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SOMAPL1H

Nutrition & Metabolism

Questions:
All 100

OBJ 2739 — Metabolism & Synthesis

5 questions

OBJ 2740 — Glycolysis / TCA / ETS

16 questions

OBJ 2741 — Lipid Metabolism

13 questions

OBJ 2742 — Protein Metabolism

10 questions

OBJ 2743 — Nucleic Acid Metabolism

5 questions

OBJ 2744 — Balanced Diet

8 questions

OBJ 2745 — Vitamins & Minerals

14 questions

OBJ 2746 — Caloric Value

7 questions

OBJ 2747 — Metabolic Rate / BMR

8 questions

OBJ 2748 — Thermoregulation

10 questions

OBJ 2749 — Age-Related Changes

4 questions

★ Final Score — SOMAPL1H

Score by Objective

Nutrition & Metabolism

Martini, Ober, Bartholomew — Essentials of Anatomy & Physiology (Pearson, 2013) · Chapter 17

SOMAPL1HOBJ 2738–274912 Lesson Steps
2738
Medical Vocabulary — Nutrition and Metabolism
Define the medical vocabulary components related to nutrition and metabolism.

Word Roots & Meanings

Root / PrefixMeaningExample Term
anabolea building upanabolism — synthesis of new organic molecules
katabolea throwing downcatabolism — breakdown of organic molecules for energy
glykussweetglycolysis — the breakdown (loosening) of glucose (sweet)
lysisa looseningglycolysis, lipolysis — breakdown of glucose, lipids
liposfatlipogenesis — synthesis of fat
genesisan origin, creationgluconeogenesis — creation of new glucose; thermogenesis — creation of heat
neo-newgluconeogenesis — new glucose creation from non-carbohydrate sources
thermeheatthermogenesis — heat production; thermoregulation — heat regulation
vitalifevitamin — essential organic nutrients for life
2739
Metabolism — Definition and Why Cells Synthesize
Communicate the definition of metabolism and why cells need to synthesize new organic structures.

Core Definitions

  • Metabolism — ALL the chemical reactions that occur in the body. Includes both catabolism and anabolism.
  • Energetics — the study of the flow of energy and its transformation from one form to another.
  • Catabolism — the breakdown of organic molecules, releasing energy that can be captured as ATP. First steps occur in the cytosol; most energy is generated in mitochondria.
  • Anabolism — the synthesis of new organic molecules, requiring energy (ATP).
  • Nutrients — essential substances absorbed by the digestive tract: water, vitamins, mineral ions, carbohydrates, lipids, and proteins.

Energy Capture Efficiency

Mitochondria capture roughly 40% of the energy released during catabolism as ATP. The remaining 60% escapes as heat that warms the cell and surrounding tissues.

Four Reasons Cells Synthesize New Organic Components

1
Structural maintenance and repairs. Most cell structures are temporary. Continuous removal and replacement = metabolic turnover.
2
Support growth. Cells preparing to divide increase in size and synthesize extra proteins and organelles.
3
Produce secretions. Secretory cells must manufacture their products and deliver them to the interstitial fluid.
4
Build nutrient reserves. Cells store nutrients for emergencies: muscle stores glycogen, adipocytes store triglycerides, liver stores both.

Fuel Priority Order

Energy Source PriorityWhen a cell has excess carbohydrates, lipids, and amino acids and needs energy, it breaks down: carbohydrates FIRST (least processing needed) → lipids SECONDamino acids LAST (seldom broken down if other sources available, because proteins form essential structures). Nucleic acids are almost never catabolized for energy.
2740
Glycolysis, the Citric Acid Cycle, and the Electron Transport System
Identify the basic steps in glycolysis, the TCA cycle, and the electron transport system.

Glycolysis

Glycolysis = breakdown of one 6-carbon glucose molecule into two 3-carbon pyruvate molecules. Occurs in the cytosol. Anaerobic (does not require oxygen).

Requirements: (1) glucose, (2) cytoplasmic enzymes, (3) ATP and ADP, (4) NAD (nicotinamide adenine dinucleotide) — a coenzyme that removes hydrogen atoms.

1
Glucose enters the cytosol → a phosphate group is attached (costs 1 ATP).
2
A second phosphate group is attached (costs another ATP). Total investment: 2 ATP.
3
The 6-carbon chain is split into two 3-carbon molecules.
4
Each 3-carbon molecule gains a phosphate group; 2 NADH are generated from NAD.
5
Each 3-carbon molecule produces 2 ATP (total: 4 ATP).

