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F M Ashcroft

Publications and source records attributed to F M Ashcroft.

140 records · Page 8Linked to original sources
PubMed1987

A microflow superfusion system for use with excised membrane patches.

A new method for rapidly changing the solution superfusing excised membrane patches is described. The main advantage of this method over previous rapid exchange methods is that it is possible to use very small quantities of solution (minimal volume about 100 microliters). The method consists of inserting the pipette tip, after obtaining an excised patch, into a small tube which can be independently perfused. Air bubbles are used to separate different solutions and to produce rapid "step" changes of solution. To test this method we examined the rate of change of: the pipette resistance produced in response to changing to a solution of lower conductivity, the amplitude of single K-channel currents in response to changing external K. The results suggest that the solution exchange is essentially a step function and is complete within 10-20 ms. The recording is briefly interrupted during the time taken for the passage of the air bubble past the pipette tip (less than 250 ms). In general, the passage of the air bubble did not affect the seal resistance. This method will be particularly useful for studies of the interactions of single ionic channels with chemicals which can only be obtained in small quantities.

Animals↗
PubMed1987

Effects of 2-ketoisocaproate on insulin release and single potassium channel activity in dispersed rat pancreatic beta-cells.

1. The effects of the insulin secretagogue 2-ketoisocaproate, and of arginine, on insulin release, intracellular adenosine triphosphate (ATP) concentration and the activity of single K channels in cell-attached membrane patches have been studied in primary cultures of beta-cells from adult rat islets of Langerhans. 2. Insulin secretion was significantly increased by 2-ketoisocaproate (20 mM). The time course of this release was biphasic. Arginine (20 mM) did not stimulate insulin secretion. 3. In the absence of 2-ketoisocaproate (or arginine), two kinds of K channel were regularly observed in cell-attached membrane patches held at the cell resting potential: a channel of approximately 20 pS conductance and a channel of 50 pS conductance ([K]o = 140 mM, room temperature). 4. Addition of 2-ketoisocaproate (20 mM) to the bath suppressed the activity of the 50 pS channel and initiated action potentials. Arginine (20 mM) was without effect. 5. The intracellular concentration of ATP was increased significantly by 2-ketoisocaproate (20 mM) but not by arginine (20 mM). 6. It is suggested that, like glucose, 2-ketoisocaproate depolarizes the beta-cell and mediates insulin secretion by reducing the open probability of the 50 pS K channel. The results are also consistent with the idea that both secretagogues inhibit this channel by increasing the cytoplasmic concentration of ATP.

Action Potentials↗
PubMed1986

The ATP-sensitivity of K+ channels in rat pancreatic B-cells is modulated by ADP.

ATP-sensitive K+ channels in inside-out membrane patches from dispersed rat pancreatic B-cells were studied using patch-clamp methods. The dose-response curve for ATP-induced channel inhibition was shifted to higher concentrations in the presence of ADP (2 mM). In glucose-free solution, the total intracellular concentration of ATP was 3.8 mM and of ADP 1.5 mM; glucose (20 mM) increased ATP and decreased ADP by approx. 40%. These results suggest that both ADP and ATP may be involved in regulating the activity of the glucose-sensitive K+ channel in intact B-cells.

Adenosine Diphosphate↗
PubMed1985

Inward rectification in the transverse tubular system of frog skeletal muscle studied with potentiometric dyes.

