KH Metab 2016

Carbohydrate Metabolism
siufui hendrawan – Dept. of Biochemistry and Molecular Biology

Faculty of Medicine -Tarumanagara University
Jakarta, 2016
Learning Objective
Memahami berbagai macam makanan sumber
karbohidrat, struktur karbohidrat, serta metabolismenya
pada tingkat seluler hingga hasil akhir metabolisme
tersebut.
CARBOHYDRATES ARE ALDEHYDE OR KETONE
DERIVATIVES OF POLYHYDRIC ALCOHOLS
• Carbohydrates are
widely distributed in
plants and animals;
they have important
structural and
metabolic roles.
• Animals can synthesize

carbohydrates from
amino acids, but most
are derived ultimately
http://sevenscience.weebly.com/relationships-in-the-
from plants. ecosystems.html
Energy balance
The structures of common dietary carbohydrates. For disaccharides
and greater, the sugars are linked through glycosidic bonds between
the anomeric carbon of one sugar and a hydroxyl group on another
sugar.
Glucose
• central to all of metabolism
• universal fuel for all types of human cells
• the source of carbon for the synthesis of most
other compounds.
• precursor for the synthesis of other sugars
compounds, such as lactose, cell surface antigens,
nucleotides, or glycosaminoglycans.
• precursor of noncarbohydrate compounds; it can
be converted to lipids (including fatty acids,
cholesterol, and steroid hormones), amino acids,
and nucleic acids.
Dietary carbohydrates are converted to glucose, galactose, and
fructose in the digestive tract
In tissues, fructose and galactose are converted to
intermediates of glucose metabolism. Thus, the
fate of these sugars parallels that of glucose.
Monosaccharides are absorbed from the intestine, enter the blood, and travel to the
tissues where they are metabolized.
Glucose uptake by cell
The role of insulin
After glucose is transported into cells, it is phosphorylated by a
hexokinase to form glucose 6-phosphate. Glucose 6-phosphate
can then enter a number of metabolic pathways. The three that
are common to all cell types are glycolysis, the pentose
phosphate pathway, and glycogen synthesis
• The major fate of glucose 6-
phosphate is oxidation via the
pathway of glycolysis, which
provides a source of ATP for all
cell types.
• Cells that lack mitochondria

cannot oxidize other fuels. They
produce ATP from anaerobic
glycolysis (the conversion of
glucose to lactic acid).
• Cells that contain mitochondria

oxidize glucose to CO2 and H2O
via glycolysis and the TCA cycle.
Some tissues, such as the brain,
depend on the oxidation of
glucose to CO2 and H2O for
energy because they have a
limited capacity to use other
fuels.
Glucose produces the
intermediates of glycolysis
and the TCA cycle that are
used for the synthesis of
amino acids and both the
glycerol and fatty acid
moieties of
triacylglycerols.
• Another important fate of
glucose 6-phosphate is
oxidation via the pentose
phosphate pathway, which
generates NADPH. The
reducing equivalents of
NADPH are used for
biosynthetic reactions and
for the prevention of
oxidative damage to cells
• In this pathway, glucose is

oxidatively decarboxylated to
5-carbon sugars (pentoses),
which may reenter the
glycolytic pathway. They also
may be used for nucleotide
synthesis
• Glucose 6-phosphate is also
converted to UDP-glucose,
which has many functions in
the cell. The major fate of UDP-
glucose is the synthesis of
glycogen, the storage polymer
of glucose.
• Although most cells have

glycogen to provide emergency
supplies of glucose, the largest
stores are in muscle and liver.
Muscle glycogen is used to
generate ATP during muscle
contraction.
• Liver glycogen is used to

maintain blood glucose during
fasting and during exercise or
periods of enhanced need.
• All cells are continuously
supplied with glucose under
normal circumstances; the
body maintains a relatively
narrow range of glucose
concentration in the blood
(approximately 80-100 mg/dL)
in spite of the changes in
dietary supply and tissue
demand as we sleep and
exercise. This process is called
glucose homeostasis.
• Low blood glucose levels

