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Menthol Inhibits Detrusor Contractility Independently of TRPM8 Activation

Menthol Inhibits Detrusor Contractility Independently of TRPM8 Activation

  • Antonio Celso Saragossa Ramos-Filho, 
  • Ajay Shah, 
  • Taize Machado Augusto, 
  • Guilherme Oliveira Barbosa, 
  • Luiz Osorio Leiria, 
  • Hernandes Faustino de Carvalho, 
  • Edson Antunes, 
  • Andrew Douglas Grant
PLOS
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Abstract

Agonists such as icilin and menthol can activate the cool temperature-sensitive ion channel TRPM8. However, biological responses to menthol may occur independently of TRPM8 activation. In the rodent urinary bladder, menthol facilitates the micturition reflex but inhibits muscarinic contractions of the detrusor smooth muscle. The site(s) of TRPM8 expression in the bladder are controversial. In this study we investigated the regulation of bladder contractility in vitro by menthol. Bladder strips from wild type and TRPM8 knockout male mice (25–30 g) were dissected free and mounted in organ baths. Isometric contractions to carbachol (1 nM–30 µM), CaCl2 (1 µM to 100 mM) and electrical field stimulation (EFS; 8, 16, 32 Hz) were measured. Strips from both groups contracted similarly in response to both carbachol and EFS. Menthol (300 µM) or nifedipine (1 µM) inhibited carbachol and EFS-induced contractions in both wild type and TRPM8 knockout bladder strips. Incubation with the sodium channel blocker tetrodotoxin (1 µM), replacement of extracellular sodium with the impermeant cation N-Methyl-D-Glucamine, incubation with a cocktail of potassium channel inhibitors (100 nM charybdotoxin, 1 µM apamin, 10 µM glibenclamide and 1 µM tetraethylammonium) or removal of the urothelium did not affect the inhibitory actions of menthol. Contraction to CaCl2 was markedly inhibited by either menthol or nifedipine. In cultured bladder smooth muscle cells, menthol or nifedipine abrogated the carbachol or KCl-induced increases in [Ca2+]i. Intravesical administration of menthol increased voiding frequency while decreasing peak voiding pressure. We conclude that menthol inhibits muscarinic bladder contractions through blockade of L-type calcium channels, independently of TRPM8 activation.

Introduction

Overactive bladder (OAB) affects millions of people worldwide. Although first-line pharmacological interventions are efficacious [1], their unpleasant side effects have stimulated the search for novel targets to modulate bladder contractions. Many recent studies have investigated the effects of agonists and antagonists of the Transient Receptor Potential (TRP) family of ion channels on bladder function. Instillation of the TRP Melastatin-8 (TRPM8) agonist menthol into the bladder is suggested to activate bladder sensory afferents [2], whilst inhibiting muscarinic contractions of the detrusor smooth muscle (DSM) [3]. However, the dependence of these menthol effects on TRPM8 activation has only been investigated through the use of receptor antagonists [4], with no previous studies examining menthol effects in the bladders of TRPM8 knockout mice.

The nonselective cation channel TRPM8 was first identified for its activation by moderate cooling [5], [6]. It is permeable to both Na+ and Ca2+, and is activated by diverse stimuli including cool temperatures (<25°C), menthol and icilin [5], [7]. Menthol is commonly used in topical analgesic, antipruritic, and antiseptic therapies as a consequence of the sensation of cooling it produces, mediated by TRPM8 activation [8]. However, the pharmacology of menthol is complex, and it can interact with multiple targets independently of TRPM8 [9], [10], [11].

The precise sites of expression and functions of TRPM8 in the bladder remain unclear. In human bladder samples, TRPM8 mRNA was detected in the urothelium but not in the DSM layer [12]. TRPM8 immunoreactive nerve fibres, both unmyelinated and myelinated, were identified in the suburothelium of human bladder biopsies, with immunoreactivity also in urothelial cells [13]. The density of innervation correlated well with pain and urinary frequency in patients with overactive bladder or painful bladder syndrome [13]. Menthol and icilin both produced inwards currents and an increase in cytosolic Ca2+ in a proportion of cultured rat urothelial cells [14]. However, in cultured mouse urothelial cells TRPM8 mRNA was below the detection level, and no TRPM8 currents or increase in cytosolic Ca2+ were observed following exposure of the cells to menthol [15].

