The Role of Membrane Potential for the Control of Elongation Growth of Vigna Hypocotyl: Response of a Hollow Cylinder to Osmotic and Ionic Stress

We have devised an experimental system of perfusion througha hollow cylinder of a Vigna hypocotyl to examine the controlmechanism of plant stem elongation. When the cylinder was subjectedto osmotic stress, it began to shrink and then spontaneouslyresumed elongation. Not only the membrane potential differencebetween the parenchyma symplast and the central bore (V_px),but also that between the parenchyma symplast and the organsurface (V_ps), showed hyperpolarization a few minutes afterthe cylinder began to shrink. Removal of the stress caused animmediate increase in elongation rate followed by depolarizationof both membrane potentials a few minutes later. When the cylinderwas subjected to KCl stress, V_px showed transient depolarizationand recovery, while V_ps showed only immediate hyperpolarization.Increasing the KCl concentration caused V_px to depolarize, andthe cylinder simultaneously to cease to elongate for about 5min,even when the osmotic concentration of the perfusion solutionwas kept almost constant. An inverse reaction was observed whenthe KCl concentration was decreased. These two reversible responses suggest that control of V_px mayregulate the elongation of hollow cylinders, and that the xylempump plays an important role in the regulation of intact stemelongation. (Received January 7, 1987; Accepted April 30, 1987)     

Structure and function of the elongation sink in the stems of higher plants I. Effects of anoxia and IAA on the growth rate and the spatially separate electrogenic ion pumps

Two spatially separate membrane potentials of the parenchymasymplast (7, 8) and the rate of elongation growth were measuredsimultaneously in bean hypocotyl segments. Both the membrane potentials, V_ps (electric potential differencebetween parenchyma symplast and organ surface) and V_px (electricpotential difference between parenchyma symplast and xylem),were rapidly depolarized by anoxia, and were repolarized withre-aeration. Anoxia reduced the growth rate by about 85%, andre-aeration restored it. Changes in the membrane potentialspreceded those in the growth rate by 30–50 sec. About 8 min after the application of aerosol generated from10^–3 M indole acetic acid (IAA) solution to the segments,V_ps began to hyperpolarize, and the growth rate increased witha delay of several minutes after the potential change and subsequentlybecame ten times the control rate. This hyperpolarization ofV_ps was due to the increase in the activity of the respiration-dependentelectrogenic ion pump at the outer surface membrane of the parenchymasymplast. A clear correlation was observed between the growthrate and pump activity (V_ps) with the change in IAA concentration. (Received December 6, 1979; )     

Distribution of electric potential and ion transport in the hypocotyl of Vigna sesquipedalis VI. The dual structure of radial electrogenic activity

The electrophysiological structure in bean hypocotyl was investigatedby the intracellular electrode method in combination with surfaceelectric potential (V_s) measurement and respiratory inhibitionby anoxia, with special reference to the membrane transportof ions and the formation of an absorption centre in the elongating(E) zone. The radial potential difference (V_sx: electric potentialdifference between the organ surface and a xylem vessel), onwhich axial distribution of V_a was dependent, comprised twocomponents; V_ax=V_px–V_ps. |V_px| (the potential differencebetween the inside of a parenchyma symplast and a xylem vessel)was at a maximum in the E-zone, while |V_ps| (the intracellularelectric potential with respect to the organ surface) was largestin the G-zone (mature zone), resulting in the characteristicdistribution pattern of V_s with a minimum in the E-zone. Therewere two independent electromotive forces which were both partiallydependent on respiration; one corresponding to V_ps located atthe surface of the parenchyma symplast (P) and the other toV_px located between P and the xylem (X). The electrogenic componentof Vpx was relatively small both in the hook (H) zone and theG-zone, but maximal in the E-zone of the hypocotyl. This resultwas consistent with the emergence of a maximum pH differencebetween P and X in the E-zone, where accumulation of K⁺ andwater were at a maximum, suggesting maximum activity of an H⁺-pumpextruding protons from P into X in exchange for K⁺. (Received July 17, 1978; )     

