Midterm 2 Flashcards

1
Q

Development of the CNS

A
  1. 3rd week – human brain is a hollow tube present in the ball of cells
    a. Rises from ectoderm – outer layer of cells
    b. Neuralation
  2. 4th week – specializes in the anterior end
    a. 4 main divisions
    i. Forebrain
    ii. Midbrain
    iii. Hindbrain
    iv. Spinal cord
  3. 4-6 weeks – large increase in cells organized into new structures
    a. Forebrain
    i. Cerebrum
    ii. Diencephalon
    b. Midbrain
    c. Hindbrain
    i. Pons & cerebellum
    ii. Medulla oblongata
  4. 11 weeks – tube has enlarged and bent
    a. Cerebrum – large increase in cells; wraps around to diencephalon
    b. Hindbrain
    i. Pons – ventral
    ii. Cerebellum – dorsal
    - Looks like mini brain
    iii. Medulla – transition into spinal cord
    - Nucleus of the solidary tract
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2
Q

Derivatives of each section

A

Forebrain

i. Cerebrum
- Cerebral hemispheres
- lateral ventricles
- Basal ganglia
ii. Diencephalon
- Thalamus
- Hypothalamus
- 3rd ventricle

Midbrain

i. Superior and inferior colliculus
ii. Substantia nigra

Hindbrain

i. Pons
ii. Cerebellum
iii. Medulla

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3
Q

Ventricles
- specialized for what

  • remnants of
  • location
  • structure
A

Fluid filled cavities within the brain, remnants of the “hollow tube” from which the brain developed

4 ventricles

a. Cerebrum
- third – will be around the hypothalamus
- lateral
b. Hindbrain
- fourth – very small

Structure

a. Filled with CSF – part of the protection of brain
b. Continuous with the central canal – hollow tube in the spinal cord
c. Lined by ependymal cells – glial cells; contribute to BBB (water tight barrier)
- Specialized for transport – allow the movement of certain solutes across

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4
Q

White matter vs grey matter

  • where are they present in the brain
A

Grey matter: Unmyelinated cell bodies, axon terminals, dendrites, and synapses

a. Clusters of neuronal cell bodies are most often found clustered together in nuclei, or on the outer surface of the brain as the cerebral cortex.
i. Nuclei – clusters of cell bodies
- Groups of neurons that do similar things are grouped together – nucleus
ii. Ganglia – “knot” of cells; collection of cell bodies in PNS
- Some groups within CNS are also called a ganglia
b. Outermost layer of cerebrum
c. Thalamus (2)
d. Hypothalamus (3)

White matter: Myelinated axons

a. Make up much of the cerebral cortex
- Large amount of information transfer – signal conduction & information processing

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5
Q

Protection of CNS

  • what is a cat scan
A

CNS is fragile – protective components

a. Bony skull and vertebral column
b. Meninges – three protective and nourishing membranes
- CAT scan – x ray that takes sequential pictures (computerized tomography); gives 3D structure of brain
c. Cerebrospinal fluid (CSF)
d. Blood-Brain barrier

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6
Q

Meninges

  • layers
  • menginitis
  • head injuries
A

Layers
1. Dura mater – outermost layer; tough leathery layer; tough mother
a. Functions
• Immediately within skull – helps hold in place
• Protective – if skull is cracked, it will protect brain
b. Forms reservoir within – important in circulation
i. Dural sinus – cavity; part of the circulatory system
o Continuous with veins – blood is being collected when draining from brain
o Emissary veins – drains blood from Dural sinus
ii. Any cuts in skull
o Place for bacteria to enter and access venous system and cause infection – can be life threatening
2. Arachnoid membrane – middle; connected to pia mater via fibrous structures
a. Arachnoid trabeculae – webs; hold arachnoid to pia mater
• Arachnoid – spider webs
b. Arachnoid villi – project into Dural sinus; play role in movement of CSF
3. Pia mater – directly on surface of brain; soft and delicate

Meningitis – contagious bacteria, viral, or fungal infection
o Causes swelling of meninges – puts pressure on CNS
o More common in large groups of people

Head injuries – can cause bleeding between layers; really bad really fast

a. epidural bleeding – between the skull and dura
- epi – above dura
- ski accident of actress – killed her after hitting her head on a bunny hill
b. subdural bleeding – between the dura and arachnoid
- sub – beneath dura
c. subarachnoid bleeding – between the arachnoid membrane and the pia mater)
- sub – beneath arachnoid

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7
Q

Cerebrospinal fluid

  • circulation
  • importance
A

Circulation

  1. Produced by choroid plexus – specialized cells within ventricles
  2. Exits the 4th ventricle through pores – foramen of Magendie (median) and foramen of Luschka (lateral)
    - Inters into subarachnoid space
  3. Some circulates around the spinal cord, some circulates into subarachnoid space
  4. Enters arachnoid villi from subarachnoid space – enters into dural sinus
    - Arachnoid villi – granulations; extensions from subarachnoid space into subdural space and dural sinus
    - Dural sinus – collects into venous blood; allows movement of waste from brain into circulatory system

Importance

a. Help maintain proper solute concentrations in the ISF surrounding neurons
- Ex. if there is high [K+] – some will move into CFS to keep within set point
b. Waste removal
c. Cushion from brain – prevent physical damage; brain won’t hit the skull

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8
Q

Blood brain barrier

  • structure
  • neuronal vs non-neuronal blood vessels
  • examples of substances that can move through
  • function
A

Barrier between the interstitial fluid of the brain and the plasma of circulatory system

Structure

a. Endothelial cells – have tight junctions (proteins); prevent movement between cells
b. Astrocyte cells – surround the endothelial cells
- End feet – projections that surround all vessels; prevent movement of solutes
c. Non-neural blood vessels
- Not connected via tight junctions
- Fenestrations – pores connecting luminal and extraluminal side

Function

a. Keeps unwanted materials out, keeps wanted materials in.
- Prevents leakage of materials from circulation into brain
- Keeps neurotrophic factors from leaving neural tissue into circulatory
b. Permeability
i. Hydrophobic substances – can diffuse across and directly contact neurons
- Ex. ethanol, steroids, nicotine, Benadryl
- Benadryl – allergy medicine; can come into contact with neurons and inhibit activity by affecting histamine receptors (antagonist)
- This is why is causes drowsiness
ii. Hydrophilic substances – must be transported across cellular layers to make it into neurons
- Ex. glucose or peptide based hormone, insulin, Na+

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9
Q

Spinal cord

  • 4 levels
  • internal circulatory - what types of movement
  • meningeal layers
A

Major pathway between the CNS & PNS; brain and skin, muscle, joints, and organs.

