Module 8 - Cell-Cell Interactions Pt2 Flashcards

1
Q

Where do we get fat from

A

from consuming too many calories from sugar, fat or protein

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2
Q

WHat are sources of acetyCoA

A

Pyruvate breakdown, breakdown of fats (beta oxidation), ketone bodies and some amino acids

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3
Q

What is structure of triglycerides, what do they do in our body

A

●Fats are stored in the body as triacylglycerols (aka triglycerides)
●Triglycerides made of 3 fatty acids that have been esterified with glycerol
Usually made of 2 or more types of fatty acids

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4
Q

Where is fat stored

A

found in adipose tissue in specialized cells called adipocytes
- some muscle also as small amounts of fat

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5
Q

Where are triglycerides broken down

A

In adipocytes

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6
Q

How are triglycerides broken fown

A

● Lipase is enzyme which releases the free fatty acids from the glycerol moiety by hydrolyzing the ester bonds

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7
Q

What causes lipase to be stimulated

A

●When glucose levels are low, hormone glucagon is released and stimulates the lipase to breakdown fats to provide energy
●Beta oxidation allows free fatty acids will be broken down and oxidized to generate reducing equivalents NADH, FADH2 and acetylCoA, which feeds into the citric acid cycle to make energy in the form of GTP and even more reducing equivalents

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8
Q

Where do fatty acids go when theyre NOT beta oxidized

A

● Fatty acids from lipase leave the adipose tissue and enter the bloodstream to be delivered to other tissues
● Fatty acids are carried through the bloodstream bound to protein albumin, which keeps fatty acids soluble

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9
Q

What happens to fatty acids that get takedup into tissue

A

● Fatty acids taken up into tissues are broken down to acetylCoA via beta oxidation pathway

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10
Q

What happens to the glycerol from triacylglycerol

A

● The glycerol moiety is also unstable energy and leaves the adipose tissue to be taken up by liver which is where gluconeogenesis takes place (converted into glucose)
● Glycerol is a substrate for gluconeogenesis entering the gluconeogenic pathway at midpoint

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11
Q

Where in body are fatty acids used

A

preferred fuel for muscles at rest

Liver uses fat for energy

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12
Q

What must happen before fatty acid enters beta oxidation pathway

A

Must be activated

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13
Q

How are fatty acids activated and what does this allow

A
  • Attaching attaching a long chain hydrocarbon of fatty acid to coenzymeA
  • similar to pyruvate becoming acetyl CoA
  • Now acyl CoA is ready to be transported into mitochondrial matrix to be oxidized
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14
Q

Where are enzymes of beta oxidation located and where does it occur

A

● Enzymes of beta oxidation are all located in the matrix

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15
Q

What happens during Beta Oxidation of Fatty acids

A

● One round of beta oxidation involves sequential removal of two carbons at a time from the acyl group
- Cleaving bond involves series of four reactions that occur in single round beta oxidation
●you make 1NADH and 1 FADH and acetylCo
●Beta oxidation since it cleaves the carbon-carbon bond adjacent to beta carbon
●Then shortened acylCoA starts the process again entering a subsequent round of beta oxidation and cleaves two more carbons
●The process reapers until all of the acyl group is cut into two carbon acetylCoAs (for even-numbered fatty acids)

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16
Q

What is an alternate fate for AcetylCoA then the citric acid cycle

A

under starvation → ketogenesis
●Convert fatty acids to ketone bodies in the liver and during fasting or starvation with low glucose since bodies glycogen stores are depleted, can use ketone bodies for energy in brain

17
Q

What happens to Ketone bodies during fasting

A

during faster enter bloodstream and cross blood-brain barrier and be taken up by brain and broken back down into acetylCoA which can enter citric acid cycle and produce energy

18
Q

Does anabolic fat synthesis share any of the same enzymes

A

No unlike glycolysis and gluconeogenesis

19
Q

What happens conceptually during fat synthesis

A

the process is reverse of beta oxidation

● Two carbons originating from acetylCoA are added one at a time to elongating fatty acyl chain

20
Q

When do bodies synthesize fat

A
  1. Bodies are in mode of synthesizing fat when we have excess intake of carbohydrates (replenish stores then excess broken down via glycolysis and pyruvate dehydrogenase rxn to make acetylCoA) → where acetyl CoA originates from
21
Q

What does the anabolic process of fat synthesis involve/need

A
  1. Anabolic process = reductive → we have to inject or donate e= into newly synthesized compound (in this case fatty acid)
22
Q

Where must acetyl CoA be for fat synthesis to take place and how does it get there

A
  1. Tricarboxylate transport system must remove acetylCoA via citrate intermediate out of mitochondrial matrix into cytosol (that’s where fat synthesis takes place)
23
Q

What does fatty acid synthetase do

A

catalyzes synthesis of fatty acids

24
Q

What do enzymes elongases and desaturases do

A

Elongase - can make longer chain fatty acids

desaturases - create double bonds in unsaturated fatty acids

25
Q

What happens once fatty acids are synthesized

A

they are esterified with glycerol to form triacylglycerols used to make membrane lipids

26
Q

What happens to fatty acid metabolism after a meal

A

●Insulin activates fat synthesis in the liver and simultaneously inhibits fat breakdown in adipose tissue
●Futile cycling: we want to avoid breaking down fats when glucose is plentiful and body is in mode of synthesizing fats

27
Q

What happens to fatty acid metabolism during periods of low glucose

A

● Glucagon released during low glucose which is insulins counter hormone
● It stimulates fat breakdown by stimulating lipase in adipose tissue
● Then fats broken down to acetylCoA used for energy or acetylCoA diverted to ketone body synthesis (although not ideal)

28
Q

What else is AcetylCoA a precursor for

A

for cholesterol synthesis and synthesis of some amino acids

29
Q

What does HMG-CoA reductase do

A

help lower cholesterol levels in those afflicted with high levels of “bad cholesterol”, LDL

30
Q

Can amino acids made AcetylCoA or pyruvate

A

Yes certain amino acids can become acetyl CoA while others can become Pyruvate by either entering the citric cycle or directly becoming pyruvate or acetyl CoA

31
Q

what does Aconitase do

A
  • an enzyme called aconitase converts citrate into isocitrate
  • Aconitase contains an iron-sulfur center which acts both in the binding of the substrate at the active site and in the catalytic addition or removal of H2O.