Title: PHASE 1 Revision
1 IMMS (2)
- PHASE 1 Revision
- Akanksha Sinha
- Regina Sarbaratnam
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2Aims - Overview
- METABOLISM
- (Carbohydrates, Protein, Lipid, Alcohol,
Glycogen) - ATP
- (ATP-ADP cycle, Glycolysis, Krebs cycle,
Oxidative Phosphorylation) - FATTY ACID OXIDATION/KETONES
- (Beta oxidation, Ketogenesis)
- ACID/BASE/BUFFER (Henderson-Hasselbach equation)
- OXYGEN TOXICITY (ROS, Haber-Weiss and Fenton
reactions) - HISTOLOGY (Stains, Epithelia)
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3Metabolism
- The chemical processes that occur within a living
organism in order to maintain life
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4Metabolism
4 main energy sources Carbohydrates Starch,
fructose, sucrose, glucose, lactose Mainly come
from starchy foods and fruit. Proteins Largely
come from meat ,dairy ,pulses , fish Alcohol
typically ethanol Lipids triacylglycerols
4kcal/g 4kcal/g 7kcal/g 9kcal/g
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5What happens to the excess energy intake?
- 1. Stored as triglycerides (approximately 15kg)
- 2. Stored as glycogen (approximately 200g in
liver, 150g in muscle) - 3. Stored as protein (approximately 6kg)
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6BMR
Energy needed to stay alive at rest
- Increase BMR
- Increased body weight
- Hyperthyroidism
- Low ambient temperature
- Fever/infection
- Caffeine/stimulant intake
- Pregnancy
- Decrease BMR
- Increased age
- Being female
- Dieting/Starvation
- Hypothyroidism
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7ATP
ATP Adenosine Triphosphate Structure
components Adenine, Ribose, 3 Phosphate
How does it provide Energy?
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8ATP
- -The ATP molecule has two phosphoanhydride bonds.
- These are RELATIVELY WEAK bonds, hence require
relatively less energy to break - Overall more energy is released in forming the
products that used to break bonds in the
reactants
ATP
Hydrolysis
ADP
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9ATP-ADP Cycle
ATP
CO2
Respiration Energy production Carbohydrate Lipid
Protein
Energy utilization Biosynthesis of
macromolecules Muscle contraction Active ion
transport Thermogenesis
ADP Pi
O2
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10ATP- ways to generate ATP?
- Glycolysis
- Krebs cycle
- Oxidative phosphorylation
- Substrate level phosphorylation
- Via electron transport chain
- Beta oxidation (Discussed in fatty acid oxidation)
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11Glycolysis
- Glycolysis
- Pathway of 10 steps
- Takes place in cytoplasm
- In short Glucose ?
- 2Pyruvate 2ATP 2NADH (AEROBIC)
- 2Lactate 2ATP (ANAEROBIC)
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12Glycolysis
Energy Investment Phase - 2 ATP
Energy Generation Phase 4 ATP
Glycolysis generates a NET 2 ATP plus 2 NADH
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13Step 1
- Facilitated diffusion of Glucose into cell
mediated by Insulin - Phosphorylation of Glucose by Hexokinase
- -ATP
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14Step 2
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15Step 3
- F6P? F1,6BP
- Via phosphofructokinase (PFK is primary regulated
step of glycolysis responds to both cellular
energy and hormonal regulation) - -ATP
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16Step 6-10
- 6 NADH (x2) produced
- 7 ATP (x2) produced
- 8
- 9
- 10 2Pyruvate ATP (x2) produced
- Remember all the enzymes
- Good Gracious, Father Franklin Did Go By Picking
Pumpkins (to) Prepare Pies
Pyruvate enters the TCA cycle
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17Acidosis affecting glycolysis
- PFK1 is pH dependent
- Inhibited in acidosis
- Control of glycolysis via
- Step 1
- Step 3 -key regulatory step in glycolysis
Positive regulators AMP
Negative regulators H, ATP, Citrate, hormonal
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18Krebs/ TCA cycle
In Mitochondrial matrix Acetyl CoA can come from
glycolysis/ fatty acid breakdown/ amino acids
carbon skeletons
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19Krebs/TCA cycle
- Inhibited by ATP, NADH, succinyl CoA
- Activated by ADP
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20Electron Transport Chain
- The electron transport chain (ETC) is a process
in which the NADH and FADH2 produced during
glycolysis, ß-oxidation, and other catabolic
processes are oxidized - thus releasing energy in the form of ATP. The
mechanism by which ATP is formed in the ETC is
called chemiosmotic phosphorylation
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21The chemiosmotic theory
- Based on the following
- -inner mitochondrial membrane is impermeable to
protons, hence the mitochondrial matrix is a
closed environment - -the proton pumping of the ETC leads to the
proton motive force which in turn provides the
energy for ATP synthesis (Proton flow through the
ATP synthase protein drives ATP synthesis)
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22The chemiosmotic theory
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23Substrate level phosphorylation
- some ATP can be made in the cytoplasm through a
process called substrate-level phosphorylation - With this type of phosphorylation you have an
adenosine diphosphate (ADP), which is a unit of
adenosine attached to two (di) phosphate groups
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24- oxidative phosphorylation
-
- Oxidative phosphorylation is the metabolic
pathway in which the mitochondria in cells use
their structure, enzymes, and energy released by
the oxidation of nutrients to reform ATP - (involves ETC!!!)
