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1.
The effects induced by lead ions on the short-circuit current (SCC) and on the potential difference (V) of the toad Pleurodema thaul skin were investigated. Pb2+ applied to the outer (mucosal) surface increased SCC and V and when applied to the inner (serosal) surface decreased both parameters. The stimulatory effect, but not the inhibitory action, was reversible after washout of the metal ion. The amiloride test showed that the increase was due principally to stimulation of the driving potential for Na+ (V-ENa+) and that inhibition was accompanied by a reduction in the V-ENa+ and also by a significant decrease in skin resistance indicating possible disruption of membrane and/or cell integrity. The effect of noradrenaline was increased by outer and decreased by inner administration of Pb2+. The results suggest that mucosal Pb2+ activates toad skin ion transport by stimulating the V-ENa+ and that serosal Pb2+, with easier access to membrane and cellular constituents, inactivates this mechanism, revealing greater toxicity when applied to the inner surface of the skin.
Abbreviations: SCC – short-circuit current; V – potential difference; V-ENa+– driving potential for Na+; ENaC – epithelial sodium channel; RNa+– active sodium resistance; RS – passive or shunt resistance; GNa– active sodium conductance; GS – passive or shunt conductance; Gmax – total conductance; EC50– half-maximal excitatory concentration; IC50– half maximal inhibitory concentration; NA – noradrenaline. 相似文献
2.
Summary Segments of descending colon obtained from rabbits, that had been maintained on drinking water containing 25mm NaCl and an artificial diet which contains 1% Na and is nominally K-free, respond to aldosterone in vitro (after a 30 to 60-min lag period) with a marked increase in the short-circuit current (I
sc
), an equivalent increase in the rate of active Na absorption (J
net
Na
) and a decline in tissue resistance (R
t
). Aldosterone also brings about a marked increase in the unidirectional influx of Na into the cells across the mucosal membrane (zero-time rate of uptake) which does not differ significantly from the increase inI
sc
. Treatment of control tissues with amphotericin B brings about sustained increases inI
sc
andJ
net
Na
to levels observed in aldosterone-treated tissues. However, addition of amphotericin B to the mucosal solution of aldosteronetreated tissues does not result in a sustained increase inI
sc
orJ
net
Na
and these values do not differ markedly from those observed in control tissues treated with amphotericin B. These findings, together with other evidence that Na entry in the presence of amphotericin B is sufficiently rapid to saturate the active Na extrusion mechanism at the baso-lateral membrane, are consistent with the notion that the aldosterone-induced protein increases the permeability of the mucosal membrane to Na but does not increase the saturation level of the active Na pump within the time-frame of these studies (3 hr).Finally, aldosterone has no effect on the bidirectional or net transepithelial movements of K under short-circuit conditions, suggesting that the enhanced secretion of K observed in vivo is the result of increased diffusion of K from plasma to lumen via paracellular pathways in response to an increased transepithelial electrical potential difference (lumen negative). 相似文献
3.
Summary The unidirectional influx of Na from the mucosal solution into the epithelium ofin vitro descending rabbit colon (J
me
Na
) determined under short-circuit conditions, is comprised of two components: one represents entry of Na into transporting epithelial cells and is abolished by amiloride which also abolishes Na absorption (J
net
Na
). The other represents diffusional Na entry into paracellular pathways traversing the epithelium. In all instances, exposure of the mucosal surface to amphotericin B increased tissue conductance andJ
me
Na
and elicited K secretion. Tissues showing a spontaneousI
sc of approximately 4 eq/cm2hr did not respond to amphotericin B with increasedI
sc andJ
net
Na
. However, in tissues characterized by a lowerI
sc under control conditions, amphotericin B increasedI
sc andJ
net
Na
to approximately 4eq/cm2hr. These findings suggest that amphotericin increasesJ
net
Na
and elicits K secretion by disrupting the normal permselectivity of the mucosal membrane. Under these conditions the extrusion of Na from cell-to-serosal solution becomes the rate limiting step in transepithelial Na transport. Finally, a close correlation betweenJ
me
Na
andJ
net
Na
was observed when the rate of Na absorption varied either spontaneously or experimentally with amiloride, suggesting that the backflux of Na from cell-to-mucosal solution is undetectably small. 相似文献
4.
