Cellular mechanism of force development in cat middle cerebral artery by reducedPCO2

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 pH_o followed a slower time course but did not change with time. These studies demonstrate that both elevated pH_o 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 pH_i or mediated through different mechanisms. It is possible that pH_o andPCO₂ can modify cerebral arterial tone by direct mechanisms and not necesarily by their effect on pH_i. It is clear, however, that reduction ofPCO₂ and elevation of pH_o both activate cerebral arterial muscle by a mechanism which includes reduction ofg _k.This study was supported by NIH grant no. HL-32871. Dr. Harder is an established investigator of the American Heart Association     

Further investigation of ionic diffusive properties and of NH 4 + pathways inXenopus laevis oocyte cell membrane

To study the ionic diffusive properties and the NH ₄ ⁺ pathways in theXenopus laevis oocyte cell membrane, we recorded the effects of various inhibitors on membrane potential (V _m) and membrane resistance (R _m); intracellular acidification was taken as an index of NH ₄ ⁺ influx from the bath to the cytoplasm. The following results were obtained: in the control state, barium and quinine (Q) ions depolarizedV _m and raisedR _m, consistent with inhibition of K⁺ conductance(s). Diphenylamine-2-carboxylic acid (DPC), 3, 5-dichlorodiphenylamine-2-carboxylic acid (DCDPC) and gadolinium ions hyperpolarizedV _m and increasedR _m, suggesting the inhibition of nonselective cationic conductance(s). In the presence of 20 mmol/l NH₄Cl,V _m depolarized,R _m fell, and intracellular pH (pH_i) decreased, consistent with an NH ₄ ⁺ influx. In the presence of DPC, the same manoeuvre induced a biphasicV _m change (i.e. a spike depolarization followed by a membrane hyperpolarization) and a fall ofR _m; in most oocytes, intracellular acidification persisted and was reversible upon adding ouabain (Oua). These results indicate that a DPC-sensitive conductance is not the unique NH ₄ ⁺ pathway and that Na, K-ATPase may also mediate NH ₄ ⁺ influx. However, Oua did not prevent theR _m decrease, suggesting that ouabain-insensitive rheogenic pathway(s) are activated. Thus, we investigated theV _m change induced by NH₄Cl addition in the presence of DPC: the spike depolarization followed by secondary hyperpolarization became a plateau depolarization when Q was added, suggesting involvement of Q-sensitive pathway(s) in the above described biphasicV _m change. In the presence of DPC, Q, and Oua, intracellular acidification upon adding NH₄C1 persisted consistent with further NH ₄ ⁺ influx through quinine-, DPC- and Oua-insensitive pathway (s).     

Effect of NH4 +/NH3 on cytosolic pH and the K+ channels of freshly isolated cells from the thick ascending limb of Henle's loop

The conductance properties of the luminal membrane of cells from the thick ascending limb of Henle's loop of rat kidney (TAL) are dominated by K⁺. In excised membrane patches the luminal K⁺ channel is regulated by pH changes on the cytosolic side. To examine this pH regulation in intact cells of freshly isolated TAL segments we measured the membrane voltage (V _m) in slow-whole-cell (SWC) recordings and the open probability (P _o) of K⁺ channels in the cell-attached nystatin (CAN) configuration, where channel activity and part of V _m can be recorded. The pipette solution contained K⁺ 125 mmol/l and Cl^– 32 mmol/l. Intracellular pH was determined by 2,7 bis(2-carboxyethyl)-5,(6)-carboxyfluorescein (BCECF) fluorescence. pH changes were induced by the addition of 10 mmol/l NH₄ ⁺/NH₃ to the bath. In the presence of NH₄ ⁺/NH₃ intracellular pH acidified by 0.53±0.11 units (n=7). Inhibition of the Na⁺2Cl^– K⁺ cotransporter by furosemide (0.1 mmol/l) reversed this effect and led to a transient alkalinisation by 0.62±0.14 units (n=7). In SWC experiments V _m of TAL cells was -72±1 mV (n=70). NH₄ ⁺/NH₃ depolarised V _m by 22±2 mV (n=25). In 11 SWC experiments furosemide (0.1 mmol/l) attenuated the depolarising effect of NH₄ ⁺ from 24±3 mV to 7±3 mV. Under control conditions the single-channel conductance of TAL K⁺ channels in CAN experiments was 66±5 pS and the reversal voltage for K⁺ currents was 70±2 mV (n=35). The P _o of K⁺ channels in CAN patches was reduced by NH₄ ⁺/NH₃ from 0.45±0.15 to 0.09±0.07 (n=7). NH₄ ⁺/NH₃ exposure depolarised the zero current voltage of the permeabilised patches by-9.7±3.6 mV (n=5). The results show that TAL K⁺ channels are regulated by cytosolic pH in the intact cell. The cytosolic pH is acidified by NH₄ ⁺/NH₃ exposure at concentrations which are physiologically relevant because Na⁺2Cl^–K⁺(NH₄ ⁺) cotransporter-mediated import of NH₄ ⁺ exceeds the rate of NH₃ diffusion into the TAL. K⁺ channels are inhibited by this acidification and the cells depolarise. In the presence of furosemide TAL cells alkalinise proving that NH₄ ⁺ uptake occurs by the Na⁺2Cl^–K⁺ cotransporter. The findings that, in the presence of NH₄ ⁺/NH₃ and furosemide, V _m is not completely repolarised and that K⁺ channels are not activated suggest that the respective K⁺ channels may in addition to their pH regulation be inhibited directly by NH₄ ⁺/NH₃.     

