Identification of neurons that express ghrelin receptors in autonomic pathways originating from the spinal cord
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  • 作者:John B. Furness (1) j.furness@unimelb.edu.au
    Hyun-Jung Cho (1)
    Billie Hunne (1)
    Haruko Hirayama (1)
    Brid P. Callaghan (1)
    Alan E. Lomax (2)
    James A. Brock (1)
  • 关键词:Autonomic ganglia &#8211 ; Ghrelin &#8211 ; Immunohistochemistry &#8211 ; Preganglionic neurons &#8211 ; Retrograde tracing &#8211 ; Mouse
  • 刊名:Cell and Tissue Research
  • 出版年:2012
  • 出版时间:June 2012
  • 年:2012
  • 卷:348
  • 期:3
  • 页码:397-405
  • 全文大小:1.0 MB
  • 参考文献:1. Andrews ZB (2011) The extra-hypothalamic actions of ghrelin on neuronal function. Trends Neurosci 34:31–40
    2. Asmus SE, Parsons S, Landis SC (2000) Developmental changes in the transmitter properties of sympathetic neurons that innervate the periosteum. J Neurosci 20:1495–1504
    3. Ferens DM, Yin L, Bron R, Hunne B, Ohashi-Doi K, Sanger GJ, Witherington J, Shimizu Y, Furness JB (2010a) Functional and in situ hybridisation evidence that preganglionic sympathetic vasoconstrictor neurons express ghrelin receptors. Neuroscience 166:671–679
    4. Ferens DM, Yin L, Ohashi-Doi K, Habgood M, Bron R, Brock JA, Gale JD, Furness JB (2010b) Evidence for functional ghrelin receptors on parasympathetic preganglionic neurons of micturition control pathways in the rat. Clin Exp Pharmacol Physiol 37:926–932
    5. Fujimiya M, Asakawa A, Ataka K, Chen C-Y, Kato I, Inui A (2010) Ghrelin, des-acyl ghrelin, and obestatin: regulatory roles on the gastrointestinal motility. Int J Pept 2010:1–8
    6. Furness JB, Costa M (1979) Projections of intestinal neurons showing immunoreactivity for vasoactive intestinal polypeptide are consistent with these neurons being the enteric inhibitory neurons. Neurosci Lett 15:199–204
    7. Furness JB, Hunne B, Matsuda N, Yin L, Russo D, Kato I, Fujimiya M, Patterson M, McLeod J, Andrews ZB, Bron R (2011) Investigation of the presence of ghrelin in the central nervous system of the rat and mouse. Neuroscience 193:1–9
    8. Gibbins IL (1991) Vasomotor, pilomotor and secretomotor neurons distinguished by size and neuropeptide content in superior cervical ganglia of mice. J Auton Nerv Syst 34:171–184
    9. Grkovic I, Edwards SL, Murphy SM, Anderson CR (1999) Chemically distinct preganglionic inputs to iris-projecting postganglionic neurons in the rat: a light and electron microscopic study. J Comp Neurol 412:606–616
    10. Hirayama H, Shiina T, Shima T, Kuramoto H, Takewaki T, Furness JB, Shimizu Y (2010) Contrasting effects of ghrelin and des-acyl ghrelin on the lumbo-sacral defecation center and regulation of colorectal motility in rats. Neurogastroenterol Motil 22:1124–1131
    11. Howard AD, Feighner SD, Cully DF, Arena JP, Liberator PA, Rosenblum CI, Hamelin M, Hreniuk DL, Palyha OC, Anderson J, Paress PS, Diaz C, Chou M, Liu KK, McKee KK, Pong SS, Chaung LY, Elbrecht A, Dashkevicz M, Heavens R, Rigby M, Sirinathsinghji DJ, Dean DC, Melillo DG, Patchett AA, Nargund R, Griffin PR, DeMartino JA, Gupta SK, Schaeffer JM, Smith RG, Van der Ploeg LH (1996) A receptor in pituitary and hypothalamus that functions in growth hormone release. Science 273:974–977
    12. Keast JR (1999) Unusual autonomic ganglia: connections, chemistry, and plasticity of pelvic ganglia. Int Rev Cytol 193:1–69
    13. Kojima M, Hosoda H, Date Y, Nakazato M, Matsuo H, Kangawa K (1999) Ghrelin is a growth-hormone-releasing acylated peptide from stomach. Nature 402:656–660
    14. Langley JN, Anderson HK (1895) The innervation of the pelvic and adjoining viscera. IV. The internal generative organs. J Physiol (Lond) 19:122–130
    15. Lindh B, H枚kfelt T, Elfvin LG (1988) Distribution and origin of peptide-containing nerve fibers in the celiac superior mesenteric ganglion of the guinea-pig. Neuroscience 26:1037–1071
    16. Lomax AE, Sharkey KA, Furness JB (2010) The participation of the sympathetic innervation of the gastrointestinal tract in disease states. Neurogastroenterol Motil 22:7–18
    17. Lundberg JM, H枚kfelt T, Anggard A, Terenius L, Elde R, Markey K, Goldstein M, Kimmel J (1982) Organization principles in the peripheral sympathetic nervous system: subdivision by coexisting peptides somatostatin-, avian pancreatic polypeptide-, and vasoactive intestinal polypeptide-like immunoreactive materials. Proc Natl Acad Sci USA 79:1303–1307
    18. Maccarrone C, Jarrott B (1985) Differences in regional brain concentrations of neuropeptide Y in spontaneously hypertensive SH and Wistar Kyoto WKY rats. Brain Res 345:165–169