Potassium Channels at Chara Plasmalemma

Exposure to high K⁺ medium transforms Chara plasmalemma into[K⁺]_osensitive state (K⁺ state). The current-voltage (I/V)characteristicsunder such conditions display a negative conductance region.This feature results from the complex time and voltage dependenceof K⁺ channel opening At potentials more negative than a thresholdp.d. the channels are closed and the I/V characteristics becomelinear with a low slope conductance of 0.8 S m² and only a weakdependence on [K⁺]_o. Such behaviour is usually associated witha non-specific leak current The threshold level for K⁺ channelclosing depends on [K⁺]_o. In 2.0 mol m^–3 and 5.0 mol m^–3K⁺ medium the membrane resting p.d. follows E_K, but hyperpolarizesgradually if the [K⁺]_o is lowered. The proton pump thus appearsto be non-operative, while the cell is in the K⁺ state, andrecovers slowly as the cell is returned to a low K⁺ medium.Excitation currents decline if the cells are kept in K⁺ statefor some hours. Key words: K⁺ channels, Chara corallina, Proton pump, Current/, oltage characteristics, Conductance     

Wild Oat/Barley Interactions: Varietal Differences in Competitiveness in Relation to K+ Supply

Eight cvs of barley (Hordeum vulgare L.) were separately plantedwith Wild Oats (Avena fatua L., genetically pure line CS40)in a sand culture with two external K⁺ concentrations. Substantialdifferences were observed among barley cvs in their abilityto compete with wild oat. The variety Fergus was highly competitiveat both high and low [K⁺]_e, whereas Steptoe was competitiveonly at high [K⁺]_e, and Compana was only weakly competitivewith wild oat. The differences between barley cvs were relatedto their previously reported efficiencies of K⁺ uptake and utilization. Hordeum vulgare L., Avena fatua L., barley, wild oat, competition, K⁺ nutrition, utilization efficiency     

Efficiency of K+ Utilization by Barley Varieties: Activation of Pyruvate Kinase

Barley (Hordeum vulgare L.) varieties differed in their raponseto [K⁺]₀, in terms of their utilization efficiencies (UE = freshweight. concentration of [K⁺]₁^–1). At low [K⁺]₀, Compana,an efficient-non-responder demonstrated superior utilizationof absorbed K⁺. On the other hand, at high [K⁺]₀, Fergus (anefficient responder) and BT 334 (an inefficient responder) hadhigher UE values for K⁺ than Compana which performed poorlyat this [K⁺]₀. Kinetic parameters for K⁺ activation of the enzyme pyruvatekinase from 12 barley varieties, representing a range of UEvalues, were determined. Varieties showed substantial differencesin their V_max values (P<0·01). Compana, an efficientvariety, had the highest V_max (31 µmol g^–1 freshwt. h^–1) which was about 50% higher than that of Mingo,an inefficient variety. By contrast, K_m values for the enzymeswere not significantly different among varieties The mean valuesfor all varieties (3·9±0·15 mol m^–3K⁺) is far below the estimated cytoplasmic [K⁺] (100-200 molm^–3). It is, therefore, unlikely that differences in theutilization of K⁺ by these varieties can be explained on thebasis of differential requirements for (K⁺) activation of theseenzymes. Alternative possibilities for differences in the utilizationof K⁺ are discussed. Key words: K⁺ utilization efficiency, Pyruvate kinase, Barley varieties     

Mechanisms of solute efflux from seed coats: whole-cell K+ currents in transfer cell protoplasts derived from coats of developing seeds of Vicia faba L.

In developing seed ofVicia faba L., solutes imported throughthe phloem of the coats move symplastically from the sieve elementsto a specialized set of cells (the thin-walled parenchyma transfercells) for release to the seed apoplast. Potassium (K⁺) is thepredominant cation released from the seed coats. To elucidatethe mechanisms of K⁺ efflux from seed coat to seed apoplast,whole-cell currents across the plasma membranes of protoplastsof thin-walled parenchyma transfer cells were measured usingthe whole-cell patch-clamp technique. Membrane depolarizationelicited a time-dependent and an instantaneous outward current.The reversal potential (E_R of the time-dependent outward currentwas close to the potassium equilibrium potential (E_K and itshifted in the same direction as E_K upon changing the externalK⁺ concentration, indicating that this current was largely carriedby an efflux of K⁺. The activation of the time-dependent outwardK⁺ current could be well fitted by two exponential componentsplus a constant. The instantaneous outward current could alsobe carried by K⁺ efflux as suggested by ion substitution experiments.These K⁺ outward rectifier currents elicited by membrane depolarizationare probably too small to represent the mechanism for the normalK⁺ efflux from seed coat cells. Membrane hyperpolarization morenegative than –80 mV activated a time-dependent inwardcurrent. K⁺ influx was responsible for the inward current asthe current reversed at membrane voltage close to E_K and shiftedin the same direction as E_K when external [K⁺] was varied. Activationof this K⁺inward rectifier current was well fitted with twoexponential components plus a constant. A regulating functionfor this current is suggested. Key words: Potassium outward rectifier, potassium inward rectifier, transfer cell protoplast, seed coat, Vicia faba L     

