The effects of leptin hormone on locomotor activity in Syrian hamsters (Mesocricetus auratus)

The suprachiasmatic nucleus (SCN) generates and controls the circadian rhythms in mammals including the rhythm of locomotor activity. Leptin is a hormone secreted by adipose tissue that informs the brain about the fat stores. SCN neurons express leptin receptors. Here we investigated the effects of 3 different leptin administrations on the locomotor activity of the Syrian hamsters maintained in constant darkness. Animals were intraperitoneally (ip) injected (4 µg/kg), subcutaneously (sc) infused (4 µg/kg), or intra-SCN infused (0.4 µg/kg) with leptin for 3 days at circadian time 10 whereas the controls received saline (0.9% NaCl) at the same time in order to eliminate stress factors. Our results demonstrate that the locomotor activity of the hamsters can be phase advanced by the external leptin administrations. Leptin affected the level of phase-shifts in an administration method-dependent manner. The biggest phase advance was observed in intra-SCN infusion (P = 0.001), and the smallest was in the ip injection (P = 0.041) group. The wheel-turn amounts did not change significantly in the groups before and after the leptin administrations (P = 0.233); however, the period lengths increased (P = 0.011) significantly after leptin administrations. These results suggest for the first time that in vivo leptin administrations may change the rhythm of locomotor activity in adult male Syrian hamsters.

The effects of leptin hormone on locomotor activity in Syrian hamsters (Mesocricetus auratus)

The suprachiasmatic nucleus (SCN) generates and controls the circadian rhythms in mammals including the rhythm of locomotor activity. Leptin is a hormone secreted by adipose tissue that informs the brain about the fat stores. SCN neurons express leptin receptors. Here we investigated the effects of 3 different leptin administrations on the locomotor activity of the Syrian hamsters maintained in constant darkness. Animals were intraperitoneally (ip) injected (4 µg/kg), subcutaneously (sc) infused (4 µg/kg), or intra-SCN infused (0.4 µg/kg) with leptin for 3 days at circadian time 10 whereas the controls received saline (0.9% NaCl) at the same time in order to eliminate stress factors. Our results demonstrate that the locomotor activity of the hamsters can be phase advanced by the external leptin administrations. Leptin affected the level of phase-shifts in an administration method-dependent manner. The biggest phase advance was observed in intra-SCN infusion (P = 0.001), and the smallest was in the ip injection (P = 0.041) group. The wheel-turn amounts did not change significantly in the groups before and after the leptin administrations (P = 0.233); however, the period lengths increased (P = 0.011) significantly after leptin administrations. These results suggest for the first time that in vivo leptin administrations may change the rhythm of locomotor activity in adult male Syrian hamsters.

