Significance of KATP channels, L-type Ca2+ channels and CYP450-4A enzymes in oxygen sensing in mouse cremaster muscle arterioles In vivo
© Ngo et al.; licensee BioMed Central Ltd. 2013
Received: 24 October 2012
Accepted: 8 May 2013
Published: 12 May 2013
ATP-sensitive K+ channels (KATP channels), NO, prostaglandins, 20-HETE and L-type Ca2+ channels have all been suggested to be involved in oxygen sensing in skeletal muscle arterioles, but the role of the individual mechanisms remain controversial. We aimed to establish the importance of these mechanisms for oxygen sensing in arterioles in an in vivo model of metabolically active skeletal muscle. For this purpose we utilized the exteriorized cremaster muscle of anesthetized mice, in which the cremaster muscle was exposed to controlled perturbation of tissue P O2.
Change from “high” oxygen tension (P O2 = 153.4 ± 3.4 mmHg) to “low” oxygen tension (P O2 = 13.8 ± 1.3 mmHg) dilated cremaster muscle arterioles from 11.0 ± 0.4 μm to 32.9 ± 0.9 μm (n = 28, P < 0.05). Glibenclamide (KATP channel blocker) caused maximal vasoconstriction, and abolished the dilation to low oxygen, whereas the KATP channel opener cromakalim caused maximal dilation and prevented the constriction to high oxygen. When adding cromakalim on top of glibenclamide or vice versa, the reactivity to oxygen was gradually restored. Inhibition of L-type Ca2+ channels using 3 μM nifedipine did not fully block basal tone in the arterioles, but rendered them unresponsive to changes in P O2. Inhibition of the CYP450-4A enzyme using DDMS blocked vasoconstriction to an increase in P O2, but had no effect on dilation to low P O2.
We conclude that: 1) L-type Ca2+ channels are central to oxygen sensing, 2) KATP channels are permissive for the arteriolar response to oxygen, but are not directly involved in the oxygen sensing mechanism and 3) CYP450-4A mediated 20-HETE production is involved in vasoconstriction to high P O2.
In the microcirculation, the arterioles regulate tissue blood flow to maintain a close relationship between oxygen supply and demand . Changes in oxygen tension due to changes in the metabolic activity of tissues, particularly in skeletal muscle undergoing vast changes in performance, are believed to be crucial in the regulation of local blood flow. For example, skeletal muscle arterioles dilate/constrict when exposed to a decrease/increase in oxygen tension, thereby controlling the local blood flow to the tissue [1, 2].
The mechanisms by which changes in oxygen tension are sensed and converted into downstream signals that lead to vasomotor responses is known as oxygen sensing. Because of the importance of oxygen sensing for adjusting skeletal muscle blood flow, several studies have sought to determine its underlying molecular mechanisms. A number of studies have provided evidence which suggests the involvement of ATP-sensitive K+ channels (KATP channels) in the process [3–6], but a similar number of studies from other groups have failed to find evidence to support this notion [7–9]. As an alternative it has been suggested that hypoxia may act on the voltage-dependent L-type Ca2+ channels reducing the Ca2+ influx into the vascular smooth muscle cells (VSMCs) causing hypoxic vasodilation [9, 10]. Nitric oxide (NO) and certain prostaglandins are known to be important endothelium-derived vasodilators and may therefore also play a role in hypoxic vasodilation.
Hypoxic vasodilation may be viewed as a single O2-sensitive effector mechanism operating to continuously modify the basal tone of the vessel. However, the operation of dual control mechanisms, i.e. both hypoxic vasodilation and a separate mechanism primarily activated during high oxygen tension to cause vasoconstriction may contribute to an even more elaborate and efficient regulation of local blood flow. The vasoconstrictor 20-hydroxy-eicosatetraenoic acid (20-HETE), which is a ω-hydroxylation product of arachidonic acid produced by the CYP450-4A enzyme system in the presence of molecular oxygen, may be such a mechanism involved in hyperoxic vasoconstriction [11–14].
Many studies have been performed in vitro, and have focused on determining the role of a single mechanism for oxygen sensing. However, by examining several proposed mechanisms in an in vivo animal model during controlled physiological conditions we are able to study the integrated roles of the different mechanisms for oxygen sensing.
In the present study, we used the exteriorized cremaster muscle in anesthetized male mice. The influence of experimental procedures was minimized by doing only mild surgery under the influence of neurolept anesthesia, which is not known to have any major effects on cardiovascular function , and the diameter responses to local tissue oxygen perturbations were observed by intravital microscopy.
Since considerable controversy remains regarding the specific mechanisms responsible for oxygen sensing in skeletal muscle, the main purpose of this study was to address the specific roles of KATP channels, NO, prostaglandins, 20-HETE and L-type Ca2+ channels in this process.