TRPM8 agonists are also able to alter bladder function. Intravesical menthol administration increased micturition pressure and decreased the volume threshold for micturition in anaesthetized guinea pigs, suggesting that it activates C-fibres [16]. Intravesical menthol also decreased the volume threshold for micturition in rats, with no change in micturition pressure [3]. In the same study, incubation with menthol inhibited carbachol-induced contractions of isolated bladder strips [3]. In pig detrusor and mucosal strips, both menthol and icilin inhibited carbachol-induced contractions [17]. Moreover the TRPM8 antagonist AMTB attenuated the rat bladder micturition reflex to filling, an effect attributed to its actions on the afferent innervation [18].

It has been suggested that some of the biological effects of menthol are due to mechanisms independent of TRPM8 activation, possibly through an inhibition of voltage-depedent calcium influx [9]. Additionally, it has been proposed that menthol inhibits nicotinic receptors [10] and voltage-gated sodium channels [11] in cultured sensory neurons. In this study we investigated the modulation of muscarinic bladder strip contractions by menthol, and investigated its underlying molecular mechanisms.

Materials and Methods

Animals

TRPM8 wild type (+/+) and knockout (−/−) mice were bred in house at King's College London. C57BL/6J mice were bred and housed at the University of Campinas, Brazil. Male mice (25–30 g) aged at least 2 months were used in these studies. All animals were maintained on normal diet, with free access to food and water, on a 12 h/12 h light/dark cycle, in a climate-controlled environment. All procedures were carried out in accordance with the UK Animals (Scientific Procedures) Act, 1986, UK and Brazilian College for Animal Experimentation (COBEA) guidance. They were approved by the Animal Welfare and Ethical Review Body at KCL and by the Committee for Ethics in Animal Research (CEEA-UNICAMP, protocol number 3313-1) at UNICAMP. Mouse tissues and cells used in this study were collected from animals euthanased with pentobarbital.

Tissue preparation and organ bath set-up

Mice were euthanized with an overdose of sodium pentobarbital (1 mg/g). The bladder dome was removed above the level of the ureters, and cut into 2 longitudinal strips. Unless otherwise stated, experiments were performed on bladder strips with intact mucosa. These were suspended in a 10 mL organ bath containing Krebs' solution (117 mM NaCl, 4.7 mM KCl, 2.5 mM CaCl2, 1.2 mM MgSO4, 1.2 mM KH2PO4, 24.8 mM NaHCO3 and 11 mM glucose, pH 7.4) at 37°C and bubbled with a mixture of 95% O2 and 5% CO2. Changes in isometric force were recorded using a Power Lab v.4 system (AD Instruments, UK). The resting tension was adjusted to 5 mN at the beginning of the experiments. The equilibration period was 60 min, during which the Krebs' solution was replaced every 20 min.

Electrical-field stimulation-induced bladder strip contractions

Prior to pharmacological stimulation, electrical-field stimulation (EFS) was performed with parallel electrodes positioned on either side of the bladder strips. Contractile responses to EFS were obtained at frequencies of 8, 16 and 32 Hz. The tissues were stimulated for 10 s with pulses of 1 ms width at 80 V, with 3 min intervals between stimulations. Following carbachol additions (described below), the tissues were incubated with menthol (30 or 300 µM), icilin (1 µM), nifedipine (1 µM) or vehicle (0.3% DMSO) for 15 min. The tissue was again electrically stimulated at 8, 16 and 32 Hz. Frequency-response data was also obtained in the presence of the voltage-gated sodium channel blocker, tetrodotoxin (1 µM, 30 min) to confirm the neurogenic nature of the contractions.

Concentration-response curves to carbachol

Following EFS, cumulative concentration-response curves to the muscarinic agonist carbachol (1 nM - 30 µM) were constructed in one-half log unit increments. After the first full curve was constructed, menthol (30 or 300 µM), icilin (1 µM), the neuronal Na+ channel blocker tetrodotoxin (TTX; 1 µM), nifedipine (1 µM) or vehicle (0.3% DMSO) were added to the organ baths and allowed to incubate for 15 min. A further cumulative concentration-response curve to carbachol was then constructed. The participation of sodium flux in the response to menthol was also investigated by replacing the sodium chloride and sodium bicarbonate in the Krebs' solution with the impermeant cation N-Methyl-D-glucamine (NMDG) and buffer HEPES, in equimolar concentrations. In a further series of experiments, TRPM8 +/+ urothelium denuded bladder strips were obtained by using ophthalmic scissors with the aid of a stereomicroscope. Denuded bladder strips were then mounted in the organ baths, and the above was repeated.

