SIBC511 integration of metabolism printout - Siriraj · PDF fileINTEGRATION OF METABOLISM...
Transcript of SIBC511 integration of metabolism printout - Siriraj · PDF fileINTEGRATION OF METABOLISM...
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SIBC511SIBC511-- INTEGRATION OF METABOLISMINTEGRATION OF METABOLISMAssistant Professor Dr. Chatchawan Srisawat
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INTEGRATION OF METABOLISM
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INTEGRATION OF METABOLISM
• The metabolism of carbohydrate, lipid, and protein are coordinated and well regulated to meet the bodily requirements, especially the energy need, under various conditions.
Fed stateFed state
Fasting stateFasting state
Dietary intake
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• GLUCOSE
• FAT (TRIACYLGLYCEROL)
Major metabolic fuels:
(glycerol + fatty acids)
INTEGRATION OF METABOLISM
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GLUCOSEGLUCOSE
• During the fasting state, the glucose level is prevented from dropping too low.
Normal range
Hunger, sweating, trembling
Convulsion, coma
Permanent brain damage (if prolonged)Death
Various cellular and hormonal regulations of the metabolic pathways work togther to preserve glucose as a fuel for the important organs (e.g., brain, RBC) and shift the source of fuel in other tissues to fatty acids and ketones.
Various cellular and hormonal regulations of the metabolic pathways work togther to preserve glucose as a fuel for the important organs (e.g., brain, RBC) and shift the source of fuel in other tissues to fatty acids and ketones.
INTEGRATION OF METABOLISM
• An important fuel for most tissues (e.g. muscle, red blood cells, and particularly neurons*).
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GLUCOSEGLUCOSE
Normal range
Hunger, sweating, trembling
Convulsion, coma
Permanent brain damage (if prolonged)Death
INTEGRATION OF METABOLISM
• During the fed state, the glucose level is also kept from rising too high (as it can be harmful to the body).
• An important fuel for most tissues (e.g. muscle, red blood cells, and particularly neurons*).
Various cellular and hormonal regulations of the metabolic pathways work togther to accelerate glucose utilization as a fuel and store the excess as glycogen and triacylglycerol.
Various cellular and hormonal regulations of the metabolic pathways work togther to accelerate glucose utilization as a fuel and store the excess as glycogen and triacylglycerol.
Diabetes mellitus
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Fed stateFed state Fasting stateFasting state
Dietary intake
• utilize & restore foodstuff(e.g. glycogen, fat, protein)
• release foodstuff(e.g. glucose, fatty acid, amino acid)
Glycogenesis
Lipogenesis
Glycolysis
Glycogenolysis
Lipolysis
Gluconeogenesis
Protein synthesis
Protein breakdown
INTEGRATION OF METABOLISM
Ketogenesis, ketolysis
INSULIN glucagon, epinephrinegrowth hormone, cortisol
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FED STATEFED STATE
• Insulin – secreted from β cells in the islet of Langerhan in pancreas
• Its secretion can be stimulated by various compounds (e.g. neuro-transmitters, neuropeptides, amino acids) but the most importantone is glucose
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• Insulin can reduce blood glucose by:
uptake of glucose in adipose tissue, muscle
* insulin-independent glucose transport in brain, liver, kidney, RBC
Glucose
CARBOHYDRATE METABOLISM DURING FED STATE - GLUCOSE TRANSPORT
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GLUT 1, GLUT 3 : basal glucose uptake in many tissues, e.g., brain, nerve, RBC
GLUT 4 : insulin-stimulated glucose uptake in adipose tissue and muscle
* In muscle, more GLUT4 can be recruited to the cell membrane during exercise independent of insulin actions to promote glucose uptake and utilization.
