TY - JOUR
T1 - Inhibition of neuronal M2 muscarinic receptor function in the lungs by extracellular nitric oxide
AU - Golkar, Laleh
AU - Yarkony, Kathryn A.
AU - Fryer, Allison D.
PY - 2000
Y1 - 2000
N2 - 1. These experiments were carried out to test whether neuronal M2 muscarinic receptor function in the lungs is affected by nitric oxide (NO) and whether the source of the NO is epithelial or neuronal. 2. In pathogen free, anaesthetized guinea-pigs, the muscarinic agonist pilocarpine inhibited vagally induced bronchoconstriction demonstrating functional neuronal M2 muscarinic receptors. In the presence of the NO donor, 3-morpholino-sydnonimine (SIN-1), pilocarpine no longer inhibited vagally induced bronchoconstriction. In contrast, inhibiting endogenous NO with N(G)-monomethyl-L-arginine methyl ester (L-NMMA) did not affect the ability of pilocarpine to decrease vagally induced bronchoconstriction. 3. In isolated tracheas, pilocarpine inhibited contractions induced by electrical field stimulation demonstrating that neuronal M2 muscarinic receptors function in vitro. As in the anaesthetized guinea-pigs, SIN-1 shifted the pilocarpine dose response curve to the right, demonstrating decreased neuronal M2 receptor function. However, in vitro, L-NMMA shifted the pilocarpine dose response curve to the left, demonstrating that endogenous NO was inhibiting the ability of the M2 receptors to decrease acetylcholine (ACh) release. 4. Both haemoglobin (Hb), which scavenges NO, and epithelial removal also shifted the pilocarpine dose response curve to the left, demonstrating that the NO inhibiting neuronal M2 receptor function was extracellular and probably of epithelial origin. 5. In conclusion, extracellular NO appears to inhibit the ability of the M: receptors to decrease ACh release from the parasympathetic nerves in the lungs in viva and in vitro in pathogen free guinea-pigs. However, while the neuronal M2 receptors will respond to NO (from SIN-1) in vivo, there does not appear to be an endogenous source of NO since L-NMMA had no effect in vivo.
AB - 1. These experiments were carried out to test whether neuronal M2 muscarinic receptor function in the lungs is affected by nitric oxide (NO) and whether the source of the NO is epithelial or neuronal. 2. In pathogen free, anaesthetized guinea-pigs, the muscarinic agonist pilocarpine inhibited vagally induced bronchoconstriction demonstrating functional neuronal M2 muscarinic receptors. In the presence of the NO donor, 3-morpholino-sydnonimine (SIN-1), pilocarpine no longer inhibited vagally induced bronchoconstriction. In contrast, inhibiting endogenous NO with N(G)-monomethyl-L-arginine methyl ester (L-NMMA) did not affect the ability of pilocarpine to decrease vagally induced bronchoconstriction. 3. In isolated tracheas, pilocarpine inhibited contractions induced by electrical field stimulation demonstrating that neuronal M2 muscarinic receptors function in vitro. As in the anaesthetized guinea-pigs, SIN-1 shifted the pilocarpine dose response curve to the right, demonstrating decreased neuronal M2 receptor function. However, in vitro, L-NMMA shifted the pilocarpine dose response curve to the left, demonstrating that endogenous NO was inhibiting the ability of the M2 receptors to decrease acetylcholine (ACh) release. 4. Both haemoglobin (Hb), which scavenges NO, and epithelial removal also shifted the pilocarpine dose response curve to the left, demonstrating that the NO inhibiting neuronal M2 receptor function was extracellular and probably of epithelial origin. 5. In conclusion, extracellular NO appears to inhibit the ability of the M: receptors to decrease ACh release from the parasympathetic nerves in the lungs in viva and in vitro in pathogen free guinea-pigs. However, while the neuronal M2 receptors will respond to NO (from SIN-1) in vivo, there does not appear to be an endogenous source of NO since L-NMMA had no effect in vivo.
KW - Airway epithelium
KW - L-NMMA, pilocarpine
KW - Nitric oxide
KW - SIN-1
UR - http://www.scopus.com/inward/record.url?scp=0033778215&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033778215&partnerID=8YFLogxK
U2 - 10.1038/sj.bjp.0703542
DO - 10.1038/sj.bjp.0703542
M3 - Article
C2 - 10991925
AN - SCOPUS:0033778215
SN - 0007-1188
VL - 131
SP - 312
EP - 318
JO - British Journal of Pharmacology
JF - British Journal of Pharmacology
IS - 2
ER -