Neurons interneurons

The third class of neurons includes the intemeurons, which lie entirely within the CNS. Because the human brain and spinal cord contain well over 100 billion neurons, interneurons account for approximately 99% of all the neurons in the body taken together. Intemeurons lie between afferent and... 

Westenbroek, R.E., Hoskins, L., Catterall, W.A. Localization ofCa2+ channel subtypes on rat spinal motor neurons, interneurons, and nerve terminals, J. Neurosci., 1998, 18, 6319-6330. 

Sensory neurons transduce physical stimuli, such as smell, light, or sound, into action potentials, which are then transmitted to the spinal cord or brain. Sensory neurons, which bring information into the central nervous system, are also referred to as afferent neurons. Motor neurons transmit nerve impulses away from the brain and spinal cord to muscles or glands and are also called efferent neurons. Intemeurons transmit nerve impulses between sensory neurons and the motor neurons. Interneurons are responsible for receiving, relaying, integrating, and sending nerve impulses. Intemeurons are found exclusively in the central nervous system and account for almost 99% of all the nerve cells in the body. 

Figure 1.3 Some possible basic neurotransmitter-synaptic arrangements for the excitation and inhibition of different neurons, (a) The single NT activates neuron B and inhibits neuron C by being able to activate both excitatory and inhibitory receptors or, more probably, acting on one receptor linked to both events. There is potential, however, for the NT to activate any inhibitory receptors that may be on B or excitatory receptors on C. (b) The same NT is used as in (a) but the excitatory receptors are now only on dendrites and separated from the inhibitory receptors only on the soma. There is less chance of unwanted mixed effects, (c) Neuron A releases distinct excitatory and inhibitory NTs from its two terminals each acting on specific and morphologically separated receptors. But this depends on a neuron being able to release two NTs. (d) Neuron A releases the same NT from both terminals. It directly excites B but inhibits C through activating an inhibitory interneuron (I) which releases an inhibitory NT onto specific receptors on C. This last scheme (d) is clearly more functional and is widely used...

Fortunately there is another way in which one neuron can excite and inhibit different neurons using just one NT. Neuron A could excite B and inhibit C by the introduction of an inhibitory interneuron the activation of which by A, using the same excitatory NT as at B, automatically inhibits C (Fig. 1.3(d)). This form of inhibition is quite common in the CNS and in fact much inhibition is mediated by these so-called short-axon interneurons and a neuron may inhibit itself through feedback via an axon collateral synapsing onto an adjacent inhibitory short-axon interneuron (Fig. 1.2). 

These approaches are, in any case, only suitable for classical neurotransmitters. Those with slow background effects will probably not be released in large amounts. For such substances we require a measure of their utilisation, or turnover, over a much longer period of time. With NTs released from short-axon interneurons there are no pathways to stimulate and it becomes necessary to activate the neurons intrinsically by field stimulation, which is of necessity not specific to the terminals of the interneurons. 

ACh is released from the large non-spiny striatal interneurons (Fig. 15.10) which only represent some 5% of total striatal neuron number. Since ACh is excitatory and DA inhibitory on striatal neurons, various schemes have been proposed to balance their antagonistic action but the role of ACh in striatal function (and PD) appears to be relatively minor. 

Lamina II is also known as the substantia gelatinosa (SG) and can be divided into two layers, the outer layer (IIo) and the inner layer (Ili). This layer is densely packed with small neurons and lacks myelinated axons. Neurons with cell bodies in Hi receive inputs from low-threshold mechanoreceptive primary afferents, while those in IIo respond to inputs from high-threshold and thermoreceptive afferents. The intrinsic cells which comprise the SG are predominantly stalk and islet cells. Stalk cells are found located in lamina IIo, particularly on the border of lamina I, and most of their axons have ramifications in lamina I although some also project to deeper layers. These cells are thought to predominantly relay excitatory transmission. Islet cells, on the other hand, are located in Hi and have been demonstrated to contain the inhibitory neurotransmitters, y-aminobutyric acid (GABA), glycine and enkephalins in their dendrites. Hence these cells have been proposed to be inhibitory interneurons. 

The cells comprising lamina V are more diverse than those of lamina IV and their dendrites extend vertically toward the superficial layers. Cell bodies in lamina V contribute to three projection pathways, the SCT, PSDC and STT. However, the STT cells appear to be predominant in this lamina. Lamina V plays an important role in nociception since it receives both A - and C-fibre inputs. Some cells in lamina V also respond to cutaneous low- and high-threshold mechanical stimuli and receive nociceptive inputs from the viscerae. Many of these neurons also project onto mononeurons and so act as interneurons in the polysynaptic withdrawal reflex to noxious stimuli. 

Distinguish among the three types of neurons afferent neurons, efferent neurons, and interneurons... 

Interneurons are found in all areas of the spinal cord gray matter. These neurons are quite numerous, small, and highly excitable they have many interconnections. They receive input from higher levels of the CNS as well as from sensory neurons entering the CNS through the spinal nerves. Many intemeurons in the spinal cord synapse with motor neurons in the ventral hom. These interconnections are responsible for the integrative functions of the spinal cord including reflexes. 

Interneurons that transmit impulses to motor neurons... 

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