Intracellular Ca2+ inactivates an outwardly rectifying K+ current in human adenomatous parathyroid cells

We have used whole-cell patch-clamp techniques to study the conductances in the plasma membranes of human parathyroid cells. With a KCl-rich pipette solution containing Ca²⁺ buffered to a concentration of 0.1 mol/l, the zero current potential was –71.1±0.5 mV (n=19) and the whole-cell current/ voltage (I/V) relation had an inwardly rectifying and an outwardly rectifying component. The inwardly rectifying current activated instantaneously on hyperpolarization of the plasma membrane to potentials more negative than –80 mV, and a semi-logarithmic plot of the reversal potential of the inward current (estimated by extrapolation from the range in which it was linear) as a function of extracellular K⁺ concentration ([K⁺]_o) revealed a linear relation with a slope of 64 mV per decade change in [K⁺]_o, which is not significantly different from the Nernstian slope, demonstrating that the current was carried by K⁺ ions. The conductance exhibited a square root dependence on [K⁺]_o as has been observed for inward rectifiers in other tissues. The current was blocked by the presence of Ba²⁺ (1 mmol/l) or Cs⁺ (1.5 mmol/l) in the bath. The outwardly rectifying current was activated by depolarization of the membrane potential to potentials more positive than –20 mV. It was inhibited by replacement of pipette K⁺ with Cs⁺, indicating that it also was a K⁺ current: it was partially (42%) blocked when tetraethylammonium (TEA⁺, 10 mmol/l) was added to the bath. The outwardly rectifying, but not the inwardly rectifying K⁺ current, was regulated by intracellular free Ca²⁺ concentration ([Ca²⁺]_i) such that increasing [Ca²⁺]_i above 10 nmol/l inhibited the outwardly rectifying current, the half-maximum effect being seen at 1 mol/l. Since it is known that increases in [Ca²⁺]_o produce increases in [Ca²⁺]_i, and that they depolarize parathyroid cells by reducing the membrane K⁺ conductance, we suggest that it is the reduction of the outwardly rectifying K⁺ conductance by increases in [Ca²⁺]_i which is responsible for the reduction in K⁺ conductance seen when [Ca²⁺]_o is increased.     

pH dependence of K+ conductances of rat cortical collecting duct principal cells

The K⁺ channels of the principal cells of rat cortical collecting duct (CCD) are pH sensitive in excised membranes. K⁺ secretion is decreased with increased H⁺ secretion during acidosis. We examined whether the pH sensitivity of these K⁺ channels is present also in the intact cell and thus could explain the coupling between K⁺ and H⁺ secretion. Membrane voltages (V _m), whole-cell conductances (g _c), and single-channel currents of K⁺ channels were recorded from freshly isolated CCD cells or isolated CCD segments with the patch-clamp method. Intracellular pH (pH_i) was measured using the pH-sensitive fluorescent dye 2-7-bis(carboxyethyl)-5-6-carboxyfluorescein (BCECF). Acetate (20 mmol/l) had no effect on V _m, g _c, or the activity of the K⁺ channels in these cells. Acetate, however, acidified pH_i slightly by 0.17±0.04 pH units (n=19). V _m depolarized by 12±3 mV (n=26) and by 23±2 mV (n=66) and g _c decreased by 26±5% (n=13) and by 55±5% (n=12) with 3–5 or 8–10% CO₂, respectively. The same CO₂ concentrations decreased pH_i by 0.49±0.07 (n=15) and 0.73±0.11 pH units (n=12), respectively. Open probability (P _o) of all four K⁺ channels in the intact rat CCD cells was reversibly inhibited by 8–10% CO₂. pH_i increased with the addition of 20 mmol/l NH₄ ⁺/NH₃ by a maximum of 0.64±0.08 pH units (n=33) and acidified transiently by 0.37±0.05 pH units (n=33) upon NH₄ ⁺/NH₃ removal. In the presence of NH₄ ⁺/NH₃ V _m depolarized by 16±2 mV (n=66) and g _c decreased by 26±7% (n=16). The activity of all four K⁺ channels was also strongly inhibited in the presence of NH₄ ⁺/NH₃. The effect of NH₄ ⁺/NH₃ on V _m and g _c was markedly increased when the pH of the NH₄ ⁺/NH₃-containing solution was set to 8.5 or 9.2. From these data we conclude that cellular acidification in rat CCD principal cells down-regulates K⁺ conductances, thus reduces K⁺ secretion by direct inhibition of K⁺ channel activity. This pH dependence is present in all four K⁺ channels of the rat CCD. The inhibition of K⁺ channels by NH₄ ⁺/NH₃ is independent of changes in pH_i and rather involves an effect of NH₃.     

l-Alanine andl-phenylalanine activate Na+ and K+ conductance pathways in the exocrine mouse pancreas

