Literature DB >> 8528561

Nitric oxide, an enteric nonadrenergic-noncholinergic relaxant transmitter: evidence using phosphodiesterase V and nitric oxide synthase inhibition.

S J Williams1, M E Parsons.   

Abstract

1. The effects of NG-nitro-L-arginine (L-NOARG), a nitric oxide synthase inhibitor, and SK&F 96231, a phosphodiesterase type V inhibitor, on electrical field stimulated (EFS) nonadrenergic noncholinergic (NANC) relaxations of rat fundal strips, guinea-pig isolated ileum longitudinal muscle with intact myenteric plexus, and guinea-pig taenia caeci were investigated. 2. Reproducible repeated control random EFS frequency-response curves were obtained for all three tissues. 3. Depending on the frequency of stimulation, L-NOARG (10(-4)-5 x 10(-3) M) caused either a complete or partial inhibition of the NANC-induced relaxations of the rat fundal strips and the guinea-pig isolated ileum longitudinal muscle with intact myenteric plexus, but not of the guinea-pig taenia caeci. The inhibitory action of L-NOARG was partially or totally reversed, depending on the tissue, by L-arginine (5 x 10(-3) M). 4. SK&F 96231 (10(-6)-10(-4) M) caused a concentration- and frequency-dependent potentiation of both the size and duration of the EFS-induced NANC relaxant response of rat fundal strips and guinea-pig isolated ileum longitudinal muscle with intact myenteric plexus, but not of the guinea-pig taenia caeci. 5. Zaprinast, another phosphodiesterase type V inhibitor (10(-6)-10(-4) M) caused a concentration- and frequency-dependent potentiation of the NANC relaxant responses to EFS of rat fundal strips. 6. SK&F 96231 and zaprinast alone (10(-6)-10(-4) M) caused a concentration-dependent relaxation of the agonist-induced tone of all three tissues with the maximum degree of relaxation found to be in the order stomach < ileum < caecum. This is the reverse order for ability of SK&F 96231 to potentiate relaxant responses to EFS. 7. These results suggest NO is involved in the NANC nerve-mediated relaxation of rat fundal strips and guinea-pig isolated ileum longitudinal muscle with intact myenteric plexus, but not the guinea-pig taenia caeci.

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Year:  1995        PMID: 8528561      PMCID: PMC1909085          DOI: 10.1111/j.1476-5381.1995.tb16664.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  37 in total

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4.  Inhibitory innervation of the gut.

Authors:  G Burnstock; M Costa
Journal:  Gastroenterology       Date:  1973-01       Impact factor: 22.682

5.  Release of nitric oxide upon stimulation of nonadrenergic noncholinergic nerves in the rat gastric fundus.

Authors:  G E Boeckxstaens; P A Pelckmans; J J Bogers; H Bult; J G De Man; L Oosterbosch; A G Herman; Y M Van Maercke
Journal:  J Pharmacol Exp Ther       Date:  1991-02       Impact factor: 4.030

6.  Nitric oxide mediating NANC inhibition in opossum lower esophageal sphincter.

Authors:  A Tøttrup; D Svane; A Forman
Journal:  Am J Physiol       Date:  1991-03

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Authors:  C G Li; M J Rand
Journal:  Clin Exp Pharmacol Physiol       Date:  1989-12       Impact factor: 2.557

8.  Human lower oesophageal sphincter relaxation is associated with raised cyclic nucleotide content.

Authors:  M S Barnette; F C Barone; P J Fowler; M Grous; W J Price; H S Ormsbee
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Authors:  G E Boeckxstaens; P A Pelckmans; H Bult; J G De Man; A G Herman; Y M Van Maercke
Journal:  Eur J Pharmacol       Date:  1990-11-06       Impact factor: 4.432

10.  VIP as a possible neurotransmitter of non-cholinergic non-adrenergic inhibitory neurones.

Authors:  R K Goyal; S Rattan; S I Said
Journal:  Nature       Date:  1980-11-27       Impact factor: 49.962

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4.  Tonic inhibitory action by nitric oxide on spontaneous mechanical activity in rat proximal colon: involvement of cyclic GMP and apamin-sensitive K+ channels.

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