Chapter 25: Metabolism and Nutrition Flashcards
Define metabolism and differentiate between catabolism and anabolism
Metabolism is all the chemical reactions that occur in the body
Catabolism (decomposition) are chemical reactions that break down complex organic molecules into simples ones; they are exergoic in that they produce more energy then they consume
Anabolism (synthesis) combine simple molecules and comonomer to form the body complex structural and functional components; they are endergonic in they consume more energy then they produce
How does ATP link anabolism and catabolism?
When the terminal P group is split off ATP = ADP + P
Some of the energy released is used to drive anabolic reactions
In addition, energy from complex molecules is used in catabolic reactions to combine ADP + P + energy = ATP
Describe oxidation-reduction reactions
Oxidation - the removal of electrons from an atom or molecule; the result is decrease in the potential enemy of the atom/molecule
Reduction - the addition of elections to a molecule resulting in an increase in the potential energy of a molecule
These reactions are always couples as each time one stubsance is oxidized, another is simultaneously reduced known as oxidation-reductional reactions
What is nicotinamide adenine dinuclotide (NAD)
A derivative of the B vitamin niacin that is a common coenzyme used by animal cells to carry H atoms
Define phosphorylation and describe the 3 mechanisms of phosphorylation to generate ATP
phosphorylation - addition of a P group to a molecule to increase energy
- Substrate-level phosphorylation - generates ATP by transferring a high-energy P group from an intermediate metabolic compound (a substrate) directly to ATP; occurs in cytosol
- Oxidative phosphorylation - removes electrons from organic compounds and passes them through a seers of election acceptors called the electron transport changes, to molecules of O2l occurs in mitochondria
- Photophosphorylation - occurs only in chlorophyll-containing plant cells
Describe the following ways glucose is used in the body:
ATP production
Amino acid synthesis
Glycogen synthesis
Triglyceride synthesis
ATP production - glucose is oxidized to produce immediate ATP
Amino acid synthesis - use glucose to form several anino acids which can then be incorporated into proteins
Glycogen synthesis - glycogenesis where hundreds of glucose monomers are combined to form the polysaccharide glycogen
Triglyceride synthesis - hepatocytes can transform glucose to glycerol and fatty acids that can be used for lipogenesis, the synthesis of triglycerides
How does glucose move into cells?
Absorption in the GI tract is accomplished via secondary active transport (Na+ - glucose symporters)
Entry into most other body cells occurs via GluT molecules, a family of transporters that bring glucose into cells via facilitated diffusion
High levels of insulin increases insertion of GluT, increasing levels of facilitated diffusion
Define cellular respiratory and its 4 sets of reactions
Cellular respiration - oxidation of glucose to produce ATP
- Glycolysis - set of reactions in which one glucose molecule is oxidized and two molecules of pyretic acid are produce; results in 2 ATP molecules and 2 energy-containing NADH+H+
- Formation of acetyl coenzyme - prepares pyretic acid from extract into Krebs cycle; produces energy-containing NADH+H+ and CO2
- Krebs cycle reaction - oxidize acetyl coenzyme A and produce CO2, ATP, energy-containing NADH+H+ , and FADH2
- Electron transport chain reactions - oxidize energy-containing NADH+H+ and FADH2 and transfer their electrons through a series of electron carriers
Define anaerobic glycolysis
when oxygen is present, all four phases of cellular respiration occur: glycolysis, formation of acetyl coenzyme A, the Krebs cycle, and the electron transport chain.
However, if oxygen is not available or at a low concentration, pyruvic acid is converted to a substance called lactic acid, this is called anaerobic glycolysis
Which of the 4 processes of cellular respiration produces the most ATP?
Electron transport chain
Describe the 3 ways glucose takes part in or is formed in anabolic reactions
Glycogenesis - the synthesis of glycogen; glucose is phosphorylated to glucose 6-phosphate which is then covered into glucose 1-phosphate and then to uridine diphosphate and finally glycogen
Glycogenolysis - the splitting of glycogen into glucose; begins by splitting off glucose molecules from the branches glycogen molecule via phoshoprlation to form glucose 1-phosphate; stimulated by glucagon and epinephrine
Gluconeogensisi - glucose is formed from noncarbohydrate sources when low of glycogen; stimulated by cortisol
Define lipoproteins and deceive the four major classes
Lipoproteins- combination of lipids and proteins
- Chylomicrons - form from mucous epithelial cells of the small I, transport dietary lipids to adipose tissues for storage, enter lacteals of intestinal villi and are carried by lymph into venous blood and then into systemic circulation
Very low density lipoproteins (VLDLs) - form in hepatocytes, contain mainly endogenous lipids, transport triglycerides synthesized in hepatocytes to adipocytes for storage
Low density lipoproteins (LDLs) - carry about 75% of total cholesterol in blood and deliver it to cells throughout the body for use in repair of cell membranes and synthesis of steroid hormones and bile salts, enters cells via receptor-mediated endocytosis where it is broken down (bad cholesterol)
High density lipoproteins (HDLs) - remove excess cholesterol from body cells and the blood and transport it to the liver for elimination (good cholesterol)
What are the sources of significance of blood cholesterol?
