Terminology (Lecture 3) Flashcards

1
Q

Cholecystokinin (CCK) effect

A

Causes Gallbladder and Pancreas to contract and release enzymes + bile

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2
Q

Secretin Effect

A

Causes gastric acid secretion

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3
Q

Mixed Micelles

A

Amphipathic - hydrophobic inside, hydrophilic outside

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4
Q

Brush Border Membrane

A

In Enterocytes

Primary site of lipid absorption

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5
Q

In what organelle are broken down lipids resynthesized?

A

Endoplasmic Reticulum

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6
Q

Chylomicrons are surrounded by

A
  1. Phospholipids
  2. Unsterified Cholesterol
  3. Apolipoprotein
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7
Q

How do lipids enter the bloodstream?

A

Chylomicrons exocytized from enterocytes into the lacteals (lymph vessels) and then enter bloodstream

too large to enter bloodstream from any source other than the lymph

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8
Q

What tissues absorb chylomicrons from blood?

A

Fat and Muscle cells

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9
Q

Glycerol use

A

—> G3P in the Liver for glycolysis or Gluconeogenesis

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10
Q

Main Fatty Acid Esters

A

Triacylglycerol
Cholesterol Esters
Phospholipids

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11
Q

Location of unsterified (free) FA’s

A

Transported in circulation with albumin protein

“Listening to albums feeling free, driving in circles”

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12
Q

Fatty Acid chain lengths

A

12 to 20

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13
Q

Main Fatty Acid components

A

Carboxylic acid on one end (monocarboxylic acid)

No Double bonds (saturated)

Double bonds (unsaturated)

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14
Q

Why are unsaturated FA’s liquid at RT?

A

Contain cis double bonds which lengthen structure and lower bp

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15
Q

How far are double bonds spaced?

A

If more than one, they are spaced every 3 carbons

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16
Q

20:4 (5,8,11,14)

A

20 Carbons long
4 double bonds (5–6, 8-9, 11-12, 14-15)

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17
Q

Omega Terminology for Linoleic Acid 18:3 (9,12,15)

A

18:3w-3

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18
Q

Alpha-Linolenic Acid Derivatives

A

Omega-3 FA’s

3 parts to name

Essential

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19
Q

Linoleic Acid derivatives

A

Omega-6 FA’s

Essential

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20
Q

How are excess proteins + carbs stored?

A

Triacylglycerols

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21
Q

FA Synthesis locations

A
  1. Mostly liver
  2. Lactating mammary glands
  3. Adipose tissue
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22
Q

FA Synthesis Step 1

A

Acetyl-CoA converted into citrate, transported to cytosol and reconverted

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23
Q

FA Synthesis step 2

A

A) Acetyl-CoA —> Acetyl-ACP

B) Acetyl-CoA —> Malonyl-CoA

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24
Q

FA Synthesis Step 3

A

A) Acetyl-ACP —> Acetyl-Synthase

B) Malonyl-CoA —> Malonyl-ACP

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25
Q

FA Step 4

A

Acetyl-Synthase and Malonyl-ACP combine, undergoing energy consuming reactions to form Palmitate

uses Fatty Acid Synthase (FAS)

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26
Q

FA Synthesis Cont.

A

End product Palmitate can be added to, 2 carbons at once in the smooth ER

Uses NADPH

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27
Q

Desaturation of FA’s

A

In the Smooth ER

Cis double bonds inserted by Desaturases

Can only introduce between carbons 9 and 10 (no further)

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28
Q

Storage of FA’s

A

(1-3) FA’s esterified to a molecule of glycerol… = Monoglycerol, Diglycerol, and Triglycerol

  1. Usually Saturated
  2. Usually Unsaturated
  3. Either

Form anhydrous droplets in adipocytes

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29
Q

Cystolic Lipid Droplets (made of TAG’s)

