Life Functions
Maintain boundaries (skin, mucosa)
Organization:
Movement
Responsiveness
Digestion
Metabolism
Excretion
Reproduction
Growth
Lining => epithelia
Interface => basal lamina
Support => connective (interface Fascia)
Muscle (smooth, cardiac, skeletal) => tube/layer/organ (muscle, bone, joints)
Nervous system, endocrine
(G.I. trace)
(tissues, liver)
(Urinary, GI)
(genitalia)
Cavity formation: Cranial, Dorsal, Vertebral, Mediastinal, Thoracic, Pericardial, Ventral, Pleural, Abdominal, Pelvic
Defined by Membranes
Maintaining a consistent range.
Receptor, Control center, effector
Negative (-ve) & positive (+ve) feedback
Plasma membrane proteins:
Receptors
Transmembrane proteins
Channels/transporters
Adhesion molecules
Enzymes
Cell: Cell recognition
Tight junctions
Zipperlike
Apical edge
Prevents paracellular diffusion.
Gap Junctions
Transmembrane protein, lateral sides
Fluid-filled channel = ease of ion movement between cells.
Desmosomes
Snap-like connections
Loose
Allows diffusion between cells.
Hemidesmosomes
Attachment to basal lamina.
Microfilaments
Actin, FXN: Support (m), microvilli
Intermediate filaments
Actin tetramers FXN: Cell strength
Microtubules
Tubulin FXN: Move organelles, Chromatin
Diffusion - Concentration/electrical gradient
Passive transport - Channels/pores
Active transport → transporters (ATP needed).
Ectoderm => nervous system, special senses, oral & anal mucosas \ Living (skin epidermis
Mesoderm => Cardiovascular, Muscle, bone, adipose
Endoderm => GI tract mucosa, Urogenital tract, respiratory.
Planes through: Sagittal, Frontal, Transverse, Oblique, Longitudinal, Cross, Oblique
Organs
FXN: Protection, Secretion, absorption
Simple = 1 layer thick
Stratified = 2+ layers
NOT VASCULARIZED
Relies on diffusion of gases etc. through cell layers & interstitial fluid.
Thin & flat
Diffusion (blood vessels, alveoli)
Secretory (serous)
Secreted
Absorb
Kidneys, Acini
Secrete
Nuclei basal
Stomach, GI tract.
Keratin - filled
Upper layers
Waterproof
Dead
FXN: Epidermis
Secrete & propel
Mucous
Trachea, epididymis
Moist, slippery
FXN: vagina, oral mucosa, cornea, anus, tongue, esophagus.
Sweat, sperm
Hormones
Uterus, male urethra
Round-flat when stretched
Ureter, bladder
Exocrine - To outside the body/tissue e.g. Sweat, gastric, sebaceous.
Endocrine - Into blood stream.
Serous - Thin, watery
Mucous - Mucus, mucin-rich
Cytogenic - Release whole cells.
Holocrine - Cells disintegrate to make secretion.
Merocrine - Product released via exocytosis (sweat).
Apocrine - Modified mesocrine, mammary glands.
Layer of adhesive proteins between tissue types.
Laminin - adhesive, e.g., between epithelia & connective tissue.
Proteoglycans - bonds Cells & extracellular matrix (ECM)
Fibrillin - adhesive
Glycosaminoglycans (GAGS) - attract H2O, hold H2O, maintain osmolarity
Fibroblasts
Loose connective
Areolar (Underline epithelia
Between muscle
Reticular (Lymph nodes)
Adipose Red bone marrow
Dense connective
Regular (tendons, Ligaments)
Irregular (e.g. dermis)
Chondroblast - Cartilage
Hyaline (trachea)
Elastic (Pinna)
Fibro- (Symphysis)
Osteoblast - Bone
Compact
Spongy
Hemopoietic Stem Cell - All formed elements of blood (Red, white & platelets)
Scab, artery, capillary, WBC
Inflammation
Swelling, redness, heat, pain
Edema contains pathogen, stabilizes injury
Redness & heat from vasodilation
Bring nutrients & O_2 for healing
Remove debris/wastes
WBC to eliminate pathogen
Pain stops you injuring further
Regenerating epithelium (calls divide & migrate in)
Vascular supply.