Pharmacological evaluation of contraction to extracellular calcium influx

Cumulative concentration response curves to CaCl2 (1 µM to 100 mM) using one log unit increments in depolarizing conditions were constructed, as previously described [19]. Briefly, the strips were prepared and mounted in 10 mL organ baths containing Ca2+-free Krebs' solution with EGTA (1 mM) to sequester Ca2+ ions. Preparations were contracted with carbachol (10 µM) to deplete intracellular Ca2+. The initial bathing solution was removed and replaced by Ca2+-free Krebs' solution containing KCl (80 mM) with cyclopiazonic acid (CPA; 10 µM) to block sarcoplasmic reticulum Ca2+ stores. After an equilibration period of 30 min, the cumulative concentration response curve to CaCl2 was obtained in the absence or presence of nifedipine (1 µM) or menthol (300 µM). Each strip preparation was used to construct one CaCl2 concentration–response curve.

Reversal of KCl contraction of bladder strips by the addition of menthol

Following pre-contraction of the tissue strips with KCl (40 mM), a cumulative concentration–relaxation curve to menthol (10 nM–1 mM, one log unit increments) was constructed in the absence or presence of a cocktail of potassium channel blockers (charybdotoxin 100 nM, apamin 1 µM, glibenclamide 10 µM and tetraethylammonium 1 µM).

Primary Culture of DSM Cells and [Ca2+]i determination

Five bladders were dissected from six weeks old C57BL/6J mice and cut into sections in Hank's Balanced Salt solution (HBSS; Sigma Aldrich) containing 2% penicillin (10,000 units/mL) and streptomycin (10 mg/mL). The tissue was then incubated in RPMI1640 containing 1 mg/mL collagenase type I from Clostridium histolyticum (Gibco), 2% penicillin (10,000 units/mL) and 10 mg/mL streptomycin under constant stirring for 4 hours at 37°C. The resultant solution was centrifuged at 479 g and the pellet resuspended in 1 mL of trypsin/EDTA solution (Sigma Aldrich) for 5 min at 37°C. Trypsin was inactivated by adding 2 mL of RPMI1640 with 10% of fetal bovine serum. Dissociated bladder cells were counted, and 2×105 cells were plated in Petri dishes (CellView, 35 mm, four compartments, glass bottom, Greiner Bio-one) containing complete medium (RPMI1640, 10% fetal bovine serum, 2% penicillin/streptomycin and 0.14% insulin), then maintained at 37°C. The culture medium was changed every 48 hours. All the experiments were done in the first cell passage. The smooth muscle phenotype of these cells was confirmed immunocytochemically by their expression of smooth muscle myosin heavy chain.

The intracellular Ca2+ concentration was assessed as previously described [20]. Briefly, once bladder smooth muscle cells (SMCs) achieved about 60–70% confluence, they were washed two times in HBSS (Sigma Aldrich). They were incubated in HBSS with EGTA (1 mM) and carbachol (10 µM) for 10 min at 37°C. Next, cells were washed in HBSS, loaded with 10 µM of the Ca2+-sensitive dye FluoForte-AM (Enzo Life Sciences, Inc., USA) and incubated with 10 µM CPA for 45 min at 37°C. Over the last 25 min menthol (30 and 300 µM), nifedipine (1 µM) or vehicle (DMSO 0.1%) were added to the medium. Changes in [Ca2+]i were monitored in real time using a confocal microscope (Zeiss LSM780-NLO, Carl Zeiss AG, Germany). Immediately before the beginning of fluorescence recording, CaCl2 (1 mM) was added to the HBSS. The fluorescence of individual cells was recorded at excitation 490 nm and emission 520 nm for 2–4 minutes, when the calcium influx was stimulated with addition of KCl (40 mM), or carbachol (CCh; 10 µM) to the medium. [Ca2+]i was expressed as (F-Fmin)/(Fmax-Fmin), the fluorescence intensity normalized to the individual maximal fluorescence for each cell. 30 cells per image were randomly chosen and defined as responding if (F-Fmin)/(Fmax-Fmin) exceeded 0.1 during the application of carbachol/KCl.

Cystometry

Mice were anaesthetized with an intraperitoneal injection of urethane (1.8 g.kg-1). Once surgical anesthesia was reached, a 1 cm incision was made along the midline of the abdomen. The bladder was exposed and a butterfly cannula (25 G) was inserted into the bladder dome. The cannula was connected to a three-way tap, one port of which was connected to a pressure transducer and the other to the infusion pump through a catheter (PE50). Before starting the cystometry, the bladder was emptied via the third port.

