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ULTIMATE COMPUTING - Quantum Consciousness Studies

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From Brain to Cytoskeleton 63<br />

Figure 4.2: Schematic diagram of brain functional components. By Paul<br />

Jablonka.<br />

The sequence of events liberating neurotransmitter molecules from nerve<br />

endings is remarkably uniform at all synapses. Transmitter molecules are stored<br />

inside presynaptic nerve terminals in small vesicles that are analogous to the<br />

secretory granules of gland cells. The amount of neurotransmitter in one vesicle is<br />

considered a “quantum” and in neuromuscular synapses each quantum consists of<br />

one thousand to five thousand molecules of acetylcholine. Each action potential<br />

reaching the presynaptic terminal releases a number of vesicle quanta ranging<br />

from a few to several hundred. The coupling mechanism between the action<br />

potential and vesicle release involves both calcium and the cytoskeleton. As an<br />

action potential impulse arrives at the presynaptic nerve terminal, calcium ions<br />

enter the cytoplasm through the membrane by way of voltage gated channels. In<br />

presynaptic nerve terminals, inward ionic current of the action potential is thus<br />

carried partially by sodium and partially by calcium. Free calcium in the<br />

cytoplasm of the terminal causes vesicles to fuse with the surface membrane and<br />

to expel their contents. The mechanisms by which calcium triggers the release of<br />

vesicles from the presynaptic terminal is not clearly understood, however<br />

cytoskeletal proteins including contractile actin, myosin, and other filamentous<br />

proteins are involved. Calcium mediates dynamic contractile activities in flagella<br />

and skeletal muscle and appears to trigger cytoskeletal expulsion of<br />

neurotransmitters from nerve terminals.<br />

After release, transmitter molecules diffuse across the synaptic cleft and bind<br />

reversibly with the postsynaptic membrane receptors. The distance between the<br />

two membranes is sufficiently small such that the diffusion takes about a<br />

millisecond-a relatively slow event compared to switching in semiconductors.<br />

Whenever a transmitter molecule binds to the postsynaptic membrane, it causes a<br />

small voltage change in the postsynaptic membrane called the miniature endplate<br />

potential which can be either excitatory or inhibitory depending on the<br />

neurotransmitter molecule and postsynaptic receptor. In the resting state there are

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