Background
Dopamine is a ubiquitous endogenous catecholamine neurotransmitter in the mammalian central nervous system, where it controls a variety of physiological responses including emotion, cognition, and endocrine functions [
1‐
3]. This catecholamine also modulates cardiovascular function, hormone secretion, vascular tone, renal function, and gastrointestinal motility through the specific dopamine receptor subtypes expressed in peripheral organs and tissues [
3‐
7]. The dopamine receptor is a member of the large family of 7 transmembrane spanning domain G protein-coupled receptors (GPCRs). The five known subtypes of dopamine receptors have been subdivided into two distinct subclasses, “D
1-like” receptors (D
1 and D
5) which couple to the G
s protein and “D
2-like” receptors (D
2, D
3 and D
4) which couple to G
i[
3,
8].
Inhaled dopamine induces bronchodilation during bronchial obstruction in asthmatic patients [
9‐
11]. The dopamine-induced bronchodilation has been thought to be mediated via β
2-adrenoceptors because this effect is partially blocked by the β-adrenoceptor antagonist propranolol [
12]. However, a recent study suggested that the dopamine D
1-like receptor antagonist SCH23390 inhibited the bronchodilator effect of dopamine in acetylcholine-contracted rat tracheal rings suspended in organ baths [
13], suggesting that the dopamine D
1-like receptor is expressed on airway smooth muscle and induces bronchodilation. Although chronic activation of the dopamine D
2 receptor has been shown to sensitize adenylyl cyclase and facilitate forskolin-induced airway smooth muscle relaxation [
14], the functional expression of the dopamine D
1-like receptor subtype on airway smooth muscle has not been described.
Activation of G
s-coupled receptors leads to stimulation of adenylyl cyclase activity resulting in an increase in cellular cyclic AMP (cAMP) levels. Increase in intracellular cAMP levels activates cAMP-dependent protein kinase (PKA). PKA has many intracellular targets including the phosphorylation of myosin light chain kinase (MLCK), which classically promotes airway smooth muscle relaxation [
15,
16]. In addition, exchange proteins directly activated by cAMP (Epac) have recently been identified on airway smooth muscle as novel cAMP sensors able to elicit airway smooth muscle relaxation in human and guinea pig [
17,
18]. These findings led us to hypothesize that functional dopamine D
1-like receptors could respond to dopamine in airway smooth muscle and promote its relaxation through cellular cAMP’s activation of multiple potential signaling pathways.
In the present study, the expression of the dopamine D1-like receptor was assessed in native human and guinea pig airway smooth muscle tissue and cultured human airway smooth muscle (HASM) cells. In addition, cAMP production and dopamine D1 receptor effects on ex vivo contractile tone were assessed to confirm its physiological role in airway smooth muscle.
Materials and methods
Materials
M-199 smooth muscle medium, human fibroblast growth factor, human epidermal growth factor, fetal bovine serum (FBS), and antibiotic-antimycotic were purchased from Life Technologies (Grand Island, NY). Lysates of human brain cerebral cortex and kidney used as positive protein controls on immunoblots were obtained from BD Biosciences (Palo Alto, CA). Protease inhibitor cocktail III was purchased from EMD Biosciences (San Diego, CA). A68930 and SCH39166 were purchased from Tocris Bioscience (Ellisville, MO). NSC45576 was a kind gift from the Open Clinical Repository of the National Cancer Institute’s Developmental Therapeutics Program. HitHunter™ cAMP XS+ assay kit was purchased from DiscoveRx (Fremont, CA). All other chemicals were obtained from Sigma (St. Louis, MO) unless otherwise stated.
