Metabolism and Organ Function Practice Flashcards
Metabolic Processes and the Starvation Cycle
The Body's Resource Consumption Sequence:
When the body is fasting or starving, it follows a specific hierarchy of energy source utilization.
Carbohydrates and Glycogen: The body first uses all available carbohydrate stores, including any sugar stores and glycogen.
Proteins: Once sugar stores are exhausted, the body enters a phase of "eating itself." It begins to break down proteins for energy, starting with the muscles.
Fats: Fat stores are metabolized after the body has begun utilizing protein reserves.
Gluconeogenesis and Nutritional Strategies
Definition of Gluconeogenesis: This is the process of generating glucose from non-carbohydrate sources, specifically protein breakdown.
Organ Site: Gluconeogenesis occurs primarily in the liver.
Bodybuilding and Muscle Preservation:
If an individual does not eat carbohydrates, they can lose muscle mass because the body will utilize proteins for fuel via gluconeogenesis.
Bodybuilders are advised to eat a combination of carbohydrates and significantly more proteins.
Mechanism: Carbs are consumed to be used as primary fuel, allowing the dietary protein to go toward building muscle walls and tissue rather than being "cut" or used for energy production.
Fundamental Principle: "You can't grow without eating."
Fasting Caution: It is emphasized that one should not eat too quickly or excessively after a fast, as metabolic processes need to stabilize. Additionally, when trying to metabolize or exercise, consuming too much fat is discouraged.
Lactic Acid and Tissue Perfusion
Tissue Perfusion: Defined simply as "flow" or circulation. Poor tissue perfusion means inadequate blood circulation.
Shock and Anaerobic Glycolysis:
Patients in shock experience poor tissue perfusion, leading to a rise in lactic acid.
The rise in lactic acid is explained by cells utilizing anaerobic glycolysis.
Mechanism: When cells lack oxygen (anaerobic conditions), they break down sugar without oxygen, which produces lactic acid as a byproduct.
Lipids: Triglycerides, Structures, and Functions
Triglyceride Composition: Triglycerides consist of one glycerol molecule (which is a glucose) and three fatty acids.
Sugar and Fat Relationship: Excessive sugar consumption leads to high triglycerides because sugar turns into fat. Without the sugar molecule, there is no binding with the fatty acids to form the triglyceride.
Storage: Triglycerides are stored as fuel and eventually become adipose tissue.
Functional Roles of Lipids:
Insulation: Adipose tissue keeps the body warm during cold temperatures.
Cell Walls: Lipids help secure cell walls; specifically, cell membranes are made out of phospholipids.
Transport: Lipids travel through the blood as LDOs (low-density lipoproteins) and HDOs (high-density lipoproteins).
Steroid Production: Lipids are essential for making steroids, including cholesterol, Vitamin D, and sex hormones such as testosterone.
Metabolic Breakdown: Lipids break down into fatty acids, which then break down into Ketones.
Protein Metabolism and Liver Function
The Liver as a Protein Factory: The liver is responsible for producing a wide array of essential proteins.
Synthesized Proteins:
Hemoglobin
Antibody (Antibodies)
Enzymes
Albumin
Clinical Correlation (Liver Cirrhosis):
Damage to the liver (e.g., via alcohol consumption) disrupts these functions.
Failure to produce proteins like albumin leads to issues with water regulation in the tissues (edema).
Knowledge of organ function is prerequisite to understanding signs and symptoms of diseases.
Nitrogenous Waste and the Urea Cycle
Amino Acid Breakdown: When proteins/amino acids are broken down in the liver, they produce nitrogenous waste.
Chemical Components: The body is made of "CHON" (Carbon, Hydrogen, Oxide, Nitrogen). Nitrogen is a byproduct of the 90% protein breakdown occurring in the liver.
The Waste Pathway:
Protein Consumption: Protein is eaten and moves to the small intestines.
Absorption: The small intestines absorb amino acids and send them to the liver.
Liver Processing: The liver breaks down amino acids, recycling some and turning others into nitrogenous waste.
Ammonia Production: The liver makes ammonia (a toxic gas).
Urea Conversion: The liver converts ammonia into urea.
Kidney Excretion: The urea is sent to the kidneys and excreted as urine.
Clinical Lab Values and Diagnostics
Creatinine: Used to check kidney function.
Normal range: to
Levels above indicate potential kidney failure.
BUN (Blood Urea Nitrogen):
Normal range: to
Levels above are highly concerning for kidney failure. Elevated levels (e.g., ) may simply indicate dehydration.
Albumin: Used to check for liver failure.
Normal range: to
A level of indicates the liver is not functioning correctly.
Ammonia: Used to check for liver dysfunction.
Normal range: Generally under . Anything greater than is noted as elevated.
Hepato Encephalopathy and Mental Status
Hepato Encephalopathy: A condition where high ammonia levels ( > 75) affect brain circulation.
Symptoms: Irritability to the brain and changes in mental status (acting "crazy" or not like themselves).
Metabolic Assessment for Mental Change: When an elderly patient has a mental status change, always check:
Oxygen levels.
Glucose levels.
Ammonia levels.
Check for UTIs (Urinary Tract Infections).
Questions & Discussion
Q: What are amino acids?
A: Proteins (the building blocks of proteins).
Q: Where does gluconeogenesis happen in? What organ?
A: The liver.
Q: If you don't eat carbs, can you lose your muscles?
A: Yes, because of gluconeogenesis.
Q: Why is lactic acid building up in a shock patient?
A: Because the cells have no oxygen; they are using anaerobic glycolysis.
Q: What do triglycerides consist of?
A: One glycerol and three fatty acids.
Q: Which organ makes ammonia?
A: The liver.
Q: Which organ turns ammonia into urea?
A: The liver.
Q: Which organ gets rid of urea?
A: The kidneys.
Q: Where does nitrogen come from?
A: Protein breakdown.
Q: Any question on LDOs and HDOs?
A: [No response recorded].