Net gain: 2 ATP + 2 NADH per glucose molecule.

Cells Without MitochondriaRed blood cells lack mitochondria and derive ALL their ATP from glycolysis alone (2 ATP per glucose). Skeletal muscle fibers also rely on glycolysis during intense contraction when O₂ supply is insufficient.

The Citric Acid Cycle (TCA Cycle / Krebs Cycle)

Occurs in the mitochondrial matrix. Requires oxygen (aerobic).

Preparatory step: Each pyruvate + NAD + Coenzyme A → acetyl-CoA (2-carbon) + CO₂ + NADH. This reaction is irreversible — acetyl-CoA cannot be converted back to pyruvate.

The acetyl group (2C) combines with a 4-carbon molecule → citric acid (6C). One complete revolution removes the 2 added carbons as CO₂, regenerating the 4-carbon starting molecule.

Primary function: Remove hydrogen atoms from organic molecules and transfer them to coenzymes NAD and FAD. The hydrogen-loaded coenzymes (NADH, FADH₂) carry electrons to the ETS.

Per turn: 1 GTP (→ 1 ATP) + 3 NADH + 1 FADH₂ + 2 CO₂. Two turns per glucose molecule.

The Electron Transport System (ETS)

Located in the inner mitochondrial membrane. Consists of cytochromes (protein-pigment complexes). Provides roughly 95% of the ATP cells need.

1
Hydrogen atoms from NADH and FADH₂ are split into electrons and protons (H⁺).
2
Electrons pass along cytochrome chain, releasing energy at each step.
3
Released energy drives H⁺ pumps → H⁺ moves from matrix into intermembrane space → concentration gradient.
4
H⁺ flows back through ATP synthase channels → kinetic energy drives ADP + P → ATP. This process = chemiosmosis.
5
Oxygen is the final electron acceptor → combines with electrons + H⁺ → water (H₂O).

Total ATP Yield Per Glucose

SourceATP
Glycolysis (cytosol, anaerobic)2 ATP (net)
Citric acid cycle (2 turns)2 ATP (via GTP)
ETS (from all NADH and FADH₂)32 ATP
TOTAL36 ATP per glucose

Gluconeogenesis

Gluconeogenesis = synthesis of glucose from non-carbohydrate precursors (lactate, glycerol, some amino acids). Uses different enzymes than glycolysis. Acetyl-CoA cannot be used to make glucose because the pyruvate → acetyl-CoA step is irreversible. Fatty acids and many amino acids break down to acetyl-CoA, so they cannot be used for gluconeogenesis either.

Glycogen is an important energy reserve stored in liver and skeletal muscle — compact, insoluble granules of glucose.

⚠ Critical IrreversibilityThe reaction pyruvate → acetyl-CoA removes a CO₂ molecule that CANNOT be reattached. This is why fatty acids (which break down to acetyl-CoA) cannot be converted to glucose. This single irreversible step has massive metabolic consequences.
2741
Lipid Metabolism
Identify the pathways involved in lipid metabolism.

Lipid Catabolism (Lipolysis)

Lipolysis = lipid breakdown. A triglyceride is first split by hydrolysis into 1 glycerol + 3 fatty acids.

  • Glycerol → converted to pyruvate in the cytosol → enters the citric acid cycle
  • Fatty acids → enter mitochondria → beta-oxidation clips them into 2-carbon fragments (acetyl-CoA), also generating NADH and FADH₂

One 18-carbon fatty acid yields approximately 144 ATP — almost 1.5 times the energy from three 6-carbon glucose molecules (3 × 36 = 108 ATP).

Why Lipids Are Slow EnergyLipid droplets are large and insoluble → water-soluble enzymes have difficulty accessing them. Most lipid processing occurs in mitochondria, limited by oxygen availability. Result: lipids cannot provide large amounts of ATP quickly. Good for sustained low-intensity activity; not for sprints.

Fuel switching: Resting skeletal muscle uses fatty acids. Active skeletal muscle switches to glucose (faster ATP).

Lipid Synthesis (Lipogenesis)

Lipogenesis begins with acetyl-CoA. Almost any organic molecule (carbs, lipids, amino acids) can be converted to acetyl-CoA and used to build lipids. Essential fatty acids (linoleic acid, linolenic acid) cannot be synthesized by human cells and must come from the diet. They are needed for prostaglandin and phospholipid synthesis.

Lipid Transport

Free fatty acids (FFA) bind to albumin in blood. Released from adipose tissue during fasting/starvation.

