Literature DB >> 1908732

Bioassay of nitric oxide released upon stimulation of non-adrenergic non-cholinergic nerves in the canine ileocolonic junction.

G E Boeckxstaens1, P A Pelckmans, I F Ruytjens, H Bult, J G De Man, A G Herman, Y M Van Maercke.   

Abstract

1. The release and the nature of the inhibitory non-adrenergic non-cholinergic (NANC) neurotransmitter was studied in the canine ileocolonic junction. A circular muscle strip of the canine ileocolonic junction served as donor tissue in a superfusion bioassay in which rings of rabbit aorta with the endothelium removed served as detector tissue. 2. The ileocolonic junction released a labile factor with vasodilator activity upon stimulation of non-adrenergic non-cholinergic (NANC) nerves in response to electrical impulses and the nicotinic receptor agonist 1,1-dimethyl-4-phenylpiperazinium (DMPP). This release was respectively frequency- and concentration-dependent. 3. The release was reduced by the blocker of neuronal conductance, tetrodotoxin, and by the inhibitor of the nitric oxide (NO) biosynthesis NG-nitro-L-arginine. The biological activity was enhanced by superoxide dismutase and eliminated by haemoglobin. Hexamethonium abolished only the release in response to DMPP. 4. Injection of adenosine 5'-triphosphate (ATP) or vasoactive intestinal polypeptide (VIP) onto the cascade induced relaxations of the rabbit aorta but they were different from those induced by NO or the transferable factor. 5. Based on organ bath experiments in which the reactivity of different parts of the circular smooth muscle layer of the ileocolonic junction was investigated, a muscle strip of superficial circular muscle with submucosa was chosen as the detector strip in the bioassay cascade. 6. The ileocolonic junction dose-dependently relaxed in response to nitroglycerin and NO. NO was much more potent in the rabbit aorta than in the canine ileocolonic junction. 7. In conclusion, our results demonstrate the release of a transferable vasorelaxant factor in response to NANC nerve stimulation which behaves pharmacologically like NO but not like ATP or VIP. Therefore, we suggest that NO or a NO releasing substance is the inhibitory NANC neurotransmitter in the canine ileocolonic junction.

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Year:  1991        PMID: 1908732      PMCID: PMC1908082          DOI: 10.1111/j.1476-5381.1991.tb12304.x

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


  43 in total

Review 1.  Biosynthesis and metabolism of endothelium-derived nitric oxide.

Authors:  L J Ignarro
Journal:  Annu Rev Pharmacol Toxicol       Date:  1990       Impact factor: 13.820

2.  Electrical pacemakers of canine proximal colon are functionally innervated by inhibitory motor neurons.

Authors:  T K Smith; J B Reed; K M Sanders
Journal:  Am J Physiol       Date:  1989-03

Review 3.  The non-adrenergic non-cholinergic nervous system.

Authors:  G Burnstock
Journal:  Arch Int Pharmacodyn Ther       Date:  1986-04

4.  Acetylcholine is an indirect inhibitory transmitter in the canine ileocolonic junction.

Authors:  P A Pelckmans; G E Boeckxstaens; Y M Van Maercke; A G Herman; T J Verbeuren
Journal:  Eur J Pharmacol       Date:  1989-11-07       Impact factor: 4.432

5.  Interaction of two electrical pacemakers in muscularis of canine proximal colon.

Authors:  T K Smith; J B Reed; K M Sanders
Journal:  Am J Physiol       Date:  1987-03

6.  Origin and propagation of electrical slow waves in circular muscle of canine proximal colon.

Authors:  T K Smith; J B Reed; K M Sanders
Journal:  Am J Physiol       Date:  1987-02

7.  Selective blockade of endothelium-dependent and glyceryl trinitrate-induced relaxation by hemoglobin and by methylene blue in the rabbit aorta.

Authors:  W Martin; G M Villani; D Jothianandan; R F Furchgott
Journal:  J Pharmacol Exp Ther       Date:  1985-03       Impact factor: 4.030

8.  Formation of nitric oxide from L-arginine in the central nervous system: a transduction mechanism for stimulation of the soluble guanylate cyclase.

Authors:  R G Knowles; M Palacios; R M Palmer; S Moncada
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

9.  Nitric oxide as an inhibitory non-adrenergic non-cholinergic neurotransmitter.

Authors:  H Bult; G E Boeckxstaens; P A Pelckmans; F H Jordaens; Y M Van Maercke; A G Herman
Journal:  Nature       Date:  1990-05-24       Impact factor: 49.962

10.  L-arginine is the physiological precursor for the formation of nitric oxide in endothelium-dependent relaxation.

Authors:  R M Palmer; D D Rees; D S Ashton; S Moncada
Journal:  Biochem Biophys Res Commun       Date:  1988-06-30       Impact factor: 3.575

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  26 in total

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3.  Role of nitric oxide in non-adrenergic, non-cholinergic inhibitory junction potentials in canine ileocolonic sphincter.

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5.  Projections of nitric oxide synthesizing neurons in the guinea-pig colon.

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6.  Localization of nitric oxide synthase in canine ileocolonic and pyloric sphincters.

Authors:  S M Ward; C Xue; K M Sanders
Journal:  Cell Tissue Res       Date:  1994-03       Impact factor: 5.249

7.  Comparison of the effects of hydroxocobalamin and oxyhaemoglobin on responses to NO, EDRF and the nitrergic transmitter.

Authors:  M La; C G Li; M J Rand
Journal:  Br J Pharmacol       Date:  1996-03       Impact factor: 8.739

8.  Non-adrenergic, non-cholinergic relaxation of the bovine retractor penis muscle: role of S-nitrosothiols.

Authors:  X Liu; J S Gillespie; W Martin
Journal:  Br J Pharmacol       Date:  1994-04       Impact factor: 8.739

9.  Differential effects of lumenal L-arginine and NG-nitro L-arginine on blood flow and water fluxes in rat ileum.

Authors:  D Mailman
Journal:  Br J Pharmacol       Date:  1994-05       Impact factor: 8.739

10.  Distribution of P2X(3) receptor immunoreactivity in myenteric ganglia of the mouse esophagus.

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