283-294.
9. Brooks CM, Ishikawa T, Koizumi K. Autonomic system control of the pineal gland and the role of this complex in the integration of body function. Brain Res 1975; 87: 181-90.
10. Peschke D, Peschke E, Mess B. Circannual rhythm and increase of body weight and food intake in the young Wistar rat following pinealectomy and ganglionectomy. Neuroendocrinol Lett 1987; 9: 321-7.
11. Granneman JG, Stricker EM. Food intake and gastric emptying in rats with streptozotocin-induced diabetes. Am J Physiol 1984; 247: R1054-R-1061.
12. Smith JC, Gannon KS. Ingestion patterns of food, water, saccharin and sucrose in streptozotocin-induced diabetic rats. Physiol Behav 1991; 49: 189-99.
13. Vanderweele DA. Insulin and satiety from feeding in pancreatic- normal and diabetic rats. Physiol Behav 1993; 54: 477-85.
14. Baydas G, Canatan H, Turkoglu A. Comparative analysis of the protective effects of melatonin and vitamin E on streptozotocin-induced diabetes mellitus. J Pineal Res 2002; 32: 225-30.
15. Angers K, Haddad N, selmaoui B, Thibault L. Effect of melatonin on total food intake and macronutrient choice in rats. Physiol Behav 2003; 80: 9-18.
16. Wolden-Hanson T, Mitton DR, McCants RL, Yellon SM, Wilkinson CW, Matsumoto AM et al. Daily melatonin administration to middle-aged male rats suppresses body weight, intraabdominal adiposity, and plasma leptin and insulin independent of food intake and total body fat. Endocrinology 2000;141: 487-97.
17. Clifton PG. Meal patterning in rodents: psychopharmacological and neuroanatomical studies. Neuroscience & Biobehavioral Reviews 2000; 24: 213-22.
18. Tolkamp BJ, Kyriazakis I. To split behaviour into bouts, logtransform the intervals. Anim Behav 1999; 57: 807-17.
19. Keppler CA & Decker K. Glycogen determination with amyloglucosidase. In: Bergmeyer HU, editor. Methods in Enzymology. New York:Academic Press; 1974, pp. 1127-1131.
20. González E, Rosello-Catafau J, Jawerbaum A, Novaro V, Gómez G, Gelpi E, et al. Influence of nitric oxide synthase and kinin antagonists on metabolic parameters in chronic streptozotocininduced diabetes mellitus. Prostaglandins 1997; 53: 321-36.
21. Stadler K, Jenei V, Von Bolcshazy G, Somogyi A, Jakus J. Increased nitric oxide levels as an early sign of premature aging in diabetes. Free Rad Biol Med 2003; 35: 1240-51.
22. Sprangers F, Sauerwein HP, Romijn JA, van Woerkom GM, Meijer AJ. Nitric oxide inhibits glycogen synthesis in isolated rat hepatocytes. Biochem J 1998; 330: 1045-9.
23. Escames G, León J, Macías M, Khaldy H, Acuña- Castroviejo D. Melatonin counteracts lipopolysaccharide-induced expression and activity of mitochondrial nitric oxide synthase in rats. Faseb J 2003; 17: 932-4.
24. Sudnikovich EJ, Maksimchik YZ, Zabrodskaya SV, Kubyshin VL, Lapshina EA, Bryszewska M et al. Melatonin attenuates metabolic disorders due to streptozotocin-induced diabetes in rats. Eur J Pharmacol 2007; 569: 180-7.
25. Montilla López P, Vargas JF, Tunez I, Muñoz de Agueda MC, Valdelvira ME, Cabrera ES. Oxidative stress in diabetic rats induced by streptozotocin: protective effects of melatonin. J Pineal Res 1998; 25: 94-100.
26. Abdel-Wahab MH, Abd-Allah ARA. Possible protective effect of melatonin and/or desferrioxamine against streptozotocininduced hyperglycaemia in mice. Pharmacol Res 2000; 41: 533-7.
27. Anwar MM, Meki AMA. Oxidative stress in streptozotocininduced diabetic rats effects of garlic oil and melatonin. Comp Biochem Physiol A 2003; 135: 539-47.
28. Sailaja Devi MM, Suresh Y, Das UN. Preservation of the antioxidant status in chemically-induced diabetes mellitus by melatonin. J Pineal Res 2000; 29: 108-15.
29. Baydas G, Yilmaz O, Celik S, Yasar A, Gursu MF. Effects of certain micronutrients and melatonin on plasma lipid, lipid peroxidation, and homocysteine levels in rats. Arch Med Res 2002;33: 515-9.
