Not Confident Yet Flashcards

1
Q

Four types of tissue

A

Neural, connective, muscle, epithelial

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2
Q

Three types of connective tissue

A

Connective tissue proper
Fluid connective tissue
Supportive connective tissue

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3
Q

Functions of epithelial tissue

A

Provides sensation
Physical protection
Produces secretions
Controls permeability

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4
Q

Types of cell junctions

A

Gap junctions) connected by cannexons, allows movement of ions and small molecules
Tight junctions) prevents movement of water and solutes between cells, protects basal surface in digestive tract
Desmosome) allows stretch, usually in skin. Linking of cells by CAMs and proteoglycans to the cytoskeleton

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5
Q

How to maintain the integrity of the epithelia

A

Connections between cells) tight junctions, gap junctions, desmosome
Attachment to the basement membrane) hemidesmosomes
Maintenance and repair of the epithelium) division of stem cells at basement membrane to offer protection

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6
Q

8 Types of epithelium and features

A

Simple squamous) diffusion. Lines body cavities and heart/ blood vessels. Alveoli
Stratified squamous) protection. In skin
Simple cuboidal) secretion and absorption. In salivary glands
Stratified cuboidal) rare, involved in protection, secretion and absorption. Lines some ducts of sweat glands.
Transitional) tolerates repeated cycles of stretching and recoiling. In urinary bladder. Appearance changes from cuboidal to squamous when stretched.
Simple columnar) absorption, protection, secretion. Has microvilli to increase SA. Generally in digestive tract
Pseudistratifued columnar) protection, secretion, absorption. looks stratified but all cells actually attach to basement membrane, has cilia. respiratory epithelium
Stratified columnar) rare, protection, in eyelids.

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7
Q

Two components of connective tissues

A

Extracellular part) ground substance and protein fibres

Cellular part) specialised cells

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8
Q

3 roles of connective tissue

A

Connection) supports and surrounds other tissues
Protection) protects and insulates internal organs
Storage) energy reserves

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9
Q

Types of cells in connective tissue proper

A

Fibrocytes) secretary’s protein and hyaluronon
Fibroblasts) maintain fibres, produce collagen
Adipocytes) fat cells
Mesenchymal cells) divide when injury occurs and differentiate into other cells types
Others) macrophages, mast cells, lymphocytes, microphages

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10
Q

Four types of membranes

A

Synovial) produces synovial fluid, protects articulating bone, lacks true epithelium
Serous) lines cavities but do not open to the outside, has visceral and parietal portion
Mucous) lines passageways, have external connections, moist epithelial surface
Cutaneous) skin, thick waterproof and dry

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11
Q

Neuroglia of CNS and PNS

A

CNS)
astrocytes) regulates environment, maintains blood brain barrier, forms scar tissue
ependymal cells) produce, secrete and monitor cerebrospinal fluid
oligendrocytes) form myelin, insulate axons
microglia) clean cellular debris, waste products and pathogens

PNS
Schwann cells) produce myelin, insulate axons
Satellite cells) similar to astrocytes, regulate environment
Myelin

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12
Q

What is the propagation of an action potential called on an unmyelinated neuron called?

A

Continuous propagation

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13
Q

Two types of synapses

A

Electrical) cells are in direct physical contact at gap junctions. Action potential transmitted quickly and efficiently

Chemical) cells not in contact, uses neurotransmitters. Most common type

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14
Q

Steps to neurotransmission

A

Action potential arrives at axon terminal
Voltage gated calcium channels open
Calcium ions released, increasing cellular calcium ion concentration
Synaptic vesicles fuse with membrane
Neurotransmitter released into cleft
Neurotransmitter diffuses to post synaptic terminal

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15
Q

Excitory vs inhibitory neurotransmitters

A

Excitory) makes cell membrane potential more positive, depolarisation, promotes generation of action potentials
Eg ACh

Inhibitory) makes membrane potential more negative, hyper-polarisation, inhibits generation if an action potential
Eg GABA

