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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical and experimental pharmacology and physiology 23 (1996), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Melbourne, Australia : Blackwell Science Pty
    Clinical and experimental pharmacology and physiology 27 (2000), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 1. Arachidonic acid (AA) is metabolized by cytochrome P450 (CYP)-dependent pathways to epoxyeicosatrienoic acids (EET) and 20-hydroxyeicosatetraenoic acid (20-HETE) in the kidney and the peripheral vasculature.2. The present short review summarizes the renal and cardiovascular actions of these important mediators.3. Epoxyeicosatrienoic acids are vasodilators produced by the endothelium that hyperpolarize vascular smooth muscle (VSM) cells by opening Ca2+-activated K+ (KCa) channels. 20-Hydroxyeicosatetraenoic acid is a vasoconstrictor that inhibits the opening of KCa channels in VSM cells. Cytochrome P450 4A inhibitors block the myogenic response of small arterioles to elevations in transmural pressure and autoregulation of renal and cerebral blood flow in vivo. Cytochrome P450 4A blockers also attenuate the vasoconstrictor response to elevations in tissue PO2, suggesting that this system may serve as a vascular oxygen sensor. Nitric oxide and carbon monoxide inhibit the formation of 20-HETE and a fall in 20-HETE levels contributes to the activation of KCa channels in VSM cells and the vasodilator response to these gaseous mediators. 20-Hydroxyeicosatetraenoic acid also mediates the inhibitory actions of peptide hormones on sodium transport in the kidney and the mitogenic effects of growth factors in VSM and mesangial cells. A deficiency in the renal production of 20-HETE is associated with the development of hypertension in Dahl salt-sensitive rats.4. In summary, the available evidence indicates that CYP metabolites of AA play a central role in the regulation of renal, pulmonary and vascular function and that abnormalities in this system may contribute to the pathogenesis of cardiovascular diseases.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] In most arterial beds a significant endothelium-dependent dilation to various stimuli persists even after inhibition of nitric oxide synthase and cyclo-oxygenase. This dilator response is preceded by an endothelium-dependent hyperpolarization of vascular smooth muscle cells, which is sensitive ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 394 (1982), S. 182-185 
    ISSN: 1432-2013
    Keywords: Rat middle cerebral artery ; pH,P CO 2 ; Membrane potential ; K+ conductance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Some membrane electrical properties of muscle cells from the middle cerebral artery of the rat were recorded with intracellular microelectrodes. The resting membrane potential (E m) of this preparation was −63 mV. Reduction of extracellular pH to 7.0 in the face of a constantP CO 2of 40 mm Hg had no significant effect onE m. Similarly the slope of the steady-state voltage/current curves was not different at pH 7.0 compared to control at pH 7.4. In marked contrast, whenP CO 2was elevated to around 60 to 70 mm Hg there was a rapid hyperpolarization and reduction in the slope of the voltage current curve suggesting an increased conductance for one or more ionic species. In addition elevation ofP CO 2increased the slope of theE m vs. log[K]0 curve from 46 mV/decade to 59 m V/decade which is in good agreement with a Nernstian potential for a K+ selective membrane. These data suggest that while the smooth muscle cells of rat cerebral arteries are relatively insensitive to a small reduction in extracellular pH; reduction of intracellular pH by elevatingP CO 2induces hyperpolarization by increasing K+ conductance (g k). However, it is not clear from these experiments if theP CO 2effects are mediated entirely by changes in pH or if there is a direct membrane action of CO2.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 378 (1978), S. 111-119 
    ISSN: 1432-2013
