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  • ¹®È­¡¤°æÁ¦ | Cases and Studies of Culture & Economy in Lottery & Gambling | Ùþûù & 经济

    date : 2015-05-20 01:10|hit : 2606
    Article] VAGAL AFFERENT INNERVATION OF THE RAT FUNDIC STOMACH - MORPHOLOGICAL CHARACTERIZATION OF THE GASTRIC TENSION RECEPTOR
    DocNo of ILP: 8381

    Doc. Type: Article

    Title: VAGAL AFFERENT INNERVATION OF THE RAT FUNDIC STOMACH - MORPHOLOGICAL CHARACTERIZATION OF THE GASTRIC TENSION RECEPTOR

    Authors: BERTHOUD, HR; POWLEY, TL

    Full Name of Authors: BERTHOUD, HR; POWLEY, TL

    Keywords by Author: MECHANORECEPTOR; IN-SERIES TENSION RECEPTOR; STRETCH RECEPTOR; GASTRIC DISTENSION; GASTRIC SMOOTH MUSCLE INNERVATION; NODOSE GANGLION; DIL, DIA

    Keywords Plus: PLEXUS MUSCULARIS PROFUNDUS; MOUSE SMALL-INTESTINE; INTERSTITIAL-CELLS; NERVE-FIBERS; GASTROINTESTINAL-TRACT; OPOSSUM ESOPHAGUS; MECHANORECEPTORS; CHOLECYSTOKININ; DISCHARGE; SPHINCTER

    Abstract: Although the gastric tension receptor has been characterized behaviorally and electrophysiologically quite well, its location and structure remains elusive. Therefore, the vagal afferents to the rat fundus (forestomach or nonglandular stomach) were anterogradely labeled in vivo with injections of the carbocyanine dye Dil into the nodose ganglia, and the nerves and ganglia of the enteric nervous system were labeled in toto with intraperitoneal Fluorogold injection. Dissected layers and cryostat cross sections of the fundic wall were mounted in glycerin and analyzed by means of conventional and laser scanning confocal microscopy. Particularly in the longitudinal, and to a lesser extent in the circular, smooth muscle layers, Dil-labeled fibers and terminals were abundant. These processes, which originated from fibers coursing through the myenteric ganglia and connectives, entered either muscle coat and then ran parallel to the respective muscle fibers, often for several millimeters. They ran in close association with the Fluorogold-labeled network of interstitial cells of Cajal, upon which they appeared to form multiple spiny appositions or varicosities. In the myenteric plexus, two different types of afferent vagal structures were observed. Up to 300 highly arborizing endings forming dense accumulations of small puncta similar to the esophageal intraganglionic laminar endings (Rodrigo et al., '75 Acta Anat. 92:79-100) were found in the fundic wall ipsilateral to the injected nodose ganglion. They often covered small clusters of myenteric neurons or even single isolated ganglion cells (mean = 5.8 neurons) and tended to extend throughout the neuropil of the ganglia. In a second pattern, fine varicose fibers with less profuse arborizations innervated mainly the central regions of myenteric ganglia. Camera lucida analyses established that single vagal afferent fibers had separate collaterals in both a smooth muscle layer and the myenteric ganglia. Finally, Dil-labeled afferent vagal fibers were also found in the submucosa and mucosa. Control experiments in rats with supranodose vagotomy as well as rats with Dil injections directly in the distal cervical vagus ruled out the possibility of colabeling of efferent fibers of passage. In triple labeling experiments, in conjunction with Dil labeling of afferents and Fluorogold labeling of enteric neurons, the carbocyanine dye DiA was injected into the dorsal motor nucleus of the vagus to anterogradely label the efferent vagal fibers and terminals. The different distributions and morphological characteristics of the vagal afferents and efferents could be simultaneously compared. In some instances the same myenteric ganglion was apparently innervated by an afferent laminar ending and an efferent terminal. Given their locations, distributions, and morphology, we suggest that the intramuscular afferents are gastric tension receptors. It seems probable that their intramuscular collaterals associated with the interstitial cell network are responsible for detecting tension of the gut wall. The function of the highly arborizing intramyenteric vagal afferent endings is not known. We suggest that they are collaterals of intramuscular tension receptors with either an efferent function, to serve local reflex action, or a chemoreceptive function to detect blood borne factors (such as CCK) or messengers released locally by myenteric ganglia.