Michael E. Duffey Klaus Turnheim Raymond A. Frizzell Stanley G. Schultz 《The Journal of membrane biology》1978,42(3):229-245
Summary Intracellular chloride activities, (Cl)c, in rabbit gallbladder were determined by using conventional (KCl-filled) microelectrodes and Cl-selective, liquid ionexchanger, microelectrodes. The results indicate that in the presence of a normal Ringer's solution, (Cl)c averages 35 mM; this value is 2.3 times that predicted for an equilibrium distribution across the mucosal and baso-lateral membranes. On the other hand, when the tissue is bathed by Na-free solutions, (Cl)c declines to a value that does not differ significantly from that predicted for an equilibrium distribution.These results, together with those of Frizzellet al. (J. Gen. Physiol.
65:769, 1975) provide, for the first time, compelling evidence that (i) the movement of Cl from the mucosal solution into the cell is directed against an electrochemical potential difference (23 mV); and (ii) this movement is energized by coupling to the entry of Na down a steep electrochemical potential difference.Finally, our data suggest that (i) Cl exit from the cell across the basolateral membrane may be coupled to the co-transport of a cation or the countertransport of an anion; and (ii) the mechanism responsible for active Na extrusion from the cell across the baso-lateral membrane is rheogenic (electrogenic), and is not the result of a neutral Na-K exchange. 相似文献
5.
Summary Effects of a potent synthetic glucocorticoid, methylprednisolone (MP), on transepithelial Na transport were examined in rabbit descending colon. Current-voltage (I–V) relations of the amiloride-sensitive apical Na entry pathway were measured in colonic tissues of control and MP-treated (40 mg im for 2 days) animals. Tissues were bathed mucosally by solutions of various Na activities, (Na)m, ranging from 6.2 to 75.6mm, and serosally by a high K solution. TheseI–V relations conformed to the constant field flux equation permitting determination of the permeability of the apical membrane to Na,P
Na
m
, and the intracellular Na activity, (Na)c. The following empirical relations were observed for both control and MP-treated tissues: (i) Na transport increases hyperbolically with increasing (Na)m obeying simple Michaelis-Mentin kinetics; (ii)P
Na
m
decreased hyperbolically with increasing (Na)m, but was unrelated to individual variations in (Na)c; (iii) (Na)c increased hyperbolically with (Na)m; (iv) both spontaneous and steroid-stimulated variations in Na entry rate could be attributed entirely to parallel variations inP
Na
m
at each mucosal Na activity. Comparison of these empirical, kinetic relations between control and MP-treated tissues revealed: (i) maximal Na current andP
Na
m
were greater in MP tissues, but the (Na)m's at which current andP
Na
m
were half-maximal were markedly reduced; (ii) (Na)c was significantly increased in MP tissues at each (Na)m while the (Na)m at half-maximal (Na)c was unchanged. These results provide direct evidence that glucocorticoids cause marked stimulation of Na absorption across rabbit colon primarily by increasing the Na permeability of the apical membrane. While the mechanism for the increased permeability remains to be determined, the altered relation betweenP
Na
m
and (Na)m suggests possible differences in the conformation or environment of the Na channel in MP-treated tissues. 相似文献
6.
