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Reticular Theory
Nerves communicate through a continuous nerve net
Neuron Doctrine
The nervous system is made up of discrete, individual cells
Central Nervous System
Made up of the brain and spinal cord, protected inside bones
Peripheral Nervous System
Cranial and spinal nerves, extends beyond the bony skull and vertebral column
Dynamic Polarity
Electrical signals within a neuron flow in one direction
Dendrites
Receive input
Some
Important for integration of signal
Axon
Important for signal propagation
Axon Terminal
Site of signal output
Synaptic Vesicle
Contain, store, and release neurotransmitters
Ecto/Endosome
Deliver proteins to plasma membrane (ecto) and remove proteins from the plasma membrane (endo)
Lysosome
Breakdown waste and debris
Dendrites and Spines
Number of dendritic branches correlates with the number of inputs, spines increase the number of input locations
Axons
Propagate electrical signals between neurons, form presynaptic terminals of synapses
Myelin
Wraps axons like insulation to keep electricity from escaping
Nodes of Ranvier
Breaks in myelin with concentrated channels
Sensory Receptor Neurons
Change sensory input into electrical signals
Projection Neurons
Communicate with other neurons located in a different or distant CNS regions (between brain areas, between spinal cord and sensor/motor stuctures)
Interneurons
Communicate with other neurons located in the same or nearby CNS region
Glial Cells
Support system for neurons, more numerous than neurons
Astrocytes
Restricted to CNS, help maintain the proper extracellular chemical environment necessary for neural signaling, comprise the blood brain barrier
Oligodendrocytes
In the CNS, myelinate several parts of several axons
Schwann Cells
In the PNS, each cell myelinates one part of a single PNS axon
Microglia
Scavenger cells that remove debris from sites of injury, modulate inflammation, cell survival, and cell death, very plastic
Meninges
3 layers of tissues provide protection to the brain and spinal cord
Dura mater
Outermost meninges layer, tough and leathery
Arachnoid mater
Middle meninges layer, fairly delicate and impermeable. Separated from the dura by subdural space and from the pia by the subarachnoid space (filled with cerebrospinal fluid)
Pia mater
Innermost meninges layer, adheres to the surface of the brain, appears glossy and is so thin it is almost invisible to the naked eye
Ventricular System
Cerebrospinal fluid is derived from the choroid plexus on the walls of ventricles
CSF leaves the ventricles through foramina
CSF enters the subarachnoid space
CSF drains into the subdural sinuses then back to the general blood flow
Cerebrospinal Fluid
Needed for brain buoyancy and protection
Hydrocephalus
Results from a block of CSF drainage, can be treated through surgical implantation of a shunt to drain fluid
Concussions
Most often caused by blows to the head, result in temporary disorientation or short-term memory loss
Blood-Brain Barrier
Protects the brain from substances in the blood, formed by tight junctions between capitally endothelial cells, anything that is both small and lipid-soluble for which specific transporters exist can get through
Circumventricular Organs
Not protected by the blood-brain barrier, serve to detect presence of toxins in the blood
White Matter
Myelinated axons
Gray Matter
Mostly cell bodies and dendrites
Spinal Cord
Within the vertebral column, transfers information between the CNS and PNS, sensory information enters the dorsal portion and motor commands exit the ventral side
Cranial Nerves
12 pairs, emerge from the brain and send motor commands to and receive sensory information from the head to the neck
Medulla
Neurons that maintain normal, rhythmic breathing
Brainstem
Pons Regions
Allows cerebellum to communicate with the brainstem and the cerebral cortex
Brainstem
Midbrain
Localization of visual and auditory stimuli
Brainstem
Brainstem
Contains sensory and motor axons
Cerebellum
Motor planning and learning
Diencephalon
Thalamus relays information going to and coming from the neocortex, hypothalamus regulates autonomic nervous system and hormone release
Cerebral Cortex (Neocortex)
Processing of sensory input, initiation/planning of movement, memory, cognition, language
Occipital Lobe
Early-stage vision
Cerebral Cortex
Parietal Lobe
Somatosensory, late-stage vision
Cerebral Cortex
Temporal Cortex
Memory, hearing, language comprehension
Cerebral Cortex
Central Sulcus
Separates parietal and frontal lobes
Lateral Fissure
Separates the temporal lobe from those surrounding it
Longitudinal Fissure
Separates the two hemispheres of the brain
Postcentral Gyri
Directs caudal to the central sulcus, contains the primary somatosensory cortex
Precentral Gyri
Directly rostral to the central sulcus, contains the primary motor cortex
Neocortex Layer 4
Receives main input from thalamus
Neocortex Layer 5
Sends projections to other parts of the neocortex and to other brain regions
Limbic System
Sexual behavior, formation of memory, primary reward and punishment centers, site of action of drugs which produce euphoria
Hypothalamus
Regulates many motivates function, sleep/wake cycle, pituitary gland activity
Limbic System
Hippocampus
Memory consolidation and provide the organism’s context
Limbic System
Amygdala
Coordinates autonomic responses with emotional states
