the liver
DESCRIPTION
The Liver. 1450 cm 3 of blood flows through the liver every minute. 1450 cm 3 of blood flows through the liver every minute. 1)Amino acids to glucose. Wide range of functions;. 7) Detoxification. 2)Metabolism of fat. 6) Production of bile. 3) Synthesis of Triglycerides. - PowerPoint PPT PresentationTRANSCRIPT
The Liver
1450 cm3 of bloodflows through theliver every minute.
Wide range offunctions;
1)Amino acids to glucose.
1450 cm3 of bloodflows through theliver every minute
2)Metabolism of fat.
3) Synthesis of Triglycerides.
4) Synthesis & regulationof cholesterol.
5) Deamination/transamination/urea formation
6) Production ofbile.
7) Detoxification
A – Liver
B – Hepatic vein
C – Hepatic artery
D – Portal vein
E – Bile duct
F – Stomach
G – Cystic duct
H – Gall bladder
Blood enters the liver through twovessels:
1)Hepatic artery2)Portal vein
3x the blood enters via the Portal vein.
The blood here comes from the small intestineit is rich is dissolved nutrients.
The blood here is deoxygenated and at low pressure compared to the hepatic artery
Small intestine
Liver
Stomach
Pancreas
AORTA
VENA CAVA
Histology of the liver……
2mm
Liver Lobule.
Central vein
HP vein
Hepatic arteryBile duct
Histology of the liver……
There are 10,000 lobules one adult liver
Blood flows up thru.HPV & hepatic art.
HPV
HA
Blood then flows thru.into Central vein thru.SINUSOIDS
Lobules are made of Cells called HEPATOCYTES
Blood then flows tohepatic vein & out
2mm
Histology of the liver……
Bile ducts
Special cells producebile, which flows thru.BILE CANALICULI.
Special cells (KUPFFER)are macrophages that eat bacteria that come in bloodFrom the HPV
CBH metabolism in the liver……Liver stores glycogen and
Hepatocytes respond to insulin& glucagon
GLUCOSE
GLYCOGENGLUCAGON & ADRENALINE
INSULIN
GLYCOGEN25% LIVER
75% MUSCLES
High bloodGlucose level
βcells in the Islets ofLangerhans secrete INSULIN
INSULIN
Glycogen formed
Blood glucosedrops
This occurs inHEPATOCYTES
Low bloodglucose level
αcells in the Islets ofLangerhans secrete GLUCAGON
GLUCAGON & ADRENALINE
Glycogen
This occurs inHEPATOCYTES
High bloodglucose level
CBH metabolism in the liver……
……GLUCONEOGENESIS
Gluconeogenesis – literally ‘making new glucose’
3 biological molecules can be broken down to form glucose;AMINO ACIDS, LACTATE & LIPIDS.
3 biological molecules are initially broken down to formtriose sugars (3C), which are then metabolised into glucose.
There are 3 biochemical pathways, each of which are only used when glucose concentrations are low.
CBH metabolism in the liver……
……GLUCONEOGENESIS
Excess aminoacids Glucose
DEAMINATION
Amino Grp (-NH2) removed
Urea formed
Pyruvate Triose phosphate
CBH metabolism in the liver……
……GLUCONEOGENESIS
Excess lipids
Glucose
HYDROLYSIS
Fatty Acids
Triose phosphate
Glycerol
CBH metabolism in the liver……
……GLUCONEOGENESIS
Lactate GlucoseTriose
phosphate
Pyruvate
What is Lactate?By product of anaerobic respiration, very common in large muscles.
Lipid metabolism in the liver……
Gluconeogenesis only occurs when blood glucose levels are low. When glucose levels are high, lipids are produced.
So excess glucose forms lipids, lipids are needed for;
Energy store in adipose cells
Used in respiration to produce ATP
Cell structures (membranes)
Formation of steriods, which then form hormones
Lipids as an energy source……
Lipids are used as energy sources even when blood glucose levels are high.
Often fatty acids are used as a preferred energy source, this is particularly true of cardiac muscle.
Triglycerides are broken down into glycerol and fatty acids (hepatocytes),the fatty acids are broken down into acetyl coenzyme A, this is then fed into the Krebs Cycle, producing ATP.
Glycerol3 fatty acids
TRIGLYCERIDE
GlycerolGlucose
Triose phosphate1
2
AcetylCoenzyme
A
ATP
KREBSCYCLE
Lipids as an energy source……
Synthesising triglycerides……Once lipids are synthesised, they are converted toTRIGLYCERIDES and then stored in adipose tissue.But, lipids are insoluble in water, meaning they are difficult to transport.They are converted to LIPOPROTEINS as low density lipoproteins (LDLs)
For each fat that needs transporting, there is specificlipoprotein that does the job – the all have different densities.
Synthesising & regulating cholesterol……
The liver makes cholesterol.Cholesterols functions are:1) Cell membrane stability.2) Cell membrane fluidity.3) Membrane barrier tohydrophilic substances.
4) Synthesis of steroid hormones (oest/test)
5) Deposited under skin, making it waterproof.
6) Involved in Vit D synthesis.
7) Involved in synthesis of bile salts.