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16
Q

How do long bones form? (6 steps)

A

Endochondral ossification

1 Cartilage forms from stem cells
2 Cartilage grows due to bursting of cells in the centre, which causes a shift in PH and trigger calcification
3 Primary ossification centre forms, nutrient arteries penetrate the centre of cartilage and sponges bone forms since bone mineral matrix covers spongey bone
4 Medullary cavity forms when bone mineral is reshaped and reformed
5 Secondary ossification centre formed as blood vessels enter the epiphyses (around time of birth) Spongey bone is formed here, but no medullary cavity
6 Cartilage remains of ends of bones/ joints as articulate cartilage

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17
Q

How do long bones get longer?

A

1 Cartilage grows on growth plate, on the epiphyseal side
2 Cartilage cells are destroyed and replaced by bone at the metaphysis
3 bone gets longer
4 bone stops growing when the growth plate becomes too thin, this leaves an epiphyseal line

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18
Q

Growth of flat bones

A

Intramembranous Ossification

Bone grows directly from osteoblasts, no growth plate or cartilage formation involves
Fibroblasts differentiate into osteoblasts
Skull plates grow towards each other over time

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19
Q

What is bone made up of?

A

10% organic collagen matrix
65% mineral (hydroxyapatite, insoluble salt of calcium and phosphorus)
25% water
Trace amounts of magnesium, sodium and bicarbonate

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20
Q

4 Types of bone cells

A

Osteoblasts) bone forming cells, secrete type 1 collagen (make the collagen chains that form the new matrix), on surface of bone, control deposition of mineral, becomes osteocytes or undergo apoptosis
Osteoclasts) bone resorbing cells, large cells with many nuclei, umbrella shaped, secrete acids and enzymes that degrade bone, undergo apoptosis when finished
Osteocytes) born from osteoblasts that cipher stuck in matrix, maintains bone matrix, has canniculi, forms gap junctions w neighbouring cells, detects changes in environment
Bone lining cells) flat elongated cells, generally inactive, lines surfaces of inactive bone

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21
Q

How does vitamin D help bone growth?

A

Promotes calcium and phosphorus absorption at the intestine
Regulates osteoblast and osteoclast function

22
Q

Structure of muscle from big to small components

A

Muscle (surrounded by epimysium)
Fascicle (surrounded by perimysium)
Fibre (surrounded by sarcolemma)
Myofibfil
Sarcomere

23
Q

Overview of muscle contraction

A

An action potential is the stimulus that arrives to the muscle
Calcium ions released from sarcoplasmic reticulum
Calcium ions bind to top onion on action filaments
Tropomyosin moves out the way, G actin binding sites becomes exposed
Myosin heads on thick filaments bind to G actin binding sites, Cross bridge formed
ATP on myelin head broken down into ADP and Pi
Power stroke occurs, head pivots and pulls filaments together
Creates a contraction, tension is produced
Another ATP attaches to myosin, cross bridge detaches
Myosin is reactivated

24
Q

Termination of a muscle contraction

A

ACh is broken down
No more generation of action potentials
Calcium ions are reabsorbed into sarcoplasmic reticulum
Active sites are covered, no more cross bridge formation
Contraction ends
Muscle relaxes to resting length

25
Q

Effect of exercise on bone

A

Exercise places compression on bone
Osteocytes act as mechano-sensors that respond to intermittent pressure
Fluid that surrounds osteocytes and canniculi is compressed and creates fluid shear stress
Osteocytes produce nitric oxide
Nitric oxide triggers production of a factor that causes osteoblasts to produce collagen and bone mineral
Leads to increase bone mineral density

26
Q

What to hemopoetic stem cells differentiate into

A

Myeloid stem cells, gives rise to WBS, RBC, platelettes
Lymphoid stem cells, gives rise to lymphocytes

27
Q

What hormone regulates RBC production?