The effects of some amino acids,l-alanine,l-phenylalanine,dl-alanine,d-alanine and -alanine on membrane potential, membrane current, amylase secretion and⁴⁵Ca and⁸⁶Rb fractional efflux in isolated mouse pancreatic segments were investigated. A two micro-electrode voltage clamp technique was applied to study the effects of the amino acids on membrane current. The amino acids evoked dose-dependent (0.05–0.5 mmole) and reversible membrane depolarization and increases in membrane current. The relative potencies of the actions of the amino acids were:l-alanine>dl-alanine>l-phenylalanine>d-alanine>-alanine. A more detailed study of the action ofl-alanine showed that the relationship between thel-alanine-evoked membrane current and membrane potential was virtually linear with reversal of current polarity being observed at a membrane potential of about +30 mV. While thel-alanine-induced increase in membrane conductance was dose-dependent, the reversal potential (E _l-ala) was independent of thel-alanine concentration used. Replacement of the normal Na-rich superfusion fluid by a low Na solution (5 mM) markedly reduced thel-alanine-elicited inward current at the normal resting potential. Thel-alanine-evoked conductance increase was also reduced in low Na solution and the E _l-ala was close to 0 mV. During the exposure of pancreatic segments to Cl free solution (sulphate substitution) E _l-ala was about 12 mV more positive (+43.7±0.8 mV) than during exposure to control solution (+31.5±1.0 mV). Calculations based on the Goldman-Hodgkin-Katz equations taking into account the values of E _l-ala in the different ionic situations, indicate that the relative permeability of the ionic pathway opened up in the presence ofl-alanine isP _Na/P _Cl/P _K=7.5/1.5/1.0 The pathway is therefore Na selective, but with some leak permeability for Cl and K. In the physiological range of membrane potentials (–15 to –40 mV) the current evoked byl-alanine is virtually entirely carried by Na. Measurements of amylase secretion and⁴⁵Ca fractional efflux show that none of the amino acids (all at 10 mM concentrations) had significant effect whereas pentagastrin (Pn; 10^–6 M) elicited marked increases in amylase output and⁴⁵Ca release. Both pentagastrin andl-alanine stimulated the release of⁸⁶Rb from prelabelled tissue whereasdl-alanine,l-phenylalanine,d-alanine and -alanine had little or no effect. The present results indicate that although the amino acids have no effect on either amylase secretion or calcium metabolism, they nevertheless open conductance pathways in the acinar plasma membrane mainly permeable to Na.     

Crypt base cells show forskolin-induced Cl− secretion but no cation inward conductance

Whole-cell patch-clamp studies in base cells of isolated colonic crypts of rats pretreated with dexamethasone were performed to examine the effects of stimulation by forskolin (10 mol/1). The experiments were designed in order to distinguish between two postulated effector mechanisms: the activation of a non-selective cation channel and the activation of Cl^– channels. As shown in an accompanying report, forskolin depolarizes the membrane voltage (V _m) by some 40–50 mV and enhances the whole-cell membrane conductance (G _m) substantially in these cells. In this report all experiments were performed in the presence of forskolin. A reduction of the bath Na⁺ concentration from 145 to 2 mmol/1 led to a hyperpolarization ofV _m by some 20–30 mV This hyperpolarization occurred very slowly suggesting that the hyperpolarization produced by the low-Na⁺ solution was caused indirectly and not by a change in the equilibrium potential for Na⁺,E _Na ⁺. A complete kinetic analysis of the effect on voltage of bath Na⁺ revealed a saturation-type relation with a high apparent affinity for Na⁺ of around 5–10 mmol/1. A reduction in bath Cl^– concentration from 145 to 32 mmol/1 caused a depolarization ofV _m from –34 ± 3 to –20 ± 4 mV (n = 13) in the presence of a high bath Na⁺ concentration, but had the opposite effect at low (5 mmol/1) Na⁺ concentrations:V _m was hyperpolarized from –46 ± 4 to –62 ± 6 mV (n = 13). If the effect of Na⁺ onV _m was caused by a non-selective cation channel the opposite would have been expected. To test directly whether the Na⁺2Cl^–K⁺ cotransporter was responsible for the effects of changes in bath Na⁺ onV _m, the effects of increasing concentrations of several loop diuretics were examined. Furosemide, piretanide, torasemide and burnetanide (up to 0.1–0.5 mmol/1) all hyperpolarizedV _m, albeit only by less than 10 mV. Another subclass of loop diuretics containing a tetrazolate in position 1 [e.g. azosemide, no. 19A and no. 20A from Schlatter E, Greger R, Weidtke C (1983) Pflüger Arch 396: 210–217] were much more effective. Azosemide hyperpolarizedV _m from –46 ± 3 to –74 ± 2 mV (n = 18) and reducedG _m from 11 ± 1 to 4 ± 1 nS (n = 14). These data indicate that forskolin stimulates Cl^– secretion in these cells by a mechanism fully compatible with the current scheme for exocrine secretion involving the Na⁺2Cl^–K⁺ cotransporter.     