Continuous cystometry (CMGs) was carried out by infusing saline into the bladder for 30–35 min at a rate of 0.6 ml.h−1. After completion of the first CMG, the pump was stopped and the bladder was emptied. A further cystometric recording was then carried out with instillation of menthol (30 µM or 300 µM). The following parameters were assessed: Pressure threshold (the intravesical pressure immediately before micturition); Voiding pressure (the peak pressure reached during micturition); Capacity (the volume of saline needed to induce the first micturition); Voiding frequency (the number of voids per minute).

Drugs and reagents

Apamin, carbachol, charybdotoxin, cyclopiazonic acid, DMSO (dimethyl sulphoxide), EGTA (ethylene glycol-bis (2-amino-ethylether)- N,N,N′,N′-tetra-acetic acid), glibenclamide, (-)-menthol, NMDG (N-Methyl-D-glucamine), tetraethylammonium and tetrodotoxin were obtained from Sigma Aldrich, UK or Sigma Aldrich, USA. All drugs were dissolved and administered in Krebs' solution.

Analysis of data

Nonlinear regression analysis was performed to determine the pEC50 using GraphPad Prism (GraphPad Software, San Diego, CA, USA) with the constraint that Φ = 0. All concentration–response data were evaluated for a fit to a logistic function in the form: where Emax is the maximal response produced by agonists; c is the logarithm of the EC50, the concentration of drug that produces a half-maximal response; x is the logarithm of the concentration of the drug; n, the exponential term, is a curve-fitting parameter that defines the slope of the concentration– response line and Φ is the response observed in the absence of added drug.

Data are expressed as mean ± SEM of n experiments. The cumulative concentration and frequency-response data are expressed as mean of the contraction in mN mg−1 of wet strip weight ± SEM of n experiments to control for variances in bladder strip size. Cumulative concentration–response curves to CaCl2 are expressed as percentage of contractions to 10 µM carbachol. Instat (GraphPad Software, San Diego, CA, USA) was used for statistical analysis. One-way Analysis of Variance (ANOVA) followed by Tukey's test was used in all groups, and p<0.05 was accepted as significant.

Results

EFS-induced contractions are inhibited by menthol in both wild type and TRPM8 knockout bladder strips

EFS (8–32 Hz) elicited bladder contractions in bladder strips, and these contractions were unaffected by preincubation for 15 minutes with 30 µM menthol. In contrast, preincubation with 300 µM menthol or 1 µM nifedipine significantly inhibited contractions (Figure 1A). Contractions to EFS were of similar magnitude in bladder strips from TRPM8 −/− mice (Figure 2A). Incubation for 15 minutes with menthol (300 µM) significantly decreased EFS-induced contractions at all frequencies tested in bladder strips of both genotypes (Figure 2A; P<0.05). Incubation with icilin (1 µM, 15 min) had no effect on the contractions to EFS (Figure 2B).

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Figure 1. Electrical field stimulation (EFS; 8, 16 and 32 Hz; 80 V, 1 msec pulses) and carbachol (1 nM–30 µM) induced contractions of bladder strips that were inhibited by 300 µM menthol or 1 µM nifedipine.

(A) The effect of incubation with menthol (15 min; 30 µM or 300 µM) or nifedipine (15 min; 1 µM) on EFS-induced contractions. (B) The effect of incubation with menthol (15 min; 30 µM or 300 µM) or nifedipine (15 min; 1 µM) on carbachol-induced contractions. (C) Comparison of maximal responses (Emax) to carbachol in the experimental groups. *  =  P<0.05 compared with control group (one-way ANOVA followed by Tukey's post-test).

https://doi.org/10.1371/journal.pone.0111616.g001

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Figure 2. Electrical field stimulation (EFS)-induced contractions (8, 16 and 32 Hz; 80 V; 1 msec pulses) of bladder strips from TRPM8 +/+ and −/− mice in the absence or presence of TRPM8 agonists.