Four levels
o	Cervical – neck 
o	Thor – chest 
o	Lumbar – lower back 
o	Sacral/coccygeal – tail bone 

Has its own internal circuitry
a. Mediates simple reflexes
b. Generates complicated control programs – rhythmic patterns
i. Ex. used for walking
• Input is initially needed from brain – rhythmic movements are from spinal cord
ii. Ex. patellar reflex – stimulates its own contraction; only travels to spinal cord & does not require brain

Same meningeal layers as brain
o Pia mater – directly on spinal cord
o Arachnoid membrane
o Dura mater

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10
Q

Segments of spinal cord

  • autonomic ganglia
A

Each segment has bilateral sets of roots

  1. Dorsal – sensory into CNS
    a. Differentiated by ganglia – bulge
    b. Neurons
    o Dendrites – in the PNS
    o Cell bodies – in the ganglia
    o Axons – will collect and form spinal nerves
    c. Autonomic ganglia – contain neurons that regulate ANS
  2. Ventral – control/motor away from CNS

31 pairs of spinal nerves – axons from ventral and dorsal root pairs converge and form
a. After L1-L2, the spinal cord consists of cauda equina – thick elongated nerve endings
• Most nerves have diverged somewhere else – what is left
• “horsetail”

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11
Q

Grey & white matter in spinal cord

A

White – outside (reverse of brain); myelinated axons

a. Ascending tracts – dorsal surface and outer lateral
- Sensory info
b. Descending tracts – ventral and interior lateral positions
- Somatic & autonomic

Grey – inside (butterfly); neuronal cell bodies, dendrites, unmyelinated synapses 
a.	Sensory nuclei – dorsal horn
i.	Somatic – first cluster  
•	Cell body of second order sensory neurons – receive info from synaptic terminal of first order sensory neurons (within CNS) 
ii.	Visceral – second cluster 
•	Info from organs and viscera 
b.	Motor nuclei – ventral horn 
i.	Autonomic – more lateral in horn 
•	Control of organs and homeostasis 
ii.	Somatic – more medial in horn 
•	Controls skeletal muscle
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12
Q

Brainstem

  • phylogenetically
  • consists of
  • cranial nerves (what do they control)
  • reticular formation
A

Phylogenetically – oldest region of the brain – primate ancestors still have
o Transition of brain to spinal cord

Consists of
1. Midbrain – critical relay for visual and auditory info
a. Neurons that control movement of eyes & constriction/dilation of pupils
b. Gives rise to groups of diffuse modulatory neurons
2. Pons – acts as a relay station for cerebellum and cerebrum (neither are part of brainstem)
a. Plays role in regulating muscle reflexes involved in equilibrium and posture
b. Proximity to cerebellum – critical in posture, balance, and equilibrium
• Integrating area from cortex
• Allows maintenance of equilibrium with posture
• NOT part of brainstem! – hindbrain only; developmentally in the same area
3. Medulla – contains nuclei that control heart and blood vessel function, respiration, and many digestive functions
a. Vital and nonvital functions

Most of cranial nerves (10/12 pairs) arise from brainstem

a. Cranial nerves – pairs of nerves emerging from CNS
- Sensory, motor, or both
- Controls mouth, tongue, movement of eyes, balance, functioning of organs

Reticular formation – diffused; no real structure/not a tight collection of cell bodies

a. Receives and integrates incoming sensory input – plays critical role in arousal
- Arousal – wakefulness; whether you can focus on certain kinds of info
b. Gives rise to groups of diffuse modulatory neurons

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13
Q

Diffuse modulatory neurons

A

Neurotransmitters – can have neuromodulatory functions
o Long, slow regulation of neurons – usually through the actions of GPCR
o Ex. no ligand gated ion channels for norepinephrine

Spread axons throughout brain – do not just project to a single location

Nt: histamine, serotonin, norepinephrine, acetylcholine, dopamine

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14
Q

Cerebellum

  • processes sensory info from where
A

Integrating center; “mini brain”

Processes sensory info from muscles, joints, vestibular system, eyes – integrates position and movement of body with intent to move body
1. Important in maintaining balance and controls eye movements
a. Eye movements are important for sense of balance
• Standing on one foot and closes eyes – balance in inhibited
2. Enhances muscle tone and coordinates skilled – voluntary movements
a. Coordinated movement of hands, arms, fingers when picking up a pencil
3. Plays role in planning and initiating voluntary activity by providing input to cortical motor areas
4. Stores procedural memories
a. Motor learning – learning how to do something (ex. a perfect pitch)

Also has recently discovered function in cognition & emotional processing

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15
Q

Diencephalon

  • structures
  • their functions
A

Thalamus – main relay center for most types of information

  1. Receives information from almost every area of the CNS, and sends information to these same areas.
    a. Sensory info – often makes first synaptic relay in thalamus & sent to cortex
  2. Sensory, emotional, motor, arousal
    a. The whole point of more synaptic connections – have more information processing and integrating info
    - Helps contextualize information because it’s combining

Hypothalamus – homeostasis
Functions
1. Controls body temperature
2. Controls thirst and urine output
3. Controls food intake
4. Controls anterior pituitary hormone secretion
5. Produces vasopressin & oxytocin (neuroendocrines)
6. Controls uterine contractions and milk ejection
7. Serves as a major ANS coordinating center
8. Plays role in emotional and behavioral patterns, including reproduction, sexual orientation?

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16
Q

Hypothalamus and sexuality

A

1991 – Simon LeVay published a paper indicating a morphological difference in a nucleus of the hypothalamus between gay and straight men (INAH3)
o The area in gay men was anatomically more similar to females.

