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PSA523 Nervous System Mechanics PDF

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Document Details

FragrantMossAgate

Uploaded by FragrantMossAgate

Loughborough University

2023

Loughborough University

Dr Clare Holley

Tags

nervous system physiology neuroscience biology

Summary

This document is a handout from a lecture on the mechanics of the nervous system given on February 15, 2023, at Loughborough University. It covers the structure of the nervous system, resting neurons, action potentials, and different components of the nervous system.

Full Transcript

15/02/2023 PSA523 2: Mechanics of the nervous system Dr Clare Holley [email protected] 1 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron Action potential Reading 2 Last week 1: The brain through the ages What can you remember? 3 1...

15/02/2023 PSA523 2: Mechanics of the nervous system Dr Clare Holley [email protected] 1 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron Action potential Reading 2 Last week 1: The brain through the ages What can you remember? 3 1 15/02/2023 Lecture objectives  Describe the structure of the nervous system  Understand why ions are important and recognise their distribution inside and outside of the neuron  Identify the characteristics of an action potential  Explain how action potential signal moves along an axon 4 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron Action potential Reading 5 The nervous system (NS) Network of neurons in the brain, spinal cord and periphery  Central Nervous System (CNS) • Brain and Spinal Cord  Peripheral Nervous System (PNS) • Nerves (Cranial and Spinal) • Ganglia (a mass of nerve cell bodies) 6 2 15/02/2023 CNS: Brain 7 CNS: Cerebrum 8 CNS: Spinal cord  Continuous with brain stem  Long conical structure  Thickness of adult’s little finger  Mediates information transmission between brain & body below the neck 3 major functions:  Coordinating certain reflexes  Conduit for sensory and motor information 9 3 15/02/2023 CNS: Spinal cord  Protected by vertebrae (24 vertebra)  Core of grey matter surrounded by white matter Dorsal Ventral 10 CNS: Spinal cord  Spinal nerves split into dorsal & ventral roots before entering spinal cord  Afferent neuron axons enter cord in dorsal root & terminate in dorsal horn  Efferent neurons have a cell body in ventral horn & axons leave cord in ventral root Reproduced with permission from Pearson Education From Physiology & Behavior (9th Ed.) by N Carlson 11 PNS: Function Afferent neurons Receptors Efferent neurons CNS Effectors  Connects CNS to limbs & organs via cranial and spinal nerves  Conveys info from environment to CNS (afferent neurons)  Conveys messages from CNS to muscles and glands (efferent neurons) 12 4 15/02/2023 PNS: Nerves  Neuron axons grouped into bundles  Only present in the PNS  43 pairs • 12 cranial nerve pairs • 31 spinal nerve pairs 13 PNS: Cranial nerves  12 pairs • 10 → brainstem • I & II → forebrain  Information between the brain and body above the neck • Exception: Vagus nerve 14 PNS: Spinal nerves  31 pairs  Each pair is associated with a particular segment of spinal cord  Named dependent on vertebral level they attach  Spinal nerves can contain sensory & motor fibres Reproduced with permission from Pearson Education From Physiology & Behavior (9th Ed.) by N Carlson 15 5 15/02/2023 Divisions of the PNS Peripheral Nervous System Somatic Nervous System Sympathetic Nervous System Autonomic Nervous System Parasympathetic Nervous System Enteric Nervous System 16 Somatic NS  Voluntary control of body movement  Receives sensory information and controls spinal nerves that innervate skin, joints & muscles • Afferent neurons carry sensory info from skin (sensory neuron) • Efferent neurons control skeletal muscles via (motor neuron)  Neurons are excitatory 17 Autonomic NS  Controls involuntary functions and internal environment  Afferent neurons carry sensory info from internal organs to CNS  Efferent neurons control smooth muscle, cardiac muscle & glands  Neurons are excitatory or inhibitory  Has three further sub-divisions: 1. Sympathetic Nervous System, 2. Parasympathetic Nervous System and 3. Enteric