THE KETONE BODIES: FROM PROVIDERS OF ENERGY FOR LIFE TO FATAL KILLERS By Prof Morsi Arab University...
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Transcript of THE KETONE BODIES: FROM PROVIDERS OF ENERGY FOR LIFE TO FATAL KILLERS By Prof Morsi Arab University...
THE KETONE BODIES: FROM PROVIDERS OF ENERGY FOR
LIFE TO FATAL KILLERS
ByProf Morsi Arab
University of Alexandria, Egypt
Storage
The Fed State
Body Energy in {The Fed State}
1. Provision of Energy : by continuous supply from ingested glucose and fat.
2. Storing of Energy : In the liver: (Glycogen ) up to 1000 Kcal In Fat Depots (TG) up to 100000 Kcal
3 Tissue utilization of fuel for Energy: All Tissues can use glucose or FA . Except the Brain , only glucose .
In The { Fasting } and { Starvation } States
I. In An Over night Fast 1 .Glycogen stores are depleted …….(shortage of
glucose) 2 .Fat has to be utilized for energy : (TG)
FA + Glycerol) oxidation for energy) (is used for neoglucogenesis
in the liver( Acetyl CoA
Ketone Bodies (KB) ………………… up to 0.1 - 0.4 mM
II. In Prolonged Fasting ( Starvation ) … up to 7-10 mM
Adipose Tissue Blood
InsulinLipolysis
FFA
Delivery
KB
X
FFA
Muscles Brain
Utilization
Liver
Ketogenesis
Glucagon
Insulin
Ketogenesis What is it and What For?
Ketogenesis is the conversion of long chain FA to the Four carbon acetoacetate and 3 hydroxy butyrate ( Ketone Bodies: KB).
The primary utility of ketogenesis is to provide a universally accepted * fuel for energy production… ( an adaptive response in starvation)
* The Brain oxidizes KB but not Fat.* Other Tissues oxidize KB and Fat.
Ketosis or Keto-Acidosis
A large accumulation of KB is dangerous, because it leads to profound metabolic acidosis.
The physiologic Ketogenesis of fasting and
the adaptive ketosis in starvation never progress to life threatening acidosis
The Chemical Sequence from FA to KB (through Acetyl Co A)
• 2 Acetyl Co A2 Acetoacetyl CoA+CoA• Aceto acetyl Co A +Acetyl Co A Hydoxymethyl Glutaryl Co A3. Hyrdoxymethyl Glutaryl Co A Acetoacetate + Acetyl Co A4. Acetoacetate + NADH = H2 3-Hydroxy Butyrate
The “Mitochondria” and the “Carnitine CoA Shuttle”
• The mitochondria play a major role in ketogenesis.
• Medium chain FA easily enter the mitochondria , but Long chain FA require a shuttle to get inside (The Carnitine CoA Shuttle)
Carnitine Shuttle
The Carnitine CoA Shuttle Reaction
LCFA (outside MC)----------------- Carnitine) Carnitine Palmitoyl Transferase I- CPT I(
Carnitine -----------------LCFA (inside MC )) Carnitine Palmitoyl Transferase II – CPT II(
..………………………………………………Therefore , the CPT I enzyme is a key control in FA oxidation and in Ketogenesis
Carnitine FA
Malonyl CoA
KB
X
Acetyl Co A
Glucagon
CPT1
CPT IIX
Co A
The role of “Malonyl Co A” in Ketogenesis
Malonyl Co A is derived from Acetyl Co A
A high level of Malonyl Co A in the hepatocyte inhibits the activity of CPT I
and so it damps down ketogenesis.
Insulin increases the production of Malonyl
Co A from Acetyl Co A
The Role of Insulin in Ketogenesis
Lack of insulin has been long known to be related to development of ketosis.
The presence of Insulin blocks Lipolysis, the source of FFA delivery to the liver, the substrate needed for ketogenesis.
Insulin increases poduction of Malonyl Co A
(so, inhibits CPT I …damps ketogenesis, inspite of any increased substrate FFA delivery)
Glucagon and Ketogenesis
Diabetes is not only a disease of Insulin deficiency but also excess Glucagon.
Glucagon has ketogenic activity . It plays this role in regulation of ketogenesis independent from insulin .. ( It activates FA oxidation at the expense of TG synthesis
The Glucagon / Insulin ratio is more important than the absolute value of either, in determining the metabolic events in the hepatocyte
The main factors which control Ketogenesis in the liver
1. Availability of the substrate (Long Chain Fatty Acids) : from increased production by lipolysis with increased delivery of FA to the liver.
2. The level of Malonyl Co A in the liver, with its influence to inhibit the Carnitine Palmitoyl Transferase I (CPT I)
3. The Glucagon / Insulin Ratio : a high ratio increases lipolysis and activation of oxidative ketogenesis , a low ratio counteracts ketogenisis
Ketogenesis under Patho- physiolocal states
•
Ketone Bodies in Obesity
1. In obesity, FFA and KB levels are elevated (independent on normal or impaired glucose tolerance)
2. KB Clearance is also diminished.
3. But, following an oral glucose load FFA and KB levels are lowered.
Ketone Bodies in Type 2 Diabetes
1 FFA and KB are usually elevated (circulating KB may increase 3 folds in non obese diabetics even if FFA are normal.)
N.B. Why KB level is increased in type 2 diabetes inspite of increased insulin (which should counteract ketogenesis ) ?
- because of an also increased Glucagon, (with finally a lower Insulin / Glucagon ratio)
Ketone Bodies in Type 1 Diabetes
1.Insulin is deficient2. FFA and KB are increased , ketogenesis is
activated to provide energy source substitute.3. FFA uptake across the splancnic area is
increased . Delivery of FFA substrate to the liver is not blocked (absence of the blocking effect of insulin )
3. KB Clearance is diminished.4. An unrestricted KB accumulation leads to
metabolic acidosis (Diabetic Keto-acidosis )
Ketone Bodies in Hyperthyroidism
1. Increased lipolysis ( more FFA) =
augmented substrate delivery
2. Increased lipid oxidation .
All levels of FFA, Glycerol and KB are elevated .
Alexandrie – Palais du Montazah
Thank You