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This does not occur because of the action of Na+,K+-ATPase, transferring potassium ions from the intercellular liquid into the axon and sodium ions in the opposite direction, through hydrolysis of ATP When the nerve cells are excited by an electric impulse (either 'natural', from another nerve cell or another site on the axon, or 'artificial', from an electrode), the membrane potential changes, causing an increase in the frequency of opening of the gates of the sodium channels Thus, the flux of sodium ions increases and the membrane potential is shifted towards the Nernst potential value determined by sodium ions, which considerably differs from that determined by potassium ions, as the concentration of sodium ions in the extracellular space is much greater than in the intracellular space, while the concentration ratio of potassium ions is the opposite.

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Figure 8.14. Chemical structure of H-bonded supramolecular LC polymer lm and scheme of the strategy for selective detachment of Az unit after the relief formation.

The potential shift in this direction leads to a further opening of the sodium gates and thus to 'autocatalysis' of the sodium flux, resulting in a spike which is stopped only by inactivation of the gates In spite of the fact that the overall currents flowing across the cell membranes consist of tiny stochastic fluctuating components, the resulting dependences, as shown in Figs 619 and 620, are smooth curves and can be used for further analysis (the situation is, in fact, analogous to most of phenomena occurring in nature) Thus, the formation of a spike can be shown to be a result of gradual opening and closing of very many potassium and sodium channels (Fig 624) According to Fig 6.

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The mass migration is readily formed also for this supramolecular system. This fact implies an important issue that the covalent linkage of the Az unit to the polymer chain is not necessary to cause the ef cient phototriggered material transfer, but H-bonding can be the exact alternative. As a control experiment, 8Az-4ImBr (Fig. 8.14), a precursor compound of the imidazol compound, is also examined. No SRG formation is observed, obviously showing the importance of H-bond formation.

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17 the nerve cell is linked to other excitable, both nerve and muscle, cells by structures called, in the case of other nerve cells, as partners, synapses, and in the case of striated muscle cells, motor endplates (neuromuscular junctions) The impulse, which is originally electric, is transformed into a chemical stimulus and again into an electrical impulse The opening and closing of ion-selective channels present in these junctions depend on either electric or chemical actions The substances that are active in the latter case are called neurotransmitters A very important member of this family is acetylcholine which is transferred to the cell that receives the signal across the postsynaptic membrane or motor endplate through a.

The selective extraction of 8Az-4Im from the lm is performed after the chemical post xation of the SRG structure. The H-bonded acceptor 8Az-4Im is extracted selectively by ethanol or THF from the lm with retention of the periodic structures. Figure 8.15 shows the UV-vis spectrum, and topographical AFM images taken from the sample after the cross-linking procedure (initial) and

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Fig. 6.24 A hypothetic scheme of the time behaviour of the spike linked to the opening and closing of sodium and potassium channels. After longer time intervals a temporary hyperpolarization of the membrane is induced by reversed transport of potassium ions inside the nerve cell. Nernst potentials for Na+ and K+ are also indicated in the figure. (According to A. L. Hodgkin and A. F. Huxley)

1.2.6.1. Photoswitches. As already pointed out, the azo isomerization can be used to photoswitch a wide variety of other properties (at numerous size scales). In addition to the optical changes already described, it is worth noting that the transient change in material refractive index (owing to the different n of cis and trans) can itself act as a photoswitch (Barley et al., 1991). The azo photochromism

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