    Keywords: Arterial vascular smooth muscle ; Membrane potentials ; Potassium conductance ; Barium effect ; Tetraethylammonium effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Some electrical membrane properties of an isolated small artery, namely, the superior mesenteric artery of the guinea pig, were studied by intracellular microelectrodes. The mean resting membrane potential (E m) was −54 mV. The average slope of theE m vs. log [K]o curve (between 10 and 100 mM [K]o) was 32 mV/decade, and the curve extrapolated to a [K]i of 160 mM. The ratio of Na+ permeability to K+ permeability (P Na/P K) at 4.0 mM [K]o calculated from the Goldman constant-field equation (assuming Cl− to be passively distributed) was 0.18 (E m=−46 mV after a 5 min exposure to ouabain to suppress any electrogenic pump potential). The normal input resistance (R in) averaged 8.5 mΩ. Choline substitution for Na+ or amiloride, an agent known to depressP Na, hyperpolarized the muscle to about −63 mV without a significant change inR in. Ba2+ (0.5 mM) depolarized the muscle to −37 mV, increasedR in to 15 mΩ, and produced spontaneous action potentials in this normally quiescent artery; tetraethylammonium (TEA, 5 mM) enabled large overshooting action potentials to be produced upon stimulation. Glutamate of NO 3 − substitution for Cl− produced an initial depolarization followed by a return to the original resting potential within 10 min; readdition of 25 mM Cl− transiently hyperpolarized the muscle markedly, followed by a return to the originalE m. These data indicate that Cl− is passively distributed and does not contribute to the steady-state resting potential in this vascular muscle. The data also suggest that the relatively lowE m in this arterial muscle is not due to a low [K]i, but is due to a highP Na/P K ratio, presumably related to a low K+ conductance (g K). Since Ba2+ and TEA+ are known to decrease restingg K and K+ activation, the data also suggest that K+ activation could inhibit action potential generation.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-2013
    Keywords: Cerebral circulation ; Vasodilation ; Hypoxia ; Ca2+-sensitive K+ channel ; Patch clamp
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The cellular mechanisms mediating hypoxia-induced dilation of cerebral arteries have remained unknown, but may involve modulation of membrane ionic channels. The present study was designed to determine the effect of reduced partial pressure of O2, PO 2, on the predominant K+ channel type recorded in cat cerebral arterial muscle cells, and on the diameter of pressurized cat cerebral arteries. A K+-selective single-channel current with a unitary slope conductance of 215 pS was recorded from excised inside-out patches of cat cerebral arterial muscle cells using symmetrical KCl (145 mM) solution. The open state probability (NP o) of this channel displayed a strong voltage dependence, was not affected by varying intracellular ATP concentration [(ATP]i) between 0 and 100 μM, but was significantly increased upon elevation of intracellular free Ca2+ concentration ([Ca2+]i). Low concentrations of external tetraethylammonium (0.1–3 mM) produced a concentration-dependent reduction of the unitary current amplitude of this channel. In cell-attached patches, where the resting membrane potential was set to zero with a high KCl solution, reduction of O2 from 21% to 〈 2% reversibly increased the NP o, mean open time, and event frequency of the Ca2+-sensitive, high-conductance single-channel K+ current recorded at a patch potential of + 20 mV. A similar reduction in PO2 also produced a transient increase in the activity of the 215-pS K+ channel measured in excised inside-out patches bathed in symmetrical 145 mM KCl, an effect which was diminished, or not seen, during a second application of hypoxic superfusion. Hypoxia had no effect on [Ca2+]i or intracellular pH (pHi) of cat cerebral arterial muscle cells, as measured using Ca2+- or pH-sensitive fluorescent probes. Reduced PO2 caused a significant dilation of pressurized cerebral arterial segments, which was attenuated by pre-treatment with 1 mM tetraethylammonium. These results suggest that reduced PO2 increases the activity of a high-conductance, Ca2+-sensitive K+ channel in cat cerebral arterial muscle cells, and that these effects are mediated by cytosolic events independent of changes in [Ca2+]i and pHi.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 390 (1981), S. 296-298 
    ISSN: 1432-2013
    Keywords: Dopamine ; Rabbit Basilar Artery ; Membrane Depolarization ; Force Development
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Intracellular membrane potential (Em) and force development were measured in rabbit basilar artery to help elucidate the mechanism of action of dopamine in this preparation. There was a strong correlation between membrane depolarization and contraction (r=0.95) between 3×10−7 M to 10−4 M dopamine. When the vascular muscle cells were depolarized by elevating [K]o there was a Em dependent decrease in force development in response to dopamine. Significant reduction of dopamine stimulated force development was observed when the vessel was depolarized by 5–6 mV by excess extracellular K+ and 90% inhibition was seen when the artery was depolarized to −20mv. When Ca++ influx was blocked, dopamine no longer induced force development. Such findings suggest that dopamine cotracts rabbit basilar artery by a mechanism involving membrane depolarization. This process may involve an influx of extracellular Ca++ through voltage sensitive channels.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-2013
