BioElectricity Local Currents (graded Potential) Action Potentials Flashcards

1
Q

Electricity and Bioelectricity

Electricity and Bioelectricity

A

Electricity - Flow of electrons
* Force is an electrical gradient

Bioelectricity - Flow of ions
* Force is a chemical gradient and eletrical gradient combined

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2
Q

Transmembrane Potential

Transmembrane Potential

A
  • Driving force for ion flow across the cell membrane
  • Extracellular fluid - higher concetration of NA ions and CL ions and Ca2+ ions
  • Intracellular Fluid - higher concentration of K ions and Proteins (A-)
  • Concentration gradient maintained by active transport of sodium ions out of cell and postassium ions into cell
  • NA/K ATPase exchange pump
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3
Q

Gated Ion Chanels

Gated Ion Chanels
(on/off switched for bioelectricity)

A

Pathway for ion flow across the cell membrane
* Chemically gated (Neurotransmitters and Hormones)
* Voltage gated
* Mechanically Gates ( presure on cell membrane)

Gated chanels open in response to various signals (stimuli)
* Ions flow across membrane by difsuiion down their concentration gradient
* Typically stay open only Briefly

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4
Q

Bioelectricity

Bioelectricity

A

Ion Flow across a membrane requires:
* Chemical and or electrical concentration gradient (driving force)
* Transmembrane poteantial
* Pathway
* Ion chanel through the membrane

Ion flow through the cytoplasm or interstitial fluid (local current) requires:
* Chemical and or electrical concentration gradient (driving force)

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5
Q

Local Current - Graded Potential

Local Current - Graded Potential

A

Driving force is concentration gradient created by ions coming across membran through open chanels
* ions travel a short distance through cytoplasm or or interstitial fluid
* Cytoplasm and interstitial fluid have high resistance to ion flow
* Depolarization or hyperpolarization effect decreases with distance from open chanel

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6
Q

Bioelectricity and conduction of electrical signals in nervoussystem

Bioelectricity and conduction of electrical signals in nervoussystem

A

local currents (graded potentials) transmit bioelectric signals over short distances
* Typical of dendrites and cell bodies in NS

Action Potentials need to transmit bioelectric signals over long distances
* Typical of Axons
* Typical of long dendrites of unipolar and Bipolar sensory neurons
* Unique to excitible cells
* An unstoppable chain reaction of small local currents

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7
Q

Action Potential of Voltage Gated Chanels

Action Potential of Voltage Gated Chanels

A

Sodium ion Channel
* Open rapidly in response to depolarization (-60mV threshold)
* Inactivate or close rapidly after opening and can not reopen until return to resting rate
* Absolute refractory period - can not reopen

Potassium Ion Channel
* Open slowley in response to depolirization (at +30mV)
* Close slowley after repolarization

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8
Q

Action Potentials

Action Potentials

A

Steps involved:
* Membrane depolarization stimulus occurs
* Sodium Channel activates - NA ions flow into cell, duter depolarizing
* Sodium chanel innactivation - NA ions stop flowing
* Potasium channel activates - K+ ions flow out of the cell, repolarizing and then hyperpolarizing the membrane
* Return to normal permeability - Both channels are inactivated

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9
Q

Action Potentials

Action Potentials

A

Ion Restoration
* Only a small amount of sodium ions and potassium ions cross the membrane
* Transmembrane potential (like a battery) can power many action potentials before becoming depleated
* Sodium-Potassium ATPase exchange pump maintains transmembrane potential over time but is not needed each action potential

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10
Q

Action Potentials

Action Potentials

A

Generation of action potential follows all or none principle
* Requires threshold depolarization to initiate an action potential
* Threshold depolarization - amount of depoloarization needed to open voltage gted sodium chanels
* Threshold depolarization comes from local current spreading throughout the cytoplasm

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11
Q

Action Potentials

Action Potentials

A

Continuous Propagation
* Unmylenated axons
* Propagation of action potential along entire membrane in series of small steps

Saltatory Propegation
* Myelinated axons
* Porpagation of action potential from node to node, skipping internodal membrane

