ERJ
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (12)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tournoy, K.G.
Right arrow Articles by Joos, G.F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tournoy, K.G.
Right arrow Articles by Joos, G.F.
Eur Respir J 2003; 21:3-10
Copyright ©ERS Journals Ltd 2003

Modulatory role of tachykinin NK1 receptor in cholinergic contraction of mouse trachea

K.G. Tournoy1, K.O. De Swert1, P.G. Leclere2, R.A. Lefebvre2, R.A. Pauwels1 and G.F. Joos1

1 Dept Respiratory Diseases, Ghent University Hospital, and 2 Heymans Institute of Pharmacology, Ghent University, Faculty of Medicine, De Pintelaan, Ghent, Belgium

CORRESPONDENCE: K. De Swert, Dept Respiratory Diseases, Ghent University Hospital, De Pintelaan 185, B-9000, Ghent, Belgium. Fax: 32 92402341. E-mail: Katelijne.Deswert@rug.ac.be

Keywords: airway contraction, knockout mice, neuropeptides, substance P receptor, tachykinins

Received: January 31, 2002
Accepted August 5, 2002

This study was supported by the Concerted Research Initiative of Ghent University (GOA Project 98-6). K.G. Tournoy was supported by the Fund for Scientific Research Flanders. K.O. De Swert was supported by the Concerted Research Initiative of Ghent University (GOA Project 98-6).


   Abstract
TOP
 Abstract
Materials and methods
 Results
 Discussion
 Acknowledgements
 References
 
The role of the NK1 receptor in airway contraction induced by electrical field stimulation (EFS) was evaluated by comparing the response in NK1 receptor knockout mice (NK1R–/–) with that of NK1 receptor wild-type controls (WT).

A frequency/response curve on tracheas from NK1R–/– mice and NK1R WT littermates was constructed. After incubation with [3H]choline, [3H]acetylcholine release upon EFS was measured by high-performance liquid chromatography and liquid scintillation counting. The effects of atropine (1x10–6 M), tetrodotoxin (1x10–6 M) and a specific NK1R antagonist (SR140333, 1x10–8 M) were studied, as well as the effects of substance P (1x10–5 M) on precontracted tracheas.

Upon EFS, NK1R–/– mice had a significant lower trachea contractility than the NK1R WT animals, accompanied with less [3H]acetylcholine release. Pretreatment with atropine or tetrodotoxin abolished the EFS-induced contraction in both strains. Pretreatment with the NK1R antagonist SR140333 significantly reduced the contractility in the NK1R WT but not in the NK1R–/– mice. Substance P caused a small contraction in both NK1R WT and NK1R–/– mice. Substance P induced a relaxation in precontracted tracheas in NK1R WT but not in NK1R–/– mice.

The data presented here provide direct evidence that the NK1 receptor augments cholinergic neurotransmission in mouse trachea.

Substance P is a member of the tachykinin peptide family and is localised to the sensory nerves of the airways in various species including mice. This peptide has effects that are potentially relevant in the pathogenesis of asthma, such as bronchoconstriction, bronchial vasodilatation, plasma extravasation, augmentation of airway secretions and effects on inflammatory and immune cells 1. The bronchoconstrictor effects of substance P are mediated via a direct effect on airway smooth muscle and via indirect effects on nerves and inflammatory cells.

Direct and indirect evidence exists that substance P has a facilitatory role in the release of acetylcholine from postganglionic cholinergic nerves in guinea pig 2–4, rabbit 5, 6 and human 7, 8 airways. In guinea pigs, both exogenous and endogenous tachykinins may facilitate cholinergic neurotransmission. Through the use of specific antagonists, it has been suggested that NK1 receptors may be involved in this facilitation 9.

Conversely, tachykinins also exhibit additional biological effects that may protect against pro-asthmatic actions. In mouse and rat airways, substance P is involved in the tachykinin NK1 receptor-mediated airway relaxations due to epithelium-derived prostaglandin (PG)E2 10–12.

The present study was designed to evaluate the effects of endogenous tachykinins acting through the NK1 receptor 13, 14 on the cholinergic neurotransmission in mouse trachea in vitro. Electrical field stimulation (EFS)-induced contractions and acetylcholine release were measured in tracheas of tachykinin NK1 receptor knockout mice (NK1R–/–) versus NK1 receptor wild-type control mice (WT). The results provide direct evidence that tachykinins facilitate cholinergic transmission in mouse trachea in vitro through the NK1 receptor. Furthermore, this study has confirmed and extended previous findings that NK1 receptors are also involved in the substance P-induced relaxation of precontracted smooth muscle cells 10–12, 15.


