BackNutrition, Metabolism, and Energy Balance: Study Notes for Human Anatomy & Physiology
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Protein Metabolism
Overview of Protein Metabolism
Proteins in the body are constantly being broken down and replaced. Unlike carbohydrates and fats, proteins are not stored for future use. When dietary proteins are in excess, amino acids are either oxidized for energy or converted to fat for storage.
Deamination: The first step in amino acid breakdown, where the amine group (NH2) is removed.
Fate of Amino Acids: After deamination, amino acids are converted into pyruvic acid or keto acid intermediates of the citric acid cycle.
Three Events of Amino Acid Degradation
Transamination: Transfer of an amine group from an amino acid to α-ketoglutaric acid, forming glutamic acid and a keto acid.
Oxidative Deamination: In the liver, the amine group of glutamic acid is removed as ammonia (NH3), which combines with CO2 to form urea, excreted in urine.
Keto Acid Modification: Keto acids are altered to produce metabolites (e.g., pyruvic acid, acetyl CoA) that enter the citric acid cycle or contribute to gluconeogenesis.

Example: During fasting, muscle proteins are broken down, and amino acids are used for gluconeogenesis in the liver.
Catabolic-Anabolic Steady State
Dynamic Metabolic State
The body is in a continuous state of breaking down (catabolism) and rebuilding (anabolism) organic molecules. Nutrient pools of amino acids, carbohydrates, and fats are interconvertible, with the liver, adipose tissue, and skeletal muscle directing these conversions.
Amino Acid Pool: Used for protein synthesis, amino acid derivatives, and gluconeogenesis.
Carbohydrate and Fat Pools: Easily interconverted and directly oxidized for energy; excess can be stored, but amino acids cannot be stored as proteins.

Metabolic States of the Body
Absorptive (Fed) State
The absorptive state lasts about four hours after eating, during which anabolism exceeds catabolism and nutrients are stored.
Carbohydrates: Glucose is used for energy or stored as glycogen/fat.
Triglycerides: Hydrolyzed and used for energy or stored in adipose tissue.
Amino Acids: Used for protein synthesis or converted to fat if in excess.

Hormonal Control: Insulin is the primary hormone, promoting glucose uptake, glycogen and fat synthesis, and protein synthesis.

Postabsorptive (Fasting) State
When the GI tract is empty, the body relies on stored reserves. Catabolism exceeds anabolism, and the goal is to maintain blood glucose for organs like the brain.
Sources of Blood Glucose: Glycogenolysis (liver and muscle), lipolysis (adipose tissue), and protein catabolism (during prolonged fasting).
Glucose Sparing: Most tissues use fatty acids, sparing glucose for the brain; ketone bodies are produced during prolonged fasting.

Hormonal Control: Glucagon is the main hormone, stimulating glycogenolysis, gluconeogenesis, and lipolysis. The sympathetic nervous system and other hormones also play roles.

Hormonal Influences on Metabolism
Hormone | Effect on Metabolism |
|---|---|
Insulin | Stimulates glucose uptake, glycogenesis, lipogenesis, protein synthesis; inhibits gluconeogenesis and glycogenolysis |
Glucagon | Stimulates glycogenolysis, gluconeogenesis, lipolysis |
Growth Hormone | Stimulates protein synthesis, lipolysis |
Thyroxine | Increases metabolic rate, stimulates glucose and fat metabolism |
Cortisol | Stimulates gluconeogenesis, protein breakdown |
Testosterone | Stimulates protein synthesis |

Metabolic Role of the Liver
Functions of the Liver in Metabolism
The liver is central to metabolic regulation, processing nutrients, regulating cholesterol, storing vitamins/minerals, and detoxifying substances.
Metabolic Process | Function |
|---|---|
Carbohydrate Metabolism | Glycogen storage, glucose release, gluconeogenesis |
Fat Metabolism | Beta-oxidation, lipoprotein synthesis, cholesterol synthesis |
Protein Metabolism | Deamination, urea formation, plasma protein synthesis |
Vitamin/Mineral Storage | Stores vitamins A, D, B12, iron, copper |
Biotransformation | Detoxifies drugs, hormones, bilirubin |

Cholesterol Metabolism and Regulation
Cholesterol Transport and Lipoproteins
Cholesterol is essential for cell membranes, bile salts, and steroid hormones. It is transported in the blood by lipoproteins:
HDLs (High-Density Lipoproteins): Remove excess cholesterol from tissues to the liver.
LDLs (Low-Density Lipoproteins): Deliver cholesterol to tissues; high levels are linked to atherosclerosis.
VLDLs (Very Low-Density Lipoproteins): Transport triglycerides from the liver to tissues.
Chylomicrons: Carry dietary lipids from the intestine to tissues.

Recommended Levels: Total cholesterol < 200 mg/dl, HDL > 60 mg/dl, LDL < 100 mg/dl.
Energy Balance and Regulation of Food Intake
Energy Balance
Energy intake must equal energy output for weight stability. Energy output includes heat, work, and storage. Nearly all food energy is eventually converted to heat, which maintains body temperature and allows metabolic reactions.
Regulation of Food Intake
Food intake is regulated by hypothalamic centers, neural and hormonal signals, and psychological factors. Short-term controls include neural signals from the GI tract and nutrient levels; long-term controls involve hormones like leptin.

Short-term: Vagal signals, blood glucose, gut hormones (insulin, CCK, ghrelin).
Long-term: Leptin from adipose tissue suppresses appetite.
Metabolic Rate and Body Temperature Regulation
Metabolic Rate
Metabolic rate is the total heat produced by the body. Basal metabolic rate (BMR) reflects energy needed for essential activities and is influenced by age, gender, temperature, stress, and thyroxine.
Body Temperature Regulation
Body temperature is maintained by balancing heat production and loss. The hypothalamus acts as the main thermoregulatory center, receiving input from peripheral and central thermoreceptors.

Heat Production: Basal metabolism, muscular activity, thyroxine, and temperature effects.
Heat Loss: Radiation, conduction/convection, evaporation.

Clinical Correlations and Disorders
Diabetes Mellitus: Inadequate insulin leads to high blood glucose, protein/fat catabolism, and metabolic acidosis.
Obesity: Defined by BMI; increases risk for cardiovascular disease, diabetes, and other conditions.
Metabolic Syndrome: Cluster of risk factors (waist circumference, blood pressure, glucose, triglycerides, HDL) that increase risk for heart disease and diabetes.

Developmental Aspects and Inborn Errors
Phenylketonuria (PKU): Inability to metabolize phenylalanine, leading to neurotoxicity.
Galactosemia: Inability to convert galactose to glucose, causing mental deficits.
Glycogen Storage Disease: Deficiency in enzymes for glycogen breakdown.
Additional info: Metabolic rate declines with age, and various medications and lifestyle factors can influence nutrition and metabolism.