Cell culture
Cultures of HASM cells came from three sources. Primary cultured HASM cells were obtained from (1) Lonza (Walkersville, MD), and (2) were a kind gift from Dr. Reynold A Panettieri, Jr. (University of Pennsylvania, PA), which were obtained from lung transplant donors in accordance with procedures approved by the University of Pennsylvania Committee on Studies Involving Human Beings as previously described [
19]. (3) Cultures of immortalized HASM cells were a kind gift from Dr. William Gerthoffer (University of South Alabama, Mobile, AL) and have previously been characterized [
20]. Cells were grown in culture medium M-199, supplemented with 10% FBS, 1 ng/ml human fibroblast growth factor, 250 pg/ml human epidermal growth factor, and an antibiotic-antimycotic mix (100 units/ml penicillin G sodium, 100 μg/ml streptomycin sulfate, 0.25 μg/ml amphotericin B) at 37°C in 95% air/5% CO
2.
Isolation of smooth muscle from human and guinea pig trachea
All Studies were approved by Columbia University’s Institutional Review Board (IRB) and deemed not human subjects research under 45 CFR 46. Human trachea was obtained from discarded regions of healthy donor lungs harvested for lung transplantation at Columbia University. Human tissue was transported in cold buffer as described [
14].
All guinea pig studies were approved by the Columbia University Institutional Animal Care and Use Committee. These studies were also reviewed by the Committee on the Ethics of Animal Experiments in Tohoku University School of Medicine, and they were carried out in accordance with both the Guidelines for Animal Experiments issued by the Tohoku University and The Law (No. 105) and Notification (No. 6) issued by the Japanese Government. Adult male Hartley guinea pigs (approx. 400 g body weight) were deeply anesthetized by intraperitoneal pentobarbital (50 mg/kg). The chest cavity was opened, and the guinea pigs were exsanguinated. The entire trachea and whole brain (positive control for immunoblot) were surgically removed and immersed in cold (4°C) KH buffer. The exteriors of either the human or guinea pig trachea were carefully dissected free of adherent connective tissue under a microscope. Epithelium was left intact for immunohistochemistry but removed for organ bath experiments and immunoblotting.
Isolation of RNA and reverse transcriptase polymerase chain reaction
Total RNA was extracted from freshly dissected native human airway smooth muscle, and primary cultured HASM cells (Lonza, Walkersville, MD) using TRIzol Reagent (Ambion, Austin, TX) according to the manufacturer’s recommendations. Total RNA from whole human brain (Clontech, Mountain View, CA) was used as a positive control. The extracted RNA from freshly dissected native human airway smooth muscle and primary cultured HASM cells were treated enzymatically with DNase I (Life Technologies, Grand Island, NY) to digest contaminating genomic DNA according to the manufacturer’s instructions. cDNA was synthesized using SuperScript VILO cDNA Synthesis Kit (Life Technologies, Grand Island, NY). Briefly, 1 μg of DNase I-treated total RNA was reverse transcribed at 42°C. The reaction was terminated by heating to 85°C for 5 min and then cooled at 4°C.
PCR was performed and analyzed as described (1) with sense and antisense primers corresponding to the “D
1 subgroup (D
1 and D
5) of dopamine receptors (Table
1). Two-step PCR (annealing and extension at same temperature) was performed with Mastercycler ep gradient S thermal cycler (Eppendorf, Hamburg, Germany) for all PCR reactions and all reactions included an initial denaturation step at 94°C for 1 min followed by 40 cycles of denaturation (94°C for 10 s) and annealing/extension at 72°C for 1 min. Dopamine D
1 primers were designed to anneal in two separate exons spanning a large intron to ensure that amplified PCR products resulted from amplified cDNA and not contaminating genomic DNA. Since the dopamine D
5 receptor gene is intronless, complete removal of genomic DNA from the RNA samples was verified by performing negative control reactions in which reverse transcriptase was omitted from the cDNA synthesis reaction (-RT controls). PCR products were electrophoresed on 5% nondenaturing polyacrylamide gel in Tris, acetate, EDTA buffer. The gel was stained with ethidium bromide, and visualized using ultraviolet illumination. The gel image was captured with a model Powershot A570 digital camera (Canon, Tokyo, Japan).
