GTP和GDP类似物对棉铃虫神经细胞高电压敏感钙通道的调节作用

以Ba²⁺为载流子,采用全细胞膜片钳法,研究了在电极液中分别加入G蛋白稳定 激活剂GTPγS（GTP类似物）和抑制剂GDPβS（GDP类似物）对棉铃虫Helicoverpaarmigera 3龄幼虫神经细胞高电压敏感钙通道的调节作用。Ba²⁺电流记录时间为20 min。对照组 和实验组的Ba²+电流在记录的初期均出现电流的增加现象,随后电流衰减,即“rundown ”。对照组峰电流在第20 min时降为初始值的(72.09±12.80)%。电极内液中加入2 mmol/L GTPγS可缓解电流的衰减现象,在第20 min时,峰电流为初始值的(95.99±7.93)%,明显大 于对照组的峰电流(P<0.01),而且电流 电压（I-V）关系曲线向正电压方向移动。相反 ,电极内液加入2 mmol/L GDPβS则导致峰电流衰减更加严重,第20 min时,峰电流仅为初始水 平的(41.95±9.32)%,显著小于对照组（P<0.01）,但未见电流 电压（I-V）关系曲 线的明显漂移。结果表明,棉铃虫神经细胞钙通道活动受G蛋白激活剂GTPγS和G蛋白抑制剂GDPβS的影响,提示G蛋白活动水平的改变调节钙通道的电流幅值和电压依赖性。     

Ferri- and Ferrocyanide Salts Change the Current/Voltage Relations of Chara corallina: No Correlation with the Transmembrane Redox System

The current/voltage {I/V) relations of the plasma membrane ofChara corallina cells are characteristic when the bathing mediumhas elevated (5-0 mM) concentrations of potassium Addition ofeither 0-5 mM femcyanide or 0-5 mM ferrocyanide usually induceda qualitatively similar increase in the ‘leak’ current,with a concomitant increase in membrane conductance. Both redoxreactants failed for unknown reasons to affect the I/V profileof some of the cells tested In the sensitive cells, femcyanidewas unable to generate extra current over that found upon additionof ferrocyanide Because the feiTocyanide oxidation rate of thecells is only 10% of the femcyanide reduction rate, we concludethat both forms, fern- and ferrocyanide, affect the 'leak' conductanceindependent of the redox state of the reactants, i e ferrocyanidedoes not act indirectly via an oxidation to femcyanide Hence,under the experimental conditions, we were unable to detecta current that could be assigned to the operation of a transmembraneredox system Furthermore, the fern- and ferrocyanide inducedshift in the I/V profile only reversed slowly after withdrawalof the redox reactants. This suggests that the elicited currentis independent of the presence of an extracellular electronacceptor, i.e on the continuous operation of a proposed transmembraneredox system Key words: Current/voltage curves, transmembrane reductase, voltage clamp, femcyanide, ferrocyanide, Chara     

光学活性拟除虫菊酯对棉铃虫神经细胞钠通道电流的影响

用全细胞膜片钳技术对比分析了alpha体氯氰菊酯与theta体氯氰菊酯对棉铃虫Helicoverpa armigera幼虫离体培养中枢神经细胞Na⁺通道门控过程的影响。结果表明,alpha体氯氰菊酯作用后,神经细胞Na⁺通道电流（I_Na）先增大,同时通道的激活电压向负电位方向移动约10 mV,提示alpha体氯氰菊酯使通道激活电位降低,通道更容易被激活。药剂作用约10 min后,I_Na又迅速降低,表明alpha体氯氰菊酯对开放状态的Na⁺通道有抑制作用。另外,alpha体氯氰菊酯使I_Na到达峰值的时间缩短,但对失活时间无明显影响。Theta体氯氰菊酯也使I_Na激活电位左移,幅值降低,但降低速率较慢。总的结果表明alpha体氯氰菊酯与theta体氯氰菊酯对棉铃虫中枢神经细胞处于关闭和开放状态的钠通道均有作用,且alpha体氯氰菊酯对钠通道电流的抑制作用强于theta体氯氰菊酯。     

A hyperpolarization- and acid-activated nonselective cation current in Xenopus oocytes