Suggested “sexual orientation has a biological substrate”
Often misinterpreted
1. Religious right – said being gay is a form of brain damage
2. Pro gay people – there is a “genetic cause”
• Also not what he said – only found correlation and biological substrate

Very controversial findings
a. Accused him of having an agenda – he was gay
• LeVay accused of being biased
b. In early 90s and 80s – terrible time to be gay
• AIDS epidemic – no effective treatment
• Fear and anger against gay people

His study was statistically well done – credited for being the pioneer of these kinds of study

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17
Q

Cerebrum

  • evolutionarily
  • how large
  • surface area
  • components
A

Evolutionarily, the newest
o Largest and most distinct part of human brain (makes up about 80% of total brain weight)

Intelligence comes from large surface area compared to other animals
o Gyri and sulci – folds; these are used as landmarks; increases surface area
a. Gyri – ridges
b. Sulci – valleys

Components

  1. Cortex
    - Lateralization
    - Wernicke’s and Broca’s area
  2. White matter
  3. Basal ganglia
  4. Limbic system
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18
Q

Localization of function in the cerebral cortex

  • outdated ideology
A

Lateralization – side do not have mirror functions; halves are not identical
o Ex. Left-handed persons brain is not a mirror image of right-handed person’s

Many functions are localized to one side – not always the case
1. Left side – for most people; language processing, math processing
a. Very little language processing on right side for most people
• 95% right handed people left dominant for language
• But only 80% left handed people left dominant for language
- many lefties process language on both sides (i.e. it’s complicated_
b. Speech – often
c. General interpretive center – language and math
2. Right side – for most people; spatial recognition, face recognition, aspects of emotion processing and artistic functions
a. Generalizations – not all people process on right side

Lateralization does not refer to right brain person (creative, artistic) vs left brain (logical and analytical) – this idea from 1960’s is considered scientifically unsound
o Stems from phrenology – brain functions were correlated with lumps on skull and brain

Some functions are not localized
o Auditory and visual cortex – both sides

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19
Q

Broca’s and Wernicke’s area

A

Connected via reciprocal connections (axons go both ways and communicate with each other)

Input for language processing – come from audio or visual information.

a. Listening or reading language
b. Sensory input goes from audio or visual cortex -> Wernicke’s -> Broca’s.
- Integration occurs between these two areas (back and forth)
- Information from Broca’s is then sent to motor cortex to initiate spoken or written action

Damage to either area can be devastating to communication – aphasia
a. Aphasia – inability to comprehend or formulate language
b. Many kinds – not always straight forward & one kind
• Lots of subtle variations – very complex
• Older textbooks may give very defined signs and symptoms

Damage to Wernicke’s area – generalized

a. Receptive aphasia – difficulty understanding spoken or visual language
- Sensory info goes here first
- Can be both spoken and visual language or just one or the other
b. Speech may be nonsensical because of trouble connecting words with meaning (word salad, Jargon aphasia)
- Wernickes = words strung together illogically (real words but don’t make sense structurally)

Damage to Broca’s area

a. Expressive aphasia – difficulty expressing ideas; “can’t get a sentence out”
- They know what they want to say
- May not be able to speak or write or both
b. Often can interpret simple words or sentences – may have trouble with more complicated ones with several elements.
- Having numerous elements in a single sentence
c. Words “distorted” – gibberish; mangle the sounds of the words
- No damage in motor areas (still functioning) – there is a disconnect in how they form proper words

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20
Q

Basal ganglia

  • components & functions
  • loss resulting in damage
A

Ganglia – collections of cell bodies (= nuclei).
o The neurons within basal ganglia communicate with each other, and with other brain areas

Several components – form a complex circuit between the motor cortex, premotor cortex, cerebellum, thalamus, and other areas.

a. Through communication with each other and other areas
b. Largely involved in movement
- Pre and motor cortex & cerebellum areas – specifically involved in movement
- Thalamus – relay center between sensory and motor

Loss of any parts of the basal ganglia is devastating – often result in disorders of movement
1. Parkinson’s disease – loss of dopaminergic neurons in BG; causes tremors, loss of ability to move, cognitive deficits.
a. Loss of ability to initiate movement
• Ex. have difficulty getting up from a chair
b. Too much medication – overstimulates neurons; can cause Huntington’s like symptoms
• Ex. Michael J Fox
2. Huntington’s disease – loss of cholinergic neurons in BG
a. Activates the neurons that are lost in Parkinson’s – dopamine movement
b. Causes uncontrollable movements (chorea), loss of coordination, dementia
• Chorea – to dance

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21
Q

Limbic system

  • phrenologically
  • components & what do components do
  • functions
A

Phrenologically – oldest part of the cerebrum
o Connected with many homeostatic control centers
o Very deep within brain

Components

a. Includes – amygdala, hippocampus, cingulate gyrus
- Hippocampus – learning and memory
- Amygdala and cing gyrus – emotional processing
b. Strongly connected with other areas – thalamus, hypothalamus, parts of the midbrain & parts of brainstem

Function – links higher processing with primitive emotions such as fear, aggression, reward, social and sexual behaviour.
a. “animal brain” – basic animal instinct emotions
b. Regulating basic emotional responses
i. Sensory stimulus – will be arousing stimuli of primitive emotions
• Ex. seeing a bear
ii. Cerebral cortex passes to limbic – processes and sends back to cortex
• Evokes emotion of fear – feedback processing
iii. Hypothalamus and brainstem
• Homeostatic response: Autonomic response – fight or flight activation pathway
• Long term stresses – can alter immune responses
• Somatic motor responses – will feel need to run from bear immediately

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22
Q

Damage to frontal lobe

A

A lot of what we know about the brain – came from bad situations

a. Ancient Greeks/romans/Persians – doctors and medics in battle
b. Damage to brain and how it affected their behaviour
- Many early scientists thought heart was the “brain”

Phineas gage
a. His job was to put dynamite into drilled holes – tamping down dynamite charge; caused rod to be driven through his brain
b. He survived
- Abolished a large portion of frontal cortex
- He got an infection – he made the recovery
c. Before accident – he was a very smart and nice person
i. After recovery – his personality was very different
• He became argumentative and difficult – swearing
• He changed jobs numerous times – couldn’t do a single thing a long time
d. Historically important cases – stimulated an entire area of research
- Another example – HM in the hippocampus

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23
Q

Conscious senses
- 2 subtypes

Unconscious senses
- 2 subtypes

A

Conscious Senses
1.. Somatic senses (somatosensory)
a. Touch (texture, vibration..)
b. Temp
c. Pain
d. Itch
e. Proprioception – where is my body and where are my limbs
i. Positioning of body and limbs in space and in regard to other things in your environment
• Ex. grabbing coffee cup – need to know where limbs are
• Feedback mechanisms

  1. Special senses**
    a. Vision
    b. Hearing
    c. Taste
    d. Smell
    e. Balance

Unconscious Senses

  1. Visceral – you can’t get an accurate conscious perception of these things
    a. Blood pressure
    b. GI distension
    c. Glucose
    d. Osmolarity
    e. Oxygen/CO2 content of blood
    f. Many others
  2. Somatic stimuli
    a. Muscle tension
    b. Proprioception
    i. Ex. You don’t always think about position of legs when running
    • Spinal cord processes this information
24
Q

