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长链烷烃衍生物的异构体与神经冲动阻断

Isomers of long-chain alkane derivatives and nervous impulse blockage.

作者信息

Requena J, Velaz M E, Guerrero J R, Medina J D

出版信息

J Membr Biol. 1985;84(3):229-38. doi: 10.1007/BF01871386.

Abstract

The potency to block nervous impulse of members of normal aliphatic homologous series of primary and secondary isomers of functional derivatives of alkanes was tested in bundles of a few axons from sciatic nerves of the toad Bufo marinus. For the primary substituted functional derivates of pentane, the relative potency series was I greater than H approximately equal to Br greater than Cl greater than COOCH3 greater than F greater than CH2OH greater than COCH3 greater than OH approximately equal to NH2 greater than COOH. For the homologous series of primary alkanols, and from saturated Ringer's solutions, the time required to reversibly reduce the amplitude of the action potential to one-half its initial value were determined. The cut-off effect was detected at the level of dodecan-1-ol, while for the primary bromoalkanes it was bromooctane. However, solutions of the secondary isomer of the inactive primary homologues, such as tridecan-5-ol and tridecan-7-ol or 2-bromononane, were able to block nervous impulse conduction reversibly. From the concentration required for an equipotent effect it was calculated that the standard free energy for adsorption of primary alkanols was -705 cal mol- CH2. Similarly, for primary bromoalkanes a value of -733 cal mol-1 CH2 was obtained. The concentration required for an equipotent effect for primary isomer (either of alkanols or bromoalkanes) is lower than those obtained for the secondary isomers. Therefore, the latter are less potent than the former. Among secondary isomers the potency decreases as the functional group is moved away from the terminal carbon. The differential effect of structural isomers of long-chain alkane derivates around the point of cut-off cannot be explained in terms of differences in chemical properties, concentration in aqueous and membrane phases, or mean molecular volume. It is concluded that a volume related to that of the hydrophobic region of the agent and not its mean molecular volume should be responsible for an expansion of the target region.

摘要

在海蟾蜍(Bufo marinus)坐骨神经的几根轴突束中,测试了烷烃官能衍生物的伯、仲异构体的正常脂肪族同系物成员阻断神经冲动的能力。对于戊烷的伯取代官能衍生物,相对效力顺序为:I大于H约等于Br大于Cl大于COOCH3大于F大于CH2OH大于COCH3大于OH约等于NH2大于COOH。对于伯链烷醇同系物,在饱和林格氏溶液中,测定了将动作电位幅度可逆地降低至其初始值一半所需的时间。在十二烷 - 1 - 醇水平检测到截止效应,而对于伯溴代烷烃,截止效应出现在溴辛烷。然而,无活性伯同系物的仲异构体溶液,如十三烷 - 5 - 醇和十三烷 - 7 - 醇或2 - 溴壬烷,能够可逆地阻断神经冲动传导。根据等效效应所需的浓度计算得出,伯链烷醇吸附的标准自由能为 - 705 cal mol- CH2。同样,对于伯溴代烷烃,得到的值为 - 733 cal mol-1 CH2。伯异构体(链烷醇或溴代烷烃)等效效应所需的浓度低于仲异构体。因此,后者的效力低于前者。在仲异构体中,随着官能团远离末端碳,效力降低。长链烷烃衍生物的结构异构体在截止点周围的差异效应不能用化学性质、水相和膜相中的浓度或平均分子体积的差异来解释。得出的结论是,与药剂疏水区域相关的体积而非其平均分子体积应负责靶区域的扩展。

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