The Neuroendocrine System of the Gut

Reference

• Tatemoto K, Mutt V. Isolation of two novel candidate hormones using a chemical method of finding naturally occurring polypeptides. Nature 1980; 285: 417
   PubMed Web of Science ®Google Scholar
• Tatemoto K, Mutt V. Isolation and characterization of the intestinal peptide porcine PHI (PHI-27), a new member of the glucagon-secretin family. Proc Natl Acad Sci USA 1981; 78: 6603
   PubMed Web of Science ®Google Scholar
• Tatemoto K, Rökaeus Å, Jörnvall H, McDonald T, Mutt V. Galanin—a novel biologically active peptide from procine intestine. FEBS Lett 1983; 164: 124
   PubMed Web of Science ®Google Scholar
• Gluschankof P, Cohen P. Proteolytic enzymes in the post-translational processing of polypeptide hormone precursors. Neurochem Res 1987; 12: 951
   PubMed Web of Science ®Google Scholar
• Brownstein MJ. Peptide processing: An overview. Biogenetics of Neurohormonal peptides., R Håkanson, J Thorell. Academic Press, London 1985; 105
   Google Scholar
• Joose J. Functional and evolutionary perspectives of neuropeptides and their precursors. Integrative neuroendocrinology: Molecular, cellular and clinical aspects, S M McCann, R I Weiner. Karger, Basel 1987; 176
   Google Scholar
• Sundler F, Alumets J, Ekblad E, Böttcher G, Håkanson R. Coexistence of peptides in the neuroendocrine system. Biogenetics of neurohormonal peptides, R Hakanson, J Thorell, 1986; 213
   Google Scholar
• Itoh N, Obata K I, Yanaihara N, Okamoto H. Human preva-soactive intestinal polypeptide contains a novel PHI-27-like peptide, PHM27. Nature 1983; 304: 547
   PubMed Web of Science ®Google Scholar
• Nawa H, Hirose T, Takashima H, Inayama S, Nakanishi S. Nucleotide sequences of cloned cDNAs for two types of bovine brain substance P precursor. Nature 1983; 306: 32
   PubMed Web of Science ®Google Scholar
• Bell G I, Santerre R F, Mullenbach RT. Hamster preproglucagon contains the sequence of glucagon and two related peptides. Nature 1983; 302: 716
   PubMed Web of Science ®Google Scholar
• Furness J B, Costa M. The enteric nervous system. Churchill Livingstone, Edinburgh 1987
   Google Scholar
• Hökfelt T, Fried G, Hansen S, Holets V, Lundberg J M, Skirboll L. Neurons with multiple messengers distribution and possible functional significance. Progr Brain Res 1986; 65: 115
   PubMed Web of Science ®Google Scholar
• Ekblad E, Håkanson R, Sundler F. VIP and PHI coexist with an NPY-like peptide in intramural neurons of the small intestine. Regul Pept 1984; 10: 47
   PubMedGoogle Scholar
• Furness J B, Costa M, Rökaeus Å., McDonald T J, Brooks B. Galanin-immunoreactive neurons in the guinea-pig small intestine: their projections and relationships to other enteric neurons. Cell Tissue Res 1987; 250: 607
   PubMed Web of Science ®Google Scholar
• Melander T, Hökfelt T, Rökaeus Å, Fahrenkrug J, Tatemoto K, Mutt V. Distribution of galanin-like immunoreactivity in the gastrointestinal tract of several mammalian species. Cell Tissue Res 1985; 239: 253
   PubMed Web of Science ®Google Scholar
• Ali-Rachedi A, Varndell I M, Adrian T E, et al. Peptide YY (PYY) immunoreactivity is co-stored with glucagon-related immunoreactants in endocrine cells of the gut and pancreas. Histochemistry 1984; 80: 487
   PubMedGoogle Scholar
• Böttcher G, Sjölund K, Ekblad E, Håkanson R, Schwartz T W, Sundler F. Coexistence of peptide YY and glicentin immunoreactivity in endocrine cells of the gut. Regul Pept 1984; 8: 261
   PubMed Web of Science ®Google Scholar
