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高浓度乙酰胆碱对蛙终板离子通道的激活作用。

Activation of ion channels in the frog end-plate by high concentrations of acetylcholine.

作者信息

Colquhoun D, Ogden D C

机构信息

Department of Pharmacology, University College London.

出版信息

J Physiol. 1988 Jan;395:131-59. doi: 10.1113/jphysiol.1988.sp016912.

DOI:10.1113/jphysiol.1988.sp016912
PMID:2457675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1191987/
Abstract
  1. The equilibrium relationship between acetylcholine (ACh) concentration and response (fraction of channels open), corrected for the effects of desensitization, has been estimated by single-ion-channel recording at the adult frog skeletal neuromuscular junction. At high ACh concentration channel openings occur in well-defined clusters separated by long desensitized intervals. The response, po, was estimated as the proportion of time for which a single channel was open during a cluster. 2. At negative membrane potential (-120 mV) po reached a maximum value of 0.9 at 100 microM-ACh and was half-maximum at 15 microM with a Hill slope of 1.6 at this point. At concentrations higher than 200 microM-ACh, po declined as a result of open-channel block by free ACh itself. 3. At positive membrane potentials (+100 mV) there was little channel block by ACh; po reached a maximum value of 0.41 at 500 microM-ACh, with half-maximum activation at 50 microM and Hill slope of 1.2 at this point. 4. Particular mechanisms for channel activation by ACh were fitted to the data by the method of least squares. Fits were fully determinate only if the two binding sites for ACh were assumed to be equivalent with no co-operativity in the ACh binding reactions. At negative potential the microscopic equilibrium constant for binding was K1 = K2 = 77 microM and the equilibrium constant for channel opening (opening/closing rates, beta/alpha) was 32. At positive potential the affinity was slightly higher, K = 32 microM, which confirms the view that the binding sites for ACh are outside the membrane electric field. The equilibrium constant for channel opening was reduced to 0.7 mainly as a result of the much shorter open lifetime (increased closing rate alpha) at positive potentials. 5. The data were also fitted well by very high values of beta/alpha together with a high degree of negative co-operativity or non-equivalence in ACh binding affinity (K2 much greater than K1). A good fit could also be obtained with moderate positive co-operativity combined with non-equivalence of the binding sites. 6. A mechanism that postulates a receptor with two independent gating subunits provided a poor fit to the data at negative potential. 7. The rate constants for channel opening and ACh dissociation were estimated by constraining the fitted parameters so that the burst length for channel opening was equal to its observed value at low concentrations of ACh.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 已通过成年青蛙骨骼肌神经肌肉接头处的单离子通道记录,估算了经脱敏作用校正后的乙酰胆碱(ACh)浓度与反应(通道开放分数)之间的平衡关系。在高ACh浓度下,通道开放以明确的簇状出现,中间间隔着长的脱敏期。反应值po被估算为单个通道在一个簇状开放期间的时间比例。2. 在负膜电位(-120 mV)时,po在100 μM - ACh时达到最大值0.9,在15 μM时为最大值的一半,此时希尔斜率为1.6。在高于200 μM - ACh的浓度下,由于游离ACh自身对开放通道的阻断,po下降。3. 在正膜电位(+100 mV)时,ACh对通道的阻断作用很小;po在500 μM - ACh时达到最大值0.41,在50 μM时激活达到最大值的一半,此时希尔斜率为1.2。4. 通过最小二乘法将ACh激活通道的特定机制与数据进行拟合。只有当假定ACh的两个结合位点等效且ACh结合反应中无协同性时,拟合才是完全确定的。在负电位时,结合的微观平衡常数为K1 = K2 = 77 μM,通道开放的平衡常数(开放/关闭速率,β/α)为32。在正电位时,亲和力略高,K = 32 μM,这证实了ACh的结合位点在膜电场之外的观点。通道开放的平衡常数降至0.7,主要是由于正电位时开放寿命短得多(关闭速率α增加)。5. 通过非常高的β/α值以及ACh结合亲和力中的高度负协同性或不等效性(K2远大于K1),数据也能得到很好的拟合。中等程度的正协同性与结合位点的不等效性相结合也能得到良好的拟合。6. 一种假设具有两个独立门控亚基的受体的机制,在负电位时对数据的拟合较差。7. 通过约束拟合参数来估算通道开放和ACh解离的速率常数,以使通道开放的爆发长度等于在低ACh浓度下观察到的值。(摘要截取自400字)

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本文引用的文献

1
The antagonism between tubocurarine and substances which depolarize the motor end-plate.筒箭毒碱与使运动终板去极化的物质之间的拮抗作用。
J Physiol. 1960 Jul;152(2):309-24. doi: 10.1113/jphysiol.1960.sp006489.
2
A study of the desensitization produced by acetylcholine at the motor end-plate.一项关于乙酰胆碱在运动终板产生脱敏作用的研究。
J Physiol. 1957 Aug 29;138(1):63-80. doi: 10.1113/jphysiol.1957.sp005838.
3
Interaction at end-plate receptors between different choline derivatives.不同胆碱衍生物在终板受体处的相互作用。
Proc R Soc Lond B Biol Sci. 1957 May 7;146(924):369-81. doi: 10.1098/rspb.1957.0018.
4
Relationship between reversible antagonist occupancy and the functional capacity of the acetylcholine receptor.可逆性拮抗剂占有率与乙酰胆碱受体功能容量之间的关系。
J Biol Chem. 1981 Jul 10;256(13):6692-9.
5
Physiological and pharmacological manipulations with light flashes.用光闪烁进行生理和药理操作。
Annu Rev Biophys Bioeng. 1982;11:151-75. doi: 10.1146/annurev.bb.11.060182.001055.
6
Acetylcholine receptor: evidence for a voltage-dependent regulatory site for acetylcholine. Chemical kinetic measurements in membrane vesicles using a voltage clamp.乙酰胆碱受体:乙酰胆碱电压依赖性调节位点的证据。使用电压钳对膜囊泡进行化学动力学测量。
Biochemistry. 1983 Dec 6;22(25):5973-8. doi: 10.1021/bi00294a042.
7
Acetylcholine receptor: evidence for a regulatory binding site in investigations of suberyldicholine-induced transmembrane ion flux in Electrophorus electricus membrane vesicles.乙酰胆碱受体:在对南美电鳗膜囊泡中辛二酰二胆碱诱导的跨膜离子通量的研究中,关于一个调节性结合位点的证据。
Biochemistry. 1983 Dec 6;22(25):5967-73. doi: 10.1021/bi00294a041.
8
Agonists block currents through acetylcholine receptor channels.激动剂可阻断通过乙酰胆碱受体通道的电流。
Biophys J. 1984 Aug;46(2):277-83. doi: 10.1016/S0006-3495(84)84022-9.
9
Conductances of single ion channels opened by nicotinic agonists are indistinguishable.烟碱样激动剂打开的单离子通道的电导无法区分。
Nature. 1984;309(5964):160-2. doi: 10.1038/309160a0.
10
Activation of a nicotinic acetylcholine receptor.烟碱型乙酰胆碱受体的激活。
Biophys J. 1984 Jan;45(1):175-85. doi: 10.1016/S0006-3495(84)84146-6.