   Materials and methods
TOP
 Abstract
 Materials and methods
Results
 Discussion
 Acknowledgements
 References
 
Animals
NK1R–/– and NK1R WT mice were derived from the mating of heterozygous NK1R+/– mice, as described previously 16. The targeting construct was derived from a mouse 129/sv strain genomic library and targeted clones were injected into C57BL/6 blastocysts. Chimaeric males were mated with C57BL/6 females. The mice were bred from successive generations of sibling knockout and NK1R WT mice and can be thought of as representing a recombinant inbred strain. The respective NK1R–/– and WT breeding pairs were provided by the lab of S. Hunt (Cambridge, UK). The animals were bred locally and maintained under germ-free conditions in a conventional animal house in the animal research facilities of the Dept of Respiratory Diseases of the University Hospital, Ghent, Belgium, and received food and water ad libitum.

General procedure
The mice were killed by an intraperitoneal injection of pentobarbital (100 mg·kg–1 Nembutal®; Sanofi, Libourne, France). The trachea was gently excised and the adhering connective tissue was carefully dissected and removed under microscopy guidance. The whole tracheas were mounted in 2 mL organ baths containing Krebs solution (KS) (composition in mM: NaCl 118, KCl 4.6, CaCl2 2.5, MgSO4 1.15, NaHCO3 24.9, KH2PO4 1.15 and glucose 5.5), which was maintained at 37°C and bubbled with carbogen (5% carbon dioxide, 95% oxygen (O2)). The optimal resting tension on the trachea of this mouse strain was 0.7 g, as determined by length-tension experiments. The tracheas were allowed to stabilise for 15 min at this resting tension. After this stabilisation period, increasing concentrations of carbachol were added to the organ bath in a noncumulative way (3.3x10–7, 1x10–6 and 3.3x10–6 M) in order to stabilise the tissues. The contact time for each concentration was 15 min. An interval of 10 min was inserted between the administrations while the bathing medium was changed. The contractions were measured isometrically with Grass FT03 transducers (Grass Instruments Co., Quincy, MA, USA) and recorded on a Graphtec Linearecorder type WR3701 (Graphtech Corp., Tokyo, Japan).

Transmural nerve stimulation
The tracheal rings were suspended between two platinum field bar electrodes (15 mm distance) in 2 mL organ baths containing KS. Responses to EFS were studied by applying monophasic square wave pulses from a Grass S44 stimulator (Grass Instruments Co.), using a supramaximal voltage of 50 V, 230 mA and a pulse duration of 0.5 ms. Frequency/response curves were generated using a frequency range of 0.1–30 Hz. One 10-s train at increasing frequency was given at 2-min intervals, while the Krebs solution was refreshed after two stimulus trains to prevent disturbances of the ion balance. Preliminary experiments showed that, both in NK1R WT and NK1R–/– mice, two frequency/response curves could be constructed, with a 30-min interval, without the occurrence of tachyphylaxis. The effect of atropine (1x10–6 M), tetrodotoxin (TTX, 1x10–6 M; Alomone Labs, Jerusalem, Israel) and SR140333 (a specific NK1R antagonist, 1x10–8 M; X. Emonds-Alt, Sanofi Recherche, Montpellier, France) 17 was evaluated by incubating tracheal tissue from both mouse strains for 20 min before the construction of the second frequency/response curve.

[3H]acetylcholine release
Two tracheas were mounted vertically between 2 platinum wire electrodes (40x0.5 mm, distance 5 mm) in a 2 mL organ bath containing KS supplemented with cholinechloride (1x10–6 M) and ascorbic acid (57x10–6 M). During a 30-min equilibration period, the tissues were superfused at a rate of 2 mL·min–1, using a peristaltic pump (Gilson Minipuls, Villers Le Bel, France). During the last 10 min, the tracheas were subjected to a continuous EFS (Grass S88 Stimulator; Grass Instruments Co.), characterised by 0.5 ms monophasic square wave pulses of 0.1 Hz at 40 V to liberate the stores of neurotransmitter. After this equilibration period, the superfusion was stopped. The neuronal stores of acetylcholine were labelled with [3H]choline (5 µCi·mL–1; [methyl-3H]-choline chloride (2775 GBq·mmol–1); NEN, Boston, USA) under field stimulation delivered at 0.1 Hz during 30 min (40 V, 0.5 ms). To remove loosely bound radioactive choline, the tissues were superfused (2 mL·min–1 for 60 min) with KS supplemented with hemicholinium-3 (1x10–7 M; hemicholinium-3-bromide; RBI, USA), physostigmine (1x10–7 M; physostigmine salicylate; Federa, Brussels, Belgium) and atropine (1x10–6 M). These substances were added to prevent the re-uptake of choline, the hydrolysis of acetylcholine and the presynaptic auto-inhibition of acetylcholine release. Presynaptic muscarinic autoreceptors have indeed been demonstrated in the trachea of different species 18–20 and preliminary experiments in the absence or presence of atropine during stimulation phase 3 (S3, see below) showed that no acetylcholine release could be detected in the mouse trachea without atropine. After this 60-min washout period, the content of the organ baths (1 mL from now on) was collected and replaced every 3 min for a total of 30 collections. The tracheal rings were stimulated three times (S1, S2 and S3) for 30 s (10 Hz at 40 V with 0.5 ms pulses). S1 started 13 min (5th sample), S2 43 min (15th sample) and S3 73 min (25th sample) after the end of the washout period. A total of 500 µL of all collected samples was fixed with 2 mL Ultima Gold (Canberra Packard, Meriden, CT, USA). The radioactivity of all samples was measured by liquid scintillation counting (Packard Tri-Carb TR; Canberra Packard) (fig. 1aGo). The stimulation-induced increase in tritium overflow was calculated by subtracting the basal tritium overflow. The basal tritium overflow during the period of stimulation was calculated by fitting a regression line through the values of the four samples before S1 and through the values of the samples starting from where the overflow had returned to basal values after S1, S2 and S3. The amounts of [3H]acetylcholine, [3H]choline and [3H]phosphorylcholine were measured by reverse-phase high-performance liquid chromatography (HPLC) (Hyperchrome-HPLC-column, 250x4.6 mm, prepacked with hypersil-ods 5.0 µm; Bischoff Chromatography, Leonberg, Germany), as previously described 21. Briefly, a 0.1 M phosphate buffer (pH 4.7) containing methanol (8 vol %; Lab-Scan, Dublin, Ireland) and tetramethylammonium (0.2 mM; Merck-Schuchardt, Hohenbrunn, Germany) was used with a flow of 0.5 mL·min–1. The collection of the effluent was in 1-min fractions. HPLC was performed on one basal fraction before S1, S2 and S3 and on the fractions with the highest radioactivity after the stimulations. A total of 100 µL of the samples was injected into the HPLC and 27 fractions were collected and mixed with 2.5 mL Ultima Gold. The fractions 6–11 contained the peaks with phosphorylcholine and choline, while fractions 14–24 contained the acetylcholine (fig. 1bGo) (proven by the preliminary HPLC on the standards, results not shown). The real amount of choline, phosphorylcholine and acetylcholine expressed as percentages was calculated by subtraction of the background counting. The background counting was estimated by fitting a regression line through the values of the first five fractions and fractions 26–27 22.



