Appetite, Metabolic Syndrome And DOHD Flashcards

1
Q

Describe how the location of the arcuate nucleus is ideal for controlling appetite

A
  • Located at base of hypothalamus

- Can sense substances such as appetite hormones from bloodstream e.g. Ghrelin, fatty acids, Leptin

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2
Q

Explain how the primary neurones in the arcuate nucleus control appetite

A
  • 2 types: excitatory and inhibitory
  • Excitatory neurones contain NPY and AgRP which promote HUNGER
  • Inhibitory neurones contain POMC (yields neurotransmitters α-MSH and β-endorphin) which promote SATIETY
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3
Q

Describe how feeding behaviour can be altered

A

Primary neurones synapse with secondary neurones in other regions of the hypothalamus and the signals are INTEGRATED

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4
Q

What 2 substances promote hunger?

A
  • NPY (neuropeptide Y)

- AgRP (Agouti-related peptide)

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5
Q

What substance in the inhibitory primary neurones promote satiety?

A
  • POMC (pro-opiomelanocortin)

- Yields several neurotransmitters including α-MSH and β-endorphin (involved in pleasure)

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6
Q

What hormone detected in the arcuate nucleus promotes hunger and where is it released from?

A
  • GHRELIN
  • Released from stomach wall when empty
  • Stimulates excitatory primary neurones in arcuate nucleus, promoting hunger
  • Filling of stomach inhibits release of ghrelin
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7
Q

What hormone released in the colon promote satiety?

A
  • PEPTIDE TYROSINE TYROSINE (PYY)
  • Short 36AA peptide released from ILEUM OF COLON in response to feeding
  • Stimulates inhibitory primary neurones and inhibits excitatory primary neurones
  • SUPPRESSES APPETITE
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8
Q

Describe the affect of LEPTIN on appetite

A
  • Released by adipocytes
  • Stimulates inhibitory primary neurones (POMC)
  • Inhibits excitatory primary neurones (NPY and AgRP)
  • SUPPRESSES APPETITE
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9
Q

Explain the action of LEPTIN in mitochondria

A
  • Induces expression of UNCOUPLERS - uncouple electron transport from ATP synthesis
  • Increases permeability of inner membrane to H+
  • Energy from PMF is dissipated as heat
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10
Q

Name 4 hormones that suppress appetite

A
  • PYY
  • Leptin
  • Insulin
  • Amylin
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11
Q

Define METABOLIC SYNDROME

A

A group or recognisable pattern of symptoms or abnormalities that indicate a particular trait or disease
- CLUSTER of the most dangerous risk factors associated with cardiovascular disease

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12
Q

What risk factors may be associated with metabolic syndrome/CVD?

A
  • Abdominal obesity
  • High blood pressure
  • Insulin resistance
  • High fasting plasma glucose
  • Dyslipidaemia (⬇️HDL cholesterol, ⬆️TAGs)
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13
Q

Describe the aetiology of metabolic syndrome

A
  • Exact underlying cause UNKNOWN

- Insulin resistance and abdominal (central) obesity are significant risk factors

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14
Q

Explain how insulin resistance can cause metabolic syndrome

A
  • Cells less sensitive to insulin so glucose is not efficiently utilised
  • High plasma glucose leads to increased insulin production and eventually β cells wear out
  • Type II diabetes
  • Risk of micro/macrovascular damage due to glycosylation of vessels
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15
Q

Describe the treatment methods associated with metabolic syndrome

A
  • PRIMARY methods include change to diet and lifestyle by moderate calorie restriction and increase daily exercise
  • SECONDARY methods (when primary methods are unaffective) involves drug intervention e.g. Statins. anti hypertensive drugs (lower BP) and antidiabetic drugs (lower BG)
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16
Q

What is meant by EPIGENETICS?

A
  • Changes in the organism that result from modifications in expression of genes rather than the genetic code itself
  • MODIFICATIONS CAN BE INHERITED
17
Q

State 5 factors that can affect epigenetic mechanisms

A
  • Development in childhood
  • Environmental chemicals
  • Drugs
  • Ageing
  • Diet
18
Q

Describe how methylation of DNA can affect gene expression

A
  • METHYLATION OF DNA
  • Additional methyl group added to DNA structure (but DNA sequence is unchanged)
  • Can affect expression or inhibition of genes
  • Methylation pattern can be INHERITED from one generation to the next
19
Q

State 3 epigenetic mechanisms that can affect the expression of genes

A
  • Methylation of DNA
  • Phosphorylation of histone tails
  • Non coding RNA initiation of mRNA degradation
20
Q

Name the 6 distinct nuclei of the hypothalamus

A

PADAVS:

  • Paraventricular
  • Anterior
  • Dorsomedial
  • Arcuate
  • Ventromedial
  • Supraoptic
21
Q

Explain what is meant by the THRIFTY PHENOTYPE HYPOTHESIS

A
  • States that reduced fetal growth is strongly associated with development of chronic conditions later on in life such as obesity, diabetes and CVD
  • If mother experiences low nutrition during pregnancy then child is “programmed” to expect a similar life
  • If child experiences plentiful nutrition, the adaptations can result in development of metabolic syndrome and other chronic conditions
22
Q

What is the clinical importance of understanding DOAHaD?

A
  • Potentially understand the origins of some diseased states

- Highlights importance of ANTENATAL CARE in terms of adequate nutrition

23
Q

What are the potential socioeconomic issues surrounding DOAHaD?

A

Women with greatest risk of poor nutrition during pregnancy (those who come from a low socioeconomic background) may be least likely to present for antenatal care