|Year : 2015 | Volume
| Issue : 4 | Page : 204-210
Vasorelaxation of goat mesenteric artery is mediated by endothelial Na+-K+-ATPase
R Sathiskumar1, Bimal Prasanna Mohanty2, Subas Chandra Parija1
1 Department of Pharmacology and Toxicology, Orissa University of Agriculture and Technology, Bhubaneswar, Odisha, India
2 FREM Division, Central Inland Fisheries Research Institute, ICAR, Kolkata, West Bengal, India
|Date of Submission||06-Mar-2015|
|Date of Decision||09-Aug-2015|
|Date of Acceptance||09-Sep-2015|
|Date of Web Publication||15-Dec-2015|
Subas Chandra Parija
Department of Pharmacology and Toxicology, College of Veterinary Sciences and Animal Husbandry, Orissa University of Agriculture and Technology, Bhubaneswar - 751 003, Odisha
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Objective: To examine the role of Na+-K+-ATPase and K+ channels in mediating vasorelaxation in the superior mesenteric artery of Capra hircus. Materials and Methods: Goat superior mesenteric artery (GSMA) was cut into 1.5–2 mm circular rings and mounted in a thermostatically controlled (37°C ± 0.5°C) organ bath containing 20 ml of modified Krebs-Henseleit saline (MKHS) (pH 7.4), with continuous aeration under 1.5 g tension for 90 min. Endothelium-intact (ED+) or endothelium-denuded (ED−) GSMA ring was contracted with phenylephrine (PE) or 5-hydroxytryptamine (5-HT) (1µM–0.1 mM) in the absence or presence of ouabain (0.1 µM). KCl (1µM–10 mM) was added cumulatively to K+-free MKHS-pre-contracted (ED+/−) rings in the absence or presence of ouabain (0.1µM) or barium (1µM) or 4-aminopyridine (1µM). Results: Ouabain did not alter the basal tone of the arterial ring. The contractile response induced by PE (Emax: 50.46 ± 2.68, pD2: 5.53 ± 0.04) and 5-HT (Emax: 30.86 ± 1.33, pD2: 6.17 ± 0.03) in ED+ ring was significantly (P < 0.001) augmented in ED− rings (PE: Emax: 93.30 ± 2.11, pD2: 6.41 ± 0.04; 5-HT: Emax: 95.07 ± 0.99, pD2: 6.27 ± 0.03). The contractile response induced by PE and 5-HT in ED+ or ED− rings in the presence of ouabain was almost identical with that of ED− rings. Vasorelaxation of KCl (Emax: 2.90 ± 1.14, pD2: 3.9 ± 0.03) was significantly attenuated in the presence of ouabain (Emax: 73.8 ± 5.16, pD2: 4.3 ± 0.04), Ba2+ (Emax: 16.34 ± 4.7, pD2: 3.22 ± 0.02), 4-AP (Emax: 18.16 ± 2.4, pD2: 3.68 ± 0.03), ouabain and Ba2+ (Emax: 70.09 ± 3.66, pD2: 4.41 ± 0.04), and ouabain and 4-AP (Emax: 66.98 ± 4.61, pD2: 4.13 ± 0.06). Conclusion: The vasorelaxation in GSMA is mediated by the endothelium-derived hyperpolarizing factor (EDHFs) such as ouabain-sensitive Na+-K+-ATPase, KIRand Kvchannels.