View larger version (18K):
[in this window]
[in a new window]
  		Fig. 1.— Example of acetylcholine release measurements. a) Measurement of the released radioactivity in samples collected every 3 min for 90 min. Tracheas were stimulated three times (#: S1; : S2; and +: S3). b) Measurement of the stimulation-induced efflux of choline (§), phosphorylcholine (f) and acetylcholine (##) after high-performance liquid chromatography separation of sample no. 25. The fractions 6–11 contained the peaks with phosphorylcholine and choline while the fractions 14–24 contained acetylcholine. dpm: disintegrations per minute.

 
Effects of carbachol, substance P and Sar9,Met(O2)11-substance P on the tracheal ring tension
Increasing concentrations of carbachol (1x10–8 to 1x10–4 M) were added to the organ bath in a cumulative way (in steps of 0.5 log[concentration]), whereby the contact time for each concentration was ≥4 min. Concentration/response curves to substance P (Peninsula Laboratories Ltd, St Helens, UK) and Sar9,Met(O2)11-substance P (a selective NK1R agonist; Peninsula Laboratories Ltd) were constructed by adding increasing concentrations to the organ bath in a noncumulative way (1x10–8 M to 1x10–4 M) after the stabilisation period with carbachol. The contact time for each concentration was ≥4 min. Isolated mouse airways do not exhibit intrinsic tone, thus airway segments were contracted to 50–75% of carbachol maximum with 3.3x10–7 M carbachol to allow a possible relaxation to substance P and Sar9,Met(O2)11-substance P (1x10–5 M). Whether the observed relaxation effects of substance P were mediated through the production of nitric oxide (NO) or prostaglandin E2 was analysed by measuring the effect of a pretreatment with 2x10–4 M N{omega}-nitro-l-arginine methyl ester (l-NAME) or 1x10–6 M indomethacin (Indocid ®; MSD, Brussels, Belgium) on the substance P-induced relaxation in carbachol precontracted tissue. A positive control of the relaxation in indomethacin pretreated tracheal tissue was performed by means of the ß-adrenergic compound isoproterenol (Isuprel®; Abbott, Ottignies, Belgium) at 1x10–5 M.

Statistical analysis
The results of the in vitro analyses of airway responsiveness and acetylcholine release are reported as mean±sem. Frequency/response curves in the absence and presence of antagonists, atropine and TTX (multiple comparisons) were compared by analysis of variance (ANOVA). The differences in acetylcholine release were evaluated using the nonparametric Mann-Whitney U-test. Differences were regarded as significant when p<0.05.