Table 1
primer sequences for dopamine D
1
-like receptor subtypes
Human Dopamine D1 | FP: 5′-CCA GCG AAG TCC ACA TTC CAA GCT CC-3′ | 207 |
(NM_000794) | RP: 5′-GCC TCT GCT CTG CTA GTC AGT TGC AAT CAC-3′ | |
Human Dopamine D5 | FP: 5′- CTG GTG TGC GCA GCC ATC GT-3′ | 173 |
(NM_000798) | RP: 5′- ACC CAG ACG TCG CAG AAC GC-3′ | |
Immunoblot analysis
Confluent cultures of HASM cells were rinsed with cold phosphate-buffered saline (PBS), and mechanically scraped from the surface of the T75 culture flask in the presence of protease inhibitor cocktail III. Cells were pelleted (500 g, 10 min, 4°C) and lysed in cold lysis buffer [50 mM Tris–HCl, pH 8.0, 1% Nonidet P-40, 0.5% sodium deoxycholate, 0.1% SDS, 150 mM NaCl, 1 mM EDTA, 1:200 dilution of protease inhibitor cocktail III, 1 mM Na3VO4, 1 mM NaF]. Lysed cells were centrifuged (15,000 g, 15 min, 4°C) and an aliquot of the supernatant was subjected to protein analysis and storing at -80°C. Freshly dissected native human and guinea pig airway smooth muscle, and guinea pig brain cerebral cortex was homogenized (Tekmar Ultra Turrax T25 high-speed homogenizer set at top speed for 30 s) in cold (4°C) buffer (50 mM Tris, 10 mM HEPES, pH 7.4, 1 mM EDTA with a 1:200 dilution of protease inhibitor cocktail III). The homogenate was filtered through 125-μm Nitex mesh and centrifuged twice at 500 g for 15 min. The supernatant was transferred into new tubes and centrifuged at 50,000 g for 30 min at 4°C. The final membrane pellet was resuspended in the same buffer for protein concentration determinations and stored at -80°C. Each sample was solubilized by heating at 95°C for 10 min in sample buffer before use.
All the samples and positive controls were electrophoresed (8% SDS-PAGE) and transferred to PVDF membranes. 5% membrane blocking agent (GE Healthcare, RPN2125V, Waukesha, WI) in Tris-buffered saline with 0.1% Tween 20 (TBST) was used to block non-specific binding for 1 hr at room temperature. Membranes were then probed with antibodies directed against the dopamine D1 receptor protein (rabbit monoclonal 1:1,000; Epitomics, 2192-1, Burlingame, CA) or the dopamine D5 receptor protein (rabbit polyclonal 1:500; Santa Cruz, sc-25650, Santa Cruz, CA) overnight at 4°C. After washing three times with TBST, membranes were incubated for 1 hr at room temperature with HRP-labeled secondary anti-rabbit antibodies (1:5,000; GE Healthcare, NA934V, Waukesha, WI). The signals from the immunoreactive bands were detected by ECL Plus (GE Healthcare, Waukesha, WI) and were captured using chemiluminescent image analyzer (LAS 4000 Mini; GE Healthcare, Waukesha, WI).
