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4 Characteristics of Muscles |
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Specialized for contractility Has action potential. (Only cell capable of movement) Large volume of body (large energy requirements) Move by interaction of filaments (actin, myosin) |
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Striated cardiac: Involuntary Striated skeletal: Voluntary, somatic Smooth: Long, tapered, uni-nucliate, contract slowly |
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Aligned protein structures running lengthwise in cell. Composed of 2 kinds of filaments |
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Basic structural/functional unit of striated muscle. Area between 2 Z-lines |
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Length of thick filament (dark) Fixed width |
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Area of thin filament Change width (light) |
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Bisects I-band Place where thin filaments attach |
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Bisects H-zones Cross-links centers of thick filaments |
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How do the bands interact during contraction? |
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Thin filaments are pulled into the A-band. The I-band and H-zone will decrease. |
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Outer membrane with numerous invaginations (T-tubules) |
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Bring action potential to the interior of muscle fiber Have extracellular fluid Surround myofibrils between the A & I bands |
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Smooth ER of muscle fibers Intracellular site for storage, uptake, and release of Calcium |
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Parts of the SR that surround the T-tubules at A-I Junctions in mammals |
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Describe skeletal muscle cytoplasm |
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Mitochondria and glycogen granules between myofibrils (glycogen forms rosettes) Other organelles clustered at ends of elongated peripheral nuclei |
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4 Steps to muscle contraction |
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1. Nerve impulse makes action potential; travels along sarcolemma; enters cell via T-tubles 2. Depolarization of T-tubules releases Ca from Terminal Cisternae 3. Ca binds to actin pulling thick and thin filaments together toward A-band 4. SR re-accumulates Ca; muscle relaxes |
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Red: Type I (slow twitch) White: Type II (fast twitch) Intermediate: Between red and white |
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Myosatellite cells (reserve cells) on surface grow and divide after injury Resulting cells fuse with each other and pre-existing muscle *Capacity for repair is limited. Large injuries use connective tissue instead. |
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Myo-satellite cells fuse to produce more fibers |
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Increased use causes increased cytoplasm making cells larger (working out) |
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Due to inactivity or denervation, cells get smaller cytoplasmic mass |
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Adds/removes sarcomeres, making them longer or shorter |
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Motor neuron + all fibers it innervates Ranges from 2-hundreds of fibers Fewer fibers = more control |
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Neuromuscular Junction (Motor End Plate) |
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Axon branch of SE neurons contact fibers at motor end plates Sarcolemma is highly folded: Junctional Folds Each muscle fiber has only one motor neuron! |
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What do junctional folds do/ |
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Increase surface area of synaptic cleft |
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Sensory receptors (sense degree of stretch) Fusiform structures within most muscles CT Capsule surrounds intrafusal fibers |
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2 types of fibers in muscle spindles |
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Nuclear bad: Larger, clustered nuclei Nuclear chain: Smaller, distributed nuclei |
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Functions of Smooth Muscle |
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Contractility Conductivity Regeneration |
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Contain actin and myosin (acidophilic) To transverse bands Involuntary movement Location: Arteries, GI/Repro tract, Iris... Parenchyma = functional cell Stroma = connective tissue |
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Smooth Muscle Appearance (under LM) |
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Long, spindle shaped cells (thick in middle) Tapered (smallest muscle type) Central nuclei; 1 per cell Small amount of connective tissue |
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Smooth muscle appearance (EM) |
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Sarcolemma has invaginations (caveolae) that release Ca to initiate contraction Activate a kinase that phosphorylates myosin Dark Bodies Gap Junctions |
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Dense Bodies (Smooth muscle EM) |
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Dark staining patches in cytoplasm Attachment sites for intermediate and myosin filaments |
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Gap Junctions (Smooth muscle EM) |
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Allows ionic coupling (communication) |
