Liv4 Flashcards

1
Q

surface anatomy

A

mainly upper R quadrant

protected by rib cage

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2
Q

gross anatomy

A
4 lobes 
R biggest
L/
caudate lobe in middle 
quadrate lobe below it 
falciform ligament - attach to diaphragm 
common bile duct - lead to gall bladder
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3
Q

blood in liver

A

hepatic portal vein and artery to liver

hepatic vein - away

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4
Q

functional anatomy

A

cauinaud classification
8 functionally independent sections - own blood supply and venous drainage
central - HPV artery and bile duct
periphery - hepatic vein

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5
Q

blood supply

A

25% CO
dual - 20% hepatic artery, oxygenated and 80% HPV - deoxygenated from gut
HPV and artery mixed = overall poor oxygenation
hepatic vein drains into vena cava

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6
Q

purpose of hepatic artery

A

oxygen and nutrients

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7
Q

purpose of HPV

A

take breakdown products of gut

liver has a high metabolic rate

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8
Q

morphological anatomy

A

lobules
HPV and artery combine in sinusoid
lined by epithelia - substances can diffuce across into hepatocytes
sinusoid pass through lobule to central vein to vena cava
portal triad/tract - bile duct, HPV and artery
centrilobular hepatocyte - centre of lobe
periprotal hepatocyte

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9
Q

portal triad

A

around edge of lobule

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10
Q

acinus

A

functional
less well defined
unit of hepatocytes divided into zones dependant on proximity to arterial blood supply
zone 1-3
1 near portal triad - risk of viral infection
3 near central vein - risk of ischemia

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11
Q

hepatocytes

A

80% of the mass
large cell
pale and round nuclei
radiate from the central vein

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12
Q

which cells appear to be in sinusoids

A

kuppfer/stellate
flattened
dense nuclei

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13
Q

histology of non-parenchymal cells

A

endothelial cells - nuclei red and flat
Kupffer cells - cytoplasm blue, nuclei red
hepatocytes - nuclei red and round

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14
Q

stellate cells

A

vitamin A storage
activation = ECM formation - fibrinogenesis
respond to proinflammatory environment
important in cirrhosis - fibrotic lesion

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15
Q

sinusoidal endothelial cells

A

fenestrated - allow lipid and large molecule movement to and from hepatocytes

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16
Q

Kupffer cells

A

phagocytosis
including RBC breakdown
secretion of cytokines that promote stellate cell activation - fibrinogenesis

17
Q

four functions of liver

A

control synth and met of protein
maintenance of blood sugar
lipid met
Metabolism and excretion of bilirubin and bile acids.

18
Q

control synth and met of protein

A

albumin
transferrin - transport and carrier proteins
coagulation factors and complement
degradation of aa -> urea

19
Q

Maintenance of blood sugar

A

release glucose
breakdown glycogen
synth glucose from aa or glycerol

20
Q

Lipid metabolism.

A

manufacture most cholesterol -> make bile salts

synth lipoproteins and triglycerides

21
Q

Metabolism and excretion of bilirubin and bile acid

A

bile acids are from cholesterol

22
Q

metabolism of carbohydrates

A

store of glycogen only available for 24hrs
glucose enter muscle = TCA cycle/lactate production
lactate converted to pyruvate in liver via lactate dehydrogenase
pyruvate is converted to glycose by gluconeogenesis
requires 6ATP

23
Q

synthesis of protein

A

aa from diet or muscle break down
enter liver
liver makes secreted proteins eg plasma proteins, clotting factors and lipoproteins

24
Q

transamination

A

transfer essential to non-essential AA
keto acids are a go between
alanine transaminase

25
Q

different transamination reactions

A

depends on the transaminase
a keto-glutarate –> glutamate, proline, arginine
pyrivate –> alanine, valine, leucine
oxaloacetate –> aspartate, methionine, lysine

26
Q

why is deamination needed

A

muscle can use AA to produce glucose
but energy required to convert pyruvate to glucose and remove nitrogen
so job is given to liver

27
Q

deamination

A

glucose-alanine cycle
pyruvate and glutamate form alanine in muscle alanine converted to glutamate and pyruvate in the liver
pyruvate converted back to glucose with addition of 6ATP - TCA
glutamate broken into urea by addition of 4ATP - utilised to make glucose

28
Q

triglyceride metabolism

A

adipose tissue: triglyceride into FA
liver: FA vie B oxidation to acetyl CoA to TCA
OR liver generate ketones: 2x acetyl CoA -> acetoacetate - leave the liver as tissue energy source

29
Q

lipoprotein synthesis

A

glucose enters converted to glycerol and pyruvate
pyruvate –> acetyl CoA
acetyl CoA –> FA and cholesterol
glycerol –> triacylglycerol
triacylglycerol+ apoproteins and phospholipids + cholesterol –> lipoproteins

30
Q

action of lipoproteins

A

VLDL - transport FA to tissues
VLDL –> LDL
LDL converts chol to tissues
HDL - pick up excess chol, have few FA

31
Q

storage

A

fat sol vit - A, E, D, K
A D E store sufficient for 6 month
store iron as ferratin - available for erythropoiesis

32
Q

detoxification

A

phase 1 - P450 make more hydrophilic so easier to secrete in urine
phase 2 - attach water soluble side chain to make less reactive so less likely to leave blood until reaches kidney