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25TOTAL ATP
- Total ATP made from one molecule of glucose
- 34 ATP
- But this is very debatable
- Some sources will say 30 or 32 ATP
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26Fatty acid oxidation/ Beta oxidation
- Examples of fatty acids
-
- Palmitoleic acid
- Linoleic acid
- Palmitic acid
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27Fatty acid oxidation/ Beta oxidation
Fatty Acid
Acetyl CoA (used in TCA/Krebs cycle)
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28Fatty acid oxidation/ Beta oxidation
ATP
PPi
Fatty Acid
Acyl adenylate
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29Fatty acid oxidation/ Beta oxidation
CoA
AMP
Acyl adenylate
Acyl CoA
Acyl CoA synthetase
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30Fatty acid oxidation/ Beta oxidation
The carnitine shuttle !!!
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31The Carnitine Shuttle
Carnitine
CoA
Acyl CoA
Acyl Carnitine
Carnitine Acyl Transferase I
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32Inner mitochondrial membrane
CoA
Carnitine
Acyl Carnitine
Acyl CoA
Carnitine Acyl Transferase II
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33Fatty acid oxidation/ Beta oxidation
Acetyl CoA
Acyl CoA
Acyl CoA 2C
- Sequential removal of 2- carbon units
- Each round of ß-oxidation produces
- 1 mole of NADH
- 1 mole of FADH2
- 1 mole of acetyl-CoA
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34Ketogenesis
- The process by which ketone bodies are produced
as a result of fatty acid breakdown. - Ketones are used for energy at low fat states.
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35Ketogenesis
2 Acetyl-CoA
CoA-SH
thiolase
Acetoacetyl-CoA
Acetyl-CoA H20
HMG-CoA synthase
CoA-SH
HMG-CoA
HMG-CoA lyase
Acetyl-CoA
Acetoacetate
Acetone
ß- hydroxybutyrate
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36I know, no pathology
Diabetic ketoacidosis
- Reduced supply of glucose due to a significant
decline in circulating insulin and an associated
increased in circulating glucagon. - The increased production of Acetyl-CoA leads to
ketone body production - This lowers the pH of the blood
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37Acid/Base/Buffer
- Acid proton (H) donor
- HA ? H A-
- Base proton (H) acceptor
- B H ? BH
- Buffer weak acids or bases that act to maintain
H concentration
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38Acid/base/buffer
- Acidosis can either be respiratory or metabolic
- Alkalosis can either be respiratory or metabolic
- pH range is 7.35-7.45. But ideal pH is 7.4
- Compensation metabolic is slow, respiratory is
fast.
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39Henderson-Hasselbalch equation
- Hendersons formula-
- H x HCO3 - K x pCO2
- Hasselbalch converted it to pH
- pH pK log (HCO3 - / CO2)
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40Acidosis
Carbonic anhydrase
- Respiratory
- Insufficient ventilation retains CO2 so there is
more carbonic acid in the blood leading to
acidosis - Causes include COPD (chronic bronchitis
emphysema), asthma
- Metabolic
- Low bicarbonate levels leading to acidosis
- Causes include bicarbonate losses from the GI
tract e.g. diarrhoea, DKA, lactic acidosis
(anaerobic respiration), renal failure
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41Alkalosis
- Respiratory
- Blowing off too much CO2 leading to alkalosis
- Causes hyperventilation, pink puffers COPD (i.e.
type 1 respiratory failure), anxiety, fever
- Metabolic
- Loss of H or too much bicarbonate leading to
alkalosis - gastric secretions contain large quantities of
hydrogen ions. - Causes include excess vomiting (because youre
losing H), pyloric stenosis, anorexia nervosa,
ingestion of bicarbonate
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42Anion Gap
- The anion gap is calculated by subtracting the
serum concentrations - of ANIONS (Cl- and HCO3-) from the concentrations
of CATIONS (Na and K) - BUT
- Â potassium concentrations, being very low,
usually have little effect on the calculated gap.