   Results
TOP
 Abstract
 Materials and methods
 Results
Discussion
 Acknowledgements
 References
 
Comparison of carbachol- and electrical field stimulation-induced tracheal contractions in NK1R–/– and corresponding NK1R WT mice
No differences in tracheal contractions were observed between NK1R–/– and NK1R WT mice during a cumulative concentration response curve to carbachol (fig. 2Go). In contrast, the EFS-induced contraction of the trachea was significantly lower in the NK1R–/– mice (fig. 3Go). Pretreatment with SR140333 at 1x10–8 M was able to reduce the EFS-induced contraction in the NK1R WT mice (n=5) (fig. 4aGo). At a concentration of 1x10–8 M, SR140333 had no effect on the EFS-induced contraction of the NK1R–/– trachea (n=4) (fig. 4bGo). At a higher concentration (1x10–7 M) of SR140333, a small decrease of EFS-induced contractions was observed in the NK1R–/– mice (results not shown). The EFS-induced contractions were completely abolished by pretreatment with TTX (n=2) (fig. 5aGo) as well as by pretreatment with atropine (n=6) (fig. 5bGo).



View larger version (13K):
[in this window]
[in a new window]
  		Fig. 2.— In vitro response to carbachol of tracheal smooth muscle from NK1 receptor knockout mice (----) versus NK1 receptor wild-type control mice (––) (n=6). Data are presented as mean±sem. There were no differences between the two strains in terms of their in vitro responses to this agonist (ns).

 


View larger version (13K):
[in this window]
[in a new window]
  		Fig. 3.— In vitro response to electrical field stimulation (EFS; 50 V, 230 mA, 0.5 ms) of tracheal smooth muscle from NK1 receptor knockout mice (NK1R–/–; ----) versus NK1 receptor wild-type control mice (NK1R WT; ––) (n=12). Data are presented as mean±sem. Tracheas from NK1R WT mice responded significantly more to EFS than tracheas from NK1R–/– mice (p<0.001).

 


View larger version (15K):
[in this window]
[in a new window]
  		Fig. 4.— a) In vitro response to electrical field stimulation (EFS; 50 V, 230 mA, 0.5 ms) of tracheal smooth muscle from NK1 receptor wild-type control mice in the presence (––) or absence (----) of 1x10–8 M SR140333 (n=5). Data are presented as mean±sem. p<0.05. b) In vitro response to EFS (50 V, 230 mA, 0.5 ms) of tracheal smooth muscle from NK1 receptor knockout mice in the presence (––) or absence (----) of 1x10–8 M SR140333 (n=4) (ns).

 


View larger version (18K):
[in this window]
[in a new window]
  		Fig. 5.— In vitro response to electrical field stimulation (EFS; 50 V, 230 mA, 0.5 ms) of tracheal smooth muscle from NK1 receptor knockout mice (NK1R–/–; ----) versus NK1 receptor wild-type control mice (NK1R WT; ––) in the presence ({square}) or absence ({blacksquare}) of a) tetrodotoxin (n=2) or b) atropine (n=6). Responses are fully abrogated in the presence of these substances. p<0.001.

 
Comparison of acetylcholine release of tracheas from NK1R–/– and corresponding NK1R WT mice
In NK1R WT as well as NK1R–/– mice, the authors studied whether activation of the NK1R pathway resulted in differences of acetylcholine release. After labelling with radioactive choline, EFS of tracheas of both NK1R–/– and NK1R WT mice resulted in the release of a radioactive signal in the organ bath. The first stimulation released more radioactive signal into the organ bath than the second. No significant difference was observed between the second and the third stimulation (results not shown). The tracheas of the NK1R WT mice released 36% more radioactive signal than the NK1R–/– mice (2,306±305 versus 1,595±260 disintegrations per min·mg wet weight (ww)–1, ns, n=6) during the third stimulation. Performing HPLC on a sample of the organ bath taken just before S3 revealed a similar basal leakage of [3H]choline and [3H]phosphorylcholine in the tracheas of both strains, but no detectable basal [3H]acetylcholine release. In contrast, during S3, tracheas of both strains released a detectable amount of [3H]acetylcholine. The NK1R WT mice released significantly more acetylcholine than the NK1R–/– counterparts during S3 (fig. 6Go).



View larger version (40K):
[in this window]
[in a new window]
  		Fig. 6.— Acetylcholine (ACh) release from tracheas of NK1 receptor knockout mice (NK1R–/–) versus NK1 receptor wild-type control mice (NK1R WT) caused by stimulation 3 (10 Hz at 40 V with 0.5 ms pulses) after high-performance liquid chromatography separation. Tracheas from NK1R WT mice released significantly larger amounts of ACh, compared with tracheas from NK1R–/– mice. **: p<0.01. dpm: disintegrations per minute.

 
Effect of substance P and the NK1R agonist Sar9,Met(O2)11-substance P on tracheal ring tension
Tracheas of both mouse strains were exposed to increasing doses of substance P (1x10–8–1x10–4 M). Both NK1R WT and NK1R–/– mice reacted with a comparable small, but significant contractile response only at the highest concentration of substance P (fig. 7Go). In contrast, no contractile response was observed upon administration of the specific tachykinin NK1 receptor agonist Sar9,Met(O2)11-substance P in either mouse strain (n=6, data not shown). In a second set of experiments, the effect of these molecules on the trachea, precontracted by carbachol (3.3x10–7 M) was evaluated. Upon administration of substance P, a relaxing response was observed in the NK1R WT mice (fig. 7Go), averaging 78.52±8.70% of the carbachol-induced contraction (n=4). In contrast, the tracheas of NK1R–/– mice (fig. 7Go) failed to relax (0.0±0.0%) (n=4). The NK1R agonist, Sar9,Met(O2)11-substance P induced a relaxation in precontracted trachea (carbachol 3.3x10–7 M) of NK1R WT mice (86.6±44.62%) but not in precontracted trachea (carbachol 3.3x10–7 M) of NK1R–/– mice (0.0±0.0%) (n=4).



