Mangiferin Prevents Guinea Pig Tracheal Contraction via Activation of the Nitric Oxide-cyclic Gmp Pathway

Previous studies have described the antispasmodic effect of mangiferin, a natural glucoside xanthone

An extract obtained via the decoction and drying of mango stem bark was developed at industrial scale in Cuba for use as a nutritional supplement and phytomedicine [13]. VimangH is the brand name of this commercial preparation, and it contains a standardised mixture of terpenoids, steroids, fatty acids and polyphenols, including phenolic acids, phenolic esters and the predominant component mangiferin [13].
Similar to other polyphenol compounds, such as anthocyanins, curcumin and resveratrol, mangiferin has a broad spectrum of pharmacological effects. The most prominent and best-studied property of this class of phytochemicals is their antioxidant activity [1,14]. The ability to scavenge and decrease the formation of reactive oxygen species, as well as to activate enzymatic antioxidant systems, seems to be crucial for the outstanding antioxidant activity of mangiferin [1,14,15]. Apart from its capacity to interfere with oxidative stress, mangiferin exhibits a number of other properties, including immune-modulatory [16][17][18], anti-inflammatory [19][20][21] and anti-cancer [11,22,23] activities, suggesting that this substance could be used as a molecular template for innovative therapeutic applications.
The free radical nitric oxide is a neurotransmitter of the inhibitory nonadrenergic noncholinergic respiratory system [24,25]. It is produced by neural fibres that innervate airway smooth muscle cells, epithelial ciliated cells, type II alveolar cells and macrophages, and nitric oxide has been described as an effective antispasmodic mediator in the airway [26]. The molecular mechanism underlying the antispasmodic effect of nitric oxide is the direct activation of soluble guanylate cyclase and subsequent elevation of intracellular cGMP levels [27].
The aim of the present study was to assess the potential protective effect of mangiferin on the contractile response presented by the rat tracheal smooth muscle, following exposure to distinct pro-spasmodic agents, such as histamine, 5-hydroxytryptamine (5-HT), carbachol and allergen in vitro. All these spasmogens are supposed to play important role in the pathogenesis of airway obstruction noted in atopic asthmatics. Indeed, earlier investigations have shown that M. indica stem bark aqueous extract is an effective inhibitor of rat tracheal contraction caused by acetylcholine [28,29] and histamine [29]. However, exactly how the extract is acting to induce anti-contraction effects and whether or not this effect is accounted for by mangiferin has not been studied. Furthermore, our intention with this study was to test the hypothesis that mangiferin might be acting as an antispasmodic agent via activation of the nitric oxide-cGMP pathway. The results show that mangiferin can indeed inhibit smooth muscle spasms triggered by immunological and nonimmunological stimuli. Such an effect is associated with nitric oxide production by epithelial cells, up-regulation of intracellular cGMP and the opening of K + ATP and small-conductance Ca 2+activated K + channels in airway smooth muscle cells.

Ethics Statement
Experimental conditions and procedures involving animals were performed with direct approval of the Committee on Use of Laboratory Animals of the Oswaldo Cruz Foundation under license no. CEUA-FIOCRUZ 00085-01.

Animals
Male guinea pigs (300-400 g) were obtained from the Oswaldo Cruz Foundation breeding unit (Rio de Janeiro, Brazil). They were housed under conditions of constant temperature and controlled illumination, and food and water were available ad libitum.

Isolated Tracheal Preparation and Measurement of Tension
Guinea pigs used for anaphylactic contraction assays were presensitised with a subcutaneous injection of 0.2 ml of a suspension containing ovalbumin (50 mg) and Al(OH) 3 (5 mg). The animals were sacrificed in a CO 2 atmosphere 14 days after sensitisation, and their tracheal segments were removed and quickly immersed in Krebs' nutritional solution (118 mM NaCl, 4.8 mM KCl, 2.5 mM CaCl 2 , 1.2 mM MgSO 4 , 1.2 mM KH 2 PO 4 , 24 mM NaHCO 3 , and 11 mM glucose). Adhering fat and connective tissue were dissected away from the trachea, and the trachea was then cut into rings. The tracheal rings were mounted in isolated organ baths filled with 10 ml of Krebs' solution, maintained at 37uC, and aerated with 95% O 2 and 5% CO 2 . To achieve a steady spontaneous tone level, an initial tension of 1 g was applied. Contractions were measured with an isometric force-displacement transducer (Ugo Basile, Comerio, Italy) and recorded by an Isolated Organs Data Acquisition program (Proto5; Letica Scientific Instruments, Barcelona, Spain).

