Advances in Clinical and Experimental Medicine

Title abbreviation: Adv Clin Exp Med
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ISSN 1899–5276 (print)
ISSN 2451-2680 (online)
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Advances in Clinical and Experimental Medicine

2019, vol. 28, nr 6, June, p. 737–746

doi: 10.17219/acem/95039

Publication type: original article

Language: English

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Expression profile of Galp, alarin and their receptors in rat adrenal gland

Marianna Tyczewska1,A,B,C,D,E,F, Paulina Milecka2,B,C,F, Marta Szyszka1,B,C,F, Piotr Celichowski1,B,C,F, Karol Jopek1,B,C,F, Hanna Komarowska3,B,C,F, Ludwik Kazimierz Malendowicz1,E,F, Marcin Ruciński1,A,F

1 Department of Histology and Embryology, Poznan University of Medical Sciences, Poland

2 Central Laboratory of Microbiology, H. Swiecicki Clinical Hospital at the Poznan University of Medical Sciences, Poland

3 Department of Endocrinology, Metabolism and Internal Medicine, Poznan University of Medical Sciences, Poland

Abstract

Background. Galanin-like peptide (Galp) and alarin (Ala) are 2 new members of the galanin peptide family. Galanin (Gal), the “parental” peptide of the entire family, is known to regulate numerous physiological processes, including energy and osmotic homeostasis, reproduction, food intake, and secretion of adrenocortical hormones. Galp and Ala are known to regulate food intake. In the rat, Galp mRNA has been found in the brain, exclusively in the hypothalamic arcuate nucleus (ARC) and median eminence, which are involved in the regulation of energy homeostasis. Alarin-like immunoreactivity is present in the locus coeruleus (LC) and the ARC of rats and mice.
Objectives. The aim of the study was to investigate the expression of Ala, Galp and their receptors in the organs of the hypothalamo–pituitary–adrenal (HPA) axis of the rat.
Material and Methods. The expression of the examined genes was measured in different models of adrenal growth of the rat in vivo (postnatal ontogenesis, compensatory adrenal growth, adrenocortical regeneration, adrenocorticotropic hormone (ACTH) administration). The expression was evaluated using the Affymetrix® microarray system or quantitative polymerase chain reaction (qPCR).
Results. The expression of Ala gene was observed in each organ of the HPA axis (the hypothalamus, hypophysis and adrenal gland). The elevated level of expression of this gene was observed in the pituitary of 2-day rats, while very low levels of Ala mRNA were observed in the adrenals. Galp mRNA expression was observed only in the hypothalamus and the hypophysis during postnatal ontogenesis. The expression of Gal receptors was demonstrated in the hypothalamus, the hypophysis and the adrenal gland. In different compartments of the adrenal glands of adult, intact male and female rats, the expression of Ala, Galp and galanin receptor 1 (Galr1) genes was negligible, but the expression of galanin receptor 2 (Galr2), galanin receptor 3 (Galr3) and neurotrophic receptor tyrosine kinase 2 (Ntrk2) genes was noticeable.
Conclusion. The examined genes showed different expression levels within the studied HPA axis; some of them were neither expressed in the hypothalamus or the pituitary gland, nor in the adrenal gland.

Key words

galanin-like peptide, alarin, adrenal gland

References (40)