View larger version (9K):
[in this window]
[in a new window]
  		Fig. 7.— Individual tracings showing a) in vitro response to substance P (1x10–4 M) in NK1 receptor wild-type control mice (NK1R WT), b) in vitro response to substance P (1x10–4 M) in NK1 receptor knockout mice (NK1R–/–), c) in vitro response to substance P (1x10–5 M) of precontracted tracheas from NK1R WT mice and d) in vitro response to substance P (1x10–5 M) of precontracted tracheas from NK1R–/– mice. Solid arrow: carbachol; arrow: substance P.

 
Two potential mediators of the substance P-induced relaxation were investigated in this respect. Pretreatment of the tracheas of the NK1R WT mice with l-NAME (2x10–4 M), a specific NO-synthase inhibitor, did not inhibit the relaxing effect of substance P (results not shown). In contrast, pretreatment of the NK1R WT tracheas with the cyclooxygenase inhibitor indomethacin (1x10–6 M) completely abolished the substance P-induced relaxation (from 78.52±8.70% to 0.03±0.03% in the presence of indomethacin, p<0.05) (n=6). The ß2-adrenergic-mediated isoprenaline-induced relaxation was not affected by indomethacin pretreatment (data not shown).


   Discussion
TOP
 Abstract
 Materials and methods
 Results
 Discussion
Acknowledgements
 References
 
In this study, the role of the NK1R in cholinergic neurotransmitter-mediated contraction of mouse trachea has been evaluated in vitro. In mice lacking the NK1R, the contractile response of the trachea to EFS was significantly decreased. An NK1R antagonist partially reduced the EFS-induced responses in the NK1R WT mice. The responses to EFS were completely blocked by the neurotoxin TTX and by atropine, establishing that stimulation of cholinergic neural elements within the airways mediated these contractile responses. Upon EFS, the NK1R–/– mice produced less acetylcholine compared to the WT littermates. These results suggest that endogenous tachykinins, coreleased during EFS, signal through the NK1R on cholinergic nerve endings to augment acetylcholine release.

The lower tracheal contraction to electrical stimulation in the NK1R–/– mice cannot be explained by a lower sensitivity to cholinergic agonists. A cumulative concentration response curve to carbachol revealed no differences between the trachea of the NK1R WT and NK1R–/– mice. The ECSO values of both curves were very similar for both strains. Moreover, the maximal response to carbachol was somewhat higher in the NK1R–/– mice (compared to NK1R WT) (fig. 2Go).

Endogenous tachykinins (e.g. substance P) do not seem to be involved in mediating direct contractile responses through the NK1R, as only high concentrations of exogenous substance P were able to induce a small contraction in both strains. Moreover, as substance P-induced contraction in both NK1R WT and NK1R–/– mice, it is likely that this effect is mediated through another tachykinin receptor, probably the NK2R. This is supported by the lack of a contractile effect for the specific NK1R agonist, Sar9,Met(O2)11-substance P. Moreover, pretreatment with atropine completely abolished the EFS-induced contractions, suggesting that these contractions were mediated only through acetylcholine release, excluding a direct effect by endogenously released tachykinins on smooth muscle cells.

In the NK1R–/– mice a significantly lower release of acetylcholine was observed after EFS, in comparison to the WT mice. These results provide direct evidence that the NK1R is involved in the augmentation of cholinergic neurotransmission in the mouse in vitro. These present findings are in agreement with data obtained in other species, such as rabbits and guinea pigs. In rabbits, a significant increase in acetylcholine release in vitro was observed upon application of substance P, which could be abolished by the addition of a specific NK1R antagonist 6. In guinea pigs, functional evidence exists for the presence of facilitatory tachykinin NK1 receptors on postganglionic nerve terminals 2–4, 9. In humans, NK1 receptors were occasionally found in nerves by the use of immunostaining with specific antibodies 23. NK1 receptor immunoreactivity has also been found in the epithelium, particularly on cell surfaces of the upper half of the epithelial layer 24.