Protocols for Measurement of Tension Development
The experimental protocols were previously described [30]. Briefly, the tracheal rings were allowed to stabilise for 60 min, whereas the bathing solution was exchanged at 10 min intervals. At the end of the equilibration period, isolated tracheal rings, in absence or presence of epithelium, were contracted with carbachol (2.5 mM), and once the contractions had reached a plateau, various concentrations of vehicle (DMSO) or mangiferin (0.1-1000 mM) were added. All relaxations are expressed as the percentage of the maximal carbachol-induced contractile responses.
We also investigated the spasmolytic effect of mangiferin on isolated tracheal rings. At the end of the equilibration period, the response to carbachol (2.5 mM) was recorded. After carbachol was washed out and a stable baseline tone was re-established, the tissues were exposed to carbachol (0.01-100 mM), histamine (0.1-1000 mM), 5-HT (0.01-30 mM), or antigen (ovalbumin; 0.001-100 mg/ml) in the presence or absence of mangiferin (0.1-10 mM). The preparations were pre-incubated with mangiferin for 15 min before the addition of each spasmogen. All responses were expressed as a percentage of the initial response to 2.5 mM carbachol. In some experiments, the epithelial cells were removed mechanically by rubbing the internal tracheal surface with a fine silver wire (200 mm in diameter), as described previously [31]. During the experiment, the contractile response to carbachol (0.01-100 mM) was measured before and after exposing intact or denuded epithelium tracheal rings to 10 mM mangiferin for 15 min.
To evaluate the putative interference of mangiferin with calcium influx, Ca 2+ concentration-response curves were established. Briefly, the responses of tracheal ring segments from naive guinea pig to 2.5 mM carbachol were recorded. After the carbachol was washed out and a stable baseline tone was reestablished, the tissues were exposed to successive cycles of 60 mM KCl stimulations/washouts in Ca 2+ -free Krebs' solution containing 2 mM EGTA until complete desensitisation to the 60 mM KCl-evoked contractile response was achieved. Next, the tracheal rings were immersed in Ca 2+ -free Krebs' solution containing 60 mM KCl, and the extracellular Ca 2+ concentration was increased stepwise by the cumulative addition of CaCl 2 (0.01-30 mM), in the presence or absence of mangiferin (0.1-10 mM) or vehicle (0.1% DMSO). All responses were expressed as a percentage of response to 2.5 mM carbachol.
To further investigate the mechanisms of action of mangiferin, the tracheal rings were pretreated 10 min before mangiferin application with 10 mM ODQ, an inhibitor of guanylate cyclase; 100 mM L-NAME, an inhibitor of NOS; 100 mM SQ22536, an inhibitor of adenylate cyclase; 10 mM TEA, a nonselective K + channel blocker; 1 mM glibenclamide, a K + ATP channel blocker or 1 mM apamin, Ca 2+ -dependent K + channel blocker of small conductance. All responses were expressed as a percentage of the response to 2.5 mM carbachol.

Western Blotting for NOS3
Three pools of three 3 rat tracheas were incubated with 10 mM mangiferin or vehicle (0.1% DMSO) for 15 min., and then homogenized in ice cold lysis buffer containing the protease inhibitor cocktail Complete (F.Hoffmann-La Roche Ltd., Basel, Switzerland) and 0.1% Triton X-100 in PBS. The lysate was centrifuged at 13.0006g for 10 min at 4uC. Supernatant was recovered and protein concentration was determined using the BCA assay (Sigma-Aldrich Corp., St Louis, USA). Equal amounts of sample protein (100 mg/lane) were separated by SDS-PAGE using polyacrylamide gels and proteins were transferred to nitrocellulose membranes (GE Healthcare, Little Chalfont, UK). Nonspecific binding was blocked with 5% (w/v) skimmed milk