Lawrence G. Palmer 《The Journal of membrane biology》1985,83(1-2):57-69
Summary The Na conductance of the apical membrane of the toad urinary bladder was measured at different concentrations of Na both in the external medium and in the cell. Bladders were bathed in high K-sucrose medium to reduce basal-lateral resistance and voltage, and the transepithelial currents measured under voltage-clamp conditions. Amiloride was used as a specific blocker of the apical Na channel. At constant external Na, the internal Na concentration was increased by blocking the basallateral Na pump with ouabain. With high Na activity in the mucosal medium (86mm), increases in intracellular Na activity from 10 to over 40mm increased the amiloride-sensitive slope conductance at zero voltage while apical Na permeability, estimated from current-voltage plots using the constant field equation, decreased by less than 20%. Lowering the serosal Ca concentration from 1 to 0.1mm had no effect on the change inP
Na with increasing Nac, but increasing serosal Ca to 5mm enhanced the reduction inP
Na with increasing Na
c
, presumably by increasing Ca influx into the cell.P
Na was also reduced by serosal vanadate (0.5mm), a putative blocker of ATP-dependent Ca extrusion from the cell, and by acute exposure to CO2, which presumably acidifies the cytoplasm. Current-voltage relationships of the amiloridesensitive transport pathway were also measured in the absence of a Na gradient across the apical membrane. These plots show that outward current passes through the channels somewhat less easily than does inward current. The shape of theI-V relationships was not significantly altered by changes in cellular Na, Ca or H, indicating that the effects of these ions onP
Na are voltage independent. 相似文献
7.
Summary Ion-sensitive glass microelectrodes, conventional microelectrodes and isotope flux measurements were employed inNecturus gallbladder epithelium to study intracellular sodium activity, [Na]
i
, electrical parameters of epithelial cells, and properties of active sodium transport. Mean control values were: [Na]
i
: 9.2 to 12.1mm; transepithelial potential difference,
ms
: –1.5 mV (lumen negative); basolateral cell membrane potential,
es
: –62 mV (cell interior negative); sodium conductance of the luminal cell membrane,g
Na: 12 mho cm–2; active transcellular sodium flux, 88 to 101 pmol cm–2 sec–1 (estimated as instantaneous short-circuit current). Replacement of luminal Na by K led to a decrease of the intracellular sodium activity at a rate commensurate to the rate of active sodium extrusion across the basolateral cell membrane. Mucosal application of amphotericin B resulted in an increase of the luminal membrane conductance, a rise of intracellular sodium activity, and an increase of short-circuit current and unidirectional mucosa to serosa sodium flux. Conclusions: (i) sodium transport across the basolateral membrane can proceed against a steeper chemical potential difference at a higher rate than encountered under control conditions; (ii) the luminal Na-conductance is too low to accommodate sodium influx at the rate of active basolateral sodium extrusion, suggesting involvement of an electrically silent luminal transport mechanism; (iii) sodium entry across the luminal membrane is the rate-limiting step of transcellular sodium transport and active sodium extrusion across the basolateral cell membrane is not saturated under control conditions. 相似文献
8.
(1) The active transport of Na+ across the turtle bladder epithelial cell layer consists of a passive entry step through a Na+-selective path in the apical membrane and an active extrusion step through Na+ pump-containing path in the basal-lateral membrane together with some back-leakage through the paracellular spaces and tight junctions between the epithelial cells. This hypothesis has now been verified qualitatively and to some extent, quantitatively by the use of an intracellularly-located microelectrode in conjunction with a conventional assembly of extracellularly-located macroelectrodes mainly in short-circuited bladders bathed by Na+-rich Ringer media. Under these conditions, the intracellular potential (Vsc) averaged 38.4 mV with the cell electronegative; the fractional resistance of the apical membrane () averaged 0.55; while the concomitant transepithelial parameters, short circuiting current (Isc) and electrical conductance (Gt), average 68.6 μA/cm2 and 0.98 mS/cm2, respectively. (2) The relation between these parameters and the transepithelial flow of Na+ (orIsc) is evoked by blocking Na+ entry into the cell (by the mucosal addition of amiloride or removal of mucosal Na+). Amiloride-induced blockade of the Na+ entry step results in a rapid hyperpolarization of the cell interior during which Vsc = —79.1 mV and . Isc and Gt (equivalent to the shunt conductance under these conditions) averaged 5 μA/cm2 and 0.35 mS/cm2, respectively. The entire process is reversible on re-admission of Na+ entry into the cell. (3) A slow depolarization of the cell interior in the period of blocked transapical Na+ entry is opposite to that expected from an electroneutral Na+-K+ exchanging pump; but instead is the predictable response of an electrogenic Na+ pump in parallel with a passive K+-selective conductance in the basal-lateral membrane. (4) The electrogenicity concept is substantiated after pretreatment of the bladder with serosal ouabain, which changes the response of Vsc to amiloride (from the aforementioned biphasic response) to a step-function response, attributable mainly to the development of a slowly dissipating K+ diffusion potential across the basallateral membrane. (5) Under open-circuit conditions, the electronegativity of cell to mucosa (Va) is a linear inverse function of the electropositivity of serosa to mucosa (Vt). For Vt ? 100 mV, Va is positive; and for Vt between ?30 and 90 mV, Va is negative. 相似文献
9.
