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Chapter 24: Nutrition, Metabolism, and Energy Balance – Anatomy & Physiology II Study Notes

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Nutrition and Dietary Guidelines

Macronutrients and Micronutrients

Nutrition is the process by which the body converts nutrients into energy and building blocks for growth, maintenance, and repair. Nutrients are classified as macronutrients (carbohydrates, lipids, proteins) and micronutrients (vitamins, minerals). Water is also considered a nutrient due to its essential role in physiological processes.

  • Macronutrients: Provide energy and structural components. Includes carbohydrates, lipids, and proteins.

  • Micronutrients: Required in small amounts. Includes vitamins and minerals.

  • Essential nutrients: Must be obtained from the diet because the body cannot synthesize them.

  • Energy value: Measured in kilocalories (kcal). 1 dietary "Calorie" = 1 kcal.

Basic dietary principles emphasize balanced intake of fruits, vegetables, whole grains, and proteins, while minimizing processed foods and excess calories.

USDA MyPlate dietary guidelines

Macronutrient Metabolism

Carbohydrates

Carbohydrates are primarily derived from plant sources and serve as the main fuel for cellular ATP production. They are classified as simple (sugars) and complex (starches, fibers).

  • Dietary sources: Grains, vegetables, fruits, sugarcane, honey, milk.

  • Role: Glucose is the preferred fuel for neurons and red blood cells.

  • Dietary requirements: 45–65% of total calories, mainly from complex carbohydrates.

Lipids

Lipids include triglycerides, phospholipids, and cholesterol. They provide energy, structural components, and are involved in hormone synthesis.

  • Dietary sources: Saturated fats (meat, dairy), unsaturated fats (seeds, nuts, vegetable oils), cholesterol (egg yolk, meats).

  • Essential fatty acids: Linoleic acid (omega-6) and linolenic acid (omega-3).

  • Dietary requirements: 20–35% of total caloric intake; saturated fats limited to 10% or less.

Proteins

Proteins are vital for structural and functional roles in the body. Complete proteins contain all essential amino acids, while incomplete proteins lack one or more.

  • Dietary sources: Animal products (eggs, milk, fish, meats), soybeans, legumes, nuts, cereals.

  • Uses: Structural (keratin, collagen), functional (enzymes, hormones).

  • Dietary requirements: 0.8 g per kg body weight per day.

Protein synthesis depends on the presence of all essential amino acids, adequate caloric intake, and hormonal regulation.

Essential amino acids and sources

Micronutrients: Vitamins and Minerals

Vitamins

Vitamins are organic compounds that function as coenzymes in metabolic reactions. They are classified by solubility:

  • Water-soluble: B complex, C; not stored, excess excreted.

  • Fat-soluble: A, D, E, K; stored in body, excess can be toxic.

  • Antioxidants: Vitamins C, E, A, and mineral selenium neutralize free radicals.

Vitamin

Major Dietary Sources

Major Functions

Deficiency Symptoms

Vitamin A

Liver, fish, dairy, carrots

Vision, epithelial health

Night blindness

Vitamin D

Eggs, dairy, sunlight

Calcium absorption

Rickets

Vitamin E

Vegetable oils, nuts

Antioxidant

Neurological issues

Vitamin K

Green vegetables

Blood clotting

Bleeding

B complex

Whole grains, meats

Energy metabolism

Anemia, neurological issues

Vitamin C

Citrus fruits

Collagen synthesis

Scurvy

Table of vitamins, sources, functions, and deficiencies

Minerals

Minerals are inorganic elements required for various physiological functions, including bone formation, nerve function, and electrolyte balance.

