- Open Access
Apamin inhibits NO-induced relaxation of the spontaneous contractile activity of the myometrium from non-pregnant women
© Modzelewska et al; licensee BioMed Central Ltd. 2003
- Received: 24 January 2003
- Accepted: 5 February 2003
- Published: 5 February 2003
There is now considerable evidence for the involvement of K+ channels in nitric oxide (NO) induced relaxation of smooth muscles including the myometrium. In order to assess whether apamin-sensitive K+ channels play a role in NO – induced relaxation of the human uterus, we have studied the effect of specific blockers of these channels on the relaxation of myometrium from non-pregnant women. In vitro isometric contractions were recorded in uterine tissues from non-pregnant premenopausal women who had undergone hysterectomy. Apamin (10 nM) and scyllatoxin (10 nM) did not alter spontaneous myometrial contractions. However, 15-min pretreatment of the myometrium strips with apamin completely inhibited relaxation caused by diethylamine-nitric oxide (DEA/NO). The pretreatment with scyllatoxin significantly reduced (about 2.6 times) maximum relaxation of the strips induced by DEA/NO (p < 0.05). These results strongly suggest that, beside Ca2+ and voltage dependent charybdotoxin-sensitive (CTX-sensitive) K+ channels, apamin-sensitive K+ channels are also present in the human non-pregnant myometrium. These channels offer an additional target in the development of new tocolytic agents.
- Nitric Oxide
- Organ Bath
- Spontaneous Contraction
- Physiological Salt Solution
- Small Conductance
Nitric oxide has been shown to be a potent inhibitor of spontaneous contractile activity of the myometrium from non-pregnant women. It has recently been shown that contrary to the finding in some smooth muscle, in the myometrium from non-pregnant women, there was no causal relationship between the relaxation induced by NO donors and the elevated production of cGMP [1, 2]. A number of recent studies on both vascular and uterine smooth muscle have provided evidence for the involvement of potassium (K+) channels in relaxation induced by nitric oxide (NO) donors [3–8].
In smooth muscle, K+ channels play an important role in regulation of cell membrane excitability and contractile activity of the tissue [3–8]. K+ channels consist of a diverse group of proteins with disparate structural features and controlling mechanisms. Calcium (Ca2+)-dependent K+ channels have been found in many smooth muscles including myometrium from different species [4, 9–12]. Ca2+-activated K+ channels up to now identified in human myometrium represent the type of large-conductance and voltage-dependent channels (BK) blocked by charybdotoxin (CTX) and iberiotoxin [11, 13]. However, other classes of Ca2+-activated K+ channels may exist in smooth muscle cells including K+ channels with intermediate (IK) and small unitary conductance (SK) [14, 15].
Ca2+-activated K+ channels with small conductance found in different visceral smooth muscles [4, 16, 17] have so far not been identified in human myometrium. These channels, so called apamin-sensitive K+ channels are specifically blocked by a bee venom toxin, apamin [18, 19] and scyllatoxin (leiurotoxin I), a toxin from the venom of the scorpion Leiurus quinquestriatus Hebraeus [20, 21]. Calcium-dependent apamin-sensitive SK channels and CTX-sensitive BK channels can apparently co-exist in the same cell [18, 22]. Recently, it has been demonstrated that the intermediate conductance K+ channels, sensitive to both apamin and charybdotoxin exist in mouse intestinal smooth muscles and rat renal arterioles [14, 15].
Although, inhibition of smooth muscle contraction by K+ channels openers is a well-recognized mechanism, information on the expression and characteristics of various channels is needed to develop tissue and channel type specific K+ channel openers. In order to assess whether apamin-sensitive K+ channels play any role in NO induced relaxation, we have in this study examined the effect of specific blockers of these channels on the relaxation of myometrium from non-pregnant women.
Human uterine tissues were collected from 14 non-pregnant premenopausal women (age, 41–50 years; median, 46 years) who had undergone hysterectomy because of either dysfunctional bleeding, benign uterine tumors or cervical malignancy. All women were recruited from patients of the Department of Gynecology, Medical Academy of Bialystok, Poland. The women were informed about the nature and procedure of the study and gave their written consent. The local ethics committee approved the study. Myometrial samples were excised transversally from the fundus of uterus, placed in an ice-cold physiological salt solution and immediately transferred to the laboratory where processed as previously described . Briefly, 4–8 strips, 6–7 mm in length and 2 × 2 mm of cross section area were obtained under a dissecting microscope. The strips were then mounted in an organ bath containing 20 ml of physiological salt solution (PSS) at 37°C, pH 7.4 and bubbled with carbogen (95% O2 + 5% CO2). Strips were left for the equilibration period of 1–2 hours. During that period the passive tension was adjusted to 3 mN.