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12
Q

Continuous Propagation of an AP

Continuous Propagation of an AP

A
  1. Threshold level of local current spreads to AP initation site
  2. AP is initiated in small segement of axon
    * Voltage gated NA+ ion chanels open, and NA+ ions flow in, Channels inactivate
    * Voltage Gated K+ ion channels ope, K+ flows out of the cell casuing repolarization which closes the potasium channel
  3. High Concentration of NA+ ions produce local current that spread down cytoplasm, bringig adjacent segemnt of axon to threshold
  4. AP is initiated in the adjacent small segement of axon
  5. Propagation
    * Cycle is repeated - local current spreading from each action potential creates an AP in the next adjcent segment
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13
Q

Saltatory Propagation of an AP

Saltatory Propagation of an AP

A
  1. Threshold level of local current spreads to AP initation site
  2. AP is initiated in small segment of axon
  3. High concentration of NA+ ions produces local current that spread relativley down cytoplasm, bringing adjacent noed of axon to threshold
  4. AP is initiated in these adjacent nodes
  5. Porpagation
    * Cycle is repeated, local current spreading from each action potential creates an AP in the next adjacent nodes
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14
Q

Clasification of Nerve Fibers

Clasification of Nerve Fibers

A

Large Fibers
* Type A Fibers: Largest Diamater, mylinated, fastest (140m/s)
* Motor Neurons to skeletal muscles
* Fastest Sensory informartion

Slower, small fibers
* Type B Fibers: Small diamater, myleinated, moderate speed (18m/s)
* Type C Fibers: Small diamater, unmylenated slowest (1m/s)
* Efferent neurons sending action potentials to smooth, caridac muscle, and gland cells
* Slow sensory information

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15
Q

Synapse

Synapse

A

Synapse - cell to cell
* Presynaptic cell
* Postsynaptic cell
* Neuron, muscle, or gland (fat cells)

Eletrical synapses or Chemical synpses

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16
Q

General Properties of Synapses

General Properties of Synapses

A

Eletrical synapses
* Rare in nervous system
* Pre- and postsynaptic cells are bound by interlocking membrqane proteins (gap junctions)
* Ion current flows directly from presynaptic cell to postsysnaptic cell

17
Q

General Properties of Synapses

General Properties of Synapses

A

Chemical Synapses
* Neurotransmitter released from axon terminal to postsymanptic neuron
* Neurotransmitter difueses across synptic cleft (synaptic gap)
* Neurotransmitter binds to receptors of chemically gated ion channel
* Neurotransmitter is removed from celft by diffusion, reuptake, and or degredation (enzyme ex: AchE)

18
Q

Mechansims of chemically gated ion channels

Mechansims of chemically gated ion channels

A

Direct acting - fast
* Neurotransmitter binds to receptor site that is part of the gated channel

Indirect Acting - Slow
* Neurotransmitter bindws to receptor that cpntrolls gated channel via intracellular secondary messenger
* G-Protein Coupled Receptor
* Primary Messenger - neurotransmitter
* Secondary Messenger - Intracellular Molecule, often Cyclic AMP or Cyclic GMP

19
Q

Effect on Postsynaptic cell

Effect on Postsynaptic cell

A

Excitatory Post-synaptic Potential (EPSP)
* Gated channel opens for NA+ ion
* Depolarining synaptic potential
* Bringing axon hillock closer to threshold
* Promotes action potential initiation

Inhibitory Post-synaptic Potential (IPSP)
* Gated Chaneel opens for potassium or chloride ion channels
* Hyperpolarizing synaptic potential
* Supress action potential initiation

20
Q

Information Processing

Information Processing

A

Simplest level of information processing occurs at the cellular level
* Excitatory and Inhibitory potentials are integrated and determine weither or not an action potential in intitated

EPSP and IPSP local ion currents combine through summation
* Temporal Summation (time)
* Spatial Summation (Space)

21
Q

Neurotransmitters

Neurotransmitters

A

PNS Neurotransmitters
* Acetylcholine (ACh) - Cholinergic synapses
* Norepinephrine (NE) - Adrenergic Synapses

22
Q

Cholinergic Synapses

Cholinergic Synapses

A
  • Presynaptic cell contains vesicles of acetylcholine (ACh)
  • Postsynaptic cell has chemically gated ion channels and receptors for ACH
  • Synaptic cleft has AChE enzyme that breaks down ACH
23
Q