5 general properties of sensory systems

A
  1. Receptors are most sensitive to certain forms of energy or stimuli - modality
  2. receptors transduce sensory info to graded potentials
  3. sensory neurons have receptive fields
  4. CNS integrates sensory info
  5. coding and processing distinguish stimulus properties
25
Q

Receptors are most sensitive to certain forms of stimuli

  • definitions of receptors (& where is trigger zone)
  • types of modalities
  • types of receptors
A

Ex. light, sound, pressure waves

Receptor – two meanings in neuroscience

i. Protein that binds a ligand
- Ex. receptors channels & GPCR & intracellular receptors etc..
ii. “structure” that detects sensory info – originates in psychology branch
- Can be many things for different types of stimuli
- Also often ion channels
- Trigger zone – the area immediately adjacent to the receptor, where the dendrites join the axon

Modalities detected by “receptors”

a. Chemoreceptor – taste, smell, o2 concentration in blood
b. Mechanoreceptor – pressure & somatosensory; angle of joint
i. Hearing – also depends upon
- Depends on pressure waves that move structures – a mechanosensation
c. Thermoreceptor – whether something is colder or warmer than body temperature
d. Photoreceptor – vision; detects photons of light

3 types of receptors

  1. Simple
    a. Free nerve endings – can detect pH, temp, o2 levels
    - Found at bare nerve ending of primary sensory neuron – brings sensory info back into CNS
  2. Complex – ensheathed by non neuronal accessory cells/tissue
    a. Specialized
    b. Ex. vibration
  3. Special senses – they require 2 cells
    a. Specialized transducer cell – will detect its preferred modality
    i. There is a synapse between
    ii. Neuroepithelial – ectodermal embryonic origin
    - Some properties of neurons – can release synaptic vesicles
    b. Primary sensory neuron
    c. Ex. smell, vision
26
Q

Cortex Lobes

A
  • Outer surface – highly convoluted; highest, most complex integrating area of the brain
  • Plays key role in most sophisticated neural functions
  • Math, language, music
  • Each half of cortex divided into five major lobes
  1. Frontal – lots of motor/skeletal movement & coordination of movement
    Motor cortex
    a. Pre motor – motor association area
    i. Planning – receive information from basal ganglia, cerebellum, and somatosensory cortex
    - Sensory info about the position of muscles and movement that must occur
    - Thinking about an action – will activate neurons in premotor
    ii. Will not activate motor neurons unless you actually initiate action
  2. Primary motor cortex – executing
    a. Receives input from premotor cortex neurons
    b. Neuron cell bodies in grey matter
    • Sent through white matter & spinal cord
    • Make contact with neuron in spinal cord that controls skeletal muscle
  3. Parietal – sensory info
    a. Central sulcus – delineates frontal and parietal
    b. Primary somatosensory cortex – processing of textures, touch, temp
    i. Information from sensory neurons – enters into primary somatic sensory area
    o First area of processing – ability to discriminate between simple properties of stimulus (ex. smooth vs rough)
    ii. Sends to sensory association areas
    o Second area of processing – able to associate with other stimuli and determine what that stimulus is

3, Temporal – processing auditory info (more notes)

a. Primary/auditory cortex – first place info is sent to
b. Auditory association area – info is sent

  1. Occipital – first place visual info is processed
    a. Primary – first layer of processing
    • This item is red/round
    b. Info is sent to adjacent neurons – association areas
    • Higher level processing
    • Info comes together – it’s a red ball
  2. Insular – processing taste and smell (more notes)
    a. “insulated” – not obvious by looking at brain; not always included in text
    b. Has primary and association areas
27
Q

Receptors transduce sensory info into graded potentials

  • what stimulates GP
  • receptor potential
  • adaquate stimulus
  • intensity of the stimulus
  • receptor threshold
A

There is always a process of converting one form of energy/stimulus into GP and AP

The transduction process involves changes in membrane potential of sensory neurons

  1. Graded potential from
    a. Ligand gated channels (chemical)
    - Ex. olfactory
    b. Mechano-, thermo-gated channels (touch, temp, pressure, hearing and balance)
  2. Channels modulated through second messenger pathways (vision)

Changing ion channel activity in the sensory receptor causes a graded potential – receptor potential

  1. adequate stimulus – the preferred type of stimulus for a receptor
    a. Not a stimulus that passes threshold
    b. Preferred
    - Photoreceptor is light
    - Mechanoreceptor is pressure
  2. intensity of the stimulus – encoded by the magnitude of the graded potential produced
    a. Not encoded by amplitude of AP
    b. Amplitude of GP – translated to frequency of AP in higher order neurons
  3. Receptor threshold – the minimum stimulus to activate a receptor
    a. Minimum intensity of light & pressure
28
Q

sensory neurons have receptive fields

  • somatosensory maps
  • convergence
A

gather info from very specific areas

Receptive field – region of space in which the presence of a stimulus will alter the firing of a sensory neuron
i. Ex. sensory neuron in skin – will have a limited area of skin it innervates

Primary sensory neurons – converge onto secondary neurons; allows summation (simultaneous subthreshold stimuli to initiate AP)

i. May need to stimulate multiple primary receptive fields in order to bring secondary sensory neuron to threshold
ii. Convergence influences sensitivity
- Increased convergence = larger receptor field = lower acuity
iii. 2 point discrimination
- 2 stimuli that fall within the same secondary receptive field – perceived as single point; only one signal to brain
- lower acuity = lower spatial resolution

Somatotopic map – more area = greater acuity
i. Ex. finger takes up same amount of space as arm – greater acuity; less convergence

29
Q

CNS integrates sensory info

  • where are visceral reflexes processed
  • somatosensory processing (perceptual threshold)
A

Some sensory info processed in spinal cord/brainstem levels – unconscious perception

a. Brainstem – HR and BP
- Often don’t have a conscious perception of it
- Directly to brain stem via cranial nerves
b. Visceral reflexes integrated in brain stem or spinal cord usually do not reach conscious perception

Some sensory info processed in cortex – consciously aware

a. A stimulus may activate a primary sensory neuron by causing receptor potential and AP in sensory neuron – may not have enough intensity to surpass perceptual threshold
i. Perceptual threshold – level of stimulus necessary to be aware of particular sensation
- Can change in heightened states of arousal
- ex. hair blowing on arms from breeze – not surpassing threshold
- vs watching documentary on spiders – a small breeze that moves hairs; you will now notice

30
Q

Coding and processing distinguish stimulus properties

  • properties that must be determined
  • groups in the brain associated with
  • labelled line processing
  • lateral inhibition
  • how are properties coded
A