Immunohistochemistry
Human and guinea pig tracheal rings were fixed, paraffin embedded, sectioned and rehydrated as previously described [
14]. Heat-mediated antigen retrieval, blockade of endogenous peroxidase, protein blocking and avidin-biotin blocking was performed as described [
14] and slides were incubated overnight at 4°C in primary antibody against the dopamine D
1 receptor protein (rabbit monoclonal 1:2,000; Epitomics, 2192-1, Burlingame, CA) or dopamine D
5 receptor protein (rabbit polyclonal 1:2,000; Santa Cruz, sc-25650, Santa Cruz, CA), in 2% normal goat serum in PBS with 0.1% Triton X-100 (PBST). A parallel tracheal ring section was incubated with an isotype-specific rabbit IgG antibody as a negative control. After overnight incubation at 4°C, slides were washed three times with PBST and primary antibodies were detected using biotinylated anti-rabbit antibodies (Vector Laboratories, Peterborough, UK) at a concentration of 1:100. After incubation with ABC-HRP complex (Vector Laboratories, Peterborough, UK) for 30 min, the antigen antibody complex was then visualized with the peroxidase substrate kit (DAB) (SK-4100, Vector Laboratories, Peterborough, UK). Sections were counterstained with hematoxylin (Vector Laboratories, Peterborough, UK), dried, dehydrated in a graded alcohol series and xylene, and cover slipped using Poly-mount (Polysciences, Warrington, PA).
cAMP assays
The dopamine D1 receptor-mediated cAMP production in primary cultured HASM cells (Lonza; Walkersville, MD) was measured using a HitHunter™ cAMP XS+ Assay kit according to the manufacturer’s instructions. Briefly, HASM cells in white 96-well plates were washed twice with warm PBS (37°C). The cells were incubated with dopamine (1 μM), or the dopamine D1-like receptor agonists (A68930 or SKF38393) (1 μM) for 20 min at 37°C. To examine the effect of dopamine on cAMP production in the presence of dopamine D2 receptor blockade, the cells were pretreated with the dopamine D2 receptor antagonist L-741626 (1 μM) for 30 min followed by incubation with dopamine (1 μM) for 20 min at 37°C. Incubation of the cells with L-741626 (1 μM) alone was also performed to determine whether L-741626 by itself exerts any effect on cAMP production. To examine the dose-dependent and time-course effects of the dopamine D1-like receptor agonist A68930 on cAMP production, the cells were incubated with A68930 (1 nM - 100 μM) for 10 - 60 min at 37°C. In separate experiments, the cells were pretreated with the dopamine D1-like receptor antagonists [SCH23390 (1 μM) or SCH39166 (1 μM)] or vehicle (PBS) for 30 min followed by incubation with A68930 (1 μM) for 20 min at 37°C. Then cAMP XS antibody reagent followed by the mixture of enzyme donor (ED)/Lysis/chemiluminescence (CL) working solution was added to each well. After incubation for 60 min at room temperature, cells were further incubated with the enzyme acceptor (EA) reagent for 3 hrs at room temperature. Luminescence signals were detected using a multimode microplate reader (Appliskan, Thermo Fisher Scientific, Waltham, MA).
In vitro assessment of dopamine D1receptor agonist effect on guinea pig airway smooth muscle relaxation after contraction with acetylcholine
Guinea pig tracheas were dissected and equilibrated in organ baths as described [
21]. All rings were precontracted with 10 μM N-vanillylnonanamide (capsaicin analogue) and then 2 cycles of cumulatively increasing concentrations of acetylcholine (0.1 μM - 1 mM) with extensive buffer washes and resetting of the resting tension to 1.0 g between cycles. Rings were pretreated with 1 μM tetrodotoxin and 10 μM pyriliamine to eliminate the confounding effects of neural depolarizations and histamine release, respectively. Rings were then contracted with acetylcholine (an individual EC
50 or EC
75 calculated for each ring). Following the achievement of a stable contraction (typically 15 min), cumulatively increasing concentrations of dopamine (1 μM – 100 μM), the dopamine D
1-like receptor agonist A68930 (1 μM - 100 μM) or the β-adrenoceptor agonist isoproterenol (0.5 nM – 1 μM) was incrementally added to the buffer in the baths. Control-contracted rings received vehicle (KH buffer) to serve as time controls for the A68930-induced relaxation. In separate experiments, rings were pretreated for 15 min with the dopamine D
2 receptor selective antagonist L-741626 (10 μM), PKA inhibitor Rp-cAMPS (100 μM), large-conductance calcium-activated potassium (BK
Ca) channel blocker iberiotoxin (100 nM) or the Epac antagonist NSC45576 (250 μM) before the addition of cumulatively increasing concentrations of A68930 (1 μM – 100 μM) or isoproterenol (0.5 nM – 1 μM) to assess their effects on airway smooth muscle force.