Role of K+ and Cl- in Osmotic Adjustment in Roots and Hypocotyls of Intact Mung Bean Seedlings

It was confirmed that osmotic adjustment occurred in young intactmung bean (Vigna mungo (L.) Hepper) seedlings exposed to highosmotic pressure stress. Root growth was not affected by osmoticpressure of less than 200 mOsra in the external solution, althoughhypocotyl growth was conspicuously reduced. Under this moderateosmotic stress, intracellular K⁺ concentration, [K⁺]_i, increaseddramatically during the osmotic adjustment in all the regionsof the root, but the intracellular Cl^– concentration,[Cl^–]_i, increased only in the aged mature region of theroot (28–33 mm from the root tip). About a half of theintracellular osmotic pressure in the aged mature region ofthe root could be ascribed to the contributions of [K⁺]_i and[Cl^–]_i, but in the hypocotyl, [K⁺]_i only contributed slightlyto the osmotic adjustment. (Received June 18, 1986; Accepted August 26, 1986)     

Efficiency of Potassium Utilization by Barley Varieties: The Role of Subcellular Compartmentation

Memon, A. R., Saccomani, M. and Glass, A. D. M. 1985. Efficiencyof potassium utilization by barley varieties: The role of subcellularcompartmentation.?J. exp. Bot. 36: 1860–1876. The subcellulardistributions of K⁺ in roots of three barley (Hordeum vulgareL.) varieties, grown at 10 and 100 mmol m^–3 external K⁺([K⁺]_o) were estimated by compartmental analyses. In general,increased [K⁺]_o caused a 2–3 fold increase in vacuolar[K⁺], but cytoplasmic [K⁺] increased only slightly. Nevertheless,the three varieties, which had been selected for study on thebasis of their different rates of K⁺ utilization, showed distinctdifferences in the allocation of K⁺ between cytoplasm and vacuole.At 10 mmol m^–3 [K⁺]_o var. Betzes exhibited typical K⁺deficiency symptoms while var. Fergus and var. Compana did not,even though Betzes had higher [K⁺] in shoots and roots. Theinefficient utilization of K⁺ in this variety appears to beassociated with a failure to mobilize vacuolar K⁺ into the cytoplasmiccompartment (the ratio of vacuolar: cytoplasmic K⁺ contentsfor Betzes was 4.1 compared to 2.7 and 2.5, respectively, forFergus and Compana). Fergus and Betzes, which demonstrate pronouncedgrowth responses to increased [K⁺]₀ between 10 and 100 mmolm^–3, showed significant increases of cytoplasmic [K⁺]in this range of [K⁺]_o. By contrast, cytoplasmic [K⁺] in Compana,a variety whose growth is not stimulated by increased [K⁺]₀(from 10 to 100 mmol m^–3) showed virtually no increase.It is suggested that the efficiency of K⁺ utilization and thegrowth response to [K⁺]₀ in these varieties are functions ofthe subcellular distribution of this ion between cytoplasm andvacuole. Key words: Barley varieties, K⁺ subcellular compartmentation, utilization efficiency     

K+ Channel in the Chora Plasmalemma: Estimations of K+ Channel Density and Single K+ Channel Conductance

The electromotive force E and the conductance G of the Characorallina plasmalemma were measured under voltage clamp conditions.In the depolarized voltage range less negative than –60mV, E changed according to the Nerhst equation for K⁺, and Gincreased with the external K⁺ concentration [K⁺]_o and alsowith the depolarization of the membrane potential. This is attributedto the voltage-dependent opening of the K⁺ channels in the largelydepolarized voltage region. The voltage-dependent increase ofG was due to the increase of the number of open K⁺ channelsper unit area. The density of the total K⁺ channels in the C. corallina plasmalemmawas estimated to be about 6.50/(10 µm)2. The single K⁺channel conductance _K changed with the external [K⁺]_o; it was79.3, 86.1, 105.9, 119.0 pS for external [K⁺]_o of 0.2, 0.5,2.0 and 5.0 mu respectively. (Received May 22, 1986; Accepted August 22, 1986)     

