Serum leptin profiles, food intake, and body weight in melatonin-implanted Syrian hamsters (Mesocricetus auratus) exposed to long and short photoperiods

We have shown that circadian changes in leptin concentrations are inversely linked to circulating melatonin levels in the Syrian hamster. The present study aimed to assess the effects of subcutaneous melatonin implants under different photoperiodic conditions: did the implants affect serum leptin levels, body weight, food consumption, and/or testicular weight? Male hamsters were exposed to long and short photoperiods for 10 weeks and received subcutaneous melatonin implants (1 mg in 24 mg beeswax) every 2 weeks. Blood samples were collected every week at midday (1200 hours) or midnight (0000 hours) to assess leptin and melatonin concentrations. Testes were measured to calculate weight. Body weight and food intake were determined every week. Melatonin implants blocked the testicular regression produced by short photoperiods. No differences in body weight were observed among any of the groups. Food consumption increased only with the melatonin implant in the short photoperiod. Serum leptin levels in both photoperiods remained constant. Differences were apparent between noon and night leptin profiles. Noon leptin levels were high (16-18 ng/mL) compared to night leptin levels (8-11 ng/mL) in untreated controls. On the other hand, serum leptin concentrations declined in melatonin-implanted hamsters in both photoperiods. The effects of melatonin on leptin hormone profiles are very pronounced, and melatonin seems to have both physiologically and pharmacologically suppressive effects on leptin production by direct or indirect mechanisms.

Serum leptin profiles, food intake, and body weight in melatonin-implanted Syrian hamsters (Mesocricetus auratus) exposed to long and short photoperiods

We have shown that circadian changes in leptin concentrations are inversely linked to circulating melatonin levels in the Syrian hamster. The present study aimed to assess the effects of subcutaneous melatonin implants under different photoperiodic conditions: did the implants affect serum leptin levels, body weight, food consumption, and/or testicular weight? Male hamsters were exposed to long and short photoperiods for 10 weeks and received subcutaneous melatonin implants (1 mg in 24 mg beeswax) every 2 weeks. Blood samples were collected every week at midday (1200 hours) or midnight (0000 hours) to assess leptin and melatonin concentrations. Testes were measured to calculate weight. Body weight and food intake were determined every week. Melatonin implants blocked the testicular regression produced by short photoperiods. No differences in body weight were observed among any of the groups. Food consumption increased only with the melatonin implant in the short photoperiod. Serum leptin levels in both photoperiods remained constant. Differences were apparent between noon and night leptin profiles. Noon leptin levels were high (16-18 ng/mL) compared to night leptin levels (8-11 ng/mL) in untreated controls. On the other hand, serum leptin concentrations declined in melatonin-implanted hamsters in both photoperiods. The effects of melatonin on leptin hormone profiles are very pronounced, and melatonin seems to have both physiologically and pharmacologically suppressive effects on leptin production by direct or indirect mechanisms.

