Muscle Contraction and Muscle Fiber Types
Neuromuscular Junction and Muscle Contraction
- Three steps lead to muscle contraction, as reviewed in labs.
- These steps primarily lead to muscle contraction.
Summary of Muscle Contractions
- Neuromuscular junction connection is always necessary.
- Junction: space.
- Neuromuscular: nervous system and muscular system.
- Somatic motor neurons connect with skeletal muscle.
Excitation Contraction Coupling
- Excitation: excitability.
- Contraction: contractility.
- Conversion of electrical signal into contractile motion.
- Primary signal: calcium.
- Increase in intracellular calcium from the SR (sarcoplasmic reticulum) leads to:
- Sliding filament theory (majority of contractions).
- Muscle twitch.
- Muscle twitches are usually signaled by fatigue or stimulus.
EMG (Electromyogram)
- Used to test skeletal muscle.
- Generates signals to witness contractions.
EKG/ECG (Electrocardiogram)
- Used to measure the electrical activity of the heart.
- Same thing; EKG is German, ECG is American terminology.
- German uses 'K' for cardio.
- Muscle twitch can indicate contraction, excessive stimulation, or pathology.
- Magnesium glycinate can help reduce the effects of stress.
- Stress depletes magnesium reserves.
- Low magnesium can cause nerves to be unable to relax, leading to muscle twitch or tetany.
- Excessive stress depletes magnesium reserves.
- Lack of magnesium prevents nerves from relaxing, leading to muscle twitches or tetany.
Neuromuscular Junction (NMJ)
- Connection between neuron and muscle.
- Purpose: Creating specialized neurotransmitters to connect neurons to muscles.
- Common neurotransmitter: Acetylcholine (ACh).
- ACh: A cholinergic molecule responsible for signaling.
NMJ and EC Coupling
- Acetylcholine needs to be exocytosed for release.
- Exocytosis: active transport requiring energy.
- Action potentials open voltage-gated calcium channels.
- Voltage-gated: Channels open when stimulated by electrostatic force (action potential).
- Calcium influx (diffusion) through facilitative diffusion.
- Calcium influx leads to depolarization (cell becomes positive).
- Unfavorable state; cell converts energy to return to resting potential via exocytosis.
- Acetylcholine released into the synapse or junction.
- Acetylcholine binds to its receptor on the cell surface (sarcolemma).
- Acetylcholine acts as a ligand.
- Binding of acetylcholine to the receptor initiates depolarization of the sarcolemma. Muscles are excitable and contractible.
- Muscle can depolarize because it is excitable and can be stimulated.
- Sodium channels open, and sodium rushes in (more sodium outside).
- The influx of sodium causes further depolarization.
- Depolarization is transmitted through T-tubules.
- T-tubules stimulate DHP (dihydropyridine) calcium channels.
- DHP channel opening stimulates RYR (Ryanodine receptor), a mechanically gated channel, to release calcium from the sarcoplasmic reticulum (SR).
- Extracellular calcium sensed by the DHP receptor triggers the opening of the SR to release intracellular calcium.
- This step is called EC coupling.
- Responsible for opening calcium release to begin the sliding filament theory.
Muscle Cramps
- Muscle cramp: excessive contraction.
- Often due to issues with repolarization, potentially lacking potassium.
- Potassium is needed for relaxation.
- Bananas are recommended for cramps, as they are high in potassium.
- Channel opens in contracted state, intracellular calcium influx occurs, relaxation closes the channel.
- Calcium returns to the SR via active transport, requiring energy as it moves against the gradient.
Sliding Filament Theory
- Key elements: Calcium and ATP.
- ATP is responsible for detachment.
- Hydrolyzed ATP (ADP) leads to realignment.
- Myosin head is static and acts as an anchor, pushing actin during contraction/relaxation.
- Contraction doesn't always mean angle changes; can involve resisting force, like lowering a weight.
Troponin and Tropomyosin
- Myosin head contains ATPase.
- ATP is responsible for detachment.
- Hydrolyzed ATP (ADP) allows reattachment.
- Contraction: sliding.
- Tension: Resistant force related to the angle and weight.
Rigor State
- No ATP, ADP, or inorganic phosphate present in the myosin head.
- Myosin head tightly bound.
- Rigor mortis: muscle freeze due to lack of ATP, which is needed for detachment.
G Actin vs F Actin
- G actin: Globular actin.
- F actin: Filament actin (e.g., tropomyosin).
Rigor Mortis
- Skeletal muscle issue.
- Smooth muscle has different pathways without sarcomeres.
- Smooth muscle lacks sarcomeres.
- Nervous system shuts down upon death.
- Sphincters relax.
Energy for Skeletal Muscle
- Multiple ways to receive ATP.
- Aerobic (with oxygen) vs. anaerobic (without oxygen) respiration.
- Slow oxidative (aerobic) vs. fast glycolytic (anaerobic).
- Fast glycolytic provides immediate energy.
- Slow oxidative generates more ATP (35-37 ATP) than fast glycolytic (2 ATP).