《Molecular membrane biology》2013,30(3-4):339-365
In rat small intestine, the active transport of organic solutes results in significant depolarization of the membrane potential measured in an epithelial cell with respect to a grounded mucosal solution and in an increase in the transepithelial potential difference. According to the analysis with an equivalent circuit model for the epithelium, the changes in emf's of mucosal and serosal membranes induced by active solute transport were calculated using the measured conductive parameters. The result indicates that the mucosal cell membrane depolarizes while the serosal cell membrane remarkably hyperpolarizes on the active solute transport. Corresponding results are derived from the calculations of emf's in a variety of intestines, using the data that have hitherto been reported. The hyperpolarization of serosal membrane induced by the active solute transport might be ascribed to activation of the serosal electrogenic sodium pump. In an attempt to determine the causative factors in mucosal membrane depolarization during active solute transport, cell water contents and ion concentrations were measured. The cell water content remarkably increased and, at the same time, intracellular monovalent ion concentrations significantly decreased with glucose transport. Net gain of glucose within the cell was estimated from the restraint of osmotic balance between intracellular and extracellular fluids. In contrast to the apparent decreases in intracellular Na+ and K+ concentrations, significant gains of Na+ and K+ occurred with glucose transport. The quantitative relationships among net gains of Na+, K+ and glucose during active glucose transport suggest that the coupling ratio between glucose and Na+ entry by the carrier mechanism on the mucosal membrane is approximately 1:1 and the coupling ratio between Na+-efflux and K+-influx of the serosal electrogenic sodium pump is approximately 4:3 in rat small intestine. In addition to the electrogenic ternary complex inflow across the mucosal cell membrane, the decreases in intracellular monovalent ion concentrations, the temporary formation of an osmotic pressure gradient across the cell membrane and the streaming potential induced by water inflow through negatively charged pores of the cell membrane in the course of an active solute transport in intestinal epithelial cells are apparently all possible causes of mucosal membrane depolarization. 相似文献
10.
Hoegni J. Baerentsen Ove Christensen Grove Per Thomsen Thomas Zeuthen 《The Journal of membrane biology》1982,68(1):215-225
Summary A simple numerical model for theNecturus gallbladder epithelium is presented. K+, Na+ and Cl– cross the mucosal and serosal membranes as well as the junctions by means of electrodiffusion; furthermore the mucosal membrane contains a neutral entry mechanism for NaCl and the serosal membrane contains an active pump for K+ and Na+. The values which have been used for the model are taken from the literature. The model can only attain steady states if the resistance of the serosal membrane is lower than 1000 cm2. Values reported in the literature for the resistance of this membrane vary from about 3000 to about 100 cm2. We shall argue, however, that the higher estimates are in error because they are derived from a model of the tissue in which each membrane and the junction are modeled by a resistor; this procedure is invalid because the resistance of the lateral intercellular space relative to the resistance of the tight junctions is neglected and consequently the resistance of the serosal membrane is overestimated by a factor of about four. Apart from predicting a realistic steady state at normal external concentrations the model can predict quantitatively several experimental results obtained from the living epithelium. We have focused on the experiments which test the permeabilities of the serosal membrane and the properties of the pump:i) Replacement of serosal Cl– by an impermeant ion.ii) Replacement of serosal K+ by Na+.iii) Inhibiting the (Na+, K+)-pump. The best correspondence between model and experiments is obtained when the pump is assumed to be electrogenic (or rheogenic) with a ratio of coupling between Na+ and K+ of 32. In this case both model and direct experiments (also presented in this paper) show an initial abrupt depolarization of 6 to 7 mV. The model also shows that it cannot be concluded fromi andii that the Cl– permeability of the serosal membrane is low. The model explains, even with high passive Cl– permeabilities, why the intracellular Cl– concentration is relatively unaffected by paracellular currents, a fact which in other epithelia has been taken as an implication of a low Cl– permeability of the serosal membranes. 相似文献
11.