Keywords: EDHF, goat, KIR, KV,mesenteric artery, ouabain, pump, sodium pump
|How to cite this article:|
Sathiskumar R, Mohanty BP, Parija SC. Vasorelaxation of goat mesenteric artery is mediated by endothelial Na+-K+-ATPase. J Pharmacol Pharmacother 2015;6:204-10
|How to cite this URL:|
Sathiskumar R, Mohanty BP, Parija SC. Vasorelaxation of goat mesenteric artery is mediated by endothelial Na+-K+-ATPase. J Pharmacol Pharmacother [serial online] 2015 [cited 2020 Jan 27];6:204-10. Available from: http://www.jpharmacol.com/text.asp?2015/6/4/204/171884
| Introduction|| |
Na +-K +-ATPase is an integral membrane enzyme, ubiquitously distributed in the plasma membrane of all eukaryotic cells. It plays an important role in generation and maintenance of electrochemical gradient by extrusion of three sodium ions and influx of two potassium ions across the cell membrane by utilizing the energy derived from ATP hydrolysis. Endothelium has also been shown to regulate the Na +-K +-ATPase activity either by release of nitric oxide (NO) or endothelial diffusible factors like leukotrienes and prostaglandins., The role of the endothelium in sodium pump induced vasorelaxation varies between vascular beds and species. The vasorelaxation induced by vascular sodium pump has been reported to be endothelium dependent in human placental vessels, mice femoral artery, and rat aorta  and endothelium independent in goat ruminal artery  and rabbit aorta. In small arteries like mesenteric bed, where the ratio of endothelium/smooth muscle increases, the endothelium plays a more important role in modulation of the expression of Na +-K +-ATPase.
In addition to the role of sodium pump, the activation of vascular endothelial K + channels hyperpolarizes and relaxes the underlying vascular smooth muscle; hence, K + acts as the endothelium-derived hyperpolarizing factor (EDHF). Endothelium-derived K + is also reported to function as a local intravascular vasodilator , as observed in rabbit aorta, rat resistance arteries  and rabbit arcuate arteries, and rat mesenteric artery, whereas findings from other studies conflicted with the proposed role of K + ion as an EDHF in porcine coronary arteries  and rat mesenteric artery. KCl-induced relaxation in vascular smooth muscles may involve activation of sarcolemmal Na +-K +-ATPase  or inward rectifier K + channels  or even both the mechanisms.
In view of the contradicting evidences with respect to the activity of Na +-K +-ATPase and K + channel is linked to the endothelium in different vascular beds, we hypothesized that vasorelaxation in ruminant mesenteric artery could be contributed by endothelium-dependent Na +-K +-ATPase and K + channels such as KIR and KV channels. In order to establish it, we selected superior mesenteric artery of goat (Capra hircus) as a ruminant vascular model and conducted functional studies to characterize the Na +-K +-ATPase in endothelium-intact (ED+) and –denuded (ED−) vessels using K +-induced relaxation in K +-free solution as an activator of vascular Na +-K +-ATPase.
| Materials and Methods|| |
Preparation of superior mesenteric artery and tension recording
After careful exposure of goat intestinal mesentery, a branch of superior mesenteric artery adjacent to the duodenum and jejunum just before it branches into the inferior branch was dissected out and placed in cold, aerated, modified Krebs-Henseleit saline (MKHS) solution. Arteries were cleared of fat and connective tissues. Endothelium was removed by rubbing it with horse hair. The arterial rings of 1.5–2 mm were then mounted between two fine, L-shaped hooks made of stainless steel and kept under a resting tension of 1.5 g in a thermostatically controlled (37.0°C ± 0.5°C) automatic organ bath (Pan Lab) of 20 ml capacity containing MKHS and aerated continuously with air. The arterial rings were equilibrated for 90 min before recording the muscle tension. During this period, the bathing fluid was changed every 15 min. This experiment was repeated for both ED+ and ED− vessels. The change of isometric tension was measured by a highly sensitive isometric force transducer (Model MLT0201; AD instrument, Sydney, Australia) and analyzed using Chart 7.1.3 software.
Acetylcholine (1 µM) on 5-hydroxy tryptamine–induced sustained contractile response
In order to examine intact functional endothelium, a single sub-threshold concentration of 5-hydroxy tryptamine (5-HT; 0.1 µM) was added to the bath to obtain a sustained contraction and observed for inhibitory effect of ACh (1 µM) for 1 min.
