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CARBOHYDRATE METABOLISM
- Carbohydrates are normally transported as glucose substances
- BUT glucose is not suitable for storing in liver and muscle cells
- so its converted into Glycogen
- So as the Blood glucose level rises
- Beta cells in the Islet of Langerhans (Tissue in Pancreas)
- Secretes Insulin
- This stimulates the conversion of glucose in Glycogen
- Insulin also has this effect on muscle cells and fat in the adipose tissue
- it increases the rate at which glucose is metabolised so the blood levels return to normal
- IF the level is too low
- then the Alpha Cells in the Islets of Langerhans secrete Glucagon
- Glucogon converts the stored glycogen into glucose
- It does this by binding to glycoprotein receptors on the plasma membranes of hepatocytes
- This results in a series of events of Glycogenolyisis
- The glucose then passes out of the hepatocytes raising the blood level
- ADRENAL GLANDS also play a part
- Adrenaline has the same effect of Glucogen
- Under Stress glycogen is broken down into Glucose
- So the respiratory substrate is available as extra fuel - adrenaline associated with fight or fly thing? so it prepares body for the "fight"
- GLUCONEOGENESIS - Conversion of Amino acids, lipids, pyruvates and Lactate into glucose
- This happens is response to glucogen when all glycogen in liver and muscle cells has been exhausted
- Amino acids are converted into glucose by deamination
- the nitrogen containing part is converted to urea and excreted by the kidneys
- The rest are molecules are pyruvates which are converted to molecules of Triose Phosphates and then into glucose
- The Lactate is used in anaerobic respiration in the muscles
- It is then taken in by hepatocytes and converted into Pyruvates
- the Pyruvates are then converted into Triose Phophates then into glucose
- the lipids (Glycerol) is converted into Triose Phosphates which are then converted into glucose
- FATTY ACIDS NOT CONVERTED
PROTEIN METABOLISM
- TRANSAMINATION is the conversion of one type of amino acid to another
- However some amino acids can only be obtained from diet (Essential amino acids)
- Excess amino acids cannot be stored by the body so are converted into urea in the ORNITHINE CYCLE
- the NH3 is deaminated from amino acids
- ONLY THE NH3 GROUP IS EXCRETED
- NH3 + CO2 + ATP react with ORNITHINE. Another ATP molecule is used to form CO(NH2)2 = UREA which is released by hepatocytes into the blood and excreted via the kidney
- Ornithine is reproduced and the cycle repeats
MUSCLE CONTRACTION
- OK so muscle contraction is when the actin filaments slide into the Myosin filaments
- This will cause the sarcomere to decrease in length
- The actin filament has two extra proteins
- In the myosin head, there are enzymes called ATPases which catalyse the reaction of
- ATP --> ADP + Pi
- When a nerve impulse arrives the usual thing happens between the presynaptic and post synaptic membrane - which happens to be the muscle fibre
- Due to the arrival of action potential, Calcium channels open
- Inlux of Ca2+ - cause vesicles of Acetylcholine (ACh) to fuse with presynaptic membrane - EXOCYTOSIS
- ACh bind to receptors in sarcolemma and sodium channels open
- Na+ ions flood through - Action potential is continued across the membrane
- This depolarisation spreads to the T- tubule
- Causes Ca2+ channels to open - Ca2+ diffuse out of Sarcoplasmic reticulum
- Ca2+ binds to tropomyosin and troponin
- This causes the Tropomyosin and troponin to move ans expose the myosin head and its binding sites
- the Actin filament can now bind to myosin head.
- The Myosin head tilts (45 deg.) so the actin filaments move
- this causes the release of ADP + Pi
- Now ATP binds to myosin head
- Enzymes in myosin head hydrolyse ATP --> ADP + Pi
- this relseases energy causing the myosin head and actin filament to unbind
- Actin filament moves back and myosin head flips away
Comments
These notes are aimed at people studying Edexcel Biology A Level, but will be suitable for other exam boards too.
Originally written by DBSK<3 on TSR Forums.