Ex. pitches of sounds, is it moving away or coming towards you

All stimuli are converted to action potentials

Properties of stimulus that need to be determined:

  1. Modality of stimulus – specific receptors only activated by specific stimuli
    a. Receptors – have a preferred modality or adequate stimulus
    i. Specific groups of neurons within the brain are associated with specific modalities
    - Occurs through development – group of primary SN that only detect light or heat etc
    b. Perception of a stimulus depends on the neural pathway that brings it to the CNS, not the receptor that transduced the signal
    i. Labeled Line processing – each modality has its own “wiring system” from the receptor to higher processing centre
    c. Ex somatic senses – primary neurons innervate a patch of skin
    i. Spinal cord – brainstem – thalamus – cortex
    - Primary somatosensory cortex – processed here
    d. Ex. eye
    i. Photoreceptors – thalamus – occipital cortex
    ii. If you moved photoreceptors from the eye
    - You will not “see” through your fingers when activated by light
    - You will perceive is as some sort of touch because it’s processed in somatosensory cortex

Location of stimulus – determined by what receptor fields are activated

  1. Location of perceived stimulus – determined by labeled line processing
    a. Stimulus from adjacent areas of the body are most often processed in adjacent areas of the brain (somatotopic maps)
    i. Ex. sensory info from fingers are processed in adjacent areas in sensory cortex (thumb is beside pointer)
  2. Lateral inhibition – mechanism to increase contrast between activated receptive fields and non-activated ones; used to discriminate between adjacent receptor fields processed in adjacent areas of the brain
    a. Steps (ex. stimulating skin with pin)
    i. Directly activates primary sensory neuron B
    - With enough pressure – can activate A and C
    - Not as activated – B has the highest frequency of AP
    ii. Secondary sensory neurons – have axon collaterals
    - Collaterals – can inhibit what is occurring in adjacent sensory neurons (presynaptic inhibition)
    - Will inhibit A and C downstream
    iii. Neurons A and C – will have a lower frequency of AP than they normally would
    - B – enhanced perceptual stimulus

Properties are coded by Intensity and duration of the stimulus – reflected by graded potential and action potentials

31
Q

Receptor adaptation

A
  1. Tonic – AP are being stimulated the whole time a stimulus is present
    a. Purposes
    i. Joints – need to be aware of position of body for coordinated movements
    ii. Pain – protective
  2. Phasic – main kind; only see AP occurring at the beginning and the end (changing)
    a. Reflexive change in the stimulus
    i. Accommodation – adapting to constant stimulus
    b. Purposes
    i. Olfactory – often only notice changes in smells
    ii. Pacinian corpuscles – detect vibration
32
Q

Skin mechanoreceptors

  • types of skin
  • types of receptors
  • peripheral nerve
A

Types of skin
o Glabrous skin – no hair
o Hairy

Types of receptors – within epidermis (outer) and dermis (inner)
1. Bare nerve ending
a. bare nerve ending surrounding hair receptor – will detect the movement of hair and sends info back through primary sensory neurons; within dermis
b. bare nerve ending right below epidermis as well
• multi modal – many stimuli can activate (ex. temp)
2. Meissner’s corpuscle – located right below epidermis
a. encapsulated in connective tissues (collagen)
b. rapidly adapting
• modality – flutter and light strokes
3. Pacinian corpuscle – deep within dermis
a. Surrounded by layers of connective tissue – looks like onion
b. Rapidly adapting
• Main modality – vibrations
4. Ruffini ending – within dermis
a. Enlarged nerve endings
• Attached to connective tissue – stretching tissues activates receptors
b. Slowly adapting
i. Modality – detects stretching of the skin
o Positioning of joints and things that may be touching skin
5. Merkel disk receptors – superficial (very close to epidermis)
a. Enlarged nerve endings
b. Slow adaptation
• Modality – detects textures (that’s why its so shallow)

peripheral nerve – contains bundle of axons

33
Q

Temperature and pain receptors

  • which do we have more of
  • where are they found and on what type of neurons
  • nobel peace prize
A

Temperature receptors – are ion channels; all are found on free nerve endings
a. Activators in mouth
• Mint activates cold receptors – ion channels opened by cold temperatures
• Capsaicin activates warm receptors – ion channels opened by warm/hot temperatures
• Hot wings – does not change the temp of your mouth
b. Family of ion channels: TRP channels – detect ranges of temp
• Found in primary sensory neurons – causes GP and stimulates perception to a range of temperatures
• Ex. TRPA1 – below 15C it will open; get perception that its cold

More cold receptors than warm receptors
a.	Activated relative to body temp 
•	Cold – activated below body temp
•	Warm – 37 to 45 °C – slightly above normal body temp 
•	Pain – above 45 °C

Nobel prize for physiology or medicine in 2021
a. Awarded to David Julius and Ardem Patapoutian for their discoveries of receptors for temperature and touch
• Discovered the molecular structure of TPR channels
• Important for salt and water regulation
• Some families – variations can cause diseases

34
Q

Skin nociceptors

  • what are nociceptors
  • types
A

Nociceptors – detect pain; always bare nerve ending (never encapsulated)
a. Can be activated by:
• Strong noxious stimuli that may damage tissue
• Noxious – things we find unpleasant
• Extreme temperature – painful hot, painful cold
• Arachidonic acid and prostaglandins – may activate TRPV2 ion channels and GPCR to cause graded potentials in nociceptive neurons

Different types of axons/fibers carry pain info – pain can be perceived in different ways
a. A-beta – fastest pain
• Medium diameter myelinated – fastest due to size and myelination
• Usually slightly larger than A delta
b. A delta – fast pain
• Medium myelinated
c. C fibres – slow pain
• Small unmyelinated
• Pain is more intense and longer lasting
• Ex. second wave of pain after stubbing toe

35
Q

2 sensory pathways

A

Fine touch, vibration, proprioception
a. Nerve ending in PNS – cell body in dorsal root ganglion
b. Axon is in dorsal horn (primary sensory neuron)
• Travels up spinal cord ipsilaterally – same side
c. In brainstem – synapses with secondary sensory neuron
• Desiccates in brainstem
d. In thalamus – synapses with tertiary sensory neuron
• Travels to cortex

Nociception, & temp
a. Nerve ending in PNS – cell body in dorsal root ganglion
b. Dorsal horn – synapses with secondary sensory neuron
• Desiccates in spinal cord – contralateral
• Travels through brainstem
c. In thalamus – synapses with tertiary sensory neuron
• Travels to cortex