5-HT and phenylephrine (1 ηM)–induced contraction in ED+ and ED− goat superior mesenteric artery rings in the absence or presence of ouabain
Experiments with K +-free physiological solution
K +-induced relaxation of arterial rings exposed to K +-free MKHS is an experimental protocol for the functional assessment of vascular sodium pump. In order to study the regulation of sodium pump by vascular endothelium in goat superior mesenteric artery (GSMA), the arterial rings were equilibrated in MKHS for 90 min and then the tissue viability was checked with 5-HT (1.0 µM). The endothelial integrity was examined by applying ACh (1 µM) to the vessels pre-contracted with 5-HT (1 µM). After a period of wash for 30 min in MKHS, tissues were incubated in K +-free solution and all the subsequent experimental protocols were carried out in K +-free solution. This experiment was repeated for both ED+ and ED− vessels.
KCl-induced relaxation in K +-free MKHS in the presence of ouabain or 4-aminopyridine or barium, or ouabain and 4-AP, or ouabain and barium
The arterial ring was incubated in K +-free MKHS pre-incubated with either 0.1 µM ouabain or 1 µM 4-aminopyridine (4-AP) or 1 µM Ba 2+, or 0.1 µM ouabain and 1 µM 4-AP, or 0.1 µM ouabain and 1 µM Ba 2+ for 30 min to obtain a sustained contraction and, subsequently, KCl was added (1 µM–10 mM) to the bath cumulatively at an interval of 1 min to record the contractile response.
The results were analyzed by interactive non-linear regression through the computer program GraphPad Prism (GraphPad Prism Software, San Diego, CA, USA). Statistical analysis was done using unpaired Student's “t” test with GraphPad Software Quick Calcs. P values <0.05 and <0.001 were considered statistically significant.
Acetylcholine chloride, ouabain, phenylephrine and 5-hydroxy tryptamine (Sigma Aldrich, USA), barium chloride and 4-aminopyridine (Qualigens and HiMedia, India) were employed in this study.
| Results|| |
Effect of ACh on 5-HT (0.1 μM)-induced contraction
5-HT pre-contracted the arterial ring, reaching a steady level (1.28 ± 0.25 g, n = 14) within 2–3 min. ACh (1 µM) inhibited the 5-HT–induced sustained contraction by 44.51 ± 9.37% (n = 7), suggesting the presence of functional endothelium. In contrast, ACh did not inhibit the 5-HT–induced sustained contraction in ED− GSMA rings.
Effect of KCl (1 µM–10 mM) in ED+ and ED− GSMA rings in K+ -free MKHS
Exposure of arterial ring to K +-free solution caused a rise in basal tone that reached the maximum (1.43 ± 0.27 g, n = 22) in about 25–30 min and, subsequently, a sustained contraction was observed within 2–3 min. Cumulative addition of KCl inhibited sustained contraction in a concentration-dependent manner in both ED+ and ED− rings. The concentration related contractile (CRC) response curve of K + (pD2 3.9 ± 0.03, Emax 2.90 ± 1.14%) in ED+ rings was shifted to the right with a significant (P < 0.001) decrease in pD2 (3.32 ± 0.02) and increase in Emax (66.78 ± 1.49%) in ED− rings [Figure 1].