  1. Hökfelt T, Tatemoto K. Galanin – 25 years with a multitalented neuropeptide. Cell Mol Life Sci. 2008;65(12):1793–1795.
  2. Lang R, Gundlach AL, Kofler B. The galanin peptide family: Receptor pharmacology, pleiotropic biological actions, and implications in health and disease. Pharmacol Ther. 2007;115(2):177–207.
  3. Ohtaki T, Kumano S, Ishibashi Y, et al. Isolation and cDNA cloning of a novel galanin-like peptide (GALP) from porcine hypothalamus. J Biol Chem. 1999;274(52):37041–37045.
  4. Lang R, Berger A, Santic R, et al. Pharmacological and functional characterization of galanin-like peptide fragments as potent galanin receptor agonists. Neuropept. 2005;39:(3)179–184.
  5. Santic R, Fenninger K, Graf K, et al. Gangliocytes in neuroblastic tumors express alarin, a novel peptide derived by differential splicing of the galanin-like peptide gene. J Mol Neurosci. 2006;29(2):145–152.
  6. Krasnow SM, Fraley GS, Schuh SM, Baumgartner JW, Clifton DK, Stei­ner RA. A role for galanin-like peptide in the integration of feeding, body weight regulation, and reproduction in the mouse. Endocrinol. 2003;144(3):813–822.
  7. Patterson M, Murphy KG, Thompson EL, et al. Microinjection of galanin-like peptide into the medial preoptic area stimulates food intake in adult male rats. J Neuroendocrinol. 2006;18(10):742–747.
  8. Juréus A, Cunningham MJ, McClain ME, Clifton DK, Steiner RA. Galanin-like peptide (GALP) is a target for regulation by leptin in the hypothalamus of the rat. Endocrinol. 2000;141(7):2703–2706.
  9. Larm JA, Gundlach AL. Galanin-like peptide (GALP) mRNA expression is restricted to arcuate nucleus of hypothalamus in adult male rat brain. Neuroendocrinol. 2000;72(2):67–71.
  10. Takatsu Y, Matsumoto H, Ohtaki T, et al. Distribution of galanin-like peptide in the rat brain. Endocrinol. 2001;142(4):1626–1634.
  11. Gundlach AL. Galanin/GALP and galanin receptors: Role in central control of feeding, body weight/obesity and reproduction? Eur J Pharmacol. 2002;440(2–3):255–268.
  12. Crawley JN, Austin MC, Fiske SM, et al. Activity of centrally administered galanin fragments on stimulation of feeding behavior and on galanin receptor binding in the rat hypothalamus. J Neurosci. 1990;10(11):3695–3700.
  13. Shiba K, Kageyama H, Takenoya F, Shioda S. Galanin-like peptide and the regulation of feeding behavior and energy metabolism. FEBS J. 2010;277(24):5006–5013.
  14. Corder R, Pralong F, Turnill D, Saudan P, Muller AF, Gaillard RC. Dexamethasone treatment increases neuropeptide Y levels in rat hypothalamic neurones. Life Sci. 1988;43(23):1879–1886.
  15. Malendowicz LK, Tortorella C, Nussdorfer GG. Orexins stimulate corticosterone secretion of rat adrenocortical cells, through the activation of the adenylate cyclase-dependent signaling cascade. J Steroid Biochem Mol Biol. 1999;70(4–6):185–188.
  16. Tortorella C, Neri G, Nussdorfer GG. Galanin in the regulation of the hypothalamic-pituitary-adrenal axis (Review). Int J Mol Med. 2007;19(4):639–647.
  17. Jopek K, Tyczewska M, Celichowski P, Malendowicz LK, Rucinski M. Transcriptome profile in unilateral adrenalectomy-induced compensatory adrenal growth in the rat. Int J Mol Sci. 2018;19(4):1111.
  18. Rucinski M, Ziolkowska A, Szyszka M, Hochol A, Malendowicz LK. Evidence suggesting that ghrelin O-acyl transferase inhibitor acts at the hypothalamus to inhibit hypothalamo–pituitary–adrenocortical axis function in the rat. Peptides. 2012;35(2):149–159.
  19. Trejter M, Jopek K, Celichowski P, Tyczewska M, Malendowicz LK, Rucinski M. Expression of estrogen, estrogen related and androgen receptors in adrenal cortex of intact adult male and female rats. Folia Histochem Cytobiol. 2015;53(2):133–144.
  20. Paschke L, Zemleduch T, Rucinski M, Ziolkowska A, Szyszka M, Malendowicz LK. Adiponectin and adiponectin receptor system in the rat adrenal gland: Ontogenetic and physiologic regulation, and its involvement in regulating adrenocortical growth and steroidogenesis. Peptides. 2010;31(9):1715–1724.