Synthesising & regulating cholesterol……
Meat, eggs and other
diary products have high cholesterol.
When you eat lots of these foods, your liver synthesises lessless cholesterol.
This is called dietary cholesterol.
High levels of dietary cholesterol
stops……
Acetyl Coenzyme
A
CHOLESTEROL
..Enzymes
So high levels of DIETARY CHOLESTEROL
does not always lead to high BLOOD CHOLESTEROL
Synthesising & regulating cholesterol……
Alternatively, if your diet contains high
levels of SATURATED FATS…
…synthesis of cholesterol increases.
No C-C double bonds,
e.g. all C-H bonds
Lots of evidence to suggest that
geneticsHas a role to play
Transporting cholesterol……
Cholesterol is a lipid, therefore not
water soluble.
It is also transported in LIPOPROTEINS.
It is transported as either…….
High Density Lipoproteins HDLs
These are good for you.Protecting you from LDLs
May also remove LDLs
Low Density Lipoproteins LDLs
These are not good for you.They deposit cholesterol on
walls of arteries (AKA plaques)
Protein metabolism……
Convert one amino acid to another -
AKATRANSAMINATION.
Removing excess amino acids - AKA
DEAMINATION.
Production of urea – linked to
DEAMINATION.
Production of 3 blood proteins – FIBRINIGEN/ALBUMIN/GOBULIN
S
TRANSAMINATION - converting one amino acid to another.
If our dietary intake of amino acids does not match the bodies requirements, then the liver has the ability to add/remove elements from R groups inorder to make new amino acids.
There are a group of amino acids that the body can not do this with, they are called ESSENTIAL AMINO ACIDS.
DEAMINATION – removing excess amino acids.
If our dietary intake of amino acids exceeds the bodies requirements, then the excess needs to be removed.Deamination removes the AMINE GRP (-NH2), with the rest of the molecule being converted to CBH or fat.The AMINE GRP (NH2) is converted to AMMONIA (NH3) – this is very soluble and toxic, so is not around for long!
It is then combined with CO2 using ATP to produce UREA (CO(NH2)2 this occurs in the ornithine cycle.
The ORNITHINE CYCLE. Deamination NH3
CO2
ATP
ATP
UREACO(NH2)2
SYNTHESIS of PLASMA PROTEINS………
There are 3 important proteins in blood;•Fibrinogen•Globulin•Albumin
Each of these proteins are globular and are produced in the liver.
Hwrk: Read and make notes on
GLOBULIN & ALBUMIN (pg 24).
SYNTHESIS of PLASMA PROTEINS………
Damage to blood vesselsleads to the collagen fibres
being exposed, this stimulatesplatelets.
Prothrombin
Thrombin
Fibrinogen
Fibrin
Thrombin – an enzyme, which catalyses the removal of AA from fribrinogen, to allow it to polymerase and form FIBRIN.
Fibrin is an insoluble protein that forms long fibres, they tangle up trapping rbcs and leading to a clot.
Production of BILE………
2mm
Bile ducts
Special cells producebile, which flows thru.BILE CANALICULI.
1000cm3 of bile is produced each day
Cholesterol made in theLiver is needed to prd. bile
Bile to gallbladder
Production of BILE………
BILE is composed of water & BILE SALTS.
BILE SALTS emulsify fats, then LIPASE can act on thelarger surface area.
BILE SALTS also contain cholesterol – if there is too muchcholesterol or not enough water, gall stones can form.
They can block bile duct and interfere with lipase digestion.
BILE & dead RBCs………
RBCs only live for about 120 days, then they are broken down in the spleen.(below the heart, lower than the diaphragm).
HAEMOGLOBIN is broken down in the LIVER into HAEM &GLOBIN.GLOBIN is broken down into its constituent AA, these are then recycled.
HAEM is broken down into iron and the greenish yellow product called BILIRUBIN – this is excreted into bile.
DETOXIFICATIONMany drugs/dangerous substances are broken down in thesmooth endoplasmic reticulum of hepatocytes.Metabolising alcohol•Alcoholic drinks contain ethanol (C2H5OH)
•It is lipid soluble, so moves thru. cells very easily.
•Alcohol dehydrogenase catalyses the breakdown of ethanol to ethanal.
•Aldehyde dehydrogenase then catalyses the breakdown of ethanal to ethanoate
•Ethanoate can then enter the Krebs cycle to produce ATP.
ETHANOL ETHANAL ETHANOATE
The KREBS CYCLE
ALCOHOLDEHYDROGENASE
ALDEHYDEDEHYDROGENASE
Oxidised NAD
Reduced NAD
Reduced NAD
Oxidised NAD
DETOXIFICATION of ALCOHOL
If you drink too much, reduced NAD builds up and levels of oxidised NAD become low. These means fatty acids build and a condition called ‘fatty liver’ develops.
DETOXIFICATION of ALCOHOL
Drinking too much leads to......•Low levels of oxidised NAD, failure to metabolise fatty acids and ‘fatty liver’ develops.
•Destruction of hepatocytes, leads to replacement with inferior hepatocytes.
•Reduced blood supply to the lobules
•This is called CIRRHOSIS
The liver can not function properly, e.g. NH3 builds up and canLead to coma and death in extreme cases