Summary

This document covers chapter 10 on muscle tissue, including its functions, properties, types (skeletal, cardiac, and smooth), anatomy, and metabolism. It details the sliding filament mechanism of contraction, as well as the production of ATP in muscles. The document also discusses the nerve stimulus of skeletal muscle and neuromuscular junction.

Full Transcript

CHAPTER 10 - MUSCLE TISSUE Chemical energy  mechanical energy to 1 generate force, perform work, produce movement Myology Prefixes – myo, mys, & sarco all refer to muscle 5 FUNCTIONS OF MUSCLE TISSUE 1. Body movement 2. Maintenance of posture 3. Pro...

CHAPTER 10 - MUSCLE TISSUE Chemical energy  mechanical energy to 1 generate force, perform work, produce movement Myology Prefixes – myo, mys, & sarco all refer to muscle 5 FUNCTIONS OF MUSCLE TISSUE 1. Body movement 2. Maintenance of posture 3. Protection & Support 4. Storage & Movement of materials Peristalsis taking place in the Heat production intestine of a horse. Viewed during 5. laparoscopic surgery. 2 5 SPECIAL PROPERTIES OF MUSCLE TISSUE 1. Excitability 2. Conductivity (Action potentials) 3. Contractility 4. Extensibility 5. Elasticity 3 3 TYPES OF MUSCLE TISSUE 1. Skeletal muscle –  attaches to bone, skin or fascia  striated  voluntary control of contraction & relaxation http://www.cretin-derhamhall.org/Departmental/Science/AFroehle/skeletal_muscle2.gif 4 http://www.css.edu/users/tboone2/asep/dexp/anatpics.htm 3 TYPES OF MUSCLE TISSUE 2. Cardiac muscle http://www.cretin-derhamhall.org/Departmental/Science/AFroehle/cardiac4.gif striated involuntary autorhythmic (pacemaker) 5 3 TYPES OF MUSCLE TISSUE 3. Smooth muscle  Arrector pili  Wallsof hollow organs  Non-striated  Involuntary 6 GROSS ANATOMY OF SKELETAL MUSCLE: CONNECTIVE TISSUE A muscle = one organ  Hypodermis  Fascia  Connective tissue sheaths include:  epimysium  perimysium  endomysium 7  Tendon GROSS ANATOMY OF SKELETAL MUSCLE: NERVE AND BLOOD SUPPLY  Skeletal muscle supplied by nerves, arteries & veins  Somatic motor neuron  Neuromuscular junction 8 FUSION OF MYOBLASTS INTO MUSCLE FIBERS  Maturemuscle developed from > 100 myoblasts  Mature muscle cells can not divide  Satellitecells retain ability to regenerate new cells 9 MUSCLE FIBER OR MYOFIBERS  Sarcolemma  Sarcoplasm filled w/ myofibrils & myoglobin 10 Muscle organization: Muscle  muscle fibers (cells)  myofibrils  sarcomere  myofilaments (actin & myosin) SARCOMERE  Smallest contractile unit of a muscle  region of myofibril between 2 successive Z discs  Composed of myofilaments made up of contractile proteins  Myofilaments: thick (myosin) & thin (actin) 11 Muscle organization: Muscle  muscle fibers (cells)  myofibrils  sarcomere  myofilaments (actin & myosin) MYOFIBRILS & MYOFILAMENTS  Myofibrils separated by SR  Myofilaments = contractile proteins of muscle 12 SARCOPLASMIC RETICULUM (SR)  System of tubular sacs (sER) encircles myofibril  Regulates Ca+2 levels  Stores Ca+2 in relaxed muscle (attached to calmodulin & calsequestrin), Ca+2 pump  releases Ca+2 during contraction via voltage gated Ca+2 channels 13 TRANSVERSE TUBULES  Invaginations of the sarcolemma into cell  Filled w/ extracellular fluid  Carry AP down into cell  Mitochondria lay near muscle proteins that use ATP 14 FILAMENTS & SARCOMERE  Striations = I bands & A bands  Overlap region  Supporting proteins  M line, titin & Z disc anchor thick & thin filaments in 15 place REGIONS OF A SACROMERE OF A MYOFIBRIL 16 THE PROTEINS OF MUSCLE