GLUT 2 : liver and the islet β cells
Glucose
Note
CARBOHYDRATE METABOLISM DURING FED STATE - GLUCOSE TRANSPORT
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Glucose
Glucose-6-phosphate
Fructose-6-phosphate
Fructose-1,6-bisphosphate
Glyceraldehyde-3-phosphate
1,3-bisphosphoglycerate
3-phosphoglycerate
2-phosphoglycerate
Phosphoenolpyruvate
Pyruvate
Glycolysis converts 1 molecule of glucose (C6) into 2 molecules of pyruvate (C3)
- yields 2 ATP, 2 NADH, and 2 pyruvate per one glucose molecule
+ATP
+ATP
+NADH
- Glycolytic intermediates are important for the biosynthesis of various compounds (e.g. glycerol, acetyl-CoA, 2,3-BPG)
- Major energy-producing pathway in RBC, brain
location: cytosol
functions:
CARBOHYDRATE METABOLISM DURING FED STATE - GLYCOLYSIS
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Glucose
Glucose-6-phosphate
Fructose-6-phosphate
Fructose-1,6-bisphosphate
Glyceraldehyde-3-phosphate
1,3-bisphosphoglycerate
3-phosphoglycerate
2-phosphoglycerate
Phosphoenolpyruvate
Pyruvate
+ATP
+ATP
+NADH
PFK1*
**
***
phosphofructokinase 1 (rate-limiting step)*
important enzymes:
phosphofructokinase 2 (activated by insulin, inhibited by glucagon)
CARBOHYDRATE METABOLISM DURING FED STATE - GLYCOLYSIS
F-2,6-P
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Mechanisms of enzyme regulation
Allosteric regulation – fructose-2,6-bisphosphate, AMP, ADP, ATP etc.Covalent modification – phosphorylation (e.g. through actions of hormones)
CARBOHYDRATE METABOLISM DURING FED STATE - GLYCOLYSIS
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Glucose
Glucose-6-phosphate
Fructose-6-phosphate
Fructose-1,6-bisphosphate
Glyceraldehyde-3-phosphate
1,3-bisphosphoglycerate
3-phosphoglycerate
2-phosphoglycerate
Phosphoenolpyruvate
Pyruvate
+ATP
+ATP
+NADH
PFK1*
**
***
important enzymes:
glucokinase/hexokinase **phosphofructokinase *pyruvate kinase ***
Three irreversible reactions inglycolytic pathway
Need new sets of enzymes to operate in the opposite direction, i.e., the gluconeogenetic pathway.
CARBOHYDRATE METABOLISM DURING FED STATE - GLYCOLYSIS
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pyruvate lactate
Anaerobic glycolysis
In cells deprived of oxygen supply or in RBC (lacking mitochondria), pyruvate can be converted to lactate by lactate dehydrogenase (LDH)to regenerate NAD+ from NADH to be reused in glycolysis.
NADH + H+ NAD+
Lactate is released into the bloodstream and taken up by the liver to convert it to pyruvate and glucose.
CARBOHYDRATE METABOLISM DURING FED STATE - GLYCOLYSIS
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pyruvate
pyruvate
acetyl CoA
oxaloacetatecitrateKrebs
cycle
Aerobic glycolysis
When oxygen supply is adequate, pyruvate enters mitochondria and is converted into acetyl CoA by pyruvate dehydrogenase (PDH).
NADH + H+
NAD+
*Note
• PDH contains thaimine (vit B1), lipoic acid, CoA, FAD (vit B2), NAD (niacin or vit B3) as coenzymes.
• Disease association
Wernicke-korsakoff
B1 deficiency (beri-beri)
CARBOHYDRATE METABOLISM DURING FED STATE - GLYCOLYSIS
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pyruvate
pyruvate acetyl CoA
oxaloacetatecitrateNADH
FADH2GTP
TCAcycle
aerobic glycolysis
-+Pyruvate
carboxylase
Pyruvate dehydrogenase
Important feedback controls of acetyl CoA:
- inhibits Pyruvate dehydrogenase- activates Pyruvate carboxylase
CARBOHYDRATE METABOLISM DURING FED STATE - GLYCOLYSIS
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KREBS CYCLE
location: mitochondria
functions: - Complete oxidation of acetyl CoAacetyl CoA 2CO2 + 3NADH + FADH2 + GTP
Cindy Is Kinky So SheFornicates More Often
kinky = marked by unconventional sexual preferences or behavior, as fetishism, sadomasochism, or the like
Krebs orCitric acid or
tricarboxylic acid cycle
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important enzymes:
isocitrate dehydrogenase (rate-limiting step – inhibited by NADH)
***
KREBS CYCLE
Krebs orCitric acid or
tricarboxylic acid cycle
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* Krebs cycle intermediates are linked with the metabolic pathways of many important compounds (e.g. amino acids, fatty acids, nucleic acids, etc).