Nervous System 18 6 15/02/2023 ANS: Sympathetic NS (SNS)  Any responses for activities which expend energy  Coordinates Fight or Flight response 19 ANS: Parasympathetic NS (PSNS)  Activities involved with increase in the body’s supply of stored energy  Coordinates Rest and Relax response 20 ANS: Enteric NS (ENS)  The “second brain”  Lines your gastrointestinal tract from oesophagus to rectum  Main role is controlling digestion • swallowing • release of enzymes • control of blood to facilitate nutrient absorption 21 7 15/02/2023 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron • Structure and general function • Movement of ions • Resting potential Action potential Reading 22 Neurons  Transmit information to other neurons, muscle of gland cells  80% of neurons are in the brain 23 Neuron structure Dendrites Axon Terminal/ Terminal Boutons Axon Cell body/soma Structure and general function • Recommended reading pp. 31-34 24 8 15/02/2023 1: Sensory neurons  Part of PNS  Contain sensory receptors for detecting sensory changes  Sends information about these changes to CNS  Cell body in PNS, axon enters CNS (axon terminals located in CNS) 25 2: Motor neurons  Part of PNS  Synapses to skeletal muscle to command movement or onto glands to release hormones  Relays signal from CNS to PNS  Dendrites & cell body in CNS, axon enters PNS 26 3: Interneurons  In CNS  Receives info from sensory neurons  Sends info to motor neurons  Integrate / change signal • Integrate: inputs from multiple afferent neurons – average signal • Change: Interneurons can provide excitatory or inhibitory signals 27 9 15/02/2023 Neuronal membrane  Made of two layers of lipid molecules  Lipid molecules • Hydrophilic (water loving) heads • Hydrophobic (water hating) tails  Barrier: water soluble molecules cannot pass through  Particularly impermeable to ions hydrophilic "head" region hydrophobic "tail" regions hydrophilic "head" region Author Jerome Walker 28 Fluid environment  Fluid environment containing ions • Intracellular fluid • Extracellular fluid Cations (+ve) Anions (-ve) Sodium (Na+) Organic ions (A-) Predominantly extracellular Only intracellular Potassium (K+) Chloride (Cl-) Predominantly intracellular Predominantly extracellular 29 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron • Structure and general function • Movement of ions • Resting potential Action potential Reading 30 10 15/02/2023 Movement of ions  Ions move because of: Concentration gradients (via diffusion) Electrical force (via electrostatic pressure) 31 Electrical polarity of neurons Neuron is polarised  At rest, neurons are -ve charged compared to extracellular fluid  -ve charge occurs if there are less +ve ions and/or more –ve ions inside cell  Whilst there is a difference in charge, an electrical force tends to move ions across the membrane Extracellular Neuron –70 mV 0 mV 32 Border guards Ion channels (leak channels): • Passive ion specific conduits • Selected ions rush down gradients of concentration & electric potential • Controlled by a gate Ion pumps: • Energy consuming • Active transport – against gradient • Maintains and builds gradients • Slower 33 11 15/02/2023 Net force Extracellular Fluid K+ Neuron -ve Na+ +ve → concentration gradient → electrostatic gradient 34 Potassium ions (K+) Diffusion  K+ highly concentrated in cell • K+ wants to move out of cell down concentration gradient  At rest, K+ leak channels allows K+ to leave neuron down concentration gradient  Inside cell becomes more –ve Electrostatic pressure • Not a lot of K+ moves out Ions will stop moving when opposing forces are equal (at equilibrium)  NB: this happens in a resting cell 35 Chloride ions (Cl-) Diffusion  Cl- highly concentrated outside cell  Cl- wants to move into cell down concentration gradient Electrostatic pressure  Inside of cell is -ve charged  Cl- also wants to move out of cell due to repel of electric charge Net force for Cl - = stay where it is 36 12 15/02/2023 Sodium ions (Na+) Diffusion  Na+ is highly concentrated outside cell  Na+ wants to move into cell down concentration gradient Electrostatic pressure  Inside of cell is -ve charged  Na+ also wants to move into cell due to electric charge attraction Net force for Na+ = move into cell Note: There are few sodium channels so ion movement is slight 37 Sodium/Potassium Pump How does extracellular Na+ remain greatest? 