The present findings contrast with data from a recently published study in which it was shown that tachykinin NK2 receptors are involved in the facilitation of acetylcholine release from guinea pig trachea 25. These differing results may be the consequence of species specificity or due to limitations of the experimental methods used. The study on guinea pig trachea was carried out with the use of specific agonists for the NK1, NK2 and NK3 receptors. However, only an NK2 receptor antagonist was used to evaluate the involvement of the NK2 receptor. The present results do not exclude a possible involvement of the NK2 receptor, but the involvement of the NK1 receptor is incontestable by the use of an NK1 receptor knockout model. Moreover, the functional results observed upon EFS in the NK1R–/– trachea were mimicked by application of a specific NK1 receptor antagonist (SR140333) 17 on NK1R WT tracheas. However, the reduction of the EFS-induced contractions by SR140333 in NK1R WT mice seemed less pronounced than the decrease in response to EFS in the NK1R–/– mice. It is possible that the concentration of SR140333 used (1x10–8 M) did not fully block the NK1 receptor. Indeed, higher concentrations, such as 1x10–7 M, are needed to inhibit NK1-agonist-induced effects in a human astrocytoma cell line 26. Higher concentrations are also used in the brain tissue of mice 27, 28. However, higher concentrations of SR140333 induced nonspecific effects in the preparation reported here, which precluded the performance of a concentration/response curve for SR140333.

Besides its pro-asthmatic effects, substance P also exhibits the capacity to exert a protective effect. Elevated levels of substance P may play a protective role in the responses of rat airways to chronic exposure of inhaled irritants like sulphur dioxide and ozone 29–31. A relaxing effect of substance P on the airways has been demonstrated in Sprague-Dawley rats and mice 10–12, 15, 32–34. In rat trachea, the importance of the presence of the epithelium and the NK1 receptor has been demonstrated. Through the use of specific inhibitors and measurements of mediator release, PGE2 was found to be the relaxing factor 10, 15, 33. This phenomenon has also been described in mice. A specific NK1 receptor agonist, [Pro9]-substance P sulphone, and exogenously administered as well as endogenously released substance P mediate relaxation of precontracted mouse main bronchi. The specific NK1 receptor antagonist, CP96345, can block this effect. The relaxation induced by substance P was inhibited by indomethacin 11. This hypothesis was further confirmed by the use of EP2 (one of the four PGE2 receptor subtypes)-deficient mice. Mice lacking the EP2 receptor have a defect in PGE2-mediated relaxation of smooth muscle tissue. Relaxation to substance P was significantly reduced in tracheas of these mice. However, the release of PGE2 induced by substance P was not impaired 12. The current study in the NK1R–/– mice and their corresponding NK1R WT littermates confirm that substance P-induced relaxation in mouse trachea is mediated solely through the NK1 receptor. Moreover, the specific NK1R agonist, Sar9,Met(O2)11-substance P was able to induce relaxation of the precontracted NK1R WT tracheas. The relaxation of precontracted tracheas of NK1R WT animals could be blocked by the addition of indomethacin, suggesting that an inhibitory metabolite of arachidonic acid derived from cyclooxygenase is involved. As the relaxing capacity of the tracheas, as measured by application of isoprenaline, was not influenced by indomethacin, the present observations, together with previous findings of other groups 10, 11, suggest that PGE2 is the relaxing factor. In addition, it was reported that guinea pig tracheal tube preparations relax by stimulation of epithelial NK1 receptors via NO release 35, 36.

It is important to note that relaxation occurred 30 s after the addition of substance P in the NK1R WT tracheas. As in the functional studies, the tracheas were stimulated during 10 s whereby an immediate contractile response was observed, and therefore relaxation cannot interfere with these EFS-induced contractions.

In conclusion, by using NK1 receptor knockout mice, the authors have evaluated the modulatory role of the NK1 receptor pathway in cholinergic contractions of mouse trachea. Through functional studies and direct acetylcholine release experiments in an NK1 receptor knockout model, the authors conclude that tachykinin NK1 receptor activation augments cholinergic neurotransmission upon electrical field stimulation. Exogenously applied NK1 receptor agonists do not induce contraction but can influence tracheal tone by induction of relaxation of precontracted tracheas.


   Acknowledgements
TOP
 Abstract
 Materials and methods
 Results
 Discussion
 Acknowledgements
References
 
The authors would like to thank S. Hunt (Cambridge, UK) for kindly providing the NK1 receptor wild-type controls and knockout breeding pairs and X. Emonds-Alt (Sanofi Recherche, Montpellier, France) for providing the specific NK1 receptor antagonist, SR140333. They also gratefully acknowledge the skilful technical assistance of G. Van der Reysen and E. Castrique for the excellent care of the animals.