36
Q

Protection of eye

A

Bony socket

Eyelids – act like shutters to protect eye from environmental hazards

Eyelashes – trap fine, airborne debris such as dust before it can fall into eye

Tears – cleanses, lubricates, bactericidal (prevents growth of bacteria and fungus)
a. Continuously produced by lacrimal glands and conjunctiva
• Conjunctiva – mucous membrane; runs over surface of eye and under eyelid
o Conjunctivitis – pink eye

37
Q

3 Tissue layers of the eye

  • what else is present in second layer
A

1.Sclera/cornea
a. Sclera –tough outer layer of connective tissue; forms visible white part of the eye
• continuous with the cornea
• not transparent
b. Cornea –anterior, transparent outer layer, allows passage of light rays
• still a lot of connective tissues – it’s transparent & allows light through

2.Choroid/ciliary body/iris
a. Choroid – middle layer underneath sclera; contains blood vessels that nourish retina
i. Forms ciliary body and sensory ligaments
o Ciliary body – under the iris; connected to the suspensory ligaments
o Sensory ligaments – connect to lens
ii. Forms Iris – muscles around pupil; controls the amount of light entering the eye
o Contains two sets of smooth muscle
1. Circular = constrictor
2. Radial = dilator
b. Contains dark pigment (melanin) under retina – absorbs stray photons of light

3.Retina
a. Innermost layer under choroid
b. Consists of:
• Outer pigment cells
• Rods and cones – photoreceptors
• Axons of visual nerve fibres – will exit the eye
• RD

38
Q

Fluid filled cavities

Pupil
Lens

A

Interior – two fluid-filled cavities separated by the lens

a. Posterior cavity – between lens and retina (most of the eye)
- Vitreous humor – gelatinous
b. Anterior cavity – between cornea and lens (very small)
- Aqueous humor – similar to normal extracellular fluid

Pupil – opening through which light enters the eye
- Can constrict and dilate depending on smooth muscles of iris

Lens – can change shape to focus on objects near or distant; focuses light

39
Q

Tapertum Lucidum

A

Tapetum lucidum – reflective layer in many vertebrates; light is reflected back towards retina & photoreceptors; improves sensitivity of vision in low light
o Many vertebrates have less melanin
o May cause blurriness

Humans do not have

40
Q

Dilating and constricting pupil

  • effects of changing the pupil size
  • autonomic ns
A

Effects of changing pupil size
1. Controls the amount of light entering the eye
a. Optimization for light and dark conditions.
• Very bright – pupil constricts; keeps photoreceptors from being saturated
• Dark – dilate to allow more light and activation of photoreceptors
b. Gives the eye a wide “dynamic range” (range of useful light conditions)
2. Controls “depth of field”
a. Size of aperture
i. a small aperture – gives large depth of field; used to view close objects
o pupil is constricted – circular muscle
o items in the background are also in focus, so if object moves, it will remain in focus – we would otherwise be constantly refocusing
ii. a large aperture – reduces depth of field; used to view far away objects
o pupil is dilated – radial muscle
o background is blurry but item is focused; can be sharper focus than smaller aperture – tradeoff
• Smartphone does this digitally with “portrait mode”

Autonomic NS – controls pupil dilation; antagonistic control
1. Parasympathetic stimulation – causes constriction
a. CN III (oculomotor) (Ach) – circular constrictor muscle
• Circular – “circles” around pupil
• Constriction – will make pupil smaller
2. Sympathetic stimulation – causes dilation
a. Superior cervical ganglion (norepinephrine) – radial muscle
• Radial – point radially
• Constriction – “pulls” pupil open

41
Q

Accommodation

  • distance and close up (where does light converge onto)
  • ANS input & speed
A

When light enters eye:
1. From distant source – parallel
a. Will all converge and focus in one specific spot
b. Lens will be flatter and weaker – ciliary muscle not contracted
2. From closer – light rays will be bent differently; light rays are no longer parallel
a. Focal length will become longer – image distance will be behind retina
b. Lens will be rounder/stronger and increase curvature – ciliary muscle is contracted
• shortens focal length to move towards retina

Parasympathetic NS control (acetylcholine/Ach) – no sympathetic; tonic control
a. Very fast – 350ms to change
b. Influences ciliary muscle – circular (contraction will tighten)
- Natural shape of lens is strong and rounded – ciliary muscles pull into flatter, weaker shape
- Lens is attached to ciliary muscle via suspensory ligaments (zonules)
c. Effects
i. Relaxed – ligaments pull on and flatten the lens
• Decreases parasympathetic activity
ii. Contraction – releases tension on the ligaments; becomes rounded
• Increased parasympathetic activity – release of Ach causes contraction

42
Q

Nearsighted vs farsighted

A

Myopia – near sighted

a. Focal point is in front of retina
b. Fixed with concave lens
- Will cause light to diverge/split slightly – focuses on retina

Hyperopia – far slighted

a. Convex lends
- Bends light inward slightly/converges light before it gets to lends

43
Q

Organization of the Retina

A

Direction of light – back to front
o Light travels through cell layers – arrives at photoreceptors
o Photoreceptors propagate forward – through bipolar and ganglion cells

Cell layers
1. Photoreceptors
a. Rods
i. More
ii. Larger – higher sensitivity due to size
o Used in situations of low light – night vision
o Low acuity – more convergence onto ganglion cells
iii. Grayscale vision – not really “black and white” only
iv. Mainly located in peripheral retina
o Most sensitive part of retina – has high concentration of cones
a. Cones
i. Fewer
ii Smaller than rods – lower sensitivity
o Day vision
o Higher acuity – less convergence
iii. Color vision (at least three varieties)
o Differ by pigments
iv. Mainly located in the fovea

  1. Bipolar cells – primary sensory neuron
    a. Bipolar neurons – 2 processes off cell body
    b. Activated via nt released by photoreceptors
    c. Synapse onto ganglion cells
  2. Ganglion cells – secondary sensory neuron
    a. Axons form optic nerve
44
Q

Posterior eye:

Fundus
Macula & fovea
Optic disc
Pigment epithelium

A

Fundus – the back of the eye; where light may strike the retina (back half ish)
o if you looked through someones eye and took a picture, you would be looking at the fundus (fundus scope)

The macula – an area of a high concentration of cones; images focused here to ensure highest resolution (cones have less convergence); light and image will be focussed here
o Generally darker when looking at fundus – due to high concentration of cones

Fovea – spot in macula; light strikes the photoreceptors directly, because overlying neurons are pushed aside
a. Allows light to be focused almost directly onto photoreceptors
b. The very highest density of cones is found at the fovea
• There is very little convergence of sensory neurons at the fovea – single photoreceptors synapse with bipolar neurons that synapse onto single ganglion cells.