Myofibrils built of 3 kinds of protein: 1. Contractile= myosin & actin 2. Regulatory = troponin & tropomyosin 3. Structural = titin, myomesin, nebulin & dystrophin 17 THICK FILAMENTS - COMPOSED OF MYOSIN 18 THIN FILAMENTS - ACTIN, TROPONIN, & TROPOMYOSIN  Myosin-binding site covered by tropomyosin in relaxed muscle  Thin filaments held in place by Z lines 19 OTHER STRUCTURA L PROTEINS  Titin anchors thick filament to M line & Z disc  Role in recovery of muscle from being stretched  M line (myomesin) - connects to titin & adjacent thick filaments  Nebulin - inelastic protein helps align thin filaments  Dystrophin - links thin filaments to sarcolemma & 20 transmits tension generated to tendon SLIDING FILAMENT MECHANISM OF CONTRACTION  Myosin cross bridges pull on thin filaments  Thin filaments slide inward  Z Discs come toward each other  Sarcomeres shorten  Muscle fiber shortens  muscle shortens 21 MUSCLE GROSS ANATOMY SUMMARY Myofibril Myofilament: Organelle Actin & Myosin 22 Muscle Fiber (Cell) Muscle fiber (cell) (organelles) 23 24 Myofilament: organelle 25 EXCITATION CONTRACTION COUPLING SUMMARY 1. Motor Neuron excites muscle cell at NMJ 2. AP spreads across sarcolemma & t-tubules 3. SR releases Ca++ into sarcoplasm 4. Ca++ enters myofibril organelles & binds to Troponin 5. Troponin removes tropmyosin from actin 6. Myosin heads attach to actin beads 7. Sarcomere, myofibril, muscle 26 fiber, fascicle, & muscle shorten -pull on tendon/bone CONTRACTION CYCLE  Repeating sequence of events that cause thick & thin filaments to move past each other (when ATP & Ca+2 available)  4 steps to contraction cycle 1. Cross bridge formation (attach) 2. Power stroke (pull) 3. Release of myosin head (cross-bridge detachment) 4. Reset (“cocking” of) myosin head 27 SEQUENTIAL Myosin head (high-energy EVENTS OF configuration) CONTRACTIO N 1 Myosin cross bridge attaches to actin myofilament Thin filament ADP +P (inorganic phosphate) released i Thick filament 4 2 Working stroke—myosin head pivots & bends as it pulls on the actin As ATP is split into ADP + P , cocking of myosin head i filament, sliding it toward M line occurs Myosin head (low-energy configuration) 28 3 As new ATP attaches to myosin head, cross bridge detaches 29 RIGOR MORTIS  State of muscular rigidity  3-4hours postmortem  Lasts about 24 hours  Afterdeath Ca+2 ions leak out of SR & allow myosin heads to bind to http://kadokami.hp.infoseek.co.jp/E.Sendoiji.htm actin  ATP synthesis has ceased  crossbridges cannot detach from actin until proteolytic 30 enzymes begin to digest decomposing cells NERVE STIMULUS OF SKELETAL MUSCLE  Motor neurons of somatic nervous system  Axons in nerves  muscle cells  Branch profusely as they enter muscles  Axonal branch forms neuromuscular junction w/ single muscle fiber  Neuromuscular junction is formed from:  Axonal endings  Motor end plate of a muscle  Synaptic cleft 31 STRUCTURES OF NMJ REGION  Synaptic end bulbs  Synaptic vesicles (Acetylcholine)  Motor end plate 32  Nerve signal events EXCITATION OF SKELETAL MUSCLE FIBER  nn 33 EXCITATION-CONTRACTION COUPLING 34 EXCITATION-CONTRACTION COUPLING 35 OVERVIEW OF SKELETAL MUSCLE CONTRACTION . 