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  • Stetson MH, Watson-Whitmyre M. Nucleus suprachiasmaticus: Th e biological clock in the hamster? Science 191: 197-199, 1976.
  • Gillette MU, Mitchell JW. Signaling in the suprachiasmatic nucleus: selectively responsive and integrative. Cell Tissue Res 309: 99-107, 2002.
  • Refi netti R, Kaufman CM, Menaker M. Complete suprachiasmatic nuclei lesions eliminate circadian rhythmicity of body temperature and locomotor activity in golden hamsters. J Comp Physiol 175: 223-232, 1994.
  • Le Sauter J, Silver R. Suprachiasmatic nucleus lesions abolish and fetal SCN graft s restore circadian gnawing rhythms in hamsters. Res Neuro Neurosci 6: 135-143, 1994.
  • Challet E, Caldelas I, Graff C et al. Synchronization of the molecular clockwork by light-dark and food-related cues in mammals. Biol Chem 384: 711-719, 2003.
  • Rusak B. Biological rhythms: from physiology to behaviour. In: Montplaisir J, Godbout R. eds. Sleep and Biological Rhythms. Oxford University Press, New York; 1990: pp. 11-24.
  • Francis AJP, Coleman GJ. Th e eff ect of ambient temperature cycles upon circadian running and drinking activity in male and female laboratory rats. Physiol Behav 43: 471-477, 1988.
  • Goel N, Lee TM. Social cues accelerate reentrainment of circadian rhythms in diurnal female Octodon degus (Rodentia: Octodontidae). Chronobiol Int 12: 311-323, 1995.
  • Prosser RA, Bergeron HE. Leptin phase advances the rat suprachiasmatic circadian clock in vitro. Neurosci Letters 336: 139-142, 2003.
  • Ahima RS, Prabakaran D, Mantzoros C et al. Role of leptin in the neuroendocrine response to fasting. Nature 382: 250-252, 1996.
  • Ahima RS, Prabakaran D, Flier JS. Postnatal leptin range and regulation of circadian rhythm of leptin by feeding. Implications for energy homeostasis and neuroendocrine function. J Clin Invest 101: 1020-1027, 1998.
  • Gündüz B. Daily rhythm in serum melatonin and leptin levels in the Syrian hamster (Mesocricetus auratus). Comp Biochem Physiol 132: 393-401, 2002.
  • Kalsbeek A, Fliers E, Romijn JA et al. Th e suprachiasmatic nucleus generates the diurnal changes in plasma leptin levels. Endocrinology 142: 2677-2685, 2001.
  • Karakas A, Gündüz B. Suprachiasmatic nuclei may regulate the rhythm of leptin hormone release in Syrian hamsters (Mesocricetus auratus). Chronobiol Int 23: 225-236, 2006.
  • Prolo P, Wong ML, Licinio J. Leptin. Int J Biochem Cell Biol 30: 1285-1290, 1998.
  • Guan XM, Hess JF, Yu H et al. Diff erential expression of mRNA for leptin receptor isoforms in the rat brain. Mol Cell Endocrinol 133: 1-7, 1997.
  • Carter DS, Goldman BD. Antigonadal eff ects of timed melatonin infusion in pinealectomized male Djungarian hamsters (Phodopus sungorus sungorus): duration is the critical parameter. Endocrinology 113: 1261-1267, 1983.
  • Hao J, Cabeza de Vaca S, Carr KD. Eff ects of chronic ICV leptin infusion on motor-activating eff ects of D-amphetamine in food-restricted and ad libitum fed rats. Physiol Behav 83: 377-381, 2004.
  • Choi YH, Li CL, Hartzell DL et al. ICV leptin eff ects on spontaneous physical activity and feeding behavior in rats. Behav Brain Res 188: 100-108, 2008.
  • Wittert GA, Turnbull H, Hope P. Exogenously administered leptin leads to weight loss and increased physical activity in the marsupial Sminthopsis crassicaudata. Physiol Behav 85: 613- 620, 2005.
  • Banks WA, Kastin AJ, Huang W et al. Leptin enters the brain by a saturable system independent of insulin. Peptides 17: 305- 311, 1996.
  • Burguera B, Couce ME, Curan GL et al. Obesity is associated with a decreased leptin transport across the blood-brain barrier in rats. Diabetes 49: 1219-1223, 2000.
  • Horton TH, Buxton OM, Losee-Olson S et al. Twenty-four- hour profi les of serum leptin in Siberian and golden hamsters: photoperiodic and diurnal variations. Horm Behav 37: 388- 398, 2000.
  • Schwartz MD, Nunez AA, Smale L. Diff erences in the suprachiasmatic nucleus and lower subparaventricular zone of diurnal and nocturnal rodents. Neuroscience 127: 13-23, 2004.
  • Bouret SG, Draper SJ, Simerly RB. Trophic action of leptin on hypothalamic neurons that regulate feeding. Science 304: (5667) 108-110, 2004.
  • Buijs RM, Scheer FA, Kreier F et al. Organization of circadian function: interaction with the body. Prog Brain Res 153: 341- 360, 2006.
  • Gooley JJ, Schomer A, Saper CB. Th e dorsomedial hypothalamic nucleus is critical for the expression of food- entrainable circadian rhythms. Nature Neuroscience 9: 398- 407, 2006.
  • Turek FW, Joshu C, Kohsaka A et al. Obesity and metabolic syndrome in circadian Clock mutant mice. Science 308: 1043- 1045, 2005.
  • Miyasaka K, Ichikawa M, Momose K et al. Physiological and pathological age-associated changes in diurnal rhythm of energy expenditure in rats. Arch Gerontol Geriatr 39: 83-91, 2004.
  • Krieger DT. Restoration of corticosteroid periodicity in obese rats by limited A.M. food access. Brain Res 171: 67-75, 1979.
  • Richardson GS. Circadian rhythms and aging. In: Schneider EL, Rowe JW. eds., Handbook of the Biology of Aging. Academic Press, San Diego; 1990: pp. 275-305.
Turkish Journal of Biology-Cover
  • ISSN: 1300-0152
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

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Production, purification, and characterization of a-amylase by Bacillus subtilis and its mutant derivates

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The effects of leptin hormone on locomotor activity in Syrian hamsters (Mesocricetus auratus)

Bülent GÜNDÜZ, Alper KARAKAŞ

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Mehmet Burçin MUTLU, Kıymet GÜVEN