Lipoproteins = lipid-protein complexes (triglycerides + cholesterol inside a coating of phospholipids + proteins):

LipoproteinOriginFunction
ChylomicronsIntestinal epithelial cellsLargest lipoproteins; ~95% triglycerides; transport dietary fats from gut to bloodstream
LDLs ("bad cholesterol")LiverDeliver cholesterol TO peripheral tissues; may deposit in arterial walls → plaques → atherosclerosis
HDLs ("good cholesterol")LiverTransport excess cholesterol FROM peripheral tissues back to liver for storage/excretion in bile
Clinical — Ketone BodiesWhen acetyl-CoA accumulates (from excessive lipid or protein catabolism), the liver converts excess to ketone bodies (including acetone). Liver cells do NOT catabolize ketone bodies — they diffuse into circulation for use by peripheral tissues. Excessive ketone production = ketosis. If pH-buffering is overwhelmed, ketoacidosis occurs (pH below 7.05 = coma, arrhythmias, death). Most dangerous form: diabetic ketoacidosis.
2742
Protein Metabolism
Communicate protein metabolism and the use of proteins as an energy source.

Amino Acid Catabolism

The first step is removal of the amino group, requiring a coenzyme derived from vitamin B₆ (pyridoxine). Two pathways:

Transamination

Transfers an amino group from one amino acid to another carbon chain → creates a NEW amino acid. Enables cells to synthesize many amino acids needed for protein synthesis. Active in liver, skeletal muscle, heart, lung, kidney, brain.

Deamination

Removes the amino group, generating a toxic ammonium ion (NH₄⁺). The carbon skeleton can enter the citric acid cycle or be converted to ketone bodies. Liver cells convert toxic ammonium ions to urea (relatively harmless, water-soluble, excreted in urine).

Three Reasons Protein Catabolism Is Impractical for Quick Energy

1
Proteins are more difficult to break apart than carbohydrates or lipids.
2
Ammonium ions (a by-product) are highly toxic to cells.
3
Proteins form the most important structural and functional components of any cell. Extensive protein catabolism threatens homeostasis.

Essential vs. Nonessential Amino Acids

Of 20 amino acids, 10 are essential (must come from diet). Eight cannot be synthesized at all (isoleucine, leucine, lysine, threonine, tryptophan, phenylalanine, valine, methionine). Two more (arginine, histidine) can be synthesized but in insufficient amounts for growing children. The remaining 10 are nonessential (synthesized on demand via amination or transamination).

If even ONE essential amino acid is missing, protein synthesis halts completely — all amino acids must be present at the ribosome simultaneously.

Clinical — Phenylketonuria (PKU)Inherited defect in phenylalanine hydroxylase enzyme → cannot convert phenylalanine to tyrosine. Tyrosine is a precursor for norepinephrine, epinephrine, and melanin. If undetected in infancy, PKU causes severe brain damage.
2743
Nucleic Acid Metabolism
Communicate nucleic acid metabolism.

DNA vs. RNA Catabolism

  • DNA is NEVER catabolized for energy, even during starvation. The genetic information is absolutely essential to cell survival.
  • RNA is regularly broken down and replaced. mRNA lasts minutes to hours; rRNA lasts about 5 days; tRNA is also replaced regularly.

Nucleotide Breakdown

When nucleotides are broken down, only sugars, cytosines, and uracils can enter the citric acid cycle for ATP production. Adenine and guanine cannot be catabolized — they are deaminated and excreted as uric acid.

Nitrogenous Wastes

WasteSourceSolubility
UreaAmino acid deamination (liver converts NH₄⁺ + CO₂ → urea)Highly water-soluble; excreted in urine
Uric acidPurine (adenine/guanine) breakdown from nucleotide catabolismPoorly soluble; can form crystals
Clinical — GoutElevated uric acid in blood = hyperuricemia. Uric acid crystals deposit in joints = gout (painful inflammation). Most cases linked to impaired renal excretion of uric acid, not overproduction.
2744
Balanced Diet
Identify what constitutes a balanced diet and why it is important.

Definition

Nutrition = the absorption of essential nutrients from food. A balanced diet contains all the nutrients needed to maintain homeostasis: adequate energy substrates, essential amino acids and fatty acids, minerals, vitamins, and sufficient water. It prevents malnutrition (unhealthy state from inadequate OR excessive intake of one or more nutrients).

