further notes on nutrition & metabolism
coupled reactions
free energy
ΔF for oxidation of 1 mol glucose = 686 kcal
at STP ~-bond ΔF = 7.3 kcal, but 12 kcal at body conditions
facilitated diffusion
active sodium cotransport
GI cell membrane
renal tubule membrane
facilitation of glucose transport by insulin
phosphorylation of glucose
glucokinase in liver
hexokinase elsewhere
glycogenesis
g6p → g1p → UDPg
sources include convertible monosaccharides
lactic acid, glycerol, pyruvic acid, some amino acids
glycogenolysis
activation of phosphorylase by Epi and glucagon
increase of cAMP
glucose + 2 ADP + 2 PO43- → 2 pyruvic acid + 2 ATP + 4 H
amount of energy lost from glucose, 56 kcal, efficiency 43%
2 pyruvic acid + 2 CoA → 2 Acetyl-CoA + 2 CO2 + 4 H
2 Acetyl-CoA + 6 H2O + 2 ADP → 4 CO2 + 16 H + 2 CoA + 2 ATP
chemiosmotic mechanism of the mitochondria
ionization of hydrogen
2 H + NAD+ → NADH + H+
electron transport chain
flavoprotein, ubiquinone, cytochromes
cytochrome A3, cytochrome oxidase
ATP synthase
allosteric inhibition of phosphofructokinase
excess citrate
formation of lactic acid
reconversion of lactic and pyruvic acids to glucose
expenditure: 6 ATP
glucose + 12 NADP+ + 6 H2O → 6 CO2 + 12 H + 12 NADPH
5 for 6
lipoproteins
nonessential and essential amino acids
synthesis of cellular components
muscular contraction
membrane active transport
glandular secretion
nerve conduction
~-bond contains 8.5 kcal at STP, 13 kcal at body conditions
nutrients
major nutrients
kilocalories (kcals)
essential nutrients
complex carbohydrates (starch)
monosaccharides (simple sugars)
triglycerides
essential fatty acids - linoleic and linolenic acid
dietary requirements
phospholipids
prostaglandins
cholesterol
complete proteins
dietary requirements
incomplete proteins
essential amino acids
daily intake
synthesis and hydrolysis
all-or-none rule
nitrogen balance
hormonal control
anabolic hormones accelerate protein synthesis
only vitamins D, K, and B are synthesized in the body
water-soluble vitamins (B-complex and C)
fat-soluble vitamins (A, D, E, and K)
bind to ingested lipids and are absorbed with their digestion products
seven minerals are required in moderate amounts
calcium, phosphorus, potassium, sulfur, sodium, chloride, and magnesium
at least a dozen are required in trace amounts
cellular respiration
anabolic reactions
catabolic reactions
stages of metabolism
digestion
anabolism
oxidative breakdown
oxidation-reduction (ReDox) reaction
oxidized substances lose energy
reduced substances gain energy
coenzymes
nicotinamide adenine dinucleotide (NAD+)
flavin adenine dinucleotide (FAD)
substrate-level phosphorylation
glycolysis and the Krebs cycle
oxidative phosphorylation
is carried out by the electron transport proteins in the cristae of the mitochondria
oxidation of glucose:
c6H12O6 + 6O2 → 6H2O + 6CO2 + 36ATP + heat
three pathways
glycolysis
citric acid (Krebs) cycle
electron transport chain and oxidative phosphorylation
a three-phase pathway:
glucose is oxidized into pyruvic acid
NAD+is reduced to NADH + H+
ATP is synthesized by substrate-level phosphorylation
pyruvic acid:
moves on to the Krebs cycle
reduced to lactic acid
glycolysis: phases 1 and 2
sugar activation
two ATP molecules activate glucose into
fructose-1,6-diphosphate
sugar cleavage
dihydroxyacetone phosphate
glycolysis: phase 3
oxidation and ATP formation
final products:
two pyruvic acid molecules
two reduced NAD+ (NADH + H+) molecules
net gain of two ATP molecules
preparatory steps
occurs in mitochondrial matrix
pyruvic acid is converted to acetyl CoA in steps:
decarboxylation
oxidation
formation of acetyl CoA
