Horm Metab Res 2008; 40(6): 398-403
DOI: 10.1055/s-2008-1065330
Animals, Clinical

© Georg Thieme Verlag KG Stuttgart · New York

Effect of Constant Light on Prolactin and Corticosterone Rhythms Evaluated Using a Noninvasive Urine Sampling Protocol in the Rat

B. Claustrat 1 , 2 , J.-L. Valatx 3 , C. Harthé 1 , J. Brun 1
  • 1Service de Radioanalyse, Centre de Médecine Nucléaire, GHE 59 blvd Pinel, Bron, France
  • 2INSERM, U846, Stem Cell and Brain Research Institute, Department of Chronobiology, Bron, France
  • 3INSERM U628, Faculty of Medicine, 8 avenue Rockefeller, Lyon, France
Further Information

Publication History

received 10.07.2007

accepted 28.11.2007

Publication Date:
14 April 2008 (online)

Abstract

Circadian prolactin and corticosterone rhythms are usually investigated in the rat by analysis of plasma hormone profiles. In order to develop a nonstressful methodology for long-term studies, we validated prolactin and corticosterone radioimmunoassays in rat urine samples. Among the criteria of validation, prolactin was identified in urine by Western blot whereas both prolactin and corticosterone levels were undetectable in the urine of hypophysectomized rats. The determination of prolactin and corticosterone levels on serial urine samples showed daily variations in male rats entrained by the light-dark cycle. The acrophases of the 24-hour prolactin and corticosterone profiles were located at 03:26 h and 23:32 h respectively, a delay of 3-4 hours compared with the values of the 24-hour plasma profiles reported in the literature. Corticosterone and prolactin rhythms were abolished or dramatically delayed after 3 weeks of constant illumination. As expected, constant light suppressed the rhythm of 6-sulfatoxymelatonin, the major hepatic metabolite of melatonin. The noninvasive and nonstressful methodology we developed could be of interest for studying the regulation of hormone rhythms and their mutual endocrine interactions in physiological conditions, especially their evolution in the aging process.