Heterologous expression of avariety of membrane proteins in Xenopus oocytes sometimesresults in the appearance of a hyperpolarization-activated inwardcurrent. The nature of this current remains incompletely understood.Some investigators have suggested that this current is a Cl current,whereas others have identified it as a nonselective cation current. Thepurpose of this investigation was to characterize this current in moredetail. The hyperpolarization-activated inward current(I_IN) present in native oocytes wascomposed of a current carried at least partly by Ca and Mg underphysiological ionic conditions plus a Ca-activated Cl current. TheCa-activated Cl current was blocked by chelation of cytosolic Ca with1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid.When Cl currents were blocked, the cation current could be carried byCa, Mg, or Co, but not appreciably by Ba, Mn, or Cd.I_IN was stimulated by intracellularacidification. The properties of I_IN were quitedifferent from those of the store-operated Ca current. Heterologousexpression of transient receptor potential-like gene product (TRPL),one of the members of the transient receptor potential family ofputative store-operated Ca channels, apparently resulted in alterationof the voltage sensitivity of the endogenous I_IN.

     

Voltage--Current Characteristics of Chara australis During Changes of pH and Exchange of Ca-Mg in the External Medium

Chara australis was the subject of voltage-clamp experimentsin which external calcium, magnesium, and hydrogen were varied.The voltage clamp was applied across the combined plasmalemma,cytoplasm, and tonoplast of internodal cells. Calcium is necessaryin the batching medium for transient currents to occur duringa depolarizing voltage clamp. Magnesium cannot replace calciumas mediator in this function. Lowering the medium pH appearsto affect more than one variable in the membrane system. Weargue that more than one ion is responsible for the transientcurrent; large increases in membrane current of sodium, potassium,and chloride occur.     

苦皮藤素Ⅳ和Ⅴ对棉铃虫幼虫神经细胞钠通道的影响

电压门控钠通道是神经细胞兴奋传导的基础,也是杀虫剂最主要的作用靶标。具有二氢沉香呋喃多元酯骨架的苦皮藤素Ⅳ和Ⅴ是卫矛科植物苦皮藤的主要杀虫活性成分,苦皮藤素Ⅳ和Ⅴ处理后昆虫的中毒症状分别表现为麻醉和兴奋。本实验应用全细胞膜片钳技术就苦皮藤素Ⅳ和Ⅴ对棉铃虫Helicoverpa armigera幼虫离体培养神经细胞钠离子通道的影响进行了比较。结果表明：苦皮藤素Ⅳ对TTX-敏感钠通道电流的抑制明显具有浓度和时间依赖性,高浓度（10 μmol/L和1 μmol/L）条件下,峰值电流迅速减小而被抑制,在较中间浓度（0.1 μmol/L）时缓慢降低,而在低浓度（0.01 μmol/L）下,峰值电流先增加然后再缓慢降低;苦皮藤素Ⅳ对激活电压无明显影响,但使峰值电压向正电位方向移动,在高浓度移动迅速,低浓度移动缓慢。苦皮藤素Ⅴ对TTX-敏感钠通道电流峰值有明显的增大作用,也有一定的浓度依赖性;对激活电压无明显影响,峰值电压在高浓度下变化不明显,在较低浓度(0.1 μmol/L和 0.01 μmol/L)下向正电位方向移动明显。结果说明,苦皮藤素Ⅳ和Ⅴ可能在钠通道上有一个相同的靶标位点,但由于它们化学结构上的差异,可能对钠通道动力学的修饰 不同,导致不同的生理效应,昆虫表现出不同的神经中毒症状。     

苦参碱对棉铃虫幼虫神经细胞钠通道的影响

用全细胞膜片钳技术研究了生物碱类植物杀虫剂苦参碱对棉铃虫Helicoverpa armigera幼虫离体培养中枢神经细胞钠离子通道门控过程的影响。结果表明： 苦参碱对棉铃虫幼虫神经细胞所表达的TTX （tetradotoxin, 河豚毒素)敏感钠通道具有浓度依赖性阻滞作用,1,10和100 μmol/L的苦参碱作用5 min后,分别使钠电流峰值较给药前下降（12.49±1.67）%、（18.79±2.16）%和（43.15±8.17）% (n=8, P<0.05)。苦参碱使钠电流的电流 电压关系曲线上移,但并不改变其激活电压、峰电压和电流电压关系曲线的形状。苦参碱对钠通道的阻滞作用可能是其具有某些毒理效应的离子基础。     

