Urothelium-dependent modulation of urinary bladder smooth muscle contractions by menthol
Paduraru OM, Filippov IB, Boldyriev OI, Vladymyrova IA, Naĭd'onov VH, Shuba IaM
Bogomoletz Institute of physiology NAS of Ukraine, Kyiv, Ukraine
DOI: https://doi.org/10.15407/fz57.06.015
Abstract
TRPM8 cold receptor/channel is considered amongst the variety of receptors that support and modulate sensory function of urothelium, although the information regarding this is still quite contradictory. Here we have studied the effects of nonspecific TRPM8 activator menthol on the contractions of the smooth muscle strips of the rat bladder with intact and removed urothelium, and assessed the expression in them of TRPM8 mRNA using semi-quantitative RT-PCR. Menthol (100 uМ) decreased the basal tone and the amplitude of spontaneous contractions only in the strips with intact urothelium.Irrespective of the presence of urothelium it similarly inhibited (by ~45 %) the contractions evoked by high-potassium depolarization. Contractions induced by muscarinic agonist carbachol (1 uМ) were inhibited by menthol much stronger (by ~63 %) if the urothelium was present than without it (by ~12 %). Expression of TRPM8 mRNA in urothelium was not detected, whilst in detrusor smooth muscle it was found very low. We conclude that modulation of contractile responses by menthol is most likely explained by its blocking action on voltage-gated calcium channels of detrusor smooth muscle cells (SMC) and by menthol-stimulated release from urothelium of some factor(s) with relaxant effects on SMCs. Stimulation of the secretion of these factors from urothelial cells most likely involves menthol-induced, TRPM8-independent mobilization of calcium.
Keywords:
bladder, urothelium, detrusor, smooth muscles,menthol, cold receptor TRPM8.
References
- Baylie R.L., Cheng H., Langton P.D., James A.F. Inhibition of the cardiac L-type calcium channel current by the TRPM8 agonist, (-)-menthol . J. Physiol. Pharmacol. 2010. 61, N 5. P. 543-50.
- Birder L.A. Urinary bladder urothelium: molecular sensors of chemical. thermal. mechanical stimuli . Vascul. Pharmacol. 2006. 45, N 4. P. 221-226.
CrossRef
PubMed
- Birder L.A. TRPs in bladder diseases . Biochim. and Biophys. Acta. 2007. 1772, N 8. P. 879-884.
CrossRef
PubMed PubMedCentral
- Birder L.A, de Groat W.C. Mechanisms of disease: involvement of the urothelium in bladder dysfunction . Nat. Clin. Pract. Urol. 2007. 4, N 1. P. 46-54.
CrossRef
PubMed PubMedCentral
- Birder L.A, Nakamura Y., Kiss S., Nealen M.L., Barrick S., Kanai A.J., Wang E., Ruiz G., De Groat W.C, Apodaca G., Watkins S., Caterina M.J. Altered urinary bladder function in mice lacking the vanilloid receptor TRPV1 . Nat. Neurosci. 2002. 5, N 9. P. 856-860.
CrossRef
PubMed
- Colyer J. Phosphorylation states of phospholamban . Ann. NY Acad. Sci. 1998. 853. P. 79-91.
CrossRef
PubMed
- Dietrich A., Chubanov V., Kalwa H. Rost B.R., Gudermann T. Cation channels of the transient receptor potential superfamily: their role in physiological and pathophysiological processes of smooth muscle cells . Pharmacol. Ther. 2006. 112, N 3. P. 744-760.
CrossRef
PubMed
- Everaerts W., Gevaert T., Nilius B., De Ridder D. On the origin of bladder sensing: Tr(i)ps in urology . Neurourol. Urodyn. 2008. 27, N 4. P. 264-273.
CrossRef
PubMed
- Everaerts W., Sepblveda M.R., Gevaert T., Roskams T., Nilius B., De Ridder D. Where is TRPV1 expressed in the bladder, do we see the real channel? . Naunyn Schmiedebergs Arch. Pharmacol. 2009. 379, N 4. P. 421-425.
CrossRef
PubMed
- Gevaert T., Vriens J., Segal A., Everaerts W., Roskams T., Talavera K., Owsianik G., Liedtke W., Daelemans D., Dewachter I., Van Leuven F., Voets T., De Ridder D., Nilius B. Deletion of the transient receptor potential cation channel TRPV4 impairs murine bladder voiding . J. Clin. Invest. 2007. 117, N 11. P. 3453-3462.
CrossRef
PubMed PubMedCentral
- Gudermann T., Hofmann T., Mederos Y, Schnitzler M., Dietrich A. Activation, subunit composition and physiological relevance of DAG-sensitive TRPC proteins . Novartis Found. Symp. 2004. 258, P. 103-118.
CrossRef
- Lee K.P., Jun J.Y, Chang I.Y, Suh S.H., So I., Kim K.W. TRPC4 is an essential component of the nonselective cation channel activated by muscarinic stimulation in mouse visceral smooth muscle cells . Mol. Cells. 2005. 20, N 3. P. 435-441.
- Mahieu F., Owsianik G., Verbert L., Janssens A,m De Smedt H., Nilius B., Voets T. TRPM8-independent menthol-induced Ca2+ release from endoplasmic reticulum and Golgi . J. Biol. Chem. 2007. 282, N 5. P. 3325-3336.
CrossRef
PubMed
- Marshall I. Mechanism of vascular relaxation by the calcitonin gene-related peptide . Ann NY Acad Sci. 1992. 657. P. 204-215.
CrossRef
PubMed
- Palade P. Drug-induced Ca2+ release from isolated sarcoplasmic reticulum. II. Releases involving a Ca2+-induced Ca2+ release channel . J. Biol. Chem. 1987. 262, N 13. P. 6142-6148.
- Sanguinetti M.C., Krafte D.S., Kass R.S. Voltage-dependent modulation of Ca channel current in heart cells by Bay K8644 . J. Gen. Physiol. 1986. 88, N 3. P. 369-392.
CrossRef
PubMed PubMedCentral
- Streng T., Axelsson H.E., Hedlund P, Andersson D.A., Jordt S.E., Bevan S., Andersson K.E., Hogestatt E.D., Zygmunt P.M. Distribution and function of the hydrogen sulfide-sensitive TRPA1 ion channel in rat urinary bladder . Eur. Urol. 2008. 53, N 2. P. 391-399.
CrossRef
PubMed
- Swandulla D., Carbone E., Schafer K., Lux H.D. Effect of menthol on two types of Ca currents in cultured sensory neurons of vertebrates . Pflug. Arch. 1987. 409. P. 52-59.
CrossRef
PubMed
- Thebault S., Lemonnier L., Bidaux G., Flourakis M., Bavencoffe A., Gordienko D., Roudbaraki M., Delcourt P., Panchin Y, Shuba Y, Skryma R., Prevarskaya N. Novel role of cold. menthol-sensitive transient receptor potential melastatine family member 8 (TRPM8) in the activation of store-operated channels in LNCaP human prostate cancer epithelial cells . J. Biol. Chem. 2005. 280, N 47. P. 39423-39435.
CrossRef
PubMed
- Wang P., Luthin G.R., Ruggieri M.R. Muscarinic acetylcholine receptor subtypes mediating urinary bladder contractility and coupling to GTP binding proteins . J. Pharmacol. Exp. Ther. 1995. 273, N 2. P. 959-966.
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