Role of extracellular [Ca2+] in fatigue of isolated mammalian skeletal muscle

The possiblerole of altered extracellular Ca²⁺concentration([Ca²⁺]_o)in skeletal muscle fatigue was tested on isolated slow-twitch soleusand fast-twitch extensor digitorum longus muscles of the mouse. Thefollowing findings were made. 1) Achange from the control solution (1.3 mM[Ca²⁺]_o)to 10 mM[Ca²⁺]_o,or to nominally Ca²⁺-freesolutions, had little effect on tetanic force in nonfatigued muscle.2) Almost complete restoration oftetanic force was induced by 10 mM[Ca²⁺]_oin severely K⁺-depressed muscle(extracellular K⁺ concentration of10-12 mM). This effect was attributed to a 5-mV reversal of theK⁺-induced depolarization andsubsequent restoration of ability to generate action potentials(inferred by using the twitch force-stimulation strength relationship).3) Tetanic force depressed bylowered extracellular Na⁺concentration (40 mM) was further reduced with 10 mM[Ca²⁺]_o.4) Tetanic force loss at elevatedextracellular K⁺ concentration (8 mM) and lowered extracellular Na⁺concentration (100 mM) was partially reversed with 10 mM[Ca²⁺]_oor markedly exacerbated with low[Ca²⁺]_o.5) Fatigue induced by using repeatedtetani in soleus was attenuated at 10 mM[Ca²⁺]_o(due to increased resting and evoked forces) and exacerbated at low[Ca²⁺]_o.These combined results suggest, first, that raised[Ca²⁺]_oprotects against fatigue rather than inducing it and, second, that aconsiderable depletion of[Ca²⁺]_oin the transverse tubules may contribute to fatigue.

     

Voltage-dependent stimulation of the Na(+)-K(+) pump by insulin in rabbit cardiac myocytes

Insulin enhancesNa⁺-K⁺ pump activity in various noncardiactissues. We examined whether insulin exposure in vitro regulates Na⁺-K⁺ pump function in rabbit ventricularmyocytes. Pump current (I_p) was measured using thewhole-cell patch-clamp technique at test potentials(V_ms) from 100 to +60 mV. When theNa⁺ concentration in the patch pipette([Na]_pip) was 10 mM, insulin caused aV_m-dependent increase in I_p.The increase was ~70% when V_m was at nearphysiological diastolic potentials. This effect persisted afterelimination of extracellular voltage-dependent steps and whenK⁺ and K⁺-congeners were excluded from thepatch pipettes. When [Na]_pip was 80 mM, causingnear-maximal pump stimulation, insulin had no effect, suggesting thatit did not cause an increase in membrane pump density. Effects oftyrphostin A25, wortmannin, okadaic acid, or bisindolylmaleimide I inpipette solutions suggested that the insulin-induced increase inI_p involved activation of tyrosine kinase,phosphatidylinositol 3-kinase, and protein phosphatase 1, whereasprotein phosphatase 2A and protein kinase C were not involved.

     

Regulation of K+ Influx in Barley: Evidence for a Direct Control of Influx by K+ Concentration of Root Cells

Siddiqi, M. Y. and Glass, A. D. M. 1987. Regulation of K⁺ influxin barley: Evidence for a direct control of influx by K⁺ concentrationof root cells.—J. exp. Bot. 38: 935–947. The kinetics of K⁺ (⁸⁶Rb⁺) influx into intact roots of barley(Hordeum vulgare L. cv. Fergus) seedlings having different combinationsof root and shoot [K⁺], different growth rates and differentroot:shoot weight ratios were studied. K⁺ influx was stronglycorrelated with root [K⁺]; shoot [K⁺], growth rates, and root:shoot ratios appeared to have little effect on K⁺ influx. Adetailed study showed that both V_max and K_m for K⁺ influx wereaffected by root [K⁺] but not by shoot [K⁺]. We have suggestedthat factors such as growth rates and root: shoot ratio mayaffect K⁺ influx indirectly primarily via their influence onroot factors such as root [K⁺]. We have reiterated that othertypes of kinetic control, e.g. increased or decreased synthesisof ‘carrier systems’, may operate in addition todirect (allosteric?) control of K⁺ influx by root [K⁺]. Thenegative feedback signal from root [K⁺] appeared to be the primeeffector in the regulation of K⁺ influx. Key words: Barley, K⁺ influx     

Dependence of Na+-K+ pump current-voltage relationship on intracellular Na+, K+, and Cs+ in rabbit cardiac myocytes