(hypoglycemia) are prevented
by a release of glucose from
the large glycogen stores in the
liver (glycogenolysis); by
synthesis of glucose from
lactate, glycerol, and amino
acids in liver (gluconeogenesis)
• High blood glucose levels
(hyperglycemia) are
prevented both by the
conversion of glucose to
glycogen and by its
conversion to triacylglycerols
in liver and adipose tissue.
• Thus, the pathways for

glucose utilization as a fuel
cannot be considered as
totally separate from
pathways involving amino
acid and fatty acid
metabolism
The release of insulin and glucagon by the pancreas aids in the
body’s use and storage of glucose.
Intertissue balance in the utilization and storage of

glucose during fasting and feeding is accomplished
principally by the actions of the hormones of
metabolic homeostasis—insulin and glucagon
Glycolysis
• Sequence of reactions that converts glucose into
pyruvate
 Relatively small amount of energy produced

 Glycolysis reactions occur in cytoplasm
 Does not require oxygen
Lactate (anaerobic)
Glucose → Pyruvate
Acetyl-CoA (TCA cycle)
Glycolysis
Anaerobic Metabolism of Pyruvate
• Solution:
• Turn NADH back to NAD+ by making lactate (lactic acid)
(reduced) (oxidized)
NADH + H+ NAD+
COO– COO–
C O HC OH
Lactate dehydrogenase
CH3 CH3
Pyruvate Lactate
(oxidized) (reduced)
Pyruvate Dehydrogenase Complex (PDH)
• Prepares pyruvate to enter the TCA cycle
Aerobic Conditions
Electron TCA Cycle
Transport
Chain
Electron Transport Chain
Electron Transport Chain
• NADH + H+ and FADH2 enter ETC

• Travel through complexes I – IV
• H+ flow through ETC and eventually attach to O2
forming water
NADH + H+ 3 ATP
FADH2 2 ATP
Glikogenesis and Glikogenolisis
Gluconeogenesis
• Synthesis of glucose from non-carbohydrate
precursors during fasting in monogastrics
 Glycerol
 Amino acids
 Lactate Supply carbon skeleton
 Pyruvate
 Propionate
 There is no glucose synthesis from fatty acids
• Occurs primarily in liver, but can also occur in

kidneys and small intestine
Pentose Phosphate Pathway
• Secondary metabolism of glucose
• Produces NADPH
• Required for fatty acid synthesis
• Glutathione reduction
• Generates essential pentoses
• Ribose
• Used for synthesis of nucleic acids
Carbohydrate metabolism in different cell
types
Metabolic abnormalities
Frequently caused by faulty endocrine regulation (e.g.,
diabetes mellitus) or genetic defects of enzymes
(enzymopathies)
Abnormalities of carbohydrate metabolism
Diabetes mellitus is caused by an absolute or relative lack of insulin
that, among other consequences, leads to an increase in plasma glucose
concentration
Daftar Pustaka
• Murray RK, et al. (2009) Harper’s Illustrated Biochemistry,
28th Edition. New York: McGraw-Hill Lange.
• Silbernagl S, Despopoulos A. (2008) Color Atlas of
Physiology, 6th Edition. New York: Thieme.
• Silbernagl S, Lang F. (2000) Color Atlas of Pathophysiology.
New York: Thieme.
• Marks AD, Lieberman MA. (2005) Marks’ Basic Medical
Biochemistry: A Clinical Approach, 4th Edition. Philadelphia:
Lippincott Williams & Wilkins.
Thank You

KH Metab 2016

Uploaded by

Copyright:

Available Formats

KH Metab 2016

Uploaded by

Document Information

Original Description:

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

KH Metab 2016

Uploaded by

Copyright:

Available Formats

Carbohydrate Metabolism

siufui hendrawan – Dept. of Biochemistry and Molecular Biology

• Animals can synthesize

• Cells that lack mitochondria

• Cells that contain mitochondria

• In this pathway, glucose is

• Although most cells have

• Liver glycogen is used to

• Low blood glucose levels

• Thus, the pathways for

Intertissue balance in the utilization and storage of

 Relatively small amount of energy produced

• Prepares pyruvate to enter the TCA cycle

• NADH + H+ and FADH2 enter ETC

• Occurs primarily in liver, but can also occur in

You might also like