KREBS CYCLE
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Electron transport system
NADH + H+NAD+
FADH2O2
H2O
ATP
ADP + Pi
NADHFADH2
aerobic glycolysis
KREBS CYCLE
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• Excess glucose during the fed state is
also stored as glycogen in liver and
muscle (Glycogenesis).
glycogen synthase (rate-limiting step)activated by insulin
glucose-6-phosphate
glycogen synthasebranching enzyme
Glycogen
glucose
location: cytosol
important enzymes:
CARBOHYDRATE METABOLISM DURING FED STATE - GLYCOGENESIS
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Pentose phosphate pathway
• NADPH
• Ribose
Glucose-6-phosphate dehydrogenase *
- synthesis of fatty acid, cholesterol, nucleotides
- DNA & RNA synthesis
glucose
glucose-6-phosphate
• In addition, excess glucose also enters the pentose phosphate pathway (Hexose monophosphate shunt)
location: cytosol
functions: generate
important enzymes:
- coenzymes of antioxidant enzymes
glucose-6-phosphate dehydrogenase G6PD (rate-limiting step)
CARBOHYDRATE METABOLISM DURING FED STATE –PENTOSE PHOSPHATE PATHWAY
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adipocyte
pyruvate
acetyl CoA
oxaloacetatecitrateKrebs
cycle
glucose
glycolysis acetyl CoA
fatty acid glycerol
triacylglycerol
• Stored as triacylglycerol
lipoprotein (VLDL)
liver
• During the fed state, the increased glucose and insulin levels stimulate the syntheses of fatty acid and triacylglycerol (Lipogenesis).
NADPH
DHAP
malonyl CoAacetyl CoA carboxylase
- Excessive intake of high carbohydrate diet can lead to obesity.
FATTY ACID SYNTHESIS AND LIPOGENESIS
- On average, a 70-kg man stores ~ 12 kg of fat, which can provideenough energy for 2 months during starvation (fat gives 9 kcal/g).
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adipocyte
pyruvate
acetyl CoA
oxaloacetatecitrate
glucose
glycolysis acetyl CoA
fatty acid glycerol
triacylglycerol
• Stored as triacylglycerol
lipoprotein (VLDL)
liver
NADPH
DHAP
malonyl CoAacetyl CoA carboxylase
Fatty acid synthesislocation: cytosol
Krebscycle
FATTY ACID SYNTHESIS AND LIPOGENESIS
Therfore, acetyl CoA has to be transported into the cytosol as citrate, which is then converted back to acetyl CoA in the cytosol by citrate lyase.
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adipocyte
pyruvate
acetyl CoA
oxaloacetatecitrate
glucose
glycolysis acetyl CoA
fatty acid glycerol
triacylglycerol
• Stored as triacylglycerol
lipoprotein (VLDL)
liver
NADPH
DHAP
malonyl CoAacetyl CoA carboxylase
Fatty acid synthesis
important enzymes:
acetyl CoA carboxylase (rate-limiting step) activated by insulin and citrate
fatty acid synthase (use NADPH derived from the pentose phosphate pathway)
Krebscycle
FATTY ACID SYNTHESIS AND LIPOGENESIS
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adipocyte
pyruvate
acetyl CoA
oxaloacetatecitrate
glucose
glycolysis acetyl CoA
fatty acid glycerol
triacylglycerol
• Stored as triacylglycerol
lipoprotein (VLDL)
liver
NADPH
DHAP
malonyl CoAacetyl CoA carboxylase
• The newly-synthesized fatty acids are combined with glycerol-3-phosphate (a glycolytic intermediate) to generate triacylglycerol, which is then transported into the bloodstream and peripheral tissues in the forms of lipoprotein VLDL.
Krebscycle
FATTY ACID SYNTHESIS AND LIPOGENESIS
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CHOLESTEROL SYNTHESIS
HMG CoA
lipoprotein (VLDL)
HMG CoA reductase
mevalonate
cholesteroltransported into the bloodstream
location: cytosol important enzymes:
During the fed state, the cholesterol synthesis is also increased due to the action of insulin and the availability of acetyl CoA in the cytosol.