A

Erythropoietin

28
Q

Types of blood cells

A

RBC (erythrocytes), high SA to V ratio, no nucleus or mitochondria, contains haemoglobin, discs bend to enter capillaries, biconcave discs
WBC (leukocytes) nucleated, no haemoglobin, short lived, for inflammation and infection.
Platelets (thrombocytes) no nucleus, replaced by spleen, disc shaped cell fragments, for clotting

29
Q

Hemostasis (clotting process)

A

Vascular phase) smooth muscle wall of vessel damaged, vascular spasm, platelets activated and release vasoconstrictors, response initiated by pain receptors
Platelets phase) platelets form a plug, extend projections to each other, release clotting compounds
Coagulation phase) clotting factors promote formation of prothrombinase, turns into thrombinase, forms thrombin. Thrombin converts fibrinogen into fibrin. Fibrin is meshwork around the plug to stabilise it. Needs calcium.

30
Q

Three layers of heart wall

A

Epicardium) visceral layer on heart
Myocardium) cardiac muscle fibres that provides pumping action. Has high aerobic capacity, lots of mitochondria and glycogen deposits. Contains intercalated discs maintain structure and conduct action potentials.
Endocardium) outer parietal lining

31
Q

2 types of cardiac muscle fibres

A

Autorhythmic fibres) initiate and conduct action potentials

Contractile fibres) provide mechanical pumping action

32
Q

Components of the conducting system in order

A

Sinoatrial node (pacemaker) , spontaneously generates an action potential (depolarises 80-100 times per min)

Atrioventricular node , stimulus spread across atria and reach AV node. Atria contract AV nodal delay allows time for atria to contract and fill the ventricles
(spontaneously depolarises 40-60 times per min)

Action potential spreads across:
Atrioventricular bundle, Right and left branches, Perkinje fibres

Action potential relayed across ventricles and ventricles contract.

33
Q

Cardiac action potential

A

Resting membrane potential is -90mV
1 Rapid depolarisation , voltage gated sodium channels open and influx of sodium ions until 30mV
2 plateau , sodium Chanel’s close rapidly and calcium channels open slowly for a long time. Calcium influx and sodium efflux, balances slow sodium outflow until 0mV
3. Calcium Chanel’s close, voltage gated slow potassium channels open. Potassium efflux until resting -90mV

34
Q

Factors effecting cardiac output

A

HR) hormones (adrenaline, noradrenaline) and autonomic innervation (cardiac centres)
SV) EDV (preload, filling time, venous return) and ESV (preload, afterload, contractility)

35
Q

Blood vessels vs diameter, blood pressure, cross sectional area and velocity of blood flow

A

diameter, veins highest, arteries 2nd highest
blood pressure , arteries highest, veins lowest
cross sectional area , capillaries highest, bell curve
velocity of blood flow , arteries highest, veins second highest

36
Q

Types of lung diseases

A

Obstructive - difficultly to expire
Restrictive - difficulty to inspire

37
Q

Neural control of respiration
Chemical control of respiration
Voluntary control of respiration

A

Neural - involuntary establishment of basic breathing rhythm from medullary oblongata
Dorsal respiratory group - inspiratory centre only, quiet and forced breathing
Ventral respiratory group - inspiratory and expiratory centres, forced breathing only
The neurons in the pons fine tune to adjust breathing rate and depth

Chemical - detects changes in pH, PCO2 and PO2, exert secondary control over breathing
Peripheral chemoreceptors - in aorta and carotid arteries, detect changes in plasma pH
Central chemoreceptors - in medulla, detect changes in pH of cerebrospinal fluid

Voluntary
Cerebral cortex

38
Q

4 Types of receptors

A

Ion channels - allows movement of ions across membrane, usually associated with a activities that reply on transmission of action potentials
Transmembrane receptors with linked enzymatic domains - usually associated with cancer. Ligands binds to receptors and linked enzymatic domain becomes activates and carries out a response.
G protein coupled receptors - crosses the membrane, has seven different transmembrane domains. ligand binds to receptor and activates a G protein, initiates a response.
Intracellular - in cytoplasm and nucleus, binds to DNA and prevent transcription/protein production