Fibroblasts migrate in & deposit collagen.
Macrophages remove debris - granulation tissue.
Organization
Regenerated epithelium
Fibrosed area matures & Contracts (can take months)
Epithelium thickens
Regeneration
Scarring
Erythematous - Fed from neovascularization
Hypertrophic - Over growth that reduces with time.
Atrophic - Indented.
Cell body with long projections (axons, dendrites).
Peripheral nerves can regenerate if cell body remains intact, cannot divide
Smooth
Cardiac & striated, cardiac has intercalated discs.
Skeletal.
Hypertrophy = ↑ cell size, rarely cell #
Atrophy = ↓ cell size or cell #
Skin
Epidermis
Stratum corneum-Keratinized outer layer-waterproofing
Stratum lucidum-thick skin only
Stratum granulosum-Keratinohyalin
Stratum spinosum-Keratinocytes
Stratum basale-stem cells (keratinocyte melanocytes pigment-touch receptors)
Dermis
Dense irregular CT- nerves, blood vessels, hair follicles sweat & sebaceous glands
Hypodermis
Adipose-larger blood vessels
Stratum basale divides pushing Cells up. cells gradually filled with Keratin & lose Cell function until completely dead. Dead cells exfoliated.
Fibrous Sheath
Shaft
Circular shaft = straight
Oval shaft = curly.
Pigment
Eumelanin = brown/black.
Pheomelanin = yellow
Medulla (balance of both
Cortex (pigmented) - shades) -tighter curl).
Inner root sheath.
Outer root sheath.
Papilla - for proper hair growth the papilla MUST be intact, & hair follicle straight to guide hair through epidermis. No papilla = NO HAIR
Growth
Anagen - active growth
Catagen - shrinking follicle - hair separates from papilla. (2-3 wks)
Telogen - resting (1-3 mnths) No growth - bulb & papilla reconnect
Blocked follicle == ingrown hair.
Fold
Root
Free edge.
Nail bed.
Stem cells in Nail bed - as cells pushed out, Keratin added - nail bed adds Keratin = thickens nails.
Nails & sensitivity of touch receptors to pressure by providing resistance
Long, short, flat, irregular shaped.
Epiphysis, metaphysis (growth / epiphyseal Plate - ONE END, ONLY., diaphysis (shaft)
Cartilage spongy Bone with red bone marrow compact bone periosteum. Yellow bone marrow endosteum
Periosteum outer compact bone spongy bone + red bone marrow. Holes = trabeculae. Inner compact bone.
Osteogenic cells
Osteoblasts
Osteocytes
Osteoclasts
3-50 fused stem cells.
Lie under periosteum
Ruffled border- H^+ pumped into space between ruffled border & bone - Ca^{2+} follows = dissolves Minerals, acid phosphatase digests collagen - NEEDS ACID TO WORK
In endosteum, periosteum, Central canals => osteoblasts mineralize matrix using osteonectin & Ca^{2+} & PO_4^{2-}
Osteoblasts trapped in matrix - Lacunae (hole cell in) cells connected by gap junctions in projections = Canaliculi
Canaliculi
Perforating / Volkmann Canals - Canals turning perpendicular to central canal for blood vessels - blood vessels, nerves
Central osteocyte canal - growth of osteon OUTSIDE IN.
Flat bones - FROM SCRATCH
Mesenchyme condenses into trabeculae
Osteoblasts lay down matrix
Hydroxyapatite deposited
Osteoclasts carve out marrow cavities, blood vessels grow into hiles/cavities
Osteoblasts form compact bone at surfaces
Formation of periosteum.
Other bone types - uses hyaline cartilage as scaffold
Perichondrium -> BV -> Osteoblasts -> Bony collar -> 1° Ossification Center (1°OC) in middle -> vascularization, chondrocytes swell & die
2° Ossification Center (2°OC) epiphysis Meta-/Diaphysis articular Cartilage, spongy bone EP Plate Enlarge marrow cavity
Birth -> enlarged marrow Cavities - enlarging, chondrocytes swell & die 2°OC cavities in one epiphysis
Epiphyseal Plate Growth
Resting Zone - Reserve Cartilage
Proliferating Zone - Chondrocytes dividing
Degenerating Zone - older chondrocytes - older chondrocytes (hypertrophy & enlarged)
Ossification Zone - adding moss hydroxyappatite, Fully mineralized. Simulate osteoclasts prepare surface- osteoblasts replace bone, - Cover with lining calls
Wolff's Law
Resorption
Reversal
Formation
Resting
Cartilage Fully mineralized.