Cremaster muscle preparation
All procedures and protocols were approved by the Danish Animal Care and Use Committee. Male C57BL/6J mice (body weight = 27.6 ± 0.7 g, n = 28; Taconic, DK-8680 Ry, Denmark) were anesthetized by i.p. injection with a mixture of droperidol (30.8 mg/kg), midazolam (4.0 mg/kg) and fentanyl (0.2 mg/kg) dissolved in saline (total volume given was 20 ml/kg). This same anesthetic mixture was used to maintain anesthesia, by continuous i.v. infusion with the rate of 20 ml/kg/h (syringe pump model 100, serial no. 671, KD Scientific, U.S.A). The mice were tracheotomized to maintain airway patency and the jugular vein was cannulated to allow for infusion of anesthesia and saline, while resting on top of the heated microscope stage. Using gentle dissection, the cremaster muscle with its blood perfusion intact was placed flat on top of a coverslip and fixed by sutures (Prolene 6-0, Ethicon Inc., Somerville, New Jersey, U.S.A.) attached to a silicone bank.
Superfusion of the cremaster muscle
The Krebs’ solutions (118.4 mM NaCl, 4.8 mM KCl, 2.5 mM CaCl2, 1.2 mM MgSO4, 25.0 mM NaHCO3 and 1.2 mM KH2PO4, pH range 7.35-7.45) were vigorously bubbled with 95% N2/5% CO2 or 21% O2/74% N2/5% CO2 gas mixtures to yield low or high oxygen tension Krebs’ solutions respectively. To minimize gas exchange between the superfusate in the supply tubing and the atmospheric air, the length of the tubing was kept at a minimum and thick-walled polyurethane tubing was used (Flexible Tubing 85 Durometer Polyurethane AP01T122PENA, Ark-Plas Products, Inc. Flippin, Arkansas). The superfusate was heated through an inline heater system (Inline heater Model SH-27B, automatic temperature controller TC-324B, Warner Instrument Corporation, Hamden, Connecticut) to a temperature of 34-36°C.
Vessel diameter measurement
The microcirculation of the cremaster muscle was visualized using a motorized Olympus BX50WI microscope with a fixed stage enabling free positioning of the 4× air- or 20× water-immersion objectives on top of the exteriorized cremaster muscle. The field was viewed on a monitor (Triniton, PWM 1442 QM, Sony, Tokyo, Japan) using a monochrome CCD camera (CCD72S, Dage-MTI Michigan City, IN), and images were recorded on a HDD-recorder (Pioneer DVD recorder DVR-530H) for later off-line analysis. The final magnification (20× objective) of the image was ~700× and the final pixel size was ~0.6 μm. The vessel diameter of the arteriole was measured offline as the external diameter in micrometers (μm).
Oxygen tension measurement
A fiber-optic oxygen microsensor system (Tapered tip sensor, tip diameter < 50 μm, Microx TX3 Oxygen Meter, PreSens, Regensburg, Germany) was used to measure oxygen tensions in the cremaster muscle microcirculation. The oxygen microsensor consists of a fiber-optic cable with a luminophore at the tip. The luminophore is excited by photons from the oxygen meter. Depending on the presence of molecular oxygen, either photons are reemitted from the luminophore and these are subsequently registered by the oxygen meter, or the energy from the activated luminophore is transferred to the oxygen molecules in the surrounding solution. Thus, the probe does not consume oxygen during the measurements, and consequently, does not by itself affect the oxygen levels within the cremaster muscle tissue. Calibration of the microsensor was performed with a two-point calibration in oxygen-free water prepared by diluting 4 g sodium dithionite (Na2S2O4) in 60 ml water in a beaker, and water vapor-saturated air prepared by placing wet cotton wool in another beaker. The output of the oxygen sensor is given as the partial oxygen tension in mmHg. All oxygen tension measurements were done with the tip of the oxygen microsensor placed on top of the cremaster muscle in the intersection between the cremaster muscle and the superfusate in close proximity (< 100 μm) to the arterioles under study. The tip, which is the active part of the oxygen microsensor, was always covered by Krebs’ solution and continuous measurements were done throughout the whole experiment with a 1 Hz sampling rate.