    Cate of OECD: Basic medicine

    Year of Publication: 1992

    Business Area: other

    Detail Business: medicine & science

    Country: USA

    Study Area:

    Name of Journal: JOURNAL OF COMPARATIVE NEUROLOGY

    Language: English

    Country of Authors: PURDUE UNIV,DEPT PSYCHOL SCI,REGULATORY PSYCHOBIOL LAB,W LAFAYETTE,IN 47907

    Press Adress:

    Email Address:

    Citaion:

    Funding:

    Lists of Citation: ANDREWS PLR, 1980, J PHYSIOL-LONDON, V298, P513; ANDREWS PLR, 1986, PROG BRAIN RES, V67, P65; ANDREWS PLR, 1980, J PHYSIOL-LONDON, V307, P401; BARBER WD, 1983, AM J PHYSIOL, V245, pG242; BERTHOUD HR, 1991, AM J PHYSIOL, V260, pR200; BERTHOUD HR, 1991, GASTROENTEROLOGY, V100, P627; BERTHOUD HR, 1990, J COMP NEUROL, V301, P65, DOI 10.1002/cne.903010107; BERTHOUD HR, 1992, IN PRESS J AUTONOM N; BERTHOUD HR, 1991, BRAIN RES, V553, P336, DOI 10.1016/0006-8993(91)90846-N; BLACKSHAW LA, 1987, J AUTONOM NERV SYST, V18, P19; BLACKSHAW LA, 1987, J AUTONOM NERV SYST, V18, P225; Cajal SR, 1893, CR SOC BIOL PARIS, V45, P217; Cannon WB, 1912, AM J PHYSIOL, V29, P441; CHRISTENSEN J, 1987, J AUTONOM NERV SYST, V19, P137, DOI 10.1016/0165-1838(87)90007-5; CLERC N, 1987, BRAIN RES, V424, P216, DOI 10.1016/0006-8993(87)91464-8; COTTRELL DF, 1984, J PHYSIOL-LONDON, V354, P457; DANIEL EE, 1984, AM J PHYSIOL, V246, pG305; DAVISON JS, 1978, J PHYSIOL-LONDON, V284, P69; DAVISON JS, 1988, AM J PHYSIOL, V255, pG55; DOCKRAY GJ, 1986, PROG BRAIN RES, V67, P133; EWART WR, 1983, AM J PHYSIOL, V244, pG613; GABELLA G, 1974, CELL TISSUE RES, V153, P63; GRUNDY D, 1988, J AUTONOM NERV SYST, V22, P175, DOI 10.1016/0165-1838(88)90104-X; HARDING R, 1973, J PHYSIOL-LONDON, V228, P73; IGGO A, 1955, J PHYSIOL-LONDON, V128, P593; IGGO A, 1986, PROG BRAIN RES, V67, P29; JANSSON G, 1968, ACTA PHYSL SCAND, V75, P245; KOLOSSOW NG, 1963, Z MIKROSK ANAT FORSC, V70, P427; MILOCHIN A A, 1963, Z Mikrosk Anat Forsch, V69, P615; MORAN TH, 1982, AM J PHYSIOL, V242, pR491; NEUHUBER WL, 1987, J AUTONOM NERV SYST, V20, P243, DOI 10.1016/0165-1838(87)90153-6; PAINTAL AS, 1954, J PHYSIOL-LONDON, V126, P255; PHIFER CB, 1986, AM J PHYSIOL, V250, pR807; POWLEY TL, 1991, J NEUROSCI METH, V36, P9, DOI 10.1016/0165-0270(91)90132-J; POWLEY TL, 1987, AM J PHYSIOL, V253, pR61; RICHARDSON DC, 1958, AM J ANAT, V103, P99; RODRIGO J, 1982, ACTA ANAT, V112, P47; RODRIGO J, 1975, ACTA ANAT, V92, P79; RUMESSEN JJ, 1982, ANAT REC, V203, P129, DOI 10.1002/ar.1092030112; RUMESSEN JJ, 1982, ANAT REC, V203, P115, DOI 10.1002/ar.1092030111; SATO M, 1987, BRAIN RES, V400, P101, DOI 10.1016/0006-8993(87)90657-3; SMITH GP, 1985, AM J PHYSIOL, V249, pR638; WILSON AJ, 1987, CELL TISSUE RES, V247, P497, DOI 10.1007/BF00215742

    Number of Citaion: 43

    Publication: WILEY-LISS

    City of Publication: NEW YORK

    Address of Publication: DIV JOHN WILEY & SONS INC 605 THIRD AVE, NEW YORK, NY 10158-0012

    ISSN: 0021-9967

    29-Character Source Abbreviation: J COMP NEUROL

    ISO Source Abbreviation: J. Comp. Neurol.

    Volume: 319

    Version: 2

    Start of File: 261

    End of File: 276

    DOI: 10.1002/cne.903190206

    Number of Pages: 16

    Web of Science Category: Neurosciences; Zoology

    Subject Category: Neurosciences & Neurology; Zoology

    Document Delivery Number: HR227

    Unique Article Identifier: WOS:A1992HR22700005

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