Exam II Neuroscience
Glycine- inhibitory Neurotransmitter
more localized than GABA
about 50% of inhibitory snapses ise glycine
Synthesis
From serine (Enzyme: serine hydroxymeythyltransferase)
Inactivation
reuptake into presynaptic membrane by glycine transporters
Receptors
ligand gated Cl- channels
Biogenic Amines - regulate brain functions and are active in PNS
Catecholamine synthesis
All derives from tyrosine
tyrosine turns into DOPA by adding hydroxyl group ( tyrosine hydroxylase)
DOPA dearboxylase removes CO2 creating DOPAMINE
dopamine hydroxylase adds OH creating NOREPINEPHRINE
Phenylethanolamine N-methyltransferase (CH3) creating EPINEPHRINE
Dopamine(DA)
coordination of movement
motivation/ reward pathways
motor control
cognition
impulse control
risk of addicton ( loss of D2 receptors)
Inactivation
uptake into glial cells or Presynaptic neuron by sopamine transporter (DAT)
enzymatic degradation (MAO) (COMT)
DA participates in almost all centrally controlled movement
Dopamine receptor action
metabotropic receptors ONLY
location and subtype determine action
ALL work through G- proteins to stimulate/ inhibit adenylyl cyclase
Adenylyl Cyclase changes ATP→ cAMP
Norepinnephrine (noradrenaline)
brainstem projections to forebrain structures
made in Locus Coeruleus
responsible for attention, wakefulness, feeding behavior
uses sympathetic ganglion as a peripheral transmitter
inactivation
reuptake by norepinephrine transporter (NET)
Enzymatic degradation ( MAO) (COMT)
Act at metatropic receptors
alpha and beta adrenergic receptors
Alpha1 recep. slows depolarization due to inhibiton of K+ channels
Alpa2 recep. slows hyperpolarization to due activation of K+ channels
3 subtypes of beta receptors ( 2 found in neurons)
Epinephrine (adrenaline)
found in brain at lower levels than other catecholamines
metabolism similar to norepinephrine
bind to alpha and beta adrenergic receptors
made in axon terminal
inactivation
uses NET for reuptake
enzymatic degradation (MAO & COMT)
Histamine
found in hypothalamus neurons that project to brain and spinal cord
wake- promoting and attention
controls reactivity of vestibular ( balance) system
act through metabotropic receptor
Synthesis
Histidine → Histidine decarboxylase (CO2) → Histamine
Inactivation
MAO and histamine methyltransferase
Serotonin
AKA 5- hydroxytryptamine ( 5-HT)
derived from tryptophan
found in the pons and upper brainstem region
regulates sleep and wakefulness
most receptors are metabotropic
ONE ionotropic (5-HT3)
Inactivation
reuptake by serotonin transporter (SERT)
MAO degradation
ATP and other purines
ATP is an excitatory NT
Motor neurons of spinal cord
action in CNS
metabolized to adenosine (NOt a NT)
3 classes of receptors
P2x ionotropic receptors (faster)
allowing exit/ entrance of non-selectove cations
Two classes of purigenic metabotropic receptors
Peptide neurotransmitters
synthesis is similar to protein production on non-neuronal cells
generally bind to Metatrobic receptors
ex: Substance P, endorphins, enkephalins, etc)
five categories based on amina acid sequence
Brain- gut peptides (CCK, substance P, )
opioid peptides ( enkephalins, endorphins)
pituitary peptides (ADH, TSH)
hypothalamic- releasing peptides (CRH, GHRH)
miscellaneous peptides
Pre-propeptides: inactive form of final NT
synthesized in ER
signal sequence to let cell know it will be secretes
pro-peptide: polypeptide after signal sequence is removed
protein can be modified and cleaved multiple times before reaching final NT form to make different products
pro-peptide makes multiple active peptides
inactivation
degradaded by peptidases
Somatic sensory system
afferent fibers reside in ganglia alongsidete spinal cord and brainstem
afferent= PNS→ CNS (travels TO CNS)
efferent = signals leaving CNS
dorsal root ganglia (body info)
cranial nerve ganglia ( head info)
supplys sensory information from periphery→ CNS
Trigeminal ganglia- sensory ganglia for facial sensation (HSV hides here)
sensory afferent neurons are pseudounipolar
Have cell body, one projection that splits
pseudounipolar: continuous fiber that has a single attachment to the cell body
Action potentials are generated by changes in the skin or muscle
goes to synaptic terminal to communicate with CNS
Sensory transduction: converting exernal stimuli into electrical signals that the nervous system can use ( touch, feel,hear)
similar in all somatic afferents
generates a depolarization recepor potential
Sensory receptors
mechanoreceptors (touch, pressure)
Merkel cells- found in tips of epidermal ridges
slow adapting
highest spatial resolution
fine touch and pressure
meissner’s corpuscle- dermal papillae
rapidly adapting
detect low frequency vibration while object in motion
important for grip control
pancinian corpuscle
rapidly adapting
deep in dermis and subcut- layer
detect high vibration of objects that we are gripping ( writing )
Ruffini afferent
slow adapting
located in ligaments and tendons ; parallel to skin
detect how the skin stretches
specialized receptor tht encapsulates afferent fibers
lower threshold than unencapsulated afferents
Free nerve endings
afferent fibers that lack specialized receptor cells ( merkel, pacinian, etc.)