To study the mechanisms of oxygen sensing, different drugs were used. Cromakalim (1 and 5 μM), an activator of KATP channels, glibenclamide (10 and 100 μM), an inhibitor of KATP channels and nifedipine (3 and 30 μM), a Ca2+ antagonist, which inhibits voltage-dependent L-type Ca2+ channels, were used to study the role of KATP channels and L-type Ca2+ channels. Dibromo-dodecenyl-methylsulfimide (DDMS, 10 μM), an inhibitor of the cytochrome P450-4A enzyme system (CYP450-4A), was used to study the role of 20-HETE. The role of prostaglandins was studied by using indomethacin (28 μM), an inhibitor of cyclooxygenase. L-NAME (100 μM), an inhibitor of NO-synthases, was used to study the role of NO. Papaverine (100 μM), a smooth muscle cell relaxant, was used to maximally dilate the arterioles to obtain the passive diameter of the arterioles. Cromakalim, glibenclamide and indomethacin were dissolved in dimethyl sulfoxide (DMSO, 0.3%) prior to adding to the Krebs’ solution. The other drugs were dissolved directly in Krebs’ solution. Cromakalim, glibenclamide, indomethacin, L-NAME, nifedipine and papaverine were bought from Sigma-Aldrich, Copenhagen, Denmark, whereas DDMS was bought from Cayman chemical, Michigan, USA.
After preparation of the exteriorized cremaster muscle, the tissue was superfused with low oxygen Krebs’ solution and the preparation was allowed to rest for the next 15-20 minutes to obtain steady state. Subsequently, hyperoxic vasoconstriction and hypoxic vasodilation was induced by superfusing the cremaster muscle with Krebs’ solution containing high or low oxygen tension, respectively. Among several cremaster muscle arterioles (diameter < 40 μm) showing both hyperoxic vasoconstriction and hypoxic vasodilation, one or two arterioles were randomly picked for further study.
The experimental protocol was as follows. During the control period the cremaster muscle was exposed to low oxygen tension followed by high oxygen tension two or three times. Then the cremaster muscle was exposed to low oxygen tension and high oxygen tension in the presence of drugs, and this was repeated at least once. In some experiments two different drugs were added, in other experiments cumulative concentrations of the same drug were added. Afterwards the cremaster muscle was exposed to low oxygen and high oxygen tensions without drugs (wash-out period). At the end of the experiments papaverine was superfused to yield the maximal vessel diameter.
One or two arterioles were studied per mouse and the outer vessel diameters (D) were measured. ΔD = D low oxygen – D high oxygen , where D low oxygen is vessel diameter during low oxygen tension and D high oxygen is vessel diameter during high oxygen tension. All results are presented as mean ± SEM. Statistical comparisons were performed by paired two-tailed Student’s t- test or one-way ANOVA repeated measures with Holm-Sidak method as post-hoc analysis. P-values < 0.05 were considered as statistically significant.
The summarized effects of exposure to low, high oxygen tension and during application of 100 μM papaverine on arteriolar diameter (Mean ± SEM, *p < 0.05 vs. high oxygen and papaverine, †p < 0.05 vs. low oxygen and papaverine, ‡p < 0.05 vs. low oxygen and high oxygen, n = 28)
n = 28
100 μM papaverine
32.9 ± 0.9 μm *
11.0 ± 0.4 μm †
37.5 ± 1.3 μm ‡
13.8 ± 1.3 mmHg
153.4 ± 3.4 mmHg
21.5 ± 1.9 mmHg
Role of KATP channels
Role of 20-HETE
Role of L-type Ca2+ channels
Both KATP channels and 20-HETE [4, 11] cause vasomotor responses through changes in VSMC membrane potential and voltage-dependent L-type Ca2+ channels are therefore a central part of their signaling pathways. Moreover, L-type Ca2+ channels have been proposed to be sensitive to changes in the oxygen tension [9, 10].
Role of prostaglandins and NO-synthase
According to a prominent hypothesis for the mechanism of oxygen sensing in the microcirculation, low oxygen tension opens KATP channels in VSMCs due, at least in part, to an increase in the ADP/ATP concentration ratio. This leads to efflux of K+ and hyperpolarization of the cell, which in turn inhibits the influx of Ca2+ through the voltage-gated L-type Ca2+ channels leading to smooth muscle relaxation and eventually vasodilation [3, 18, 19]. In apparent agreement with this notion the present study shows that hypoxic vasodilation was completely inhibited by glibenclamide, and the reactivity could be restored gradually by increasing concentrations of the KATP channel activator cromakalim (1 μM and 5 μM cromakalim). Likewise cromakalim alone caused maximal vasodilation and a complete loss of hyperoxic vasoconstriction, which was gradually restored by application of 10 μM and 100 μM glibenclamide.
Importantly, however, studies by Jackson have provided evidence against the direct involvement of KATP channels in hypoxic vasodilation . Jackson showed that low oxygen tension, in a glibenclamide sensitive manner, inhibited norepinephrine-induced contraction in VSMCs from hamster cremaster muscle arterioles. However, the effect of low oxygen tension was neither associated with a change of the whole-cell conductance nor of the membrane potential of the VSMCs , which clearly argues against the opening of K+ channels. Instead it was suggested that the reported effect of glibenclamide was unspecific, possibly related to a drug-induced membrane depolarization .