Effects of cell differentiation on ion conductances and membrane voltage in LLC-PK1 cells

LLC-PK1 cells serve as a widely used model for the renal proximal tubule. Until now, little has been found out about their membrane voltage (V _m) and ionic conductances (g). Several studies have shown changes in cell properties during differentiation and ageing. The aim of this study was to examine the relationship between V _m or g and the age of these cells. Therefore, we investigated single cells, subconfluent and confluent monolayers of LLC-PK1 cells aged 1–8 days with the slow-whole-cell patch-clamp technique. The V _m of all cells was-34±2 mV (n=75) and the membrane conductance (g _m) was 2.3±0.3 nS (n=30). V _m in cells aged up to 2 days was-24±3 mV (n=22) whereas V _m in cells aged 5–8 days was -50±3 mV (n=15). An increase of extracellular K⁺ from 3.6 to 18.6 mmol/l led to a depolarization in all cells of 4±1 mV (n=31) and an increase of g _m by 17±13% (n=15). Complete replacement of extracellular Na⁺ by N-methyl-D-glucamine (NMDG) led to a hyperpolarization of 19±2 mV (n=38) and g_m was lowered by 27±14% (n=17). A reduction in extracellular Cl^– from 147 to 32 mmol/l showed no significant effect on V _m (n=16) or g _m (n=11). Amiloride (10 mol/l) had no significant effect on V _m (n=13) or g _m (n=7). The reduction of the extracellular osmolarity from 290 to 160 mosmol/l led to a hyperpolarization of 11±1 mV (n=18) and an increase in g _m by 326±117% (n=12). There was no significant correlation between g _m and cell age. LLC-PK1 cells used in this study have a K⁺ conductance and a non-selective cation conductance in parallel. With increasing age, LLC-PK1 cells became more and more conductive for K⁺ and lost their nonselective cation conductance. There is no evidence for a significant amiloride-sensitive Na⁺ or Cl^– conductance in these cells. The K⁺ conductance could be activated by osmotically induced cell swelling.     

Effect of secretin and inhibitors of HCO3 −/H+ transport on the membrane voltage of rat pancreatic duct cells

The aim of the present study was to study the effect of secretin on the electrophysiological response of pancreatic ducts. Furthermore, we investigated the effects of lipid-soluble buffers and inhibitors of HCO₃ ^–/H⁺ transport. Ducts obtained from fresh rat pancreas were perfused in vitro. Secretin depolarized the basolateral membrane voltage, V _bl, by up to 35 mV (n=37); a halfmaximal response was obtained at 3×10^–11 mol/l. In unstimulated ducts a decrease in the luminal Cl^– concentration (120 to 37 mmol/l) had a marginal effect on V _bl, but after maximal secretin stimulation it evoked a 14±2 mV depolarization (n=6), showing that a luminal Cl^– conductance G _Cl- was activated. The depolarizing effect of secretin on V _bl was often preceded by about a 6 mV hyperpolarization, most likely due to an increase in the basolateral G _K+. Perfusion of ducts with DIDS (4,4 — diisothiocyanatostilbene — 2,2 — disulphonic acid, 0.01 mmol/l) or addition of ethoxzolamide (0.1 mmol/l) to the bath medium diminished the effect of secretin. Acetate or pre-treatment of ducts with NH₄ ⁺/NH₃ (10 mmol/l in the bath) depolarized the resting V _bl of –65±2 mV by 16±4 mV (n=7) and 19±3 mV (n=10), respectively. The fractional resistance of the basolateral membrane (FR _bl) doubled, and the depolarizing responses to changes in bath K⁺ concentrations (5 to 20 mmol/l) decreased from 22±1 to 11±2 mV. The Na⁺/H⁺ antiporter blocker EIPA (5-[N-ethyl-N-isopropyl]-amiloride, 0.1 mmol/l) also depolarized V _bl by 10±1 mV, FR_bl increased and the response to K⁺ concentration changes decreased (n=7). Effects of EIPA and ethoxzolamide on V _bl were greater in ducts deprived of exogenous HCO₃ ^–/CO₂. Taken together, the present study shows that secretin increased the basolateral G _K+ and the luminal G _Cl-. The depolarizing effect of secretin was diminished following inhibition of HCO₃ ^– transport (DIDS), or HCO₃ ^–/H⁺ generation (ethoxzolamide). Manoeuvres that presumably led to lowered intracellular pH (NH₄ ⁺/NH₃ removal, acetate, EIPA) decreased the basolateral G _K+. The present data support our previously published model for pancreatic HCO₃ ^– secretion, and indicate that the basolateral membrane possesses a pH-sensitive G _K+.     

Transmitter-induced changes of the membrane voltage of HT29 cells

The colonic carcinoma cell line HT₂₉ was used to examine the influence of agonists increasing cytosolic cAMP and Ca²⁺ activity on the conductances and the cell membrane voltage (V _m). HT₂₉ cells were grown on glass cover-slips. Cells were impaled by microelectrodes 4–10 days after seeding, when they had formed large plaques. In 181 impalements V _m was –51±1 mV. An increase in bath K⁺ concentration from 3.6 mmol/l to 18.6 mmol/l or 0.5 mmol/l Ba²⁺ depolarized the cells by 10±1 mV (n=49) or by 9±2 mV (n=3), respectively. A decrease of bath Cl^– concentration from 145 to 30 mmol/l depolarized the cells by 11±1 mV (n=24). Agents increasing intracellular cAMP such as isobutylmethylxanthine (0.1 mmol/l), forskolin (10 mol/l) or isoprenaline (10 mol/l) depolarized the cells by 6±1 (n=13), 15±3 (n=5) and 6±2 (n=3) mV, respectively. In hypoosmolar solutions (225 mosmol/l) cells depolarized by 9±1 mV (n=6). Purine and pyrimidine nucleotides depolarized the cells dose-dependently with the following potency sequence: UTP > ATP > ITP > GTP > TIP > CTP = 0. The depolarization by ATP was stronger than that by ADP and adenosine. The muscarinic agonist carbachol led to a sustained depolarization by 27±6 mV (n=5) at 0.1 mmol/l, and to a transient depolarization by 12±4 mV (n=5) at 10 mol/l. Neurotensin depolarized with a half-maximal effect at around 5 nmol/l. The depolarization induced by nucleotides and neurotensin was transient and followed by a hyperpolarization. We confirm that HT₂₉ cells possess Cl^–- and K⁺-conductive pathways. The Cl^– conductance is regulated by intracellular cAMP level, cytosolic Ca²⁺ activity, and cell swelling. The K⁺ conductance in HT₂₉ cells is regulated by intracellular Ca²⁺ activity.Supported by DFG Gre 480/10 and GIF Proj. no. I-86-100.10/ 88     