Statistical analysis
Statistical analysis was performed using repeated measures of ANOVA, followed by Bonferroni posttest comparison using GraphPad Instat 3.0.6 software (GraphPad Software Inc., San Diego, CA). Data are presented as mean ± SEM; P < 0.05 was considered significant.
Discussion
The major finding of the present study is that functional dopamine D1 receptors are expressed in both human and guinea pig airway smooth muscle. The dopamine D1 receptors were detected at the level of mRNA and protein, and a dopamine D1-like receptor-selective agonist facilitated relaxation against acetylcholine-induced contraction in airway smooth muscle through cAMP production and PKA activation.
In addition to the expression in the central nervous system, numerous studies have also demonstrated the expression of functional dopamine D
1 receptors in peripheral organs and tissues such as the myocardium, pulmonary artery, renal tubules, gastrointestinal tract, and the zona glomerulosa cells of the adrenal cortex [
4‐
7,
24‐
27]. Identification of mRNA in freshly dissected human airway smooth muscle ensures that native expression of the dopamine D
1-like receptor (D
1 and D
5) is being examined. However, a limitation of this approach is that even with careful dissection, freshly isolated tissue could be contaminated by other cells types that could give rise to cDNA products during sensitive RT-PCR amplification. To confirm the expression of dopamine D
1–like receptor in airway smooth muscle itself, we also evaluated its expression in primary cultured HASM cells which are a homogenous population of airway smooth muscle cells. In the present study, there was good agreement between the expression of dopamine D
1-like receptor in freshly isolated native airway smooth muscle and from cultured HASM cells. These findings were in accordance with the previous findings using expression microarrays in that mRNA of both dopamine D
1-like receptor subtypes was expressed in HASM cells [
28]. Moreover, in agreement with these mRNA analyses, the dopamine D
1 receptor protein was also identified in airway smooth muscle from native human airway smooth muscle, and cultured HASM cells from three independent sources. Immunohistochemical analysis also confirmed the expression of dopamine D
1 receptor on airway smooth muscle in both human and guinea pig airway smooth muscle. On the other hand, the dopamine D
5 receptor protein was not identified in both human and guinea pig native airway smooth muscle tissue, and cultured HASM cells by immunoblotting and immunohistochemistry. The discrepancy of the results obtained from RT-PCR and protein analyses on the expression of dopamine D
5 receptor on airway smooth muscle is likely due to posttranscriptional regulation, differences in mRNA and protein turnover rates [
29,
30], or detection of small amounts of dopamine D
5 mRNA by sensitive PCR techniques that does not translate into detectable levels of dopamine D
5 protein. Several studies also described the correlation between mRNA and protein expression as moderately or weakly positive with correlation coefficients ranging from 0.2 to 0.5 [
30‐
33].