The results of the present study are therefore difficult to reconcile with a direct role for KATP channels in oxygen sensing in cremaster muscle arterioles. The most likely explanation of the present results appears to be that the effects of glibenclamide and cromakalim, both when applied alone and in combination, are mediated indirectly through changes in the membrane potential. In cremaster muscle VSMCs glibenclamide applied alone closes KATP channels, and depolarizes the cell membrane . This will activate the L-type Ca2+ channels, and constrict the vessels. We hypothesize that if the membrane depolarization is pronounced, the activation of the L-type channels will be sufficient, even in the presence of hypoxia, to elicit maximal vasoconstriction. The addition of cromakalim antagonizes the effect of glibenclamide and the membrane potential will gradually become more negative as the KATP channels are reactivated . This will partially deactivate the L-type Ca2+ channels due to the steep voltage-dependence of their gating behavior in the physiological range of membrane potentials (–60 to –30 mV), and eventually render them responsive towards the effects of hypoxia. When cromakalim is added alone to maximally activate the KATP channels, the membrane will be hyperpolarized and the L-type Ca2+ channels closed. The vessel will therefore be close to maximally dilated, and once more irresponsive to changes in oxygen levels.
These apparently competitive actions of glibenclamide and cromakalim on the KATP channels are in line with previous ex vivo as well as in vivo observations. In isolated porcine coronary artery, the concentration-response curve of glibenclamide was right-shifted in the presence of cromakalim demonstrating a competitive action of these drugs on KATP channels . In an elaborate in vivo study in rats, Gardiner et al showed that the hindquarter skeletal muscle blood flow was increased significantly by levcromakalim, and that this was reversibly antagonized by glibenclamide, demonstrating that glibenclamide and a cromakalim analogue have reversible and competitive actions on local blood flow in rat skeletal muscle in vivo. Similar effects were obtained in the mesenteric and renal circulations . However, in an early pharmacological study glibenclamide (IC50 148 nM) was able to block cromakalim (0.5 μM) induced relaxation of isolated rabbit superior mesenteric artery . As we have used much higher concentrations of these drugs due to the fact that it was an in vivo study, we speculate that only at sufficiently high concentrations are cromakalim able to compete with the actions of glibenclamide on KATP channels. We find it unlikely that the observed effects represent unspecific effects due to the high concentrations of the respective drugs. However, we cannot rule out this possibility, and it is clearly a limitation of the present in vivo study.
The results of the glibenclamide/cromakalim experiments show that oxygen sensing depends critically on the level of the membrane potential, and this suggest that voltage gated L-type Ca2+ channels could play a central role in the mechanism. As is apparent from Figure 6, this was indeed the case. In the presence of medium (3 μM) to high (30 μM) concentrations of nifedipine, there was no significant difference in vessel diameter between high and low oxygen tension. The failure to dilate in response to hypoxia was not due to a complete loss of vessel tone as indicated by the fact that even in the presence of 3 μM nifedipine, the vessels were still able to dilate further when papaverine was added to the superfusate. L-type Ca2+ channels are only one of several Ca2+ entry mechanisms in VSMCs, and it is therefore not surprising that the vessels are able to retain tone despite the presence of nifedipine. This suggests that the failure to dilate in response to hypoxia was not due to a complete loss of vessel tone, but rather due to the inhibition of the L-type Ca2+ channels. When given at a high concentration (30 μM) nifedipine had a more pronounced effect on vascular tone, and this effect was irreversible within the time limit of the washout period. The fact that changes in Ca2+ influx through the L-type channels appears to be involved in oxygen sensing does not indicate that the change in influx is mediated by changes in the membrane potential. Previous studies have suggested that hypoxia could induce vasodilation by acting directly on the voltage operated L-type Ca2+ channels, reducing Ca2+ influx [9, 10]. Our findings therefore show that L-type Ca2+ channels are central for the oxygen sensing mechanism, but they do not allow us to discriminate between a direct action of oxygen on the channels, and an indirect effect mediated through changes in membrane potential.
