Causes of diabetes Flashcards

1
Q

Insulin

A

Secreted by beta cells in pancreas

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2
Q

Sodium and potassium

A

3:2
Na:K

Netflow charge -70mm
Outside more positive than inside

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3
Q

ATP

A

Binds to potassium channel and closes it, stops movement of K. K accumulates in cell, equalises charge across membrane

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4
Q

Charge in membrane

A

Increased uptake of glucose leads to increase ATP:ADP

Increased ATP closes K channel and membrane

Depolarisation leads to opening of Calcium channel

Increase in cytosolic Calcium promotes secretion of insulin via exocytosis

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5
Q

Insulin signalling pathway

A

Binding of insulin to insulin receptor leads to receptor auto phosphorylation

Phosphorylated residues act as binding sites for Insulin receptor protein substrates

IR phosphorylates 4 tyrosin residues in IRS proteins

Lipid kinase, phosphoinositide 3-kinase binds to residue and converts PIP2 to PIP3

PIP3 activates PDK1, which phosphorylates and activates PKB

Activated PKB diffuses through cell and activates glucose transport

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6
Q

Glucose transport mechanism

A

Insulin stimulates glucose uptake into adipocytes and skeletal muscle

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7
Q

Insulin in adipocytes

A

Glucose transporter GLUT4 contained inside storage vesicle cells

Protein AS160 retains vesicles

Activation of PKB phosphorylates AS160 and inactivates it

Allows GLUT4 vesicles to fuse with plasma membrane

Increased levels of glucose transporters at cell surface

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8
Q

Gluconeogensis

A

Fox01 synthesised in cytosol, targeted to nucleus
Regulates expression genes mediating gluconeogenesis (PEPCK, G6Pase)

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9
Q

Fox01 prevention from nucleus

A

PKB phosphorylation prevents Fox01 from moving to nucleus

Insulin signalling leads to activation of PKB

PKB phosphoryltaes Fox01

Fox01 absence from nucleus leads to loss of expression of gluconeogenic genes

Loss of glucose production

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10
Q

Loss of glucose metabolism

A

Loss of insulin-stimulated uptake into target cells (adipocytes)

Loss of insulin-mediated repression of gluconeogenesis in liver

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11
Q

Type 1 diabetes genetic cause

A

Risk of T1D

Human Leukocytes Antigen (HLA) region contains genes that encode components of major histocompatibility complex

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12
Q

Autoantibodies in type 1

A

Presence of autoantibodies against beta cell antigens is risk for development of T1D

-Glutamic acid decarboxylase-65
-Insulin
-IA-2
-ZnT8

20% risk if 1 present
75% risk if 2 present

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13
Q

T1D development

A

Enteroviruses (coxsackie viruses)

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14
Q

Autoimmune destruction of beta cells

A

Islet of Langerhans contain alpha, beta, delta cells

Effector T cell recognises peptides from beta cell and kills it

Glucagon and somatostatin produced by alpha and delta cells, no insulin made

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15
Q

Type 1 diabetes treatment

A

Insulin injections

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16
Q

Type 2 diabetes characteristics

A

Insulin resistance of target tissues
Beta cell dysfunction

17
Q

Mechanism inhibiting insulin signalling pathway

A

Protein tyrosine phosphatase 1B (PTP1B) dephosphorylates insulin receptor, leading to loss of IRS binding

PTEN dephosphorylates PIP3 back to PIP2

IRS proteins inactivated by phosphorylation of serine residues by PKC
PKC - serine phosphorylation

Prevents IR from phosphorylating tyrosine residues on IRS

18
Q

Insulin resistance

A

Lipid overflow into liver, muscle, epicardium

Excess fat leads to increased intracellular lipid signalling intermediate DAG and ceramide into cytoplasm

Ceramide = Inhibits PKB
PKC = Inhibits IRS

19
Q

Adipokines

A

Adiponectin secreted from adipocytes promotes insulin sensitivity

Affects sphingolipid metabolism

Decreased in obesity

20
Q

Obesity

A

Decrease of adiponectin

Increased cytokines

TNF Alpha cytokine cells affect adipokines

21
Q

Increased TNF levels

A

Contribute to insulin sensitivity

Induces expression of PTP1B, dephosphorylates insulin receptor

Activates JNK, causes serine phosphorylation and inactivation of IRS proteins

22
Q

PTP1B

A

Dephosphorylates IR leading to loss of IRS binding