Calcitonin - Influence osteoblasts to deposit hydroxyapatite, & CaCO_3 - Ca^{2+} out from plasmic.
Calcitriol - activated Vitamin D UV light -> cholecalciferol D_3 -> LIVER -> calcidiol -> KIDNEY -> Calcitriol ↑ Ca^{2+} absorption in GI & from bone, stem cell differentiation to OSTEOCLASTS, rescrption of Ca^{2+} in Kidney.
Parathyroid Hormone (PTH) - ↑ Ca^{2+} in serum. Causes RANKL release from Osteoblast to ↑ Osteoclast number - ↑ Ca^{2+} resorption & Calcitriol production -& Collagen synthesis by osteoblasts.
Hematoma Formation - Hematoma (granulation tissue)
Soft Callus Formation - Soft callus - fibrocartilage
Hard Callus Formation - Ossification of Gibro-cartilage by OSTEOBLASTS, spongy bone/hard callus
Remodelling - spongy bone -> Compact bone by osteoblasts, Gradients removed by osteoclasts continuous marrow cavity.
Bone ends
1) Bony - Fusion of bones e.g. Frontal bones (Synostosis)
2) Fibrous - Fibers connect bones e.g. SUTURES (serrate, lap, plane)
3) Cartilaginous - Castilage forms joint.
Hyaline cartilage ribs to sternum (Synchondrosis)
Fibro cartilage - Pubic symphysis (semiphysis), Intervertebral discs.
4) Synovial - Synovial Membrane LIGAMENT attach bone to bone.
Joint cavity filled with synovial fluid - lubrication, feeds cartilage.
Fibrous capsule continuous with periosteum
Synovial membrane Subintima - Loose areolar/ Gatty/fibrous, Intima -Fibroblasts secrete HYALURONAN & LUBRICIN - macrophages remove debris from Synovium Underneath HIGHLY VASCULAR.
Functional Classification - How much movement exists.
Synostosis (bony) - Fused bone - NO MOVEMENT (or very little over time).
Gomphoses - Teeth jaw
Syndesmoses - e.g. Tibia fibula.
Sutures
Synchondrosis - rib to sternum
Semiphysis - pubic symphysis - SOME MOVEMENT
Ball & socket (Hip)
Hinge (elbow)
Saddle (Thumb)
Gliding (Intercarpel)
Pivot (ulnaradial)
Condyloid (Metacarpale
Extension of joint capsule connective tissue lined it synovial membrane around tendons so easily slide over muscle to bone. individual tendons.
Mechanical advantage - MA = \frac{Length :of: effort: arm}{Length: of: resistance: arm}
MA => 1 low advantage effort
How much effort goes in alters how easily you you get moving
Low power, high speed moving e.g. bicep /brachialis -forearm (elbow joint).
MA < 1 high advantage low speed
High power, e.g: Temporalis (TMJ)-mylohyoid-digastrics, Atlantooccipital joint e.g. TMJ opening & closing.
1st class Lever - fulcrum in middle
2nd Class Lever - Effort in the middle/Ulna/humerus
3rd class lever - Effort is farthest from the movement/bone
Tendon (Insertion) attachment of muscle to the bone that MOVES
Continuation of tendon around whole belly
Epimysium - around bundles of cells.
Perimysium - around bundles of cells.
Endomysium - around individual cells.
Origin - attachment of muscle to bone that DOES NOT MOVE.
Belly - Thickest part of muscle
Agonist/Prime mover - Muscle putting in initial effort to move bone, contributes most effort.
Synergist - Aids agonist in completing movement
Antagonist - Works in opposition to agonist.
Fixator - Stabilizes bone & joint.
T-tubule, sarcoplasmic reticulum, mitochondria, H band, Z disc - Sarcomere, Actin, I band, myosin
Titin - actin-tropomyosin-troponin- myosin head
A band - thick filament region
I band - thin filament region
Nerve (1) and the number of muscle fibers it innervates
Fine motor
A few fibers (nerve more innervation - conscious thought, longer to learn).
