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How are these bioelectrical signals transmitted into the body?
One method is Frequency Modulation - Radio and television waves are electromagnetic waves that are generated by the production of oscillating electrical charges (Jones and Childers, 1990).

All radio and television stations in the United States are assigned a specific broadcast frequency by the Federal Communications Commission (FCC). The frequency that radio and television stations always broadcast on is known as the carrier wave and is the frequency that a person tunes into on their radio or TV (Jones and Childers, 1990).

It has been known for over a hundred years that a carrier wave can be used to piggyback other waves, which are known as the signal waves. The signal waves carry the information that is being transmitted such as sound or pictures (Carr, 2001).

The superimposition of a signal wave on a carrier wave is known as modulation. Modulation can be accomplished in a number of ways. Two of the most widely used methods are amplitude modulation (AM) and frequency modulation (FM). In (AM) modulation the amplitude of the carrier wave is modulated by the information signal. In frequency modulation (FM) the frequency of the carrier wave is modulated by the information signal (Jones and Childers, 1990).

Proper operation of such a system requires a transmitter that sends out the combined carrier and signal waves and a receiver that contains a tuning circuit that can be set to resonate at the correct frequency. The reception of the broadcast signal induces a small voltage in the receiving antenna. When the signal that is transmitted matches the tuner frequency it then passes through the tuning circuit to be amplified.

From the point of view of the electronic biology of the human body, the cells of the body contain liquid crystal components (proteins, membranes, membrane receptors, DNA, and RNA) that possess the electronic capability of resonating to certain specific frequencies like antennas (Beal, 1996a, 1996b). In a sense the body is constructed of liquid crystal oscillators. The biological liquid crystal molecules of the cell are organized in complex structures that exhibit cooperative behavior (Ho, 1998). When the correct specific bioelectrical frequencies are supplied to the cells of the body these liquid crystal molecules will resonantly absorb energy and information (Adey, 1988, 1993a; Beal, 1996a, 1996b).

The cellular components of the body behave as electrical circuits (since they have capacitive, inductive and resistive elements, biopotential voltage sources and ionic and electron current flows). This allows electricity and information that is carried by the frequencies of bioelectrical signals to pass into and out of the cells. Cells also have components composed of membranes, membrane receptors and cytoskeletal protein complexes that behave as tuning circuits. These cellular tuning circuits allow detection, resonant absorption and amplification of very specific bioelectrical signals that are in certain frequency and amplitude windows (Adey, 1981, 1988, 1993a; Garnett, 1998, 2002; Ho, 1998).

Frequency modulation of cell membrane receptors that function as electrical antennas/transducers results in voltage fluctuations across cell membranes at the frequency of the stimulus (Dallos, 1986; Russell et al., 1986). Frequency modulation will activate the receptors of cell membranes that respond to voltage changes and these receptors are in turn coupled to other membrane proteins that regulate the electrical, contractile and metabolic activity of cells. Voltage changes in cell membranes are believed to drive protein-based motors located in the lateral cell wall of outer hair cells in the cochlea of the ear (Santos-Sacchi and Dilger, 1988; Holley and Ashmore, 1990; Hallworth et al., 1993). Protein based motors are also located in muscle fibers, mitochondrial membranes and other locations in the body (Rayment et al., 1993, Spudich, 1994; Neupert and Brunner, 2002).

Numerous writers such as Fritjof Capra have noted that nature conserves mechanisms that work (Capra, 2002). In the author's opinion bioelectrical forces such as voltage changes in cell membranes and inward current flows may in fact drive all of the protein/enzyme-based motors in the body. This opinion is based on the fact that an inward current is known to exist between the cell membrane and other cell structures such as the mitochondria and DNA (Garnett, 1998). In addition, electrical currents can enter the cell through ion channels in the cell membrane that act as electrical rectifiers resulting in the entry of minerals such as potassium or calcium ions, which produces a signal amplifying effect (Nicholls et al., 2001). Some of the electrical charges that compose these inward electrical currents travel through an intracellular oscillating biological electrical circuit composed of liquid crystal semiconducting proteins of the cells cytoskeleton (Oschmann, 2000).

The interior of every cell is composed of an integrative structure composed of cytoskeletal proteins that have been shown to form hardwired connections between the cell membrane and the DNA and the mitochondria. The fact that these liquid crystal cytoskeletal proteins also possess semiconducting properties allows them to transfer charges (current) from the cell membrane to internal structures like DNA and the mitochondria. The cytoskeleton of cells in a sense hardwires all of the components of the cell into a solid-state biological computer.



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