Characterization of the rat Na+/nucleoside cotransporter 2 and transport of nucleoside-derived drugs using electrophysiological methods

The Na⁺-dependent nucleoside transporter 2 (CNT2) mediates active transport of purine nucleosides and uridine as well as therapeutic nucleoside analogs. We used the two-electrode voltage-clamp technique to investigate rat CNT2 (rCNT2) transport mechanism and study the interaction of nucleoside-derived drugs with the transporter expressed in Xenopus laevis oocytes. The kinetic parameters for sodium, natural nucleosides, and nucleoside derivatives were obtained as a function of membrane potential. For natural substrates, apparent affinity (K_0.5) was in the low micromolar range (12–34) and was voltage independent for hyperpolarizing membrane potentials, whereas maximal current (I_max) was voltage dependent. Uridine and 2'-deoxyuridine analogs modified at the 5-position were substrates of rCNT2. Lack of the 2'-hydroxyl group decreased affinity but increased I_max. Increase in the size and decrease in the electronegativity of the residue at the 5-position affected the interaction with the transporter by decreasing both affinity and I_max. Fludarabine and formycin B were also transported with higher I_max than uridine and moderate affinity (102 ± 10 and 66 ± 6 µM, respectively). Analysis of the pre-steady-state currents revealed a half-maximal activation voltage of about –39 mV and a valence of about –0.8. K_0.5 for Na⁺ was 2.3 mM at –50 mV and decreased at hyperpolarizing membrane potentials. The Hill coefficient was 1 at all voltages. Direct measurements of radiolabeled nucleoside fluxes with the charge associated showed a ratio of two positive inward charges per nucleoside, suggesting a stoichiometry of two Na⁺ per nucleoside. This discrepancy in the number of Na⁺ molecules that bind rCNT2 may indicate a low degree of cooperativity between the Na⁺ binding sites. two-electrode voltage clamp; concentrative nucleoside transport; presteady-state currents     

ACTION POTENTIAL OF NITELLA INTERNODES

The ionic current during a non-propagating action potentialis analysed from the voltage clamp experiments. The shape ofthe action potential of the Nitella internode can be reconstructedfrom the data of the voltage clamp experiments. The N-shapedcurrent-voltage characteristics (I-V curve) of the Nitella membraneis not constant with time as it is in the tunnel diode, butdecays with time, converging finally into a delayed rectificationcurve. The temporal locus of the potential at which each I-Vcurve crosses the voltage axis coincides almost exactly withthe action potential. The membrane resistance which is calculatedfrom the slope of the I-V curve at each intersection with thevoltage axis also changes in parallel to the action potential.Such correlations are found in the Nitella not only in the pondwater, but also in high Na, high Ca or high Mg medium, wherethe shape of the action potential is modified in various ways.It is highly probable that the action potential is a locus ofthe change of the membrane potential so that the net membranecurrent may be maintained at zero after the transient modificationof the membrane structure by stimulation. (Received June 30, 1966; )     