• Grube D, Aunis D, Bader F, Cetin Y, Jörns A, Yoshie S. Chromogranin A (CGA) in the gastroentero-pancreatic (GEP) endocrine system. I. CGA in the mammalian endocrine pancreas. Histochemistry 1986; 85: 441
   PubMedGoogle Scholar
• Lassmann H, Hagn C, Fischer-Colbrie R, Winkler H. Presence of chromogranin A, B and C in bovine endocrine and nervous tissues: a comparative immunohistochemical study. Histochem J 1986; 18: 380
   PubMedGoogle Scholar
• O'Connor D T, Burton D, Delftos LJ. Immunoreactive human chromogranin A in diverse polypeptide hormone-producing human tumors and normal endocrine tissues. J Clin Endocrinol Metab 1983; 57: 1084
   PubMed Web of Science ®Google Scholar
• Rindi G, Buffa R, Sessa F, Tortora O, Solcia E. Chromogranin A, B and C immunoreactivities of mammalian endocrine cells. Distribution, distinction from costored hormones/ prohomones and relationship with the argyrophil component of secretory granules. Histochemistry 1986; 85: 19
   PubMedGoogle Scholar
• Håkanson R, Sundler F. The design of the neuroendocrine system: a unifying concept and its consequences. TIPS 1983; 4: 41
   Web of Science ®Google Scholar
• Lundberg J M, Hökfelt T. Coexistence of peptides and classical neurotransmitters. Trends Neurosci 1983; 6: 325
   Web of Science ®Google Scholar
• Sundler F, Håkanson R, Lorén I, Lundquist I. Amine storage and function in peptide hormone-producing cells. Invest Cell Pathol 1980; 3: 87
   PubMedGoogle Scholar
• Sundler F, Håkanson R, Ekblad E, Uddman R, Wahlestedt C. Neuropeptide Y in the peripheral adrenergic and enteric nervous systems. Int Rev Cytol 1986; 102: 243
   PubMed Web of Science ®Google Scholar
• Alumets J, Håkanson R, Sundler F, Chang KJ. Leu-enkephalin-like material in nerves and enterochromaffin cells in the gut. Histochemistry 1978; 56: 187
   PubMedGoogle Scholar
• Sundler F, Alumets J, Håkanson R. 5-Hydroxytryptamine-containing enterochromaffin cells: Storage site of substance P. Acta Physiol Scand 1977; 452: 121, Suppl
   Google Scholar
• Sjölund K, Sandén G, Håkanson R, Sundler F. Endocrine cells in human intestine: An immunocytochemical study. Gastroenterology 1983; 85: 1120
   PubMed Web of Science ®Google Scholar
• Sundler F, Håkanson R. Peptide hormone-producing endo-crine/paracrine cells in the gastro-entero-pancreatic region. Handbook of chemical neuroanatomy. The peripheral nervous system., A Björklund, T Hökfelt, C Owman. Elsevier, Amsterdam 1988; 6: 219
   Google Scholar
• Solcia E, Capella C, Buffa R, Usellini L, Fiocca R, Sessa F. Endocrine cells of the digestive system. Physiology of the gastrointestinal tract, L T Johnson. Raven Press, New York 1987; 111
   Google Scholar
• Grube D, Forssmann WG. Morphology and function of entero-endocrine cells. Horm Metab Res 1979; 11: 589
   PubMed Web of Science ®Google Scholar
• Håkanson R, Ekelund M, Sundler F. Activation and proliferation of gastric endocrine cells. Evolution and tumour pathology of the neuroendocrine system, S Falkmer, R Håkanson, F Sundler. Elsevier, Amsterdam 1984; 371
   Google Scholar
• Håkanson R, Blom H, Carlsson E, Larsson H, Ryberg B, Sundler F. Hypergastrinaemia produces trophic effects in stomach but not in pancreas and intestines. Regul Pept 1986; 13: 225
   PubMedGoogle Scholar
• Håkanson R, Böttcher G, Ekblad E, et al. Histamine in endocrine cells in the stomach: A survey of several species using a panel of histamine antibodies. Histochemistry 1986; 86: 5
   PubMedGoogle Scholar
• Böttcher G, Håkanson R, Nilsson G, Seensalu R, Sundler F. Effects of long-term hypergastrinemia on the ultrastructure of of entero chromaffin-like cells in the stomach of the rat, hamster and guinea-pig. Cell Tissue Res 1989, In press.
