Lyposlysis, Fatty Acid Oxidation, and Metabolism Flashcards
Triglyceride Lipases
Break triglycerides into fatty acids and glycerol via lypolysis
Both products of this reaction are released into plasma
FA circulate bound to albumin and are called free fatty acids
Enzymes for lypolysis
ATGL (adipose triglyceride lipase) major one
HSL (hormone sensitive lipase) mainly for diglycerides
MGL (monoglyceride lipase) for monoglycerides
Lipoprotein lipase
Acts with circulating TG rich molecules (VLDL, chylomicrons) to facilitate uptake of FA into adipocyte.
This enzyme is made and secreted by adipocytes and gets lodged in EC capillary endothelium.
NEFA (non-esterified fatty acids)
Free fatty acids
Fate of triglycerides
Fatty acids become as oxidative fuel or ketone bodies in liver.
Glycerol becomes available for gluconeogenisis in liver and kidney.
Location of fatty acid metabolism
In mitochondria. Leads to preferred source of oxidative metabolism in muscle.
CD36
protein involved in taking FA into cells. Process not known.
Fatty-Acyl CoA
What fatty acids taken into the cell are turned into by Fatty-Acyl CoA Synthases.
Carnitine
Zwitterion attached to fatty acid instead to Acyl-CoA by Carnitine-Acyl transferases I (CAT1) to allow fatty acid to go into mitochondrion.
CAT2 is on the outer side of the inner mitochondrial membrane.
Malonyl-CoA
Allosterically inhibits CAT1.
Establishes inverse relationship between FA synthesis and FA oxidation in liver
Presence of Malonyl-CoA governs the switch from using glucose of FA for energy
ACC-B (Acetyl-CoA Carboxylase-B)
Makes Malonyl-CoA in the process of FA synthesis
This happens most when glucose is readily available
Carnitine-Acyl transferase 2
Enzyme on the matrix side of mitochondria, reforms fatty acyl-CoA
Beta-oxidation pathway
Once inside mitochondrial membrane, the 16-Carbon Palmitoyl-CoA undergoes 7 oxidation cycles to yield 8 Acyl CoAs, each with 2 Cs.
-Each oxidation cycle produces 1 FADH2 in first step and 1 NADH in 2nd step, to be used in ETC.
-8 Acyl-CoAs are available for combustion in Krebs cycle
if oxaloacetate is present (means some glucose is still needed)
Ketone bodies
- Acetoacetate and B-hydroxybutyrate made in liver via ketogenesis (organic acids)
- can be made available to brain
- adaptation to starvation
-when glucose and therefore oxaloacetate is low, acetyl-CoA can’t be used in the citrate cycle, the latter is taken through ketogenesis.
Monocarboxylase transporter (MCT1)
Takes ketone bodies into cells.
Ketones are oxidized mainly in muscle and brain