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     

K+ transport and capacitance of the basolateral membrane of the larval frog skin

Skin from larval bullfrogs was mounted in an Ussing-type chamberin which the apical surface was bathed with a Ringer solution containing 115 mM K⁺ and thebasolateral surface was bathed with a Ringer solution containing 115 mMNa⁺. Ion transport was measured asthe short-circuit current(I_sc) with alow-noise voltage clamp, and skin resistance(R_m) wasmeasured by applying a direct current voltage pulse. Membrane impedance was calculated by applying a voltage signal consisting of 53 sine wavesto the command stage of the voltage clamp. From the ratio of theFourier-transformed voltage and current signals, it was possible tocalculate the resistance and capacitance of the apical and basolateralmembranes of the epithelium(R_a andR_b,C_a and C_b,respectively). With as the anion,R_m decreasedrapidly within 5 min following the addition of 150 U/ml nystatin to theapical solution, whereasI_sc increasedfrom 0.66 to 52.03 µA/cm² over a60-min period. These results indicate that nystatin becomes rapidlyincorporated into the apical membrane and that the increase inbasolateral K⁺ permeabilityrequires a more prolonged time course. Intermediate levels ofI_sc were obtainedby adding 50, 100, and 150 U/ml nystatin to the apical solution. Thisproduced a progressive decrease in R_a andR_b whileC_a andC_b remainedconstant. With Cl as theanion, I_sc valuesincreased from 2.03 to 89.57 µA/cm² following treatment with150 U/ml nystatin, whereas with gluconate as the anionI_sc was onlyincreased from 0.63 to 11.64 µA/cm². This suggests that theincrease in basolateral K⁺permeability produced by nystatin treatment, in the presence of morepermeable anions, is due to swelling of the epithelial cells of thetissue rather than the gradient for apicalK⁺ entry. Finally,C_b was notdifferent among skins exposed toCl,, or gluconate, despite the largedifferences inI_sc, nor didinhibition of I_scby treatment with hyperosmotic dextrose cause significant changes inC_b. These resultssupport the hypothesis that increases in cell volume activateK⁺ channels that are alreadypresent in the basolateral membrane of epithelial cells.

     

Angiotensin regulates the selectivity of the Na+-K+ pump for intracellular Na+

Treatment of rabbits with angiotensin-converting enzyme (ACE)inhibitors increases the apparent affinity of theNa⁺-K⁺pump for Na⁺. To explore themechanism, we voltage clamped myocytes from control rabbits and rabbitstreated with captopril with patch pipettes containing 10 mMNa⁺. When pipette solutions wereK⁺ free, pump current(I_p) formyocytes from captopril-treated rabbits was nearly identical to thatfor myocytes from controls. However, treatment caused a significantincrease in I_pmeasured with pipettes containingK⁺. A similar difference wasobserved when myocytes from rabbits treated with the ANG II receptorantagonist losartan and myocytes from controls were compared.Treatment-induced differences in I_p wereeliminated by in vitro exposure to ANG II or phorbol 12-myristate 13-acetate or inclusion of the protein kinase C fragment composed ofamino acids 530-558 in pipette solutions. Treatmentwith captopril had no effect on the voltage dependence ofI_p. We concludethat ANG II regulates the pump's selectivity for intracellularNa⁺ at sites near the cytoplasmicsurface. Protein kinase C is implicated in the messenger cascade.

     

Temperature dependence of human ether-a-go-go-related gene K+ currents

The function of voltage-gated human ether-à-go-gorelated gene (hERG) K⁺ channels is critical for both normal cardiac repolarization and suppression of arrhythmias initiated by premature excitation. These important functions are facilitated by their unusual kinetics that combine relatively slow activation and deactivation with rapid and voltage-dependent inactivation and recovery from inactivation. The thermodynamics of these unusual features were examined by exploring the effect of temperature on the activation and inactivation processes of hERG channels expressed in Chinese hamster ovary cells. Increased temperature shifted the voltage dependence of activation in the hyperpolarizing direction but that of inactivation in the depolarizing direction. This increases the relative occupancy of the open state and contributes to the marked temperature sensitivity of hERG current magnitude observed during action potential voltage clamps. The rates of activation and deactivation also increase with higher temperatures, but less markedly than do the rates of inactivation and recovery from inactivation. Our results also emphasize that one cannot extrapolate results obtained at room temperature to 37°C by using a single temperature scale factor. potassium channel; kinetics; voltage-dependent gating     

The electromotive force of the Chara membrane during the hyperpolarizing response

The hyperpolarizing response of the Chara internodal cell wasstudied by applying the voltage clamp and constant current techniques.By assuming the membrane as an electromotive force (emf) inseries with a resistance r (which is the sum of a series resistancer_s and the membrane resistance r_m), it was shown that the hyperpolarizingresponse was brought about not only by the increase in membraneresistance but by the increase in membrane emf. The time dependentcurrent-voltage (I–V_m) curve obtained under the voltageclamp during the hyperpolarizing response showed a negativeresistance. The hyperpolarizing response is also an excitation,since it is a transition process of the membrane across a negativeresistance region. (Received July 22, 1974; )     

Selectivity of ion channels: competitive catalysis versus independent electrodiffusion

