Metabolism Flashcards
Cellular metabolism
All controlled chemical reactions that occur inside a cell
Anabolic metabolism
Reactions that join molecules together
Catabolic metabolism
Reactions that break molecules apart
Body weight and energy balance
Weight is determined by energy balance and generally has a homeostatic set point
In humans this set pint can vary quite dramatically between individuals
Influence regulation of weight and set point
Hereditary, environmental influence
Appetite - short term regulators
Ghrelin
• Secreted by parietal cells in the fundus of the stomach.
• Produces hunger.
• Stimulates the hypothalamus to secrete GHRH.
Peptide YY (PYY)
• Secreted by enteroendocrine cells of the ileum and colon.
•Primary effect is to signal satiety. ( full and don’t need to eat)
Cholecystokinin (CCK)
• Secreted by enteroendocrine cells in the duodenum and jejunum.
• Stimulates secretion of bile and pancreatic enzymes.
• Stimulates the brain via the vagus nerve to produce an appetite-suppress
Amylin
• Hormone secreted by beta cells of pancreatic islets.
• Produces satièty.
• Slows digestive activities of the stomach.
Appetite - long term regulators
Govern the average rate of calorie intake and energy expenditure over weeks and years.
• Inform the brain about the volume of adipose tissue in the body.
• Activate mechanisms to either add or remove adipose tissue.
Leptin
•Secreted by adipocytes.
•Its level is proportional to an individual’s fat storage.
•Assists the brain in determining the amount of body fat present.
Insulin
•Provides similar functions to leptin.
•Acts as an index of the body’s fat stores.
Metabolism
Metabolism
Represents the total of all chemical reactions in the body.
•Comprises two main processes:
Catabolism
Anabolism
Catabolism
Catabolism
•Energy-releasing process.
•Large molecules are broken down into smaller ones.
•The released energy is utilized for:
•Driving various reactions.
• Processes such as active transport and muscle contraction.
Anabolism
Anabolism
•Energy-requiring process.
•Small molecules are combined to form larger ones.
•Occurs in cells, especially during:
Cell division to produce new cells.
• Formation of substances like fat and protein.
Which of the following is a catabolic process?
C. Breaking down large molecules into smaller ones.
What is the primary characteristic of anabolism?
• C. Energy-requiring.
A monosaccharide is formed from a polysaccharide in what kind of reaction?
Catabolic reaction
Carbohydrates
•Storage in a well-nourished adult:
• Total: Approximately 440g of CHO
• Muscle glycogen: 325g
• Liver glycogen: 90-100g
• Blood glucose: 15-20g
•Functions:
• Mainly serves as fuel for the body
•Some participate in the structural components of other molecules
•Energy Demands:
• Most cells fulfill their energy needs through CHO and fats
• Certain cells rely almost exclusively on CHO, such as:
• Erythrocytes
• Neurons
•Blood Glucose Regulation:
• Achieved through the interplay of glucagon and insulin.
Fats
Adults derive 80-90% of their resting energy requirements from fat.
Fat represents the primary form of stored energy in the body.
Essential roles of specific fats:
• Phospholipids and cholesterol:
Play vital structural roles in cell membranes.
• Have significant physiological functions within the body.
Advantages of Fat over Carbohydrates (CHO):
• Hydrophobic nature:
Offers a higher energy source.
Provides greater energy yield than CHO.
• Glucose and protein sparing effect:
When sufficient fat is available, glucose is reserved primarily for cells that rely heavily on it, such as neurons.
Role in Vitamin Absorption:
• Vitamins A, D, E, and K require fat for effective absorption.
Consequences of Inadequate Fat Intake:
• Insufficient dietary fat can lead to deficiencies in fat-soluble vitamins.
Protein
Constituent in the Body:
• Makes up approximately 12-15% of body mass.
• 65% of this is found in skeletal muscle.
Functional Roles:
• Enables muscle contraction. Cause muscles are made of it
• Facilitates the motility of cilia and flagella.
• Plays a significant role as a structural component in cellular membranes and other structures.
•Provides pH stability in blood. Buffering effect
• Assists in blood clotting.
• Aids in gas transportation in the blood.
Specific Protein Types:
• Structural Proteins:
• Collagen: Provides structural strength to connective tissues.
