causes of diabetes Flashcards

1
Q

insulin secretion

A
  • increased uptake and metabolism of glucose leads to an increase in ATP-ADP ratio
  • increased ATP-ADP leads to closure of ATP-sensitive K+ channels and membrane depolarisation
  • depolarisation of membrane leads to opening of voltage-gated Ca2+ channels
  • resulting increase in cytosolic Ca2+ promotes secretion of insulin via exocytosis of insulin granules
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2
Q

insulin signalling pathways

A
  • binding of insulin to insulin receptor (IR) leads to receptor auto-phosphorylation
  • phosphorylated residues on the IR act as binding sites for insulin receptor substrate (IRS) proteins
  • IR phosphorylates 4 tyrosine residues in IRS proteins
  • the lipid kinase, phosphoinositide 3 kinase binds to phosphorylated residues on IRS proteins and converts PIP2 to PIP3
  • binding to PIP3 activates PDK1 which then phosphorylates and activates kinases such as PKB/Akt
  • activated PKB/Akt can then diffuse through cell and activate processes such as glucose transport and glycogen synthesis
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3
Q

glucose transport into adipocytes/skeletal muscle

A
  • glucose transporter GLUT4 is contained inside cell in storage vesicles
  • the protein AS160 acts to retain these vesicles in the cell
  • activated PKB phosphorylates AS160 and inactivates it
  • allowing GLUT4 vesicles to fuse with plasma membrane leading to increased levels of glucose transporter at cell surface
  • this is how insulin stimulates glucose uptake into adipocytes/muscle
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4
Q

insulin inhibiting gluconeogenesis

A
  • insulin signalling leads to activation of PKB
  • PKB phosphorylates Fox01
  • phosphorylation of Fox01 prevents it from entering the nucleus leading to a loss of expression of gluconeogenic genes and hence a loss of glucose production
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5
Q

Fox01

A

synthesised in the cytosol but is targeted to the nucleus where it regulates expression of genes that mediate gluconeogenesis

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6
Q

genetic risk factors for type 1 diabetes

A
  • risk of T1D is 15x higher for first degree relatives of someone with type 1
  • HLA (human leukocyte antigen) region is critical susceptibility locus for T1D
  • contains genes that encode components of major histocompatibility complex (MHC)
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7
Q

autoantibodies

A
  • presence of autoantibodies against beta cell antigen is a risk factor for developing T1D
    examples:
  • glutamic acid decarboxylase-65 (GAD-65)
  • insulin
  • IA-2 (islet antigen 2)
  • AnT8 (zinc transporter 8)
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8
Q

enteroviruses and T1D

A

striking similarity between the 2C protein of coxsackie virus and GAD-65 suggests molecular mimicry might be involved of aetiology of T1D

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9
Q

auto-immune destruction of beta cells

A
  • the islets of langerhans contain several cell types secreting distinct hormones, each cell expresses different tissue-specific proteins
  • in T1D an effector T-cell recognises peptides from a beta cell specific protein and kills the beta cell
  • glucagon and somatostatin are still produced by alpha/beta cells but insulin cannot be made
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10
Q

mechanisms that inhibit insulin signalling pathway

A
  • protein tyrosine phosphatase 1B dephosphorylates the insulin receptor IR leading to a loss of IRS binding
  • PTEN (phosphate and tensin homologue) dephosphorylates PIP3 back to PIP2
  • IRS proteins are inactivated by phosphorylation of serine residues by PKC which prevents IR from phosphorylating tyrosine residues on IRS
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11
Q

obesity affecting insulin resistance

A
  • a consequence of obesity is that the amount of triacylglycerols exceeds the storage capacity of adipose cells as a result fat starts to accumulate in other tissues such as liver and muscle
  • excess fat leads to increased levels of intracellular lipid signalling intermediates diacylglycerol (DAG) and ceramide (component of sphingolipids) in the cytoplasm of cells, both formed from fatty acids
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12
Q

adiponectin

A

secreted from adipocytes and promotes insulin sensitivity

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13
Q

adipokines and insulin resistance

A
  • insulin-sensitising effects of adiponectin are related to its effects on sphingolipid metabolism
  • adiponectin secretion is decreased in obesity which contributes to insulin resistance
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14
Q

obesity

A
  • pro-inflammatory condition in which hypertrophied adipocytes and adipose-resident immune cells contribute to increased circulating levels of pro-inflammatory cytokines
  • in obesity more inflammatory cytokines are released such as TNFa (tumour necrosis factor alpha)
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15
Q

increased TNF and insulin resistance

A
  • induces expression of PTP1B which can dephosphorylate the insulin receptor
  • activates JNK (jun-N-terminal kinase) which causes serine phosphorylation and inactivation of IRS proteins
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16
Q

loss of insulin secretion in type 2 diabetes

A
  • dysregulation of insulin secretion linked to accumulation of fat in pancreas
  • over time beta cell mass decreases
    25% decrease 5 years after diagnosis
    50% decrease >15 years after diagnosis
17
Q

beta cell destruction

A
  • beta cells respond to prevailing insulin resistance by synthesising more insulin
  • this puts endoplasmic reticulum under stress and cells can no longer fold and process new insulin
  • activates unfolded protein response (UPR)
  • eventually results in apoptosis and beta cell death