2 sources: some is present in foods but most is synthesized by hepatocytes
1) High intake of dietary fats stimulates reabsorption of cholesterol containing bile back into the blood and 2) when saturated fats are broken down in the body, hepatocytes use some of the breakdown products to make cholesterol
As total cholesterol levels increase, the risk of coronary artery disease begins to rise (above 200 mg/dL heart attack chance doubles every 50 mg/dL increase)
Describe the fate of lipids
They can be oxidized to produce immediate ATP or can be stored in adipose tissue throughout the body and the liver
How are triglycerides stored?
Chylomicrons and VLDLs remove triglycerides and store them until they are needed for ATP production
Adipose tissues contsitture 98% of the bodies reserve as they are hydrophobic and store easily
Triglycerides in adipose tissues are continually broken down and resyntheisized and continually released, transported in the blood, and redeposited into other adipose tissue cells
Describe lipolysis
aka lipid catabolism - triglycerides are split into glycerol and fatty acids, a process that is catabolized by lipases - Epi and NE enhance triglyceride breakdown into fatty acids and glycerol
If ATP supply is high, glyceraldehyde 3-phosphate is converted into glucose
If ATP supply is low, glyceraldehyde 3-phosphate enters the catabolic pathway to pyruvic acid
Fatty acids undergo beta oxidation and enter the Krebs cycle via acetyl
coenzyme A
Describe lipogenesis
aka lipid anabolism - liver cells and adipose cells synthesize lipids from glucose or amino acids, a process stimulated by insulin
This occurs when individuals consume more carols than are needed to satisfy their ATP needs
amino acids -> acetyl CoA -> fatty acids -> triglycerides.
The use of glucose to form lipids takes place via two pathways:
(1) glucose -> glyceraldehyde 3-phosphate -> glycerol
(2) glucose -> glyceraldehyde 3-phosphate -> acetyl CoA -> fatty acids.
Describe the fate of proteins in the body
Active transport of amino acids into body cells is stimulated by insulin like growth factors (IGFs) and insulin
Almost immediately after digestion, amino acids are reassembled into proteins
What are the possible fates of the amino acids from protein catabolism
Hepatocytes convert some animo acids to fatty acids, ketone bodies, or glucose
Cells throughout the body oxidize a small amount of amino acids to generate ATP via the Krebs cycle and the electron transport chain - they must first be covered to molecules that are part of the Krebs cycle or can enter (CoA)
How are essential and nonessential amino acids different?
Essential (10 of 20) - must be present in the diet because they cannot be synthesized in the body in adequate amounts
Nonessential - can be synthesized by body cells, formed by transamination - transfer of an amino group from an amino acid to pyretic acid or to an acid in the Kreb’s cycle
Where is protein anabolism carried out?
Carried out on the ribosomes of almost every cell in the body directed by the cells DNA and RNA
IGF, thyroid hormones, insulin, estrogen, and testosterone all stimulate protein synthesis
What group is removed from an amino acid before it can enter the Krebs cycle, and what is this process called?
Amino group must be removed - process is called deamination which occurs in hepatocytes and produces ammonia
Briefly describe the difference between metabolism during the absorptive state and post absorptive state
absorptive state - ingested nutrients are entering the bloodstream, and glucose is readily available for ATP production; stimulated by insulin
postaborptive state - absorption of nutrients from the GI tract is complete and energy needs must be met by fuels already in the body; stimulated by Epi, NE, cortisol, and glucagon
Describe the dominant reactions that occur during the absorptive stage
- 50% of glucose is oxidized to produce ATP via glycolysis, Krebs cycle, and the electron transport chain
- Most glucose that enters hepatocytes is converted to glycogen; small amounts may be used for synthesis of fatty acids and glyceraldehyde 3-phosphate
- Some fatty acids and triglycerides synthesized in the liver remain there but hepatocytes package most into VDLs for storage in adipose tissues
- Adipocytes take up glucose no picked by liver and covert it into triglycerides for storage
- Most dietary lipids are stored in adipose tissue; only small portion is used for synthesis reactions
- Many absorbed amino acids that enter hepatocytes are delaminated to keto acids, which can either enter the Kreb’s cycle for ATP production or be used to synthesize glucose or fatty acids
- Some amino acids enter hepatocytes and a re used to synthesize proteins
- Amino acids not taken up by hepatocytes are used in other body cells for synthesis of proteins or regulatory chemicals