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High conductance potassium channels activation by acid exposure in rat aorta is endothelium-dependent
BMC Research Notes volume 8, Article number: 462 (2015)
We investigated, previously, the mechanism by which extracellular acidification promotes relaxation in rat thoracic aorta. These studies suggested that extracellular acidosis promotes vasodilation mediated by NO, KATP and SKCa, and maybe other K+ channels in isolated rat thoracic aorta. This study was carried out to investigate the paxilline-mediated hyperpolarization induced by acid exposure.
The relaxation response to HCl-induced extracellular acidification (7.4–6.5) was measured in rat aortic rings pre-contracted with phenylephrine (PE, 10−6 M). The vascular reactivity experiments were performed in endothelium-intact and denuded rings, in the presence of paxilline (10−6 M), which is an inhibitor of high calcium conductance potassium BKCa channels. In rings with endothelium, paxilline inhibits relaxation, triggered by acidification at all pH values lower than 7.2 and had no effect on rings without endothelium, showing that the activation of BKCa is endothelium-dependent.
High conductance potassium channel activation induced by acid exposure is endothelium-dependent.
We investigated, previously, the mechanism by which extracellular acidification promotes relaxation in rat thoracic aorta. The extracellular acidosis failed in inducing any changes in the vascular tone of rings pre-contracted with potassium chloride (KCl). However, it caused endothelium-dependent, and endothelium-independent, relaxations in rings pre-contracted with PE. These relaxations were inhibited by L-NAME, apamin, and glibenclamide, but not by indomethacin. These results suggested that extracellular acidosis promotes vasodilation mediated by NO, KATP and SKCa, and maybe other K+ channels in the isolated rat thoracic aorta . In rings with endothelium, paxilline inhibits relaxation induced by acidification at all pH values lower than 7.2. Otherwise, paxilline had no effect on rings without endothelium, showing that the activation of BKCa is endothelium-dependent. After an extensive literature search, we assumed this data as original. Therefore, the rationale of the present study was to test a hypothesis that the relaxation induced by extracellular acidification includes the activation of high conductance BKCa potassium channels.
The experimental procedures and animal handling were reviewed and approved by the Institutional Animal Care Review Board (CETEA—Ethics Committees of Animal Experiments of the Faculty of Medicine of Ribeirão Preto—University of São Paulo). This investigation conforms with the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85-23, revised 1996). Before the experiments, the rats were housed under standard laboratory conditions (12 h light/dark cycle at 21 °C), with free access to food and water. Male Wistar rats (230–280 g) were anesthetized with thiopental sodium (40 mg/kg, intraperitoneal injection), followed by a laparotomy for exsanguination via the abdominal aorta and a thoracotomy for thoracic aorta harvesting. The thoracic aorta was carefully dissected free of connective tissue and immediately immersed in Krebs. For the vascular reactivity studies, Krebs solution with the following composition (mM) was employed: NaCl—118.0, KCl—4.7, CaCl2—2.5, KH2PO4—1.2, MgSO4—1.66, glucose—11.1, NaHCO3—25.0 (pH 7.4).
The thoracic aorta was cut into rings (4–5 mm in length). The endothelium was removed from some rings by gently rubbing the intimal surface of the blood vessel with a pair of watchmaker’s forceps. This method removes the endothelium, but it does not affect the ability of the vascular smooth muscle to contract or relax. Then, these rings were placed in isolated organ baths (10 mL) filled with Krebs solution, maintained at 37 °C, and bubbled with 95 % O2/5 % CO2 (pH 7.4). Each arterial ring was suspended by two stainless steel clips placed through the lumen. One clip was anchored to the bottom of the organ bath, while the other was connected to a strain gauge for measurement of the isometric force with the aid of the Grass FT03 equipment (Grass Instrument Company, Quincy, MA, USA). Each ring was stretched to a resting tension of 1.5 g and allowed to equilibrate for 60 min. During this period, tissues were washed every 15 min. The efficacy of the procedure for endothelium removal was confirmed by the lack of relaxant effects induced by acetylcholine (10−6 M) in rings pre-contracted with PE (10−6 M—EC80). Endothelium was considered to be present when the Ach-induced relaxation was at least 80 %. Then, each ring was washed and re-equilibrated for 30 min. Aortic rings were then pre-contracted with PE (10−6 M), and pH-response curves were obtained after a stable plateau was reached. The pH-response curves allowed assessment of the relaxation response to HCl-induced (1N) extracellular acidification (7.4, 7.3, 7.2, 7.1, 7.0, 6.9, 6.8, 6.7, 6.6, 6.5). For this purpose, an electrode (Analion G2134, Ribeirão Preto, SP, Brazil) connected to a pH-meter (MS tecnopon MPA 210, Piracicaba, SP, Brazil) was immersed in the organ bath, enabling real-time analysis of the Krebs solution pH, each point of the curve was obtained by adding a sufficient volume (approximately 2–3 μL) of HCl to the preparation, in order to decrease the pH in 0.1 units. The time elapsed between consecutive additions of acid was 1–2 min, which was necessary for observation of the effect of pH-changes and achievement of the plateau. Considering that the pH curve ranged from 7.4 to 6.5, the total final volume of HCl added to the organ bath was about 30 μL. The paxilline added to the bath was 10−6 M. Preparations were kept in contact with the drugs for an incubation period of 30 min. Phenylephrine (PE) and paxilline were purchased from Sigma Chemical Company (St. Louis, MO, USA). All the drugs were prepared with distilled water.