|Figure 1: KCl (1 µM–10 mM)–induced concentration-dependent contractile response curve elicited in either endothelium-intact [ED+ (○)] or endothelium-removed [ED− (•)] GSMA rings pre-contracted with K+-free solution|
Click here to view
Effect of ouabain in 5-HT and PE (1 ηM–0.1 mM)-induced CRC response curves in ED+ and ED− vessels
5-HT–induced CRC response curve was shifted to the left with insignificant alteration in pD2 (6.27 ± 0.03) and significant (P < 0.05) increase in Emax (95.07 ± 0.99%) in ED− rings as compared to ED+ rings (pD2 6.17 ± 0.03, Emax 30.86 ± 1.33). In the presence of ouabain, 5-HT–induced CRC response curve was shifted to the left with significant (P < 0.05) increase in pD2 (6.82 ± 0.02) in ED− rings as compared to ED+ (pD2 6.25 ± 0.02) rings [Table 1] and [Figure 2]a,[Figure 2]b,[Figure 2]c. PE-induced CRC response curve was shifted to the left with significant (P < 0.001) increase in pD2 (6.41 ± 0.04) and Emax (93.30 ± 2.11%) in ED− rings as compared to ED+ rings (pD2 5.53 ± 0.04, Emax 50.46 ± 2.68%). In the presence of ouabain, PE-induced CRC response curve was shifted to the left with significant (P < 0.001) increase in pD2 (6.34 ± 0.05) in ED− rings as compared to ED+ (pD2 5.2 ± 0.05) rings [Table 1] and [Figure 3]a,[Figure 3]b,[Figure 3]c.
|Table 1: Effect of ouabain (0.1 µM) on 5-HT-induced and PE (1 nM-0.1 mM)-induced CRC response curves in endothelium-intact (ED+) and endothelium-denuded (ED-) vessels|
Click here to view
|Figure 2: (a) Effect of endothelium removal on 5-HT (1 ηM–0.1 mM)-induced concentration-related contractile response presented in curves labeled as 5-HT, ED+ (○) and 5-HT, ED− (□). Effect of pre-incubation of ouabain (0.1 µM) on 5-HT (1 ηM–0.1mM)-induced concentration-related contractile response curves in endothelium-intact (•) and endothelium-removed (▪) GMSA rings is presented in 5-HT (ED+) + 0.1 µM Ouab and 5-HT (ED−) + 0.1 µM Ouab. (b) Tracing representing the effect of ouabain (0.1 µM) on the contractile response induced by 5-HT (10 µM) in endothelium-intact goat superior mesenteric artery. (c) Tracing representing the effect of ouabain (0.1 µM) on the contractile response induced by 5-HT (10 µM) in endothelium-denudated goat superior mesenteric artery|
Click here to view
|Figure 3: (a) Effect of endothelium removal on PE (1 ηM–0.1 mM)-induced concentration-related contractile response presented in curves labeled as PE, ED+ (○) and PE, ED− (□). Effect of pre-incubation of ouabain (0.1 µM) on PE (1 ηM–0.1 mM)-induced concentration-related contractile response curves in endothelium-intact (•) and -removed (▪) GMSA rings is presented in PE (ED+) + 0.1 µM Ouab and PE (ED−) + 0.1 µM Ouab. (b) Tracing representing the effect of ouabain (0.1 µM) on the contractile response induced by PE (10 µM) in endothelium-intact GMSA rings. (c) Tracing representing the effect of ouabain (0.1 µM) on the contractile response induced by PE (10 µM) in endothelium-denudated GMSA rings|
Click here to view
Effect of ouabain (0.1 µM), barium (1 µM), 4-AP (1 µM), ouabain (0.1 µM) and barium (1 µM), and ouabain (0.1 µM) and 4-AP (1 µM) on KCl-induced relaxation
K +-induced vasorelaxation was attenuated with rightward shift of KCl-induced CRC response curve with significant (P < 0.001) increase in Emax in the presence of ouabain (73.8 ± 5.16%), Ba 2+ (16.34 ± 4.7%), 4-AP (18.16 ± 2.4%), ouabain and Ba 2+ (70.09 ± 3.66%), and ouabain and 4-AP (66.98 ± 4.61%), as compared to that of control (2.90 ± 1.14%). Similarly, pD2 (3.9 ± 0.03) of KCl-induced CRC curve was shifted to the right with a significant (P < 0.001) increase (4.3 ± 0.04), decrease (3.22 ± 0.02), decrease (3.68 ± 0.03), increase (4.41 ± 0.04), and increase (4.13 ± 0.06) in the presence of ouabain, Ba 2+, 4-AP, ouabain and Ba 2+, and ouabain and 4-AP, respectively [Table 2] and [Figure 4]a,[[Figure 4]b,[Figure 4]c.