A

Major energy reserve of the body

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30
Q

Activation of FA’s

A

Fatty acyl-CoA synthetases (thiokinases) attach CoA to activate

31
Q

Alternate storage of FA’s

A

Little TAG’s stored in liver and exported as VLDL

32
Q

Beta Oxidation

A

2-C fragments removed from carboxyl end of activated FA’s

Produces acetyl CoA, NADH, and FADH2

33
Q

Beta Oxidation Location

A

Mitochondria

34
Q

Carnitine Shuttle

A

How Long Chain Fatty Acids (LCFA’s) get to mitochondria for Beta Oxidation

35
Q

Even FA beta oxidation end products

A

Fatty acyl CoA and Acetyl CoA

NADH and FADH2

36
Q

Odd FA Beta Oxidation

A

Final 3-C molecule Propionyl CoA metabolized to Succinyl CoA —> Krebs Cycle

37
Q

Acetyl-CoA from Beta-Oxidation

A

Converted by liver mitochondria into Ketone bodies

38
Q

Ketone bodies

A

Acetoacetate, 3-hydroxybutyrate, and acetone

39
Q

Ketoacidosis symptom

A

Fruity breath from acetone

40
Q

Sphingomyelin

A

Only major Sphingophospholipid in humans

Myelin nerve fibers

Major structural component in membranes

41
Q

Phospholipid Synthesis Location

A

Occurs in Smooth ER

Then transported to Golgi, organelle membranes, plasma membranes, or exocytized

42
Q

Most Abundant Phospholipids

A

Phosphatidylethanolamine and phosphatidylcholine

43
Q

Glycolipids

A

Carb and lipid components

Derived from ceramides

Essential membrane component and nerve tissue component

Carbohydrate portion is ANTIGENIC

44
Q

Cerebrosides

A

Neutral Glycosphingolipids

Ceramide with glucose or galactose

45
Q

Acidic glycosphingolipids

A

Negative charge from
NANA acid - gangliosides
Sulfate groups - sulfatides

46
Q

Glycosyl Transferases + UDP sugar donors

A

Transfer glycosyl monomers

Make glycosphingolipids in Golgi

47
Q

Glycosphingolipid production site

A

Golgi Apparatus

48
Q

Eicosanoids stem from..

A

20+C polyunsaturated fats

49
Q

Collective name for Prostaglandins, Leukotrienes, and Thromboxanes

A

Eicosanoids

50
Q

Eicosanoids function

A

Inflammatory Response

Hypersensitivity to pathogens

51
Q

Precursor of prostaglandins and thromboxane

A

Linoleic acid (Omega-6)

52
Q

Eicosanoids include

A
  1. Leukotrienes
  2. Prostaglandins
  3. Thromboxanes
53
Q

Cholesterol functions

A
  1. Modulate membrane fluidity
  2. Precursor of bile acids, steroid hormones, and vitamin D
54
Q

What organ regulates cholesterol?

55
Q

Cholesterol enters the liver as…

A
  1. Dietary cholesterol
  2. Self-made cholesterol
  3. From extrahepatic tissues
56
Q

Cholesterol leaves the liver…

A
  1. As unmodified cholesterol in bile
  2. As bile salts secreted into the intestinal lumen
  3. As VLDL
57
Q

Sterols

A

8-10 C steroids
Branched at C17

58
Q

Cholesterol Synthesis pt. 1

A

Acetyl-CoA to HMG CoA

59
Q

Cholesterol Synthesis pt. 2

A

HMG-CoA to Squalene

60
Q

Cholesterol Synthesis pt. 3

A

Squalene to Cholesterol

61
Q

Ring structure of Cholesterol

A

Can’t be metabolized to CO2 and H2O

62
Q

How is cholesterol eliminated?

63
Q

Rate limiting step of bile acid synthesis

A

Cholesterol 7-alpha-hydroxylase

64
Q

Before bile acids leave the liver

A

Conjugated to glycine or taurine

65
Q

Bile contains

A
  1. Bile Salts
  2. Cholesterol
  3. Phospholipids
  4. Bile Pigments
66
Q

Yellow-green Bile

A

Produced by hepatocytes

Stored in the gall bladder

67
Q

Chylomicrons

A

Assembled in intestine

Transport lipids to peripheral tissues

68
Q

VLDL

A

Produced in liver

Transports lipids to peripheral tissues

Become LDLs when depleted

69
Q

LDL

A

Transport “bad cholesterol” to tissues

70
Q

HDL

A

Brings cholesterol from tissues back to liver

“Good cholesterol”

71
Q

Cholecystokinin

A

Cause contraction and enzyme release in pancreas + gallbladder

72
Q

Secretin

A

Causes enzyme release in pancreas

73
Q

Lipoprotein Lipase

A

Breaks down TAGs in bloodstream so they can cross into tissues

74
Q

Palmitic Acid

A

16 Carbons (max for fatty acid synthase)

Terminal FA in FA synthesis