Wednesday, February 11, 2015

Limbic system (neuroanatomy)

The limbic system is comprised of both cortical and subcortical brain structures that play an important role in emotions, drives, olfaction, homeostasis, autonomic control, neuroendocrine control and memory.  (I use the mnemonic “A Demon” or “Moaned” to remember these six functions)  

Most of the limbic structures lie hidden in the ventral-medial areas of the brain and diagrams of them can be seen below.  A list of the various structures of the limbic system can also be seen in the table to the right.

The olfactory system, or rhinencephalon, consists of several types of neurons.  Olfactory receptors of the (1) olfactory nerves relay information about odorants into the olfactory bulb where they synapse with (2) mitral cells and (3) tufted cells.  These cells relay information about the odorants through the olfactory tract and to the olfactory cortex.  Additional neurons called (4) periglomerular cells and (5) granule cells participate in this process.  Eventually information is received by the primary olfactory cortex, near the medial, anterior tip of the temporal lobes.  The primary olfactory cortex is comprised of the piriform and periamygdaloid cortices.  Information received by the primary olfactory cortex is then projected to several secondary olfactory areas such as the basolateral amygdala, mediodorsal nucleus of the thalamus, anterior entorhinal cortex and ultimately, the orbitofrontal olfactory areas.

The hippocampal formation is one of many different memory structures that make up the limbic system.  It’s three components are the (1) dentate gyrus, (2) hippocampus and (3) subiculum.  The anterior division of the hippocampus, known as the pes hippocampi, is the largest.  As it progresses posteriorly it tapers and wraps posteriorly around the corpus collosum until it disappears under the splenium of the corpus callosum.  A vestigial remnant continues along the dorsal surface of the corpus calossum, forming the indusium griseum. 

The hippocampal formation is unique in that it is comprised of a special type of cortical tissue named archicortex.  Archicortex is more phylogenetically ancient form of cortex that is comprised of only three layers (molecular, pyramidal and polymorphic layers in the hippocampal formation).  The majority of our cerebral cortex is comprised of six layered neocortex.

A great deal of research has been compiled on how the circuitry of the hippocampal formation contributes to memory functions.  Research suggests that pyramidal cells of the entorhinal cortex project to the hippocampal formation through the perforant and alvear pathways.

The parahippocampal gyrus includes several adjacent areas of cortex such as the entorhinal cortex (the major input/output relay between the association cortex and the hippocampal formation), the perirhinal cortex, piriform cortex, periamygdaloid cortex, presubicular cortex, prorhinal cortex and parahippocampal cortex.  As the parahippocampal gyrus travels posteriorly it tapers into the parahippocampal cortex and then into the rhinal sulcus.

The fornix is a C-shaped collection of white matter tracts that serve as a major output pathway from the subiculum of the hippocampus to the septal nuclei and mammillary bodies.  A smaller group of cholinergic neurons travel in the opposite direction from the  medial septal nuclei and diagonal band of Broca, to the hippocampal formation.

The amygdala lies just dorsal to the anterior tip of the hippocampus and plays roles in emotion, homeostasis, memory and olfaction.  However, it is best known for it’s prominent role in emotions and drives.  The amygdala is comprised of (1) corticomedial nuclei (2) basolateral nuclei (3) central nuclei and (4) bed nuclei of the stria terminalis.  The corticomedial nuclei are involved in olfaction and hypothalamic appetitive states.  The central nuclei are also involved with the hypothalamus, in addition to the brainstem and play an important role in autonomic control.  While activity in the amygdala is important in fear, anxiety and aggression, the septal area appears important for pleasureable states.  The amygdala plays an important role in attaching emotional significance to memories.  Finally, it also appears to have a role in neuroendocrinological functioning during states of altered emotional experience.

Diencephalic limbic structures (e.g. the hypothalamus, select thalamic nuclei and the nucleus accumbens) play a role in all limbic functions.

The septal nuclei play an important role in memory encoding.  The lateral septal nuclei recieve information from from the precommissural fibers of the fornix.  The medial septal nuclei send acetylcholine back in the opposite direction.  This acetylcholine then allows memories to be formed by enabling theta electrical waves in the temporal regions.