(A) The effect of incubation with menthol (15 min; 300 µM) on EFS-induced contractions. (B) The effect of incubation with icilin (15 min; 1 µM) on EFS-induced contractions. Data represents the mean ± S.E.M. for 5–7 strips in each group. *  =  P<0.05 compared with untreated +/+; #  =  P<0.05 compared with untreated −/− (one-way ANOVA followed by Tukey's post-test).

https://doi.org/10.1371/journal.pone.0111616.g002

Muscarinic contractions are inhibited by menthol in both wild type and TRPM8 knockout bladder strips

Carbachol (1 nM–30 µM) produced concentration-dependent contractions in bladder strips, and these contractions were unaffected by preincubation for 15 minutes with 30 µM menthol. In contrast, preincubation with 300 µM menthol or 1 µM nifedipine significantly inhibited contractions (Figures 1B and 1C). Contractions to carbachol were of similar magnitude in bladder strips from TRPM8 −/− mice, with no significant differences in Emax or pEC50. Incubation with menthol (300 µM, 15 min) decreased Emax in both groups (Figure 3A and 3C), whilst incubation with icilin (1 µM, 15 min) did not change any pharmacological parameter (Figure 3B). Incubation with the vehicle control DMSO (0.3%) did not affect the Emax of the carbachol-induced contractions (Basal: 0.69±0.11 mN/mg vs DMSO-treated: 0.63±0.13 mN/mg).

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Figure 3. Carbachol (1 nM–30 µM) induced concentration-dependent contractions in isolated bladder strips from TRPM8 +/+ and −/− mice in the absence or presence of TRPM8 agonists.

(A) The effect of incubation with menthol (15 min; 300 µM) on carbachol-induced contractions. (B) The effect of incubation with icilin (15 min; 1 µM). (C) Comparison of maximal responses (Emax) to carbachol in the experimental groups. Data represents the mean ± S.E.M. for 5–7 strips in each group. *  =  P<0.05 compared with untreated +/+; #  =  P<0.05 compared with untreated −/− (one-way ANOVA followed by Tukey's test).

https://doi.org/10.1371/journal.pone.0111616.g003

Menthol inhibition of carbachol contractions is independent of the urothelium

Carbachol produced similar concentration-dependent contractions in both intact and urothelium-denuded preparations (Figures 4A and 4B). Pre-treatment with menthol (300 µM) significantly inhibited contractions in both preparations (P<0.05).

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Figure 4. Effect of urothelial denudation on inhibition by menthol of carbachol-induced contraction of mouse bladder strips.

(A) Concentration-response curves for carbachol (1 nM–30 µM) contractions in mucosal-denuded, URO (−), and mucosal-intact, URO (+) bladder strips, before and after incubation with menthol (15 min; 300 µM). (B) Comparison of maximal responses (Emax) to carbachol in the experimental groups. Data represents the mean ± S.E.M. for 5–7 strips in each group. *  =  P<0.05 compared with untreated URO(−); **  =  P<0.01 compared with untreated URO (+) (one-way ANOVA followed by Tukey's test).

https://doi.org/10.1371/journal.pone.0111616.g004

Menthol inhibition of carbachol contractions is independent of neuronal activation

Neither incubation with the sodium channel inhibitor TTX (1 µM) nor replacement of the NaCl and NaHCO3 in the Krebs' buffer with the impermeant cation NMDG (130 mM) and HEPES (25 mM) affected the contractions produced by carbachol (Figure 5). However, incubation of the bladder strips with TTX or NMDG/HEPES buffer combined with menthol (300 µM) significantly inhibited carbachol-induced contraction (P<0.01) (Figure 5).

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Figure 5. Disruption of Na+ channel currents does not affect menthol inhibition of muscarinic contractions.

(A) Concentration-response curves for carbachol contractions in the presence of vehicle, TTX (1 µM) alone or TTX with menthol (300 µM). (B) Concentration-response curves for carbachol contractions in normal Krebs' solution, or following replacement of extracellular sodium with NMDG or NMDG with menthol (300 µM). (C) and (D) Comparison of maximal responses (Emax) to carbachol in the experimental groups. Data represents the mean ± S.E.M. for 3–4 strips in each group. **  =  P<0.01 compared with control (one-way ANOVA followed by Tukey's test).

https://doi.org/10.1371/journal.pone.0111616.g005

Menthol relaxation of KCl-precontracted bladder strips is independent of potassium channel activation

Menthol (10 nM–1 mM) induced a concentration-dependent relaxation of bladder strip contractions produced by 40 mM KCl (Figure 6). Pre-treatment with a cocktail of K+ channel inhibitors (100 nM charybdotoxin, 1 µM apamin, 10 µM glibenclamide and 1 µM tetraethylammonium) had no effect on the relaxation produced by menthol (Figure 6).

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Figure 6. Blockade of K+ channels does not affect relaxation of KCl-precontracted bladder strips.