K+ channels in the basolateral membrane of rat cortical collecting duct

Impalement studies in isolated perfused cortical collecting ducts (CCD) of rats have shown that the basolateral membrane possesses a K⁺ conductive pathway. In the present study this pathway was investigated at the single-channel level using the patch-clamp technique. Patch-clamp recordings were obtained from enzymatically isolated CCD segments and freshly isolated CCD cells with the conventional cell-free, cell-attached and the cell-attached nystatin method. Two K⁺ channels were found which were highly active on the cell with a conductance of 67±5 pS (n=18) and 148±4 pS (n=21) with 145 mmol/l K⁺ in the pipette. In excised patches the first channel had a conductance of 28±2 pS (n=15), whereas the second one had a conductance of 85±1 pS (n=53) at 0 mV clamp voltage with 145 mmol/l K⁺ on one side and 3.6 mmol/l K⁺ on the other side of the membrane. So far it has not been possible to characterize the smaller channel further. Excised, and with symmetrical K⁺ concentrations of 145 mmol/l, the intermediate channel had a linear conductance of 198±19 pS (n=5). After excision in the inside-out configuration the open probability (P _o) of this channel was low (0.18±0.05, n=13) whereas in the outside-out configuration this channel had a threefold higher P _o (0.57±0.04, n=12). Several inhibitors were tested in excised membranes. Ba²⁺ (1 mmol/l), tetraethylammonium (TEA⁺, 10 mmol/l) and verapamil (0.1 mmol/l) all blocked this channel reversibly. Furthermore P _o was reversibly reduced by 10 nmol/l charybdotoxin (outside-out). This K⁺ channel of the basolateral membrane was regulated by cellular pH. P _o was reduced to 26±3% at pH 6.5 (n=6) and increased to 216±18% at pH 8.5 (n=7) compared to pH 7.4. Half-maximal inhibition was reached at pH 7.0. The channel had its highest P _o at a Ca²⁺ activity of less than 10^–8 mol/l (n=13). Increasing the Ca²⁺ activity to 1 mmol/l on the cytosolic side of the membrane resulted in a reduction of P _o to 13±3% (n=11). Half-maximal inhibition was reached at a Ca²⁺ activity of 10^–5 mol/l. The high activity of both K⁺ channels of the basolateral membrane on the cell indicates that they may serve for K⁺ recirculation across the basolateral membrane.     

Properties of the luminal membrane of isolated perfused rat pancreatic ducts

The aim of the present study was to investigate by what transport mechanism does HCO ₃ ^– cross the luminal membrane of pancreatic duct cells, and how do the cells respond to stimulation with dibytyryl cyclic AMP (db-cAMP). For this purpose a newly developed preparation of isolated and perfused intra-and interlobular ducts of rat pancreas was used. Responses of the epithelium to inhibitors and agonists were monitored by electrophysiological techniques. Addition of HCO ₃ ^– /CO₂ to the bath side of nonstimulated ducts depolarized the PD across the basolateral membrane (PD_bl) by about 9mV, as also observed in a previous study [21]. This HCO ₃ ^– effect was abolished by Cl^– channel blockers or SITS infused into the lumen of the duct: i. e. 5-nitro-2-(3-phenylpropylamino)-benzoic acid (NPPB, 10^–5 M) hyperpolarized PD_bl by 8.2±1.6 mV (n=13); 3,5-dichlorodiphenylamine-2-carboxylic acid (DCl-DPC, 10^–5 M) hyperpolarized PD_bl by 10.3±1.7 mV (n=10); and SITS hyperpolarized PD_bl by 7.8±0.9 mV (n=4). Stimulation of the ducts with dbcAMP in the presence of bath HCO ₃ ^– /CO₂ resulted in depolarization of PD_bl, the ductal lumen became more negative and the fractional resistance of the luminal membrane decreased. Together with forskolin (10^–6 M), db-cAMP (10^–4 M) caused a fast depolarization of PD_bl by 33.8±2.5 mV (n=6). When db-cAMP (5×10^–4 M) was given alone in the presence of bath HCO ₃ ^– /CO₂, PD_bl depolarized by 25.3±4.2 mV (n=10). In the absence of exogenous HCO ₃ ^– , db-cAMP also depolarized PD_bl by 24.7±3.0 mV (n=10). The present data suggest that in the luminal membrane of pancreatic duct cells there is a Cl^– conductance in parallel with a Cl^–/HCO ₃ ^– antiport. Dibutyryl cyclic AMP increases the Cl^– conductance of the luminal membrane. Taking together our present results, and the recent data obtained for the basolateral membrane [21], a tentative model for pancreatic HCO ₃ ^– transport is proposed.Parts of this study have been presented at the Scandinavian Physiological Society Meeting in Copenhagen 1986 and 64th Meeting of the German Physiological Society in Homburg/Saar     

