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Neurons synapses and

Inactivation of pilocarpine is thought to occur at neuronal synapses and probably in plasma. Pilocarpine and its minimally active or inactive degradation products, including pilocarpic acid, are excreted in the urine. [Pg.1439]

Absorption decreased if faken wifh a high-faf meal. Inactivafion of pilocarpine fhoughf fo occur af neuronal synapses and probably in plasma. Excrefed in urine. Half-life 4-12 hr. [Pg.988]

Mochida S, Poulain B, Weller U, Habermann E, Tauc L (1989) Light chain of tetanus toxin intracellularly inhibits acethylcholine release at neuro-neuronal synapses, and its internalization is mediated by heavy chain. In FEBS Lett. 253 47—51 Monk JR, Fernandez JM (1994) The exocytotic fusion pore and neurotransmitter release. In Neuron 12 707-16... [Pg.189]

Inhibition of serotonin reuptake from the neuronal synapse and the subsequent increase in its functionality is one of the mainstays of the pharmacological treatment of depression. Like many amino acids, tryptophan is commercially available as a nutritional supplement or as a so-called smart drug, claiming to reduce symptoms of depression, anxiety, obsessive-compulsive disorders, insomnia, fibromyalgia, alcohol withdrawal, and migraine. However, no convincing clinical data are available to support these... [Pg.9]

Synaptic vesicles are the organelles in axon terminals that store neurotransmitters and release them by exocytosis. There are two types, the large dense-core vesicles, diameter about 90 nm, that contain neuropeptides, and the small synaptic vesicles, diameter about 50nm, that contain non-peptide transmitters. About ten vesicles per synapse are docked to the plasma membrane and ready for release, the readily releasable pool . Many more vesicles per synapse are stored farther away from the plasma membrane, the resting pool . When needed, the latter vesicles may be recruited into the readily releasable pool. Neuronal depolarization and activation of voltage-sensitive Ca2+... [Pg.1174]

In a classical neural pathway, such as that depicted in Fig. 1.3, neuron A must excite neuron B and at the same time inhibit neuron C in order to optimise the excitation of B. It could achieve this with one NT able to activate receptors linked to different events on B and C. Of course, neuron C would have other inputs, some of which would be excitatory and if the same NT was used it could activate the inhibitory mechanism on C as well. Also, the NT released from A might be able to stimulate as well as inhibit neuron C (Fig. 1.3(a)). Even the provision of separate receptors linked to excitation and inhibition would not overcome these problems since both would be accessible to the NT. One possible solution, used in the CNS, is to restrict the NT to the synapse at which it is released by structural barriers or rapid degradation. Also the inputs and receptors linked to excitation could be separated anatomically from those linked to inhibition and, in fact, there is electrophysiological and morphological evidence that excitatory synapses are mainly on dendrites and inhibitory ones on the soma of large neurons (Fig. 1.3(b)). Nevertheless, the problem of overlap would be eased if two NTs were released, one to activate only those receptors linked to excitation and another to evoke just inhibition, i.e. place the determinant of function partly back on the NT (Fig. 1.3(c)). This raises a different problem which has received much consideration. Can a neuron release more than one NT ... [Pg.11]

The function of a neuron is to communicate or relay information to another cell by way of an electrical impulse. A synapse is the site at which the impulse is transmitted from one cell to the next. A neuron may terminate on a muscle cell, glandular cell, or another neuron. The discussion in this chapter will focus on neuron-to-neuron transmission. At these types of synapses, the presynaptic neuron transmits the impulse toward the synapse and the postsyn-aptic neuron transmits the impulse away from the synapse. Specifically, it is the axon terminal of the presynaptic neuron that comes into contact with the cell body or the dendrites of the postsynaptic neuron. Most neurons, particularly in the CNS, receive thousands of inputs. As will become evident, the transmission of the impulse at the synapse is unidirectional and the presynaptic neuron influences activity of the postsynaptic neuron only. [Pg.35]

Convergence occurs when the axon terminals of many presynaptic neurons all synapse with a single postsynaptic neuron. As discussed previously, spatial summation of nerve impulses relies on the presence of convergence. Divergence occurs when the axon of a single presynaptic neuron branches and synapses with multiple postsynaptic neurons. In this way, activity in a... [Pg.40]

As discussed, the first-order neuron is the afferent neuron that transmits impulses from a peripheral receptor toward the CNS. Its cell body is located in the dorsal root ganglion. This neuron synapses with the second-order neuron whose cell body is located in the dorsal horn of the spinal cord or in the medulla of the brainstem. The second-order neuron travels upward and synapses with the third-order neuron, whose cell body is located in the thalamus. Limited processing of sensory information takes place in the thalamus. Finally, the third-order neuron travels upward and terminates in the somatosensory cortex where more complex, cortical processing begins. [Pg.68]

Synapses between the autonomic postganglionic neuron and effector tissue — the neuroeffector junction — differ greatly from the neuron-to-neuron synapses discussed previously in Chapter 5 (see Table 9.1). The postganglionic fibers in the ANS do not terminate in a single swelling like the synaptic knob, nor do they synapse directly with the cells of a tissue. Instead, the axon terminals branch and contain multiple swellings called varicosities that lie across the surface of the tissue. When the neuron is stimulated, these varicosities release neurotransmitter over a large surface area of the effector tissue. This diffuse release of the neurotransmitter affects many tissue cells simultaneously. Furthermore, cardiac muscle and most smooth muscle have gap junctions between cells. These specialized intercellular communications... [Pg.93]

Regulation of neuronal proliferation and differentiation, myelinogenesis, neuronal outgrowth, and synapse formation... [Pg.130]


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See also in sourсe #XX -- [ Pg.56 ]




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Neuron synapses

Neuronal synapses

Synapses

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