References

  • 1 Abe K, Kroning J, Greer MA, Critchlow V. Effects of destruction of the suprachiasmatic nuclei on the circadian rhythms in plasma corticosterone, body temperature, feeding and plasma thyrotropin.  Neuroendocrinology. 1979;  29 119-131
  • 2 Klein DC, Moore RY. Pineal N-acetyltransferase and hydroxyindole-o-methyl-transferase : control by the retinohypothalamic tract and the suprachiasmatic nucleus.  Brain Res. 1979;  174 245-262
  • 3 Rusak B, Zucker I. Neural regulation of circadian rhythms.  Physiol Rev. 1979;  59 449-526
  • 4 Klein DC, Weller JL. A rapid light-induced decrease in pineal serotonin N-acetyltransferase activity.  Science. 1972;  177 532-533
  • 5 Brown GM, Bar-Or A, Grossi D, Kashur S, Johannson E, Yie SM. Urinary 6-sulphatoxymelatonin, an index of pineal function in the rat.  J Pineal Res. 1991;  10 141-147
  • 6 Takahashi K, Inoue K, Takahashi Y. Parallel shift in circadian rhy-thms of adrenocortical activity and food intake in blinded and intact rats exposed to continuous illumination.  Endocrinology. 1977;  100 1097-1107
  • 7 Fischman AJ, Kastin AJ, Graf MV, Moldow RL. Constant light and dark affect the circadian rhythm of the hypothalamic-pituitary-adrenal axis.  Neuroendocrinology. 1988;  47 309-316
  • 8 Dunn J, Schering L, Millet P. Circadian variation in stress-evoked increases in plasma corticosterone.  Am J Physiol. 1972;  223 402-406
  • 9 Dunn JD, Arimura A, Schering LE. Effect of stress on circadian periodicity in serum LH and PRL concentration.  Endocrinology. 1972;  90 29-33
  • 10 Lisboa PC, Passos MCF, Bonomo IT, Denolato ATA, Reis AM, Moura EG. Leptin and prolactin, but not cortisoterone, modulate body weight and thyroid function in protein-malnourished lactating rats.  Horm Metab Res. 2006;  38 295-299
  • 11 Atkinson HC, Wood SA, Kershaw YM, Bate E, Lightman SL. Diurnal variation in the responsiveness of the hypothalamic-pituitary-adrenal axis of the male rat to noise stress.  J Neuroendocrinol. 2006;  18 526-533
  • 12 Casanueva F, Apud JA, Masotto C, Cocchi D, Locatelli V, Racagni G, Muller E. Daily fluctuations in the activity of the tuberoinfundibular GABAergic system and plasma prolactin levels.  Neuroendocrinology. 1984;  39 367-370
  • 13 Trouillas J, Girod C, Claustrat B, Joly-Pharaboz MO, Chevallier P. Spontaneous prolactin transplantable tumor in the Wistar/Furth Rat (SMtTW): a new animal model of human prolactinoma.  Cancer Res. 1990;  50 4081-4086
  • 14 Harthé C, Claustrat B, Brun J, Chazot G. Direct radioimmunoassay of 6-sulfatoxymelatonin in plasma with use of an iodinated tracer.  Clin Chem. 1991;  37 536-539
  • 15 Rodbard D, Ruder HJ, Vaitukaitis J, Jacobs HS. Mathematical analysis of kinetics of radioligand assays: improved sensitivity obtained by delayed addition of labelled ligand.  J Clin Endocrinol Metab. 1971;  33 343-355
  • 16 Faure A, Nemoz C, Claustrat B. A graphical and statistical method for investigation of time series in chronobiology according to the cosinor procedure.  Comput Biol Med. 1990;  20 319-329
  • 17 Champier J, Claustrat B, Harthé C, Chevallier P, Trouillas J. Concanavalin-A-bound and -unbound prolactin in normal and hyperprolactinaemic rats.  J Endocrinol. 1992;  134 27-32
  • 18 Kizer JS, Zivin JA, Jacobowitz DM, Kopin IJ. The nyctohemeral rhythm of plasma prolactin: effects of ganglionectomy, pinealectomy, constant light, constant darkness or 6-OH-dopamine administration.  Endocrinology. 1975;  96 1230-1240
  • 19 Gomez-Sanchez C, Holland OB, Higgins JR, Kem DC, Kaplan NM. Circadian rhythms of serum renin activity and serum corticosterone, prolactin, and aldosterone concentrations in the male rat on normal and low-sodium diets.  Endocrinology. 1976;  99 567-572
  • 20 Mhatre MC, Shah PN, Juneja HS. Effect of varying photoperiods on mammary morphology, DNA synthesis, and hormone profile in female rats.  J Nat Cancer Inst. 1984;  72 1411-1416
  • 21 Blask DE, Nodelman JL. An interaction between the pineal gland and olfactory deprivation in potentiating the effects of melatonin on gonads, accessory sex organs and prolactin in male rats.  J Neurosci Res. 1980;  5 129-136