  21. Tyczewska M, Rucinski M, Trejter M, Ziolkowska A, Szyszka M, Malendowicz LK. Angiogenesis in the course of enucleation-induced adrenal regeneration – expression of selected genes and proteins involved in development of capillaries. Peptides. 2012;38(2):404–413.
  22. Gentleman RC, Carey VJ, Bates DM, et al. Bioconductor: Open software development for computational biology and bioinformatics. Genome Biol. 2004;5(10):80.
  23. Santic R, Schmidhuber SM, Lang R, et al. Alarin is a vasoactive peptide. Proc Natl Acad Sci U S A. 2007;104(24):10217–10222.
  24. Benjamini Y, Hochberg Y. Controlling the false discovery rate: A practical and powerful approach to multiple testing. J R Stat Soc Ser B. 1995;57:289–300.
  25. Hochol A, Tortorella C, Rucinski M, Ziolkowska A, Nussdorfer GG, Malendowicz LK. Effects of neuropeptides B and W on the rat pitui-tary-adrenocortical axis: In vivo and in vitro studies. Int J Mol Med. 2007;19(2):207–211.
  26. Rucinski M, Ziolkowska A, Szyszka M, Malendowicz LK. Cerebellin and des-cerebellin exert ACTH-like effects on corticosterone secretion and the intracellular signaling pathway gene expression in cultured rat adrenocortical cells – DNA microarray and QPCR studies. Int J Mol Med. 2009;23(4):539–546.
  27. Fraley GS, Shimada I, Baumgartner JW, Clifton DK, Steiner RA. Differential patterns of Fos induction in the hypothalamus of the rat following central injections of galanin-like peptide and galanin. Endocrinol. 2003;144(4):1143–1146.
  28. Krasnow SM, Hohmann JG, Gragerov A, Clifton DK, Steiner RA. Analysis of the contribution of galanin receptors 1 and 2 to the central actions of galanin-like peptide. Neuroendocrinol. 2004;79(5):268–277.
  29. Man PS, Lawrence CB. The effects of galanin-like peptide on energy balance, body temperature and brain activity in the mouse and rat are independent of the GALR2/3 receptor. J Neuroendocrinol. 2008;20(1):128–137.
  30. Boughton CK, Patterson M, Bewick GA, et al. Alarin stimulates food intake and gonadotrophin release in male rats. Br J Pharmacol. 2010;161(3):601–613.
  31. Zhuang F, Li M, Gao X, et al. The antidepressant-like effect of alarin is related to TrkB-mTOR signaling and synaptic plasticity. Behav Brain Res. 2016;313:158–171.
  32. Lawrence CB, Baudoin FM, Luckman SM. Centrally administered galanin-like peptide modifies food intake in the rat: A comparison with galanin. J Neuroendocrinol. 2002;14(11):853–860.
  33. Lawrence CB, Williams T, Luckman SM. Intracerebroventricular galanin-like peptide induces different brain activation compared with galanin. Endocrinol. 2003;144(9):3977–3984.
  34. Seth A, Stanley S, Dhillo W, Murphy K, Ghatei M, Bloom S. Effects of galanin-like peptide on food intake and the hypothalamo-pituitary-thyroid axis. Neuroendocrinol. 2003;77(2):125–131.
  35. Takenoya F, Hirayama M, Kageyama H, et al. Neuronal interactions between galanin-like-peptide- and orexin- or melanin-concentrating hor-mone-containing neurons. Regul Pept. 2005;126(1–2):79–83.
  36. Eberhard N, Mayer C, Santic R, et al. Distribution of alarin immunoreactivity in the mouse brain. J Mol Neurosci. 2012;46(1):18–32.
  37. Lang R, Gundlach AL, Kofler B. The galanin peptide family: Receptor pharmacology, pleiotropic biological actions, and implications in health and disease. Pharmacol Ther. 2007;115(2):177–207.
  38. Otani K, Okada M, Yamawaki H. Diverse distribution of tyrosine receptor kinase B isoforms in rat multiple tissues. J Vet Med Sci. 2017;79(9):1516–1523.
  39. Yu Y, Fuscoe JC, Zhao C, et al. A rat RNA-Seq transcriptomic BodyMap across 11 organs and 4 developmental stages. Nat Commun. 2014;5:3230.
  40. Faure-Virelizier C, Croix D, Bouret S, et al. Effects of estrous cyclicity on the expression of the galanin receptor Gal-R1 in the rat preoptic area: A comparison with the male. Endocrinol. 1998;139(10):4127–4139.