Measurement of cGMP
Intracellular cGMP concentrations in guinea pig tracheal rings were assayed as described previously [30]. Isolated tracheas were cut into rings, quickly immersed in Krebs' nutritional solution, and incubated with mangiferin (0.1-10 mM), L-NAME (100 mM) or ODQ (10 mM) in the presence of 100 mM 3-isobutyl-1-methylxanthine (IBMX) for 20 min. Some tracheal rings were pretreated with 100 mM L-NAME or 10 mM ODQ for 10 min before the addiction of 10 mM mangiferin. Tissue sections were rapidly frozen in liquid nitrogen, and the frozen tracheal rings were homogenised in ice-cold 6% trichloroacetic acid (TCA). The homogenate was centrifuged at 20006g for 15 min at 4uC. To remove TCA, the supernatants were washed 4 times with 5 volumes of water-saturated diethyl ether. The top ether layer was discarded after each wash. Then, the supernatants were lyophilised, and the cGMP of each sample was determined using commercially available enzyme immunoassay kits (GE Healthcare, Chalfont St. Giles, UK).

Statistical Analysis
The results were expressed as the mean 6 S.E.M. EC 50 values were calculated by fitting the log (agonist) vs. normalised response using GraphPad Software, and the results are displayed as the negative logarithm (pEC 50 ). Significant differences were determined using one-way analysis of variance (ANOVA), followed by the Student-Newman-Keuls test. P values of 0.05 or less were considered to be statistically significant.

Epithelial Removal Impairs the Anti-Spasmodic Effect of Mangiferin
Next, we examined whether the epithelium is involved in the effect of mangiferin by mechanically removing the epithelial cells from the internal tracheal surface with a fine silver wire, as previously reported [31]. Histological examination confirmed that the epithelial layer was removed (data not shown). The relaxant effect of mangiferin on carbachol pre-contracted tracheal segments (Figure 2A) was abolished following epithelial removal ( Figure 2B). Similarly, the ability of mangiferin to impair carbachol-induced Table 1. Potency (pEC 50 ) and maximal response (E MAX ) values obtained from concentration-response curves of allergen (ovalbumin, 0.001-100 mg/ml), histamine (0.1-3000 mM), 5-HT (0.01-30 mM) or carbachol challenge (0.01-100 mM) in guinea pig tracheal rings, following co-incubation with mangiferin (0.1-10 mM) or vehicle (0.1% DMSO).    contraction ( Figure 2C) was abolished after epithelial denudation ( Figure 2D).

Inhibition of NOS or Guanylate Cyclase Prevents the Anti-Spasmodic Effect of Mangiferin
Tracheal rings were pretreated with the NOS inhibitor, L-NAME (100 mM), to examine the role of nitric oxide-mediated signalling in the antispasmodic effect of mangiferin. As shown in figure 3A, L-NAME prevented the relaxing effect of mangiferin after carbachol-induced tracheal contraction. This response was also abrogated by pre-incubation with the soluble guanylate cyclase inhibitor, ODQ (10 mM) ( Figure 3B), whereas pretreatment with the adenylate cyclase inhibitor, SQ22536 (100 mM), did not alter the protective effect of mangiferin ( Figure 3C).

Mangiferin Increases NOS3 Expression in Cultured Tracheal Rings
To determine whether NOS3 isoform was up-regulated by mangiferin treatment, western blotting analyses were performed on tracheal tissue homogenates. We found that constitutive NOS3 expression was significantly increased in cultured tracheal rings exposed to 10 mM mangiferin, as compared to vehicle exposed rings (Figure 4).

Mangiferin Increases cGMP Levels in Cultured Tracheal Rings
Next, we demonstrated that mangiferin (0.1-10 mM) upregulated the levels of cGMP in cultured guinea pig tracheal rings in a concentration-dependent manner ( Figure 5). The ability of mangiferin to elevate cGMP levels was abolished by preincubation with either 100 mM L-NAME or 10 mM ODQ ( Figure 5).

K + Channel Blockers Reduce the Antispasmodic Effect of Mangiferin
Prior studies revealed that the opening of K + channels leads to K + efflux, hyperpolarisation and relaxation of respiratory smooth muscle [32]. The nonselective K + channel blocker TEA (10 mM), the K + ATP channel blocker glibenclamide (1 mM) and the small-conductance Ca 2+ -activated K + channel blocker apamin (1 mM) were utilised to assess the potential role of K + channels in the antispasmodic activity of mangiferin. The ability of individual K + channel blockers to interfere with the protective effect of 10 mM mangiferin was evaluated in epithelia-preserved guinea pig tracheas that were stimulated with 2.5 mM carbachol. We found that a 15-min preincubation with TEA ( Figure 6A), glibenclamide ( Figure 6B) or apamin ( Figure 6C), prior to the application of mangiferin, prevented the antispasmodic effect of this compound.