20-HETE has been proposed to be involved in oxygen sensing by acting as a vasoconstrictor. It is produced in the VSMCs by the CYP450-4A enzyme system with arachidonic acid as a substrate. In the presence of oxygen, CYP450-4A oxidizes arachidonic acid to 20-HETE. The K m for oxygen is approximately 55 μM at 37°C . This value corresponds to an oxygen tension of around 40 mmHg, which is above the normal values in skeletal muscle [2, 23–25]. The synthesis of 20-HETE is therefore partially limited by the availability of oxygen, and an increased oxygen tension will lead to an increased production rate for 20-HETE. 20-HETE inhibits large-conductance Ca2+-activated K+ channels (BKCa channels) located in the plasma membrane of VSMCs, which leads to depolarization of the cell. This in turn activates voltage-dependent L-type Ca2+ channels, increasing influx of Ca2+ and causing contraction of the VSMCs and eventually vasoconstriction [11, 12, 14]. Evidence supporting this includes a patch clamp study on cat cerebral microvessel VSMCs  and an intravital microscopy study of rat cremaster muscle arterioles, showing inhibition of hyperoxic vasoconstriction by 17-octadecynoic acid (17-ODYA), an inhibitor of CYP450-4A . In our preparation, inhibition of 20-HETE production using 10 μM DDMS inhibited vasoconstriction to high oxygen tension in a reversible manner, but did not affect vasodilation to low oxygen tension (Figure 5). Previous studies have shown that vessels maintain their reactivity to vasoconstrictors (norepinephrine) following addition of DDMS , and in the present study the vessels maintained some tone after addition of DDMS. It is therefore unlikely that the lack of response to high oxygen reflects a general failure of the VSMC to contract. The results show that 20-HETE plays a role in vasoconstriction to high oxygen tension in mouse cremaster muscle arterioles, but has no role in hypoxic vasodilation. Since 20-HETE acts as a vasoconstrictor through inhibition of BKCa channels and/or stimulation of TRPC6 channels [27, 28], it is interesting that specific activation of the KATP channels using cromakalim was able to abolish hyperoxic vasoconstriction (Figure 4A & B). This further strengthens the notion that the effect on oxygen sensing of blocking the KATP channels is indirect. When the KATP channels are activated by addition of cromakalim the membrane hyperpolarizes, and we expect that inhibition of the BKCa channels by 20-HETE will not be able to depolarize the membrane sufficiently to elicit vasoconstriction.
Vasodilator prostaglandins PGE2 and PGI2 (prostacyclin) and NO released from the vascular endothelium play important roles in regulating vascular tone in the microcirculation [29–33]. Release of prostaglandins and NO has been proposed to occur during low oxygen tension, and these substances could contribute to oxygen sensing [34–38]. Evidence of prostaglandins as effectors of hypoxic vasodilation comes from in vitro studies on isolated arterioles, where inhibition of cyclooxygenase using indomethacin inhibited hypoxic vasodilation [37, 38]. Moreover, skeletal muscle contraction-induced vasodilation in hamster cremaster muscle arterioles paired with venules was blocked by indomethacin in vivo.
In our study, inhibition of prostaglandin synthesis by application of 28 μM indomethacin (Figure 7), acutely inhibited vasodilation during low oxygen, but after ~2-3 minutes (steady state) the arterioles had regained their responsiveness, and dilated to low oxygen with a response comparable to the control. The transient reduction in the vessel diameter was probably due to a sudden disruption of a constitutive release of vasodilator prostaglandins causing a transient vasoconstriction. Alternatively, the rate of vasodilation to hypoxia could be severely slowed by the acute lack of prostaglandins. However the vessels quickly regained their responsiveness to low oxygen tension, indicating that prostaglandins are not involved in the steady state mechanism of hypoxic vasodilation. In a previous in vivo study, indomethacin inhibited contraction-induced dilation of 3rd order arterioles paired to venules in the hamster cremaster muscle, but had no effect on unpaired 3rd order arterioles. It was therefore suggested that prostaglandins, released from the venules and diffusing to the arterioles, participate in the vasodilator response during muscular contraction . In our study, only unpaired 3rd order arterioles were examined, and in good agreement with the findings of Hammer et al., we did not find evidence for the involvement of prostaglandins in unpaired arterioles in hypoxic vasodilation.
In the present study we tested whether NO was released during low oxygen tension by additional application of 100 μM L-NAME, a concentration which we formerly have shown to effectively abolish bradykinin-induced vasodilation in the mouse cremaster muscle microcirculation in situ. In the presence of indomethacin and L-NAME the vessels responded with vasodilation and constriction to low and high oxygen tension as during the control, indicating that NO is not involved in hypoxic vasodilation in mouse cremaster muscle arterioles. This is in good agreement with recent studies from our laboratory, where application of L-NAME did not affect vasomotor responses to low or high oxygen tension [6, 39].
The exteriorized cremaster muscle preparation is a well-established in vivo model for studying the microcirculation of skeletal muscles. Several studies have investigated the effect of tissue oxygen tension perturbations on vascular responses caused by superfusion of the cremaster muscle with physiological salt solutions equilibrated with gas mixtures with different % O2, balanced with N2 and 5% CO2[40–42]. When the oxygen levels are low the superfusate acts as an “oxygen-sink”, and the tissue oxygen tension is reduced. Conversely, the tissue oxygen tension is increased by elevating the P O2 of the superfusate, which now behaves as an “oxygen-source” [43, 44]. We recently showed that, when the oxygen microsensor tip was placed below the cremaster muscle, a decrease or increase in oxygen tension could be measured that mirrored changes in the superfusate oxygen tension above the tissue . This provides an efficient method for studying the influence of tissue oxygen tensions in the microcirculation of a living animal, and allows changing the oxygen tension locally in the cremaster muscle independently of the oxygen supplied by the vessels. The preparation, on the other hand, does not allow us to determine whether the responses are mediated by oxygen acting directly on the proteins in question, or whether the changes in oxygen levels exert their effect through changes in the production of various metabolites. Nor is it possible to determine the specific cellular location of the signaling pathways, i.e. if they are strictly intravascular or whether they involve the parenchymal cells as well.