Optic disk – below macula
o Where all axons exit the eye – there are no photoreceptors present
o Blood vessels also leave eye here

Pigment epithelium – layer of epithelial cells posterior to photoreceptors; absorb the excess light rays that escape photoreceptors
o Prevent distracting light from reflecting inside eyes and distorting the visual image
o Black colour – comes from granules of melanin pigment

45
Q

Phototransduction

  • epithelial cells
  • photoreceptors - disks & visual pigments
  • function of rhodopsin
A

The conversion of light energy into electrical signals

Epithelial cells – in close contact with rods and cones
o Rods – rod shaped
o Cones – cone shaped

Photoreceptors – convert light energy into electrical signal

a. Most anteriorly – synapse with bipolar
- Have nucleus and cell body in the middle area
b. Disks – within outer segment of photoreceptors (posterior; closest to pigment epithelium)
- Rods – have more disks than cones
c. Visual pigments – bound to disks & convert light energy into a change in membrane potential
- Rods – rhodopsin

Function of rhodopsin – within disks of rods

  1. Rhodopsin molecule – a membrane spanning protein within disks (layers of cell membrane); converts light into other signal
    a. Made of
    i. Opsin protein
    - Modified GPCR – ligand binding
    ii. Retinal – vitamin A derivative
    - Light sensitive molecule – light is activating

In darkness – rhodopsin in inactive
1. Retinal is cis – bent
a. Opsin in inactivated
2. Levels of cGMP are high – intracellular cyclic nucleotide second messenger
a. Binds to cyclic nucleotide gated (CNG) ion channel – opens channels
• Allows movement of Na+ /Ca2+ into the cell – photoreceptors are constantly depolarized in darkness
b. Tonically releases glutamate onto bipolar cells
c. K+ channels are also open -> K+ leaving causes hyperpolarization

In light – light bleaches rhodopsin; actives it
1. changes shape of retinal from cis to trans – small conformational change; activates opsin
a. Cis – bent; in the dark
b. Trans – straight; in the light
o Activated opsin (modified GPCR) -> activates transducin (a G-protein)
2. Transducin moves along membrane -> activates phosphodiesterase (PD)
• Phosphodiesterase – amplifier enzyme; degrades cGMP
3. Decrease in cGMP (the ligand) causes CNG channels to close – hyperpolarizes the cell/photoreceptor
- Due to open K+ channels and no entering Ca2+ and Na+
- Causes less glutamate to be released onto bipolar cells
- Light = LESS nt

46
Q

Information pathway in visual pathway

  • where does depth perception come from
  • where do neurons go from thalamus
A

Photoreceptors – specialized receptors; not neurons

Bipolar cells – primary neurons

Ganglion cells (optic nerve) – secondary neurons 
o	Leave the eye via the optic disc 

Optic chiasm – axons/nerves desiccate
a. Not all of them cross over – about 80% cross over
- Aspects are processed in right and left retina – different properties
- Different visual fields are processed in different areas – spliced back together at visual cortex
b. Right and left visual overlap – allows for binocular vision/depth perception
- Losing eye = loss of depth perception
c. Animals with eyes on both sides of head – difficulty seeing in front
• Allows for larger visual fields for predators

Optic tract – between chasm and thalamus

Lateral geniculate nucleus of thalamus – synapse onto tertiary sensory neurons

a. Some neurons project into midbrain – has neurons that send axons back to the eye
- Controls gaze and pupillary reflex – used to check for damage in midbrain (no pupillary constriction indicates damage)

Optic radiation – tracts to occipital lobe

Occipital lobe

47
Q

Amblyopia

A

“Lazy eye”

Normal development of visual cortex relies on synchronous input from BOTH eyes – Intended to be able to gaze at the same structures

For young children with Amblyopia, proper development of visual cortex will not occur!!!

a. Depth perception doesn’t develop
b. Dependent on synaptic plasticity
- Requires simultaneous input from both eyes

Treatment is often to simply patch the good eye, forcing the brain to use the information from the weaker eye.

a. Narrow window – only works when people are younger
- Brains are more easily manipulated
- Earlier = more effective

Strengthen inputs from the weak eye and proper visual cortex development

48
Q

2 branches of autonomic ns

Features of ANS

  • where is information processed
  • what kind of control

Necessity of innervation on organs

A

2 branches of autonomic NS
o Sympathetic and parasympathetic
o Sensory info from the regulation of smooth muscle, glands, organs – unconscious awareness

Autonomic – “self-governed”; you don’t need to be consciously aware
1. Its actions usually involuntary (without conscious intent or awareness)
a. There are examples of “conscious control”
i. Micturation (to pee or not to pee)
o When bladder is very descended – you will pee
- You need to be a certain age in order to exert conscious control
- Body can override conscious control if bladder is too full
ii. Control of heart rate
o Swimmers, deep divers, athletes, sharp shooters, biathlon

Innervates organs whose functions are not usually under voluntary control

  1. Reflexes – important for autonomic control; you need sensory info in regards to what is occurring within your body in order to make decisions
    a. Sensory info may be processed within hypothalamus, limbic system, or even at the level of spinal cord
    b. Reflex may evoke changes in autonomic output – can change
    i. Usually negative feedback – corrects deviation from setpoint
    ii. Feedforward control – senses will activate fight or flight
    - Anticipates change and works to prevent perturbation too far from set point

Homeostatic control – effectors are often visceral organs and blood vessels

Most visceral effectors do not need the ANS to function – ANS only adjusts their activity to match the body’s needs to maintain homeostasis

a. Heart rate – your heart will beat without influence of autonomic NS
- You can remove all input from symp and para – it will still beat
- ANS allows speeding and slowing of HR – required for life

49
Q

General ANS pathway

A

CNS -> innervated organ

Two-neuron chain
a. Preganglionic fiber – synapses with cell body of second neuron
o Cell body is within CNS – synapses with post
b. Postganglionic fiber – innervates effector organ or tissue
o Cell body is often in autonomic ganglion – axons to effector

Synaptic terminal – differs

a. Axons spread over the effector
b. Varicosities – spread though with chain like connections; release nt onto target

Ganglion – mass or group of neuronal cell bodies; knot like mass of tissue
a. Chain ganglion/sympathetic trunk – parallel to spinal cord