- Anaerobic respiration byproduct: lactic acid (causes muscle soreness).
- Parts of the body do not have oxygen distributed, causing lactic acid buildup.
Heart Attack (Infarction)
- Lack of blood flow to heart muscles.
- Ischemia: Pain due to lack of blood flow and lactic acid buildup.
- Heart uses glycogen stores when transitioning from oxidative to glycolytic pathways.
Phosphocreatine Pathway
- Faster way to get ATP.
- Creatine tests are usually blood tests to assess kidney function (creatine excreted by kidneys).
- ATP is stored in a resting state by binding a phosphate to creatine, forming ADP and phosphocreatine.
- During work phase, phosphate is grabbed from phosphocreatine and bound to ADP to create ATP.
- This bypasses cellular respiration, offering immediate ATP.
- At rest, excess ATP binds to creatine to form phosphocreatine (energy storage).
- During activity, phosphocreatine donates phosphate to ADP, forming ATP.
Creatine Supplementation
- Creatine gives you a good feeling.
- Problem: Swelling, and you lose gains when you stop using creatine.
- Creatine can be obtained from meat and liver.
- Creatine dehydrates you. It converts sugar to energy, so be cautious and stay hydrated.
- Excess creatine is excreted by the kidneys.
- If you have kidney problems, you should not take creatine.
Muscle Fiber Types
- Slow twitch (oxidative) vs. fast twitch (glycolytic) fibers with intermediate fibers.
- Create a table to compare and contrast the qualities of fast twitch and slow twitching muscles.
Slow Twitch
- Oxidative, aerobic.
- Generates most ATP.
- Marathons (long range).
Fast Glycolytic
- Anaerobic.
- Fastest ATP generation.
- Sprinting, powerlifting.
- Have the least amount of mitochondria (glycolysis occurs in the cytoplasm).
- More vascularized.
- Type IIa.
- Triathletes; bike, swim, running.
- Pale pigment due to less blood flow and fewer mitochondria.
- Mitochondria have iron.
Tension Generation Relationships
- Tetanus: maximum contraction with little or no relaxation.
Motor Unit
- One motor neuron and multiple muscle fibers.
- For more precision, one has less muscle fibers.
- More precise (eyes) = more muscle fibers are required.
Length-Tension Relationship
- Fixed length provides optimal tension.
- Too much/little overlap decreases tension.
- Optimal resting length needed for highest tension (between 2-2.3 micrometers).
Isotonic vs. Isometric Contractions
- Isotonic: Changes in angle.
- Isometric: No change in angle.
Isotonic
- Concentric (shortening).
- Eccentric (lengthening).
- Lengthening while the muscles remain contracted.
Isometric
- No angular change.
- Planking.
- No angular change, but connective tissue stretches.
- Sarcomere shortens.
Tension Contractions
- Changing distance.
- Concentric: Shortening.
- Eccentric: Lengthening.
Muscle Tension
- Muscle tension plateaus, and is gradually lost over time.
- Performing a exercise for so long will eventually exhaust the muscle.
- Muscle tension does not require that much force. Forces are required to move a load to generate movement.
Smooth Muscle and Cardiac Muscle
- Smooth muscle: involuntary, mononucleated, non-striated.
Smooth Muscle Location
- Vascular, GI, urinary, respiratory, reproductive, ocular.
- Ocular: Pupil dilation. Pupils are smooth muscles.
- Blinking: Skeletal Muscle.
Contractions
- Phasic: Alternating contractions and relaxation (e.g., eating/swallowing).
- Tonic: Continuous contractions (e.g., urination/defecation).
Urination/Defecation
- Psychological aspects.
- Neurological aspects.
Single vs. Multi Units
- Looks like NMJ, but with varicosities (big storage of neurotransmitters).
- Most likely acetylcholine, to regulate smooth muscle.
- Skeletal muscle usually is not vital (diaphragm is the exception). Other smooth muscle will be vital.
- Due to specialized organs requires a higher level of regulation for chemical messengers.
Neuron Types
- Neurons that regulate smooth muscle-all are visceral.
*Visceral = involuntary response regulation - Smooth muscles activation is based off of myosin light chain.
- Instead of going through NMJ EC coupling they have their own method of light chain here.
Dense Bodies
- Responsible for smooth muscle shortening and contracting when stimulated by visceral neurons.
Smooth Muscle Regulation
- Controlled by the autonomic brain.
Paracrine Signalling
- Grabbing chemical messengers and sending to neigboring cells.
Airways
- Histamine: released during allergies. Causes vasoconstriction. Dilates blood vessels, causing redness during allergic reactions.
Nitrous Oxide
- Very potent vasodilator.
- Brings blood pressure down.
- Nitroglycerin:
- Paramedics will use nitroglycerin which will be put under the tongue.
- Prolongs the blood flow into the heart until operated on by some kind of surgical intervention.
- Most potency to carry happens when muscles are relaxed. More energy is used for resistant tension.