HMG CoA reductase (rate-limiting step)
HMG CoA = 3-hydroxy-3-methylglutaryl CoA
liver
pyruvate
acetyl CoA
oxaloacetatecitrate
glucose
glycolysis acetyl CoA
liver
Krebscycle
- activated by insulin - inhibited by antilipidemic drugs Statin
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LIPOPROTEIN TRANSPORT OF LIPID
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Gut
Protein synthesis
Nitrogenous compounds
Amino acid pool
Amino acid
AMINO ACID METABOLISM DURING FED STATE
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histamine
heme
Examples of important nitrogenous compounds
AMINO ACID METABOLISM DURING FED STATE
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Amino acid pool
Gut
Protein synthesis
Nitrogenous compounds
• After being used for the syntheses of proteins and nitrogenous compounds, the excess amino acids are undergone transmination and deamination.
Transamination &Deamination
AMINO ACID METABOLISM DURING FED STATE
• Unlike glucose or fatty acids, amino acids are not stored.
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A) Transamination
B) Deamination
AMINO ACID METABOLISM DURING FED STATE
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α-keto acids
Intermediates inmetabolic pathways (e.g. glycolysis andKrebs cycle)
During the fed state, the carbon skeletons of amino acids can be used for:
• energy production
• synthesis of fatty acid and triacylglycerol
AMINO ACID METABOLISM DURING FED STATE
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FED STATEFED STATE
GlucoseGlucose
insulin
counterregulatory hormones
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glycolysis
glycogenesis
lipogenesis
protein synthesis
FED STATEFED STATE
GlucoseGlucose
insulin
counterregulatory hormones
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glucagonepinephrines
growth hormonecortisol
glucagonepinephrines
growth hormonecortisol
counterregulatory hormones
FASTING STATEFASTING STATE
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glucose glucose-6-phosphate
glycogen phosphorylasedebranching enzyme
Glycogen
liver
• During the fasting state, glycogen in the liver is broken down to release glucose into the bloodstream, preventing the blood glucose from dropping too low (Glycogenolysis).
location: cytosol important enzymes:
glycogen phosphorylase (rate-limiting step)activated by glucagon and epinephrine
CARBOHYDRATE METABOLISM DURING FASTING STATE - GLYCOGENOLYSIS
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glucose glucose-6-phosphate
glycogen phosphorylasedebranching enzyme
glucose-6-phosphatase*
Glycogen
liver
• Glycogenesis occurs both in liver and muscle.
• However, the muslce lacks the enzyme glucose-6-phosphatase, thus unable to release glucose into the bloodstream: i.e. the muscle glycogen is stored and used only within the muscle.
CARBOHYDRATE METABOLISM DURING FASTING STATE - GLYCOGENOLYSIS
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• Therefore, glycogen is used up only within 12-24 hr after fasting.
• On average, a 70-kg man stores ~70 g of glycogen in the liver and
400 g in muscle (carbohydrate yields 4 kcal/g).
CARBOHYDRATE METABOLISM DURING FASTING STATE - GLUCONEOGENSIS
very little comparing with fat storage (~12 kg in a 70-kg man)
• To keep up the blood glucose level, new glucose must be synthesized from other compounds (e.g. amino acids, lactate, glycerol) by a process called gluconeogenesis, which is activated by the counterregulatory hormones (glucagon and epinephrine).
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pyruvate
acetyl CoA
oxaloacetatecitrateKrebs
cycle
glucose glucose-6-phosphate
fructose-6-phosphate
phosphoenolpyruvate
lactate
glycerol
amino acids
fructose-1,6-bisphosphate
(source - muscle)
liver & kidney
Lactate dehydrogenase
• Gluconeogenesis is essentially a reverse process of glycolysis except at the three irreversible steps, which require new set of enzymes operating in the opposite directions.
location: cytosol และ mitochondria
CARBOHYDRATE METABOLISM DURING FASTING STATE - GLUCONEOGENSIS
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pyruvate
acetyl CoA
oxaloacetatecitrateKrebs
cycle
glucose glucose-6-phosphate
fructose-6-phosphate
phosphoenolpyruvate
lactate
glycerol
amino acids
fructose-1,6-bisphosphate
(source - muscle)
liver & kidney
Lactate dehydrogenase
important enzymes:
12
3
4
1. pyruvate carboxylase and 2. PEP carboxykinase
3. fructose-1,6-bisphosphatase (rate-limiting step)4. glucose-6-phosphatase
CARBOHYDRATE METABOLISM DURING FASTING STATE - GLUCONEOGENSIS
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pyruvate
acetyl CoA
oxaloacetatecitrateKrebs
cycle
glucose glucose-6-phosphate
fructose-6-phosphate
phosphoenolpyruvate
lactate
glycerol
amino acids
fructose-1,6-bisphosphate
(source - muscle)
liver & kidney
Lactate dehydrogenase
12
3
4
Note: acetyl CoA (derived from the beta-oxidation of fatty acid) cannot be used as a substrate for gluconeogenesis.