To examine effects of cytosolicNa⁺, K⁺, and Cs⁺ on the voltagedependence of the Na⁺-K⁺ pump, we measuredNa⁺-K⁺ pump current (I_p)of ventricular myocytes voltage-clamped at potentials(V_m) from 100 to +60 mV. Superfusates weredesigned to eliminate voltage dependence at extracellular pump sites.The cytosolic compartment of myocytes was perfused with patch pipette solutions with a Na⁺ concentration ([Na]_pip)of 80 mM and a K⁺ concentration from 0 to 80 mM or withsolutions containing Na⁺ in concentrations from 0.1 to 100 mM and K⁺ in a concentration of either 0 or 80 mM. When[Na]_pip was 80 mM, K⁺ in pipette solutionshad a voltage-dependent inhibitory effect on I_pand induced a negative slope of theI_p-V_m relationship. Cs⁺ in pipette solutions had an effect onI_p qualitatively similar to that ofK⁺. Increases in I_p with increasesin [Na]_pip were voltage dependent. The dielectriccoefficient derived from[Na]_pip-I_p relationships at thedifferent test potentials was 0.15 when pipette solutions included 80 mM K⁺ and 0.06 when pipette solutions were K⁺ free.

     

Effects of Gibberellin on Auxin-Induced Hyperpolarization of Cell Membranes in Hypocotyls of Vigna unguiculata

Auxin activates pumping of protons from the symplast to theapoplast and causes hyperpolarization of the symplast membranein the elongation zone of Vigna stems prior to the accelerationof growth. This auxin-induced hyperpolarization has been studiedin most cases in hypocotyl segments excised from the elongationzone. In the present study, mature-zone segments were perfusedwith IAA by the xylem perfusion technique in an effort to determinewhether or not IAA has any effects in the mature zone. Althoughno hyperpolarization of the symplast membrane was observed uponthe perfusion with auxin alone, auxin-induced hyperpolarizationwas observed when mature-zone segments had been pretreated withGA₃, in the absence of an increase in the growth rate. Theseresults suggest that cells in the mature zone have lost theability to activate the proton-pumping machinery in responseto auxin but that this ability can be restored by treatmentwith GA₃. This effect of GA₃ suggests the possibility that theconcentration of gibberellin in a tissue controls one of thecell's responses to auxin, namely, activation of the protonpump. (Received January 10, 1994; Accepted June 11, 1994)     

Distribution of electric potential and ion transport in the hypocotyl of Vigna sesquipedalis V. Electrogenic activity of the parenchyma cells in hypocotyl segments

Intracellular potential of parenchyma cells (V_ps) in the hypocotylsegment of Vigna sesquipedalis was initially low after excision,then gradually increased to a more negative level. ThereafterV_ps could be remarkably reduced under anoxia then recoveredwith reaeration, accompanied by several cycles of damped oscillations.Both the rapidity of the decrease of V_ps caused by anoxia andits temperature dependency suggest an electrogenic mechanism.No marked spatial differences along the germ axis and the radiusof hypocotyl were observed in the V_ps level and its electrogeniccomponent when the reference electrode was placed on the surfaceof the hypocotyl segment. V_ps also decreased rapidly in an atmospherecontaining 80% CO+20% O₂ in the dark, then was recovered immediatelyin the light or spontaneously but very slowly in the dark. Theextent of the decrease of V_ps caused by CO depended on the growthactivity of the cell and the time lapse after excision. Theseresults suggest the possible conversion or replacement of theterminal oxidase. Sometimes phenomena resembling those of actionpotentials occurred spontaneously or during the reduction ofV_ps due to inhibition of the energy metabolism. V_ps in the elongatingregion varied transiently with the change in illumination. Interrelationshipbetween V_ps and the surface resting potential is discussed. (Received July 20, 1977; )     

Changes of action potentials and force at lowered [Na+]o in mouse skeletal muscle: implications for fatigue

We examined 1) whether the effects of lowered trans-sarcolemmal Na⁺ gradient on force differed between nonfatigued fast- and slow-twitch muscles of mice and 2) whether effects on action potentials could explain the decrease of force. The Na⁺ gradient was reduced by lowering the extracellular [Na⁺] ([Na⁺]_o). The peak force-[Na⁺]_o relationships for the twitch and tetanus were the same in nonfatigued extensor digitorum longus and soleus muscles: force was maintained over a large range of [Na⁺]_o and then decreased abruptly over a much smaller range. However, fatigue was significantly exacerbated at a lowered [Na⁺]_o that had little effect in nonfatigued soleus muscle. This finding suggests that substantial differences exist in the Na⁺ effect on force between nonfatigued and fatigued muscle. The reduced contractility in nonfatigued muscles at lowered [Na⁺]_o was largely due to 1) an increased number of inexcitable fibers and threshold for action potentials, 2) a reduction of action potential amplitude, and 3) a reduced capacity to generate action potentials throughout trains. sodium gradient; muscle contraction; action potential train; extensor digitorum longus; soleus     