Summary Rabbit erythrocytes are well known for possessing highly active Na+/Na+ and Na+/H+ countertransport systems. Since these two transport systems share many similar properties, the possibility exists that they represent different transport modes of a single transport molecule. Therefore, we evaluated this hypothesis by measuring Na+ transport through these exchangers in acid-loaded cells. In addition, selective inhibitors of these transport systems such as ethylisopropyl-amiloride (EIPA) and N-ethylmaleimide (NEM) were used. Na+/Na+ exchange activity, determined as the Na
o
+
-dependent22Na efflux or Na
i
+
-induced22Na entry was completely abolished by NEM. This inhibitor, however, did not affect the H
i
+
-induced Na+ entry sensitive to amiloride (Na+/H+ exchange activity). Similarly, EIPA, a strong inhibitor of the Na+/H+ exchanger, did not inhibit Na+/Na– countertransport, suggesting the independent nature of both transport systems. The possibility that the NEM-sensitive Na+/Na+ exchanger could be involved in Na+/H+ countertransport was suggested by studies in which the net Na+ transport sensitive to NEM was determined. As expected, net Na+ transport through this transport system was zero at different [Na+]
i
/[Na+]
o
ratios when intracellular pH was 7.2. However, at pH
i
=6.1, net Na+ influx occurred when [Na+]
i
was lower than 39mm. Valinomycin, which at low [K+]
o
was lower than 39mm. Valinomycin, which at low [K+]
o
clamps the membrane potential close to the K+ equilibrium potential, did not affect the net NEM-sensitive Na+ entry but markedly stimulated, the EIPA-and NEM-resistant Na+ uptake. This suggest that the net Na+ entry through the NEM-sensitive pathway at low pH
i
, is mediated by an electroneutral process possibly involving Na+/H+ exchange. In contrast, the EIPA-sensitive Na+/H+ exchanger is not involved in Na+/Na+ countertransport, because Na+ transport through this mechanism is not affected by an increase in cell Na– from 0.4 to 39mm. Altogether, these findings indicate that both transport systems: the Na+/Na+ and Na+/H+ exchangers, are mediated by distinct transport proteins. 相似文献
12.
Klaus Turnheim Raymond A. Frizzell Stanley G. Schultz 《The Journal of membrane biology》1978,39(2-3):233-256
Summary Ouabain abolishes the short-circuit current (I
sc
) and decreases the transepithelial conductance (G
t
) of rabbit colon. In contrast, amphotericin B elicits a maximumI
sc
and markedly increasesG
t
. However, inboth instances the amiloride-sensitive Na entry step is completely blocked, presumably due to an increase in cell Na. Conversely, when Na-depleted tissues are suddenly exposed to 140mm Na, the amiloride-sensitiveI
sc
and the amiloride-sensitive component ofG
t
(
a
G
Na
) increase abruptly to their maximum values and the decline to steady-state plateaus with a half time of 6 min; throughout the decline (I
sc/a
G
Na)=E
Na is constant at a value of 95 mV. In the presence of amphotericin B, theI
sc
abruptly rises to the same maximum but does not decline. These findings indicate that in the presence of 140mm Na the conductance of the amiloride-sensitive Na entry step can vary from a maximum value of approximately 1.6 mmhos/cm2 when cell Na is depleted, to zero when cell Na is abnormally elevated (e.g., in the presence of ouabain or amphotericin B). Our findings are consistent with a system in which the pathway responsible for transcellular Na transport parallels another cellular compartment with which it communicates. The Na capacity of the active transport pathway appears to be very small so that this compartment fills rapidly after exposure of Na-depleted cells to 140mm Na, and active transepithelial Na transport is initiated and reaches steady-state levels quickly. The Na capacity of the second compartment is much larger; the Na content of this compartment appears to be responsible for the negative feedback effect on the permeability of the amiloride-sensitive entry step. 相似文献
13.