Brainstem nuclei (i.e. interpeduncular nucleus, superior central nucleus, dorsal tegmental nucleus, ventral tegmental nucleus, parabrachial nucleus, periaquedctul gray, reticular formation, nucleus solitarius and the motor nucleus of the vagus) exert an influence on limbic pathways

Saturday, January 17, 2015

Synaptic transmission {physio}

T/F: The dendrites of a neuron have a threshold potential which, if exceeded, could initiate an action potential within the shaft of the dendrite.

True, although this threshold is far higher than at the axon hillock so it is never exceeded.

Why does the axon hillock have the lowest threshold potential?

It is the region with the highest number of voltage-gated sodium channels

What two ways can an EPSP become strong enough to initiate an AP?

Spatial summation (recruit more excitatory neurons with a stronger stimulus)
Temporal summation (add multiple EPSPs close together)

T/F: Inhibitory neurons located on dendrite shafts decrease the strength of local EPSPs while inhibitory neurons located near the axon hillock decrease the strength of the collective EPSP of the cell.

True

A measure of the change in EPSP strength compared to the original EPSP.

Synaptic strength (efficacy)

What is the principle difference between axo-somatic inhibitory synapses and axo-axonic inhibitory synapses?

Axo-somatic inhibitory synapses act by lowering the strength of the graded potential, making it harder to reach threshold. Axo-axonic inhibitory synapses act downstream of the AP and act to limit the amount of neurotransmitter release.

What is a major function of axo-axonic inhibition in the various sensory pathways?

It serves to filter out "noise" allowing the subject to focus on the important stimulus more efficiently. For example, random noise in a room when you are having a conversation.

The process of filtering out sensory "noise"

Habituation

What is the principle axo-axonic inhibitory neurotransmitter?

GABA

GABA inhibits via two receptors. What are they and how do they cause inhibition?

GABAb: close Ca++ channels and/or open K+ channels
GABAa: open Cl- channels

**think "a" is first letter, so it's the most simple. Only one ion.

These cells in the CNS "fine-tune" muscle responses.

Renshaw cells

A motorneuron sends ACh to _________ receptors at the NMJ while simultaneously sending ACh to _________ receptors on Renshaw cells.

Nicotinic (ionotropic); muscarinic (metabotropic)

Interneurons in the motor pathway use _________ as the primary inhibitory neurotransmitter.

Glycine

Motor axons are _________ while motor neuron axon collaterals are _________.

Myelinated; unmyelinated

Muscarinic receptors on Renshaw cells are blocked by this compound.

Atropine

T/F: Muscarinic Renshaw cell receptors increase K+ conductance.

False. They decrease K+ conductance

Norepinephrine, dopamine, seratonin are synthesized in the _________ of a neuron. They are neither __________ nor __________.

Terminal bouton; excitatory nor inhibitory

These are minor CNS neuromodulators that are synthesized in the soma and transported to the boutons.

Neuropeptides. Substance P (burning sensation) and enkephalin (opiate action)

Increasing/decreasing K+ conductance changes the __________ of action potentials.

Frequency (or duration)

T/F: A larger synaptic head tends to produce a stronger EPSP.

True. The larger head allows for more receptors.

T/F: Mentally retarded children will exhibit a larger number of dendritic spines in their neurons early on.

True. But these are largely immature and eventually disintegrate, leading to a lowered number of spines in adulthood (Slide 17, lecture 08)

T/F: Sanel has less LTP going on in his hippocampus than in Rick Hill's hippocampus.

:-)

What induces a LTP to form?

A strong, short stimulus

Describe the steps of LTP.

1) Activation of NMDA receptors, Ca++ flows in
2) Ca++ binds to calmodulin, activates PKC
3) More AMPA receptors are recruited to the plasma membrane, increasing synaptic strength
**Additionally, the phosphorylation state of existing AMPA receptors can be changed to modulate their activity

T/F: Genetic actin defects lead to mental retardation.

True. Actin is used to anchor AMPA receptors during LTP/LTD. A problem in this process will lead to decreased cognitive abilities.

T/F: Now that you understand the molecular basis of cognitive pathways, studying moderately over long periods of time is better than studying a lot over a short period of time.

True!

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