|Table 2: Effect of ouabain (0.1 µM), 4-AP (1 µM), barium (1 µM), ouabain (0.1 µM) and 4-AP (1 µM), and ouabain (0.1 µM) and barium (1 µM) on KCl-induced vasorelaxation|
Click here to view
|Figure 4: (a) KCl (1 µM–10 mM)–induced concentration-related contractile response curve elicited either in the absence (○) or presence of 0.1 µM ouabain (•) or 1 µM 4-AP (▪) or 0.1 µM ouabain and 1 µM 4-AP (□) or 1 µM barium (▴) or 0.1 µM ouabain and 1 µM barium (▪) in endothelium-intact GSMA rings pre-contracted with K+-free solution. (b) Tracing representing KCl (1–10,000 µM)-induced concentration-dependent vasorelaxation response elicited in endothelium-intact GSMA following pre-contraction with K+-free MKSH in the absence of ouabain. (c) Tracing representing KCl (1–10,000 µM)-induced concentration-dependent vasorelaxation response elicited in endothelium-intact GSMA following pre-contraction with K+-free MKSH in the presence of ouabain|
Click here to view
| Discussion|| |
The results obtained in the present study showed the following: (1) The vasotonic response of PE or 5-HT in ED+ GSMA rings is potentiated due to the removal of endothelium that results in termination of direct vasorelaxation of endothelial NO; (2) ouabain augmented identically the PE/5-HT–induced maximal vasotonic effect in ED+ rings, but not in ED− rings. This augmentation of agonist-induced vasotonic response in ED+ ring by ouabain could be due to abolition of vasorelaxation effect of endothelium-dependent Na +-K +-ATPase; (3) K +-induced vasorelaxation in K +-free medium of ED+ rings was attenuated by ouabain (70%), which is identical to that in ED− rings (64%) and further supports that Na +-K +-ATPase is endothelium dependent in this tissues; and (4) 4-AP, a KV channel blocker, and Ba 2+, a KIR channel blocker, inhibited KCl-induced vasorelaxation in ED+ rings only by 16–18%, which was augmented fourfold in conjunction with ouabain, but did not exceed the attenuation of maximum vasorelaxation caused by ouabain only (70%).
The net augmentation of vascular contraction induced by different agonists may be due to loss of a tonic release of vasorelaxant factors such as endothelium-dependent relaxing factors (EDRF), viz. NO. In addition, EDHF can also modulate vasorelaxation via NO, prostaglandin I2, or arachidonic acid and its metabolites, which in turn opens big conductance calcium-activated K-channels (BKCa) or Na +, K + ions on vascular smooth muscle cells., The significant augmentation of the maximal contractile responses to both 5-HT and PE in ED− rings clearly supports the active involvement of EDRF or/and EDHF in GSMA rings, which is the same as that reported in human placental vessels. Interestingly, endothelium removal in goat mesenteric artery augmented the maximal contractile response to 5-HT and PE by threefold and twofold, respectively. This result clearly explains that endothelium-derived vasorelaxation factors possibly exhibited greater inhibitory effect on vasotonic response to 5-HT than PE. In several vascular beds, endothelium-derived factors such as EDRF and endothelium-dependent contracting factor (EDCF) differentially regulated the vasotonic responses to different agonists such as nor-adrenaline (NA) and 5-HT in rat, canine, and porcine coronary arteries, Angiotensin II in rat aorta, and histamine in human internal mammary artery, PE in rat aorta and superior mesenteric artery.