In conclusion, this in vivo study supports the notion that KATP channels are permissive for the response to oxygen by controlling the membrane potential in cremaster muscle VSMCs, whereas the activity of L-type Ca2+ channels are central to the oxygen sensing mechanism. As an additional mechanism, 20-HETE mediates hyperoxic vasoconstriction. Our conclusions are highlighted by the fact that blockade of L-type Ca2+ channels, which constitute a common pathway for the two mechanisms, inhibited both vasodilation and constriction to low and high oxygen tensions, respectively. In contrast, the lack of effects of inhibiting two major endothelial-derived vasodilator metabolites, prostaglandins and NO, suggests that these pathways are not involved in hypoxic vasodilation in mouse cremaster muscle arterioles in vivo.
This study was supported by grants from the Danish Medical Research Council for Health and Disease, the Novo-Nordisk Foundation, the Lundbeck Foundation and the Danish Heart Association.
- Segal SS: Regulation of blood flow in the microcirculation. Microcirculat 2005, 12: 33-45. 10.1080/10739680590895028View ArticleGoogle Scholar
- Duling BR, Berne RM: Longitudinal gradients in periarteriolar oxygen tension. A possible mechanism for the participation of oxygen in local regulation of blood flow. Circ Res 1970, 27: 669-678. 10.1161/01.RES.27.5.669View ArticlePubMedGoogle Scholar
- Dart C, Standen NB: Activation of ATP-dependent K + channels by hypoxia in smooth muscle cells isolated from the pig coronary artery. J Physiol 1995,483(Pt 1):29-39.View ArticlePubMedPubMed CentralGoogle Scholar
- Daut J, Maier-Rudolph W, von Beckerath N, Mehrke G, Gunther K, Goedel-Meinen L: Hypoxic dilation of coronary arteries is mediated by ATP-sensitive potassium channels. Science 1990, 247: 1341-1344. 10.1126/science.2107575View ArticlePubMedGoogle Scholar
- Liu Q, Flavahan NA: Hypoxic dilatation of porcine small coronary arteries: role of endothelium and KATP-channels. Br J Pharmacol 1997, 120: 728-734. 10.1038/sj.bjp.0700939View ArticlePubMedPubMed CentralGoogle Scholar
- Ngo AT, Jensen LJ, Riemann M, Holstein-Rathlou NH, Torp-Pedersen C: Oxygen sensing and conducted vasomotor responses in mouse cremaster arterioles in situ . Pflug Arch 2010, 460: 41-53. 10.1007/s00424-010-0837-xView ArticleGoogle Scholar
- Archer SL, Rusch NJ: Potassium channels in cardiovascular biology. 2001, 505-522.View ArticleGoogle Scholar
- Gauthier KM: Hypoxia-induced vascular smooth muscle relaxation: increased ATP-sensitive K + efflux or decreased voltage-sensitive Ca2+ influx? Am J Physiol Heart Circ Physiol 2006, 291: H24-H25. 10.1152/ajpheart.00260.2006View ArticlePubMedGoogle Scholar
- Jackson WF: Hypoxia does not activate ATP-sensitive K + channels in arteriolar muscle cells. Microcirculation 2000, 7: 137-145.View ArticlePubMedPubMed CentralGoogle Scholar
- Franco-Obregon A, Urena J, Lopez-Barneo J: Oxygen-sensitive calcium channels in vascular smooth muscle and their possible role in hypoxic arterial relaxation. Proc Natl Acad Sci U S A 1995, 92: 4715-4719. 10.1073/pnas.92.10.4715View ArticlePubMedPubMed CentralGoogle Scholar
- Harder DR, Gebremedhin D, Narayanan J, Jefcoat C, Falck JR, Campbell WB, Roman R: Formation and action of a P-450 4A metabolite of arachidonic acid in cat cerebral microvessels. Am J Physiol 1994, 266: H2098-H2107.PubMedGoogle Scholar
- Harder DR, Narayanan J, Birks EK, Liard JF, Imig JD, Lombard JH, Roman RJ: Identification of a putative microvascular oxygen sensor. Circ Res 1996, 79: 54-61. 10.1161/01.RES.79.1.54View ArticlePubMedGoogle Scholar
- Kunert MP, Roman RJ, Onso-Galicia M, Falck JR, Lombard JH: Cytochrome P-450 omega-hydroxylase: a potential O(2) sensor in rat arterioles and skeletal muscle cells. Am J Physiol Heart Circ Physiol 2001, 280: H1840-H1845.PubMedGoogle Scholar