Activity of myometrium was recorded under isometric conditions by means of force transducers with digital output. The spontaneous contractile activity was treated as a control. After the recording of spontaneous activity the response of myometrium to nitric oxide and K+ channel blockers was recorded. Quantification of the responses was done by calculation of area under the curve (AUC), amplitude and frequency of contractions. The area was measured from the basal tension over a 10-min period after each stimulus. The effects were evaluated by comparing experimental responses with the controls (set as 100%).
Diethylamine-nitric oxide (DEA/NO), which has been shown previously to inhibit spontaneous activity in human [2, 24] or rat  myometrium, in a concentration-dependent manner, was used as NO donor. Three or four strips from the same uterus were studied in parallel. One of them was always treated as a control and regularly washed with PSS. DEA/NO was given cumulatively directly into the organ bath in log increments within the concentrations range 10 nM to 100 μM. The effect of DEA/NO was observed in the absence and after 15 minutes preincubation with 100 nM CTX, 10 nM apamin or 10 nM scyllatoxin. The contact time for each concentration was 10 min. Only one concentration-response curve was obtained for each strip.
DEA/NO, a generous gift of dr Larry K. Keefer from Laboratory of Comparative Carcinogenesis, National Cancer Institute, Frederick, Maryland, USA, was dissolved in a 10 mM NaOH, and kept cold until dilution with cold pH 7.4 buffer immediately before addition to a bathing medium . The concentration of NaOH in the organ bath never exceeded 0.001% v/v and had no influence on the experimental responses. Apamin and scyllatoxin, purchased from Sigma Chemical Company, were dissolved in distilled water. All substances were added directly to the organ bath containing physiological salt solution composed of (mM): NaCl 136.9; KCl 2.68; MgCl2 1.05; NaH2PO4 1.33; CaCl2 1.80; NaHCO3 25.0; glucose 5.55.
All data were analyzed statistically with PRISM 3.0 (GraphPad Software Inc., San Diego, Calif.). The data were analyzed with ANOVA, Friedman test or Wilcoxon matched pairs signed rank test, where appropriate. The statistical significance was considered when probability value was P < 0.05.
Throughout the paper the results are expressed as mean ± S.E.M. and n denotes the number of tissues obtained from different patients. In the case when the same protocol was run on two strips from the same uterus, the data were averaged.
In experiments performed on tissues taken from 10 women, we studied the effect of apamin, a blocker of Ca2+-dependent K+ channels with small conductance on DEA/NO – induced relaxation of the myometrium. Apamin at a concentration of 10 nM did not alter spontaneous myometrial contractions. In presence of apamin, the mean values of amplitude and frequency of contractions did not differ significantly from those observed before the blocker administration (Wilcoxon matched pairs rank test) (Fig. 4). However, pretreatment of myometrium strips with 10 nM apamin for 15 minutes resulted in complete inhibition of relaxation caused by a cumulative administration of DEA/NO. In the presence of apamin, the mean AUC value at the highest DEA/NO concentration in the bath medium was (97.13 ± 2.73)%. This value did not differ significantly from that calculated for the spontaneous contractions (p > 0.05) (Fig. 1C, 2A and 5).
To test this effect we used scyllatoxin, a polypeptide isolated from scorpion venom, that blocks the apamin-sensitive K+ channels in other tissues [20, 21]. In a separate group of five experiments, scyllatoxin (10 nM), like apamin, did not alter spontaneous myometrial activity (Fig. 4). However, pretreatment of tissue with 10 nM scyllatoxin considerably reduced the DEA/NO-induced relaxation of the strips (Fig. 2A and 5). In the presence of 10 nM scyllatoxin, the mean AUC value at 100 μDEA/NO in the bath medium was (81.63 ± 2.54)%. Thus, in presence of 10 nM scyllatoxin, the maximum of DEA/NO-induced relaxation of the myometrium strips was about 2.6 times smaller than that recorded in the absence of the blocker. The difference was statistically significant (P < 0.05). However, the reduction of the DEA/NO-induced relaxing effect by scyllatoxin was, lower than that observed after pretreatment with apamin After pretreatment with 10 nM scyllatoxin the AUC value calculated for 100 μM DEA/NO (81.63 ± 2.54%) significantly differed from that calculated in presence of 10 nM apamin (97.13 ± 2.73%).
The present data show that DEA/NO causes concentration-dependent decrease of AUC, amplitude and frequency of the myometrium from non-pregnant women. The blockers of both SK and BK channels reduce the DEA/NO-induced inhibition of spontaneous activity of the myometrium.