Summary Na, K-ATPase function was studied in order to evaluate the mechanism of increased colonic Na+ transport during early postnatal development. The maximum Na+-pumping activity that was represented by the equivalent short-circuit current after addition of nystatin (I
sc
N
) did not change during postnatal life or after adrenalectomy performed in 16-day-old rats.I
sc
N
was entirely inhibited by ouabain; the inhibitory constant was 0.1mm in 10-day-old (young) and 0.4mm in 90-day-old (adult) rats. The affinity of the Na, K pump for Na+ was higher in young (11mm) than in adult animals (19mm). The Na, K-ATPase activity (measured after unmasking of latent activity by treatment with sodium dodecylsulfate) increased during development and was also not influenced by adrenalectomy of 16-day-old rats. The inhibitory constant for ouabain (K
I
) was not changed during development (0.1–0.3mm). Specific [3H]ouabain binding to isolated colonocytes increased during development (19 and 82 pmol/mg protein), the dissociation constant (K
D
) was 8 and 21 m in young and adult rats, respectively. The Na+ turnover rate per single Na, K pump, which was calculated fromI
sc
N
and estimated density of binding sites per cm2 of tissue was 500 in adult and 6400 Na+/min·site in young rats. These data indicate that the very high Na+ transport during early postnatal life reflects an elevated turnover rate and increased affinity for Na+ of a single isoform of the Na, K pump. The development of Na+ extrusion across the basolateral membrane is not directly regulated by corticosteroids. 相似文献
14.
Raymond A. Frizzell Philip L. Smith Evan Vosburgh Michael Field 《The Journal of membrane biology》1979,46(1):27-39
Summary Measurements of the unidirectional influxes of Na and Cl from the mucosal solution into the epithelium (J
me
) of flounder intestine under short-circuit conditions reveal the presence of a coupled NaCl influx process at the brush border membrane which appears to be essential for the absorption of these ions.J
me
Cl
andJ
me
Na
were inhibited by replacing Na or Cl, respectively, in the bathing media with nontransported ions which also reduced the short-circuit current (I
sc) to near-zero values. Addition of furosemide to the mucosal solution alone inhibited theI
sc and reducedJ
me
Cl
andJ
me
Na
under control conditions, but not in the absence of Na or Cl, respectively. The reductions inJ
me
Cl
andJ
me
Na
elicited by ion replacement or furosemide were approximately equal, suggesting that the coupled influx mechanism mediates a one-for-one entry of these ions into the cell from the mucosal solution. Furosemide inhibited Cl absorption by reducing the unidirectional Cl flux from mucosa to serosa, consistent with its inhibition of the influx process. As in other epithelia, coupled NaCl influx is inhibited by cyclic AMP, which accounts for the decrease in Cl absorption elicited by cyclic nucleotides. These results support the notion thattranscellular NaCl transport is a neutral process and that the serosa-negative transepithelial electrical potential difference and preponderance of Cl over Na absorption under short-circuit conditions result from dissimilar permeabilities of the paracellular pathway to Na and Cl. 相似文献
15.