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General functions of the Cardiovascular system |
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Service needs of tissues (deliver nutrients, remove wastes) Maintain environment |
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Pulmonary Arc: To lungs Systemic Arc: Everywhere else Lymphatics: Afferent; joints veins to enter blood |
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3 Layers of vascular tubular wall |
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Tunica Intima Tunica Media Tunica Adventicia **Endothelium is the only constant feature in all components! |
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Contains: Endothelium, basal lamina, CT, few smooth muscle cells Fibers: Longitudinal; avascular Gets nourishment from lumen via foot processes (gap junctions) |
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Outermost part of Tunica Intima Not usually seen under LM Has gaps to allow for diffusion |
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Mostly smooth muscle and elastic Collagen and fibroblasts mixed in Perpendicular fibers Inner part nourished by tunica intima Outer part nourished by vasa vasorum and nervi vasorum |
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May be on outermost part of Tunica Media |
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Collagen and elastic (longitudinal) Mostly collagen (dense irregular CT) Vasa vasorum and nervi vasorum Often hard to distinguish outer boundary |
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Regular shape; thick walls; small lumen Tunica media is thickest High blood pressure (strong walls) |
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Irregular shape; thin walls; large lumen Thick tunica adventitia Lots of elastic fibers with collagen Low pressure (contain valves) |
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Walls lack distinct organization Lumens may have precipitate or lymphocytes Also may have valves |
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Small; muscular; 1-3 layers smooth muscle Possible IEL, NO EEL Tunica Adventitia blends with surrounding tissue Act as control valves to regulate blood flow to terminal vascular bed |
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Found near arterioles Indistinct Tunica Media and Adventitia "returning vessels" - move blood from terminal bed to larger veins |
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Shunt blood from arterioles to venules Bypass the capillary beds Thick muscular wall; longitudinal smooth muscle Circular smooth muscle can open or close Location: Skin, GI tract, erectile tissue Function: Regulate blood pressure, thermoregulation, erection |
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Found in terminal vascular bed Pluripotent cells Can differentiate into fibroblasts, smooth muscle, and mast cells Found on basement membrane |
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Thin TM; basement membrane; 1 RBC at a time Allow metabolites to enter, and waste to exit |
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Continuous: Has basement membrane Fenestrated: Has basement membrane Discontinuous: Found in endocrine glands Lymph: Many in gut (collect FA's/glycerol) |
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Most permeable part (fenestrations and incomplete tight junctions) Inflammatory response: histidine mediators Similar to capillaries, but 2-3 RBC's |
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Erectile tissue Large, round/irregular Used for blood pooling LACK smooth muscle |
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Capillary bed between 2 veins Ex: Portal vein (drains GI tract)and leads to hepatic veins |
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Capillary bed between 2 arterioles Ex: Afferent arteriole (In kidney) |
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Takes up digested carbs, AA's, lipids, vits Stores and releases: glucose, triglycerides, vits Synthesize things Detoxification Bile formation/secretion Converts T4 to T3 |
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What does the liver synthesize? |
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Albumin, prothrombin, glucose, FA/triglycerides, lipoproteins, cholesterol/phospholipids, a&B globulins |
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What does the liver detoxify? |
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Metabolites, drugs, xenobiotics (foreign material), bacteria, immunoglobulins, "warn out" cells, proteins |
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Hepatocytes: Capable of ALL functions Kupffer cells Fat-storing cells (Ito cells): Vit A Endothelial cells |
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Epithelial cells; form parenchyma of liver Polyhedral shape; arranged in cords Have central nucleus and glycogen Short microvilli on surface Actual activity depends on position in lobule and state of animal |
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Stellate shaped; line liver sinusoids Mononucleate Binds hemoglobin; breaks it down to bilirubin Can take over RBC degradation for spleen Antigen processing and presentation Fc and C' receptors |
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Fc and C': Phagocytosis of immune comlexes, immune bacteria, and non-immune particulates Other receptors: ASGP-R, MP-R, LDL-R |
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Increase in connective tissue |
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Liver lobule organization |
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6 lobes, many lobules, visible in pig Hexagon shape; around central vein Triads: artery, vein, and bile duct Blood drains toward central vein via sinusoids Bile drains away from central vein |
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3 Liver lobulation theories |
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Classic lobule Portal lobule Liver acinus |