Relaxation of many smooth muscles by NO donors involves activation of K+ current resulting in hyperpolarisation of cell membrane. K+ channels may be activated by pathways involving direct action by NO and/or cGMP-mediated mechanisms [26, 27]. In majority of smooth muscles, the relaxing effect of NO is related to opening of large-conductance Ca2+ and voltage dependent K+ channels blocked by charybdotoxin and iberiotoxin (BK). Present data show that, in the myometrium from non-pregnant women, the relaxation of spontaneous contractions induced by DEA/NO is inhibited by charybdotoxin. The same effect has been observed before . Thorough analysis revealed, however, that although CTX completely inhibited the DEA/NO-induced decrease of amplitude it was less efficient in preventing the lowering of frequency. Using contraction as the only indicator of the DEA/NO influence on the myometrium activity, we can only speculate about a mechanism of the observed effect. The concentration of CTX used in the experiments inhibits about 80% of potassium current through BK channels . That means that a fraction of this channels could remain unblocked, accessible to NO donated by DEA/NO. The fact that only the frequency of contractions is sensitive to activation of this fraction may indicate that, in presence of 100 nM CTX, other types of K+ channels play predominant role in controlling the amplitude of contractions. It also implies that NO donated by DEA/NO inhibits the spontaneous contractile activity reducing excitability of the myometrium cells by taking their membrane potential away from the threshold for action potential generation. Our data indicate that also apamin and scyllatoxin, blockers of small conductance K+ channels can counteract DEA/NO-induced relaxation. Apamin is a blocker of Ca2+ sensitive K+ channels with small conductance . In different smooth muscles the maximum effective concentrations of apamin are within the range 1 nM to 1 μM [14, 29, 30]. The lack of NO-induced inhibition of contractile activity that we observed in the presence of 10 nM apamin suggests the existence of apamin-sensitive K+ channels in cell membrane of the myometrium from non-pregnant women. On the other hand, in some smooth muscle preparations from animals intermediate conductance K+ channels exist that are sensitive to both CTX and apamin [14, 15]. The similar effects of CTX and apamin on the relaxation caused by DEA/NO suggest that the same channel may be a target for both blockers. Such a conclusion, however, is inconsistent with data obtained in presence of scyllatoxin, a blocker of Ca2+-activated K+ channels with small conductance  that has no effect on intermediate or large conductance, Ca2+-activated K+ channels . The decrease of NO-induced inhibition in presence of scyllatoxin shown here supports the suggestion that Ca2+-activated K+ channels with small conductance exist in the myometrium from non-pregnant women. The difference between effects of equimolar concentrations of apamin and scyllatoxin is in agreement with the fact that the scyllatoxin affinity to the SK channels is 10 – 20 lower than that of apamin [30, 32].
Our findings, however, are not in agreement with the data reported by others. Perez et al.  using cell membranes from myometrium from non-pregnant women that were incorporated into lipid bilayer have founded no apamin-sensitive K+ currents in this preparation. The lack of sensitivity to apamin was also observed in a beta-subunit of maxi KCa channel from human myometrium expressed in Xenopus laevis oocytes . The discrepancy between our findings and the electrophysiological observations [11, 33] may be explained by assuming that exposure to NO or metabolic activation is required to activate the apamin-sensitive K+ channels. It has been observed that the transfer of ionic channels to the artificial environment resulted in an inactivation of these channels [34, 35].
The data of the present study strongly suggest that, the apamin-sensitive K+ channels exist in the myometrium from non-pregnant women. On the basis of our data we cannot, however, preclude that in myometrium from non-pregnant women exist channels sensitive to both CTX and apamin similar to those reported in some smooth muscles [14, 15]. Further studies are necessary to verify this hypothesis.
We have previously shown that K+ATP channel openers are potent inhibitors of contractile responses of the myometrium of non-pregnant women induced by vasopressin, an agent implicated in the pathophysiology of dysmenorrhoea . Specific openers of apamin sensitive K+ channels, if developed, should have strong potential in the treatment of dysmenorrhoea.