Douglas C. Eaton A. Michael Frace S. Unglaub Silverthorn 《The Journal of membrane biology》1982,67(1):219-229
Summary The apical membrane of rabbit urinary bladder can be functionally removed by application of nystatin at high concentration if the mucosal surface of the tissue is bathed in a saline which mimics intracellular ion concentrations. Under these conditions, the tissue is as far as the movement of univalent ions no more than a sheet of basolateral membrane with some tight junctional membrane in parallel. In this manner the Na+ concentration at the inner surface of the basolateral membrane can be varied by altering the concentration in the mucosal bulk solution. When this was done both mucosal-to-serosal22Na flux and net change in basolateral current were measured. The flux and the current could be further divided into the components of each that were either blocked by ouabain or insensitive to ouabain. Ouabain-insensitive mucosal-to-serosal Na+ flux was a linear function of mucosal Na+ concentration. Ouabain-sensitive Na+ flux and ouabain-sensitive, Na+-induced current both display a saturating relationship which cannot be accounted for by the presence of unstirred layers. If the interaction of Na+ with the basolateral transport process is assumed to involve the interaction of some number of Na+ ions,n, with a maximal flux,M
max, then the data can be fit by assuming 3.2 equivalent sites for interaction and a value forM
max of 287.8pm cm–2 sec–1 with an intracellular Na concentration of 2.0mm Na+ at half-maximal saturation. By comparing these values with the ouabain-sensitive, Na+-induced current, we calculate a Na+ to K+ coupling ratio of 1.40±0.07 for the transport process. 相似文献
16.
Bruce F. Scharschmidt Edwin R. Griff Roy H. Steinberg 《The Journal of membrane biology》1988,106(1):71-81
Summary The apical surface of the retinal pigment epithelium (RPE) faces the neural retina whereas its basal surface faces the choroid. Taurine, which is necessary for normal vision, is released from the retina following light exposure and is actively transported from retina to choroid by the RPE. In these experiments, we have studied the effects of taurine on the electrical properties of the isolated RPE of the bullfrog, with a particular focus on the effects of taurine on the apical Na+–K+ pump.Acute exposure of the apical, but not basal, membrane of the RPE to taurine decreased the normally apical positive transepithelial potential (TEP). This TEP decrease was generated by a depolarization of the RPE apical membrane and did not occur when the apical bath contained sodium-free medium. With continued taurine exposure, the initial TEP decrease was sometimes followed by a recovery of the TEP toward baseline. This recovery was abolished by strophanthidin or ouabain, indicating involvement of the apical Na+–K+ pump.To further explore the effects of taurine on the Na+–K+ pump, barium was used to block apical K+ conductance and unmask a stimulation of the pump that is produced by increasing apical [K+]
0
. Under these conditions, increasing [K+]
0
hyperpolarized the apical membrane and increased TEP. Taurine reversibly doubled these responses, but did not change total epithelial resistance or the ratio of apical-to-basal membrane resistance, and ouabain abolished these responses.Collectively, these findings indicate the presence of an electrogenic Na+/taurine cotransport mechanism in the apical membrane of the bullfrog RPE. They also provide direct evidence that taurine produces a sodium-dependent increase in electrogenic pumping by the apical Na+–K+ pump. 相似文献
17.
Sodium movements in the human red blood cell 总被引:19,自引:9,他引:10
J R Sachs 《The Journal of general physiology》1970,56(3):322-341
Measurements were made of the sodium outflux rate constant, o
k
Na, and sodium influx rate constant, i
k
Na, at varying concentrations of extracellular (Nao) and intracellular (Nac) sodium. o
k
Na increases with increasing [Nao] in the presence of extracellular potassium (Ko) and in solutions containing ouabain. In K-free solutions which do not contain ouabain, o
k
Na falls as [Nao] rises from 0 to 6 mM; above 6 mM, o
k
Na increases with increasing [Nao]. Part of the Na outflux which occurs in solutions free of Na and K disappears when the cells are starved or when the measurements are made in solutions containing ouabain. As [Nao] increases from 0 to 6 mM, i
k
Na decreases, suggesting that sites involved in the sodium influx are becoming saturated. As [Nac] increases, o
k
Na at first increases and then decreases; this relation between o
k
Na and [Nac] is found when the measurements are made in high Na, high K solutions; high Na, K-free solutions; and in (Na + K)-free solutions. The relation may be the consequence of the requirement that more than one Na ion must react with the transport mechanism at the inner surface of the membrane before transport occurs. Further evidence has been obtained that the ouabain-inhibited Na outflux and Na influx in K-free solutions represent an exchange of Nac for Nao via the Na-K pump mechanism. 相似文献
18.
