Literature DB >> 3443251

Neural inhibition of gastrointestinal smooth muscle motility in guinea-pigs.

M Nawano1, E Kaneko, N Honda.   

Abstract

The neural inhibition of the gastrointestinal (GI) smooth muscle motility was studied by means of electrical transmural nerve stimulation (ETNS) in guinea-pigs. In untreated muscle strips, ETNS induced four types of response, consisting of three basic components, i.e., contraction and relaxation during ETNS, and after-contraction. Following atropinization, all the responses changed to only one type, i.e., relaxation during ETNS followed by after-contraction. The relaxation of the muscle strips induced by ETNS after atropinization was not significantly reduced under superimposing guanethidine treatment in any site of the GI tract. The maximal relaxation of the muscle strips induced by ETNS after atropine and guanethidine treatments was not uniform throughout the GI tract. The relaxation of the gastric body and colon was greater than that of the jejunum and ileum. The extent of the relaxation was significantly different even in the colon. Theophylline and phentolamine did not reduce the ETNS-induced relaxation following atropine and guanethidine treatments in the distal colon and taenia coli. The findings suggest the following: the non-adrenergic inhibitory (NAI) nerve is the main postganglionic nerve to inhibit the GI smooth muscle motility; and the role of adrenergic nerve is of little importance in respect to postganglionic inhibition. The innervation of the NAI nerve seems not to be uniform throughout the GI tract. Theophylline and phentolamine are not the specific antagonists of the NAI nerve.

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Year:  1987        PMID: 3443251     DOI: 10.1007/BF02776740

Source DB:  PubMed          Journal:  Gastroenterol Jpn        ISSN: 0435-1339


  21 in total

1.  Nervous control of the blood vessels.

Authors:  B FOLKOW
Journal:  Physiol Rev       Date:  1955-07       Impact factor: 37.312

2.  Effect of autonomic drugs on the responses of isolated preparations from the guinea-pig intestine to electrical stimulation.

Authors:  A F MUNRO
Journal:  J Physiol       Date:  1953-04-28       Impact factor: 5.182

3.  Unmasking, after cholinergic paralysis by botulinum toxin, of a reversed action of nicotine on the mammalian intestine, revealing the probable presence of local inhibitory ganglion cells in the enteric plexuses.

Authors:  N AMBACHE
Journal:  Br J Pharmacol Chemother       Date:  1951-03

4.  Reversal of nicotine action on the intestine by atropine.

Authors:  N AMBACHE; J EDWARDS
Journal:  Br J Pharmacol Chemother       Date:  1951-06

5.  Antagonism of the effects of purinergic nerve stimulation and exogenously applied ATP on the guinea-pig taenia coli by 2-substituted imidazolines and related compounds.

Authors:  D Satchell; G Burnstock; P Dann
Journal:  Eur J Pharmacol       Date:  1973-09       Impact factor: 4.432

6.  Direct evidence for ATP release from non-adrenergic, non-cholinergic ("purinergic") nerves in the guinea-pig taenia coli and bladder.

Authors:  G Burnstock; T Cocks; L Kasakov; H K Wong
Journal:  Eur J Pharmacol       Date:  1978-05-15       Impact factor: 4.432

7.  Relaxations of guinea-pig fundic strip by adenosine, adenine nucleotides and electrical stimulation: antagonsism by theophylline and desensitization to adenosine and its derivatives.

Authors:  F K Okwuasaba; J T Hamilton; M A Cook
Journal:  Eur J Pharmacol       Date:  1977-12-01       Impact factor: 4.432

8.  Theophylline antagonizes some effects of purines in the intestine but not those of intramural inhibitory nerve stimulation.

Authors:  R C Small; A H Weston
Journal:  Br J Pharmacol       Date:  1979-10       Impact factor: 8.739

9.  The effects of adrenaline, noradrenaline and isoprenaline on inhibitory alpha- and beta-adrenoceptors in the longitudinal muscle of the guinea-pig ileum.

Authors:  H W Kosterlitz; R J Lydon; A J Watt
Journal:  Br J Pharmacol       Date:  1970-06       Impact factor: 8.739

10.  Evidence that adenosine triphosphate or a related nucleotide is the transmitter substance released by non-adrenergic inhibitory nerves in the gut.

Authors:  G Burnstock; G Campbell; D Satchell; A Smythe
Journal:  Br J Pharmacol       Date:  1970-12       Impact factor: 8.739

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