38 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron • Structure and general function • Movement of ions • Resting potential Action potential Reading 39 13 15/02/2023 Resting membrane potential  Two forces act on ions  Membrane is a barrier to ion movement  At rest membrane is permeable to K + so mainly K + ions move  K + ion movement stops once opposing forces reach equilibrium  Result: unequal distribution of positive & negative ions on the inside & outside of membrane Resting membrane potential  Difference in charge across membrane at rest = −70 mV 40 Summary of ion movement http://faculty.washington.edu/chudler/ap.html Author Looie496 41 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron Action potential • Characteristics • Triggering • Movement along a neuron Reading 42 14 15/02/2023 Phases of an action potential 1. Depolarisation: inside becomes more +ve 2. Repolarisation: inside becomes more –ve 3. Hyperpolarisation: more –ve than at rest Depolarisation +ve in cell Repolarisation +ve out cell Threshold Rest Rest Hyperpolarisation +ve still moving out 43 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron Action potential • Characteristics • Triggering • Movement along a neuron Reading 44 Neuron excitability  A stimulus causes small depolarisation (moves membrane potential towards 0 from -70 mV)  Size of this depolarisation is proportional to size of stimulus  If depolarisation reaches threshold (~ -55 mV) an AP occurs automatically 45 15 15/02/2023 Features of an AP  ‘all-or-nothing’ phenomena – AP only occurs if threshold is reached (at ~ -55 mV)  Large change in membrane potential (-70 to +30 mV)  Standard size & shape  Very rapid (1-4 ms)  Frequent (100’s per s) – depending on stimulus intensity 46 What regulates strength of a response?  APs are subject to an ‘all-or-nothing’ law  Strength of a response is not dictated by size of a single AP  Strength is a function of the ‘rate’ law  Rate of neural firing 47 Depolarisation  Stimulus causes a small amount of Na + to move into the cell  Na + is +ve charged → neuron becomes less –ve (slightly depolarised)  If depolarisation changes charge by +15 mV it activates voltage-gated channels in membrane 48 16 15/02/2023 Voltage-gated channels  Activated by changes in charge of membrane  Two types important for the AP: • Voltage-gated Na+ channels • Voltage-gated K+ channels Channels open Na+ & K+ rush over membrane Rapid changes in membrane potential 49 Voltage-gated action potential 1. Voltage-gated Na + channels open. Na + influx → more +ve 2. Na + channels become refractory at peak 3. Voltage-gated K + channels open. K + efflux → less +ve 4. Open K + channels allow outflow 5. Overshoot caused by slow closing K + channels 50 Resetting  The Na+/ K+ ATPase Pump moves 3 Na+ OUT & 2 K+ IN  The pump keeps Na+ conc. low in neuron  K+ also diffuse back in to neuron  This re-establishes resting membrane potential 51 17 15/02/2023 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron Action potential • Characteristics • Triggering • Movement along a neuron Reading 52 Movement along the neuron  Signal travels away from cell body towards axon terminals  No decay  Termed AP propagation 53 AP propagation  Na+ ions spread away from site of AP, change charge in nearby area of cell to be more +ve (depolarised)  Triggers another AP in this nearby area  Next AP occurs as previous AP starts to die out  APs are triggered one after another all the way to axon terminals  If axon branches, each branch continues the AP  AP stays the same size 54 18 15/02/2023 Refractory period Why is the refractory period important?  Prevents AP travelling backwards  Determines upper limit on AP frequency 55 Lecture outline Recap of last week Objectives Structure of the nervous system The resting neuron Action potential Reading 56 Coming up Workshop  When electrical transmission goes wrong Next week’s lecture  Dr Isobelle Kennedy  Supporting the brain (structures and cells)  Reading in preparation • Chapter 5, pp. 55-61 57 19

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