Mangiferin Inhibits Ca +2 -Induced Contraction in K + -Depolarised Trachea Rings
Airway smooth muscle contraction is, in large part, regulated by intracellular Ca 2+ . Thus, we wanted to assess the effect of mangiferin on extracellular Ca 2+ -induced tracheal tension using the classical system of isolated organ bath preparations maintained in Ca 2+ -free medium and depolarised with 60 mM KCl [33]. As expected, when the extracellular Ca 2+ concentration was increased stepwise by the cumulative addition of CaCl 2 (0.01-30 mM), we observed a concentration-dependent elevation in the tracheal contractile response (Figure 7). As illustrated in Figure 7, preincubation for 15 min with mangiferin (0.1-10 mM) dramatically reduced Ca +2 -induced tracheal contraction.

Discussion
The current study shows that the xanthone glucoside mangiferin prevents the contraction of guinea pig tracheal rings induced by distinct spasmogens, including carbachol and allergen stimuli. This effect was abrogated by removal of the epithelium and exposure to the NOS inhibitor, L-NAME, or the guanylate cyclase inhibitor, ODQ. Mangiferin up-regulated NOS3 protein levels in the tracheal tissue. It also caused a dose-dependent increase in the intracellular cGMP levels of cultured tracheal rings via a mechanism that was also sensitive to L-NAME and ODQ treatments. These data suggest that mangiferin activates the nitric oxide-cGMP pathway to prevent airway smooth muscle contraction.
A previous study from Alvarez and collaborators [12] showed that asthma patients benefit from oral therapy with VimangH, the brand name of an aqueous extract of M. indica stem bark that is traditionally used in the Caribbean region to treat respiratory disorders [1,34,35]. Accordingly, there are consistent reports demonstrating the efficacy of VimangH and mangiferin, its prominent active ingredient, in preventing inflammatory changes in murine models of allergy and asthma [21,36]. Interestingly, the M. indica extract is also a potent inhibitor of histamine-and acetylcholine-induced rat tracheal contraction in in vitro settings [28,29]. Therefore, there is evidence that mangiferin has combined anti-inflammatory and airway-relaxing properties, which greatly increases the likelihood that this compound represents a potential therapeutic agent for the treatment of asthmatic conditions. To the best of our knowledge, this is the first study designed to assess the antispasmodic activity of mangiferin on the airway smooth muscle system and the first to indicate its molecular mechanism of action. Our findings revealed that mangiferin not only reduced the maximal tracheal contraction induced by distinct spasmogenic agents (allergen, histamine, carbachol and 5-HT) but also shifted the spasmogens-induced concentration-response curves to the right, clearly impacting the efficacy and potency of these agents. Moreover, it is clear that the effect of mangiferin on airway smooth muscle contractile responses is not specific for a certain type of receptor. The observation that tracheal epithelial denudation abrogated the relaxant effect of mangiferin on carbachol pre-contracted or post-contracted segments is of great importance, and it indicates that the integrity of the airway epithelial layer is essential for the antispasmodic activity of mangiferin. Epithelial cells play a paramount role in the modulation of airway tone by working as a physical barrier that protects sensory nerves and smooth muscle cells from inhaled irritants [37]. In addition, the epithelial layer has the ability to release smooth muscle relaxant factors, such as prostaglandin (PG) E2 and nitric oxide, protecting the airway from excessive bronchoconstriction [37].
Nitric oxide activates guanylate cyclase, which increases the level of intracellular cGMP, relaxing the airway smooth muscle [38]. We preincubated isolated tracheal rings with either L-NAME or ODQ to determine the putative involvement of the nitric oxidemediated signalling pathway for the inhibitory effect of mangiferin. Our findings revealed that treatment with both these agents prevented the anti-spasmodic activity of mangiferin, whereas the adenylate cyclase inhibitor SQ22536 had no effect. Because PGE 2 increases airway caliber via the activation of adenylate cyclase and subsequent elevation of intracellular cyclic AMP levels (cAMP), our findings indicated that the antispasmodic effect of mangiferin is mediated by cGMP, but not cAMP, ruling out the involvement of PGE 2 in this effect. We also measured cGMP levels in tracheal tissues exposed to mangiferin to examine whether the relaxant effect of this xanthone correlates with the accumulation of intracellular cGMP. Indeed, mangiferin raised intracellular cGMP levels in a concentration-dependent manner, and this augmentation was completely inhibited by incubation with either L-NAME or OQD. These results support the interpretation that the relaxant effect of mangiferin is dependent on the activation of the nitric oxide/cGMP signalling pathway in the airway epithelium.