Gross motor
Many fibers (1000's) less innervation required.
(8) Neuromuscular Junction (NMJ) Mitochondria, synaptic cleft, neurolemma, Ca channel, Synaptic knob sarcolemma (continuous with motor end plate membrane), K* channel, ACh acetylcholine receptors (AChR)
Electrical signal reaches Synaptic knot, Ca^{2+} Channels OPEN, Ca^{2+} INFLUX
Ach Released into cleft, Ach binds receptor Recepter opens its Channel, Na^{+}:IN :K^+:OUT End Plate Potential (EPP) - Na^+ :K^+ diffuses beneath muscle cell membrane -↑ Voltage as it goes. Voltage opens Na^+ channels
IN = DEPOLARIZE, : K^+ :channels: open = REPOLARIZE Action potential (AP) moves across muscle cell, down T-Tubules, opens Voltage operated Ca^{2+} Channels (SARCOPLASMIC RETICULUM) -Ca^{2+} binds TROPONIN - TROPOMYOSIN Changes Shape => OPENS UP ACTIVE SITE ON ACTIN
Hydrolysis of ATP-cock of myosin head-powerstroke
Cross Bridge with ACTIN - LOCK
Myosin head binds more ATP, Releases actin to cock again for further binding then cross bridging
Nerve impulses to Synapse (NICE) stop, ACh released from ACGR (disperses from Synapse, cleaved into Acetic Acid & CHOLINE by AChE
(ACETYLCHOLINESTERASE) Channel CLOSES, NO EPP,Cast release stops
Ca^{2+} returned to sarcoplasmic Reticulum via ATP operated pump- No Ca^{2+} = troponin Returns to initial position
If a muscle is too contracted already, it is not able to shorten, if strained too far already not efficient
Stimulus - latent period, contraction period, relaxation period Single twitch does NEE define all work- Single Threshold Stimulus => switches, until maximum tension is achieved
Max Contraction voltage Twitch responses- Incomplete tetany Treppe Twitch Low stimuli infrequent Muscle does not contract fully, contraction voltage each twitch- Recruit Motor Units in the motor unit.
Incomplete Tetany - Each stimulus cycles before recovery sustained fluttering contraction
Temporal summation, Tetanus NO relaxation time Smooth prolonged Contraction - Locked muscle.
Isometric - Tense muscle - NO CHANGE IN LENGTH.
Isotonic - Tension DURING Contraction & relaxation MUSCLE CHANGES LENGTH
At the start: Phosphagen system --> Aerobic respiration --> glycogen-lactic acid system --->finish
Myoglobin -> Creatine system-> ADP (myokinase) -->ADP(creatine kinase) --> glycogen
Phosphagen System
Supported by Cardiovascular changes (↑HR, RR, vasodilation), Provides O_2 in muscle for short spurts no longer than 10 sec.
Glycogen-Lactic Acid System
Anaerobic respiration, prolonged exercise - ↓ rate, vasodilation, respiration rate => ↑ O_2 to muscles.
Glycogen - depletion of Glucose, fluid & electrolyte loss - ATP Synthesis &, Na^+/K^+ pump cannot maintain membrane, - lactic acid inhibits enzymes hyperpolarizes cell.
Replace O2 supplies & reserves (myoglobin, Hb, plasma O2
Replenish phosphagen system.
Convert lactic acid glucose
↑ metabolism from ↑ body. temp; Co exhaling CO_2 (to balance pH).
Slow-Twitch Fibers (Type I)- Sustained aerobic -↑ mitochondria, myoglobin, capillaries -resistant to fatigue (Endurance Athletes)
Fast-Twitch Fibers (Type IIx) Short anaerobic bursts - ↑ glycogen/lactic acid supplies & quicker Ca^{2+} release from SR - have fewer & Quicker Ca^{2+} release from SR. (Strength athletes/sprinters)
Shape & size of muscle dependent
Length of muscle at start of contraction
Shape (think dienst vs. giant).
Size of motor unit & recruitment gross motor muscles easier to influence in terms of strength