Furthermore, to assess the role of endothelium on the contractile response to ouabain, 5-HT/PE–induced contractile response was elicited in the presence of ouabain either in ED+ or ED− vessels. In the presence of ouabain, the maximal contractile response to either 5-HT or PE was increased by about threefold in ED+ but not in ED− GSMA rings. Thus, 5-HT- or PE-induced contractile responses were not enhanced further by ouabain in ED− rings. This clearly demonstrates that the vasodilatory effect of endothelium is ouabain sensitive in goat mesenteric artery. Endogenous ouabain may play an important role in regulating arterial tone and peripheral vascular resistance. Increase in maximal contractile response to either 5-HT or PE by ouabain observed in ED+ GSMA rings, does not agree with the myogenic action of this glycoside. The reduction of vasotonic effect by ouabain is due to the release of NO from the functional endothelium in coronary artery  or stimulation of inducible NO synthase expression in rat vascular smooth muscle cells  and rat aorta, rat tail artery, and rat mesenteric artery. Our present finding clearly contradicts this action of ouabain and demonstrates that in GSMA, reduction of maximal contractile response to either 5-HT or PE in ED+ vessels is due to direct or indirect activation of Na +-K +-ATPase and this is endothelium dependent.
We observed that only in ED+ mesenteric artery, there was significant influence of extracellular K + on the activation of sodium pump, and that small increase in the extracellular concentration of K + caused concentration-dependent relaxation in K +-free medium, confirming the function of endothelium-derived K + as a local intravascular vasodilator  as observed in rabbit aorta, rat resistance arteries  and rabbit arcuate arteries, and rat mesenteric artery, whereas findings from other studies conflicted with the proposed role of K + ion as an EDHF in porcine coronary arteries  and rat mesenteric artery. In addition, the endothelium has also been shown to regulate the Na +-K +-ATPase activity either by release of NO  or endothelial diffusible factors like leukotrienes and prostaglandins. Our results confirm that K +-induced vasorelaxation in goat mesenteric artery is predominantly endothelium dependent and this is due to activation of endothelial Na +-K +-ATPase as evidenced in human placental vessels, mice femoral artery, and in rat aorta. In small arteries like mesenteric bed, where the ratio of endothelium to smooth muscle increases, the endothelium plays a more important role in modulation of the expression of Na +-K +-ATPase.
KCl-induced relaxation in vascular smooth muscles may involve activation of sarcolemmal Na +-K +-ATPase  or inward rectifier K +-channels  or even both the mechanisms. One of the distinguishing features of vascular relaxation by K + involving Na +-K +-ATPase is that the extracellular concentration of K + is less than 5 mM, whereas inward rectifier K + channels primarily mediate K +-induced relaxation above the physiological K + concentration (>5 mM). In goat mesenteric arteries, we found that extracellular K + between 1 µM and 5 mM produced graded relaxation of the vessels bathed in K +-free solution and it was significantly inhibited by ouabain, a Na +-K +-ATPase inhibitor, suggesting that vasorelaxation is mediated by endothelial Na +-K +-ATPase and is ouabain sensitive.
The Na +-K +-ATPase α isoforms contain a highly conserved ouabain-binding site that mediates sensitivity to inhibition by cardiotonic steroids, such as ouabain and digoxin. In most mammals, all the α subunits are sensitive to ouabain inhibition with notable exceptions, i.e. guinea pig small intestine  and human cardiac muscle, in which ouabain-resistant α subunits have been reported. Attenuation of Na +-K +-ATPase activity by about 70% by ouabain in ED+ GMSA rings clearly suggests that vasorelaxation in this artery could be mediated predominantly by ouabain-sensitive α1 isoforms of Na +-K +-ATPase. In ovine pulmonary artery, both α1 and α2 isoforms of Na +-K +-ATPase have been reported to be present and possess low and high affinity, respectively, for ouabain. The low, but not the high, affinity isoforms of Na +-K +-ATPase by ouabain significantly increased the basal tone and 5-HT–induced contractility in this vessel.