36 RELAXATION - ACETYLCHOLINESTERASE  1) Muscle end-plate potential ceases when  enzyme acetylcholinesterase (AchE) removes acetylcholine (Ach)  2) Muscle action potential ceases when  Na+ pumped out of cell with Na+/K+ ATPase pump  3) Cross-bridge cycling ceases when  Ca+2 release channels close & active transport pumps Ca+2 back into storage in sarcoplasmic reticulum  Ca+2 -binding protein (calsequestrin) helps hold Ca+2 in SR  In presence of ATP, Tropomyosin-troponin complex recovers 37 binding site on actin 38 PHARMACOLOGY OF THE NMJ  Botulinum toxin prevents Ach release  C. botulinum  Botulism  Curare  Blocks ACh receptors  Relaxes muscles during surgery  Neostigmine (Reversible acetylcholinesterase inhibitor)  Blocks removal of ACh from receptors  Antidote for curare  Pesticides & Nerve gas also ACh esterase inhibitors 39 MUSCLE METABOLISM : PRODUCTION OF ATP IN MUSCLE (10.4)  Muscle uses > ATP when active  3 sources of ATP production within muscle: 1. Immediate (5-6 sec): phosphagen system 1. ATPase, Myokinase, creatine kinase 2. Short-term (50-60 sec): anaerobic cellular respiration 3. Long-term (5-6 min): aerobic cellular respiration 40 IMMEDIATE SUPPLY OF ATP: PHOSPHAGEN SYSTEM 41 CREATINE PHOSPHATE  Excess ATP w/in resting muscle used to form creatine phosphate  Quick breakdown  ADP + CP  ATP  Creatine supplementation  decreases innate production 42 FERMENTATION: ANAEROBIC CELLULAR RESPIRATION  If no O2 present pyruvic acid is fermented  lactic acid  Lactic acid returns to liver where it’s turned into pyruvate when O2 available  About 2% as efficient as aerobic cellular 43 respiration ANAEROBIC VS AEROBIC CELLULAR RESPIRATION . 44 AEROBIC CELLULAR RESPIRATION  Production of ATP in mitochondria from pyruvic acid, FA’s & AA’s 45 MUSCLE FATIGUE (SECTION 10.7D)  Central fatigue - protective mechanism  Musclefatigue - Inability to contract after prolonged activity  Factors that contribute to muscle fatigue  Insufficient O2 or glycogen for aerobic cellular respiration  Buildup of lactic acid & phosphates  Insufficient release of ACh from motor neurons (reduced Ach or Ca+2 in neurons) 46  Na+, K+ imbalance in cell OXYGEN CONSUMPTION AFTER EXERCISE (10.4B)  Muscle tissue has two sources of O2:  Diffusesin from blood  Released by myoglobin inside muscle fibers  Aerobic system requires O2 to produce ATP needed for prolonged activity  Oxygen debt  elevated O2 use after exercise (O2 debt)  Hemoglobin & myoglobin  Glycogen stores  ATP & creatine phosphate stores  lactic acid is converted back to pyruvic acid to glucose  Elevated body temperature = > metabolic rate 47  bodyreactions release energy (~40% work & 60% lost as heat) SKELETAL MUSCLE FIBER TYPES (10.5)  3 fiber types present in each muscle to varying degrees  Differ with regards to ATP production & function  Know info. in red boxes (10.5B) 48 THE MOTOR UNIT (10.2C)  Motor unit = somatic motor neuron & skeletal muscle fibers it stimulates  Total strength of contraction depends on how many motor units are activated & how large motor units are 49 MOTOR UNIT RECRUITMENT (10.6B)  Motor units in a whole muscle fire asynchronously  Produces smooth muscular contraction  Precise movements require smaller contractions  Large motor units are active when large tension is needed 50 MUSCLE TONE (10.7A)  Involuntary contraction of a small # of motor units  Keeps muscles firm although they’re “relaxed”  Essential for maintaining posture (head upright)  Important in maintaining BP  Smooth muscle in blood vessels 51 WHAT TO FOCUS ON IN CH 10  Not Covering in Ch 10  USE POWER  Section 10.6a & 10.6c POINTS AS (on pages 354-356) OUTLINE  Get detailed  10.7b & 10.7c  10.8 information from lecture notes or text  10.9 & 10.10 – just what is in slides 4-6 52

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