The post-synaptic effects of the aliphatic alcohols, ethanol to hexanol, were investigated at the neuromuscular junctions of toads, with particular emphasis on the effects of ethanol. 2. The alcohols increased the amplitude and duration of miniature end-plate potentials. It is shown that this effect was due to the prolongation of the decay phase of miniature end-plate currents (m.e.p.c.s). There was no effect of alcohols on the growth phase of m.e.p.c.s. 3. The prolonged decay of m.e.p.c.s in ethanol remained exponential and was normally sensitive to membrane potential. Prolonged m.e.p.c.s were associated with an equivalent prolongation of the mean duration of elementary events, as determined from power spectra of acetylcholine noise in 0-5 M ethanol. 4. The relationship betweeen the time constant of decay of m.e.p.c.s (tau) and the concentration of an alcohol of carbon chain length N (C-N) was exponential, conforming to the equation tau equals tau-s exp (B-N-C-N), in which tau-s is the decay time constant in standard solution and B-N is a constant, different for each alcohol. 5. There was also an exponential relationship between B-N and N, which closely followed the relationship between membrane-buffer partition coefficient and carbon chain length for the different alcohols, indicating that the alcohols are active in the lipid phase of the post-synaptic membrane. 6. It is suggested that the alcohols act by causing a change in the dielectric constant of the post-synaptic membrane which forms the environment of the rate-limiting reaction responsible for the decay of the end-plate conductance. On the assumption that this reaction involves dipoles, it is shown that the small changes in dielectric constant, calculated from the partition coefficients of the alcohols and by assuming an initial lipid dielectric constant of 3, would give an exponential relationship between the time constant of decay of m.e.p.c.s and alcohol concentration. 7. The results support the hypothesis that the decay (but not the onset) of acetylcholine-induced conductance changes is rate-limited by a first-order reaction which involves dipoles and occurs in the lipid environment of the post-synaptic membrane.
摘要
研究了从乙醇到己醇的脂肪族醇类在蟾蜍神经肌肉接头处的突触后效应,尤其着重研究了乙醇的效应。2. 这些醇类增加了微小终板电位的幅度和持续时间。结果表明,这种效应是由于微小终板电流(m.e.p.c.s)衰减相的延长所致。醇类对m.e.p.c.s的增长相没有影响。3. 乙醇中m.e.p.c.s的延长衰减仍呈指数形式,且通常对膜电位敏感。延长的m.e.p.c.s与基本事件平均持续时间的同等延长相关,这是根据0 - 5 M乙醇中乙酰胆碱噪声的功率谱确定的。4. m.e.p.c.s衰减的时间常数(tau)与碳链长度为N的醇类(C - N)浓度之间的关系呈指数形式,符合方程tau等于tau - s exp(B - N C - N),其中tau - s是标准溶液中的衰减时间常数,B - N是一个常数,每种醇类各不相同。5. B - N与N之间也存在指数关系,这与不同醇类的膜 - 缓冲分配系数和碳链长度之间的关系密切相关,表明这些醇类在突触后膜的脂质相中具有活性。6. 有人提出,这些醇类的作用是通过引起突触后膜介电常数的变化来实现的,突触后膜构成了负责终板电导衰减的限速反应的环境。假设该反应涉及偶极子,结果表明,根据醇类的分配系数并假设初始脂质介电常数为3计算出的介电常数的微小变化,将给出m.e.p.c.s衰减时间常数与醇类浓度之间的指数关系。7. 这些结果支持了以下假设:乙酰胆碱诱导的电导变化的衰减(而非起始)受涉及偶极子且发生在突触后膜脂质环境中的一级反应限速。