___

  • Ahima RS, Prabakaran D, Mantzoros C, Qu DQ, Lowell B, MaratosFlier E, Flier J (1996). Role of leptin in the neuroendocrine response to fasting. Nature 382: 250–252.
  • Baltaci AK, Mogulkoc R (2007). Pinealectomy and melatonin administration in rats: their effects on plasma leptin levels and relationship with zinc. Acta Biol Hung 58: 335–43.
  • Baltaci AK, Mogulkoc R (2012). Leptin and zinc relation: in regulation of food intake and immunity. Indian J Endocrinol Metab 16: 611–616.
  • Bartness TJ, Wade GN (1984). Photoperiodic control of body weight and energy metabolism in Syrian hamsters (Mesocricetus auratus): role of the pineal gland, melatonin, gonads, and diet. Endocrinology 114: 492–498.
  • Bronson FH, Heideman PD (1994). The Physiology of Reproduction. New York, NY, USA: Raven Press.
  • Chehab FF, Lim M, Ronghua L (1996). Correction of sterility in omozygous female obese mice by treatment with the human recombinant leptin. Nature Genet 12: 318–320.
  • Choi SJ, Dallman MF (1999). Hypothalamic obesity: multiple routes mediated by loss of function in medial cell groups. Endocrinology 140: 4081–4088.
  • Dark J, Zucker I, Wade GN (1983). Photoperiodic regulation of body mass, food intake, and reproduction in meadow voles. Am J Physiol-Reg I 245: R334–R338.
  • Davis FC (1989). Daily variation in maternal and fetal weight gain in mice and hamster. J Exp Zool 250: 273–282.
  • Gündüz B (2002). Daily rhythm in serum melatonin and leptin levels in the Syrian hamster (Mesocricetus auratus). Comp Biochem Phys A 132: 393–401.
  • Hoffman RA (1983). Seasonal growth and development and the influence of the eyes and pineal gland on body weight of golden hamsters (M. auratus). Growth Factors 47: 109–121.
  • Hoffman RA, Davidson K, Steinberg K (1982). Influence of photoperiod and temperature on weight gain, food consumption, fat pads, and thyroxine in male golden hamsters. Growth Factors 46: 150–162.
  • Horton TH, Ray SL, Rollag MD, Yellon SM, Stetson MH (1992). Maternal transfer of photoperiodic information in Siberian hamsters. 5. Effects of melatonin implants are dependent on photoperiod. Biol Reprod 47: 291–296.
  • Kalsbeek A, Fliers E, Romijn JA, LaFleur SE, Wortel J, Bakker O, Endert E, Buijs RM (2001). The suprachiasmatic nucleus generates the diurnal changes in plasma leptin levels. Endocrinology 142: 2677–2685.
  • Karakas A, Camsari C, Serin E, Gündüz B (2005). Effects of photoperiod and food availability on growth, leptin, sexual maturation and maintenance in the Mongolian gerbils (Meriones unguiculatus). Zool Sci 22: 665–670.
  • Karakas A, Gündüz B (2006). Suprachiasmatic nuclei may regulate the rhythm of leptin hormone release in Syrian hamsters (Mesocricetus auratus). Chronobiol Int 23: 225–236.
  • Klingenspor M, Dickopp A, Heldmaier G, Klaus S (1996). Short photoperiod reduces leptin gene expression in white and brown adipose tissue of Djungarian hamsters. FEBS Lett 399: 290–294.
  • Klingenspor M, Niggemann H, Heldmaier G (2000). Modulation of leptin sensitivity by short photoperiod acclimation in the Djungarian hamster, Phodopus sungorus. Am J Physiol-Reg I B 170: 37–43.
  • Matthew JC, Donald LJ, Roberst AS (1999). Leptin’s actions on the reproductive axis: perspectives and mechanisms. Biol Reprod 60: 216–222.
  • Nieminen P, Mustonen AM, Asikainen J, Hyvarinen H (2002). Seasonal weight regulation of the raccoon dog (Nyctereutes procyonoides): interactions between melatonin, leptin, ghrelin and growth hormone. J Biol Rhythm 17: 75–83.
  • Ng TB, Wong CM (1986). Effects of pineal indoles and arginine vasotocin on lipolysis and lipogenesis in isolated adipocytes. J Pineal Res 3: 55–66.
  • Rasmussen DD, Boldt BM, Wilkinson CW, Yellon SM, Matsumoto AM (1999). Daily melatonin administration at middle age suppresses rat visceral fat, plasma leptin and plasma insulin to youthful levels. Endocrinology 110: 1009–1012.
  • Reiter RJ (1980). The pineal gland and its hormones in the control of reproduction in mammals. Endocr Rev 1: 109–131.
  • Reiter RJ (1991). Melatonin: that ubiquitously acting pineal hormone. News Physiol Sci 6: 223–227.
  • Rowland NE (1985). Ingestive behavior of Syrian hamsters— advantages of the comparative approach. Brain Res 15: 417– 4
  • Rusak B, Zucker I (1992). Neural regulation of circadian rhythms. Physiol Rev 59: 449–526.
  • Saladin R, Devos P, Guerremillo M, Leturque A, Girard J, Staels B, Auwerx J (1995). Transient increase in obese gene-expression after food-intake or insulin administration. Nature 377: 527– 5
  • Steinlechner S, Niklowitz P (1992). Impact of photoperiod and melatonin on reproduction in small mammals. Anim Reprod Sci 30: 1–28.
  • Stetson MH, Rollag MD, Watson-Whitmyre M, Tate-Ostroff B (1983). The effects of daily injections and constant release melatonin on the endogenous pineal melatonin rhythm in golden hamsters. Exp Biol M 74: 119–122.
  • Turek FW (1979). Effect of melatonin photic-independent and photic-dependent testicular growth in juvenile and adult male golden hamsters. Biol Reprod 20: 1119–1122.
  • Wade GN, Schneider JE, Li HY (1996). Control of fertility by metabolic cues. Am J Physiol-Reg I 270: E1–E19.
  • Wang J, Liu R, Hawkins M, Barzilai N, Rossetti L (1998). A nutrientsensing pathway regulates leptin gene expression in muscle and fat. Nature 393: 684–688.
  • Watson-Whitmyre M, Stetson MH (1985). A mathematical method for estimating paired testes weight from in situ testicular measurements in three species of hamster. Anat Rec 213: 473– 4
  • Williams LM, Morgan PJ, Hastings MH, Lawson W, Davidson G, Howell HE (1989). Melatonin receptor sites in the Syrian hamster brain and pituitary: localization and characterization using [ 125
  • I]iodomelatonin. J Neuroendocrinol 1: 315–320. Wolden-Hansen T, Mitton DR, McCants RL (2000). 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 141: 487–497.
  • Zalatan F, Krause JA, Blask DE (2001). Inhibition of isoproterenolinduced lipolysis in rat inguinal adipocytes in vitro by physiological melatonin via receptor-mediated mechanism. Endocrinology 142: 3783–3790.
  • Ziylan YZ, Baltaci AK, Mogulkoc R (2009). Leptin transport in the central nervous system. Cell Biochem Funct 27: 63–70.
Turkish Journal of Biology-Cover
  • ISSN: 1300-0152
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

