JD - Reward and Pleasure Flashcards

1
Q

What are ‘liking’ and ‘hedonic’ circuits in the brain?

A

Liking’ circuits, also called hedonic circuits, generate the pleasure of eating food.

  • Hedonic feeding is driven by the pleasure of consuming food, not metabolic need
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2
Q

What are 3 features of eating disorders

A
  • Eating disorders can include obesity, bulimia and anorexia
  • The number of severely obese and obese children has increased and almost doubled in the last ~10 years
  • Obesity is associated with a reduced life expectancy and is a risk factor for a range of diseases
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3
Q

What neural populations are present in the hypothalamus related to appetite? (2)

A
  • Orexigenic (Increase Appetite)
  • Anorexigenic (Decrease Appetite)
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4
Q

How was the reward circuit initially discovered?

A

The reward circuit was discovered through brain stimulation reward studies by Olds and Milner in 1954, where electrodes in certain brain areas of rodents induced self-stimulation behavior

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5
Q

What is the reward circuit?

A

The reward circuit is the neural network that receives and evaluates the rewarding properties of stimuli.

  • It consists of multiple interacting neural circuits.
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6
Q

Self-stimulation is observed from electrodes located in which brain areas? (4)

A
  • Nucleus Accumbens (NAcc)
  • Lateral hypothalamus (LH)
  • Ventral Tegmental Area (VTA)
  • Cortical structures
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7
Q

What are some of the key structures of the reward circuit? (4)

A
  • Medial forebrain bundle
  • Reward circuit includes axons that project from the VTA (ventral tegmental area) to the nucleus accumbens (Mesolimbic Dopamine Pathway)
  • VTA connects to the amygdala, septum and regions of the cortex
  • Hypothalamus receives inputs from structures within the reward circuitry
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8
Q

How can hedonic reactions to food be measured?

A

Affective orofacial liking reactions can be quantified to provide a readout for how much the subject likes a substance; food

Hedonic Reactions (sweet)

  • (Positive facial liking: relaxed facial expression and rhythmic tongue protrusions)

Aversive Reactions (bitter)

  • (Facial disliking expressions: gapes, turning away, head shakes)
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9
Q

Endogenous Opoids vs Endogenous endocannabinoids (6)

A

Endogenous opioids are neuropeptides and include: enkephalins, dynorphins and endorphins

  • opioid receptor subtypes include: mu, kappa and delta
  • Receptors are G-protein coupled receptors
  • Agonists include morphine; Antagonist Naloxone

Endogenous endocannabinoids are lipid molecules: anandamide and 2-arachidonoylglycerol (2-AG)

  • 2 cannabinoid receptor subtypes: CB1 and CB2.
  • Receptors are G-protein coupled receptors
  • CB1 subtype is predominantly expressed in the central nervous system
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10
Q

What role do opioids play in hedonic pathways?

A

Morphine enhances ‘liking’ responses of rats for palatable foods

Naloxone decreases food intake in rats, especially when sucrose is used

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11
Q

What did the injection of opioid receptor agonist (DAGMO) and measuring facial ‘liking’ reaction identify? (4)

A
  • Role for mu opioid receptors
  • Precise map of the nucleus accumbens (NAcc)
  • Hedonic hotspot (10% of Nacc)
  • A larger region for food intake (‘wanting’)
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12
Q

How was the functional connectivity between different hotspots mapped? (2)

A

An approach called a Fos plume was used.

  • One region of the animal’s brain is injected with the DAMGO and then the brain is removed and immunohistochemical staining was used to quantify the expression of a protein called c-Fos in regions of the brain outside of the injection site.
  • c-Fos is a protein that is expressed when neurons are activated, and so increased expression of this protein provides a readout for when neurons are being activated by the drug that is being injected.

Provided evidence that hotspots are functionally connected

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13
Q

What was another experiment to determine functional connectivity of hotspots?

A

Blocking opioid signaling in one hotspot while simultaneously stimulating another hotspot causes the suppression of enhanced liking responses

  • Recruitment of hotspots is an important mechanism for causing increased ‘liking’ responses disruption of one hotspot can disrupt liking reactions and the function of the circuit
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14
Q

How do endocannabinoids contribute to hedonic pathways?

A

Endocannabinoids like anandamide increase liking reactions when injected into the nucleus accumbens

  • There is an endocannabinoid hotspot in the NAcc that overlaps with the opioid hotspot

CB1 receptors and mu receptors have been identified as co-localizing in neurones of the nucleus accumbens

  • Function together to co-ordinate the release of neurotransmitters
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15
Q

What is the role of dopamine in reward?

A

Dopamine was found to be required for the motivational ‘wanting’ aspects of food reward, not the hedonic ‘liking’ component

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16
Q

What was the hypothesis made about dopamine action and how was it altered?

A

Hypothesis: dopamine signals reward ‘pleasure’

This hypothesis was tested using the facial expression paradigm combined with neurochemical lesions in the brain to reduce dopamine signaling

  • depletion of dopamine did not affect orofacial expression of liking in response to sweetness
  • BUT: reducing dopamine caused the rats to no longer seek out or consume food

New hypothesis: Dopamine is required for ‘wanting’ motivational aspects of food reward

17
Q

What facilitates the cross-talk between the homeostatic and reward circuits?

A

The lateral hypothalamic area is a key structure that facilitates cross-talk between the homeostatic and reward circuits

  • Orexin is a candidate signaling molecule for cross-talk between reward and homeostatic systems in the brain
18
Q

How might altered ‘wanting’ vs ‘liking’ contribute to eating disorders?

A

In some individuals, excessive ‘wanting’ that exceeds ‘liking’ could make them more vulnerable to overeating triggered by food cues