heptabilliray system Flashcards

1
Q

how many lobes in kidney

A

2

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2
Q

how are they divided

A

left and right by the middle hepatic vein

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3
Q

inflow to liver

A

hepatic artery

portal vein

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4
Q

outflow

A

bile

hepatic veins x 3

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5
Q

how many segments to the. liver

A

8

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6
Q

how are they ordered

A

clockwise

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7
Q

what is the liver made up of

A

lobules which make up portal triads

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8
Q

Hepatic lobule is

A

Hexagonal structural unit of liver tissue

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9
Q

how is a portal triad made

A

Each corner consists of a portal triad

Links with 3x adjacent lobules

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10
Q

what is located in the centre of a lobule

A

central vein

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11
Q

what does the vien do

A

Collects blood from hepatic sinusoids → hepatic veins → systemic venous system

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12
Q

what does the hepatic artery bring

A

Brings O2-rich blood into liver to support hepatocytes ↑ more energy demands

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13
Q

Branch of portal vein

A

Mixed venous blood from GIT (nutrients, bacteria & toxins) and spleen (waste products)
Hepatocytes process nutrients, detoxify blood & excrete waste

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14
Q

bile duct and where does it go

A

Bile produced by hepatocytes drains into bile canaliculi

Coalesce with cholangiocyte-lined bile ducts around lobule perimeter

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15
Q

what is larger portal vien or hepatic artery

A

portal vein

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16
Q

how do sinusoid form

A

hepatic artery and portal vein

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17
Q

where does bile floe

A

in the opposite direction

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18
Q

what is the hepatic acinus

A

Functional unit of liver

diamond shape from a central vien to another central vein

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19
Q

how many zones in the acinus

A

3- zone 1 2 3
zone 1 in the centre of the 2 lobules
2 then 3

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20
Q

point a

A

Blood into hepatic acinus via point a (on the outside of a lobule)

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21
Q

point b

A

Blood drains out of hepatic acinus via (middle of a lobule)

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22
Q

what is the significance of zone 1

A
Hepatocytes near outer hepatic lobule(zone 1) receive early exposure to blood contents:
Good components (O2)
Bad components (toxins)
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23
Q

