4. The study of synthesis (Anabolism)
and degradation (catabolism) of
biomolecules is biochemically termed as
metabolism.
Metabolism of carbohydrate
5. Structural maintenance
Support of growth
Production of secretions
Building of nutrient reserves
Anabolism
6. Breakdown of nutrients to provide energy (in the
form of ATP) for body processes
Nutrients directly absorbed
Stored nutrients
Cells break down excess carbohydrates first, then lipids, finally
amino acids if energy needs are not met by carbohydrates and fat
40% of the energy released in catabolism is captured in ATP, the
rest is released as heat
Catabolism
7. Carbohydrate Metabolism
Primarily glucose
Fructose and galactose enter the pathways at various points
All cells can utilize glucose for energy production
Liver is central site for carbohydrate metabolism
8. Glucose Metabolism
Four major metabolic pathways:
Immediate source of energy
Pentose phosphate pathway
Glycogen synthesis in liver/muscle
Precursor for triacylglycerol synthesis
11. Glycolysis
Sequence of reactions that converts
glucose into pyruvate
Relatively small amount of energy produced
Glycolysis reactions occur in cytoplasm
Does not require oxygen
Glucose 2 Pyruvate
Lactate (anaerobic)
Acetyl-CoA (TCA cycle)
12. Glycolysis pathway:
Oxidation of glucose to Pyruvate +water+
NADH2 in steps wise (10 steps).
It take place in all cells, for the break
down of glucose to provide energy.
*Glycolysis pathway occurs in most cell in
the presences of oxygen and called
(aerobic glycolysis)
An-aerobic glycolysis: occurs in the
completely absent of oxygen or partial
deficiency of oxygen.
13. An aerobic glycolysis found in:
1- Red blood cells (no mitochondria)
2-Labor (partial deficiency of oxygen)
3-Exercise muscle (partial deficiency of
oxygen)
4-Cancer cells
17. Pyruvate Metabolism
Three fates of pyruvate:
Conversion to lactate (anaerobic)
Conversion to alanine (amino acid)
Entry into the TCA cycle via pyruvate
dehydrogenase pathway (create ATP)
18. Pyruvate Metabolism
Three fates of pyruvate:
Conversion to lactate (anaerobic)
Conversion to alanine (amino acid)
Entry into the TCA cycle via pyruvate
dehydrogenase pathway
19. Anaerobic
Metabolism of
Pyruvate to Lactate
Problem:
During glycolysis, NADH is formed from NAD+
Without O2, NADH cannot be oxidized to NAD+
No more NAD+
All converted to NADH
Without NAD+
, glycolysis stops
20. Anaerobic
Metabolism of
Pyruvate
Solution:
Turn NADH back to NAD+
by making lactate (lactic
acid)
COO
C O
CH3
COO
HC OH
CH3
Lactate
Pyruvate
Lactate dehydrogenase
NADH + H+
NAD+
(oxidized) (reduced)
(oxidized)
(reduced)
21. Anaerobic
Metabolism of
Pyruvate
ATP yield
Two ATPs (net) are produced during the
anaerobic breakdown of one glucose
The 2 NADHs are used to reduce 2 pyruvate
to 2 lactate
Reaction is fast and doesnt require
oxygen
Lactate can be transported by blood to liver and
used in gluconeogenesis
23. Pyruvate Metabolism
Three fates of pyruvate:
Conversion to lactate (anaerobic)
Conversion to alanine (amino acid)
Entry into the TCA cycle via pyruvate
dehydrogenase pathway
24. Pyruvate metabolism
Convert to alanine and export to blood
COO
C O
CH3
COO
HC NH3
+
CH3
Alanine amino transferase
(AAT)
Alanine
Pyruvate
Glutamate -Ketoglutarate
Keto acid Amino acid
25. Pyruvate Metabolism
Three fates of pyruvate:
Conversion to lactate (anaerobic)
Conversion to alanine (amino acid)
Entry into the TCA cycle via pyruvate
dehydrogenase pathway
27. TCA Cycle
In aerobic conditions TCA cycle links pyruvate
to oxidative phosphorylation
Occurs in mitochondria
Generates 90% of energy obtained from food
Oxidize acetyl-CoA to CO2 and capture
potential energy as NADH (or FADH2) and
some ATP
Includes metabolism of carbohydrate, protein, and
fat
30. Electron transport chain (E.T.C):
This pathway is found in inner mitochondria
matrix, energy rich molecules, such as
glucose or fatty acids are metabolized by
series of oxidation reaction ultimately
yielding co2 and H20.
37. Pentose Phosphate Pathway
Secondary metabolism of glucose
Produces NADPH
Similar to NADH
Required for fatty acid synthesis
Generates essential pentoses
Ribose
Used for synthesis of nucleic acids
39. Energy Storage
Energy from excess carbohydrates
(glucose) stored as lipids in adipose tissue
Determined by ATP:ADP ratios
High ATP, acetyl-CoA goes to fatty acid synthesis
Low ATP, acetyl CoA enters TCA cycle to generate
MORE ATP
41. Liver
Use glycogen to export glucose to the
bloodstream when blood sugar is low
Glycogen stores are depleted after
approximately 24 hrs of fasting (in humans)
Glycogenesi
s
42. Glycogenesis
Skeletal muscle
More muscle than liver, therefore
more glycogen in muscle, overall
Use glycogen (i.e., glucose) for energy
only (no export of glucose to blood)
Use already-made glucose for synthesis
of glycogen
43. Fates of Glucose
Fed state
Storage as glycogen
Liver
Skeletal muscle
Storage as lipids
Adipose tissue
Fasted state
Metabolized for energy
New glucose synthesized
Synthesis and
breakdown occur at
all times
The relative rates of
synthesis and
breakdown change
44. Fasting Situation
Where does required glucose come from?
Glycogenolysis
Lipolysis
Proteolysis
Breakdown or mobilization of glycogen stored by glucagon
Glucagon - hormone secreted by pancreas during times of fasting
Mobilization of fat stores stimulated by glucagon and epinephrine
Triglyceride = glycerol + 3 free fatty acids
Glycerol can be used as a glucose precursor
The breakdown of muscle protein with release of amino acids
Alanine can be used as a glucose precursor
45. Low Blood Glucose
Proteins Broken
Down
Insulin
Pancreas
Muscle
Adipose
Cells
Glycogen
Glycerol, fatty acids
released
Glucose released
In a fasted state, substrates for glucose synthesis
(gluconeogenesis) are released from storage
46. Gluconeogenesis
Necessary process
Glucose is an important fuel
Central nervous system
Red blood cells
Not simply a reversal of glycolysis
Insulin and glucagon are primary
regulators
47. Gluconeogenesis
Synthesis of glucose from non-carbohydrate
precursors during fasting.
Glycerol
Amino acids
Lactate
Pyruvate
Propionate
There is no glucose synthesis from fatty acids
Supply carbon skeleton