- Wang J, Schmidt JR, Roman RJ, Anjaiah S, Falck JR, Lombard JH: Modulation of vascular O2 responses by cytochrome 450-4A omega-hydroxylase metabolites in Dahl salt-sensitive rats. Microcirculat 2009, 16: 345-354. 10.1080/10739680802698007View ArticleGoogle Scholar
- Jarnberg PO, Santesson J, Eklund J: Renal function during neurolept anaesthesia. Acta Anaesthesiol Scand 1978, 22: 167-172. 10.1111/j.1399-6576.1978.tb01294.xView ArticlePubMedGoogle Scholar
- Hammer LW, Ligon AL, Hester RL: Differential inhibition of functional dilation of small arterioles by indomethacin and glibenclamide. Hypertension 2001, 37: 599-603. 10.1161/01.HYP.37.2.599View ArticlePubMedGoogle Scholar
- Saito Y, Eraslan A, Hester RL: Role of endothelium-derived relaxing factors in arteriolar dilation during muscle contraction elicited by electrical field stimulation. Microcirculation 1994, 1: 195-201. 10.3109/10739689409148274View ArticlePubMedGoogle Scholar
- Rodrigo GC, Standen NB: ATP-sensitive potassium channels. Curr Pharm Des 2005, 11: 1915-1940. 10.2174/1381612054021015View ArticlePubMedGoogle Scholar
- Seino S, Miki T: Physiological and pathophysiological roles of ATP-sensitive K + channels. Prog Biophys Mol Biol 2003, 81: 133-176. 10.1016/S0079-6107(02)00053-6View ArticlePubMedGoogle Scholar
- Balwierczak JL, Krulan CM, Kim HS, DelGrande D, Weiss GB, Hu S: Evidence that BKCa channel activation contributes to K + channel opener induced relaxation of the porcine coronary artery. Naunyn Schmiedebergs Arch Pharmacol 1995, 352: 213-221.View ArticlePubMedGoogle Scholar
- Gardiner SM, Kemp PA, March JE, Fallgren B, Bennett T: Effects of glibenclamide on the regional haemodynamic actions of alpha-trinositol and its influence on responses to vasodilators in conscious rats. Br J Pharmacol 1996, 117: 507-515. 10.1111/j.1476-5381.1996.tb15219.xView ArticlePubMedPubMed CentralGoogle Scholar
- Meisheri KD, Khan SA, Martin JL: Vascular pharmacology of ATP-sensitive K + channels: interactions between glyburide and K + channel openers. J Vasc Res 1993, 30: 2-12.PubMedGoogle Scholar
- Boegehold MA, Johnson PC: Periarteriolar and tissue PO2 during sympathetic escape in skeletal muscle. Am J Physiol 1988, 254: H929-H936.PubMedGoogle Scholar
- Johnson PC, Vandegriff K, Tsai AG, Intaglietta M: Effect of acute hypoxia on microcirculatory and tissue oxygen levels in rat cremaster muscle. J Appl Physiol 2005, 98: 1177-1184. 10.1152/japplphysiol.00591.2004View ArticlePubMedGoogle Scholar
- Lash JM, Bohlen HG: Perivascular and tissue PO2 in contracting rat spinotrapezius muscle. Am J Physiol 1987, 252: H1192-H1202.PubMedGoogle Scholar
- Raffai G, Wang J, Roman RJ, Anjaiah S, Weinberg B, Falck JR, Lombard JH: Modulation by cytochrome P450-4A omega-hydroxylase enzymes of adrenergic vasoconstriction and response to reduced PO(2) in mesenteric resistance arteries of Dahl salt-sensitive rats. Microcirculat 2010, 17: 525-535.Google Scholar
- Basora N, Boulay G, Bilodeau L, Rousseau E, Payet MD: 20-hydroxyeicosatetraenoic acid (20-HETE) activates mouse TRPC6 channels expressed in HEK293 cells. J Biol Chem 2003, 278: 31709-31716. 10.1074/jbc.M304437200View ArticlePubMedGoogle Scholar
- Inoue R, Jensen LJ, Jian Z, Shi J, Hai L, Lurie AI, Henriksen FH, Salomonsson M, Morita H, Kawarabayashi Y, Mori M, Mori Y, Ito Y: Synergistic activation of vascular TRPC6 channel by receptor and mechanical stimulation via phospholipase C/diacylglycerol and phospholipase A2/omega-hydroxylase/20-HETE pathways. Circ Res 2009, 104: 1399-1409. 10.1161/CIRCRESAHA.108.193227View ArticlePubMedGoogle Scholar
