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Chapter Review Chapter 25 Metabolism and Energetics 995
Study Outline when cells cannot obtain enough glucose from interstitial
fluid. (Figure 25–7)
Access more chapter study tools online in the MasteringA&P Study Area:
25-3 Lipid metabolism involves lipolysis, beta-oxidation, and
• Chapter Quizzes, Chapter Practice Test, Art-labeling Activities,
Animations, MP3 Tutor Sessions, and Clinical Case Studies the transport and distribution of lipids as free fatty acids
and lipoproteins p. 973
• Practice Anatomy Lab ™ • A&P Flix ™ 12. During lipolysis (lipid catabolism), lipids are broken down
into pieces that can be converted into pyruvate or channeled
• Interactive Physiology ® • PhysioEx ™ into the citric acid cycle.
13. Triglycerides, the most abundant lipids in the body, are split
25-1 Metabolism refers to all the chemical reactions into glycerol and fatty acids. The glycerol enters the glycolytic
pathways (glycolysis and gluconeogenesis), and the fatty acids
in the body, and energetics refers to the flow and enter the mitochondria.
transformation of energy p. 962 14. Beta-oxidation is the breakdown of a fatty acid molecule into
1. Energetics is the study of the flow of energy and its change(s) 2-carbon fragments that can be used in the citric acid cycle.
from one form to another. Its focus includes understanding a The steps of beta-oxidation cannot be reversed, and the body
range of energy requirements from cells to the whole body. cannot manufacture all the fatty acids needed for normal
2. In general, during cellular metabolism, cells break down excess car- metabolic operations. (Figure 25–8)
bohydrates first and then lipids, while conserving amino acids. 15. Lipids cannot provide large amounts of ATP quickly. However,
Only about 40 percent of the energy released through catabo- cells can shift to lipid-based energy production when glucose
lism is captured in ATP; the rest is released as heat. (Figure 25–1) reserves are limited.
3. Cells synthesize new compounds (anabolism) to (1) perform 16. In lipogenesis (the synthesis of lipids), almost any organic
structural maintenance or repairs, (2) support growth, (3) pro- substrate can be used to form glycerol. Essential fatty acids
duce secretions, and (4) build and store nutrient reserves. are those that cannot be synthesized and must be included in
4. Cells “feed” small organic molecules to their mitochondria; the diet.
in return, the cells get the ATP they need to perform cellular 17. Most lipids circulate as lipoproteins (lipid–protein com-
functions. (Figure 25–2) plexes that contain large glycerides and cholesterol). The larg-
est lipoproteins, chylomicrons, carry absorbed lipids from the
25-2 Carbohydrate metabolism involves glycolysis, ATP intestinal tract to the bloodstream. All other lipoproteins are
derived from the liver and carry lipids to and from various tis-
production, and gluconeogenesis p. 965 sues of the body. (Figure 25–9)
5. Most cells generate ATP and other high-energy compounds 18. Capillary walls of adipose tissue, skeletal muscle, cardiac
muscle, and the liver contain lipoprotein lipase, an enzyme
through the breakdown of carbohydrates. that breaks down lipids, releasing a mixture of fatty acids and
6. Glycolysis and aerobic metabolism, or cellular respiration, monoglycerides into the interstitial fluid. (Figure 25–9)
provide most of the ATP used by typical cells. Glycogen can be 25-4 Protein catabolism involves transamination and
broken down to glucose molecules. In glycolysis, each mol-
ecule of glucose yields 2 molecules of pyruvic acid (as pyru- deamination, whereas protein synthesis involves
vate ions), a net 2 molecules of ATP, and 2 NADH molecules. amination and transamination p. 978
19. If other energy sources are inadequate, mitochondria can
(Figure 25–3)
7. In the presence of oxygen, pyruvate molecules enter mito- 25break down amino acids in the citric acid cycle to generate
chondria, where they are broken down completely in the ATP. In the mitochondria, the amino group can be removed by
citric acid cycle. Carbon and oxygen atoms are lost as carbon either transamination (an exchange reaction) or deamina-
dioxide (decarboxylation); hydrogen atoms are passed to tion. (Figure 25–10)
coenzymes, which initiate the oxygen-consuming and ATP- 20. Protein catabolism is impractical as a source of quick energy.
generating reaction oxidative phosphorylation. (Figure 25–4) 21. Roughly half the amino acids needed to build proteins can be
8. Cytochromes of the electron transport system (ETS) pass synthesized. There are 10 essential amino acids, which must
electrons to oxygen, resulting in the formation of water. As this be acquired through the diet. Amination, the attachment of
transfer occurs, the ETS generates ATP. (Figure 25–5) an amino group to a carbon framework, is an important step
9. For each glucose molecule processed through glycolysis, the in the synthesis of nonessential amino acids. (Figure 25–10,
citric acid cycle, and the ETS, most cells gain 36 molecules of Spotlight Figure 25–11)
ATP. (Figure 25–6)
10. Cells can break down other nutrients to provide substrates for 25-5 The body experiences two patterns of metabolic activity:
the citric acid cycle if supplies of glucose are limited.
11. Gluconeogenesis, the synthesis of glucose from noncarbohy- the absorptive and postabsorptive states p. 982
drate precursors such as lactate, glycerol, or amino acids, en- 22. No one cell of a human can perform all the anabolic and cata-
ables a liver cell to synthesize glucose molecules when carbo-
hydrate reserves are depleted. Glycogenesis is the process of bolic operations necessary to support life. Homeostasis can be
glycogen formation. Glycogen is an important energy reserve preserved only when metabolic activities of different tissues
are coordinated.
23. The body has five metabolic components: the liver, adipose
tissue, skeletal muscle, neural tissue, and other peripheral

