Revision questions - week 1 Flashcards

1
Q

What are the definition, and difference between digestion and absorption?

A

Digestion
– Process of breaking down foods componets into the molecules that be can absorbed by
enterocytes and delivered into blood or lymphatic circulation. Macronutrients are turned into monomers, micronutrients are freed from larger food particles.
Absorption
– Uptake of monomers and micronutrients from the lumen of the GIT through the absorptive cells (enterocytes), into the blood or lymph for transport to organs / cells.

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2
Q

Trace a cheese and salad sandwich through the digestive processes, naming the various anatomical structures 
and naming secretions involved in the digestion, and their role

A

?

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3
Q

Describe the different forms of absorption

A

Passive
Facilitated
Active
Endocytosis

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4
Q

How are various nutrients being absorbed and transported into the body?

A

VIA THE CARDIOVASCULAR
SYSTEM
• Water-soluble nutrients transported via capillaries in villi to portal vein, into the liver and to other organs and tissues
VIA THE LYMPHATIC SYSTEM
• Fat-soluble nutrients and larger particles packed as chylomicrons, transported via lacteals into lymph vessels to the thoracic duct where they then enter the blood circulation

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5
Q

What occurs to indigested food compounds?

A

?

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6
Q

What are prebiotics?

A

non-digestible carbohydrates that “feed bacteria and promote their growth, and result in fermentation products (SCFA such as butyrate) e.g. inulin, fructans, resistant starch, pectin etc

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7
Q

What is the starting molecule in lipogenesis

A

acetyl coa

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8
Q

what in triglcerides can be used in glucose production

A

glycerol

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9
Q

Can fatty acids be used as substrate for gluconeogenesis

A

No, they can’t
Because:
• Gluconeogenesis starts from oxaloacetate
• Oxaloacetate is formed from glucogenic amino acids carbon
backbones( GGAACB), e.g. not fatty acids, or pyruvate.
• Pyruvate is formed from glucose or GGAACB, not fatty acids
• Fatty acids are oxidised to acetyl-coA (2 carbons molecules)
• Acetyl coA cannot be converted back to pyruvate
(irreversible reaction)
• Acetyl coA enters the CAC to form citrate with oxaloacetate.
The CAC is an open cycle /circuit, meaning that the
intermediates are formed from a variety of substrates coming
from other pathways, and carbons atoms are lost all along as
CO2 . Therefore the acetyl coA 2 carbons do not “exist” by
the time oxaloacetate is formed.

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10
Q

Key factors and their role in regulation of energy metbaolism

A
    • liver - because most the reactions take place in the liver, major site of of nutirent conversion and metabolism,
    • Substrate availability dictates whether the metabolism will be anabolic or catabolic.
    • ATP levels in cell / tissue: determine activity of AMPK and whether
      catabolic states are activated to make more ATP
    • Enzymes are necessary for reactions to take place. Mutation in
      genes coding for these enzymes will impair energy metabolism
    • Hormones dictate whether anabolic pathways (insulin) or
      catabolic pathways (glucagon) take place
    • Vitamins and minerals necessary for transfer of ions (NAD and FAD) and act as cofactors to metabolism enzymes
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11
Q

metabolic shifts occur in substrate utilisation for energy metabolism for maintenance of blood glucose level, and for sparing lean body mass when fasting from a few hours to several days

A
  • ATP production relies on glycogen stores then lean body mas then fat stores and ketone bodies
  • Maintenance of BGL – glucose used up, liver glycogen , lean body mass used in gluconeogenesis to continue supply of BGL.
  • Long period of fasting result in using ketone bodies as energy source
    therefore body does not need to provide as much glucose anymore and can spare the lean body mass from being used for gluconeogenesis - fat stores primary source of energy in extended fasting
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12
Q

What are probiotics

A

Live bacteria,identical to that found in the gut, consumed as supplement or via foods (yoghurt, sauerkraut,
kimshi). They populate the gut with good bacterial species.

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13
Q

Passive

A
  • moves down the concentration gradient

- substrate concentration dependent

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14
Q

Facilitated

A
  • requires a carrier protein; saturable

- moves down the concentration gradient

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15
Q

Active

A
  • requires energy (ATP) + Na

- can transport against the concentration gradient

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16
Q

Endocytosis

A
  • the cell wall engulfs a substance by surrounding it with the cell membrane
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17
Q

Entero-hepatic recirculation

A

recycling of bile

- save burden of making new bile by making new cholesterol

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18
Q

What is the difference between IBS and IBD? (definitions, location and characteristics)

A

– IBS: Causes are not well understood: genetic, stress, allergies, autoimmunity, dietary triggers, or dysregulation in gut microbiota species. Mainly functional in characteristic
– IBD: includes Crohn’s disease and ulcerative colitis. Damage of the structure of the intestine due to unclear causes (multiple: genetic, autoimmune, dietary and other lifestyle triggers, gut microbiota profile

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19
Q

What is the difference between diverticulosis and diverticulitis?

