Neurobiology is the study of cells of the nervous system and the organization of these cells into functional circuits that process information and mediate behavior[Shepard, G. M. (1994). Neurobiology. 3rd Ed. Oxford University Press. ISBN 0195088433]. It is a subdiscipline of both biology and neuroscience. Neurobiology differs from neuroscience, a much broader field that is concerned with any scientific study of the nervous system. Neurobiology should also not be confused with other subdisciplines of neuroscience such as computational neuroscience, cognitive neuroscience, behavioral neuroscience, biological psychiatry, neurology, and neuropsychology despite the overlap with these subdisciplines. Scientists that study neurobiology are called neurobiologists.
Neurons and Glial Cells
Neurons are cells that are specialized to receive, propagate, and transmit electrochemical impulses. In the human brain alone, there are over a hundred billion neurons. Neurons are diverse with respect to morphology and function. Thus, not all neurons correspond to the stereotypical motor neuron with dendrites and myelinated axons that conduct action potentials. Some neurons such as photoreceptors for example, do not have myelinated axons that conduct action potentials. Other unipolar neurons found in invertebrates do not even have distinguishing processes such as dendrites. Moreover, the distinctions based on function between neurons and other cells such as cardiac and muscle cells are not helpful. Thus, the fundamental difference between a neuron and a nonneuronal cell is a matter of degree.
Another major class of cells found in the nervous system are glial cells. Despite the abundance of glial cells relative to neurons in the nervous system (there are ten glial cells for every single neuron), glial cells are only recently beginning to receive attention from neurobiologists for being involved not just in nourishment and support of neurons, but also in modulating synapses. For example, Schwann cells, a type of glial cells in peripheral nervous system modulate synaptic connections between the presynaptic terminal from a motor neuron and endplate muscle fiber in the neuromuscular junction.
Neuronal Function
One prominent characteristic of many neurons is excitability. Neurons generate electrical impulses or changes in voltage of two types: graded potentials and action potentials. Graded potentials is when the membrane potential depolarizes and hypolarizes in a graded fashion relative to the amount of stimulus that is applied to the neuron. An action potential on the other hand is an all-or-none electrical impulse. Despite being slower than graded potentials, action potentials have the advantage of travelling over long distances of neuronal processes such as axons with little or no decrement. Much of the current knowledge of action potentials comes from squid axon experiments by
Sir Alan Lloyd Hodgkin and
Sir Andrew Fielding Huxley.
Action Potential
The
Hodgkin-Huxley Model of an
action potential in the squid axon has been the basis for much of the current understanding of the ionic bases of action potentials. Briefly, the model states that the generation of an action potential is detemined by two ions: Na
+ and K
+. An action potential can be divided into several sequential phases: threshold, rising phase, falling phase, undershoot phase, and recovery. Following several local graded depolarizations of the membrane potential, the threshold of excitation is reached, voltage-gated sodium channels are activated, which leads to an influx of Na
+ ions. As Na
+ ions enter the cell, the membrane potential is further depolarized, and more voltage-gated sodium channels are activated. Such a process is also known as a positive-feedback loop. As the rising phase reaches its peak, voltage-gated Na
+ channels are inactivated whereas voltage-gated K
+ channels are activated, resulting in a net outward movement of K
+ ions, which repolarizes the membrane potential towards the resting membrane potential. Repolarization of the membrane potential continues, resulting in an undershoot phase or absolute refractory period. The undershoot phase occurs because unlike voltage-gated sodium channels, voltage-gated potassium channels invactivate much more slowly. Nevertheless, as more voltage-gated K
+ channels become inactivated, the membrane potential recovers to its normal resting steady state.
Structure and Formation of Synapses
Neurons communicate with one another via
synapses. Synapses are specialized junctions between two cells in close apposition to one another. In a synapse, the neuron that sends the signal is the presynaptic neuron and the target cell receives that signal is the postcynaptic neuron or cell. Synapses can be either electrical or chemical. Electrical synapses are characterized by the formation of gap junctions that allow ions and other organic compound to instantaneously pass from one cell to another
[Martin, A. R., Wallace, B. G., Fuchs, P. A. & Nicholls, J. G. (2001). From Neuron to Brain: A Cellular and Molecular Approach to the Function of the Nervous System. 4th Ed. Sinauer Associates. ISBN 0878934391]. Chemical synapses are characterized by the presynaptic release of neurotransmitters that diffuse across a synaptic cleft to bind with posynaptic receptors. A neurotransmitter is a chemical messenger that is synthesized within neurons themselves and released by these same neurons to
communicate with their postsynaptic target cells. A receptor is a transmembrane protein molecule that a neurotransmitter or drug binds. Chemical synapses are slower than electrical synapses.
Neurotransmitter Transporters, Receptors, and Signaling Mechanisms
After neurotransmitters are synthesized, they are packaged and stored in
vesicles. These vesicles are pooled together in terminal boutons of the presynaptic neuron. When there is a change in voltage in the terminal bouton, voltage-gated calcium channels embedded in the membranes of these boutons become activated. These allow Ca
2+ ions to diffuse through these channels and bind with synaptic vesicles within the terminal buttons. Once bounded with Ca
2+, the vesicles dock and fuse with the presynaptic membrane, and release neurotransmitters into the synaptic cleft by a process known as
exocytosis. The neurotransmitters then diffuse across the synaptic cleft and binds to postsynaptic receptors embedded on the postsynaptic membrane of another neuron. There are two families of receptors: ionotropic and metabotropic receptors. Ionotropic receptors are a combination of a receptor and an ion channel. When ionotropic receptors are activated, certain ion species such as Na
+ to enter the postsynaptic neuron, which depolarizes the postsynaptic membrane. If more of the same type of postsynaptic receptors are activated, then more Na
+ will enter the postsynaptic membrane and depolarize cell. Metabotropic receptors on the other hand activate second messenger cascade systems that result in the opening of ion channel located some place else on the same postsynaptic membrane. Although slower than ionotropic receptors that function as on-and-off switches, metabotropic receptors have the advantage of amplifying the signal from a single transmitter.
Postsynaptic depolarizations can be either excitatory or inhibitory. Those that are excitatory are referred to as excitatory postsynaptic potential (EPSP). Alternatively, some postsynaptic receptors allow Cl- ions to enter the cell or K+ ions to leave the cell, which results in an inhibitory postsynaptic potential (IPSP). If the EPSP is dominant, the threshold of excitation in the postynaptic neuron may be reached, resulting in the generation and propagation of an action potential in the postynaptic neuron.
Synaptic Plasticity
Synaptic plasticity is the process whereby strengths of synaptic connections are altered. For example, long-term changes in synaptic connection may result in more postynaptic receptors being embedded in the postsynaptic membrane, resulting in the strengthening of the synapse. Synaptic plasticity is also found to be the neural mechanism that underlies learning and memory.
Neural Development
Neural development is the process whereby the nervous system grows and develops. Aside from the primitive gut, the nervous system is the first organ system to develop and the last system to finish. Development of the nervous system begins when the ectotherm thickens to form a neural plate. The neural plate in turns thickens to form the neural tube. Within this neural tube, totipotent cells migrate and differentiate into neurons and glial cells.
References
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