Muscarinic receptor-mediated increase of intracellular Na+-ion activity and force of contraction

The effective membrane capacity (c _eff) of theXenopus egg has been measured integrating the membrane current transients in response to small voltage-clamp pulses. Before activationc _eff has a value of 1.34±SE. 0.13 F/cm² (apparent surface area, 13 eggs from 3 females) and is essentially constant over the voltage range between –30 and +60 mV. During artificial activation of the eggs by pricking or by addition of Ca²⁺ ionophore A23187,c _eff increases by about 60% in 2–3 min and then slowly decreases returning to near the initial value in 15–20 min. Electron microscopic observations of the egg surface at different times reveal that the capacity time course parallels the changes in plasma membrane area due to cortical granule exocytosis and to a later reduction of microvillar extension. Simultaneous measurements of capacity and conductance show that the capacity changes are slower and delayed in comparison with the transient development of the chloride conductance responsible for the activation potential. In CO₂-treated eggs the cortical granule exocytosis is prevented and, correspondingly, the transient capacity increase is strongly reduced or absent, but the development of the chloride conductance remains normal. This technique gives a method to electrophysiologically monitor the cortical granule exocytosis; moreover our results show that the exocytotic process can be blocked without affecting the membrane conductance changes.     

Effect of bradykinin and histamine on the membrane voltage,ion conductances and ion channels of human glomerular epithelial cells (hGEC) in culture

The effects of bradykinin (BK) and histamine (Hist) on the membrane voltage (V _m), ion conductances and ion channels of cultured human glomerular epithelial cells (hGEC) were examined with the nystatin patch clamp technique. Cells were studied between passage 3 and 20 in a bath rinsed with Ringer-like solution at 37°C. The mean value of V _m was –41±0.5 mV (n=189). BK (10^–6 mol/l, n=29) and Hist (10^–5 mol/l, n= 55) induced a rapid transient hyperpolarization by 15±1 mV and 18±1 mV, respectively. The hyperpolarization was followed by a long lasting depolarization by 6±1 mV (BK 10^–6 mol/l) and 7±1 mV (Hist 10^–5 mol/l). The ED₅₀ was about 5×10^–8 mol/l for BK and 5×10^–7 mol/l for Hist. In the presence of both agonists, increases of outward and inward currents were observed. A change in the extracellular K⁺ concentration from 3.6 to 30 mmol/l depolarized V _m by 8±1 mV and completely inhibited the hyperpolarizing effect of both agents (n=11). Reduction of extracellular Cl^– concentration from 145 to 30 mmol/l led to a depolarization by 2 ±1 mV (n=25). In 30 mmol/l Cl^– the depolarizations induced by BK (10^–7 mol/l) and Hist (10^–6 mol/l) were augmented to 9±2 mV (n=14) and to 10±2 mV (n=11), respectively. Ba²⁺ (5 mmol/l) depolarized V _m by 19±5 mV (n=6) and completely inhibited the hyperpolarization induced by BK (10^–6 mol/l, n=3) and reduced that of Hist (10^–5 mol/l) markedly (n=3). Preincubation with the K⁺ channel blocker charybdotoxin (1–10 nmol/l) for 3 min had no significant effect on V _m, but reduced markedly the BK(10^–6 mol/l, n=11) and Hist-(10^–5 mol/l, n=6) induced hyperpolarizations. In 10 out of 31 experiments in the cell attached nystatin patch configuration big K⁺ channels with a conductance of 247±17 pS were found. The open probability of these K⁺ channels was increased 3- to 5-fold during the hyperpolarization induced by BK (10^–7 mol/l) or Hist (10^–5 mol/l, both n= 4). In excised inside/out patches this K⁺ channel had a mean conductance of 136±8.5 pS (n=10, clamp voltage 0 mV). The channel was outwardly rectifying and its open probability was increased when Ca²⁺ on the cytosolic side was greater than 0.1 mol/l. The data indicate that BK and Hist activate a and a in hGEC. The hyperpolarization is induced by the activation of a Ca²⁺-dependent maxi K⁺ channel.     

Regulation of membrane excitability by intracellular pH (pHi) changers through Ca2+-activated K+ current (BK channel) in single smooth muscle cells from rabbit basilar artery