In order to express selectivity of ion channels, it is commonto determine the reversal voltages, V_r in the presence of differention species, and to convert these voltages to permeability ratiosby constant field equations, which are based on independentelectro-diffusion. In the case of individual ion channels, competitionrather than independence can be expected. This situation hasbeen described here in terms of a catalytic reaction cycle fora channel which may translocate K⁺ as well as Ca²⁺ . An exampleis given, where the fundamental rate constants for the K⁺ cycleand for the Ca²⁺ cycle are the same, and opposing 1:10 concentrationgradients for Ca²⁺ and for K⁺ are applied. In this case, thereversal voltage of the resultant total current is so closeto the equilibrium voltage of Ca²⁺, that constant field calculationwould yield an overestimated permeability ratio P_Ca:P_K of about10. Two limiting cases are pointed out. In the case of dilutesolution, the ions move independently and the system can obeythe constant field theory. At high concentrations, the systemapproaches complete dependence and will consequently behaveas an antiporter. Key words: Antiport, calcium permeability, channel selectivity, competitive catalysis, enzyme kinetics     

Differential contribution of sialic acid to the function of repolarizing K+ currents in ventricular myocytes

Weinvestigated the contribution of sialic acid residues to theK⁺ currents involved in the repolarization of mouseventricular myocytes. Ventricular K⁺ currents had a rapidlyinactivating component followed by slowly decaying and sustainedcomponents. This current was produced by the summation of threedistinct currents: I_to, which contributed to thetransient component; I_ss, which contributed tothe sustained component; and I_K,slow, whichcontributed to both components. Incubation of ventricular myocytes withthe sialidase neuraminidase reduced the amplitude ofI_to without alteringI_K,slow and I_ss. We foundthat the reduction in I_to amplitude resultedfrom a depolarizing shift in the voltage of activation and a reductionin the conductance of I_to. Expression of Kv4.3channels, a major contributor to I_to in theventricle, in a sialylation-deficient Chinese hamster ovary cell line(lec2) mimicked the effects of neuraminidase on the ventricularI_to. Furthermore, we showed that sialylatedglycolipids have little effect on the voltage dependence ofI_to. Finally, consistent with its actions onI_to, neuraminidase produced an increase in theduration of the action potential of ventricular myocytes and thefrequency of early afterdepolarizations. We conclude that sialylationof the proteins forming Kv4 channels is important in determining thevoltage dependence and conductance of I_to and that incomplete glycosylation of these channels could lead to arrhythmias.

     

Direct block of cloned hKv1.5 channel by cytochalasins, actin-disrupting agents

The action of cytochalasins, actin-disrupting agents on human Kv1.5 channel (hKv1.5) stably expressed in Ltk^– cells was investigated using the whole cell patch-clamp technique. Cytochalasin B inhibited hKv1.5 currents rapidly and reversibly at +60 mV in a concentration-dependent manner with an IC₅₀ of 4.2 µM. Cytochalasin A, which has a structure very similar to cytochalasin B, inhibited hKv1.5 (IC₅₀ of 1.4 µM at +60 mV). Pretreatment with other actin filament disruptors cytochalasin D and cytochalasin J, and an actin filament stabilizing agent phalloidin had no effect on the cytochalasin B-induced inhibition of hKv1.5 currents. Cytochalasin B accelerated the decay rate of inactivation for the hKv1.5 currents. Cytochalasin B-induced inhibition of the hKv1.5 channels was voltage dependent with a steep increase over the voltage range of the channel's opening. However, the inhibition exhibited voltage independence over the voltage range in which channels are fully activated. Cytochalasin B produced no significant effect on the steady-state activation or inactivation curves. The rate constants for association and dissociation of cytochalasin B were 3.7 µM/s and 7.5 s^–1, respectively. Cytochalasin B produced a use-dependent inhibition of hKv1.5 current that was consistent with the slow recovery from inactivation in the presence of the drug. Cytochalasin B (10 µM) also inhibited an ultrarapid delayed rectifier K⁺ current (I_K,ur) in human atrial myocytes. These results indicate that cytochalasin B primarily blocks activated hKv1.5 channels and endogenous I_K,ur in a cytoskeleton-independent manner as an open-channel blocker. voltage-gated K⁺ channel; heart; open channel block     