The non-penetrating potentiometric dyes NK2367 and WW375 were used to investigate the effect of inward rectification on the weighted-average tubular membrane potential in single frog muscle fibres voltage clamped using a three-Vaseline-gap method. In 100 mM-K solution, when inward rectification was activated by hyperpolarization the steady-state amplitude of the transverse tubular system (T-system) optical signal was reduced, and its rise time was faster than that recorded for an equivalent depolarization. The voltage dependence of the optical attenuation followed that of inward rectification, increasing with increasing hyperpolarization. For a voltage-clamp step of -140 mV the optical attenuation was 0.72 which corresponds to a weighted-average T-system potential change of 100 mV. When inward rectification was blocked in a Cs, TEA solution the optical attenuation was also abolished. The voltage dependence of the block of the inward currents in solutions containing low concentrations of Cs was also reflected in the T-system optical signals. Our results were satisfactorily predicted by a radial cable model of the T-system, assuming the same specific inward rectifier conductance in surface and tubular membranes. This analysis predicts that the measured optical attenuation corresponds to a decrease in the tubular space constant, lambda T, from 120 micron under passive conditions to about 40 micron when inward rectification is fully, activated. The voltage dependence of inward rectification measured at the surface membrane was reasonably well predicted by assuming that the specific conductance obeyed a Boltzmann type of voltage dependence; the major effect of tubular decrements was to reduce the steepness of the total (surface + T-system) conductance-voltage relation.

Animals↗
PubMed1983

T-system optical signals associated with inward rectification in skeletal muscle.

The resting potential of many excitable cells, including skeletal muscle, cardiac muscle, nerve cell bodies and egg cells, is determined by a resting potassium conductance which shows inward rectification, allowing potassium ions to move more readily inward across the cell membrane than outward. In skeletal muscle, where inward rectification has been extensively studied, a large part of this conductance is located in the T-system membranes. However, to date, only the kinetic and voltage-dependent properties of this conductance have been studied from analyses of the membrane potential or current recorded at the fibre surface. We report here measurements, obtained using a voltage-sensing dye, of potential changes in the T-system membranes associated with the inwardly rectifying K+ current. Our results show that this conductance alters the time course and significantly attenuates the amplitude of the potential change across the tubular membranes. These optical data provide new evidence for the presence of this conductance in the T-system and, when analysed using a radial cable model for the T-system, provide an estimate of the distribution of the inward rectifier conductance over the surface and T-system which is in agreement with estimates obtained by other techniques.

Animals↗
PubMed1983

The influence of the permeant ions thallous and potassium on inward rectification in frog skeletal muscle.

A three-electrode voltage-clamp method was used to investigate the inactivation of Tl currents through the inward rectifier of frog sartorius muscle fibres, and the interaction between the permeant ions Tl+ and K+. In 80 mM-Tl Ringer inward currents inactivated on hyperpolarization along an exponential time course, with time constants that initially increased and then fell with increasing hyperpolarization. Because of the inactivation process steady-state conductances were smaller than instantaneous conductances at all potentials in Tl Ringer. The steady-state conductance increased to a maximum value at around - 100 mV in 80 mM-Tl Ringer, and then fell with increasing hyperpolarization. In K Ringer the steady-state conductance was greater at all potentials than the instantaneous conductance because K currents activate (rather than inactivate) on hyperpolarization. Time constants of Tl inactivation were the same when measured from the decay of current during a single pulse, or from the rate of recovery from inactivation using either a two- or a three-pulse method, indicating that inactivation obeys first-order kinetics. In 80 mM-Tl Ringer steady-state inactivation increased with increasing hyperpolarization, e-fold every 48 mV. This would be consistent with the site at which inactivation occurs experiencing 0.5 of the membrane voltage field. Tl+ was more permeant than K+ through the inward rectifier, the permeability ratio PTl+/PK+ being 1.66. In solutions containing both Tl+ and K+ the membrane showed an anomalous mole-fraction dependence of conductance, the resting potential being more negative, and both instantaneous and steady-state conductances smaller than those recorded in solutions containing only Tl+ or only K+. The reduction in the amplitude of the instantaneous conductance in Tl-K mixtures was voltage-dependent, the block being initially increased and then falling with increasing hyperpolarization. Inward currents also inactivated on hyperpolarization in Tl-K mixtures. The time constants of inactivation, and the extent of inactivation which occurred, became less dependent on membrane potential in these solutions. When K+ is the major permeant ion in solution, Tl+ has a blocking effect on the currents carried by K+, and the degree of block is voltage-dependent. Increasing [Tl]o increased the block at all potentials. The results of our experiments in solutions containing both Tl+ and K+ are discussed in terms of an interaction between these ions within the channel.

