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