Oscillations in Extracellular Current, External pH and Membrane Potential and Conductance in the Alkaline Bands of Nitella and Chara

Oscillations with a period of approximately 2 min were observedin the membrane potential of Chara and Nitella upon illuminationof dark-treated cells, as well as in the extracellular currentpattern and pH values. A 2-min oscillation in the membrane potentialwas observed when the voltage electrode was placed close tothe border of an alkaline and acid region. Comparison of resultsfrom Chara and Nitella revealed an identical control mechanismfor external pattern stabilization in the effect of light onmembrane potential and conductance. Vibrating probe experimentsindicated that oscillations in the extracellular current occurredonly at the border of the alkaline band. Ion-specific pH micro-electrodesplaced within the alkaline band detected oscillations associatedwith light reactivation of the banding phenomenon. These resultsindicate that the oscillations represent a localized phenomenoninvolving spatially-dependent time-constants. More evidencefor the spatial dependence of time constants is gained fromsingle active acid regions in Nitella. Using this combinationof techniques, we have established that a light-dependent H⁺transporter is involved in this oscillation. Current-voltagecurves taken during these oscillations and relaxation, afterchanging the light intensity, confirmed this identification. Key words: Oscillation, vibrating probe, pH micro-electrode, time-constant. I/V curve, Chara, Nitella     

An Improved Method for Determining the Ionic Conductance and Capacitance of the Membrane of Chara corallina

The assumption of a single exponential change for the voltageresponse caused by a square current of subthreshold intensityis not necessarily an adequate explanation of the situationin the Chara membrane. By improving the speed of electronicsfor current clamping and the accuracy of data simulation, itwas found that an additional process, which can be generallysimulated with another exponential function, was superimposedon the voltage response. Such an additional exponential processmay be partly atributed to the response of the tonoplast, ifthe internal potential measuring microelectrode is in the vacuole.However, this additional process still remained in the voltageresponse of the plasmalemma of the Chara internode when thetonoplast and a large amount of endoplasm were removed by internalperfusion with an glycol ether diaminetetraacetic acid solution.The additional exponential component arose from the change ofthe electromotive force of the single membrane during applicationof the test current pulse. The increase of the conductance of the plasmalemma alone waslarge during excitation, while that of the elecrostatic capacitancewas negligible. On the other hand, the conductance and capacitancewhich reflect an additional exponential ionic process duringthe test pulse both increased greatly around the peak of excitation.This rise is the main reason for an apparent large increaseof membrane capacitance which was deduced from a simple approximationof the membrane with a single time constant model. (Received January 6, 1982; Accepted June 23, 1982)     

成年蜜蜂脑神经细胞的培养和电生理特征

为了研究杀虫剂等对蜜蜂毒性作用的神经机制,需在体外建立成年蜜蜂脑神经细胞的分离培养和电生理记录技术并研究其正常电生理特征,而对成年蜜蜂脑神经细胞的分离培养和电生理特性的研究报道甚少。我们采用酶解和机械吹打相结合的方法获得了数量较多且活力较好的成年意大利蜜蜂Apis mellifera脑神经细胞,并用全细胞膜片钳技术研究了成年意大利蜜蜂脑神经细胞对电流和电压刺激的反应,获得了成年意蜂脑神经细胞的基本电生理特征以及钠电流和钾电流的特性。全细胞电流钳的记录结果表明,在体外培养条件下,细胞无自发放电发生,注射电流后仅引起细胞单次放电,引起细胞放电的阈电流平均为60.8±63 pA; 细胞动作电位产生的阈电位平均为−27.4±2.3 mV。用全细胞电压钳记录了神经细胞的钠电流和钾电流。钠电流的分离是在电压刺激下通过阻断钾通道和钙通道实现。细胞的内向钠电流在指令电压为−40～−30 mV左右激活,−10 mV达峰值,钠通道的稳态失活电压V_1/2为−58.4 mV; 外向钾电流成份至少包括较小的快速失活钾电流和和较大的缓慢失活钾电流（占总钾电流的80%）,其半激活膜电位V_1/2为3.86 mV,无明显的稳态失活。结果提示缓慢失活钾电流的特征可能是细胞单次放电的机制之一。