30. Ojiro K, Kitamura H, Shimada T, Nakamura M. A morphometrical study of the postnatal development of rat pancreatic islets, with special regard to the differences between Wistar and Sprague-Dawley strains. Kaibogaku Zasshi 1993; 68: 190-203.
31. Mazepa RC, Cuevas MJ, Collado PS, Gonzalez-Gallego J. Melatonin increases muscle and liver glycogen content in nonexercised and exercised rats. Life Sci 2000; 66: 153-60.
32. Markova M, Adamekova E, Bojkova E, Kubatka P, Kassayova M, Ahlersova E et al. Effect of low-dose chronic melatonin administration on metabolic and hormonal variables in young laboratory rats. Acta Vet Brno 2004; 73: 445-53.
33. Mustonen AM, Nieminen P, Hyvarinen H. Effects of continuous light and melatonin treatment on energy metabolism of the rat. J Endocrinol Invest 2002; 25: 716-23.
34. De Castro JM, Balagura S. Relationship between endogenous, natural feeding patterns and body composition in the rat. Physiol Behav 1975; 15: 635-9.
35. Anderson LC. Effects of diabetes and dietary manipulation on rat parotid gland secretory response to sympathetic nerve stimulation. Comp Biochem Physiol A Comp Physiol 1991; 98: 363-6.
36. Peschke E, Wolgast S, Bazwinsky I, Ponicke K, Muhlbauer E. Increased melatonin synthesis in pineal glands of rats in streptozotocin induced type 1 diabetes. J Pineal Res 2008; 45: 439-48.
37. Kalra SP, Ueno N, Kalra PS. Stimulation of appetite by ghrelin is regulated by leptin restraint: peripheral and central sites of action. J Nutr 2005; 135: 1331-5.
38. Pico C, Oliver P, Sánchez J, Palou A. Gastric leptin: a putative role in the short-term regulation of food intake. Br J Nutr 2003; 90: 735-41.
39. Nakazato M, Murakami N, Date Y, Kojima M, Matsuo H, Kangawa K et al. A role for ghrelin in the central regulation of feeding. Nature 2001; 409: 194-8.
40. Mustonen AM, Nieminen P, Hyvarinen H. Preliminary evidence that pharmacologic melatonin treatment decreases rat ghrelin levels. Endocrine 2001; 16: 43-6.
41. Baltaci AK, Mogulkoc R. Pinealectomy and melatonin administration in rats: their effects on plasma leptin levels and relationship with zinc. Acta Biol Hung 2007; 58: 335-43.
42. Zorrilla EP, Inoue K, Valdez GR, Tabarin A, Koob GF. Leptin and post-prandial satiety: acute central leptin more potently reduces meal frequency than meal size in the rat. Psychopharmacology 2005; 177: 324-35.
43. Richardson BA, Studier EH, Stallone JN, Kennedy CM. Effects of melatonin on water metabolism and renal function in male Syrian hamsters (Mesocricetus auratus). J Pineal Res 1992; 13: 49-59.
44. Juszczak M, Boczek-Leszczyk E, Stempniak B. Effect of melatonin on the vasopressin secretion as influenced by tachykinin NK-1 receptor agonist and antagonist: in vivo and in vitro studies. J Physiol Pharmacol 2007; 58: 829-43.
45. Zambotti-Villela L, Yamasaki SC, Villarroel JS, Murena-Nunes C, Silveira PF. Prolyl, cystyl and pyroglutamyl peptidase activities in the hippocampus and hypothalamus of streptozotocin-induced diabetic rats. Peptides 2007; 28: 1586-95. (Pubitemid 47247968)
46. Merle A, Delagrange Ph, Renard P, Lesieur D, Cuber JC, Roche M et al. Effect of melatonin on motility pattern of small intestine in rats and its inhibition by melatonin receptor antagonist S 22153. J Pineal Res 2000; 29: 116-24.
47. Chesta J, Debnam ES, Srai SK, Epstein O. Delayed stomach to caecum transit time in the diabetic rat. Possible role of hyperglucagonaemia. Gut 1990; 31: 660-2.
48. Kim WK, Chung MK, Kang NE, Kim MH, Park OJ. Effect of resistant starch from corn or rice on glucose control, colonic events, and blood lipid concentrations in streptozotocininduced diabetic rats. J Nutr Biochem 2003; 14: 166-72.
49. European Medicines Agency (2008) EPARs for authorized medicinal products for human use.