  • 22 Vaughan MK, Johnson LY, Blask DE, Reiter RJ. Melatonin stimulation of prolactin secretion in male rats: influence of pinealectomy, castration or gonadal steroid pretreatment.  Adv Biosci. 1981;  29 165-170
  • 23 Zisapel N, Egozi Y, Laudon M. Inhibition by melatonin of dopamine release from rat hypothalamus in vitro: variations with sex and the estrous cycle.  Neuroendocrinology. 1983;  37 41-47
  • 24 Griffiths D, Bjoro T, Gautvik K, Haug E. Melatonin reduces the production and secretion of prolactin and growth hormone from rat pituitary cells in culture.  Acta Physiol Scand. 1987;  131 43-49
  • 25 Wittkowski W, Bockmann J, Kreutz MR, Böckers TM. Cell and molecular biology of the pars tuberalis of the pituitary.  Int Rev Cytol. 1999;  185 157-194
  • 26 Murphy BEP, Okouneff L, Klein GP, Ngo SC. Lack of specificity of cortisol determinations in human urine.  J Clin Endocrinol Metab. 1981;  53 91-99
  • 27 Ogle TF, Kitay JL. In vitro effects of melatonin and serotonin on adrenal steroidogenesis.  Proc Soc Exp Biol Med. 1978;  157 103-105
  • 28 Rebuffat P, Massocchi G, Gottardo G, Coi A, Menghelli V, Nussdorfer GG. An ultrastructural morphometric study of the effects of chronic melatonin administration on the zona fasciculata of rat adrenal cortex.  J Submicrosc Cytol. 1987;  19 415-421
  • 29 Oxenkrug GF, MacIntyre IM, Gershon S. Effects of pinealectomy and aging on the serum corticosterone circadian rhythm in rats.  J Pineal Res. 1984;  1 181-185
  • 30 Acuna D, Soler L, Garcia Torres I, Vargas F, Garcia del Rio C, Quesada T, Oxoria C. Inhibition of the renin angiotensin system by pinealectomy in female rats.  Rev Esp Fisiol. 1982;  38 251-256
  • 31 Malendowicz LK. Stereological studies on the effects of pinealectomy, melatonin and estradiol on the adrenal cortex of ovariectomized rats.  J Anat. 1985;  141 115-120
  • 32 Weidenfeld Y, Schmidt U, Nir I. The effect of exogenous melatonin on the hypothalamic-pituitary-adrenal axis in intact and pinealectomized rats under basal and stressed conditions.  J Pineal Res. 1993;  14 60-66
  • 33 Buijs RM, Wortel J, Heerikhuize JJ Van, Feenstra MGP, Ter Horst GJ, Romijn HJ, Kalsbeek A. Anatomical and functional demonstration of a multisynaptic suprachiasmatic nucleus adrenal (cortex) pathway.  Eur J Neurosci. 1999;  11 1535-1544
  • 34 Kooy A, Greef WJ De, Vreeburg JTM, Hackeng WHL, Ooms MP, Lamberts SWJ, Weber RFA. Evidence for the involvement of corticotropin-releasing factor in the inhibition of gonadotropin release induced by hyperprolactinemia.  Neuroendocrinology. 1990;  51 261-266
  • 35 Calogero AE, Weber RFA, D’agata R. Effects of rat prolactin on gonadotropin-releasing hormone secretion by the explanted male rat hypothalamus.  Neuroendocrinology. 1993;  57 152-158
  • 36 Frantz WL, Macindoe JH, Turkington RW. Prolactin receptors: characteristics of the particulate fraction binding activity.  J Endocrinol. 1974;  60 485-497
  • 37 Chang LL, Lo MJ, Kan SF, Huang WJS, Chen JJ, Kau MM, Wang JL, Lin H, Tsai SC, Chiao YC, Yeh JY, Wun WSA, Wang PS. Direct effects of prolactin on corticosterone release by zona fasciculata-reticularis cells from male rats.  J Cell Biochem. 1999;  73 563-572
  • 38 Perello M, Chacon F, Cardinali DP, Esquifino AI, Spinedi E. Effect of social isolation on 24-h pattern of stress hormones and leptin in rats.  Life Sci. 2006;  78 1857-1862
  • 39 Soltis J, Wegner FH, Newman JD. Urinary prolactin is correlated with mothering and allo-mothering in squirrel monkeys.  Physiol Behav. 2005;  84 295-301
  • 40 Fall CH, Clark PM, Hinmarsh PC, Clayton PE, Shiell AW, Law CM. Urinary GH and IGF-1 excretion in nine year-old children: relation to sex, current size and size at birth.  Clin Endocrinol. 2000;  53 69-76

Correspondence

B. Claustrat

Service de Radioanalyse

Centre de Médecine Nucléaire

GHE 59 blvd Pinel

69677 Bron

France

Phone: +33/4/72 35 72 93

Fax: +33/4/72 35 73 05

Email: bruno.claustrat@chu-lyon.fr

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