Lipid metabolism Flashcards

1
Q

What are two essential fatty acids?

A

Alpha-linolenic and linoleic

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2
Q

Name three precursors for fatty acid synthesis

A
Acetyl coA (which is found in the mitochondria and transported to the cytoplasm). 
Acetyl coA+ 7 Malonyl coA + 4 NADH -->palmitic acid
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3
Q

Name two enzyme complexes involved in FA synthesis

A

Acetyl coA carboxylase: catalyzes Acetyl coA to Malonyl coA (rate limiting)

Fatty Acid synthase- which catalyzes combining acetyl coA with malonyl coA to form palmitic acid

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4
Q

How is FA acid synthesis regulated?

A
  • Hormones and diet.
  • phosphorylation and dephosphorylation of acetyl carboxylase
  • malonyl coA inhibits FA oxidation
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5
Q

How are FA chains elongated?

A

same way as fatty acid synthesis. Add 2Cs per cycle. Desaturase aids in desaturation in the ER by adding double bonds

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6
Q

Where and when are TAGs made?

A

in the well fed state in the liver and the intestines

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7
Q

Where and when are FAs synthesized?

A

Everywhere except RBCs. In the cytosol. Well fed state.

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8
Q

Discuss the role of biotin in metabolism and its function in FA synthesis.

A

biotin bound to acetyl coA carboxylase carboxybiotin transfers carboxyl group to acetyl coA to form malonyl coA.

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9
Q

Discuss the overview of FA metablism

A

Fat is converted to glycerol (which goes to the liver to be converted to glucose) and Free FAs (bound to albumin). Free FAs go the the liver to be made into energy and to ketone bodies. The brain uses ketone bodies for energy. Free FAs also go to muscle to be converted to energy.

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10
Q

When and how are fats metabolized from adipose?

A

In the fasting state. TAGs are broken down to FFAs in adipocytes. glycerol goes to liver for gluconeogensis and FFA are converted in the muscle and liver to acetyl coA and undergo beta oxidation.

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11
Q

What do hormone sensitive lipase and perilipin do?

A

HSL catalyzes TAG->DAG->MAG reactions. Perilipin activates HSL.

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12
Q

What are adipokines?

A

Type of cytokine-related to inflammation and metabolic diseases. Made by adipocytes and macrophages. E.g. leptin.

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13
Q

How do FAs get into the mitochondria from the cytoplasm?

A

FA converted to acetyl coA+carnitine in cytolsol. becomes acyl carnitine, transported through CPT1 on outer mito membrane and through translocase on inner membrane. Acyl carnitine converted back to acyl coA+carnitine in mito matrix by CPTII. CPT=carnitine palmitoyl transferanse.

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14
Q

Describe beta oxidation.

A

palmitoyl coA+ 7coA+7FAD +7NAD+7H2O–>7FADH2 +7 NADH+8acetyl coA. Oxidation of C16:0 results in 28 ATP from beta ox and 80 ATP from krebs cycle (from NADH and FADH2) Total 108 ATP.

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15
Q

What are three ketone bodies? When and how are they made?

A

acetoacetate, beta-hydroxylbutyrate, and acetone (waste product). Made during the fasting state in the liver. beta ox-> acetyl coA–>acetoacetylcoA–> HMG coA –>acetoacetate –> beta hydroxybutyrate

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16
Q

How are ketone bodies utilized?

A

the skeletal muscle, heart, and brain oxidize ketone bodies to acetyl coA, which goes to krebs cycle to produce ATP

17
Q

Describe the events during starvation or in untreated diabetes when ketone bodies are used.

A

Ketoacidosis occurs because in untreated diabetes, the body doesn’t have enough insulin. Cells can’t take up glucose and compensates by oxidizing fatty acids and producing ketone bodies, which increases acidity in the blood.