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Describes: central lobular necrosis Shape: polygonal Portal canals in periphery Vein in center Emphasizes endocrine function of gland |
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Little use in modern hepatology Triangle shape Triad in center Central vein in apexes Emphasizes exocrine function of gland |
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Rappaport's lobule Oval shape Triad on central axis Veins at periphery Describes hepatic regeneration and cirrhosis Has zonation |
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Zone 1: peripheral (recieves blood w/ most nutrients) Zone 2: Mid-region (intermediate quality blood Zone 3: Centrilobular |
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Strong, specialized connective tissue Cells in gel-like substance: Chondroitin sulfate, hyaluronic acid, H2O (acidic sulfate = basophilic) Avascular; lots of collagen |
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Capsule-like sheath of dense irregular CT around cartilage NOT in fibrocartilage |
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Weight-bearing; friction-free movement Protect articulating bone sufaces Support nose, larynx, trachea, bronchi, external ear Template for bone development in extremities, vertebral column, and pelvis |
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First 2 steps in histogenesis |
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1. Mesenchymal cells become chondroblasts (make ground substance and collagen) 2. Cells isolate from each other in lacunae |
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Continued histogenesis within cartilage Adds matrix internally Mitosis of existing chondrocytes |
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Continued histogenesis growing outside Adds matrix externally Becomes perichondrium and secretes ground substance |
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Hyaline Elastic Fibrocartilage |
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Location: Articular surfaces of bones, nose, larynx, trachea, embryonic skeleton Fibers: Collagen (stains pale) |
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Location: Pinna, epiglottis, auditory tube Fibers: Elastic and little collagen |
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Location: Intervertebral disks, menisci of stifle Fibers: Collagen BUNDLES **NO perichondrium |
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Slow process; depends on age Both types of growth in young Fibrous CT used for old |
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Intervertebral disc disease |
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Small long dogs (presents as neurologic) |
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Tears of cranial cruciate in large breed dogs |
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Internal support Protect soft tissues in cavities Locomotion Framework for bone marrow Reservoir for Ca++ ions |
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Compact bone: outer shell Cancellous (spongy) bone: central region with marrow Lamellae: Longitudinal laminar structures (3 types) |
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Osteons: Surround vascular Haversian Canal Interstitial lamellae: irregular groups Circumferential lamellae: bony lamellae around internal and external surfaces of shaft |
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Osteoblasts: Bone forming (secrete tropocollagen and glycosaminoglycans) Osteocytes: Mature bone; in lacunae Osteoclasts: Large, multi-nucleate for bone resorption |
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Organic: Sulfated glycosaminoglycans, glycoproteins, collagen (9% H2O) Inorganic: Hydroxyapatite crystals keep rigidity (Ca, CO3, PO4) |
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Layers of lamellae Haversian canals connect via Volksmans canals (oblique) |
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Intramembranous Osteogenesis |
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Directly from mesenchyme (areas of vasculization) Flat bones of skull, mandible, maxilla 1. Mesenchymal cells become ostoblasts to secrete osteoid 2. Bone deposition around osteoblasts create lacunae and trabeculae 3. Fills intertrabecular space 4. Mesenchymal cells on surfaces form endosteum and periostium |
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Endochondral Osteogenesis |
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Replaces hyaline cartilage template Bones of extremities, vertebral column, pelvis, base of skull) Mesenchymal cells of fetus become skeletal system Low O2 causes chondroblast formation Chondrocytes secrete alkaline phosphate Calcification occurs; chondrocytes die Blood vessels invade; forms bone collar Periosteal bud forms; penetrates cartilage Multipotential cells become osteoblasts Forms new bone at primary ossification center |
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5 Zones on epiphyseal disk |
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Resting chondrocytes Proliferating chondrocytes Chondrocyte maturation Hypertrophic chondrocytes Calcification and ossification |
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Steps for fracture repair |
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1. Formation of callus 2. Hematoma forms at fracture site 3. Phagocytic cells and fibroblasts invade; Callus forms cartilage template 4. Vessels form internal callus 5. Vessels invade external callus and replacement begins (endochondral bone formation) |
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Have articular cartilge (NO perichondrium) Fluid in cavity Contains synovial capsule |
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Stratum fibrosum: outer layer of collagen Stratum synoviale: inneer layer of round or flat cells
Synovial fluid: Lots of hyaluronic acid |
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