   Web of Science ®Google Scholar
• Larsson H, Carlsson E, Mattsson H, et al. Plasmagastrin and gastric enterochromaffin-like cell activation and proliferation. Studies with omeprazole and ranitidine in intact and antrectomized rats. Gastroenterology 1986; 90: 391
   PubMed Web of Science ®Google Scholar
• Alumets J, Ekelund M, El Munshid H A, Håkanson R, Lorén I, Sundler F. Topography of somatostatin cells in the stomach of the rat: possible functional significance. Cell Tissue Res 1979; 202: 177
   PubMed Web of Science ®Google Scholar
• Larsson L I, Goltermann M, de Magistris L, Rehfeld J F, Schwartz TW. Somatostatin cell processes as pathways for paracrine secretion. Science 1979; 205: 1393
   PubMed Web of Science ®Google Scholar
• Håkanson R, Axelson J, Persson P, Sundler F. Which effects of antral gastrin are physiological?. Gastrin and cholecystokinin. Chemistry, physiology and pharmacology, J P Bali, J Martinez. Elsevier, Amsterdam 1987; 163
   Google Scholar
• Håkanson R, Persson P, Axelson J, Johnell O, Sundler F. Evidence that gastrin stimulates 45Ca uptake into bone through release of a novel gastric hormone. Regul Pept 1989, In press.
   Google Scholar
• Persson P, Håkanson R, Axelson J, Sundler F. Gastrin releases a blood calcium-lowering peptide from the oxyntic mucosa. Proc Natl Acad Sci USA 1989, In press.
   Web of Science ®Google Scholar
• Sharkey K A, Williams R G, Dockray GJ. Sensory substance P innervation of the stomach and pancreas. Gastroenterology 1984; 87: 914
   PubMed Web of Science ®Google Scholar
• Sternini C, Brecha N. Effect of neurotoxin pretreatment on calcitonin gene-related peptide immunoreactivity in the upper gastro-intestinal tract of the rat. Gastroenterology 1985; 88: 1600
   Web of Science ®Google Scholar
• Connors N A, Sullivan J M, Kubbs KS. Autoradiographic study of the distribution of fibers from the dorsal motor nucleus of the vagus to the digestive tube of the rat. Acta Anat 1983; 115: 266
   PubMedGoogle Scholar
• Donahue P E, Yoshida J, Polley E H, Nyhus LM. Preganglionic vagus nerve fibers also enter the greater curvature of the stomach in rats and ferrets. Gastroenterology 1988; 94: 1292
   PubMed Web of Science ®Google Scholar
• Ekblad E, Ekman R, Håkanson R, Sundler F. GRP neurons in the rat small intestine issue long anal projections. Regul Pept 1983; 9: 279
   Google Scholar
• Ekblad E, Ekman R, Håkanson R, Sundler F. Projections of peptide-containing neurons in rat colon. Neuroscience 1988; 27: 655
   PubMed Web of Science ®Google Scholar
• Ekblad E, Rökaeus Å, Håkanson R, Sundler F. Galanin nerve fibers in the rat gut: distribution, origin and projections. Neuroscience 1985; 16: 355
   PubMed Web of Science ®Google Scholar
• Ekblad E, Winther C, Ekman R, Håkanson R, Sundler F. Projections of peptide-containing neurons in rat small intestine. Neuroscience 1987; 20: 169
   PubMed Web of Science ®Google Scholar
• Costa M, Furness J B, Yanaihara N, Yanaihara C, Moody TW. Distribution and projections of neurons with immunore-activity for both gastrin-releasing peptide and bombesin in the guinea-pig small intestine. Cell Tissue Res 1984; 235: 285
   PubMed Web of Science ®Google Scholar
• Costa M, Furness JB. The origins, pathways and terminations of neurons with VIP-like immunoreactivity in the guinea-pig small intestine. Neuroscience 1983; 8: 665
   PubMed Web of Science ®Google Scholar
• Schultzberg M, Dalsgaard CJ. Enteric origin of bombesin immunoreactive fibres in the rat coeliac-superior mesenteric ganglion. Brain Res 1983; 269: 190
   PubMed Web of Science ®Google Scholar
• Delbro D. The role of substance P in the control of gut motility. Tachykinin antagonists, R Håkanson, F Sundler. Elsevier, Amsterdam 1985; 223
   Google Scholar
• Ekblad E, Ekman R, Håkanson R, Sundler F. Return of nerve fibers containing gastrin-releasing peptide in rat small intestine after local removal of myenteric ganglia. Neuroscience 1988; 24: 309
   PubMed Web of Science ®Google Scholar