    Keywords: Potassium channels ; membrane potential ; hyperpolarization ; endothelial cells ; shear stress ; inward rectifier ; ion channels ; calcium sensitivity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We investigated the response of inward rectifier K+ (IRK) currents in bovine aortic endothelial cells (BAECs) to shear stress. Shear evoked reversible hyperpolarization in current clamped BAECs. Voltage clamped BAECs exhibited large inward and small outward whole cell K+ currents blocked by cesium and increased in amplitude by exposure to shear stress. The open state probability of IRK channels in cell-attached membrane patches was increased within minutes of exposure to shear stress. IRK channels in inside-out patches were activated by increases in [Ca2+]i from 10−7 to 10−6 mM. We demonstrate that shear stress induces hyperpolarization and gating of single channel and whole cell IRK currents in BAECs.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 403 (1985), S. 402-406 
    ISSN: 1432-2013
    Keywords: Middle cerebral artery ; PCO2 ; pH ; Membrane potential ; K+ conductance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract These studies were undertaken to determine the effect of reducing aPCO2 below physiological levels on cat middle cerebral artery. Upon reduction ofPCO2 from 37 to 14 torr (pH 7.4) we observed membrane depolarization and force development. ReducingPCO2 decreased the slope of theE m vs. log [K]o curve and increased the slope of the steady-state I/V relationship suggesting that the change inE m was due to reduction of outward K+ conductance (g k). Elevation of pH from 7.37 to 7.6 had a very similar effect on these cerebral arterial muscle cells, depolarizing the muscle membrane (reducing theE m vs. log [K]o curve) and increasing the slope of the I/V relationship to statistically equivalent values as reduction ofPCO2. ReturningPCO2 from 14 to 37 torr rapidly relaxed these preparations, but only transiently. This relaxation was followed by a rebound contraction within 3 min, demonstrating a transient nature for the action of elevatingPCO2 in cerebral arteries. The response to changing pHo followed a slower time course but did not change with time. These studies demonstrate that both elevated pHo and reducedPCO2 activate cerebral arterial muscle by a mechanism which includes reduction ing k. However, it can not be determined if these similar responses and reduction, ofg k are mediated by changing pHi or mediated through different mechanisms. It is possible that pHo andPCO2 can modify cerebral arterial tone by direct mechanisms and not necesarily by their effect on pHi. It is clear, however, that reduction ofPCO2 and elevation of pHo both activate cerebral arterial muscle by a mechanism which includes reduction ofg k.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-2013
    Keywords: Hypertensive cerebral arteries ; Alkalosis and transmural pressure ; Myogenic activation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract These studies were undertaken to examine the effect of alkalosis to modify “pressure-induced” activation of isolated cerebral arteries from spontaneously hypertensive rats (SHR) and their normotensive Wistar-Kyoto (WKY) controls. At pH 7.4 andPCO2 of 34 torr elevation of transmural pressure from 0–140 mm Hg resulted in myogenic activation preceeded by membrane depolarization in both SHR and WKY. The degree of developed myogenic tone in SHR was elevated above WKY. Aklalosis (pH 7.4–7.7) depolarized and activated SHR cerebral arteries to a greater extent than WKY. Furthermore, both the electrical and mechanical responses to elevation in transmural pressure were exaggerated in SHR compared to WKY at pH 7.7 (PCO2 constant at 34 torr). Manipulation ofPCO2 at constant pH of 7.4 had similar effects on “pressure-induced” myogenic tone in both SHR and WKY. Thus, cerebral arteries from both SHR and WKY depolarize and develop myogenic tone in response to increasing transmural pressure. This response is augmented in SHR, but to a much greater extent upon elevation of extracellular pH, whilePCO2 is maintained within normal limits. The implications of these findings are discussed.
    Type of Medium: Electronic Resource
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