Oxytocin and vasopressin Flashcards

1
Q

Describe vasopressin

A
  • Also known as arginine vasopressin
    (AVP), antidiuretic hormone (ADH), or
    argipressin
  • Functions principally as a
    vasoconstrictor and antidiuretic
  • Modulates aquaporin (water channels)
    in kidney nephron increasing water
    resorption
  • Important regulator of water, glucose,
    and salt homeostasis
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1
Q

Describe oxytocin

A
  • One of only two hormones
    released from the posterior
    pituitary
  • Described in 1906 as a compound
    able to elicit uterine contraction
  • Identified and synthesized in 1953
  • Classic hormone roles in labour
    and lactation
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2
Q

Describe expression and function of OXT/AVP

A
  • Cleavage of the preproOXT/AVP polypeptides give rise to OXT and AVP and an additional carrier protein (~90 amino acids)
  • preproOXT yields Neurophysin I
  • preproAVP yields Neurophysin II
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3
Q

Describe oxytocinergic neurons

A
  • Oxytocinergic neurons project
    from the paraventricular
    nucleus of the hypothalamus
    to the forebrain and hindbrain
  • Notable innervation of the
    amygdala, NAc & VTA,
    hippocampus
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4
Q

Describe oxytocin systems

A
  • Oxytocinergic neurons project from the paraventricular nucleus of the
    hypothalamus to the forebrain and hindbrain
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5
Q

Describe microtine rodents

A

Prairie voles (Microtus ochrogaster) live in colonies and form life-long monogamous bonds.

Share huddles, grooming, nesting, and pup-
rearing responsibilities.

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6
Q

Describe microtine rodent relevance to oxytocin

A
  • Microtine voles are commonly used in a lab setting to examine social behaviours, bonding,
    and investigating the underlying neurochemistry of social behaviour.
  • Social behaviours can be measured using simple tests such as partner preference – measuring time spent interacting with a bonded partner vs a strange
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7
Q

Describe oxytocin receptor audio graph

A

OXTR binding
capacity correlates
with social behaviour
(measured by partner
preference tests)

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8
Q

Describe its link to early social interactions

A
  • Human infants with high parent-infant synchrony (i.e. enhanced capacity to respond to
    infant’s socio-affective signals) have increased OXT levels in saliva compared with low parent-
    infant synchrony
  • Effects seem to be cross-generational
  • Human parents with high parent-infant synchrony also show increased salivary OXT
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9
Q

Describe genetic manipulation of OXT

A
  • Social behaviours can be restored in OXT/R KO models by intracerebroventricular
    injection of OXT before but not after initial social exposure
  • Suggests a role of OXT in encoding but not recall of social information
  • Possible role in enhancing saliency of social information
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10
Q

Describe link between OXT and autism

A
  • Persistent deficits in social communication and interaction
  • Restricted and repetitive patterns of behaviour
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11
Q

Describe oxytocin pharmacology

A
  • Oxytocin IV is used clinically to induce labour
  • Induces uterine contractions
  • IV administration has a half-life of ~ 3 minutes
  • Oxytocin has been explored to induce or facilitate lactation
  • Intranasal oxytocin has been used to investigate behavioural effects of
    OXT
  • Intranasal administration can bypass the BBB and prolongs the bioavailability
    of OXT
  • Intranasal OXT is psychoactive and effects last 2-4 hours
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12
Q

Describe effects in healthy controls

A
  • IN-OXT increases social cognition in healthy controls
  • IN-OXT decreases emotional processing
  • IN-OXT administration increases disclosure of emotional events when recalling autobiographical
    stories
  • Using trust games such as risky-investment scenarios IN-OXT increased subjects ratings of
    ‘trustworthiness’ and generally gave more ‘money’ to trustworthy recipients
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13
Q

Describe link between social salience and oxytocin

A
  • Many facets of both pro- and anti-social behaviour are
    enhanced by OXT administration
  • IN-OXT may reinforce or exacerbate in-group/out-group differences
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14
Q

Describe stop distance paradigm

A
  • Subjects (male volunteers) are placed into an
    encounter with an attractive female experimenter
  • Distance was varied between the subject and
    experimenter until the subject reaches a
    comfortable distance (ideal distance)
  • Administration of intranasal OXT (but not placebo)
    had a specific effect on subjects in a relationship
  • Suggest OXT may reinforce fidelity
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15
Q

What are some caveats with OXT research?

A
  • Enhancing effects of IN-OXT may not reflect a direct role of OXT in behaviour