Activation of the KIR channel and conduction of an outward K + current in response to small increases in extracellular K + is thought to occur because of unique gating properties of KIR channels, and larger increases in K + (by < 30 mM) cause smooth muscle depolarization and subsequent constriction of several arteries due to marked membrane depolarization and Ca 2+ entry via voltage-operated Ca 2+ channels. In the present study, we observed that K +-induced maximal vasorelaxation in goat mesenteric artery was inhibited (16–18%) by either 4-AP or Ba 2+ only. This suggests that there is an independent involvement of KV or KIR channels in addition to Na +-K +-ATPase in the vasorelaxation, as observed in goat ruminal artery. Conversely, in rat basilar artery, it was reported that Ba 2+ completely blocked K +-induced vasorelaxation. This discrepancy in the sensitivity to Ba 2+ to K +-induced vasorelaxation versus hyperpolarization could be related to either altered vascular response specific to mesenteric artery or an influence of several mediators that participate in ruminal contraction.
| Conclusion|| |
In conclusion, the vasorelaxation of goat mesenteric artery is mediated (i) predominantly by endothelium-dependent, ouabain-sensitive Na +-K +-ATPase, which could be an EDHF in goat mesenteric artery, and (ii) by activation of KV and KIR channels.
This work has been approved by institutional animal ethical committee (IAEC) and registered under Registration No. 433/CPCSEA for conducting animal tissue experiment. It was funded by a university research grant.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Giachini FR, Carneiro FC, Lima VV, Carneiro ZN, Brands MW, Webb RC, et al
. A key role for Na +/
-ATPase in the endothelium-dependent oscillatory activity of mouse small mesenteric arteries. Braz J Med Biol Res 2009;42:1058-67.
Dias FM, Ribeiro RF Jr, Fernandes AA, Fiorim J, Travaglia TC, Vassallo DV, et al
. Na +
-ATPase activity and K +
channels differently contribute to vascular relaxation in male and female rats. PLoS One 2014;9:e106345.
Edwards G, Félétou M, Weston AH. Endothelium-derived hyperpolarising factors and associated pathways: A synopsis. Pflugers Arch 2010;459:863-79.
Garland CJ, Hiley CR, Dora KA. EDHF: Spreading the influence of the endothelium. Br J Pharmacol 2011;164:839-52.
Sánchez-Ferrer CF, Fernández-Alfonso MS, Ponte A, Casado MA, González R, Rodríguez-Mañas L, et al
. Endothelial modulation of the ouabain-induced contraction in human placental vessels. Circ Res 1992;71:943-50.
Zhang J, Lee MY, Cavalli M, Chen L, Berra-Romani R, Balke CW, et al
. Sodium pump alpha2
subunits control myogenic tone and blood pressure in mice. J Physiol 2005;569:243-56.
Chen KH, Chen SJ, Wu CC. Regulation of Na +
-ATPase in rat aortas: Pharmacological and functional evidence. Chin J Physiol 2005;48:86-92.
Kathirvel K, Parija SC. Role of Na-K ATPase enzyme in vascular response of goat ruminal artery. Indian J Pharmacol 2009;41:68-71.
Sánchez-Ferrer CF, Ponte A, Casado MA, Rodríguez-Mañas L, Pareja A, González R, et al
. Endothelial modulation of the vascular sodium pump. J Cardiovasc Pharmacol 1993;22(Suppl 2):S99-101.
Lacy PS, Pilkington G, Hanvesakul R, Fish HJ, Boyle JP, Thurston H. Evidence against potassium as an endothelium-derived hyperpolarizing factor in rat mesenteric small arteries. Br J Pharmacol 2000;129:605-11.
Quignard JF, Félétou M, Thollon C, Vilaine JP, Duhault J, Vanhoutte PM. Potassium ions and endothelium-derived hyperpolarizing factor in guinea-pig carotid and porcine coronary arteries. Br J Pharmacol 1999;127:27-34.
Doughty JM, Boyle JP, Langton PD. Potassium does not mimic EDHF in rat mesenteric arteries. Br J Pharmacol 2000;130:1174-82.