    19. Macrae LM, Furness JB, Costa M (1986) Distribution of subgroups of noradrenaline neurons in the coeliac ganglion of the guinea-pig. Cell Tissue Res 244:173–180
    20. Rocha-Sousa A, Saraiva J, Henriques-Coelho T, Falc茫o-Reis F, Correia-Pinto J, Leite-Moreira AF (2006) Ghrelin as a novel locally produced relaxing peptide of the iris sphincter and dilator muscles. Exp Eye Res 83:1179–1187
    21. Sch盲fer MKH, Schutz B, Weihe E, Eiden LE (1997) Target-independent cholinergic differentiation in the rat sympathetic nervous system. Proc Natl Acad Sci USA 94:4149–4154
    22. Sch盲fer MKH, Eiden LE, Weihe E (1998) Cholinergic neurons and terminal fields revealed by immunohistochemistry for the vesicular acetylcholine transporter. II. The peripheral nervous system. Neuroscience 84:361–376
    23. Shimizu Y, Chang EC, Shafton AD, Ferens DM, Sanger GJ, Witherington J, Furness JB (2006) Evidence that stimulation of ghrelin receptors in the spinal cord initiates propulsive activity in the colon of the rat. J Physiol (Lond) 576:329–338
    24. Szurszewski JH, Ermilov LG, Miller SM (2002) Prevertebral ganglia and intestinofugal afferent neurones. Gut 51:i6–i10
    25. Tack J, Depoortere I, Bisschops R, Delporte C, Coulie B, Meulemans A, Janssens J, Peeters T (2006) Influence of ghrelin on interdigestive gastrointestinal motility in humans. Gut 55:327–333
    26. Venables G, Hunne B, Bron R, Cho H-J, Brock JA, Furness JB (2011) Ghrelin receptors are expressed by distal tubules of the mouse kidney. Cell Tissue Res 346:135–139
    27. Vidovic M, Hill CE, Hendry IA (1987) Developmental time course of the sympathetic postganglionic innervation of the rat eye. Dev Brain Res 32:133–138
    28. Zhao T-J, Sakata I, Li RL, Liang G, Richardson JA, Brown MS, Goldstein JL, Zigman JM (2010) Ghrelin secretion stimulated by β1-adrenergic receptors in cultured ghrelinoma cells and in fasted mice. Proc Natl Acad Sci USA 107:15868–15873
  • 作者单位:1. Department of Anatomy & Neuroscience, University of Melbourne, Parkville, Victoria 3010, Australia2. Gastrointestinal Diseases Research Unit, Queen鈥檚 University, Kingston, Ontario, Canada
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Biomedicine
    Human Genetics
    Proteomics
    Molecular Medicine
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1432-0878
文摘
Functional studies have shown that subsets of autonomic preganglionic neurons respond to ghrelin and ghrelin mimetics and in situ hybridisation has revealed receptor gene expression in the cell bodies of some preganglionic neurons. Our present goal has been to determine which preganglionic neurons express ghrelin receptors by using mice expressing enhanced green fluorescent protein (EGFP) under the control of the promoter for the ghrelin receptor (also called growth hormone secretagogue receptor). The retrograde tracer Fast Blue was injected into target organs of reporter mice under anaesthesia to identify specific functional subsets of postganglionic sympathetic neurons. Cryo-sections were immunohistochemically stained by using anti-EGFP and antibodies to neuronal markers. EGFP was detected in nerve terminal varicosities in all sympathetic chain, prevertebral and pelvic ganglia and in the adrenal medulla. Non-varicose fibres associated with the ganglia were also immunoreactive. No postganglionic cell bodies contained EGFP. In sympathetic chain ganglia, most neurons were surrounded by EGFP-positive terminals. In the stellate ganglion, neurons with choline acetyltransferase immunoreactivity, some being sudomotor neurons, lacked surrounding ghrelin-receptor-expressing terminals, although these terminals were found around other neurons. In the superior cervical ganglion, the ghrelin receptor terminals innervated subgroups of neurons including neuropeptide Y (NPY)-immunoreactive neurons that projected to the anterior chamber of the eye. However, large NPY-negative neurons projecting to the acini of the submaxillary gland were not innervated by EGFP-positive varicosities. In the celiaco-superior mesenteric ganglion, almost all neurons were surrounded by positive terminals but the VIP-immunoreactive terminals of intestinofugal neurons were EGFP-negative. The pelvic ganglia contained groups of neurons without ghrelin receptor terminal innervation and other groups with positive terminals around them. Ghrelin receptors are therefore expressed by subgroups of preganglionic neurons, including those of vasoconstrictor pathways and of pathways controlling gut function, but are absent from some other neurons, including those innervating sweat glands and the secretomotor neurons that supply the submaxillary salivary glands.
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