Mineral

Major Dietary Sources

Major Functions

Deficiency Symptoms

Calcium

Dairy, leafy greens

Bone health, muscle contraction

Osteoporosis

Phosphorus

Meat, dairy

Bone, ATP formation

Weakness

Potassium

Fruits, vegetables

Electrolyte balance

Muscle cramps

Iron

Meat, legumes

Hemoglobin synthesis

Anemia

Iodine

Seafood, iodized salt

Thyroid hormone synthesis

Goiter

Table of minerals, sources, functions, and deficiencies

Metabolism: Biochemical Reactions

Anabolism and Catabolism

Metabolism encompasses all biochemical reactions in the body. Anabolism builds complex molecules, while catabolism breaks them down. Cellular respiration is a catabolic process that generates ATP from food fuels.

  • Anabolism: Synthesis of macromolecules (proteins, glycogen).

  • Catabolism: Breakdown of macromolecules (glycolysis, fatty acid oxidation).

  • Phosphorylation: Transfer of phosphate groups to activate molecules.

Stages of nutrient processing and metabolic pathways

ATP Synthesis

ATP is synthesized by two main mechanisms: substrate-level phosphorylation and oxidative phosphorylation.

  • Substrate-level phosphorylation: Direct transfer of phosphate to ADP during glycolysis and Krebs cycle.

  • Oxidative phosphorylation: Uses electron transport chain and chemiosmosis in mitochondria to generate most ATP.

Substrate-level phosphorylation mechanismOxidative phosphorylation mechanism

Carbohydrate Metabolism

Pathways of Glucose Catabolism

Complete glucose catabolism involves three pathways: glycolysis, Krebs cycle, and electron transport chain.

  • Glycolysis: Occurs in cytosol, breaks glucose into pyruvic acid.

  • Krebs cycle: Occurs in mitochondrial matrix, oxidizes pyruvic acid to CO2.

  • Electron transport chain: Occurs in inner mitochondrial membrane, produces most ATP.

Overview of glucose catabolism pathways

Glycolysis: Major Phases

  • Phase 1: Sugar activation – Glucose is phosphorylated and converted to fructose-1,6-bisphosphate.

  • Phase 2: Sugar cleavage – Fructose-1,6-bisphosphate is split into two 3-carbon fragments.

  • Phase 3: Sugar oxidation and ATP formation – 3-carbon fragments are oxidized, producing ATP and NADH.

Glycolysis phase 1: sugar activationGlycolysis phase 2: sugar cleavageGlycolysis phase 3: sugar oxidation and ATP formation

Lipid Metabolism

Fat Catabolism and Synthesis

Lipids are metabolized for energy and stored as triglycerides. Fatty acids undergo beta oxidation to form acetyl CoA, which enters the citric acid cycle.

  • Oxidation: Glycerol and fatty acids are broken down for ATP production.

  • Lipogenesis: Synthesis of triglycerides when energy and glucose are abundant.

  • Lipolysis: Breakdown of stored fats for energy.

  • Ketogenesis: Formation of ketone bodies during prolonged fasting or carbohydrate deficiency.

Protein Metabolism

Amino Acid Catabolism

Proteins are continually degraded and synthesized. Excess amino acids are oxidized for energy or converted to fat. Catabolism involves transamination, oxidative deamination, and keto acid modification.

  • Transamination: Transfer of amine group to keto acid.

  • Oxidative deamination: Removal of amine group as ammonia, converted to urea.

  • Keto acid modification: Conversion to citric acid cycle intermediates.

Amino acid catabolism pathways

Metabolic States of the Body

Absorptive State

The absorptive (fed) state occurs after eating, when nutrients are absorbed and stored. Insulin is the primary hormone regulating this state.

  • Carbohydrates: Glucose is used for energy or stored as glycogen/fat.

  • Triglycerides: Hydrolyzed and stored in adipose tissue.

  • Amino acids: Used for protein synthesis or converted to fat.

Metabolic pathways of the absorptive state

Postabsorptive State

The postabsorptive (fasting) state occurs when the GI tract is empty and energy is supplied by breakdown of reserves. Glucagon is the primary hormone regulating this state.

  • Glycogenolysis: Breakdown of glycogen to glucose.