   References
TOP
 Abstract
 Materials and methods
 Results
 Discussion
 Acknowledgements
 References
 

  1. Joos GF, Pauwels RA. Pro-inflammatory effects of substance P: new perspectives for the treatment of airway diseases?. Trends Pharmacol Sci 2000;21:131–133.[CrossRef][Medline] [Order article via Infotrieve]
  2. Hall AK, Barnes PJ, Meldrum LA, Maclagan J. Facilitation by tachykinins of neurotransmission in guinea-pig pulmonary parasympathetic nerves. Br J Pharmacol 1989;97:274–280.[ISI][Medline] [Order article via Infotrieve]
  3. Aizawa H, Miyazaki N, Inoue H, Ikeda T, Shigematsu N. Effect of endogenous tachykinins on neuro-effector transmission of vagal nerve in guinea-pig tracheal tissue. Respiration 1990;57:338–342.[ISI][Medline] [Order article via Infotrieve]
  4. Stretton D, Belvisi MG, Barnes PJ. The effect of sensory nerve depletion on cholinergic neurotransmission in guinea pig airways. J Pharmacol Exp Ther 1992;260:1073–1080.[Abstract/Free Full Text]
  5. Tanaka DT, Grunstein MM. Effect of substance P on neurally mediated contraction of rabbit airway smooth muscle. J Appl Physiol 1986;60:458–463.[Abstract/Free Full Text]
  6. Colasurdo GN, Loader JE, Graves JP, Larsen GL. Modulation of acetylcholine release in rabbit airways in vitro. Am J Physiol 1995;268:L432–L437.[ISI][Medline] [Order article via Infotrieve]
  7. Joos G, Pauwels R, Van Der Straeten M. The effect of oxitropium bromide on neurokinin A-induced bronchoconstriction in asthmatic subjects. Pulm Pharmacol 1988;1:41–45.[CrossRef][Medline] [Order article via Infotrieve]
  8. Black JL, Johnson PR, Alouan L, Armour CL. Neurokinin A with K+ channel blockade potentiates contraction to electrical stimulation in human bronchus. Eur J Pharmacol 1990;180:311–317.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  9. Watson N, Maclagan J, Barnes PJ. Endogenous tachykinins facilitate transmission through parasympathetic ganglia in guinea-pig trachea. Br J Pharmacol 1993;109:751–759.[ISI][Medline] [Order article via Infotrieve]
  10. Szarek JL, Spurlock B, Gruetter CA, Lemke S. Substance P and capsaicin release prostaglandin E2 from rat intrapulmonary bronchi. Am J Physiol 1998;275:L1006–L1012.
  11. Manzini S. Bronchodilatation by tachykinins and capsaicin in the mouse main bronchus. Br J Pharmacol 1992;105:968–972.[ISI][Medline] [Order article via Infotrieve]
  12. Fortner CN, Breyer RM, Paul RJ. EP2 receptors mediate airway relaxation to substance P, ATP and PGE2. Am J Physiol Lung Cell Mol Physiol 2001;281:L469–L474.[Abstract/Free Full Text]
  13. Quartara L, Maggi CA. The tachykinin NK1 receptor. Part I: ligands and mechanisms of cellular activation. Neuropeptides 1997;31:537–563.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  14. Quartara L, Maggi CA. The tachykinin NK1 receptor. Part II: Distribution and pathophysiological roles. Neuropeptides 1998;32:1–49.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  15. Szarek JL, Spurlock B. Antagonism of cholinergic nerve-mediated contractions by the sensory nerve inhibitory system in rat bronchi. J Appl Physiol 1996;81:260–265.[Abstract/Free Full Text]
  16. De Felipe C, Herrero JF, O'Brien JA, et al. Altered nociception, analgesia and aggression in mice lacking the receptor for substance P. Nature 1998;392:394–397.[CrossRef][Medline] [Order article via Infotrieve]
  17. Emonds-Alt X, Doutremepuich JD, Heaulme M, et al. In vitro and in vivo biological activities of SR140333, a novel potent non-peptide tachykinin NK1 receptor antagonist. Eur J Pharmacol 1993;250:403–413.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  18. Aas P, Maclagan J. Evidence for prejunctional M2 muscarinic receptors in pulmonary cholinergic nerves in the rat. Br J Pharmacol 1990;101:73–76.[ISI][Medline] [Order article via Infotrieve]
  19. Kilbinger H, Schneider R, Siefken H, Wolf D, D'Agostino G. Characterization of prejunctional muscarinic autoreceptors in the guinea-pig trachea. Br J Pharmacol 1991;103:1757–1763.[ISI][Medline] [Order article via Infotrieve]
  20. Loenders B, Rampart M, Herman AG. Selective M3 muscarinic receptor antagonists inhibit smooth muscle contraction in rabbit trachea without increasing the release of acetylcholine. J Pharmacol Exp Ther 1992;263:773–779.[Abstract/Free Full Text]
  21. Wessler I, Werhand J. Evaluation by reverse phase HPLC of [3H]acetylcholine release evoked from the myenteric plexus of the rat. Naunyn Schmiedebergs Arch Pharmacol 1990;341:510–516.[ISI][Medline] [Order article via Infotrieve]
  22. Leclere PG, Lefebvre RA. Influence of nitric oxide donors and of the {alpha}2-agonist UK-14,304 on acetylcholine release in the pig gastric fundus. Neuropharmacology 2001;40:270–278.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  23. Mapp CE, Miotto D, Braccioni F, et al. The distribution of neurokinin-1 and neurokinin-2 receptors in human central airways. Am J Respir Crit Care Med 2000;161:207–215.[Abstract/Free Full Text]
  24. Chu HW, Kraft M, Krause JE, Rex MD, Martin RJ. Substance P and its receptor neurokinin 1 expression in asthmatic airways. J Allergy Clin Immunol 2000;106:713–722.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  25. D'Agostino G, Erbelding D, Kilbinger H. Tachykinin NK2 receptors facilitate acetylcholine release from guinea-pig isolated trachea. Eur J Pharmacol 2000;396:29–32.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  26. Oury-Donat F, Lefevre IA, Thurneyssen O, et al. SR 140333, a novel, selective, and potent nonpeptide antagonist of the NK1 tachykinin receptor: characterization on the U373MG cell line. J Neurochem 1994;62:1399–1407.[ISI][Medline] [Order article via Infotrieve]
  27. Preston Z, Lee K, Widdowson L, Richardson PJ, Pinnock RD. Tachykinins increase [3H]acetylcholine release in mouse striatum through multiple receptor subtypes. Neuroscience 2000;95:367–376.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  28. Kouznetsova M, Nistri A. Facilitation of cholinergic transmission by substance P methyl ester in the mouse hippocampal slice preparation. Eur J Neurosci 2000;12:585–594.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  29. Long NC, Abraham J, Kobzik L, Weller EA, Krishna Murthy GG, Shore SA. Respiratory tract inflammation during the induction of chronic bronchitis in rats: role of C-fibres. Eur Respir J 1999;14:46–56.[Abstract]
  30. Killingsworth CR, Paulauskis JD, Shore SA. Substance P content and preprotachykinin gene-I mRNA expression in a rat model of chronic bronchitis. Am J Respir Cell Mol Biol 1996;14:334–340.[Abstract]
  31. Takebayashi T, Abraham J, Murthy GG, Lilly C, Rodger I, Shore SA. Role of tachykinins in airway responses to ozone in rats. J Appl Physiol 1998;85:442–450.[Abstract/Free Full Text]
  32. Devillier P, Acker GM, Advenier C, Marsac J, Regoli D, Frossard N. Activation of an epithelial neurokinin NK-1 receptor induces relaxation of rat trachea through release of prostaglandin E2. J Pharmacol Exp Ther 1992;263:767–772.[Abstract/Free Full Text]
  33. Szarek JL, Stewart NL, Spurlock B, Schneider C. Sensory nerve- and neuropeptide-mediated relaxation responses in airways of Srague-Dawley rats. J Appl Physiol 1995;78:1679–1687.[Abstract/Free Full Text]
  34. Mhanna MJ, Dreshaj IA, Haxhiu MA, Martin RJ. Mechanism for substance P-induced relaxation of precontracted airway smooth muscle during development. Am J Physiol 1999;276:L51–L56.[ISI][Medline] [Order article via Infotrieve]
  35. Figini M, Emanueli C, Bertrand C, Sicuteri R, Regoli D, Geppetti P. Differential activation of the epithelial and smooth muscle NK1 receptors by synthetic tachykinin agonists in guinea-pig trachea. Br J Pharmacol 1997;121:773–781.[CrossRef][ISI][Medline] [Order article via Infotrieve]
  36. Ricciardolo FLM, Trevisani M, Geppetti P, Nadel JA, Amadesi S, Bertrand C. Role of nitric oxide and septide-insensitive NK1 receptors in bronchoconstriction induced by aerosolised neurokinin A in guinea-pigs. Br J Pharmacol 2000;129:915–920.[CrossRef][ISI][Medline] [Order article via Infotrieve]