what is the o2 and toxin risk in z1

A

high

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24
Q

z2

A

middle

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25
z3
low
26
strcuture of sinosodial endothelial cell
No basement membrane | Fenestrated (discontinuous endothelium
27
what does it allow
Allow lipids & large molecule movement to and from hepatocytes
28
what is a kuppler cell
Sinusoidal macrophage cells
29
where are they
Attached to endothelial cells | within sinosoid
30
function
Phagocystosis | Eliminate & detoxify substances arriving in liver from portal circulation
31
what does a hepatic stellate cell do/function/s
Store vit A in liver cytosolic droplets Activated (fibroblasts) in response to liver damage Proliferate, chemotactic & deposit collagen in ECM
32
how do they exist
in a dormant state
33
hepatocytes strcuture
cubical
34
function
albumin, clotting factors & bile salts Drug metabolism Receive nutrients & building blocks from sinusoids
35
Cholangiocyte location
sorrounds the bile duct
36
function
Secrete HCO3- & H2O into bile
37
3 main functions of hepatocsytes
Metabolic & catabolic functions: synthesis & utilization of carbohydrates, lipids and proteins. Secretory & excretory functions: synthesis & secretion of proteins, bile and waste products. Detoxification & immunological functions: breakdown of ingested pathogens & processing of drugs
38
what is the purpose of the cori cycle
glucose is metabolized to pyruvate and then to lactate in muscle, the lactate is released into the blood and carried to the liver, where it is reconverted to pyruvate and used for gluconeogenesis, and the resulting glucose is released and travels back to muscle.
39
non esential amino acid sythesis
by transaminiation Different keto-acids can be converted into multiple amino acids depending on the transaminase enzyme (vital for production of non-essential amino acids)
40
what is the principle amino acid released from the body during starvation
alanine
41
Glucose-alanine cycle
involves muscle protein being degraded to provide more glucose to generate additional ATP for muscle contraction alanine trasnported to liver alanine is shuttled to the liver where the nitrogen enters the urea cycle and the pyruvate is used to make glucose.
42
routes of glucose in liver
glucose -> glycerol | glucose -> pyruvate -> acteyl CoA -> fatty acid or cholesterol
43
what next routes
glycerol and fatty acid to triglycerides lioprotiens and cholesterol to apoprotiens phospholipids
44
function of cholesterol
make hormones | mantain cell membrane
45
what are the fat soluble vitamins that are stores
a d e k
46
what else is stored
ferritin
47
what other vit is stored
k
48
what happens in detoxification
``` Phase 1 (modification) – more hydrophilic ``` Phase 2 (conjugation) – attach water soluble side chain to make less reactive
49
main component of bile
water
50
function of bile
Cholesterol homeostasis Absorption of lipids & lipid soluble vitamins (A, D, E, & K) ``` Excretion of: xenobiotics/drugs cholesterol metabolites adrenocortical & other steroid hormones Alkaline phosphatase ```
51
what colour is bile
yelloe
52
biliverdin
green
53
what is responsible for primary secretion of bile
hepatocystes Bile secretions reflect serum concentrations Secretion of bile salts (acids), lipids & organic ions 60%
54
what are Cholangiocytes responsible for
Secrete 40% of total bile | Secondary modification
55
what are secondary modifications
Alteration of pH (alkaline electrolyte solution) H2O drawn into bile by osmosis via paracellular junctions Luminal glucose & organic acids reabsorbed HCO3- & Cl- actively secreted into bile by CFTR (Cystic Fibrosis Transmembrane Regulator) IgA exocytosed
56
what do bile transporters do
Biliary excretion of bile salts & toxins performed by biliary transporters on apical surface & basolateral membranes of hepatocytes + cholangiocytes
57
what is bile sythesised from
cholesterol
58
what happens to 2 primary bile acids i
produced in the liver | converted to secondary bile acids by gut bacteria
59
bile salt function
Reduce surface tension of fats | Emulsify fat prior to its digestion & absorption
60
define amphipathic
2 faces
61
what are they
hydrophobic | hydrophilic
62
what causes bile storage and release
Between meals Sphincter of Oddi closed → bile diverted into gall bladder for storage Eating → Sphincter of Oddi relaxes Gastric contents (FFAs, AAs > CHOs) enter duodenum causing release of cholecystokinin (CCK) CCK causes gall bladder to contract
63
what happens to the bile
95% bile salts reabsorbed from terminal ileum | By Na+/bile salt co-transport Na+-K+ ATPase system
64
what happens to the other 5 percent
5% converted to 2o bile acids in colon: All Deoxycholic acid absorbed 99% Lithocolic acid excreted in stool absorbed B.salts back to liver & re-excreted in bile
65
how does the gall bladder (GB) constrict | and what does Gb do to the bile
``` . Stores bile (50 mls) - concentrates bile - acidifies bile . GB contraction triggered by CCK - Binds to CCKA receptors & neuronal plexus of GB wall (innervated by preganglionic parasympathetic fibres of vagus nerve) ```
66
what is free Bilirubin
BR (indirect/unconjugated) | = H2O-INSOLUBLE, yellow pigment
67
what is the source of free BR
75% BR from Hb (erythrocytes) breakdown 22% from catabolism of other haemoproteins 3% from ineffective BM erythropoiesis
68
how does free BR get conjugated
in the liver
69
how
Free BR bound to albumin in blood Most dissociates in liver & enters hepatocytes BR conjugated with 2x molecules of UDP-glucuronate → bilirubin diglucuronide (direct bilirubin) Secreted ACROSS concentration gradient into biliary canaliculi → GIT
70
what is a useful test for liver function
free BR --> low | albumin --> high
71
what happens when BR gets to the gut
85% excreted in faeces 15% enters enterohepatic circulation 1% enters systemic circulation & excreted by kidneys
72
how is Br converted to rubbish
BR → urobilinogen → stercobilinogen→ stercobilin (brown compound)
73
what gives feaces its brown colour
stercobilin
74
what happens in obstructive jaundice
bilrubin cant enter into the gut so no stercobilin pale feaces but dark urine as enters systemic circulation
75
causes of jaundice
pre hepatic -> hemoloysis intrahepatic post hepatic
76
Endoscopic Retrograde Cholangiopancreatography (ERCP)
is a procedure to diagnose and treat problems in the liver, gallbladder, bile ducts, and pancreas. It combines X-ray and the use of an endoscope
77
PTC
an x-ray procedure that involves the injection of a contrast material directly into the bile ducts inside the liver to produce pictures of the bile ducts. This procedure is usually performed by an interventional radiologist.