Five Basic Food Groups (MyPlate)

GroupKey Nutrients Provided
Grains (orange)Carbohydrates; vitamins E, thiamine, niacin, folate; calcium; phosphorus; iron; dietary fiber
Vegetables (green)Carbohydrates; vitamins A, C, E, folate; dietary fiber; potassium
Fruits (red)Carbohydrates; vitamins A, C, E, folate; dietary fiber; potassium
Dairy (blue)Complete proteins; fats; carbohydrates; calcium; vitamins A, B₁₂
Protein (purple)Complete proteins; fats; iron; zinc; vitamins E, B₆

Complete vs. Incomplete Proteins

  • Complete proteins contain ALL essential amino acids in sufficient quantities. Sources: beef, fish, poultry, eggs, milk.
  • Incomplete proteins lack one or more essential amino acids. Sources: most plants. Vegetarians must carefully combine foods to get all essential amino acids.
⚠ Vitamin B₁₂ Warning for VegansVitamin B₁₂ is available ONLY from animal products or fortified foods (fortified cereals, tofu). Strict vegans who do not supplement are at risk for B₁₂ deficiency → pernicious anemia.

The average U.S. diet contains too much sodium and too many calories, with saturated fats providing too great a proportion. This increases incidence of obesity, heart disease, atherosclerosis, hypertension, and diabetes.

2745
Vitamins, Minerals, and Other Important Nutrients
Identify the functions of vitamins, minerals, and other important nutrients.

Minerals

Minerals are inorganic ions. The body cannot synthesize them — they must come from the diet. Three categories of importance:

1
Osmotic concentration. Na⁺ and Cl⁻ determine body fluid osmolarity. K⁺ maintains intracellular concentration.
2
Physiological processes. Membrane potentials, skeletal construction, muscle contraction, action potentials, neurotransmitter release, blood clotting, gas transport, buffer systems.
3
Enzyme cofactors. Ca²⁺ and Mg²⁺ for ATP breakdown in contracting muscle. K⁺ and Mg²⁺ for glucose-to-pyruvate conversion.

Iron is a critical trace mineral — component of hemoglobin (blood O₂ transport), myoglobin (muscle O₂ storage), and cytochromes (ETS electron carriers).

Fat-Soluble Vitamins (A, D, E, K)

Absorbed with dietary lipids. Stored in body fat and liver → reserves can last months. Excess can cause hypervitaminosis (toxicity, especially fat-soluble).

VitaminKey FunctionDeficiency
AMaintains epithelia; visual pigment synthesis; immune supportNight blindness, epithelial deterioration
D (D₃)Bone growth; Ca²⁺ and PO₄³⁻ absorption. Unique: can be synthesized by skin exposed to sunlightRickets, skeletal deterioration
EPrevents breakdown of vitamin A and fatty acidsAnemia
KEssential for liver synthesis of prothrombin and other clotting factors. Produced by intestinal bacteriaBleeding disorders

Avitaminosis = vitamin deficiency disease. Rare for fat-soluble vitamins from diet alone (body stores them) but can occur from malabsorption or excessive demand.

Water-Soluble Vitamins (B Complex, C)

Most serve as components of coenzymes. Rapidly exchanged and excreted in urine, so toxicity is uncommon (except with mega-doses).

VitaminCoenzyme/FunctionDeficiency
B₁ (thiamine)Coenzyme in many pathwaysBeriberi (muscle weakness, heart disease)
B₂ (riboflavin)Part of FADEpithelial/mucosal deterioration
B₃ (niacin)Part of NADPellagra (CNS, GI, skin problems)
B₅ (pantothenic acid)Part of coenzyme ARetarded growth, CNS disturbances
B₆ (pyridoxine)Coenzyme in amino acid and lipid metabolismAnemia, convulsions
B₁₂ (cobalamin)Coenzyme in nucleic acid metabolism. Requires intrinsic factor from gastric mucosa for absorptionPernicious anemia
C (ascorbic acid)Coenzyme in many pathways. Found in citrus fruitsScurvy (epithelial/mucosal deterioration)

Intestinal bacteria produce five water-soluble vitamins plus fat-soluble vitamin K.

Water

Daily requirement: ~2500 mL (~40 mL/kg body weight). Sources: food (~48%), drinking (~40%), metabolic water from the ETS (~12%, about 300 mL/day). For each °C above normal body temperature, daily water loss increases by 200 mL.

2746
Caloric Value of Foods
Communicate the significance of the caloric value of foods.

Units of Energy

A calorie (lowercase) = energy to raise 1 g of water by 1°C. A Calorie (uppercase) = kilocalorie (kcal) = energy to raise 1 kg of water by 1°C. Food labels list Calories (kilocalories).