50
Q

Sympathetic NS

  • what part of the spinal cord
  • 2 neuron chain
  • where does it synapse
A

Sympathetic NS preganglionic neurons originate T1-L2 – cell bodies within spinal cord

a. Preganglionic fibers – most are short; synapse on post
- Release Ach – nicotinic
b. Postganglionic fibers – most are long; synapse on effector
- Most release NE – alpha or beta GPCR
- Can be muscarinic Ach – sweat glands

After exiting spinal cord:
1. Make a synapse in a sympathetic chain ganglion
2. Pass thru SCG and synapse in a collateral ganglion
3. Pass thru SCG and synapse in the Adrenal Medulla (within adrenal gland) – modified sympathetic ganglion; no post ganglionic neuron
i. Cells are developmentally neurons (from neural crest) – Ach is released onto modified neurons and causes release of neurohormones
• Releases mainly epinephrine and a little bit of norepinephrine – neurohormones

51
Q

Parasympathetic NS

  • where do neurons originate in spinal cord
  • finding
A

a. Preganglionic neurons originate from cranial and sacral areas of CNS
i. Within brainstem – cranial nerves
ii. Preganglionic fibers – longer
- Release Ach – nicotinic
b. Postganglionic fibers – very short
- Release Ach – often muscarinic; sometimes nicotinic
- Cell bodies are in terminal ganglion

Sometimes they’re difficult to find – ex on the heart (lies on the heart)

52
Q

Convergence and divergence

A

Convergence onto postganglionic neurons – occurs in both SNS and PSNS
a. Each postganglionic neuron receives synapses from many preganglionic

Divergence of preganglionic neurons – more in SNS

a. SNS – each preganglionic neuron branches many times to synapse on many different postganglionic neurons (= divergence)
- Ratio of pre to post neurons is 1:10 -1:30 (many more post than pre)
- Results in mass action – SNS tends to respond as a unit
b. PSNS – each preganglionic neuron branches to synapse on postganglionic neurons (= divergence).
- Ratio of pre to post neurons is 1:4 (lower than SNS)
- You can activate selective branches more easily

53
Q

Cranial nerves within PSNS

  • ex stomach distension
A

Mostly originate in brainstem

Functions
o Can be output axons – control muscle
o Can be sensory – ex. eye or olfactory
o Can be mixed – contain sensory axons and output axons

There are 12 – 4 have PSNS function
1. Oculomotor nerve – control the lens and pupil of the eye.
2. Facial nerve – tear glands, salivary glands, nasal glands
3. Glossopharyngeal nerve – salivary glands
4. Vagus nerve – 70-90% of all parasympathetic fibres (10th cranial nerve)
a. Innervates the viscera – most organs in body
• Many branches – innervates all organs except the adrenal medulla and some parts of the colon
b. Vagus – vagabond (someone who wanders)
c. Is part of a reflex arc – carries info both ways
i. Sensory info from viscera – sent to nucleus of the solitary tract of brain stem (NST/NTS)
ii. The sensory info is processed within the NTS – Integrated with info from other parts of brain
iii. The NTS may also project axons to “higher” parts of the brain – hypothalamus and cortex
iv. Ex. stomach is distended – stretching
- Integrated with hypothalamus
- Activates parts of PSNS
- Stimulates secretion of digestive enzymes
v. Vagus nerve carries efferent (parasympathetic) information to regulate/modulate organ function
- Cell bodies within NTS will send out axons as preganglionic

54
Q

Effects on target organs

  • lasting effects in SNS vs PSNS
  • Nt in SNS ve PSNS
  • receptors on target organs for PSNS and SNS
A

The SNS tends to have a longer lasting effect than PNS
1. Ach is quickly broken down by acetylcholinesterase
a. AChE – very efficient; Ach doesn’t last long
2. NE more persistent than Ach – 3 mechanisms; slower for NE than for Ach
a. NE transported back into the neuron
• Occurs very easily – can be reused and recycled
b. NE degrative enzymes – not as efficient as AchE
• catechol-O-methyl transferase (COMT)
• Monoamine oxidase (MAO)
c. NE picked up by blood – no degrative enzymes; will hang around much longer
• Can move around the body and bind to other cells with alpha and beta receptors

Receptors on target organs
1. SNS – NE are all GPCR; different pathways are linked with each receptor
a. 5 main types of GPCR – linked to second messenger pathways (P DIBI)
• α1 – phospholipase c
• α2 – decrease cAMP; activates phosphodiesterase
• β1 – increase cAMP
• β2 – both increase and decrease cAMP*
• β3 – increase cAMP
b. SNS activates adrenal medulla – releases large amount of epinephrine and some NE
• Both activate all receptors
c. 2nd messenger signaling often affects ion channels
2. PSNS – Ach
a. Nicotinic AChR – ligand gated ion channels
b. Muscarinic AChR – GPCR
• M1 – phospholipase c
• M2 – decrease cAMP
• M3 – phospholipase c

55
Q

ANS maintaining homeostasis

  • dual innervation
  • complimentary
  • antagonistic
  • mono
A

Can act antagonistically or cooperatively
- Usually both active to a degree – not often one is completely active and other is completely dormant

Dual innervation – input from both SNS and PSNS; not always balanced (ex. digestive has more PSNS than SNS)
1. Antagonistic
a. The heart is innervated by both
• SNS increases heart rate and force of contraction – increased circulation
• PNS decreases heart rate and force of contraction
b. The iris innervated by both
• SNS – pupillary dilator
• PNS – pupillary constrictor
c. Pancreatic juices
• SNS – inhibits secretion
• PSNS – increases production of enzymes (trypsin, pancreatic lipase, pancreatic amylase)

  1. Complimentary – activation of SNS and PNS can produce similar results
    a. Salivary glands – innervated by both SNS and PNS; both increase saliva production, but different kinds of saliva
    • SNS – mucus production; thicky sticky
    • PNS – watery, enzyme rich saliva; large volumes
    b. Male sexual response
    • Parasympathetic – erection; “point”
    • Sympathetic – ejaculation; “shoot”

Can lack dual innervation
o Only SNS – adrenal medulla, smooth muscle of most blood vessels, sweat glands

56
Q

CNS centers that contribute to ANS regulation

A

The Limbic system – integration of sensory and emotional responses with autonomic output

Hypothalamus – major control center for autonomic output
o Hunger, thirst, thermoregulation, emotions, and sexuality

Brain stem – gives rise to nuclei of cranial nerves that mediate several autonomic responses
o Limbic system and hypothalamus communicate with brainstem

Spinal cord – autonomic responses (ex. defecation and micturition reflexes) are integrated in the spinal cord