an eight-step cycle in which acetic acid is decarboxylated and oxidized, generating (times 2!):
three molecules of NADH + H+
one molecule of FADH2
two molecules of CO2
one molecule of ATP
food (glucose) is oxidized and the hydrogens:
are transported by coenzymes NADH and FADH2
enter a chain of proteins bound to metal atoms (cofactors)
combine with molecular oxygen to form water
release energy
hypothetical mechanism of oxidative phosphorylation
NADH dehydrogenase (FMN, Fe-S)
cytochrome b-c1
cytochrome oxidase (a-a3)
ATP synthase
electron energy gradient
NADH + H+ and FADH2
glycogenesis
glycogenolysis
gluconeogenesis
chylomicrons
lipids in chylomicrons are hydrolyzed by plasma enzymes and absorbed by cells
catabolism of fats involves two separate pathways
glycerol pathway
glycerol converted to glyceraldehyde phosphate
fatty acid pathway
fatty acids undergo beta oxidation
glyceraldehyde converted into acetyl CoA
acetyl CoA enters the Krebs cycle
lipolysis
ketone bodies
synthesis of structural materials
phospholipids
by the liver:
synthesizes lipoproteins for transport of cholesterol and fats
makes tissue factor, a clotting factor
synthesizes cholesterol for acetyl CoA
uses cholesterol for forming bile salts
certain endocrine organs use cholesterol for synthesizing steroid hormones
oxidation of amino acids
transamination
α-ketoglutaric acid
glutamic acid
oxidative deamination
keto acid modification
anabolism and energy storage
principal pathways
muscle
liver
adipose tissue
insulin effects on metabolism
stimulated by:
increased blood glucose
elevated amino acid levels in the blood
gastrin, CCK, and secretin
effects
diabetes mellitus
catabolism and replacement of fuels in the blood
glycogenolysis and gluconeogenesis
principal pathways
muscle
liver
hormonal and neural controls
alpha cells of pancreas secrete glucagon
glycogenolysis and gluconeogenesis
glucose sparing
sympathetic nervous system releases epinephrine
cholesterol
structural basis of bile salts, steroid hormones, and vitamin D
directs embryonic development
transported via lipoproteins
HDLs -
high-density lipoproteins have more protein content
LDLs -
low-density lipoproteins have a considerable cholesterol component
VLDLs -
very low density lipoproteins are mostly triglycerides
rate of energy output
measured directly with a calorimeter or indirectly with a respirometer
basal metabolic rate (BMR)
expressed in kcal/m2/h
total metabolic rate (TMR)
factors that influence BMR
Go to top of nutrition & metabolism notes
| Questions for thought | ||
|---|---|---|
| 1. | What is oxidative phosphorylation? What is the role of the electron transport system in this process? | |
| 2. | How are lipids broken down? How is beta-oxidation involved with lipid catabolism? | |
| 3. | How do the absorptive and post-absorptive states maintain normal blood glucose levels? | |
| 4. | Why are vitamins and minerals essential components of the diet? | |
| 5. | Many articles in popular magazines refer to “good cholesterol” and “bad cholesterol”. To which types and functions of cholesterol might these terms refer? Explain your answer. | |
| 6. | Describe the major events and outcomes of glycolysis. | |
| 7. | Pyruvic acid is a product of glycolysis, but is not the substance that enters the citric acid cycle. What is the substance, and what must occur if pyruvic acid is to be transformed into that molecule. | |
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[ Anatomy & Physiology 2 syllabus ][
Anatomy & Physiology 3 syllabus ] [ Page created 06 May 1999 ][ Last update 03 May 2007 ] [ Questions about this lecture? E-mail me ] |
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