important in pain sensation
unencapsulated
How to tell them apart:
axon diameter: determine action potential speed
Larger=faster conduction
receptive field size : area of skin surface that results in a lot of action potentials
more branching = larger field
temporal dynamics ( response timing)
Rapidly adapting afferents: rapid fire when stimulated but become muted over time ( dynamic properties)
Slowly adapting afferents: continue to fire with long term stimulation ( static properties)
ability to adapt quickly or slowly
Group 1a- supply sensory receptors in muscle
Receptor type- muscle spindle
largest and send fastest signal
instructs body how to respond
AB afferents - touch
AD and C afferents- pain and temperature
Golgi tendon organ- specialized for proprioception
force of muscle conraction acts on tendon
increases tension on collagen
compress intertwined sensory receptor ( activates Action potential)
Afferent 1b axons → local circut neurons → alpha motor neurons
acts as feedback to regulate tension ( so muscles dont fall off of bone)
More 1b =less alpha neurons
Sensory Pathways
afferent mechanoreceptor info is transmitted through connective neurons
1st order neurons: located in dorsal root ganglia and cranial nerve ganglia
afferent MCR that go from source → brainstem
cutaneous mechanoreceptora end info via neurons in trigeminal ganglion
central process from sensory roots to trigeminal BS
terminate in neurons on trigeminal brainstem
Trigmenial complex includes: Principal nucleus and spinal nucleus
Principal nucleus- info from low threshols tactile senses
spinal nucleus- Pain, Temperature, Coarse touch
2nd order neurons- located in brainstem nuclei ( Brainstem → Thalamus)
trigeminal BS axons cross midline
ascend to VPM via Trigeminal leminiscal tract
3rd order neurons: project from thalamus → cerebal cortex
VPM of thalamus projects to SI in cerebral cortex
Dorsal column-medial leminiscal system: conveys tactile info from body
Trigeminothalamic system- tactile info from face
Proprioception- mechanoreceptors tht provide information about mechanical forces withing the body
ex: muscle spindle, golgi tendon organ, joint receptor
types of lower motor neurons- any neuron that will innerviate muscle
Gamma (y) motor neurons-efferent
innerviate muscle spindle
sense stretch of muscle
Alpha (a) motor neurons- efferent
innerviate extrafusal muscle fibers
contraction of skeletal muscles
Muscle stretch reflex- stretch on muscle stimulate affterent neurons
signals are transmitted to alpha motor neuron
efferent signals travel back to muscle ( no cerebral cortex)
reflex circuit is responsible for steady level of muscle tension ( muscle tone)
spindle stimulation→ activation of sensory neuron → processing at motor neuron→activation of motor neuron → contraction of the muscle
Muscle spindles
sensory receptors ebedded in muscle
detects stretch fo muscle
not involved in muscle force
made of 4-8 intrafusal fibers
run parallel to extrafusal fibers
types of intrafusal fibers:
nuclear bag fibers
detect velocity of stretch ( dynamic) and sustained fiber stretch (static)
nuclear chain fibers
detect static length of muscle
typicle spindle is 1 static and 4-6 chain fibers
Sensory afferent neurons on muscle spindle:
Group 1a(primary)
coil around all 3 intrafusal fibers ( bags and chains)
send info to CNS about length and velocity of stretch
Group II (secondary)
innverviate nuclear chain and static nuclear bag fiber
send info about length only
fire tonically (steadily) proportional to stretch
these neurons form a monosynaptic excitatiry connection with alpha motor neurons that innerviate the same muscle (homonymous)
interneurons inhibitory connections with alpha motor neurons that innerviate the antagonsit muscle ( heteronymous)
Reciprocal innervation- rapid contaction of stretched muscle and simultaneous relaxation of antagonist muscle
gamma (y) motor neurons contol intrafusal fibers
keep intrafusal fibers taut and sensitive to stretch
contraction of intrafusal muscle must math the extrafusal muscle
stretch in parallel
during contraction pull on fibers is removed and spindle goes slack
no more firing of afferent neurons
y motor neurons cause spindle fiber to contract preventing insensitivity to stretch
co- activation of y and aplha motor neurons