39
Q

Variation in cell structure depending on type of cell

A

Fibroblasts involved in forming connective tissue, they make collagen proteins so they need lots of RER, ribosomes and nucleoli
Neurons involved in transmitting information from nervous system and need lots of microtubules to move material from axon terminal to cell body. They produce proteins so need lots of nucleoli.
Macrophages fight disease and engulf bacteria so have lots of lysosomes
Muscle cells need energy to move bone so have lots of mitochondria

40
Q

Cell life cycle

A

I - interphase
G1 - growth and regular cell functions, duplication of organelles
S - DNA replication
G2 - protein synthesis
M - mitosis and cytokinesis

41
Q

Types of active transport

A

Sodium potassium exchange pump , sodium and potassium ions move down their concentration gradients through leak channels
Secondary active transport - important for absorption of glucose and amino acids in digestion
Receptor mediated endocytosis
Phagocytosis

42
Q

Regulation of gastric activity (3 phases)

A

Cephalic phase) sense, see, smell, taste food. Directed by CNS sends submucosal plexus via vagus nerve. Increase gastric secretions from gastric glands and increase motility.
Gastric phase) undigested food arrives at stomach. Triggers stretch receptors and chemoreceptors. Increases enzyme and chemical secretions and increase motility.
Intestinal phase) chyme enters duodenum. Controls rate of chyme existing stomach to maintain efficiency of small intestine. Increases intestinal secretions.

43
Q

Vomiting reflex

A

1 deep inspiration, glottis closes
2 diaphragm and abdominal muscles contract, stomach compressed
3 gastric contents forces through relaxed gastroeosophageal sphincter
4 oesophageal distends and forces contents back down to stomach via peristalsis
5 cycle repeats, retching
6 pressure increases in oesophagus, jaw thrusts out, pharynx sphincter opens, contents forced out

44
Q

Peristalsis vs segmentation

A

Both - smooth muscle contraction in digestive system
Peristalsis is wave like contractions that propel the bolus forward. Circular muscles push forward and longitudinal muscles shorten the tract.
Segmentation is non directional cycles of muscle contraction that churn and fragment the bolus to mix with intestinal secretions and expose greater surface area to mucosa.

45
Q

Secretory cells from gastric glands

A

Chief cells, pepsinogen and gastric lipase
Parietal cells, HCl and intrinsic factor
Mucous cells, mucous
G cells, gastrin

46
Q

Physical and chemical factors that impact haemoglobin affinity to oxygen

A

pH) as pH increases, more oxygen is bound to hameglobin
Temp) as temp increases, more oxygen is unloaded for, haemoglobin
pOH) as pOH increases, the effect of pH is reduced, so more oxygen is unloaded rather than bound to haemoglobin

47
Q

Partial pressures of gases in the lungs and blood

A

Oxygen) 40mmHg in veins, 100mmHg in alveoli, 95mmHg in arteries

Carbon dioxide) 46mmHg in veins, 40mmHg in alveoli, 40mmHg in arteries

48
Q

3 parts of respiratory membranes

A

1 squamous epithelial lining of alveoli
2 endothelial cells lining an adjacent capillary
3 fused basal laminae

49
Q

Hormones that increase BP

A

Adrenaline and noradrenaline
Angiotensin II
ADH

50
Q

How to calculate mean arterial pressure

A

Cardiac output x total peripheral resistance

51
Q

Hormonal control of food intake

A

Ghrelin - appetite stimulant, produce feeling of hunger by stimulating NPY
Leptin - appetite suppressant, secreted by adipose tissue when fat stores increase. acts by inhibiting the appetite stimulant NPY
Insulin and CCK - depress hunger, feelings of fullness when food is absorbed