Glycolysis is the most common pathway for glucose metabolism.
However, other pathways exist, such as the lactate pathway.
The lactate pathway occurs when there is a lack of oxygen (anaerobic conditions).
Lactate utilization increases during oxygen deficits.
Glucose and lactate are heavily emphasized in the quiz.
Around half the test focuses on glucose and lactate.
Glucose converts to pyruvate during glycolysis.
Pyruvate then metabolizes to acetyl CoA.
Three major products of glycolysis:
Pyruvate
Acetyl CoA
Lactate
Glucose is NOT a product of glycolysis; it's the starting reactant.
Gluconeogenesis: A pathway where glucose is synthesized, essentially reversing glycolysis.
When you eat sugar, you get glucose.
Glucose goes through glycolysis (breaking down of sugar).
Glycolysis yields pyruvate, acetyl CoA, and sometimes lactate, depending on conditions.
Excess glucose is stored as glycogen in the liver.
During starvation or low glucose levels, glycogen is converted back to glucose via gluconeogenesis.
Glycogen storage and release are carefully regulated by insulin and glucagon.
Insulin increases when you eat, while glucagon is low.
When hungry (starvation mode), insulin is low, and glucagon is high (to convert glycogen back to glucose).
Insulin and glucagon are inversely proportional.
Insulin carries glucose into the cell.
Insulin is NOT needed to transport glucose to the brain; glucose diffuses freely.
Gluconeogenesis synthesizes glucose when there aren't enough carbohydrates available.
It can utilize lactate, amino acids (from protein), and fats to make glucose.
The Cori cycle occurs when muscles are at rest, contributing to glucose levels at a lesser rate.
Fatty acids are used to burn fats and obtain energy.
The fatty acids are broken down, producing acetyl CoA units.
ATP is converted to AMP during fatty acid breakdown, losing two phosphate groups (burning more energy).
ATP \rightarrow AMP (loss of two phosphate groups)
Burning fats requires a lot of energy.
Fatty acids are long chains, and their catabolic breakdown produces acetyl CoA, which helps make ATP.
Fatty acids are used as energy when there are no more carbohydrates to burn.
When not enough carbohydrates are available, the body turns to triglycerides (fats).
Beta oxidation in fatty acids produces a large amount of acetyl CoA.
The beta chain of fatty acids has a large amount of acetylcholine. For example, it produces nine acetyl CoA compared to 2 from glucose.
If the citric acid cycle cannot process all the extra acetyl CoA, it turns into ketone bodies (ketogenesis).
Small amounts of ketone bodies are fine, but large amounts cause problems.
Acetyl acetate is a ketone body, and it can turn into acetone.
Acetone breath is a byproduct of ketone bodies.
Ketone bodies are soluble in blood and urine. High levels in urine indicate ketosis and starvation.
Keto diets are generally safe because you're still eating something; the body isn't pushed to extreme acidosis.
In pure ketoacidosis (long-term starvation), acid builds up, lowering blood and urine pH.
Low blood pH denatures proteins and damages organs like kidneys.
Low pH can also affect the brain, leading to a coma as a protective mechanism.
Diabetic ketoacidosis occurs because, in diabetics, glucose doesn't enter the cell, causing cellular starvation.
This leads to ketogenesis and acid buildup.
The brain has enough glucose but shuts down due to acidity in the blood, not lack of glucose.
Diabetic ketoacidosis is more common in type 1 diabetes.
Treatment focuses on addressing the acidity with IV fluids.
Three pathways from glucose breakdown:
Pyruvate
Acetyl CoA
Intermediate pathway (e.g., lactate)
Remember, these pathways break down glucose, not create it, unless it's gluconeogenesis.