Webb RC, Bohr DF. Potassium-induced relaxations as an indicator of Na +
- ATPase activity in vascular smooth muscle. Blood Vessels 1978;15:198-207.
Weston AH, Richards GR, Burnham MP, Félétou M, Vanhoutte PM, Edwards G. K +
-induced hyperpolarization in rat mesenteric artery: Identification, localization and role of Na +
-ATPases. Br J Pharmacol 2002;136:918-26.
Prior HM, Webster N, Quinn K, Beech DJ, Yates MS. K(+) induced dilation of a small renal artery: No role for inward rectifier K +
channels. Cardiovasc Res 1998;37:780-90.
Gupta S, Sussman I, McArthur CS, Tornheim K, Cohen RA, Ruderman NB. Endothelium-dependent inhibition of Na(+)-K+ATPase activity in rabbit aorta by hyperglycemia. Possible role of endothelium-derived nitric oxide. J Clin Invest 1992;90:727-32.
Cocks TM, Angus JA. Endothelium-dependent relaxation of coronary arteries by noradrenaline and serotonin. Nature 1983;305:627-30.
Bullock GR, Taylor SG, Weston AH. Influence of the vascular endothelium on agonist-induced contractions and relaxations in rat aorta. Br J Pharmacol 1986;89:819-30.
Schoeffter P, Dion R, Godfraind T. Modulatory role of the vascular endothelium in the contractility of human isolated internal mammary artery. Br J Pharmacol 1988;95:531-43.
Rossoni LV, Salaices M, Marin J, Vassallo DV, Alonso MJ. Alterations in phenylephrine-induced contractions and the vascular expression of Na +
, K +
-ATPase in ouabain-induced hypertension. Br J Pharmacol 2002;135:177-81.
Pulina MV, Zulian A, Berra-Romani R, Beskina O, Mazzocco-Spezzia A, Baryshnikov SG, et al
. Upregulation of Na +
and Ca 2+
transporters in arterial smooth muscle from ouabain-induced hypertensive rats. Am J Physiol Heart Circ Physiol 2010;298:H263-74.
Walker DW, McLean JR. Absence of adrenergic nerves in the human placenta. Nature 1971;229:344-5.
Xie J, Wang Y, Summer WR, Greenberg SS. Ouabain enhances basal release of nitric oxide from carotid artery. Am J Med Sci 1993;305:157-63.
Pacheco ME, Maria NJ, Manso AM, Rodríguez-Martínez MA, Briones A, Salaices M, et al
. Nitric oxide synthase induction by ouabain in vascular smooth muscle cells from normotensive and hypertensive rats. J Hypertens 2000;18:877-84.
Quayle JM, Nelson MT, Standen NB. ATP-sensitive and inwardly rectifying potassium channels in smooth muscle. Physiol Rev 1997;77:1165-232.
Rocafull MA, Romero FJ, Thomas LE, del Castillo JR. Isolation and cloning of the K +
-independent, ouabain-insensitive Na +
-ATPase. Biochim Biophys Acta 2011;1808:1684-700.
Wang J, Velotta JB, McDonough AA, Farley RA. All human Na(+)-K(+)-ATPase alpha-subunit isoforms have a similar affinity for cardiac glycosides. Am J Physiol Cell Physiol 2001;281:C1336-43.
Chanda D, Krishna AV, Gupta PK, Singh TU, Prakash VR, Sharma B, et al
. Role of low ouabain-sensitive isoform of Na +
-ATPase in the regulation of basal tone and agonist-induced contractility in ovine pulmonary artery. J Cardiol Pharmacol 2008;52:167-75.
Chrissobolis S, Ziogas J, Chu Y, Frank MF, Sobey CG. Role of inwardly rectifying K(+) channels in K(+)-induced cerebral vasodilatation in vivo
. Am J Physiol Heart Circ Physiol 2000;279:H2704-12.
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2]