(A) Original tension recordings illustrating concentration-response relaxing curves for menthol (10 nM–1 mM) in pre-contracted bladder strips (KCl 40 mM) with or without cocktail of K+ channel blockers pre-treatment (20 min; 100 nM charybdotoxin, 1 µM apamin, 10 µM glibenclamide and 1 µM tetraethylammonium). (B) Summary data showing no statistical changes between menthol-curves in the absence and presence of K+ channels blockers. Data represents the mean ± S.E.M. for 4 strips in each group.

https://doi.org/10.1371/journal.pone.0111616.g006

Menthol and nifedipine both inhibit bladder strip contractions due to extracellular calcium influx

In bladder strips with intracellular Ca2+ stores depleted and depolarized with 80 mM KCl, CaCl2 (0.01–100 mM) caused concentration-dependent contractions (Figure 7A). Pre-treatment with nifedipine (1 µM) or menthol (300 µM) shifted pEC50 to the right compared with control curve (control: 3.31±0.12, nifedipine: 2.64±0.15 and menthol: 2.86±0.12), and significantly decreased maximal CaCl2 contractions (P<0.05; Figure 7B). Pre-treatment with a combination of nifedipine and menthol produced no greater inhibition than either compound alone.

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Figure 7. Inhibition of contractions to CaCl2 in depolarized bladder strips by menthol and nifedipine.

(A) Concentration-response curves for contractions to CaCl2 (0.01–100 mM) in the presence of nifedipine (1 µM), menthol (300 µM) or both compounds. (B) Comparison of maximal responses (Emax) to CaCl2 in the experimental groups. Data represents the mean ± S.E.M. for 3–4 strips in each group. *  =  P<0.05 compared with control (one-way ANOVA followed by Tukey's test).

https://doi.org/10.1371/journal.pone.0111616.g007

Menthol inhibited extracellular calcium influx in isolated SMCs

Primary cultured murine bladder smooth muscle cells were incubated in Ca2+-free solution containing CPA (10 µM). Cells were exposed to carbachol (10 µM) in the presence of external Ca2+, and an increase in [Ca2+]i was observed. A similar increase was observed in cells preincubated for 25 minutes with 30 µM menthol, but preincubation with 300 µM menthol or with 1 µM nifedipine prevented any increase in [Ca2+]i (Figure 8A-C). It is notable that cells exposed to 30 µM menthol had a higher baseline [Ca2+]i than vehicle-, 300 µM menthol- or nifedipine-treated cells. However the magnitude of the increase in [Ca2+]i from baseline was the same as in cells pre-treated with DMSO (Figure 8B). In a separate experiment, smooth muscle cells were depolarized with KCl (40 mM) in the presence of external Ca2+. Depolarization induced an increase in [Ca2+]i that was unaffected by preincubation with 30 µM menthol, but was abolished by preincubation with 300 µM menthol or 1 µM nifedipine (Figure 8D-F). Again, the cells pre-treated with 30 µM menthol had a higher baseline [Ca2+]i than other groups, but increase in [Ca2+]i from baseline was similar to that observed in DMSO-treated cells (Figure 8E).

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Figure 8. Inhibitory effect of menthol (300 µM) on intracellular Ca2+ concentration in bladder smooth muscle cells (SMCs) stimulated with carbachol (CCh; 10 µM) or KCl (40 mM).

(A, D) Intensity of emission at 520 nm recorded in SMC's pretreated with DMSO, menthol 30 and 300 µM, or nifedipine (Nifed; 1 µM), before and after carbachol (A) and KCl (D) induces calcium influx. (B, E) Sample trace from one experiment showing mean (F-Fmin)/(Fmax-Fmin) in 30 SMCs exposed to carbachol (B) or KCl (E). Percentage of responding cells to carbachol (C) or KCl (F) stimulation. Data represents the mean ± S.E.M. for 90 cells in total across n = 3 independent experiments.

https://doi.org/10.1371/journal.pone.0111616.g008

Menthol increased voiding frequency and decreased peak pressure in intact bladders

To determine the effects of menthol on bladder function in vivo, cystometry was performed on terminally anaesthetised mice. Instillation of 30 µM menthol had no effect on any of the parameters measured. In contrast, instillation of 300 µM menthol significantly increased the voiding frequency, while decreasing the bladder capacity, threshold pressure and peak contraction pressure (Figure 9).

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Figure 9. In vivo bladder function assessed by cystometry during instillation of menthol 30 µM or 300 µM.