  • Gluconeogenesis: Formation of glucose from noncarbohydrate sources.

  • Lipolysis: Breakdown of fats for energy.

  • Protein catabolism: Used during prolonged fasting.

Metabolic pathways of the postabsorptive state

Metabolic Role of the Liver

Liver Functions

The liver is central to metabolism, processing nutrients, regulating cholesterol, storing vitamins/minerals, and detoxifying substances.

  • Carbohydrate metabolism: Glycogenesis, glycogenolysis, gluconeogenesis.

  • Fat metabolism: Lipoprotein synthesis, cholesterol production, bile salt formation.

  • Protein metabolism: Deamination, urea formation, plasma protein synthesis.

Liver metabolic functions

Cholesterol and Lipoproteins

Cholesterol Transport

Cholesterol is transported in blood by lipoproteins. Types include chylomicrons, VLDL, LDL, and HDL, each with distinct roles and compositions.

Lipoprotein

Main Function

Composition

Chylomicron

Transport absorbed lipids from intestine to liver

Mostly triglycerides

VLDL

Transport triglycerides from liver to adipose tissue

High triglyceride content

LDL

Deliver cholesterol to tissues

High cholesterol content

HDL

Remove cholesterol from tissues to liver

High protein content

Lipoprotein composition and function

Energy Balance and Obesity

Energy Intake and Output

Energy balance is achieved when energy intake equals energy output. Imbalance leads to weight gain or loss. Body mass index (BMI) is used to assess obesity.

  • BMI formula:

  • Overweight: BMI 25–30

  • Obese: BMI > 30

Apple body shape and obesity risk

Regulation of Food Intake

Neural and Hormonal Controls

Food intake is regulated by neural signals, hormones, and nutrient levels. Key hormones include insulin, leptin, ghrelin, and neuropeptide Y.

  • Short-term controls: GI tract distension, nutrient signals, gut hormones.

  • Long-term controls: Leptin from adipose tissue, insulin from pancreas.

Metabolic Rate and Body Temperature

Basal and Total Metabolic Rate

Metabolic rate is the total heat produced by the body. Basal metabolic rate (BMR) reflects energy needed for essential functions and is influenced by age, gender, temperature, stress, and thyroxine levels.

  • BMR measurement: Postabsorptive state, relaxed, room temperature.

  • Factors: Age, gender, temperature, stress, hormones.

Regulation of Body Temperature

Body temperature is regulated by balancing heat production and loss. The hypothalamus acts as the main thermoregulatory center.

  • Heat production: Metabolism, muscular activity, hormones.

  • Heat loss: Radiation, conduction, convection, evaporation.

  • Core temperature: Highest in internal organs; shell temperature fluctuates.

Clinical Correlations and Disorders

Metabolic Disorders

  • Diabetes mellitus: Inadequate insulin production or abnormal receptors; leads to hyperglycemia, protein wasting, metabolic acidosis.

  • Ketosis: Accumulation of ketone bodies during starvation or diabetes.

  • Phenylketonuria (PKU): Inability to metabolize phenylalanine; neurotoxic effects.

  • Galactosemia: Deficit in converting galactose to glucose; mental deficits.

  • Glycogen storage disease: Enzyme deficiency; glycogen accumulation.

Tyrosine catabolism and PKU

Metabolic Syndrome

Metabolic syndrome is a cluster of risk factors that increase the risk of heart disease and diabetes.

  • Increased waist circumference

  • Increased blood pressure

  • Increased blood glucose

  • Increased blood triglycerides

  • Decreased HDL cholesterol

Metabolic syndrome risk factors

Developmental Aspects and Aging

Nutrition Across the Lifespan

Proper nutrition is critical during early development. Metabolic rate declines with age, and medications or chronic conditions can affect nutritional status and metabolism.

  • Early childhood: Deficiencies can cause mental deficits.

  • Aging: Reduced metabolic rate, increased risk of malnutrition, tissue stiffening.

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