CARBOHYDRATE METABOLISM DURING FASTING STATE - GLUCONEOGENSIS
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fatty acid
glycerol
triglyceride
adipocyte
free fatty acid
acetyl CoA
oxaloacetatecitrateKrebs
cycle
carnitine
β-oxidation
• Counterregulatory hormones stimulates lipolysis by activating hormone-sensitive lipase, which releases fatty acids into the bloodstream- a proces called Lipolysis. Peripheral tissues such as muscle, heart, and liver can use fatty acids as fuel, preserving glucose for the important organs like brain.
gluconeogenesis
hormone-sensitive lipase
LIPOLYSIS AND BETA-OXIDATION OF FATTY ACID
* rate-limiting step
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fatty acid
glycerol
triglyceride
adipocyte
free fatty acid
acetyl CoA
oxaloacetatecitrate
carnitine
β-oxidation
gluconeogenesis
hormone-sensitive lipase
* rate-limiting step
Beta oxidation of fatty acid
location: mitochondriaimportant enzymes:carnitine acyltransferase-1 (rate-limiting step)
LIPOLYSIS AND BETA-OXIDATION OF FATTY ACID
Krebscycle
facilitating fatty acid transport into mitochondria
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LIPOLYSIS AND BETA-OXIDATION OF FATTY ACID
β-oxidation of fatty acids
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Ketonebodies
acetoacetateβ-OH-butyrate
liver
acetone
Blood ketone
• An increase acetyl CoA in the liver from β oxidation and a low oxaloacetate, which is used for gluconeogenesis, lead to a production of ketone bodies.
free fatty acid
acetyl CoA
oxaloacetatecitrateTCA
cyclecarnitine
β-oxidation
ENERGY METABOLISM DURING FASTING STATE - KETOGENESIS
gluconeogenesisglucose
• more water soluble than fatty acids• can be easily transported to the peripheral tissues.
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Ketonebodies
acetoacetateβ-OH-butyrate
liver
acetone
Blood ketone
• The liver produces ketone bodies for other tissues (Ketogenesis) but cannot use them (Ketolysis) due to the lack of enzyme beta-ketoacyl CoA transferase).
free fatty acid
acetyl CoA
oxaloacetatecitrateTCA
cyclecarnitine
β-oxidation
ENERGY METABOLISM DURING FASTING STATE - KETOGENESIS
gluconeogenesisglucose
• Neurons cannot use fatty acids directly. However, they can adapt to use ketone bodies during prolonged fasting or starvation.
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pyruvate
acetyl CoA
oxaloacetatecitrate
TCAcycle
glucose glucose-6-phosphate
fructose-6-phosphate
phosphoenolpyruvate
lactate
glycerol
amino acids
fructose-1,6-bisphosphate
(source - muscle)
liver & kidney
Lactate dehydrogenase
• The carbon skeletons of amino acids are an important source of substrates for gluconeogenesis. They are derived from the protein breakdown as a result of a counterregulatory hormone corticosteroid action.
AMINO ACID METABOLISM DURING FASTING STATE
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Protein breakdown
Amino acid pool
counterregulatory hormones
(e.g. cortisol)
• The carbon skeletons of amino acids are an important source of substrates for gluconeogenesis. They are derived from the protein breakdown as a result of a counterregulatory hormone corticosteroid action.
AMINO ACID METABOLISM DURING FASTING STATE
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Glucogenic
VS.