- Bradley KK, Buxton IL, Barber JE, McGaw T, Bradley ME: Nitric oxide relaxes human myometrium by a cGMP-independent mechanism. Am J Physiol. 1998, 275: C1668-C1673.PubMedGoogle Scholar
- Modzelewska B, Sipowicz M, Saavedra JE, Keefer LK, Kostrzewska A: Involvement of K+ ATP channels in nitric oxide-induced inhibition of spontaneous contractile activity of the nonpregnant human myometrium. Biochem Biophys Res Commun. 1998, 253: 653-657. 10.1006/bbrc.1998.9844.View ArticlePubMedGoogle Scholar
- Anwer K, Oberti C, Perez G, Perez Reyes N, McDougall J, Monga M, Sanborn B, Stefani E, Toro L: Calcium-activated K+ channels as modulators of human myometrial contractile activity. Am J Physiol. 1993, 265: C976-C985.PubMedGoogle Scholar
- Brayden JE: Potassium channels in vascular smooth muscle. Clin Exp Pharmacol Physiol. 1996, 23: 1069-1076.View ArticlePubMedGoogle Scholar
- Hollingsworth M, Amedee T, Edwards D, Mironneau J, Savineau JP: The relaxant action of BRL 34915 in rat uterus. Br J Pharmacol. 1987, 91: 803-813.PubMed CentralView ArticlePubMedGoogle Scholar
- Kostrzewska A, Laudañski T, Batra S: Inhibition of contractile responses of human myometrium and intramyometrial arteries by potassium channel openers. Acta Obstet Gynecol Scand. 1996, 75: 886-891.View ArticlePubMedGoogle Scholar
- Lindeman KS, Fernandes LB, Croxton TL, Hirshman CA: Role of Potassium Channels in Hypoxic Relaxation of Porcine Bronchi in Vitro. Am J Physiol. 1994, 266: L232-L237.PubMedGoogle Scholar
- Loutzenhiser RD, Parker MJ: Hypoxia Inhibits Myogenic Reactivity of Renal Afferent Arterioles by Activating ATP-Sensitive K+ Channels. Circ Res. 1994, 74: 861-869.View ArticlePubMedGoogle Scholar
- Kirber MT, Ordway RW, Clapp LH, Walsh JV, Singer JJ: Both membrane stretch and fatty acids directly activate large conductance Ca2+-activated K channels in vascular smooth muscle cells. FEBS Lett. 1992, 297: 24-28. 10.1016/0014-5793(92)80319-C.View ArticlePubMedGoogle Scholar
- Kotlikoff MI, Kamm KE: Molecular mechanisms of beta-adrenergic relaxation of airway smooth muscle. Annu Rev Physiol. 1996, 58: 115-141. 10.1146/annurev.physiol.58.1.115.View ArticlePubMedGoogle Scholar
- Perez G, Toro L, Erlukar S, Stefani E: Characterization of large-conductance, calcium-activated potassium channels from human myometrium. Am J Obstet Gynecol. 1993, 168: 652-660.View ArticlePubMedGoogle Scholar
- Okawa T, Vedernikov Y, Saade G, Longo M, Olson G, Chwalisz K, Garfield R: Roles of potassium channels and nitric oxide in modulation of uterine contractions in rat pregnancy. Am J Obstet Gynecol. 1999, 181: 649-655.View ArticlePubMedGoogle Scholar
- Khan R, Smith S, Morrison J, Ashford M: Ca2+ dependence and pharmacology of large-conductance K+ channels in nonlabor and labor human uterine myocytes. Am J Physiol. 1997, 273: C1721-C1731.PubMedGoogle Scholar
- Gebremedhin D, Kaldunski M, Jacobs ER, Harder DR, Roman RJ: Coexistence of two types of Ca2+-activated K+ channels in rat renal arterioles. Am J Physiol. 1996, 270: F69-F81.PubMedGoogle Scholar
- Vogalis F, Zhang Y, Goyal RK: An intermediate conductance K+ channel in the cell membrane of mouse intestinal smooth muscle. Biochim Biophys Acta. 1998, 1371: 309-316. 10.1016/S0005-2736(98)00029-7.View ArticlePubMedGoogle Scholar
- Fujii K, Foster CD, Brading AF, Parekh AB: Potassium channel blockers and the effects of cromakalim on the smooth muscle of the guinea-pig bladder. Br J Pharmacol. 1990, 99: 779-785.PubMed CentralView ArticlePubMedGoogle Scholar
- Suzuki K, Ito KM, Minayoshi Y, Suzuki H, Asano M, Ito K: Modification by Charybdotoxin and Apamin of Spontaneous Electrical and Mechanical Activity of the Circular Smooth Muscle of the Guinea-Pig Stomach. Br J Pharmacol. 1993, 109: 661-666.PubMed CentralView ArticlePubMedGoogle Scholar
- Romey G, Hughes M, Schmid-Antomarchi H, Lazdunski M: Apamin: a specific toxin to study a class of Ca2+ – dependent K+ channels. J Physiol (Paris). 1984, 79: 256-264.Google Scholar