This article has been cited by other articles:


Home page
 Am. J. Respir. Cell Mol. Bio.Home page
S. Matsubara, C. H. Swasey, J. E. Loader, A. Dakhama, A. Joetham, H. Ohnishi, A. Balhorn, N. Miyahara, K. Takeda, and E. W. Gelfand
Estrogen Determines Sex Differences in Airway Responsiveness after Allergen Exposure
Am. J. Respir. Cell Mol. Biol., May 1, 2008; 38(5): 501 - 508.
[Abstract] [Full Text] [PDF]

Home page
 Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
X. Hua, C. J. Erikson, K. D. Chason, C. N. Rosebrock, D. A. Deshpande, R. B. Penn, and S. L. Tilley
Involvement of A1 adenosine receptors and neural pathways in adenosine-induced bronchoconstriction in mice
Am J Physiol Lung Cell Mol Physiol, July 1, 2007; 293(1): L25 - L32.
[Abstract] [Full Text] [PDF]

Home page
 Psychosom. Med.Home page
R. A. Joachim, V. Sagach, D. Quarcoo, Q. T. Dinh, P. C. Arck, and B. F. Klapp
Neurokinin-1 Receptor Mediates Stress-Exacerbated Allergic Airway Inflammation and Airway Hyperresponsiveness in Mice
Psychosom Med, July 1, 2004; 66(4): 564 - 571.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (12)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tournoy, K.G.
Right arrow Articles by Joos, G.F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tournoy, K.G.
Right arrow Articles by Joos, G.F.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS