Appetite, hunger & the physiology of the fed and fasted state Flashcards

1
Q

Identify and explain appetite

A

a psychological desire to eat

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2
Q

Identify and explain hunger

A

the biological drive to eat

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3
Q

identify and explain satiation

A

feeling of satisfaction that occurs during a meal, leading to termination of eating

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4
Q

identify and explain satiety

A

feeling of fullness persisting after a meal

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5
Q

homeostatic requirements vs hedonic mechanisms

A

hedonic - driven by the pleasure and comfort of food (sensory input)
homeostatic - driven by physical hunger

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6
Q

Arcuate hypothalamus regulates appetite - it has two distinct neuron populations:

A
  • NPY/AgRP orexigenic (appetite stim)
  • POMC anorexigenic (appetite inhib)
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7
Q

Leptin’s control mechanism

A
  • appetite inhibition and basal metabolic rate increasing effect
  • increases satiety and EE
  • inhibits NPY/AgRP
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8
Q

Leptin deficiency

A
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9
Q

Ghrelin’s control mechanism

A
  • reduces resting metabolic rate
  • reduces lipolysis and increase the storage of fats in adipocytes
  • Caloric restriction and weight loss have a strong impact on circulating ghrelin levels
    resulting in an increased appetite drive and impact on reducing metabolic rate
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10
Q

GLP-1

A
  • Anorexigenic
  • via L cells
  • reduces gastric emptying and improves insulin sensitivity and glucose uptake
  • enhances satiety
  • Butyrate and Propionate SCFA’s have role in stimulating release via L-cells
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11
Q

PYY

A
  • anorexigenic
  • secreted by L-cells of small and large intestine
    -decreased levels observed in obesity
  • like GLP-1, SCFAs have role
  • increased levels following wt. loss surgery - role in appetite suppression
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12
Q

CCK

A
  • cholecystokinin
  • anorexigenic - 1st discovered
  • released by epithelial cells the Duodenum and Jejunum
  • stimulates digestion via gall bladder contraction and pancreatic secretions
  • inhibits stomach emptying, and reduces appetite via brain
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13
Q

Fed state

A
  • anabolic
  • nutrients -> ATP for use or stored as glycogen or fat
  • increased blood glucose stimulate insulin via beta islet cells
  • high insulin/low glucagon
  • glucose energy source
  • excess glucose converted by liver to TAG - VLDL - adipocytes
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14
Q

Fasted state

A
  • catabolic
  • mobilisation of stored glycogen and fat to provide energy
  • decreased blood glucose stimulates glucagon and cortisol release via alpha islet cells
  • low insulin/high glucagon
  • glycogen exhausted
  • incl. gluconeogenesis via aa’s
  • FFA’s from lipolysis provide FFA’s for many tissues
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15
Q

stages of fed-fast states

A

fed: 0-3 hours following meal
post-absorptive: 3-18 hours
fasted: 18-48 hours
starvation: >48 hours

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16
Q

Post-absorptive

A
  • increased glucagon excretion
  • liver glycogenolysis and gluconeogenesis maintains BGLs
  • lipolysis free FFA’s as energy source
17
Q

Starvation

A
  • body prioritises protein sparing so aa’s rate of use is decreased
  • accelerated lipolysis and use of FFA’s
  • glycerol used for gluconeogenesis
  • ketone bodies become major fuel
18
Q

Intermittent fasting and its health benefits

A
  • metabolic benefits: continuous energy restriction (CER)
  • involves fasting for varying periods of time, typ 12 hours or longer
  • health benefits - wt. loss & metabolic switching
19
Q

Alternative Day Fasting

A
  • no calories on one day followed by no restrictions following day
20
Q

Alternate Day Modified Fasting

A
  • modified version of ADF
  • allows low-calorie intake during fast day
  • typ only 25% or less calories than a normal day
21
Q

5:2 and 4:3

A
  • 2- or 3-day fasts followed by normal libitum eating for another 4-5 days
  • ## gen <2000 kJ on 2 fasting days
22
Q

Eat-stop-Eat

A

a 24 hour fast once or twice a week

23
Q

Time Restricted Eating

A
  • e.g. 16/8 eating pattern
  • also called ‘circadian rhythm fasting’
  • idea is to consume food when energy is mostly efficiently metabolised e.g. earlier in day when insulin sensitivity is highest
24
Q

Long-Term Adaptations of fasting

A
  • increased:
    – insulin sensitivity
    – HRV
    – lipid metabolism
  • healthy gut microbiota
  • reduced:
    – abdominal fat
    – inflammation
    – blood pressure
  • resilience
  • disease resistance
25
Q

Fasting Safety Considerations

A
  • trigger disordered eating
  • not appropriate for some - pregnant, breastfeeding, children, ED, diabetes, some meds
  • long-term not known
  • safety in older adults not known
  • risk of excess weight loss
26
Q

The three most studied intermittent fasting approaches

A
  • alternate-day fasting
  • 5:2
  • daily time-restritced feeding
27
Q
A