A calorimeter measures food energy by completely burning a food sample in an oxygen-filled chamber and measuring the temperature rise of surrounding water.

Energy Content by Nutrient

NutrientCalories per Gram
Lipids~9.46 Cal/g
Proteins~4.32 Cal/g
Carbohydrates~4.18 Cal/g

Lipids yield roughly twice the energy per gram as carbohydrates or proteins. This makes lipids the most energy-dense nutrient and explains why excess calories are stored as fat (triglycerides in adipose tissue).

Energy BalanceIf daily intake exceeds expenditure → excess stored as triglycerides → weight gain. If daily expenditure exceeds intake → body draws on reserves → weight loss. Both calorie counting AND exercise matter for weight management.
2747
Metabolic Rate and BMR
Communicate the definition of metabolic rate and the factors involved in determining an individual's metabolic rate.

Definitions

  • Metabolic rate = the sum of ALL anabolic and catabolic processes at a given time. Varies widely with activity.
  • Basal metabolic rate (BMR) = the minimum, resting energy expenditure of an awake, alert person under standardized conditions. Average: ~70 Cal/hour (~1680 Cal/day).

Factors That Influence BMR

Even under standardized conditions, BMR varies based on: age, sex, physical condition, body weight, and genetic differences.

Activity and Energy Expenditure

Sedentary activities add minimal energy demands. One hour of competitive swimming can add 500+ Cal to daily requirements.

Recommended Caloric Proportions

For all ages: carbohydrates 55–60%, fats < 30%, proteins 11–12% of daily caloric intake. These proportions do not change with age — only total caloric amount changes.

2748
Thermoregulation
Identify the homeostatic mechanisms that maintain a constant body temperature.

Why Thermoregulation Matters

Enzymes operate within a narrow temperature range. Below 36°C (97°F): disorientation. Above 40°C (104°F): disorientation. Above 42°C (108°F): convulsions and permanent cell damage.

Four Mechanisms of Heat Transfer

MechanismDescriptionSignificance
RadiationEmission of infrared energy from warm objectsMore than half of total heat loss
ConductionDirect transfer of energy through physical contactGenerally NOT effective for heat loss
ConvectionWarm air near skin rises, replaced by cooler airResult of conductive heat loss to air
EvaporationWater changing to vapor absorbs ~0.58 Cal per gramInsensible perspiration (20–25 mL/hr, constant) = ~1/5 of resting heat loss. Sensible perspiration (sweat glands) up to 2–4 L/hr. Ineffective at 100% humidity.

The Hypothalamus — Body Thermostat

Heat-Loss Center (Parasympathetic)

Activated when temperature rises above set point:

  • Vasomotor center inhibited → peripheral vessel dilation → warm blood to skin → increased radiation/convection
  • Sweat glands stimulated → evaporative cooling
  • Respiratory centers stimulated → increased evaporation from lungs
Heat-Gain Center (Sympathetic)

Activated when temperature falls (prevents hypothermia):

  • Peripheral vasoconstriction → reduces heat loss; blood shunted to deep veins beneath subcutaneous fat
  • Shivering thermogenesis → oscillatory muscle contractions; up to 400% increase in heat generation
  • Nonshivering thermogenesisepinephrine (immediate: glycogen breakdown, increased metabolic rate) + thyroxine (gradual: develops over days to weeks)
2749
Age-Related Changes in Nutritional Requirements
Communicate the age-related changes in nutritional requirements.

Key Changes

  • Caloric requirements decrease by ~10% per decade after age 50. Associated with reduced metabolic rates, body mass, activity levels, and exercise tolerance.
  • The recommended proportions of carbs/fats/proteins do NOT change. Only the total caloric amount decreases.

Specific Nutritional Risks in the Elderly

IssueMechanismConsequence
Increased calcium needNormal age-related osteoporosis + sedentary lifestyleElevated calcium intake + supplemental vitamin D₃ needed to slow bone loss
Vitamin D₃ deficiencyElderly spend more time indoors; thinner skin produces less D₃ from sunlightReduced calcitriol → decreased calcium absorption from small intestine
Decreased appetiteNumber and sensitivity of olfactory and gustatory receptors declineFood is less appetizing → reduced food intake
Reduced absorption efficiencyMucosal lining of digestive tract becomes thinner with ageEven food that is eaten is not absorbed as efficiently
Iron deficiency anemiaFixed incomes → reduced animal protein consumption (primary iron source) + less efficient absorptionInadequate iron → anemia