Employing microfluorometric system and patch clamp technique in rabbit basilar arterial myocytes, regulation mechanisms of vascular excitability were investigated by applying intracellular pH (pH_i) changers such as sodium acetate (SA) and NH₄Cl. Applications of caffeine produced transient phasic contractions in a reversible manner. These caffeine-induced contractions were significantly enhanced by SA and suppressed by NH₄Cl. Intracellular Ca²⁺ concentration ([Ca²⁺]_i) was monitored in a single isolated myocyte and based the ratio of fluorescence using Fura-2 AM (R _340/380). SA (20 mM) increased and NH₄Cl (20 mM) decreased R _340/380 by 0.2 ± 0.03 and 0.1 ± 0.02, respectively, in a reversible manner. Caffeine (10 mM) transiently increased R _340/380 by 0.9 ± 0.07, and the ratio increment was significantly enhanced by SA and suppressed by NH₄Cl, implying that SA and NH₄Cl may affect [Ca²⁺]_i (p < 0.05). Accordingly, we studied the effects of SA and NH₄Cl on Ca²⁺-activated K⁺ current (IK_Ca) under patch clamp technique. Caffeine produced transient outward current at holding potential (V _h) of 0 mV, caffeine induced transient outward K⁺ current, and the spontaneous transient outward currents were significantly enhanced by SA and suppressed by NH₄Cl. In addition, IK_Ca was significantly increased by acidotic condition when pH_i was lowered by altering the NH₄Cl gradient across the cell membrane. Finally, the effects of SA and NH₄Cl on the membrane excitability and basal tension were studied: Under current clamp mode, resting membrane potential (RMP) was −28 ± 2.3 mV in a single cell level and was depolarized by 13 ± 2.4 mV with 2 mM tetraethylammonium (TEA). SA hyperpolarized and NH₄Cl depolarized RMP by 10 ± 1.9 and 16 ± 4.7 mV, respectively. SA-induced hyperpolarization and relaxation of basal tension was significantly inhibited by TEA. These results suggest that SA and NH₄Cl might regulate vascular tone by altering membrane excitability through modulation of [Ca²⁺]_i and Ca²⁺-activated K channels in rabbit basilar artery.     

Transmural gradient of tissue gas tensions in the canine left ventricular myocardium during coronary clamping and reactive hyperemia

Mass spectrometry was used for the continuous, simultaneous and quantitative measurement of oxygen (PO₂) and carbon dioxide (PCO₂) partial pressures in the subendocardial and subepicardial layers of the left ventricle in 11 anaesthetized ventilated dogs. Under control conditions,PO₂ was significantly lower in the subendocardium (13.5±4.5 mm Hg) than in the subepicardium (20.7±2.3 mm Hg), whereasPCO₂ did not differ significantly (43±8.8 and 51±9.2 mm Hg respectively). These variables were not correlated with blood pressure or coronary blood flow. Subendocardial and subepicardialPO₂ decreased less than 5 s after coronary occlusion. These changes were more rapid and severe in the subendocardium. After occlusion for 90 s: subendocardialPO₂ was 4.1±6.3 mm Hg while subepicardialPO₂ was 6.7±15.0 mm Hg (P<0.05).PCO₂ reached peak values of 56±25 mm Hg subendocardial and 82±22 mm Hg subepicardial at 2.67±0.71 min and 3.43±0.93 min after coronary clamping. A reactive hyperemia occurred after coronary unclamping with different time courses and amplitudes for systolic and diastolic stroke flows whilePO₂ recovered with different kinetics. SubendocardialPO₂ increased with a lower initial slope, probably in relation with the delay in the diastolic hyperemia. The observed delayed subendocardial hyperoxia, unrelated to the hyperemia, may indicate a delay in the recovery of normal work and metabolism in the inner layers of the myocardium.     

The ion conductances of colonic crypts from dexamethasone-treated rats

Whole-cell patch-clamp studies were performed in isolated colonic crypts of rats pretreated with dexamethasone (6 mg/kg subcutaneously on 3 days consecutively prior to the experiment). The cells were divided into three categories according to their position along the crypt axis: surface cells (s.c.); mid-crypt cells (m.c.) and crypt base cells (b.c.). The zero-current membrane voltage (V _m) was –56 ± 2 mV in s.c (n = 34); –76 ± 2 mV in M.C. (n = 47); and –87 ± 1 mV in b.c. (n = 87). The whole-cell conductance (G _m) was similar (8–12 nS) in all three types of cells. A fractional K⁺ conductance accounting for 29–67% ofG _m was present in all cell types. A Na⁺conductance was demonstrable in s.c. by the hyperpolarizing effect onV _m of a low-Na⁺ (5 mmol/1) solution. In m.c. and b.c. the hyperpolarizing effect was much smaller, albeit significant. Amiloride had a concentration-dependent hyperpolarizing effect onV _m in m.c. and even more so in s.c.. It reducedG _m by approximately 12%. The dissociation constant (K _D) was around 0.2 mol/l. Triamterene had a comparable but not additive effect (K _D = 30 mol/l,n = 14). Forskolin (10 mol/l, in order to enhance cytosolic adenosine 3, 5-cyclic monophosphate or CAMP) depolarizedV _m in all three types of cells. The strongest effect was seen in b. c..G _m was enhanced significantly in b.c. by 83% (forskolin) to 121% [8-(4-chlorophenylthio)cAMP]. The depolarization ofV _m and increase inG _m was caused to large extent by an increase in Cl^– conductance as shown by the effect of a reduction in bath Cl^– concentration from 145 to 32 mmol/1. This manocuvre hyperpolarizedV _m under control conditions significantly by 6–9 mV in all three types of cells, whilst it depolarizedV _m in the presence of forskolin in m.c. and in b.c.. These data indicate that s.c. of dexamethasone-treated rats possess mostly a K⁺ conductance and an amiloride- and Tramterene-inhibitable Na⁺ conductance. m.c. and b.c. possess little or no Na⁺ conductance; theirV _m is largely determined by a K⁺ conductance. Forskolin (via cAMP) augments the Cl^– conductance of m.c. and b.c. but has only a slight effect on s.c.     

