Olfaction and the Limbic System Flashcards

1
Q

What the three types of cell that makes up the olfactory epithelium?

A

Bipolar Olfactory Neurones (main neurons of smell)

Sustentacular Cells – support cells mainly providing metabolic support

Basal Cells – involved in regeneration of the bipolar olfactory neurones

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2
Q

Where is the olfactory bulb found?

A

Sitting on top of the cribriform plate

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3
Q

Which cells synapse within the olfactory bulb?

A

The bipolar cells pass their axons through the cribriform plate to synapse with the second order neurones (olfactory bulb mitral cells) in the glomerulus within the olfactory bulb

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4
Q

What structure do the second order neurones form and what does this structure split into?

A

Olfactory tract
Olfactory tract later splits to form the medial and lateral olfactory stria
slide 4 and 6

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5
Q

Where does higher processing of smell take place?

A

Piriform Cortex

Orbitofrontal Cortex

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6
Q

What is a clinical deficit in the olfactory system called?

A

Anosmia (loss of smell)

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7
Q

What is a common cause of anosmia?

A

Mid-face trauma
Impact with enough force could cause a fracture of the cribriform plate, shearing the neurones going from the olfactory epithelium to the olfactory bulb

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8
Q

The piriform cortex is found within the temporal lobe. Explain thesignificance of this with regards to epileptic patients.

A

Epilepsy is often focused in the temporal lobe
This means that some people with epilepsy will experience PRODROMAL AURA (they are made aware of an imminent seizure because they’ll smell something that’s not there)

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9
Q

Neurodegenerative disease is a relatively common cause of anosmia. State two neurodegenerative diseases that could cause anosmia.

A

Alzheimer’s disease

Parkinson’s disease

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10
Q

What is the limbic system?

A

A rim of cortex adjacent to the corpus callosum and diencephalon

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11
Q

What are the roles of the limbic system?

A

Homeostasis (mainly hypothalamic functions such as regulation of food intake and pituitary hormone release)
Agonistic behaviour (fight or flight)
Sexual and reproductive behaviour
Memory

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12
Q

State two important parts of the limbic system that are found within the temporal lobes.

A

Hippocampus and Amygdala

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13
Q

What circuit are these structures a part of?

A

Papez Circuit

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14
Q

What is the cortical representation of the limbic system?

A

Cingulate Cortex

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15
Q

What is the function of the Papez circuit?

A

It is a neural circuit for the control of emotional expression

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16
Q

Describe/draw the papez circuit.

A

Hippocampus –> Fornix –> Mammillary Bodies –> Mammillo-Thalamic Tract (MTT) –> Anterior Nucleus of the Thalamus –> Cingulate Cortex –> Cingulum Bundle –> Hippocampus

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17
Q

What conditions could damage the mammillary bodies leading to amnestic issues? (loss of memory)

A

Chronic Alcoholism

Wernicke-Korsakoff Syndrome

18
Q

What is our emotional expression ‘coloured’ by?

A

Neocortex

19
Q

What form of imaging is used to study the limbic system?

A

Digital Tensor Imaging – shows co-instant activity in different parts of the brain thus showing which parts of the brain are working together

20
Q

Describe the afferent pathway of the hippocampus.

A

Afferent Pathway = Perforant Pathway
The entorhinal cortex is linked to the hippocampus via the afferent pathway (perforant pathway)
The entorhinal cortex receives input from all other parts of the neocortex

21
Q

What is the efferent pathway of the hippocampus called?

A

Fimbria/Fornix

22
Q

What are the functions of the hippocampus?

A

Memory and Learning

23
Q

What happens to the hippocampus in Alzheimer’s disease?

A

It shrinks severely

24
Q

Describe the spatial relations of the hippocampus and the fornix to other important brain structures.

A

The hippocampus is found on the floor of the lateral ventricles
The fornix comes out of the hippocampus and passes under the corpus callosum
It then dives inferior and anteriorly towards the mammillary bodies

25
Q

Describe the appearance of advanced Alzheimer’s disease on a CT head scan in the coronal plane.

A

There will be extensive cortical atrophy
The ventricles would appear enlarged
There will also be widening of sulci

26
Q

State two microscopic hallmarks of neurodegeneration in ALZHEIMERS

A
  1. Tau immunostaining of cells. Some neurons are stained brown because their neurofilaments have been tangled up which is characteristic of alzheimers. Tau is a protein in the neurofilaments and is dysfunctional in alzheimers.
  2. Senile plaques- these are amyloid protein being deposited between cells in the brain

slide 18 and 19

27
Q

Describe the anatomical progression of Alzheimer’s disease, including the symptoms experienced.

A

Early:

  • Hippocampus and entorhinal cortex affected first
  • symptoms: Short-term memory problems is a major symptom

Moderate:

  • Parietal lobe
  • Symptoms: Dressing apraxia (inability to carry on procedures that you don’t think about eg u cant dress your self, cant do buttons)

Late:

  • Frontal lobe
  • Loss of executive skills (personality, ability to interact with loved ones etc)
28
Q

Where is the amydala found?

A

In the white matter of anterior temporal lobe

29
Q

What are the afferent connections of the amygdala?

A
Olfactory Cortex 
Septum (septal nuclei) 
Temporal Neocortex 
Hippocampus  
Brainstem
30
Q

What is the main output pathway of the amygdala?

A

Stria terminalis

31
Q

What is the function of the amygdala?

A

Fear and Anxiety (fight or flight)

32
Q

In Alzheimer’s and Parkinson’s disease, the amygdala starts showing pathology early on. What are the possible outcomes of this?

A

Patients could either become terrified of everything or they could become totally disinhibited and become quite aggressive

33
Q

State and describe a syndrome affecting the amygdala.

A

Kluver-Bucy Syndrome
Bilateral lesions of the anterior temporal lobe (including amygdaloid nucleus)
Symptoms
 Hyperorality (putting everything in mouth)
 Hypersexuality (horny all the time)
 Loss of Fear
 Visual Agnosia (agnosia= cannot interpret. Visual agnosia= can see but cannot interpret e.g cannot recognise faces but can see faces)

34
Q

State three structures associated with aggression.

A

Hypothalamus
Brainstem (periaqueductal grey matter)
Amygdala

35
Q

What are the main afferent connections of the septum (septum pellucidum)

A

Amygdala
Olfactory Tract
Hippocampus
Brainstem

36
Q

What are the functions of the septum?

A

Reinforcement and Reward

37
Q

Name another structure that is important in the reward system.

A

Nucleus Accumbens

38
Q

Describe another dopaminergic pathway other than the nigro-striatal pathway that is affected in Parkinson’s disease.

A

Ventral Tegmental Area (VTA) of the midbrain –> Median Forebrain Bundles –> Cortex + Nucleus Accumbens + Amygdala

39
Q

Name a structure that is important in drug dependence.

A

Nucleus Accumbens

40
Q

What effect do all drugs of abuse have on the nucleus accumbens?

A

They all stimulate neurons from midbrain that go to nucleus accumbens which increase dopamine release (or reduce dopamine reuptake) in the nucleus accumbens