NEURO: Motivation Flashcards

1
Q

Important brain region in motivation

A

hypothalamus

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2
Q

What is motivation?

A

Motivation is an urge to behave or act in a way that will satisfy certain conditions, such as wishes, desires, or goals.

It is a driving force to fulfil biological needs.

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3
Q

What is the function of the hypothalamus?

A

Maintains homeostasis by regulating 3 interrelated functions:

  • endocrine secretion
  • autonomic nervous system
  • emotions and drive/behaviour (motivated behaviour, e.g. drinking, eating)
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4
Q

Humoral and Visceromotor responses are regulated by

Behavioural responses are regulated by

What regulates food intake?

A

periventricular nucleus and medial hypothalamus

lateral hypothalamus

hypothalamus

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5
Q

Describe the long-term effects of feeding behaviour.

A

Normal energy balance leads to normal adiposity.

Prolonged positive energy balance leads to obesity.
Prolonged negative energy balance leads to starvation.

Body weight is normally stable. If an animal is force-fed, it will gain weight, The weight is lost, however, as soon as the animal can regulate its own food intake. Similarly, weight lost during a period of starvation if rapidly gained when good is freely available.

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6
Q

How did scientists discover that there must be something regulating food intake?

A

Parabiosis experiment:
Parabiosis is the sharing of blood circulation between animals. This means the bloodborne signals are shared and can affect the hypothalamus.

Example 1:
A genetically obese mouse (ob/ob) means that its fat cells do not produce leptin (which inhibits food intake).
It’s connected to a normal mouse (which produces leptin), and this leads to a reduction of obesity in the ob/ob mouse.

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7
Q

What is Leptin?

A

a hormone produced by adipose (fat) cells that acts as a satiety factor in regulating appetite by signalling to the hypothalamus

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8
Q

When is leptin released? And what does it act on?

A

Leptin is released during/after feeding by adipose tissue into the blood

Travels to the brain and binds to the arcuate nucleus of the hypothalamus at the base of the third ventricle to tell you to stop eating (inhibits feeding)

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9
Q

Important hypothalamic regions in regulation of food intake (hence body weight) and drinking (hence blood volume/osmolarity)

A
ventromedial hypothalamus (VMH)
the lateral hypothalamus (LH)
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10
Q

What was the conclusion of a VMH lesion?

A

It concludes that the VMH plays a role in the cessation of eating. Damage to the VMH results in prolonged and dramatic weight gain.

Lesioned VMH
Ventromedial Hypothalamic Syndrome
-over-eating and obesity

Lesioned LH
Lateral Hypothalamic Syndrome
-diminished appetite for food; anorexia

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11
Q

What is the response to elevated leptin after food intake?

A

Anorexic Response

  • leptin binds receptors in the arcuate nucleus
  • arcuate neurones activated
  • arcuate neurones project to the lateral hypothalamus (LH) releasing anorectic peptides ⍺-MSH and CART to inhibit feeding
  • arcuate neurones also project to the paraventricular nucleus (PVN) to stimulate the release of ACTH and thyrotropin from the anterior pituitary. increasing basal metabolic rate
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12
Q

What is the response to decreased leptin levels during starvation?

A

Orexigenic Response:

  • Ghrelin activates NPY/AgRP arcuate neurones, which project to the lateral hypothalamus (LH), releasing orexigenic peptides NPY and AgRP to stimulate feeding
  • arcuate neurone projections also to the paraventricular nucleus (PVN) to inhibit the release of ACTH and TSH from the pituitary, decreasing basal metabolic rate
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13
Q

Describe the competition for activation of the MC4 receptor?

A

One way that αMSH (an anorectic peptide) and AgRP (an prexigenic peptide) exert opposite effects on metabolism and feeding behaviour is via an interaction with the MC4 receptor on some hypothalamic neurons.

Stimulation of the MC4 receptor inhibits feeding behaviour.

a-MSH activates MC4 receptor in response to increased leptin to inhibit feeding

AgRP blocks MC4 receptor in response to low leptin to increase feeding

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14
Q

What do the LH neurons that stimulate feeding behaviour to contain?

A

Orexigenic neuropeptides
Melanin-concentrating hormone (MCH):
- has widespread connections in the brain
- prolongs consumption

Orexin

  • also has widespread cortical connections
  • promotes meal initiation
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15
Q

Feeding related disorders due to dysfunctional hypothalamus

A

hyperphagia
anorexia
bulimia nervosa

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16
Q

Short Term Regulation of Feeding

A

Cephalic Phase: hunger
Gastric Phase: feeling full
Substrate Phase: nutrient absorption

17
Q

What happens during the cephalic phase?