The results are shown as mean ± SEM. In the relaxation study, the changes in vascular tension are expressed as a percent of relaxation about the maximal contraction achieved by EC80 PE-stimulated contraction, a convention that corrects interanimal variability. Statistical analysis was performed using two-way repeated-measures ANOVA and Bonferroni post-test (Prism 4.0, GraphPad Software Inc, San Diego, CA, USA). Values were considered to be statistically significant at p values less than 0.05.
In rings with endothelium precontracted with PE (10−6 M), paxilline inhibits relaxation, induced by HCl acidification at all pH values lower than 7.2 (n = 6; p < 0.05) (Fig. 1).
In rings without endothelium precontracted with PE (10−6 M), paxilline did not inhibit the relaxation induced by HCl acidification at all pH values (n = 6; p < 0.05) (Fig. 2).
Several types of K+ channels have been identified in the vascular smooth muscle. These channels had been shown to be involved in the vasodilation seen in cerebral circulation under acidosis condition. KATP and KCa are the most important potassium channels engaged in the relaxant response [2–6] in the presence of decreased extracellular pH. It is known that high potassium concentrations can inhibit the activity of all potassium channels [4, 7].
To confirm the involvement of this two potassium channels in acidosis-induced vasodilation, we previously tested the specific channels KATP and KCa under acidosis condition concluding that their vascular beds actions were endothelium-independent. Vasodilation in response to acidosis was completely abolished when only one of these channels was blocked. The inhibitory effect of glibenclamide or apamin on vasodilation HCl-induced, was potenciated by endothelium removal. The association between L-NAME and specific potassium channels blockers, inhibited the HCl-relaxation almost a hundred percent. . This data is suggestive that hyperpolarization and NO/cGMP has some “cross-talked” mechanism. It has been shown that the vasodilator response to NO in rat middle cerebral artery is mediated by activation of KCa channels via a cGMP- independent pathway , a finding that is in accordance with our results about the important role of NO and KCa channel activity in acidosis.
To evaluate the involvement of BKCa, this study used paxilline , because although some studies have used charybdotoxin as a blocker of BKCa [2, 10], it is known that this drug is not unique to this channel [11–14]. The present studies, using the blocker paxilline, showed an interesting data: the effect of acidification mediated by potassium channel type BKCa is dependent on the endothelium. However, it is prudent to consider the fact that paxilline inhibit the relaxation only in rings with endothelium, suggesting that the opening of these channels should be dependent on some endothelium-derived factor. From this point of view, the paxilline BKCa channel blocker effect, by itself, should not participate in the relaxation induced by acidification. In addition, it is possible to speculate that the endothelium role is dependent on calcium conductance, since the acidosis-induced relaxation blocked by apamin (small conductance Ca2+-activated K+ channel blocker—SKCa) was endothelium-independent, and paxilline (a high calcium conductance BKCa) was endothelium-dependent.
The present study demonstrated the contribution of BKCa for dilation evoked by decreased pHo and paxilline proved to be useful as a pharmacological tool. For example, recent study about the vasorelaxant effect of cilostazol a selective inhibitor of type III phosphodiesterase (PDE3), was not affected by removal of the endothelium and the results were quite similar to the decreased pHo effect. Application of a nitric oxide synthase inhibitor and a small conductance Ca2+-activated K+ (SKCa) channel inhibitor did not affect cilostazol-induced vasorelaxation, which was endothelium-independent and only blocked by paxilline .
In conclusion, high conductance potassium channel (BKCa) activation induced by acid exposure is endothelium-dependent (Fig. 3).