Animals↗
PubMed1982

Calcium and potassium currents in muscle fibres of an insect (Carausius morosus).

1. A three electrode voltage-clamp was used to investigate membrane currents in the skeletal muscle fibres of the stick insect, Carausius morosus. Contraction was blocked by hypertonic solutions. 2. Membrane currents elicited by step depolarizations consisted of an inward current, an early outward current and a delayed outward current. 3. The reversal potential of the delayed outward current did not change when SO4(2-) was substituted for Cl-, but shifted by 14.1 mV when [K]0 was increased from 20 mM to 40 mM in SO4(2-) solution, suggesting that the delayed current is carried by K+. Both early and delayed outward currents were substantially reduced by 120 mM-tetraethylammonium (TEA) ions. 4. The small size of the shift in the reversal potential of the delayed outward current with increased pulse duration suggests that the delayed current measured flows mainly across the surface membrane. 5. Increasing [Ca]o made the apparent reversal potential for the inward current (120 mM-TEA Ringer) more positive and increased the size of the maximum inward current. However, Ca-currents showed saturation with increasing [Ca]o, indicating that there is a site to which Ca ions bind during their passage through the membrane. The dissociation constant of this site was 7.3 mM at 0 mV and was voltage-dependent. 6. Inward currents were blocked by 1 mM-La3+ or Cd2+, or by substitution of Co2+ or Ni2+ for Mg2+. Strontium and barium were able to permeate the channel but Na+ and Mg2+ appear impermeant. 7. As expected from the low intracellular Ca concentration, the instantaneous current-voltage relation of the Ca current rectified strongly in the inward direction. 8. Both constant field theory and the simplest, single site, Eyring rate theory model predict the rectification of the instantaneous current-voltage relation. The rate theory model also predicts saturation of the Ca current with [Ca]o.

Animals↗
PubMed1982

Calcium inactivation in skeletal muscle fibres of the stick insect, Carausius morosus.

1. Inactivation of Ca currents in skeletal muscle fibres of the stick insect, Carausius morosus, was studied using a three-electrode voltage-clamp method. 2. The extent of inactivation showed a voltage-dependence similar to that of the Ca current, inactivation being absent in the absence of a Ca current, maximal at potentials where Ca currents are largest, and reduced at potentials close to ECa. 3. Ca currents inactivated along a double exponential time course, both when measured from the decline of Ca current during a single pulse and when measured using a two pulse protocol. In 20 mM-Ca-Ringer the fast time constant of inactivation had a mean value of 27 msec and that of the slow time constant was 134 msec, at O mV and 5 degrees C. 4. The rate of inactivation was slowed, and its extent reduced, in low [Ca]o, where Ca currents are smaller. Similarly, inactivation was faster and more complete in high-Ca-Ringer. 5. The rate of recovery from inactivation also followed a double exponential time course, with time constants of 638 msec and 4 sec following a 500 msec inactivating pulse in 20 mM-Ca-Ringer at 5 degrees C. Recovery appeared to be related to the amount of Ca entry during the inactivating pulse, being slower in high [Ca]o and following longer inactivating pulses. 6. Inactivation was slowed and reduced in extent when Ba2+ or Sr2+ carried current. Inactivation in Ba solutions may be due to depletion of Ba2+ from the lumen of the transverse tubules. 7. Ba2+ does not compete with Ca2+ for the inactivation mechanism. 8. It is concluded that inactivation of Ca currents in stick insect muscle fibres is primarily mediated by Ca2+ entry.

Animals↗
PubMed1982

Calcium currents of frog and insect skeletal muscle fibres measured during voltage clamp.