A

1) Cephalic Phase: Hunger
>Ghrelin released when the stomach is empty
>It activates NPY/AgRP neurones in the arcuate nucleus to stimulate feeding
>there is the removal of ghrelin-secreting cells of the stomach, which is thought to cause loss of appetite
>Secretion of saliva in the mouth
>Secretion of gastric juices in the stomach
>Prepares you for food intake

18
Q

What happens during the gastric phase?

A

2) Gastric Phase: Feeling Full
>Gastric distention and CCK (released from intestines in response to certain foods) activate the vagus nerve which signals to the brain to induce satiety via activation of the nucleus of the solitary tract
>Insulin also released by β cells of the pancreas- important in anabolism
>More saliva secretions in the mouth and even greater gastric juice secretions in the stomach

19
Q

Substrate Phase

A

3) Substrate Phase

>Nutrients from food are absorbed by intestines and then into the blood circulation

20
Q

How is mood connected to food?

A

5HT in the hypothalamus:

  • rises in anticipation of food
  • spikes during a meal (with carbohydrates in particular)
  • has an association with anorexia nervosa, bulimia with depression (low serotonin)
21
Q

Why do we eat?

A

We eat because of the natural reward system. When we bite into our food, we get a release of tryptophan, a precursor for serotonin. Thus, we want to eat food again.

Hedonic Aspect
-we like food

Motivational/Drive Aspect
-we want/crave food

*liking and wanting food are mediated in part by separate brain circuits

22
Q

Which system is involved in the wanting/craving of food (motivational drive)?

A

dopaminergic system

23
Q

Natural rewards

A

Food
Water
Sex
Nurturing

24
Q

Describe the reward pathway.

A

activate mesolimbic pathway (reward system):
-dopaminergic neurones project from the ventral tegmental area (VTA) to nucleus accumbens, causing motivational drive (wanting/craving)

The ventral tegmental area (VTA) is connected to both the nucleus accumbens and the prefrontal cortex via this pathway, and it sends information to these structures via its neurones.

The neurones of the VTA contain dopamine, which is released in the nucleus accumbens and in the prefrontal cortex. This pathway is activated by a rewarding stimulus.

25
Q

Factors that release more dopamine than natural rewards

A

Drugs of abuse:

  • cocaine
  • heroine
  • alcohol
  • methamphetamine
26
Q

What is drug addiction?

A

Drug addiction is defined as a chronic relapsing disorder characterised by the compulsive seeking of the drug, loss of control over drug-taking and the emergence of negative emotional states (anxiety, dysphoria, irritability) and physical states when the drug is not provided (withdrawal symptoms).

activate the reward system much more than natural reward factors and are extremely rewarding

27
Q

The action of cocaine, heroin and nicotine on mesolimbic pathway

A

Cocaine inhibits dopamine transporters in nucleus accumbens, preventing reuptake and increasing dopamine at the synapse

Heroin induces dopamine release by activating mu-opioid receptors in VTA

Nicotine induces dopamine release by activating nicotinic receptors in VTA

28
Q

Describe the stages in the addiction cycle.

A

1) Positive Reinforcement: drug intake due to social pressures, inducing pleasurable effects which will trigger further drug administration
2) Escalating/Compulsive Use: pattern of escalating compulsive use due to tolerance
3) Dependance: characterised by a state of emotional and physical withdrawal symptoms (anxiety, depression etc) in short and sometimes long periods of abstinence.
4) Negative reinforcement: aversive, dysphoria experience of drug withdrawal now drives drug intake (not the positive hedonic property of drug)

29
Q

Reward system in dependant drug users and obese people

A

Dependent users crave drugs of abuse not necessarily to get high, but in an attempt to self-medicate because they suffer from extreme withdrawal symptoms (e.g. pain, anxiety, irritability, depression).

Has been shown that the reward system in the brain of dependent drug users and obese people is suppressed due to low D2 receptors and they don’t feel pleasure

Increased craving for drug/food to activate the suppressed reward system

30
Q

While the motivational drive (wanting/craving) is mediated by dopaminergic system, what mediates the hedonic aspect (liking)?

A

opioid system

31
Q

What is the difference between positive and negative reinforcement?

A

Positive reinforcement: anything added that follows a behaviour that makes it more likely that the behaviour will occur again in the future.

Negative reinforcement: a response or behaviour is strengthened by stopping, removing or avoiding a negative outcome or aversive stimulus.

32
Q

What is microdialysis?

A

It’s the measuring of neurotransmitter release in vivo.

It has an association with behaviour parameters.

33
Q

How is dopamine related to reinforcement?

A

Dopamine release in the nucleus accumbens is correlated with motivation but not liking (hedonic).

Its also released in anticipation of reward.
[note that dopamine also involved in movement]