Limbic System
Cerebral Cortex
Interacts with subcortical structures to guide behaviors
Limbic System
Basal Ganglia
Controls voluntary, smooth movement
Corpus Collosum
Long-range neurons that connect two halves of the brain
Neurons
Cells that are specialized for the reception, conduction, and transmission of electrochemical signals
Membrane Potential and Current
Inside of the cell is about -70mV relative to the outside, current causes membrane potential to become more positive or negative through movement of ions across the membrane through ion channels
Hyperpolarizaition
Neural potential is (or is becoming) more negative than resting membrane potential
Depolarization
Neural potential is (or is becoming) more positive than resting membrane potential
Conditions for Resting Membrane Potential
No net flux of ions across the membrane
Ions enter and leave the neuron at the same rate
Achieved by the balance of diffusive force and electrical force
Concentration Greater Outside Cell
Na+
Cl-
Concentration Greater Inside Cell
K+
Proteins
Homogenizing Forces
Forces promoting equal distribution of ions across the membrane, concentration gradients and electrostatic pressure
Opposing Forces
Differential permeability, sodium/potassium pump
Diffusion of Ions Across Membrane
Diffusive forces drives ions down the concentration gradient through ion channels, as ions move through they stick to the membrane
Electrostatic Pressure
Force exerted by attraction of oppositely charged ions or by the repulsion of similarly charged ions, promotes even distribution of forces
Differential Permeability
K+ and Cl- pass readily through the resting membrane through leak channels that are always open, Na+ has very few leak channels and membrane is therefore very slightly permeable to it
Sodium-Potassium Pump
Maintains Na+ and K+ concentration gradients
3 Na+ out of neuron for every 2 K+ into neuron, affecting resting membrane potential by making in less negative
Voltage-Gated Ion Channels
Opened and closed by changes in membrane voltage, Na+, K+, Ca2+
Threshold
When action potential becomes all-or-none, Na+ ions enter and depolarize cell opening even more Na+ channels
Upstroke
Strong Na+ influx and weak K+ efflux at low levels of membrane depolarization, net Na+ entry causes depolarization
Downstroke
Strong K+ efflux and weak Na+ influx at high levels of membrane depolarization, net K+ efflux causes repolarization
Afterhyperpolarization
Membrane potential is more negative than at rest, K+ channels are too slow to open and close to the K+ current outlasts the action potential and hyperpolarizes the membrane
Deactivation
Passive recovery from depolarization offset (K+)
Inactivation
Voltage dependent reduction in current before offset (Na+)
Absolute Refractory Period
Occurs when voltage-gated sodium channels are inactivated, it is impossible to generate another action potential no matter how much stimulation is applied
Relative Refractory Period
Time after an action potential when enough sodium channels have recovered from inactivation to trigger an action potential, but potassium efflux is still active and the cell is hyperpolarized, therefore more stimulus is needed to reach the threshold
Saltatory Conduction
Due to high resistance in internodal regions, current jumps (saltare) from node to node
Electrical Synapses
Allow passive flow of current directly though gap junctions
Gap Junctions
Aligned pairs of channels called connexons that create pores for ions to diffuse between the two cells, allow the flow of electrical current in either direction
Chemical Synapses
Transmission through the presynaptic release and postsynaptic binding of neurotransmitters
Synaptotagmin
Vesicle protein that detects calcium and interacts with the SNARE complex to trigger release
Ionotropic Receptors
Ligand gated ion channels, NT binding directly opens/closes channel causes current flow to produce postsynaptic potentials, fast
Metabotropic Receptors
G-protein couples receptors, NT binding indirectly affects ion channels, slow
Glutamate Channels
Permeable to Na+ and sometimes Ca2+, 4 subunits with at least 2 molecularly different types
GABA Receptors
Ligand-gated chloride channel, external binding site for GABA, 5 subunits with at least 2 different types, typically conduct Cl- into cell
GABA A-Type
GABA binding required, permeable to Cl- ions, Inhibitory Postsynaptic Response, Cl- enters cell causing hyperpolarization, fast acting yet short-lived
GABA B-Type
GABA binding required, activate K+ channels through G-protein cascade, Inhibitory Postsynaptic Responses, hyperpolarizing, slow acting yet long-lasting
Spatial Summation
Adding together of inputs over space/location, multiple inputs fired simultaneously will combine efforts and be greater, bringing the neuron closer to action potential threshold
Temporal Summation
Adding together of inputs over time, three firings from same input that occur in rapid succession sum together to have a larger effect
Enzymatic Degradation of Neurotransmitters
Enzymes in the synaptic cleft bind to N molecules and metabolize them into inactive molecules
Reuptake Through Active Transport
Transport proteins on the axon terminal bind to NT molecules in the synaptic cleft and move them back into the presynaptic neuron
Astrocyte Reuptake
Astrocytes express reuptake transporters for glutamate that diffuses out of the synaptic cleft