Characterization of calcium-activated potassium channels in single smooth muscle cells using the patch-clamp technique

Single-channel currents were recorded with the patch-clamp technique from freshly dissociated vertebrate smooth muscle cells from the stomach ofBufo marinus. Of the variety of channels observed, one displayed a large linear conductance of 250 pS (in symmetric 130 mM KCl) which in excised patches was shown to be highly K⁺ selective. The probability of the channel being open (P _o) increased when [Ca²⁺]_i was elevated and/or when the membrane potential was made more positive. Thus, the features of this channel resemble the large-conductance Ca²⁺-activated K⁺ channel found in a wide variety of cell types. The voltage sensitivity of the channel was studied in detail. For patches containing a single large-conductance channel a plot ofP _o versus membrane potential followed the Boltzman relationship. Increasing [Ca²⁺]_i shifted this plot to the left along the voltage axis to more negative potentials. Both the mean closed time and mean open time varied with potential as a single exponential with almost all of the voltage sensitivity ofP _o residing in the mean closed time. These results were verified with a series of experiments carried out at lowP _o (<0.1) in patches containing multiple (N) large-conductance channels. Here the ln (NP _o) was a linear function of potential with an inverse slope of 9 mV. Almost all of the potential sensitivity lay in the mean closed time the natural log of which was also a linear function of potential with an inverse slope 11 mV in magnitude. The characteristics of this channel as well as the appearance of several of them in almost every patch suggest that they underlie the large peak outward macroscopic current found with whole-cell voltage-clamp studies.     

Ba2+ and amiloride uncover or induce a pH-sensitive and a Na+ or non-selective cation conductance in transitional cells of the inner ear

The membrane potential V _m the cytosolic pH (pH_i), the transference numbers (t) for K⁺, Cl^– and Na⁺/ non-selective cation (NSC) and the pH-sensitivity of V _m were investigated in transitional cells from the vestibular labyrinth of the gerbil. V _m, pH_i, , and the pH_i sensitivity of V _m were under control conditions were –92±1 mV (n=89 cells), pH_i 7.13±0.07 (n=11 epithelia), 0.87±0.02 (n=22), 0.02±0.01 (n=19), 0.01±0.01 (n=24) and –5 mV/pH unit (n=13 cells/n=11 epithelia), respectively. In the presence of 100 mol/l Ba²⁺ the corresponding values were: –70±1 mV (n=32), pH_i 7.16±0.08 (n=6), 0.31±0.05 (n=4), 0.06±0.01 (n=6), 0.20±0.03 (n=10) and -16 mV/pH-unit (n=15/n=6). In the presence of 500 mol/l amiloride the corresponding values were: –72±2mV (n=34), pH_i 7.00±0.07 (n=5), 0.50±0.04 (n=6), 0.04±0.01 (n=11), 0.28±0.04 (n=9) and –26 mV/pH-unit (n=20/n=5). In the presence of 20 mmol/l propionate plus amiloride the corresponding values were: –61±2 mV (n=27), pH_i 6.72±0.06 (n=5), 0.30±0.02 (n=6), 0.06±0.01 (n=5) and 0.40±0.02 (n=8), respectively. V _m was depolarized and and pH_i decreased due to (a) addition of 1 mmol/l amiloride in 150 mmol/l Na⁺ by 38±1 mV (n=8), from 0.82±0.02 to 0.17±0.02 (n=8) and by 0.13±0.01 pH unit (n=6), respectively; (b) reduction of [Na⁺] from 150 to 1.5 mmol/l by 3.3±0.5 mV (n=30), from 0.83±0.02 to 0.75±0.04 (n=9) and by 0.33±0.07 pH unit (n=4), respectively and (c) addition of 1 mmol/l amiloride in 1.5 mmol/l Na⁺ by 20±1 mV (n=11) and from 0.83±0.03 to 0.53±0.02 (n=5), respectively. These data suggest that the K⁺ conductance is directly inhibited by amiloride and Ba²⁺ and that Ba²⁺ and amiloride uncover or induce a pH-sensitive and a Na⁺/NSC conductance which may or may not be the same entity.Some of the data have been presented at various meetings and appear in abstract form in [31, 35, 37]     

Comparison of arterial,end-tidal and transcutaneous PCO2 during moderate exercise and external C02 loading in humans

Summary Static relationships between arterial, transcutaneous[/p] and end-tidal PCO₂ (P _aCO₂, P _tc CO ₂, P _etCO₂) as well as the dynamic relationship between P _etCO₂ and P _tcCO₂ were studied during moderate bicycle ergometer exercise with and without external C0₂ loading. The exercise pattern consisted of 5-min intervals of constant power at 40 W and 100 W and 900 s of randomised changes between these two power levels. The external CO₂ loading was achieved by means of controlled variations of inspiratory gas compositions aimed at a constant P _etCO₂ of 6.5 kPa (49 mm Hg). The P_etO2 was regulated at 17.3 kPa (130 mm Hg). Under steady-state conditions all PCO₂ parameters showed close linear relationships. P _aCO₂/P _tcCO₂ was near to identity while the P _etCO₂ systematically overestimated changes in P _aCO₂. No relationship showed a significant influence of the exercise intensity. Transients of P _tcCO₂ are considerably slower than P _etCO₂ transients. The dynamic relationship between both parameters was found to be independent of whether internal or external C0₂ loadings were applied. It is concluded that the combination of P _etCO₂ and P _tcCO₂ measurements allows an improved non-invasive assessment of P _aCO₂. While P _etC0₂ better reflects the transients, P _tcCO₂ can be employed to determine slow changes of the absolute P _aCO₂.