• Keratin: Provides structural strength to skin.
• Transport Proteins: Help in the transport of various molecules.
• Receptor Molecules: Receive and transmit signals in the body.
Energy Role:
Can serve as an energy when others are being used least preferred. Eg starvation break down muscles to get energy
Cho metabolism
•Most dietary carbohydrates (CHO) are metabolised within a few hours after absorption.
•The catabolic reaction for glucose is:
• CgH1206 + 6 02 - 6 CO2 + 6 H20 + ATP
The primary goal of this reaction is:
• Transfer energy from Glucose to ATP
• NOT the production of carbon dioxide and water.
Glucose catabolism
Digestion & Absorption
Large nutrient molecules are broken down into smaller molecules.
• These smaller molecules are then absorbed into the blood.
ATP Synthesis
• Molecules are taken into cells and catabolised.
• The energy from catabolism is used to combine ADP and Pi, forming ATP.
• ADP + Pi + Energy = ATP
Oxidation-Reduction Reactions
• Chemical reactions transfer energy from chemical bonds in glucose to ATP.
• These reactions involve oxidation-reduction processes.
• A molecule is reduced when it gains electrons.
• A molecule is oxidised when it loses electrons.
Phosphorylation Sites
• Phosphorylation occurs in:
• The cytoplasm during glycolysis.
• The mitochondrial matrix during the Krebs cycle.
Which of the following is a monosaccharide?
Glucose
When a molecule gains electrons, it is:
C. Reduced
During which of the following processes does a molecule lose electrons?
Glucose catabolism
Pathways of Glucose Breakdown:
• Glycolysis:
•Splits one glucose molecule into two pyruvate molecules.
• Produces a net gain of 2 ATP and 2 NADH.
• Anaerobic Fermentation:
•Converts pyruvate to lactate in the absence of 02.
• Notable in muscle cells during intense activity.
• Aerobic Respiration (requires 02):
• Requires 02.
• Oxidizes pyruvate to produce COz and H2O.
• Involves the Krebs cycle and the Electron
Transport Chain in the mitochondria.
Coenzymes
• Enzymes remove electrons (H+) from compounds, but don’t bind them. They give them to coenzymes that add to other compounds in later reaction pathways.
FAD + 2 H* -> FADH,
NAD* + 2 H+-> NADH + H+
Glycolysis fist step (energy consumption stage)
2 ATPs consumed in this phase
Phosphorylation of Glucose
• Glucose + ATP -> Glucose-6-phosphate (G6P) + ADP
• Traps glucose inside the cell
Conversion to Fructose
Glucose-6-phosphate is converted to its isomer, Fructose-6-phosphate
Second Phosphorylation:
• Fructose-6-phosphate + ATP _› Fructose- 1,6-bisphosphate + ADP.
• Addition of the second phosphate prepares the sugar for cleavage in the next steps.
Glycolysis - Cleavage
Cleavage of the 6-Carbon Sugar:
• Fructose- 1,6-bisphosphate is split into two 3-carbon
molecules:
• Dihydroxyacetone phosphate (DHAP) and
Glyceraldehyde-3-phosphate (PGAL).
• DHAP is rapidly and reversibly converted into another molecule of Glyceraldehyde-3-phosphate (PGAL).
This concludes the energy-consuming phase where:
• Glucose is primed with high-energy phosphate groups
• Then divided into two 3-carbon molecules.
Glycolysis - Oxidation of PGAL
Oxidation and Phosphorylation of PGAL
Glyceraldehyde-3-phosphate (PAL) undergoes:
• Oxidation, transferring electrons and protons to NAD+, resulting in NADH + H+.
• Concurrent phosphorylation with inorganic phosphate (Pi), producing 1,3-bisphosphoglycerate (1,3-BPG).
Glycolysis - ATP Formation - dephosphorylation
ATP Formation 1
• 1,3-Bisphosphoglycerate transfers a phosphate to AD creating ATP.
• This occurs twice per glucose, yielding 2 ATPs.
ATP Formation 2
• Phosphoenolpyruvate (PEP) transfers its phosphate to
ADP, forming ATP.
• Also happens twice per glucose, yielding an additional 2 ATPs.
At the end of glycolysis, one molecule of glucose has been converted into two molecules of pyruvate.