Skeletal Muscle Physiology

Skeletal Muscle Physiology

Physiology Unit 2 Muscle Physiology In Physiology Today Skeletal Muscle • Characteristics – Striated – Multinucleated – Voluntary • Organization – Myofiber • Myofibril –Myofilament Sarcomere • Functional unit of skeletal muscle • Composed of 3 filaments – Thick filament • Myosin – Thin filament • Actin • Troponin • Tropomyosin – Elastic filament • Titin Thick and Thin Filaments Sliding Filament Theory of Contraction • Cross bridges form between the thick and thin filaments • Thin filaments slide across the thick filaments – Thin filaments will move closer together – Distance between Z lines decreases – I band and H bands shorten during contraction – A band stays the same Muscle Physiology • 2 distinct events happen which lead to muscle contraction 1.Electrical events – Action Potential – Receptor activation – EPP – AP – Electrical events trigger the mechanical events 2.Mechanical events – Developing tension in the muscle – Increase Ca2+ levels – contractile proteins moving – muscle fiber shortens Stimulus to Contraction • Stimulus – Receptor activation – Skeletal muscle: ACh binding to N-Achr – Results in an EPP • Latent period – Excitation-Contraction coupling • Contraction period – Cross-Bridge Cycling – Generates tension in the muscle • Relaxation period – Stimulus ends or cell fatigues – Muscle returns to its resting state Muscle Twitch Stimulus • Somatic motor neurons innervate skeletal muscle • Largest diameter neurons • Myelinated • High velocity AP • Upon reaching muscle, axon divides into many branches • Each branch forming a single junction with a muscle fiber = motor unit EPP to AP Action Potential to Contraction • AP lasts 1-2 ms • Completed before any mechanical activity begins • Mechanical activity (contraction) may last >100 ms • Electrical activity (action potential) does not act on contractile proteins • Produces a state of increased cytolsolic [Ca2+] – Resting [Ca2+] = 0.1 mMol/L – After AP [Ca2+] = 1 mMol/L Latent Period • Excitation-Contraction Coupling • Sequence of events from the generation of an AP across the sarcolemma to Ca2+ release inside of the myofiber • Sarcolemma is an excitable membrane – Generating an AP (from EPP) – Propagating an AP – Similar mechanisms as neurons Contraction Period • Increase in intracellular Ca2+ levels trigger the mechanical events • Ca2+ activates Cross- Bridge Cycling Sarcoplasmic Reticulum • Lateral sacs store Ca2+ • T-tubule has DHP receptors – DHP receptors are normally voltage gated Ca2+ channels – In skeletal muscle t-tubules, acts as a voltage sensor • SR has ryanodine receptors – Intracellular Ca2+ channels – When Ca2+ channels open, Ca2+ moves into cytoplasm Calcium Release • DHP receptors trigger calcium release • Ryanodine calcium channels open • Influx of calcium from SR into cytoplasm • Calcium influx triggers cross bridge cycling Activation by Ca2+ • Tropomyosin covers the myosin binding sites on actin • Troponin holds tropomyosin in place - has 3 sub-units 1. Troponin I • inhibitory 2. Troponin T • Tropomyosin binding 3. Troponin C • Calcium binding • Increase in intracellular Ca2+ levels cause Troponin C to bind to Ca2+ which exposes binding sites on actin Troponin Cross Bridge Cycling 1. Attachment of the myosin cross-bridge to actin of a thin filament 2. Movement of the cross-bridge, pulling on the thin filament – Each cross-bridge moves independently of all other cross- bridges – Asynchronous pulling action 3. Detachment of cross-bridge from the thin filament 4. Energizing the cross-bridge so it can again attach to a thin filament and repeat the cycle Cross-Bridge Cycling ATP in Muscle Metabolism Uses of ATP in Muscle Muscle Contraction Requires Contraction A Lot of ATP! • Activation of myosin • No ATP “storage” – High-energy myosin • 3 pathways for • Release of myosin head regeneration from actin molecule – Phosphagen system • Active transport of Ca2+ – Glycolysis into SR from the – Aerobic respiration sarcoplasm + ATP + H20 à ADP + pi + H + Energy Sources of ATP 1. Phosphagen System 2. Glycolysis 3. Oxidative phosphorylation Phosphagen System • Creatine – Natural produced ny the body – Made from amino acids • Creatine Phosphate – A store of high energy phosphate • Creatine Kinase – Transfers phosphate group from CP to ADP – Present at 3x higher concentration in skeletal muscle CrP + ADP + H+ ----> Cr + ATP Phosphagen System • Adenylate Kinase – A way to quickly make ATP – ADP + ADP ---- > ATP + AMP Aerobic Respiration • Primary source of ATP production for muscle during rest or light exercise • Fuel utilization by skeletal muscle – fatty acids – muscle glycogen – blood borne glucose Anaerobic Mechanisms • Oxygen consumption – Exercising muscle can consume more ATP than can be produced by aerobic respiration – Muscle cells will utilize available glucose and glycogen reserves – Glycolysis will then produce ATP to keep up with the demand of the active muscle • Lactic acid accumulates – Oxygen Debt • The amount of oxygen consumed to get the muscle cells and plasma back to normal conditions – Glucose levels – Glycogen reserves – Converting lactic acid back to pyruvic acid Smooth Muscle • single cells, no striations • circular layer arrangement • no sarcomeres or troponin • actin:myosin ratio = 13:1 • utilizes Ca2+/calmodulin mechanism • graded depolarizations • single unit vs multi-unit • autonomic innervation Smooth Muscle.

View Full Text

Details

  • File Type
    pdf
  • Upload Time
    -
  • Content Languages
    English
  • Upload User
    Anonymous/Not logged-in
  • File Pages
    29 Page
  • File Size
    -

Download

Channel Download Status
Express Download Enable

Copyright

We respect the copyrights and intellectual property rights of all users. All uploaded documents are either original works of the uploader or authorized works of the rightful owners.

  • Not to be reproduced or distributed without explicit permission.
  • Not used for commercial purposes outside of approved use cases.
  • Not used to infringe on the rights of the original creators.
  • If you believe any content infringes your copyright, please contact us immediately.

Support

For help with questions, suggestions, or problems, please contact us