Regulation of Elongation Growth of Excised segments of Vigna Hypocotyl under Osmotic Stress in the Absence or Presence of Absorbable Solute

The regulation of elongation growth in excised segments of Vignahypocotyl under osmotic stress was investigated by means ofthe xylem perfusion and pressure-jump method. When subjectedto osmotic stress in the absence of absorbable solutes (100mM sorbitol only) or in the presence of absorbable solutes (70mM sorbitol plus 30 mM sucrose, or 70 mM sorbitol plus 15 mMKC1), the hypocotyl segments immediately began to shrink. Thehyper-polarizations of the transmembrane potentials (V_px andV_ps) took place at once. Within 40–60 minutes, the segmentsresumed growth. In the presence of absorbable solute, therewas an obvious increase in the effective turgor (Pⁱ–Y'),but the physiological wall extensibility () increased only slightly.Conversely, in the absence of absorbable solute, increasedsignificantly but (Pⁱ–Y') decreased. The results suggestthat the recovery of growth of an excised segment under osmoticstress is mainly due to the change in in the absence of absorbablesolute, and to the change in (P¹–Y') in the presence ofabsorbable solute, and that the two respiration-dependent protonpumps play important roles in these recovery processes. (Received April 28, 1989; Accepted August 24, 1989)     

Membrane Potential Measurement of Protoplasts Isolated from Vigna mungo Hypocotyl Using a Fluorescent Probe, diS-C3-(5)

Membrane potentials of protoplasts isolated from Vigna mungohypocotyl segments were measured using the fluorescent probediS-C₃-(5). The fluorescence intensity changed in response tothe external K⁺ concentration. Membrane potential was estimatedto be inside negative (–85?8 mV at 0.1 mM KCl) from theNernst equation for K₊. The membrane potential was not affectedby DCCD (50 µM) or low temperature (5?C). Addition of0.5 mM Ca₂₊ to the protoplast suspension markedly depolarizedthe membrane potential, and subsequent EDTA treatment repolarizedit to the initial level. The Ca₂₊ effect on the membrane potentialmay be due to change in the permeability ratio of Cl^–to K₊. (Received December 16, 1986; Accepted April 22, 1987)     

Effects of carbon dioxide on the spatially separate electrogenic ion pumps and the growth rate in the hypocotyl ofVigna sesquipedalis

Carbon dioxide, introduced into the gas phase of the experimental chamber, has distinct effects on two spatially separate membrane potentials and the rate of elongation growth in hypocotyl segments ofVigna sesquipedalis Wight. Both membrane potentials (V _ps andV _px=the electric potential difference between the parenchyma symplast and the surface of the hypocotyl, and that between the parenchyma symplast and the xylem, respectively) hyperpolarized rapidly but transiently at the introduction of CO₂. Prolonged exposure of the hypocotyl to high concentrations of CO₂ (above 10%) caused depolarization of membrane potentials above the level before CO₂ introduction. When CO₂ was replaced with air, the membrane potentials exhibited a distinct depolarization response of transient nature. The growth rate of the hypocotyl segments exhibited similar responses to CO₂ as did the membrane potentials (the increase and the decrease of the growth rate were corresponded to the hyperpolarization and the depolarization, respectively), but these responses always followed the changes of the membrane potentials. The CO₂-induced maximum hyperpolarization ofV _ps and the maximum increase of the growth rate were closely correlated. All these responses were strictly dependent on aerobic metabolism. These results indicate that CO₂ may regulate elongation growth in two ways: by affecting the activity of the electrogenic ion pump via intracellular acidification, and also by acting via apoplastic acidification as a wall-loosening acid.Symbols and abbreviations V _sx electric potential difference between the surface (S) and the xylem (X) of the hypocotyl - V _px electric potential difference between the inside of a parenchyma cell (P) andX - V _ps electric potential difference betweenP andS - V _ps (CO₂, max) the maximum value of CO₂-induced hyperpolarization ofV _ps - GR(CO₂, max) the maximum value of CO₂-induced increase of the growth rate - IAA indole-3-acetic acid