Renal Physiology Flashcards

1
Q

what is the associated cause to chronic renal failure?

A

diabetes

hypertension

vascular disorders

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2
Q

what is glomerulosclerosis

A

continuing damage to kidney function

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3
Q

what are the 2 main drivers of CKD?

A

Proteinuria

Angiotensin II

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4
Q

what does glomerular hyperfiltration lead to ?

A

increase in glomerular capillary permeability

increase in protein level in interstitial fluid

accumulating protein levels lead to tubulointestilital injury

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5
Q

what effect goes angiotensin II does to CKD

A

promotes glomerular hypertension

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6
Q

What are the CKD manifestations?

A

Azotemia
- decrease kidney function leads to a buildup of urea and creatinine

Uremia
pathological build-up of nitrogenous waste

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7
Q

what is uremic syndrome and what could it be the impact

A

an inflammatory state associated with high levels of nitrogenous compounds

lead to:
glucose tolerance
abnormal lipid metabolism
hyperparathyroidism

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8
Q

what is acute kidney injury

A

abrupt loss within 7 days of renal function

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9
Q

what cause AKD

A

ischaemia

drugs

hypotension

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10
Q

how can the AKD be classified as?

A

Prerenal

Intrarenal

posternal

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11
Q

what is prerenal AKI

A

reduced renal blood flow –> renal hypoperfusion

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12
Q

what is intrarenal AKI

A

a disorder involving the tissue of the kidney

could lead to acute tubular necrosis

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13
Q

what is postrenal AKI

A

blockages cause an increase in pressure within the kidney

Hypertension leads to a loss of filtrtion

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14
Q

What 3 phases does AKI have?

A

initiation phase

Oliguirc phase

repair phase

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15
Q

what can AKI lead to

A

metabolic acidosis

hyperkalaemia

uremia

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16
Q

How do we know if patient have AKI?

A

increase in serum creatinine b >0.3mg/dl within 48 hours

Increase in serium to >1.5times in 7 days

Urine volume < 0.5ml/kg/h for 6 hours

17
Q

what is glomerulonephritis and what does it cause by?

A

is the damage to your tiny filters (the glomeruli)

its cause by immune system attacking its own body

18
Q

what are the form of acute glomerulonephritis

A

Post-infective

Rapidly progessive

Goodpasture’s syndrome

sytemic auto-immune conditions (i.e. SLE - Systemic lupus erythematosus)

19
Q

post-infective glomerulonoephritis

A

infaction with group A haemolytic strptococci

it is a deposition of complement and immune cell infiltration result in loss of kidney function

20
Q

symptoms of Post-infective glomerulonephritis

A

oliguria - initial stage
haematuria
proteinuria
Oedema - due to sodium retention

21
Q

what kind of stain can reveal the immune complex deposition in the capillaries

A

Anti-C3 antibody

22
Q

streptococcus pyogenes

A

gram positive organism

could cause:

  • strep throat
  • scarlet fever

can produce toxin as well !!

23
Q

Goodpasture’s syndrome

A

high aggressive form of glomerulonephritis

cause by antibodies like anti-GBM & form of IgG

HLA-DRB1 predisposition

24
Q

nephrotic syndrome

A

cause by gross proteinuria
could also lead to hypoalbuminaemia

damage the glomerular membrane

IgA nephropathy is the cause of it

25
Q

what is Berger’s disease

A

when IgA deposits builds up in the kidney, causing inflammation in the membrane and damage the kidney

26
Q

oncogenes

A

mutated formas of normal genes which can drive to malignant change

27
Q

tumour suppressor genes

A

inhibit cell growth and promotes apoptosis

28
Q

DNA repair genes

A

fix any errors which may have occured in the genome

29
Q

where can renal cancer arise from

A

adenomas (noncancerous tumors)
renal cells
renal pelvis
transitional cell carcinoma

30
Q

Wilm tumour

A

most common kidney cancer in children

strongly associated with congenital abnormalities (WT1 gene)

31
Q

what diagnosis can be used for wilm’s tumour?

A

renal biopsy

32
Q

renal clear cell carcinoma

A

arise from proximal tubular epithlial cells –> high concentrations of epithelial cells

33
Q

what kind of treatment is used in renal carcinoma?

A

surgery

targeted chemotherapeutic

cytokine infusion are used
–> inerleukin-2

34
Q

what does nivolumab do?

A

prevents the binding of ligand and receptor

35
Q

what does axitinib do?

A
small molecule tyrosine kinase inhibitor
Binds to VEFGR 1-3.
Prevents angiogenesis.
Prevents vasculogenesis.
May also promote autophagy.