Ketogenic amino acids
During the fasting state, the carbon skeletons of amino acids are used for:
• energy production
• gluconeogenesis
• ketogenesis
AMINO ACID METABOLISM DURING FASTING STATE
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Amino acid
Amino nitrogen(e.g. NH3)
transaminationdeamination
metabolic intermediates
• energy production (Fed & Fasting)
• fatty acids and lipogenesis (Fed)
• gluconeogenesis (Fasting)
• ketogenesis (Fasting)
carbon skeleton
AMINO ACID METABOLISM DURING FASTING STATE
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Very-well fedVery-well fed
GlucoseAcetyl CoA
+
Glutamate
Very-well fedVery-well fed
Amino acid
CoA SHN-acetylglutamate
synthase
N-acetylglutamate
Carbamoyl phosphate
UreacycleUreacycle
FastingFasting
Fatty acid
Diet Diet
Lipolysis
FastingFasting
Protein breakdown
+
AMINO ACID METABOLISM DURING FASTING STATE• The metabolism of amino acids are coordinated with those of carbohydrate and lipid both during the fed or fasting states.
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FASTING STATEFASTING STATEGlucoseGlucose
insulin
counterregulatory hormones
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GlucoseGlucose
insulin
counterregulatory hormones
gluconeogenesis
glycogenolysis
lipolysis
to increase blood glucose
to increase blood glucose
ketogenesis/ketolysis
to use fat as fuel, thus preserving glucose
FASTING STATEFASTING STATE
to use fat as fuel, thus preserving glucose
protein breakdown for gluconeogenesis/energy
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SUMMARY : INTEGRATION OF METABOLISM
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A 4-month-old baby girl was taken to the hospital because of a high-grade fever and drowsiness. The patient had a history of frequent hypoglycemic episodes since birth, which improved after receiving intravenous injections of glucose.
INTEGRATION OF METABOLISM – PROBLEM CASE
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Physical examination: the patient was drowsy and had an enlarged liver.
Laboratory findings:
glucose 24 mg/dl (normal 40-90 mg/dl)
ammonia 155 umol/L (normal 25-50 umol/L)
lactate 6.7 mol/L (normal 0.9-1.7 mol/L)
ketone 0 mg/L (normal 0.5-3 mg/dl)
INTEGRATION OF METABOLISM – PROBLEM CASE
plasma fatty acid
plama and urinary acylcarnitine
plasma dicarboxylic acid
Further biochemical investigations indicates theDeficiency of Medium-chain Acyl CoA Dehydrogenase (MCAD)
Further biochemical investigations indicates theDeficiency of Medium-chain Acyl CoA Dehydrogenase (MCAD)
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β-oxidation of fatty acids
• Defects in fatty acid oxidation
Less acetyl-CoA is produced.
Short chain fatty acid = C2-C4, medium chain = C6-C10, Long chain = C12-C26
INTEGRATION OF METABOLISM – PROBLEM CASE
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adipocyte
fatty acid
glycerol
triglyceride
free fatty acid
Acetyl CoA
oxaloacetate
citrateTCAcycle
carnitine
β-oxidation
• During the fasting state, lipolysis is stimulated to release fatty acids to be used as fuel by other tissues, thus preserving glucose for the brain.
INTEGRATION OF METABOLISM – PROBLEM CASE
plasma fatty acid (from increased lipolysis and decreased breakdown)
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• During the fasting state, amino acids, glycerol, lactate are used as substrates for gluconeogenesis.
gluconeogenesis
pyruvate
acetyl CoA
oxaloacetatecitrate
TCAcycle
glucose glucose-6-phosphate
fructose-6-phosphate
phosphoenolpyruvate
lactate
glycerol
amino acids
fructose-1,6-bisphosphate
(source - muscle)
liver & kidney
Lactate dehydrogenase
INTEGRATION OF METABOLISM – PROBLEM CASE
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gluconeogenesis
pyruvate
acetyl CoA
oxaloacetatecitrate
TCAcycle
glucose glucose-6-phosphate
fructose-6-phosphate
phosphoenolpyruvate
lactate
glycerol
amino acids
fructose-1,6-bisphosphate
(source - muscle)
liver & kidney
Lactate dehydrogenase
+Fatty acid
• Furthermore, gluconeogenesis can be stimulated by acetyl CoA because it is an allosteric activator of pyruvate carboxylase, resulting in an increase of oxaloacetate and glucose production.