Function of Cholinergic Synapse

Function of Cholinergic Synapse

A
  • Action potential reaches axon terminal
  • Depolirization by AP opens calcium ion channels in axon terminal, allowing CA to flow in
  • Calcium Ions cause vesicles to undergo exocytosis, releasing acetylcholine into synaptic celft
  • ACh drifts across synaptic celft, binds to receptors, causing ion channels to opne
24
Q

Function of Cholinergic Synapse

Function of Cholinergic Synapse

A
  • Synaptic delay - time required for calcium influx, neurotransmitter release and difussion, and gated ion channel opening (few miliseconds)
  • ACh is broken down by AChE - Choline reabsorbed by presynaptic neurons and recycled
  • Synaptic fatigue occurs when stores of ACh are exhausted
25
# **Neurotransmitters** **Neurotransmitters**
* **ACh - Primarley Direct** * **Serotonin - Primarley Direct** * **Aspartate - Direct or Indirect** * **Gamma-Aminobutyric Acid (GABA) - Direct or indirect** * **Glycine - Direct**
26
# **Neurotransmitters** **Neurotransmitters**
* **Norepinephrine - Indirect** * **Epinephrine - indirect** * **Dopamine - Indirect** * **Histamine - Indirect** * **Glutamine - Indirect** * All pepties listed - indirect * **Adenosine - indirect**
27
# **CNS Neurotransmitters** **CNS Neurotransmitters**
* **Acetylcholine** * **Monoamines (biogenic Amines):** * Norepinephrine, Epinephrine, Dopamine, Serotonin * **Amino Acids:** * Glutamate, Glycine, Gamma Aminobutyric Acid (GABA) * **Neuropeptides:** * Substance P, Endorphins, Enkephalins * **Purines** * ATP/GTP * **Gasses and Lipids**
28
# **Neurotransmitters and postynaptic effect** **Neurotransmitters and postynaptic effect**
* **Postsynapptic receptor properties determine effect of neurotransmitter on postsynaptic cell** * ACh produces EPSPs at some synapses and IPSPs at other synapses due to different types of postynaptic receptors **Ammount of neurotransmitter released into synaptic cleft and how long it remains determines amount of IPSPs and EPSPs current in postsynaptic cell**
29
# **Understanding effects of drugs on synaptic function** **Understanding effects of drugs on synaptic function**
**Drugs that bind to the postsynaptic receptor:** * Agonists (mimetics) - mimic effect of neurotransmitter-receptor * Antagonists (blocking agents) - block effect of neurotransmitter * Many neurotransmitters have more than one type of postsynaptic receptor **Affect removal of NT from synaptic cleft**
30
# **Cholinergic Synapses Postsynaptic Receptors** **Cholinergic Synapses Postsynaptic Receptors**
**Nicotinic Cholinergic receptors (direct Acting)** * Skeletal Muscles, Autonomic Ganglia * Excitatory * Agonist = **Nicotine** * Antagonist = **Curare** **Muscarinic Cholinergic Receptors (indirect: G-Protein coupled Receptors)** * Excitatory or Inhibitory * Visceral Muscles, Cardiac Muscles, CNS * Agonist = **Muscarine** * Antagonist = **Atropine**
31
# **Adrenergic Synapses Postsynaptic Receptors** **Adrenergic Synapses Postsynaptic Receptors**
**Alpha Adrenergic receptors** * **Alpha 1 - Excitatory effect:** on smooth muscles of blood vesels of skin and viscera, cause constriction * **Alpha 1 Blockers - reduce hypertension** **Beta Adrenergic Receptors** * **Beta 1 - excitatory on cardiac muscle** * Beta 1 blockers reduce heart rate * **Beta 2 - Inhibitory on smooth musles or respitory tract, cause relaxation** * beta 2 blockers cause respitory constriction (**Agonists)**
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# **Removal of Neurotransmitter from the Synaptic Cleft** **Removal of Neurotransmitter from the Synaptic Cleft**
1. Diffusion, Degredation, reuptake (transport proteins bring NT into pre-synaptic cell of glial cell) * **Cholingeric Synapses** * Acetylchonline Esterase degrades ACh * **Monoamine synapses (norepinephrine, Epinerphrine, dopamine, seratonin)** * Monoamine oxidase degredation * Slective reuptake into presynaptic terminal