(A, B) Representative cystometrogram recordings during the instillation of saline (first cystometrogram), menthol 30 µM (A) or 300 µM (B). Cystometric parameters analysed after treatments: voiding frequency (C), voiding pressure (D), capacity (E) and pressure threshold (F). Data represents the mean ± S.E.M. for 3 animals in each group. *  =  P<0.05 compared with saline infusion (one-way ANOVA followed by Tukey's test).

https://doi.org/10.1371/journal.pone.0111616.g009

Discussion

This study is the first to assess the role of TRPM8 in the modulation of bladder contraction in vitro to electrical field stimulation or the muscarinic agonist carbachol by menthol. Our results demonstrate that deletion of TRPM8 does not alter muscarinic bladder contractions. Menthol inhibited bladder contractions independently of any activity at TRPM8. This mechanism did not involve blockade of Na+ channels or activation of K+ channels. Contractions due to extracellular Ca2+ entry through voltage-gated Ca2+ channels were inhibited similarly by the L-type VOCC inhibitor nifedipine and menthol. Moreover menthol inhibited the increase in [Ca2+]i that occurred in cultured SMCs exposed to carbachol or depolarized with KCl. Menthol also exerted inhibitory effects on bladder smooth muscle contraction in vivo, decreasing the peak pressure produced during voiding contractions. Altogether our findings suggest that the inhibitory activity of menthol on DSM contractions is not mediated by agonist activity at TRPM8 but instead occurs through inhibition of L-type voltage-gated Ca2+ channels.

Electrical field stimulation of bladder strips activates the parasympathetic motor fibres innervating the DSM to release ACh and ATP, causing contraction [21]. The majority of the contraction is due to the activity of ACh on M3 muscarinic receptors, and is sensitive to blockade by atropine [22]. Addition of carbachol can also contract bladder smooth muscle through M3 receptor activation. EFS and carbachol caused contractions of mouse bladder strips that were unaffected by TRPM8 deletion, suggesting that tonic TRPM8 activity does not contribute to smooth muscle contraction or regulation of contraction in this tissue. Contractions in bladder strips from wild type mice were unaffected by incubation with the TRPM8 agonist icilin, further supporting this conclusion. Instillation of menthol during cystometry experiments caused an increase in the frequency of voiding contractions, similar to that observed in previous studies in the rat and guinea pig [3], [16]. This was probably due to activation of TRPM8 on sensory afferents. However, in contrast to these previous studies, we observed a decrease in the voiding pressure exerted by the bladder in the presence of menthol, whereas intravesical menthol enhanced voiding pressure in the guinea pig [16] and had no effect on pressure in the rat [3]. The reasons for this difference are unclear, but may be related to species differences in the structure of VOCCs. Alternatively the higher concentrations of menthol (600 µM and 3 mM) used in these previous studies may have produced effects at other non-TRPM8 targets to counteract the inhibition of contraction that we observed.

Recent studies have shown that the TRPM8 agonist menthol at concentrations greater than 100 µM inhibited carbachol-induced contraction of rat and pig bladder strips [3], [17]. We observed a similar inhibition of carbachol-induced contractions by 300 µM menthol, along with an inhibition of EFS-induced contractions. Inhibition occurred to the same extent in bladder strips from TRPM8 knockout mice, indicating that it is not dependent on activation of TRPM8 in the bladder strips.

TRPM8 expression in urothelial cells and on bladder sensory afferents has been proposed [12], [13]. Urothelial cells have the ability to sense intravesical changes, responding to chemical, mechanical and thermal stimuli by releasing mediators such as ATP, nitric oxide, and acetylcholine [23]. To further confirm that the inhibitory effects of menthol on muscarinic contractions are not dependent on activation of urothelial TRPM8, we compared carbachol contractions of intact bladder strips with those in strips with the mucosal layer surgically removed. Carbachol caused concentration-dependent contractions in both groups, and menthol inhibited muscarinic contractions in both groups, indicating that menthol's inhibitory effects do not depend on the presence of urothelial cells.

In cultured dorsal root ganglion (DRG) neurons, menthol inhibited voltage-gated Na+ channels (TTX-sensitive channels, along with NaV1.8 and NaV1.9) in a concentration-dependent manner [11]. To determine whether blockade of Na+ channels could contribute to the menthol inhibition of muscarinic contractions we removed sodium chloride and sodium bicarbonate and replaced them with equimolar concentrations of NMDG and HEPES. However, muscarinic contractions were unaltered in Na+-free solution, indicating that the inhibitory effects of menthol do not occur through inhibition of a sodium conductance in smooth muscle cells or through activation of an action potential to release inhibitory transmitters from bladder neurons. Further support for this conclusion comes from the observation that incubation of bladder strips with the sodium channel inhibitor TTX had no effect on muscarinic contractions or their inhibition by menthol.