Both vertebrate and invertebrate skeletal muscle fibres have Ca2+ permeability mechanisms which are turned on by depolarization of the surface membrane. In frog muscle, Ca currents are extremely slow and will be scarcely activated during the action potential that normally elicits a twitch. This Ca permeability cannot therefore play any substantial, direct role in excitation--contraction coupling. In insect (Carausius morosus) muscle, Ca currents activate within milliseconds of depolarization, even at low temperature, and may well play at least a triggering role in excitation--contraction coupling. These Ca currents show saturation with increasing [Ca]0, while the instantaneous current--voltage relation rectifies inwards, as expected from a very low [Ca]i. The Ca channel is permeable to Sr2+ and Ba2+. Inactivation of Ca currents under a maintained depolarization depends on Ca2+ carrying inward current, however, rather than on the depolarization itself.

Action Potentials↗
PubMed1981

Gating of a muscle K+ channel and its dependence on the permeating ion species.

In excitable cells, ions permeate the cell membrane through ionic channels, some of which open and close in response to changes in the potential difference across the membrane. It has been supposed that this opening and closing (or gating) process is largely independent of the permeating ion. However, we show here that the gating of the resting potassium permeability of frog skeletal muscle depends on the species of ion which carries current across the membrane. The potassium permeability investigated allows K+ to move in across the membrane more easily than out. This property is known as inward or anomalous rectification and is shared by cell membranes of skeletal muscle, egg and certain other cells. In both egg cells and skeletal muscle fibres, the group IIIB metal ion Tl+, which can replace K+ in several other systems in experimental conditions, also permeates the inward rectifier. Indeed, Tl+ is more permeant than K+ (refs 8, 9). However, when Tl+ carries current inwards across the membrane, the inward rectifier inactivates over a brief period when the membrane is hyperpolarized, whereas when K+ carries current, the permeability increases with time under hyperpolarization.

Animals↗
PubMedDate not supplied

Tissue-specific effects of sulfonylureas: lessons from studies of cloned K(ATP) channels.

Sulfonylureas stimulate insulin secretion in type-2 diabetic patients by blocking ATP-sensitive (K(ATP)) potassium channels in the pancreatic beta-cell membrane. This effect is mediated by the binding of the drug to the sulfonylurea receptor (SUR) subunit of the channel. K(ATP) channels are also present in other tissues, but often contain different types of SUR subunits (e.g., SUR1 in beta-cells, SUR2A in heart, SUR2B in smooth muscle). The sensitivity of these different types of K(ATP) channels to sulfonylureas is variable: gliclazide and tolbutamide block the beta-cell, but not the cardiac or smooth muscle, types of K(ATP) channel. In contrast, glibenclamide blocks all three types of channel with similar affinity. The reversibility of the drugs also varies, with tolbutamide and gliclazide being reversible on all three types of K(ATP) channel, while glibenclamide is reversible on cardiac, but not beta-cell, K(ATP) channels. This review summarizes current knowledge of how sulfonylureas act on the different types of K(ATP) channel found in beta-cells and in extrapancreatic tissues, and discusses the implications of these findings for their use as therapeutic agents.

Adenosine Triphosphate↗
PubMedDate not supplied

Glucose induces closure of single potassium channels in isolated rat pancreatic beta-cells.

The major physiological stimulus for the secretion of insulin from the pancreatic beta-cell is an increase in the plasma glucose concentration. It is well established that glucose-stimulated insulin secretion is associated with the appearance of electrical activity in the beta-cell; glucose concentrations above the threshold level for insulin release produce a slow membrane depolarization followed by either oscillatory bursts of action potentials (5-15 mM glucose) or continuous spiking (greater than 16 mM glucose). Tracer flux studies and microelectrode measurements using intact islets of Langerhans have indicated that the initial depolarization induced by glucose is caused by a decrease in the resting membrane permeability to potassium. Evidence also suggests that the electrical, ionic and secretory responses to glucose are mediated by the metabolism of the sugar within the beta-cell. By using cell-attached membrane patches from isolated rat pancreatic beta-cells, we have now identified a potassium channel (G-channel) that is active at the resting potential and is inhibited by glucose. Closure of this channel requires glucose metabolism. This is the first report of a potassium channel whose activity is modulated by glucose, and which may couple metabolic and ionic events involved in the secretion of insulin.

Action Potentials↗