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  • 1
    Online Resource
    Online Resource
    Milton :Taylor & Francis Group,
    Keywords: Serotonin-Physiological effect. ; Electronic books.
    Description / Table of Contents: Serotonin and Gastrointestinal Function provides a comprehensive review of current research into the mechanisms by which serotonin acts on gastrointestinal tissues. This book covers neurochemistry, physiology, pharmacology, and clinical issues relevant to serotonin in the gastrointestinal tract.
    Type of Medium: Online Resource
    Pages: 1 online resource (192 pages)
    Edition: 1st ed.
    ISBN: 9781000099331
    Series Statement: Handbooks in Pharmacology and Toxicology Series
    DDC: 612.3/2
    Language: English
    Note: Cover -- Title Page -- Copyright Page -- Preface -- The Editors -- Contributors -- Table of Contents -- Chapter 1: Serotonin in the Intestinal Tract: A Synopsis -- I. Introduction -- II. Synthesis and Distribution of 5-HT -- III. Release of 5-HT -- IV. Metabolism of 5-HT -- V. Prospective -- References -- Chapter 2: Localization and Neurochemical Aspects of Serotonin in the Gut -- I. The Intrinsic Innervation of the Gut is Autonomous and Different from that of Any Other Organ -- II. Classification of Enteric Neurons -- III. Functions of Some Classes of Enteric Neurons -- IV. Serotonin (5-HT) May be an Initiator of the Peristaltic Reflex -- V. The Bowel Contains Many 5-HT Receptors -- VI. Operational Properties Identify 5-HT1p-Mediated Effects -- VII. The 5-HT1p Receptor is Coupled to a Go -- VIII. Protein Kinase C Appears to Play a Critical Role in 5-HT1p-Mediated Responses -- IX. The 5-HT1p Receptor Plays a Critical Role in Initiating the Peristaltic Reflex -- X. Uptake by Crypt Epithelial Cells May Inactivate Mucosal 5-HT -- XI. 5-HT is a Neurotransmitter in the ENS -- XII. The Specific Role Played by Neuronal 5-HT in the Mediation of the Peristaltic Reflex Has Yet to be Identified -- XIII. Summary and Conclusions -- Acknowledgments -- References -- Chapter 3: Pharmacological Characterization of 5-Hydroxytryptamine Receptors in the Gastrointestinal Tract -- I. Introduction -- II. 5-HT1 Receptors -- A. 5-HT1A Receptors -- B. 5-HT1D Receptors -- III. 5-HT2 Receptors -- A. 5-HT2A Receptors -- B. 5-HT2B Receptors -- IV. 5-HT3 Receptors -- V. 5-HT4 Receptors -- VI. Orphan 5-HT Receptors -- References -- Chapter 4: Serotonin Modulation of Gastrointestinal Motility -- I. Introduction -- II. Pharmacological Actions Mediated by 5-HT Receptors in the Gut In Vitro -- A. 5-HT1 Receptors -- 1. Direct Actions Mediated by 5-HT1 Receptors. , a. Excitatory effects -- b. Inhibitory effects -- 2. Indirect Actions Mediated by 5-HT1 Receptors -- a. Excitatory effects on enteric neurons -- b. Inhibitory effects on enteric neurons. -- B. 5-HT2 Receptors -- C. 5-HT3 Receptors. -- 1. Indirect Actions Mediated by 5-HT3 Receptors -- a. Contractile effects -- b. Relaxing effects -- D. 5-HT4 Receptors -- 1. Indirect Actions Mediated by 5-HT4 Receptors -- a. Excitatory effects -- 2. Direct Actions Mediated by 5-HT4 Receptors -- a. Inhibitory effects -- III. Role of Endogenous 5-HT in the Modulation of Gut Motility In Vitro -- A. Functional Role of 5-HT1 and 5-HT2 Receptors -- B. Functional Role of 5-HT3 Receptors -- C. Functional Role of 5-HT4 Receptors -- IV. Role of 5-HT in the Modulation of GI Motility In Vivo -- A. Role of 5-HT in the Modulation of Gastric Motility -- 1. Gastric Emptying -- B. Role of 5-HT in the Modulation of Small Bowel Motility -- 1. Role of Serotonergic Pathways in the Regulation of the MMC -- 2. Small Bowel Transit -- C. Role of 5-HT in the Modulation of Colonic Motility -- D. The Brain-Gut Axis: Role of 5-HT -- 1. Role of 5-HT3 Receptors in Afferent Pathways from the GI Tract -- 2. Centrally Mediated Effects of 5-HT -- References -- Chapter 5: Serotonin as an Intestinal Secretagogue -- I. Introduction -- II. Origin of Serotonin in the Intestine -- III. Effects of 5-HT on Fluid Secretion -- A. Animal Experiments. -- 1. Small Intestine In Vivo -- 2. Small Intestine and Colon In Vitro -- B. Human Experiments -- IV. Effects of 5-HT on Ion Transport -- A. Animal Experiments -- 1. Small Intestine In Vivo -- 2. Small Intestine In Vitro -- 3. Effects on the Colon -- B. Human Experiments -- V. Effects of 5-HT on Mucus Secretion -- VI. Effects of 5-HT on Absorption of Fluid and Electrolytes -- VII. Effects of 5-HT on Absorption of Nutrients -- VIII. Effects of 5-HT on Blood Flow. , IX. Mechanisms of Action -- A. Calcium -- B. 5-HT2 Receptors and Phosphoinositol Metabolism -- C. Prostaglandins -- D. 5-HT3 Receptors -- E. Cyclic Nucleotides -- X. Role of 5-HT in Secretory Processes -- A. 5-HT and Enterotoxin-Induced Secretion -- B. Serotonin and Gut Withdrawal from Opiates -- C. 5-HT and Intestinal Anaphylaxis -- D. 5-HT and the Effects of Laxatives -- XI. Conclusions -- Acknowledgments -- References -- Chapter 6: Electrophysiological Studies of 5-Hydroxytryptamine Receptors on Enteric Neurons -- I. Introduction -- II. Types of Enteric Neurons -- III. Electrophysiological Responses Mediated by 5-HT Receptors -- A. 5-HT1p Receptors -- 1. 5-HT Mimics sEPSPs in Enteric Neurons -- 2. 5-HT1p Receptors and Slow Depolarizations of Enteric Neurons -- 3. 5-HT1p Receptors Mediate Some sEPSPs -- 4. Presynaptic 5-HT1p Receptors -- B. 5-HT1A Receptors -- 1. 5-HT1A Receptors on Myenteric AH Neurons: Membrane Hyperpolarization. -- 2. 5-HT1A Receptors Activate GK in Myenteric AH Neurons -- 3. Presynaptic 5-HT1A Receptors Mediate Inhibition of fEPSPs and sEPSPs in the Myenteric Plexus -- 4. 5-HT1A Receptors Mediate Presynaptic Inhibition of sEPSPs Recorded from Submucous AH Neurons -- C. 5-HT3 Receptors -- 1. 5-HT Activates a Cation Conductance to Cause Fast Depolarizations of Enteric Neurons -- 2. 5-HT3 Receptors Mediate the Fast Depolarization -- 3. 5-HT3 Receptors on Enteric Nerves are Ligand-Gated Cation Channels -- 4. 5-HT3-Mediated Synaptic Potentials in the Enteric Nervous System -- D. 5-HT4 Receptors -- 1. 5-HT Acting at 5-HT4 Receptors Facilitates Peristalsis -- 2. 5-HT4 Receptors Mediate Presynaptic Facilitation of fEPSPs -- 3. 5-HT4 Receptors do not Mediate Facilitation of Noncholinergic sEPSPs -- 4. Localization of 5-HT4 Receptors to Nerve Terminals -- IV. Summary and Conclusions -- References. , Chapter 7: Serotonin and the Afferent Innervation of the Gastrointestinal Tract -- I. Gastrointestinal Afferents and 5-HT -- II. Effect of 5-HT on Gastrointestinal Motility -- A. Effects of 5-HT3 Receptor Agonists on Gastric Motility -- B. Effects of 5-HT3 Receptor Antagonists on Gastric Motility and Emptying -- C. 5-HT Receptors in Intestinal Feedback Inhibition of Gastric Emptying -- D. 5-HT3 Receptors and Visceral Pain -- III. 5-Hydroxytryptamine and Emesis -- A. Motor and Integrative Mechanisms -- B. Afferent Pathways -- 1. Visceral Afferents and the Emetic Response to Cytotoxic Drugs -- C. Evidence of Involvement of 5-HT and 5-HT3 Receptors in Emesis -- 1. Antiemetic Effects of 5-HT3 Receptor Antagonists -- 2. Release of 5-HT by Emetic Stimuli -- 3. Induction of Emesis by 5-HT3 Receptor Agonists -- 4. Location of 5-HT3 Receptors and Site of Action of Antagonists -- D. Involvement of 5-HT4 Receptors in Emesis -- IV. Future Directions -- References -- Chapter 8: The Clinical Application of 5-HT Agonists and Antagonists in Gastrointestinal Disease -- I. Introduction -- II. Cisapride: Model of a Serotonin Agonist -- A. Non-Ulcer Dyspepsia -- B. Gastroesophageal Reflux Disease -- C. Gastroparesis -- D. Constipation -- E. Other GI Applications -- III. Serotonin Antagonists -- A. Nausea and Vomiting -- B. Chemotherapy-Induced Emesis -- C. Radiation-Induced Nausea and Vomiting -- D. Postoperative Nausea and Vomiting -- E. Other Uses - Case Reports -- References -- Index.
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillian Magazines Ltd.
    Nature 406 (2000), S. 405-410 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Transmitter-gated cation channels are detectors of excitatory chemical signals at synapses in the nervous system. Here we show that structurally distinct α3β4 nicotinic and P2X2 channels influence each other when co-activated. The activation of one channel type ...
    Type of Medium: Electronic Resource
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