Multiple ion channels are expressed by DSM cells and can regulate bladder contraction. Among them, the large conductance voltage- and Ca2+-activated K+ channels (BKCa or KCa1.1 channels) are recognised as key regulators of excitability and contractility of the DSM [24]. The SKCa channels (KCa2.1–KCa2.3) and KATP channel have also been reported to induce hyperpolarization and to decrease contractibility in urinary bladder smooth muscle from human and guinea-pig [25], [26]. Inhibition of muscarinic contractions by menthol could occur through opening of smooth muscle K+ channels to cause K+ efflux, hyperpolarisation and subsequent relaxation. However, addition of menthol to bladder strips contracted by exposure to 40 mM KCl caused a concentration-dependent relaxation. The efficacy of menthol in conditions when the concentration gradient for K+ efflux is reduced suggests that K+ channel activation does not underlie menthol-induced bladder relaxation. Further evidence that menthol acts independently of K+ channels is its continuing efficacy in the presence of a cocktail of K+ channel inhibitors.

Intracellular Ca2+ concentration is controlled by the balance between Ca2+ entry and extrusion from the cell. L-type voltage-operated Ca2+ channels (VOCCs) are found in the plasma membrane of excitable and non-excitable cells. The opening of these channels generates the upstroke phase of the smooth muscle action potential allowing for net influx of Ca2+ to initiate contraction [27]. High levels of extracellular K+ depolarize the cell membrane and activate L-type VOCCs, resulting in increased inward movement of Ca2+, which causes contraction [27], [28]. Extracellular Ca2+ influx through L-type VOCCs has been shown to play an important mechanism in generating the contractile responses to EFS and carbachol in the urinary bladder [27], [29], [30]. In our study, bladder strips treated with CPA to block sarcoplasmic reticulum Ca2+ stores and depolarized with KCl were contracted by addition of CaCl2 in Ca2+-free Krebs' solution. Incubation of the bladder strips with either menthol or nifedipine inhibited this contraction to a similar extent, and the combination of the two compounds did not increase the inhibitory effect.

In cultured SMCs menthol abolished the increase in internal Ca2+ concentration produced by carbachol or by KCl depolarization. This was most likely due to a block of VOCCs, as the effects of menthol and nifedipine were the same, preventing further Ca2+ influx and allowing the Ca2+ efflux and sequestration mechanisms to return the cytoplasmic Ca2+ concentration to its low resting level. We noted an elevated baseline [Ca2+]i in SMCs pretreated with 30 µM menthol, but this was not apparent in SMCs pretreated with 300 µM menthol, suggesting that it was a quirk of the data rather than an effect of TRPM8 stimulation in these cells. Importantly, the magnitude of the increase in [Ca2+]i from baseline following exposure of cells to carbachol or KCL was similar after pre-treatment with either 30 µM menthol or DMSO, indicating that the difference in baseline [Ca2+]i did not affect the response.

Conclusions

Together, our findings indicate that menthol inhibit muscarinic contractions of isolated mouse bladder strips through a mechanism independent of TRPM8 activation, most likely by blockade of L-type VOCCs. More broadly, the identification of menthol actions in the bladder that are independent of TRPM8 activity suggests that other studies linking biological activity of menthol in the bladder to TRPM8 activation must be interpreted with caution, unless a specific effect has been confirmed through the use of knockout mice or receptor antagonists.

Acknowledgments

We are grateful to Prof. Stuart Bevan, King's College London, for providing TRPM8 wild type and knockout mice. Antonio Celso S Ramos Filho thanks Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) for the grant fellowship. We also thank the access to equipment and assistance provided by the National Institute of Science and Technology on Photonics Applied to Cell Biology (INFABIC) at the State University of Campinas.

Author Contributions

Conceived and designed the experiments: ASCR TMA GOB LOL EA ADG. Performed the experiments: ASCR AS TMA GOB. Analyzed the data: ASCR AS GOB HFC EA ADG. Contributed reagents/materials/analysis tools: ASCR HFC EA ADG. Wrote the paper: ASCR AS EA ADG.

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