M. indica extract (Vimang), but not mangiferin, has been shown to inhibit vascular smooth muscle contraction triggered by noradrenaline, suggesting that different polyphenols present in the extract might account for the Vimang's vasodepressor effect [39]. However, it is of note that both Vimang and mangiferin share the ability to inhibit interleukin-1b-induced expression of inducible nitric oxide synthase (iNOS or NOS2) in vascular smooth muscle cells from WKY rats [39]. Accordingly, mangiferin and M. indica extract inhibit NOS2 mRNA expression and nitric oxide production in LPS-activated macrophages [40]. It is well established that despite being continuously expressed, the constitutive forms of NOS (nNOS or NOS1 and eNOS or NOS3) are also sensitive to expressional up regulation, leading to both physiological and pathophysiological consequences [41]. For instance, aminoguanidine inhibition of NOS2 activity ameliorates cerebral vasospasm after subarachnoid haemorrhage in rabbits via increase of NOS1 mRNA and protein levels [42]. While exploring the fact that respiratory epithelial cells do express NOS3 [43], we demonstrated in the current study that the treatment with mangiferin effectively increased the protein levels of this constitutive form NOS in cultured epithelium-intact tracheal tissues. These findings add support to the interpretation that mangiferin relaxant properties are closely related with activation of the nitric oxide-formation system.
The relationship between increased tissue levels of cGMP and tracheal smooth muscle relaxation in guinea pigs and other animal species has been reported [44][45][46]. Most of the nitric oxide-and cGMP-regulated signalling pathways responsible for airway smooth muscle relaxation is mediated by the opening of K + channels, including small-conductance Ca 2+ -activated K + and K + ATP channels. The activation of K + channels causes potassium ion efflux, plasma membrane hyperpolarisation, increased closure of voltage-gated calcium channels and, eventually, a decrease in intracellular calcium levels in smooth muscle cells [32,47]. In the current study, we demonstrated that the anti-spasmodic property of mangiferin is lost in the presence of the non-selective K + channel blocker TEA, suggesting the pivotal involvement of K + channels in this response. It is also noteworthy that glibenclamide, a K + ATP channel blocker, and apamin, a blocker of small conductance Ca 2+ -activated K + channels, significantly inhibited the anti-contraction effect of mangiferin. We chose these inhibitors because K + ATP channels and small conductance Ca 2+ -activated K + channels have been strongly implicated in the airway smooth muscle relaxant response. These results suggest that both small conductance K + ca and K + ATP channels play a role in the inhibitory effect of mangiferin on tracheal contraction.
There is a significant body of evidence for the existence of voltage-dependent Ca 2+ channels in airway smooth muscle [48,49]. In the guinea pig airway, tracheal contraction evoked by KCl is induced by membrane depolarisation and the influx of Ca 2+ through voltage-dependent Ca 2+ channels [50]. Mangiferin also inhibited Ca 2+ -induced contractions in K + depolarised preparations of epithelium-intact tracheal rings, suggesting that mangiferin could inhibit Ca 2+ influx by blocking voltage-dependent Ca 2+ channels. Taken together, our results indicate that the effect of mangiferin on tracheal tissue is mediated by activation of the nitric oxide cGMP pathway, leading to enhanced K + efflux with subsequent attenuation of Ca 2+ influx-associated contractility in smooth muscle cells (Figure 8).

Conclusion
Our findings emphasise the ability of mangiferin to inhibit smooth muscle spasms caused by immunological (allergen) and non-immunological (histamine, carbachol and 5-HT) stimuli. These effects seem to be strongly associated with increased NOS3 protein levels and nitric oxide production by epithelial cells, up-regulation of intracellular cGMP and the opening of K + ATP and small-conductance Ca 2+ -activated K + channels in smooth muscle cells. These changes block voltage-dependent Ca 2+ channels, resulting in smooth muscle relaxation. Taken together, these findings demonstrate that mangiferin may be beneficial for the treatment of airflow limitation in human lung diseases.