We have measured the voltage dependence of the Na/K pump in isolated adult rat cardiac myocytes using the whole-cell patch-clamp technique. In the presence of 1–2 mM Ba and 0.1 mm Cd and nominally Ca-free, Na/K pump current (I
p) was measured as the change in current due to 1 mM ouabain. Voltage dependence of I
pwas measured between –140 and +40 or +60 mV using square voltage-pulse and voltage-ramp protocols, respectively. With 150 mM extracellular Na (Na
o
) and 5.4 mM extracellular K (K
o
), we found that the Na/K pump shows a strong positive voltage dependence between –140 and 0 mV and is voltage independent at positive potentials. Removing Na
o
reduced the voltage dependence at negative potentials with no effect at positive potentials. When K
o
was reduced, a negative slope appeared in the current-voltage (I-V) curve at positive potentials. We have investigated whether Na
i
(intracellular Na) might also affect the voltage dependence of I
pby varying Na in the patch pipette (Napip) between 20 and 85 mM. We found, as expected, that I
pincreased markedly as Napip was raised, saturating at about 70 mM Napip under these conditions. In contast, while I
psaturated near +20 mV and declined to about 40% of maximum at –120 mV, there was no effect of Napip under these conditions. In contrast, while I
psaturated near +20 mV and declined to about 40% of maximum at –120 mV, there was no effect of Napip on the voltage dependence of I
p. This suggests that neither Na
i
binding to the Na/K pump nor the conformational changes dependent on Na
i
binding are voltage dependent. These results are consistent with extracellular ion binding within the field of the membrane but do not rule out the possibility that other steps, such as Na translocation, are also voltage dependent.We wish to thank Ms. Melinda Price, Ms. Meei Liu and Mr. Randall Anderson for their technical assistance. This work was supported in part by National Institutes of Health grant HL44660. 相似文献
19.
Summary Ion transport and electrical properties of rabbit and guinea pig gallbladders were investigated to gain further information about the active transport mechanism that mediates fluid absorption. The intracellular and transepithelial electrical potentials were measured simultaneously using the microelectrode technique. Exposure of the mucosal surface to Amphotericin B resulted in the prompt development of a serosa-positive electrical potential difference (PD) which could not be attributed to an alteration in ion diffusion potentials across either the cell membrane or across the tight junction. Because the Amphotericin B-inducedPD was immediately dependent on warm temperatures and O2, and was independent of NA and K concentration gradients across the cell membrane, it is suggested that active ion transport is directly responsible for thePD. Since thePD was abolished in the absence of Na in the bathing solutions, a rheogenic Na pump is postulated; this pump also appears to be operative in tissue not exposed to Amphotericin B. The specific tissue properties altered by Amphotericin B to produce a serosa-positivePD remain incompletely defined. The results of the present study indicate that ion transport by rabbit gallbladderin vitro is a consequence of a rheogenic active Na transport mechanism at the basolateral membranes which, in conjunction with a coupled NaCl influx process at the mucosal border, ultimately results in absorption of NaCl and water. 相似文献
20.
André B. Borle 《The Journal of membrane biology》1982,66(1):183-191
Summary The influence of extracellular Na (Na
o
) on cellular Ca transport and distribution was studied in rat kidney slices. Calcium efflux from prelabeled slices was depressed when Na
o
was completely replaced by choline or tetraethylammonium (TEA) ions and it was markedly stimulated when Na was reintroduced in a Na-free medium. However, reducing Na
o
(with choline or TEA as substituting ions) did not increase the total slice40Ca, their total exchangeable Ca pool, or the40Ca or45Ca of mitochondria isolated from these slices. Kinetic analyses of steady-state45Ca desaturation curves showed that reducing Na
o
depressed the exchange of Ca across the plasma membrane, slightly decreased the cytosolic Ca pool, but did not significantly affect the mitochondrial Ca pool and Ca cycling. Ouabain (10–3
m) which should reduce the Na gradient across the plasma membrane had no effect on calcium distribution and transport. These results suggest that in kidney cells low Na
o
depresses Ca influx as well as Ca efflux; there may be an interaction between Na and Ca at a possible carrier located in the plasma membrane, but there is no Na/Ca exchange as described in several excitable tissues. 相似文献