INTEGRATION OF METABOLISM – PROBLEM CASE
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gluconeogenesis
pyruvate
acetyl CoA
oxaloacetatecitrate
TCAcycle
glucose glucose-6-phosphate
fructose-6-phosphate
phosphoenolpyruvate
lactate
glycerol
amino acids
fructose-1,6-bisphosphate
(source - muscle)
liver & kidney
Lactate dehydrogenase
+Fatty acid
• Defects in fatty acid oxidation -> a decrease of acetyl CoA -> a decrease of oxaloacetate production -> impaired gluconeogenesis
HypoglycemiaHypoglycemia HyperlactatemiaHyperlactatemia
INTEGRATION OF METABOLISM – PROBLEM CASE
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• During the fasting state, ketogenesis in the liver is stimulated to produce ketones to be used as fuel by other tissues, thus preserving glucose for the brain.
Ketonebodies
acetoacetateβ-OH-butyrate
liver
acetone
Blood ketone
free fatty acid
acetyl CoA
oxaloacetate
citrateTCAcycle
carnitine
β-oxidation
INTEGRATION OF METABOLISM – PROBLEM CASE
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liver
• Defects in fatty acid oxidation -> a decrease of acetyl CoA -> impaired ketogeneis HypoketoticHypoketotic
Ketonebodies
acetoacetateβ-OH-butyrate
acetone
free fatty acid Acetyl CoA
oxaloacetate
citrateTCAcycle
β-oxidation of fatty acid
Blood ketone
INTEGRATION OF METABOLISM – PROBLEM CASE
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liver
Ketonebodies
acetoacetateβ-OH-butyrate
acetone
free fatty acid Acetyl CoA
oxaloacetate
citrateTCAcycle
β-oxidation of fatty acid
Blood ketone
• Because of the defects in β oxidation of fatty acid and low ketone in the blood, cells have to use glucose as fuel, further depleting blood glucose.
drowsiness in the patientHypoglycemiaHypoglycemia
INTEGRATION OF METABOLISM – PROBLEM CASE
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• Defect in beta oxidation -> accumulation of acyl CoA & acylcarnitine
ระดับ acylcarnitine สูงในเลือดและปสสาวะระดับ acylcarnitine สูงในเลือดและปสสาวะ
INTEGRATION OF METABOLISM – PROBLEM CASE
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• Causes of hyperammonemia
- Increase protein breakdown and deamination of amino acids to be used as substrates for gluconeogenesis during the fasting state
- Decrease synthesis of N-acetylglutamate** allosteric activator of CPSI – rate-limiting step of urea cycle
INTEGRATION OF METABOLISM – PROBLEM CASE
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- Decrease oxaloacetate production -> decrease aspartate* The nitrogen atoms of urea come from free ammonia and the amino group of aspartate.
- Increase protein breakdown and deamination of amino acids to be used as substrates for gluconeogenesis during the fasting state
- Decrease synthesis of N-acetylglutamate** allosteric activator of CPSI – rate-limiting step of urea cycle
INTEGRATION OF METABOLISM – PROBLEM CASE
• Causes of hyperammonemia
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β-oxidation of fatty acids
-O-C-CH2-CH2-CH2-C-O-
O O
dicarboxylic acid
ω-oxidationω-oxidation
C-O-
O
Fatty acid
β-oxidation in peroxisome
β-oxidation in peroxisome
INTEGRATION OF METABOLISM – PROBLEM CASE
plasma dicarboxylic acid
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The patient was received intravenous injection of glucose to correct the
hypoglycemic symptoms. The mother was advised to frequently feed
the baby and not to let her fast for too long (>12 hr). At night, feeding
the patient with corn starch was also recommended.
Briefly explain how the above therapeutic measures can resolve the patient’s problems.
Briefly explain how the above therapeutic measures can resolve the patient’s problems.
QuestionQuestion
INTEGRATION OF METABOLISM – PROBLEM CASE
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SUMMARY : INTEGRATION OF METABOLISM
Gluconeogenesis
Glycogenesis
Fatty acid synthesis
Glycolysis
Glycogenolysis
β oxidation/ketogenesis
Lipogenesis Lipolysis
InsulinCounterregulatory
hormones
• The processes are regulated to ascertain that the opposite processes do not occur at the same time.
FED FASTING
• The metabolism of carbohydrate, lipid, and protein are coordinated and well regulated to meet the bodily requirements, especially the energy need, under various conditions.
Protein synthesis Protein breakdown