A cDNA-AFLP protocol with reciprocally arranged 2-enzyme sequential digestion and silver staining detection

Mehmet Ali SÜDÜPAK

A preliminary proteomic evaluation of smooth muscle cells in thoracic aortic aneurysms

Ceyda Açilan AYHAN, Betül BAYKAL, Müge SERHATLI

Does CYP1A1 gene polymorphism affect cell damage biomarkers and ageing?

Sima Ataollahi ESHKOOR, Patimah ISMAIL, Sabariah Abd RAHMAN

The modeled structures of Deg5 and Deg8 proteases in Arabidopsis thaliana

Liangbing CHEN, Qingzhi LI, Lili LI

Genome-wide identification and analysis of growth regulating factor genes in Brachypodium distachyon: in silico approaches

Ertuğrul FİLİZ, İbrahim KOÇ, Hüseyin TOMBULOĞLU

Serum leptin profiles, food intake, and body weight in melatonin-implanted Syrian hamsters (Mesocricetus auratus) exposed to long and short photoperiods

Bülent GÜNDÜZ

Effect of water deficiency on seed quality and physiological traits of different safflower genotypes

Hajar AMINI, Ahmad ARZANI, Mostafa KARAMI

Identification and expression profiling of CLCuV-responsive transcripts in upland cotton (Gossypium hirsutum L.)

Beenish AFTAB, Muhammad Naveed SHAHID, Sania RIAZ, Adil JAMAL, Bahaeldeen Babiker MOHAMED

Temperature-induced stress response in Lymantria dispar neurosecretory neurons

Larisa ILIJIN, Milena VLAHOVIC, Vesna Peric MATARUGA, Ivana KMETIČ, Anja GAVRILOVIĆ, Dragana MATIĆ, Marija MRDAKOVIĆ

Effect of nanosized TiO2 particles on the development of Xenopus laevis embryos

Ayşe BİRHANLI, Fatma Bilge EMRE, Funda SAYILKAN, Abbas GÜNGÖRDÜ