Molecular identification of dopamine D
1 receptor on airway smooth muscle itself led us to question whether functional dopamine D
1 receptors could modulate airway smooth muscle tone. First, we sought to assess its ability to increase cyclic AMP and relax airway smooth muscle. Many studies have demonstrated that the activation of G
s-coupled receptors (e.g., β
2-adrenoceptor) stimulates adenylyl cyclase activity, which leads to cAMP accumulation in airway smooth muscle [
15,
34,
35]. Accumulation of cAMP content in airway smooth muscle facilitates relaxation [
15,
34,
35]. In accordance with the previous findings on G
s-coupled receptors, our findings demonstrate that activation of the dopamine D
1 receptor expressed on HASM cells with the endogenous ligand dopamine stimulated cAMP production in HASM cells but only when the dopamine D
2-G
i coupled receptor was inhibited with L-741626. These findings suggest that dopamine exerts its effect equally on both dopamine D
1-G
s coupled receptor and dopamine D
2-G
i coupled receptor in HASM cells, and selective stimulation of the dopamine D
1 receptor is required to stimulate cAMP production. Dopamine also relaxed acetylcholine-contracted guinea pig airway rings, however, contrary to the dopamine-stimulated cAMP production in HASM cells, the relaxation was produced without the blockade of dopamine D
2 receptor (data not shown). These findings would suggest that the dopamine D
2 receptor is more effectively coupled to G
i/adenylyl cyclase inhibition in the cultured HASM cells compared to intact tracheal rings. Another possibility is that in tracheal rings the dopamine-mediated relaxation is partially mediated through dopamine effects on β
2-adrenoceptors. It was previously reported that dopamine-mediated relaxation of acetylcholine-contracted guinea pig trachea was partially blocked by the β-adrenoceptor antagonist propranolol [
12]. These findings suggest that dopamine induces airway smooth muscle relaxation via both dopamine D
1 receptors and β
2-adrenoceptors.
To characterize the dopamine D
1 receptor-specific effects on airway smooth muscle, the selective dopamine D
1 receptor agonists A68930 and SKF38393 were used in the present study. Both agonists stimulated cAMP production in HASM cells, and A68930 induced airway smooth muscle relaxation in guinea pig tracheal rings. The specificities of A68930 (1 μM) at the dopamine D
1 receptor in the present study were further supported by the finding that two different dopamine D
1-like receptor antagonists SCH23390 or SCH39166 significantly blocked the effects of A68930 on cAMP production. However, treatment the HASM cells with A68930 at a higher concentration (100 μM) resulted in decrease in cAMP production compared with 1 μM of A68930. A68930 is a potent dopamine D
1 receptor agonist (EC
50 = 2.1 nM), but it also stimulates the G
i-coupled dopamine D
2 receptor at higher concentrations (EC
50 = 3.92 μM) [
22]. We have previously reported that the acute activation of the dopamine D
2 receptor expressed in HASM cells inhibited forskolin-stimulated adenylyl cyclase activity [
14], which consequently reduces in cellular cAMP levels. These findings indicate that A68930 at higher concentrations may lose its selectivity against dopamine D
1 receptors. This idea was further supported in the present study by demonstrating that the dopamine D
2 receptor selective antagonist L-741626 significantly augmented A68930-induced guinea pig airway ring relaxation. In the present study, the concentration of A68930 which was required to produce significant relaxation in guinea pig airway ring was higher (≧ 20 μM) than that required to produce significant cAMP production in HASM cells (≧ 100 nM). Previous reports in tissue organ bath also showed that phenylephrine-contracted human corpus cavernosum smooth muscle strip without endothelium suspended in organ bath was dose-dependently relaxed by A68930 (EC
50 = 3.5 ± 0.9 μM) [
36]. In contrast, in a cell-based cAMP assay, the EC
50 value of A68930-stimulated cAMP activity in LLC-PK
1 cells was much lower (EC
50 = 12.7 ± 2.7 nM) [
37]. These results and our findings suggest that at least 200-fold higher concentration of A68930 is needed for experiments on tissues where penetration to their site of action may not be equivalent to that achieved in a cell monolayer.
