Lecture Final: Chapter 19 Flashcards

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1
Q

Define the following

  • homology
  • analogy
  • homoplasy
A

HOMOLOGY: processes / mechanisms that are derived from a common ancestor but are in two different species
– Body shape in the seals / penguins / tuna is NOT a form of homology

ANALOGY: processes / mechanisms that are similar in species function-wise but are NOT derived from a common ancestor

    • Body shape IS a form of analogy
    • Ie. seals / penguins / tuna have streamlined bodies for swimming BUT different attachments within the body physiology → analogous; not homologous

HOMOPLASY: things just look alike
– Body shape is also HOMOPLASTIC → therefore cannot use body shapes of these organisms as a way to determine their relationship

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2
Q

Body Plan of Typical Mammal – Problem, solution, extra tidbit

A

Problem: most cells are too distant from surface to enable diffusion to exchange materials with environment

Solution: have exchange surfaces with large surface areas and thin / permeable barriers + convective transport mechanism to get gases / nutrients / wastes to sites where diffusion can occur → basically another way to maintain homeostasis

    • Lungs SA = 180 m squared
    • Digestive tract SA = 300 m squared

Consider this: tube within a tube – any material inside the alimentary / digestive tract is still considered “outside” the body

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3
Q

Types of Tissue (4)

A

composed of cells; make up organs (which make up organ systems)

  1. Connective: derived from mesoderm; bulk of the body; acts as the padding holding you together –STRUCTURAL SUPPORT → incl adipose, bone, cartilage, blood
  2. Epithelial: “epi” = top or outermost lining – PROTECTION, SECRETION, ABSORPTION
  3. Muscle: allows for MOVEMENT bc irritable and contractible
  4. Nervous: coordination center of the body bc irritable and conductive – COMMUNICATION, COORDINATION, CONTROL
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4
Q

Epithelial Tissue

  • naming
  • functions (4)
  • polarity (2 ; 2sub2)
A

Shape:

  1. Squamous: flat → ie skin
  2. Cuboidal: cube shaped → ie. lining of tubes in kidney
  3. Columnar: rectangular; used for absorption and secretion → ie. intestine, respiratory tract

Number of layers:

  1. Simple: single later; good for diffusion
  2. Stratified: many layers; good for protection

avascular but innervated (lacking blood vessels but has nerves)

  1. Barrier / Lining
  2. Secretory (glandular)
    - - Exocrine: has a duct; reaches surface of lining
    - - Endocrine: no duct; released into interstitial fluid and affects cells with appropriate receptors that respond → ie. hormones
  3. Absorptive
  4. Sensory

Apical surface: faces the LUMEN; fringe resultant of villi (purpose: increase surface area in order to maximize absorption)

Basal: faces more inward towards the body → usually has a specific proteins

    • Basal lamina: forms a place for the cells to sit and can act like a filter / assistant for diffusion
    • Specific proteins: Na+/K+ ATPase pump found in the basal surface; helps to create an electro gradient needed for contraction by creating the inside of the cell negative
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5
Q

Covering and Lining Membranes (3)

A

Continuous multicellular sheets composed of EPITHELIUM bound to an underlying layer of CONNECTIVE tissue

  1. Cutaneous: dry membrane (exposed to air) consisting of keratin (protein), stratified squamous epithelium (epidermis); derived from ECTODERM → ie skin
  2. Mucous: moist membranes that line all open body cavities (in contact with environment), consisting of either stratified squamous OR simple columnar; also derived from ECTODERM → ie lining of mouth
  3. Serous: moist membranes that line all closed body cavities, consisting of simple squamous epithelium (specifically, mesothelium) resting on a thin layer of connective tissue; derived from MESODERM
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6
Q

Proteins involved in the stitching together of the epithelium (4)

A

Tight junctions: near apical surface; SEAL THE CELL TOGETHER to prevent leakage and maintain polarity of the epithelium; act as a fence
– Membrane bound proteins wrap around BUT don’t need them where the sugar isn’t available, therefore will keep the polarity in place

Adherens junction: stabilize cells by having CADHERINS with bands of actin (cytoskeletal protein) → promotes cell to cell adhesion
– Cadherins: transmembrane proteins associated on the cytoplasmic face; spokes that act as a zipper

Desmosomes: again, spots of CADHERINS BUT will also have a protein plaque with intermediate filaments (made of protein keratin; orange fibers; also cytoskeleton protein) that provides flexion → desmosomes will be on opposite sides of the cell and will be connected by intermediate filaments, thus yielding strength to the cell

Gap junctions: Transmembrane connexons (six form a pore) from cell to cell that allow small, water soluble substances to move readily between cells and synchronize function for all cells as a unit (ie muscle contraction)

