Fatty Acid Metabolism Q6 Flashcards

1
Q

Out line exogenous process of dietary lipids entering body and transportation.

A

Bile salts emulsify in small intestine, lipases degrade triacylglycerols, fatty acids taken up in intestinal mucosa and converted into triacylglycerols, formation of chylomicrons which move through lymph and bloodstream, lipase converts triacylglycerols to fatty acids, fatty acids oxidized for fuel.

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2
Q

What are the two “structures” that fats are able to move through your system? Explain them.

A

Either carried by serum albumin if they are free fatty acids which binds several fatty acids and carries through vasculature. Or through production of lipoproteins IE chylomicron. Proteins with monolayer, cholesterol, and associated apolipoproteins.

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3
Q

What are the 4 types of lipoproteins?

A

Chylomicrons, Very low density lipoprotein (VLDL), Low density lipoprotein (LDL), High density lipoprotein (HDL).

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4
Q

What are the two pathways used to transport lipoproteins?

A

Exogenous pathway: Formation of chylomicrons (from diet). Endogenous pathway: Occurs in the liver. Uses lipoproteins. IE creates VLDLs.

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5
Q

What are the fates of lipids and fatty acids?

A

Energy substrates, precursors, structural elements, signaling molecules.

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6
Q

What is the difference between fatty acids and lipids?

A

Fatty acids are carboxylic acids with long carbon chains. Lipids have one or more fatty acids connected by linker molecule IE phosphate group.

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7
Q

Which two proteins transport cholesterol?

A

LDL and HDL.

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8
Q

How are fatty acids mobilized from adipose?

A

Pancreas releases glucagon which interacts with receptor on adipose tissue causing cAMP to activate protein kinase A. PKA phosphorylates perilipin located in lipid droplets. CGI is released and phosphorylates adipose triglyceride lipase (ATGL) which then breaks down triglycerides. PKA causes HSL converts to monoglycerides and MGL then removes glycerol molecule.

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9
Q

Where will glycerol go once it is removed from the triglyceride?

A

It will move into glycolysis.

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10
Q

What will happen to the fatty acid once removed from the triglyceride by lipase?

A

It will be turned into fatty acyl-CoA.

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11
Q

Where does the break down of triglycerides take place?

A

Cytoplasm of the cell. This is why they need to be transported into the mitochondrial matrix for oxidation.

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12
Q

How is Fatty Acyl-CoA transported to matrix?

A

Via acyl-carnitine transporter. At the outer membrane, fatty acyl is transferred to carnitine which then is transported in as a carnitine is transported out. Then the fatty acyl is transferred to a CoA molecule in matrix via carnitine acyltransferase II.

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13
Q

What are the three stages of fatty acid oxidation?

A

1- beta oxidation by breaking down chain into two carbon sections and also create NADH and FADH2 . 2-The two carbons are used to create acetyl-CoA molecules also producing NADH and FADH2. 3- The NADH and FADH@ created is then used in ETC.

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14
Q

How much ATP will be produced from palmitate?

A

108 ATP

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15
Q

What will happen to odd carbons and unsaturated fatty acids in beta oxidation?

A

They will undergo additional steps to oxidize.

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16
Q

What is the function of acyl-CoA dehydrogenase?

A

It is a component of the ETC and where beta oxidation feeds directly into the ETC through production of FADH2 and NADH.

17
Q

What are the three things that can happen with acetyl-CoA produced in the liver?

A

1- It can enter the CAC to produce energy. 2- It can create oxaloacetate for gluconeogenesis. 3- Or when the gluconeogenesis pathway becomes saturated, you can form ketone bodies.

18
Q

What are ketone bodies formed from?

A

Acetyl-CoA.

19
Q

What are the three ketone bodies?

A

Acetoacetate, Acetone, and D-b-Hydroxybutyrate.

20
Q

What are the two major sources for the formation of fatty acids?

A

Dietary carbs and proteins.

21
Q

What molecule will drive formation of excess acetyl-CoA into triglycerides?

A

Insulin.

22
Q

How is polmitoyl-CoA formed?

A

Turning Acetyl-CoA into malonyl-CoA and combining that with an acetyl-CoA.

23
Q

Where does lipid synthesis occur?

A

In the cytoplasmic space. For this reason acetyl-CoA have to be transported into the cytoplasm.

24
Q

What is the enzyme responsible for fatty acid synthesis?

A

Fatty acid synthase.

25
Q

What is the process of fatty acid synthesis?

A

acetyl-CoA transported into cytoplasm. Carboxylated into malonyl-CoA. Fatty acid synthase combine Acetyl-CoA and malonyl-CoA to start acyl chain. Fatty aid synthase adds malonyl-CoA carbons to create palmitate. Modification happens at the ER.

26
Q

How does Acetyl-CoA get from the matrix into the cytoplasm?

A

Via the citrate shuttle. Acetyl-CoA adds Acetyl group to oxaloacetate to form citrate. Citrate then donates it to Co-enzyme A in the matrix. Citrate then forms malate which can then form pyruvate, creating NADPH in the process important for acyl chains.

27
Q

How is acetyl-CoA turned into malonyl-CoA? What factor is required for this?

A

Via Acetyl-CoA carboxylase. Biotin is acquired from diet via vitamin B7.

28
Q

What are the two types of fatty acid synthase?

A

FAS I- vertebrates and fungi, only creates 16 chain carbons. FSA II- bacteria and plants.

29
Q

What is the function of acyl carrier protein? What is a vital component of it?

A

Shuttles malonyl-CoA to the fatty acid synthase. Vital component if pantothenic acid (vitamin B5)

30
Q

What is the initiation of fatty acid synthesis?

A

Acetyl-CoA donating acetyl (forms omega carbon) group to attach to the end of malonyl group. Then malonyl groups are continually added.

31
Q

Does the forming fatty acid chain become reduced?

A

Via NADPH donating hydrogen.

32
Q

In the ER what can the fatty acid chain be elongated to?

A

Stearate which is 18 carbons.

33
Q

What is responsible for regulating fatty acid synthesis?

A

Acetyl-CoA carboxylase. When there is high blood glucose, glycolysis produces acetyl-CoA which can then be formed in to malonyl-CoA by Acetyl-CoA carboxylase driving fatty acid synthesis. Insulin will activate and glucagon will phosphorylate and deactivate.

34
Q

How is phosphatidic acid formed? Why is it important?

A

Combination of glucose and glycerol. Head groups and fatty acids can then be added to form other molecules like triglycerides and phospholipids.

35
Q

How is cholesterol formed?

A

Excess acetate is converted into mevalonate which creates isoprene and formation of cholesterol. Takes place largely in the liver.

36
Q

What are some derivatives of cholesterol?

A

Bile acids, hormones.

37
Q

How does plaque form?

A

Macrophage ingesting lipoproteins undergoes apoptosis in the artery and sticks to artery wall.