- Lefebvre RA, Barthó L: Mechanism of nitric oxide-induced contraction in the rat isolated small intestine. Br J Pharmacol. 1997, 120: 975-981.PubMed CentralView ArticlePubMedGoogle Scholar
- Auguste P, Hugues M, Grave B, Gesquiere JC, Maes P, Tartar A, Romey G, Schweitz H, Lazdunski M: Leiurotoxin I (scyllatoxin), a peptide ligand for Ca2+-activated K+ channels. Chemical synthesis, radiolabeling, and receptor characterization. J Biol Chem. 1990, 265: 4753-4759.PubMedGoogle Scholar
- Legros C, Bougis PE, France M, Eauclaire M: Molecular biology of scorpion toxins active on potassium channels. Perspect Drug Discov Design. 1999, 15 (16): 1-14. 10.1023/A:1017010611685.View ArticleGoogle Scholar
- Van Renterghem C, Lazdunski M: A small-conductance charybdotoxin-sensitive, apamin-resistant Ca2+-activated K+ channel in aortic smooth muscle cells (A7r5 line and primary culture). Pflugers Arch. 1992, 420: 417-423.View ArticlePubMedGoogle Scholar
- Kostrzewska A, Laudañski T, Batra S: Potent inhibition by tamoxifen of spontaneous and agonist-induced contractions of the human myometrium and intramyometrial arteries. Am J Obstet Gynecol. 1997, 176: 381-386.View ArticlePubMedGoogle Scholar
- Buhimschi I, Yallampalli C, Dong Y-L, Garfield RE: Involvement of a nitric oxide-cyclic guanosine monophosphate pathway in control of human uterine contractility during pregnancy. AM J Obstet Gynecol. 1995, 172: 1577-1584.View ArticlePubMedGoogle Scholar
- Keefer LK: "NONOates " (1-substituted diazen-1-ium-1,2-diolates) as nitric oxide donors: convenient nitric oxide dosage forma. Methods Enzymol. 1996, 268: 281-293.View ArticlePubMedGoogle Scholar
- Carrier GO, Fuchs LC, Winecoff AP, Giulumian AD, White RE: Nitrovasodilators relax mesenteric microvessels by cGMP-induced stimulation of Ca-activated K channels. Am J Physiol. 1997, 273: H76-84.PubMedGoogle Scholar
- Koh SD, Dick GM, Sanders KM: Small-conductance Ca2+-dependent K+ channels activated by ATP in murine colonic smooth muscle. Am J Physiol. 1997, 273: C2010-2021.PubMedGoogle Scholar
- Lazdunski M: Apamin, a neurotoxin specific for one class of Ca2+-dependent K+ channels. Cell Calcium. 1983, 4: 421-428.View ArticlePubMedGoogle Scholar
- Mule F, Angelo SD, Serio R: Tonic inhibitory action by nitric oxide on spontaneous mechanical activity in rat proximal colon: involvement of cyclic GMP and apamin-sensitive K+ channels. Brit J Pharmacol. 1999, 127: 514-20.View ArticleGoogle Scholar
- Murphy EM, Brayden JE: Apamin-sensitive K+ channels mediate an endothelium-dependent hyperpolarization in rabbit mesenteric arteries. J Physiol. 1995, 723-734.Google Scholar
- Grant TL, Zuzack JS: Effects of K+ channel blockers and cromakalim (BRL 34915) on the mechanical activity of guinea pig detrusor smooth muscle. J Pharmacol ExpTher. 1991, 259: 1158-1164.Google Scholar
- Chicchi GG, Gimenez Gallego G, Ber E, Garcia ML, R Winquist, Cascieri MA: Purification and characterization of a unique, potent inhibitor of apamin binding from Leiurus quinquestriatus hebraeus venom. J Biol Chem. 1988, 263: 10192-10197.PubMedGoogle Scholar
- Wallner M, Meera P, Ottolia M, Kaczorowski GJ, Latorre R, Garcia ML, Stefani E, Toro L: Characterization of and modulation by a beta-subunit of a human maxi KCa channel cloned from myometrium. Receptors Channels. 1995, 3: 185-199.PubMedGoogle Scholar
- Van Renterghem C, Lazdunski M: Identification of the Ca2+ current activated by vasoconstrictors in vascular smooth muscle cells. Pflugers Arch. 1994, 429: 1-6.View ArticlePubMedGoogle Scholar
- Zhou X, Schlossmann J, Hofmann F, Ruth P, Korth M: Regulation of stably expressed and native BK channels from human myometrium by cGMP- and cAMP-dependent protein kinase. Pflugers Arch Eur J Physiol. 1998, 436: 725-734. 10.1007/s004240050695.View ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.