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7
Q

Connective Tissue

  • defined
  • three components (3sub3)

Connective Tissue Types Part 1

    • LOOSE CONNECTIVE (5)
    • FIBROUS CONNECTIVE (2)
A

Defined as widely dispersed throughout the extracellular medium; exist in a medium that they secrete; mostly derived from MESODERM (specifically, mesenchymal cells) → act as a padding

Three components:

  1. Cells: fibroblasts → blast = embryonic cell → osteoblast makes bones
    - - Versus CYTE: more mature cell → osteocytes: exists within the bones
  2. Excretion of ECM: made of ground substance (gel like → can be fluid like loose connective or hard like bone)
  3. Fibers: embedded in the ground substance
    - - Collagen: tensile strength
    - - Elastin: recoil ability
    - - Reticular: form a mesh support matrix

LOOSE CONNECTIVE TISSUE: aka areolar

    • Most common type in the body
    • Holds massive amount of interstitial fluid (acting as a reservoir for nutrients)
    • contains lots of fibers, immune cells (eg. mass cells that respond to infection via inflammation), fibroblasts
    • Binds epithelia to underlying surfaces
    • Vascularized and innervated

FIBROUS CON TISSUE:

    • Highly organized COLLAGEN fibers typical of tendons and ligament
    • Poorly vascularized, therefore if damaged will take longer to heal
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8
Q

Connective Tissue Types Part 2

    • CARTILAGE
    • BONE
    • ADIPOSE
    • BLOOD
A

CARTILAGE:

    • Collagen again embedded in RUBBERY matrix (chondroitin sulfate that is secreted by chondrocytes)
    • Strong and flexible due to tensile strength but poorly vascularized therefore will heal slowly as well

BONE: essentially mineralized cartilage formed by osteoblasts

    • collagen fibers resist tension and HYDROXYAPATITE CRYSTAL OF Ca2Po4 which resist compression and are insoluble at low pH
    • Vascularized and innervated!!

ADIPOSE:

    • Storage of excess nutrients; can act as a cushion / insulation for organs
    • Minimal ECM
    • Highly vascularized

BLOOD:

    • Generated in red marrow of bone → derive from mesoderm
    • Has ECM called PLASMA
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9
Q

Ground substance (2)

A

basically the foundation for the extracellular matrix, which are secreted by the fibroblasts

Proteoglycan: consist of CORE PROTEINS linked to GAG (glycosaminoglycans; polysaccharides that absorb water and become gel like → the more absorbed, the more gel-like, the more it can resist compression)

GAGs are repeating disacch that are highly negatively charge and attract water

    • versus Polysacch chains are too stiff to fold + are rly hydrophilic
    • Negatively charged GAGs will attract Na+ ions that lead to OSMOTIC SWELLING, creating turgor pressure for shape and cushioning
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10
Q

Muscle Tissue (4)

A

Derived from mesoderm; use Ca2+ to trigger contractions; can have more than one nucleus

Striations: represent the orderly arrangement of actin and myosin in sarcomeres (functional units of skeletal muscles)

Skeletal: striated and voluntary; multinucleated; cells are electrically isolated from each other → Ca2+ ions bind to troponin to allow myosin and actin binding

Smooth: non striated and involuntary; uninucleate (one nucleus per cell); cells electrically coupled together via gap junctions → Ca2+ ions bind to calmodulin to allow for myosin and actin binding

Cardiac: striated and involuntary; at most 2 nuclei per cell; cells are also electrically coupled via gap junctions → Ca2+ ions also bind to troponin to allow myosin and actin binding

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11
Q

Nervous Tissue

  • types of cells involved (2)
  • types of glial cells (4 ; 1sub2)
A

Derived from ectoderm; irritable and conductive because of connected cells
CELLS THAT ARE WIRED TOGETHER, FIRE TOGETHER

TWO CELL TYPES:

  1. Neurons: cells that communicate via electrical signals; organize the grids and circuits that work for the higher order of perceptions; used to respond to the world
  2. Glial: “glue” – the support cells for the neurons (which work 24/7); much more plentiful

TYPES OF GLIAL CELLS:

  1. NEUROGLIAL: provides insulation via myelin sheath;
    - - Schwann Cells: found in PNS; helps to accelerate nerve signal as it travels across axon due to the Nodes of Ranvier (saltatory conduction)
    - - Oligodendrocytes: found in CNS
  2. MICROGLIA: clean up cellular debris via phagocytosis
  3. ASTROCYTES: maintain blood brain barrier; support and repair neurons
  4. EPENDYMAL: form epithelial lining of fluid filled containers in the brain; also form lining of spinal column (inside of which is the cerebral spinal fluid, which they help in manufacturing)
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12
Q

Homeothermy
+ Regulators vs Conformers
+ Homeotherms vs Poikilotherms

A

HOMEOTHERMY IS REALLY EXPENSIVE!! But permits the fast nervous system that maintains ideal environment for cell processes (The warmer the system, the faster it works)
– Ie. snakes are cold blooded / move slower in cold → will react faster in warmth

Regulator: regulates internal temperature → typically will have an elevated temperature

Conformers: conforms to the temperature of the environment

Homeotherms: maintain a stable internal temperature (thermoregulate biologically and behaviorally)
– Regulated via internal mechanisms → endothermic

Poikilotherms: aka cold blooded; fluctuates to the temperature of the environment BUT CAN REGULATE by choosing location (thermoregulate behaviorally) – aka ectothermic (dependent on external heat sources)

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13
Q

Thermogenesis by Endotherms

  • Brown fat
  • pathway
A

Consider the muscle activity of SHIVERING, which is present in humans except in NEONATES
– instead have BROWN FAT present in NEONATES (5% of total body weight in human infants) to counter heat loss that would other occur due to their high SA:V ratio

Non shivering thermogenesis occurs via ENDOCRINE SIGNALLING of brown fat to produce HEAT instead of ATP:

  1. Endocrine signal NOREPINEPHRINE leads to activation of uncoupling proton 1 in inner membrane of the mitochondrion
  2. Uncoupling protein 1: aka thermogenic protein THERMOGENIN; when activated, mitochondrion will create heat from the lipids of brown adipose tissue cells instead
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14
Q

Physiological maintenance of body heat (5)

- make heat, want to keep it

A
  1. Insulation – ie fat, hair
  2. Vasoconstriction: can regulate the peripheral arterioles to keep warm blood in the CORE OF THE BODY → sacrifice extremities in order to save core organs
  3. Countercurrent heat exchanger: heat block that requires juxtaposition (right next door) of warm arteries NEXT TO COLD VEINS
    - - Heat will diffuse from the arteries into the veins versus the environment
  4. Countercurrent MULTIPLIERS generate gradients in nephrons in kidneys
  5. Vascular networks known as RETE MIRABILE (miracle net)
    - - Passive exchanger since it only MAINTAINS the gradient
    - - Prevents heat loss only ; does not generate heat (that’s another process)
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15
Q
Feedback mechanisms (2)
\+ types of change (3)
\+ Hiking everest as a tibetan example

Types of physiological change (2)

A

Negative feedback: maintain set point, contribute to homeostasis

Positive: moving towards a new set point → eg. clotting, labor ⇒ specifically, innate and adaptive immune responses
– ie. Immune system: GO HARD OR GO HOME → kill the sickness before it kills you

  1. Acute Response: short term changes; reversible
  2. Chronic: longer term changes due to acclimation; reversible
  3. Evolutionary: changes in allele frequencies over generations; acquiring of a beneficial allele; irreversible

Ie. tibetans have acclimated to climbing everest bc they live at those altitudes all their lives (evolutionary) – as opposed to westerners who can climb up then rest to acclimate then climb again in order to acclimate (chronic)

    • acclimation basically increases number of RBC and efficiency of O2 usage BUT too many RBC can coagulate and cause a heart attacks
    • Tibetans fight this by having low RBC but larger lung size and higher rates of breathing
  1. Developmental: programmed changes in physiology as indiv changes from conception to adult – ie puberty
  2. Changes controlled by periodic clock: Repeating patterns of changes in individuals physiology under control of internal clock; can be daily or seasonal – ie circadian cycle
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16
Q

Bioenergetics of an Animal (4)

A

Nutrient molecules in body cells can be used to create ATP (product) or HEAT (waste)
Every transformation of energy generates heat!!

Heat generated w every transformation of energy → 2nd law of thermodynamics

BMR = basal metabolic rate; minimum metabolic rate of a FASTING endotherm at rest in its thermoneutral zone

    • Declines as you age → numbers on manual
    • Males have higher BMR in kCal/day than female bc of skeletal muscle mass

SMR = standardized metabolic rate; USED FOR NON HOMEOTHERMS; metabolic rate of a non stressed, fasting ectotherm at rest at a particular temperature

17
Q

Surface area to volume ratio

– especially with smaller animals

A

Smaller animals have a larger SA:V – dissipate heat faster vs larger animals

Therefore, Smaller animals need to accelerate BMR to maintain the constant body temperature
– Therefore, will have higher heart rates; shorter life spans bc small heart is working harder

Heat loss proportional to SA, heat generation proportional to V