This leaves the following equation - Anion gap Na - (Cl- HCO3-) 16 meq/lit
The magnitude of this difference (i.e., "gap") in
the serum is often calculated when attempting to
identify the cause of metabolic acidosis. If
the gap is greater than normal, then high anion
gap metabolic acidosis is diagnosed (due to
increased cation H)
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43Types of Buffer systems
- Proteins (51)
- Weak acid/base groups
- Bicarbonate (43)
- CO2 removed via lungs, Bicarbonate regenerated by
kidneys - Haemoglobin (6)
- Deoxy Hb binds H ? HHb Bicarbonate
- Amine group on Deoxy Hb bind CO2
?carbaminohaemoglobin
? Most important
Haemoglobin binds both CO2 and H and so is a
powerful buffer
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44Oxygen Toxicity
- Toxic reactive oxygen derivatives with
- Free radicals
- Unpaired electrons in outer shell
- High reactivity
- OR
- DEF Chemically reactive molecules with unpaired
electrons in outer shell free radicals
(unpaired electron) derived from oxygen
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45Formation of ROS
Generates radicals with transition metals (Fenton
or Haber Weiss rx)
Produced by ETC
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46ROS
- OH (hydroxyl radical)
- Most potent radical
- Lipid soluble
- Chain reaction forms lipid peroxides organic
radicals - H202 (hydrogen peroxide)
- Not actually a radical
- Oxidising agent in presence of Fe2 or other
transition metals - Generates hydroxyl radical
- Lipid soluble
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47Formation of hydroxyl radical
Haber-Weiss reaction
Fenton reaction
-
O2
H2O2
H2O2
Fe2
H
O2
Fe3
H2O
OH
OH
OH-
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48Production of ROS
- Endogenous
- natural by-product of O2 metabolism
- Produced mainly inside cell organelles ie.
(mitochondria) - Exogenous
- UV radiation, smoking, inflammation
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49ve ROS
- Respiratory bursts
- ROS released during phagocytosis of bacteria
- Damages bacterial cell membrane
- Fentons reaction
- O2 ? O2-?H2O2Fe2?Fe3 OH- OH
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50-ve ROS
- Cellular damage
- Damage to membranes of nucleus, mitochondria,
endoplasmic reticulum cell - Increased permeability leads to influx of
calcium, water sodium
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51Anti-oxidants
- Enzymes
- Catalase H2O2 ? 2 H20 02
- Superoxide dismutase O2- ? H2O2
- Glutathione peroxidase
- Antioxidant vitamins/Free radical scavengers
(vitC, vitE, carotenoids) - Cellular Compartmentation
- Repair
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52Histology of Epithelia
- Roles of epithelia
- Protection(skin)
- Absorption(gut)
- Secretion(pancreas)
Simple Epithelium
Stratified Epithelium -Almost always squamous
Pseudo-stratified Epithelium
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53Simple squamous epithelia
Found in -Alveoli -Serosa
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54Simple cuboidal epithelia
- Found in
- -Kidney tubules
- -Ducts of glands
- Sweat
- Salivary
- Pancreatic
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55Simple columnar epithelia
- Found in
- -Small intestine
- -Gall bladder
- -Bronchus
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56Stratified epithelium
- Protection
- Continually being worn down
- Cells replaced from below
- Found in areas where there is continuous abrasion
- Squamous
- ?Keratinised skin
- ?Non keratinised mouth, oesophagus, vagina
- Cuboidal
- found in some large ducts
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57- Stratified squamous non-keratinising
- Found in
- Mouth
- Oropharynx
- Oesophagus
- Vagina
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58Stratified squamous keratinising
- Found in
- -Skin (hairy or non-hairy skin)
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59Pseudostratified columnar epithelia
- Found in
- Trachea and large airways (respiratory
epithelium) - Urinary tract
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60Cell Junctions
- 1) Adherent (tight) junctions
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61Cell Junctions
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62Cell Junctions
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63Staining
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64Alcian Blue
GAG-rich structuresMucous goblet cellsMast
cell granulesCartilage matrix
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65Staining
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66Eosin
Colloidal proteins (e.g. plasma)Keratin
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67Staining
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68Haematoxylin
NucleiRNA
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69Staining
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70PAS
Hexose sugars
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71Questions?
asinha1_at_sheffield.ac.uk rcsabaratnam1_at_sheffield.a
c.uk
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