A

diverticulosis: pockets formed in the intestinal wall from extended constipation and strain
diverticulitis: inflamed and infected pockets formed in intestinal walls (serious condition)

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20
Q

What are the possible reasons for developing GORD?

A

– Lower esophageal sphincter that loses efficiency. Excess weight putting pressure on the sphincter. Large meals resulting in slow digestion
– When taking antacids medications: reliefs pain but impairs digestion, therefore nutrients absorption

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21
Q

What are the differences between food allergies and food intolerances?

A

intolerance - Intestinal flatulence, diarrhoea, bloating
versus
allergy - acute immune response.
intolerance - Dose-dependent
versus
allergy - acute response to the smallest dose

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22
Q

What is leaky gut? What does it result in?

A

space between enterocytes; gut integrity is

compromised resulting in systemic inflammation

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23
Q

AI

A

Adequate Intake
The average daily nutrient intake level based on observed or experimentally-determined approximations or estimates of nutrient intake by a group (or groups) of apparently healthy people that are assumed to be adequate

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24
Q

RDI

A

Recommended Dietary Intake
The average daily dietary intake level that is sufficient to meet the nutrient requirements of nearly all (97-98%) healthy individuals in a particular life stage and gender group
- determined by EAR

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25
EAR
Estimated Average Requirement A daily nutrient level estimated to meet the requirements of half the healthy individuals in a particular life stage and gender group - biomarker of deficiency
26
SDT
Suggested Dietary Target | Daily intake of certain nutrients that may help prevent chronic disease
27
UL
Upper Level of Intake The highest average daily nutrient intake level likely to pose no adverse health effects to almost all individuals in the general population. As intake increases above the UL, the potential risk of adverse effects increases. 3% of population still at risk of toxicit
28
EER
Estimated Energy Requirment The average dietary energy intake that is predicted to maintain energy balance in a healthy adult of defined age, gender, weight, height and level of physical activity, consistent with good health
29
esterification
triglycerides fatty acids and/or glycerol | binding glycerol to fatty acids
30
beta oxidation
oxidation of fatty acids to acetyl coA
31
glycogenolysis
hydrolysis of glycogen to glucose
32
gluconeogenesis
phosphenolpyruvate to glucose (making new glucose)
33
glycolysis
glucose to pyruvate
34
ketogenesis
formation of ketone bodies
35
lipogenesis
hydrolysis of triglycerides into fatty acids and glycerol
36
deamination
removal of nitrogen group of AA
37
ketoxidation
ketones to acetyl coA
38
sucrase
digests table sugar
39
phospholipase A2
breaks down phospholipids
40
amylase
digests alpha 1-4 bonds in starch
41
alpha dextrinase
digests alpha 1-6 bonds in starch
42
pancreatic lipase
cleaves fatty acids from glycerol in duodenum
43
lactase
breaks down lactose | cleaves galactose from glucose
44
maltase
cleaves the glycosidic bond between two glucose molecules in one of the disaccharides digests maltose
45
cholesterol esterase
cleaves cholesterol esters
46
G6P
converts glucose-6-phosphate to glucose in glycogenolysis in the liver
47
pepsin
cleaves peptides bonds in stomach
48
ALT or AST
type of transaminase that facilitates transamination
49
alcohol dehydrogenase
converts alcohol in the first step of metabolism (moderate alcohol intake)
50
trypsin
type of protease that cleaves peptides in duodenum
51
pancreatic amylase
cleaves polysaccharides in duodenum
52
GLUT 4
allows cellular uptake of glucose upon insulin signalling
53
acetyl coA
molecule entering CAC after glycolysis | starting molecule in lipogenesis
54
acetaldehyde
intermediate of alcohol metabolism - causes hangovers
55
oxaloacetate
starting molecule for gluconeogenesis
56
ketone body
formed from 2 acetyl coA
57
starch
polysacchardie storage in plants
58
trans fatty acids
partially hydrogenated unsaturated fatty acids
59
ribose
saccharide used to form nucleotides
60
monounsat fatty acid
fatty acid with one double bond (in cisform)
61
polyunsat fatty acid
fatty acid with multiple double bonds
62
cholesterol
sterol manufactured by liver
63
phospholipids
similar to triglyceride but phosphorus replaces FAs
64
SCFA (short chain fatty acid)
produced by bacterial fermentation
65
eicosanoids
inflammatory response molecule formed from omega 3 and omega 6