- BKCa :
calcium-activated potassium channels
L-NG-nitroarginine methyl ester
- KATP :
ATP-sensitive potassium channel
- SKCa :
calcium-activated SK potassium channel
cyclic guanosine monophosphate
Celotto AC, Restini CB, Capellini VK, Bendhack LM, Evora PR. Acidosis induces relaxation mediated by nitric oxide and potassium channels in rat thoracic aorta. Eur J Pharmacol. 2011;656:88–93.
Lindauer U, Vogt J, Schuh-Hofer S, Dreier JP, Dirnagl U. Cerebrovascular vasodilation to extraluminal acidosis occurs via combined activation of ATP-sensitive and Ca2+-activated potassium channels. J Cereb Blood Flow Metab. 2003;23:1227–38.
Horiuchi T, Dietrich HH, Hongo K, Goto T, Dacey RG Jr. Role of endothelial nitric oxide and smooth muscle potassium channels in cerebral arteriolar dilation in response to acidosis. Stroke. 2002;33:844–9.
Kinoshita H, Katusic ZS. Role of potassium channels in relaxations of isolated canine basilar arteries to acidosis. Stroke. 1997;28:433–7.
Rosenblum WI. ATP-sensitive potassium channels in the cerebral circulation. Stroke. 2003;34:1547–52.
Santa N, Kitazono T, Ago T, Ooboshi H, Kamouchi M, Wakisaka M, Ibayashi S, Iida M. ATP-sensitive potassium channels mediate dilatation of basilar artery in response to intracellular acidification in vivo. Stroke. 2003;34:1276–80.
Adeagbo AS, Triggle CR. Varying extracellular [K+]: a functional approach to separating EDHF and EDNO-related mechanisms in perfused rat mesenteric arterial bed. J Cardiovasc Pharmacol. 1993;21:423–9.
Yu M, Sun CW, Maier KG, Harder DR, Roman RJ. Mechanism of cGMP contribution to the vasodilator response to NO in rat middle cerebral arteries. Am J Physiol Heart Circ Physiol. 2002;282:H1724–31.
Dabertrand F, Nelson MT, Brayden JE. Acidosis dilates brain parenchymal arterioles by conversion of calcium waves to sparks to activate BK channels. Circ Res. 2012;110:285–94.
Edwards G, Félétou M, Weston AH. Endothelium-derived hyperpolarizing factors and associated pathways: a synopsis. Pflugers Arch. 2010;459:863–79.
Vázquez J, Feigenbaum P, King VF, Kaczorowski GJ, Garcia ML. Characterization of high affinity binding sites for charybdotoxin in synaptic plasma membranes from rat brain. Evidence for a direct association with an inactivating, voltage-dependent, potassium channel. J Biol Chem. 1990;265:15564–71.
Waldron GJ, Cole WC. Activation of vascular smooth muscle K+ channels by endothelium-derived relaxing factors. Clin Exp Pharmacol Physiol. 1999;26:180–4.
Hattori K, Tsuchida S, Tsukahara H, Mayumi M, Tanaka T, Zhang L, Taniguchi T, Muramatsu I. Augmentation of NO-mediated vasodilation in metabolic acidosis. Life Sci. 2002;71:1439–47.
Ko EA, Han J, Jung ID, Park WS. Physiological roles of K+ channels in vascular smooth muscle cells. J Smooth Muscle Res. 2008;44:65–81.
Li H, da Hong H, Son YK, Na SH, Jung WK, Bae YM, Seo EY, Kim SJ, Choi IW, Park WS. Cilostazol induces vasodilation through the activation of Ca(2+)-activated K(+) channels in aortic smooth muscle. Vascul Pharmacol. 2015;70:15–22.
ACC and VKC participated in the design, performed the statistical analysis and drafted the manuscript. PRBE participated in the design, helped to draft the manuscript and made suggestions for the analyzes. AASA, LGF, TRN and APCS conceived the study and participated in its design and coordination. All authors read and approved the final manuscript.
We are thankful to Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) and Fundação de Apoio ao Ensino, Pesquisa e Assistência do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo (FAEPA/HCFMRP/USP) for financial support.
Compliance with ethical guidelines
Competing interests The authors declare that they have no competing interests.
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Celotto, A.C., Capellini, V.K., Albuquerque, A.A.S. et al. High conductance potassium channels activation by acid exposure in rat aorta is endothelium-dependent. BMC Res Notes 8, 462 (2015). https://doi.org/10.1186/s13104-015-1422-3
- Potassium channels
- Rat aortic rings