- Duffy SJ, Castle SF, Harper RW, Meredith IT: Contribution of vasodilator prostanoids and nitric oxide to resting flow, metabolic vasodilation, and flow-mediated dilation in human coronary circulation. Circulation 1999, 100: 1951-1957. 10.1161/01.CIR.100.19.1951View ArticlePubMedGoogle Scholar
- Huang A, Sun D, Koller A: Shear stress-induced release of prostaglandin H(2) in arterioles of hypertensive rats. Hypertension 2000, 35: 925-930. 10.1161/01.HYP.35.4.925View ArticlePubMedGoogle Scholar
- Koller A, Huang A: Development of nitric oxide and prostaglandin mediation of shear stress-induced arteriolar dilation with aging and hypertension. Hypertension 1999, 34: 1073-1079. 10.1161/01.HYP.34.5.1073View ArticlePubMedGoogle Scholar
- Koller A, Huang A: Impaired nitric oxide-mediated flow-induced dilation in arterioles of spontaneously hypertensive rats. Circ Res 1994, 74: 416-421. 10.1161/01.RES.74.3.416View ArticlePubMedGoogle Scholar
- Nicholson WT, Vaa B, Hesse C, Eisenach JH, Joyner MJ: Aging is associated with reduced prostacyclin-mediated dilation in the human forearm. Hypertension 2009, 53: 973-978. 10.1161/HYPERTENSIONAHA.108.121483View ArticlePubMedPubMed CentralGoogle Scholar
- Edmunds NJ, Marshall JM: Oxygen delivery and oxygen consumption in rat hindlimb during systemic hypoxia: role of adenosine. J Physiol 2001, 536: 927-935. 10.1111/j.1469-7793.2001.00927.xView ArticlePubMedPubMed CentralGoogle Scholar
- Edmunds NJ, Moncada S, Marshall JM: Does nitric oxide allow endothelial cells to sense hypoxia and mediate hypoxic vasodilatation? In vivo and in vitro studies. J Physiol 2003, 546: 521-527. 10.1113/jphysiol.2002.023663View ArticlePubMedPubMed CentralGoogle Scholar
- Edmunds NJ, Marshall JM: The roles of nitric oxide in dilating proximal and terminal arterioles of skeletal muscle during systemic hypoxia. J Vasc Res 2003, 40: 68-76. 10.1159/000068941View ArticlePubMedGoogle Scholar
- Goodwill AG, James ME, Frisbee JC: Increased vascular thromboxane generation impairs dilation of skeletal muscle arterioles of obese Zucker rats with reduced oxygen tension. Am J Physiol Heart Circ Physiol 2008, 295: H1522-H1528. 10.1152/ajpheart.00596.2008View ArticlePubMedPubMed CentralGoogle Scholar
- Messina EJ, Sun D, Koller A, Wolin MS, Kaley G: Role of endothelium-derived prostaglandins in hypoxia-elicited arteriolar dilation in rat skeletal muscle. Circ Res 1992, 71: 790-796. 10.1161/01.RES.71.4.790View ArticlePubMedGoogle Scholar
- Riemann M, Rai A, Ngo AT, Dziegiel MH, Holstein-Rathlou NH, Torp-Pedersen C: Oxygen-dependent vasomotor responses are conducted upstream in the mouse cremaster microcirculation. J Vasc Res 2011, 48: 79-89. 10.1159/000318777View ArticlePubMedGoogle Scholar
- Baudry N, Danialou G, Boczkowski J, Vicaut E: In vivo study of the effect of systemic hypoxia on leukocyte-endothelium interactions. Am J Respir Crit Care Med 1998, 158: 477-483. 10.1164/ajrccm.158.2.9701074View ArticlePubMedGoogle Scholar
- Frisbee JC, Lombard JH: Elevated oxygen tension inhibits flow-induced dilation of skeletal muscle arterioles. Microvasc Res 1999, 58: 99-107. 10.1006/mvre.1999.2169View ArticlePubMedGoogle Scholar
- Frisbee JC: Regulation of in situ skeletal muscle arteriolar tone: interactions between two parameters. Microcirculat 2002, 9: 443-462.Google Scholar
- Klitzman B, Popel AS, Duling BR: Oxygen transport in resting and contracting hamster cremaster muscles: experimental and theoretical microvascular studies. Microvasc Res 1983, 25: 108-131. 10.1016/0026-2862(83)90047-XView ArticlePubMedGoogle Scholar
- Popel AS: Mathematical-modeling of oxygen-transport near a tissue surface - effect of the surface Po2. Mathematical Biosci 1981, 55: 231-246. 10.1016/0025-5564(81)90097-3View ArticleGoogle Scholar
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