Classically, most cAMP effects have been attributed to the activation of PKA. PKA has multiple intracellular targets that favor relaxation including phosphorylation of MLCK which leads to a decrease in its affinity for the calcium-calmodulin complex [
38], resulting in airway smooth muscle relaxation [
15,
16]. As expected, the present study demonstrated that a PKA inhibitor Rp-cAMPS significantly attenuated dopamine D
1 receptor-mediated airway relaxation. However, several cAMP-mediated cellular events in airway smooth muscle are insensitive to PKA inhibition. Spicuzza
et al. suggested that β
2-adrenoceptor agonists suppressed acetylcholine-induced guinea pig airway contraction by mechanisms that are independent of PKA [
39]. Recently, Epac has been identified as cAMP-regulated guanine nucleotide exchange factors for Ras-like GTPases, such as Rap1 and Rap2 [
40], and been recognized as an alternative cAMP sensor to relax smooth muscle in addition to PKA. Roscioni
et al. demonstrated the protein expression of two isoforms of Epac (Epac 1 and Epac2) in human and guinea pig trachea, and activation of Epac relaxes airway smooth muscle by decreasing MLC phosphorylation [
17]. They also claimed that β
2-adrenoceptor agonist relaxes airway smooth muscle through Epac rather than PKA [
17]. In contrast, in the present study, the Epac selective antagonist NSC45576 did not block dopamine D
1 receptor agonist-induced airway relaxation. These results suggest that although both the dopamine D
1 receptor and β
2-adrenoceptor are G
s-coupled receptor, induce airway smooth muscle relaxation and increase cAMP, that the subsequent signaling targets of this cAMP elevation may not be identical following these receptors’ activations.
In addition to these cAMP-dependent mechanisms, a mechanism independent of cAMP is also relevant in β
2-adrenoceptor-mediated relaxation of airway smooth muscle [
23,
41], which involves the opening of the BK
Ca channel causing plasma membrane hyperpolarization facilitating relaxation [
41,
42]. However, in the present study, blockade of the BK
Ca channel with iberiotoxin did not inhibit relaxation induced by a dopamine D
1 receptor agonist.
In the present study, there are several differences in the results from the cell-based cAMP assays and intact tissue organ bath studies with the dopamine D
1 receptor agonist A68930. The first difference is that the relaxation evoked by isoproterenol and dopamine was rapid, while that evoked by A68930 was slow. These results suggest that the agonists’ interaction with the receptor can affect the speed of onset and duration of the induced relaxation. Variations in the molecular structure of agonists can affect the onset and duration of bronchodilation. For example, isoproterenol is a short-acting β agonist and has rapid onset, while the long-acting β
2-adrenoceptor agonist salmeterol causes sustained relaxation in airway smooth muscle of at least 12 hrs after a single administration [
43], but the speed of onset is much slower than short-acting agonists such as isoproterenol [
44]. There are remarkable differences in molecular structure between these agonists and these differences affect the speed of onset and duration of their effects [
45,
46]. These findings suggest that, even though the agonists act on the same receptor, the molecular structure can affect the kinetics of the drug effect at the receptor. The second difference between cell-based and tissue-based results with A68930 in the present study is the time required to reach significant relaxation in guinea pig airway rings was longer than the time required for significant stimulation of cAMP production in HASM cells. The dopamine D
1 agonists A68930 and A77636 contain an isochroman structure and are potent dopamine D
1 agonists which exert long-lasting effects compared with dopamine
in vivo. For example, A68930 elicited prolonged contralateral turning behavior in 6-hydroxydopamine lesioned rats (>20 hrs) [
47]. In contrast, several reports showed that A68930 stimulated cAMP production within 15 - 20 min [
37,
48]. However, it has not been determined whether the long-acting effects of A68930 rely exclusively on cAMP production. Thus, it is possible that sustained relaxation of airway smooth muscle is not solely mediated by increased cAMP and that other intracellular signaling events may be involved. Further studies will be needed to clarify the intracellular mechanisms by which A68930 induces airway smooth muscle relaxation.
Authors’ contributions
KM and CWE conceived and designed these studies; KM, YZ, DX, FM, FD and CWE performed experiments; KM, YZ, DX, FM, and CWE analyzed data; KM, YZ, DX, FM, and CWE interpreted results of experiments; KM and CWE prepared figures; KM, EM, and CWE drafted manuscript; KM, EM, and CWE edited and revised manuscript; All authors read and approved the final version of manuscript.