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LYMPH
Dr . LEKSHMI PRIYA J S
JR
SPECIFIC LEARNING OBJECTIVES
• LYMPH FORMATION
• COMPOSITION OF LYMPH
• LYMPHATIC SYSTEM
• LYMPH FLOW
• APPLIED ASPECTS- PATHOLOGY
SLO – 1
LYMPH FORMATION
• CAPILLARY FILTRATION
 major route of transport of fluid b/w
intravascular fluid( blood) and extra vascular
fluid ( fluid in interstitial space )
Occurs because of the difference in various
pressures
• 2 pressures promote filtration & 2 pressures
oppose filtration
1. Hydrostatic pressure of blood  ( + )
2. Osmotic pressure of interstitial fluid ( + )
3. Oncotic pressure (osmotic press of blood due to
pl.prtns)( -- )
4. Tissue hydrostatic pressure  ( -- )
Balance b/w these pressures determine net
filtration.
STARLING FORCES
1. Capillary hydrostatic pressure(Pc)- forces fluid outward through capillary
membrane
2. Interstitial fluid pressure(Pif)- force fluid inwardthroughthe capillary
membrane
3. Plasma colloid osmotic pressure(∏p)- osmosis of fluid inward through
capillary membrane
4. Interstitial fluidcolloidosmotic pressure(∏if)- osmosis of fluid outward
NET FILTRATION
Pressure diff :
At arteriole end = [(37-1)-25] = 11 mmHg;OUTWARD
At venule = [(17-1)-25] =- 9 mmHg; INWARD
• Net filtration pressure(NFP)= k[(Pc-Pif)-(∏p-∏if)]
• If NFP +ve, fluid filtration occurs across the capillary membrane
• If NFP –ve, fluid absorption into capillaries
• Usually NFP +ve
• Pc-capillary pressure
• Pif-interstitial fluid pressure
• ∏p-plasma colloid osmotic pressure
• ∏if-interstitial fluid colloid osmotic pressure
• k= capillary filtration coefficient, proportional to permeability of
capillary wall and area available for filtration; varies in different
tissues
• About 2 units of fluid are left in the interstitial
tissue space as the outward filtration at
arteriolar end is 2mmhg more than the inward
filtration at venular end.
• Usually taken up by lymphatics in interstitial
space,which is again brought back to
circulation as lymphatics finally drain to veins.
LYMPH
• Most of the fluid filtered at the arterial end of
capillary is reabsorbed at its venous end .
• Remaining 10% enters circulation through
lymphatics and is called LYMPH .
• LYMPH IS A TRANSUDATE FORMED FROM BLOOD
IN TISSUE SPACES .
• Ie, it is derived from interstitial fluid .
LYMPH PLASMA
Flows thru lymph vessels Flows thru blood vessels
Protein content 2-6 g% 6-8g%
Less coagulation factors,clots
slowly
Clots rapidly
Wbc count 1000-2000/cu mm 4000-11000/cu.mm
Fat content more Less
SLO 2
COMPOSITION OF LYMPH
• 94% WATER
• 6% SOLIDS
• Composition similar to that of plasma
• Protein content lower than plasma and depends on area it drains
• Fat content is more
• Cells chiefly lymphocytes
• Carbohydrates less than that of plasma
• Clotting factors
• Ions :Na+,k+,ca2+,Cl-,po4.
SLO 3
LYMPH FLOW
LYMPH FLOW FROM THE TISSUE
SLO 4
LYMPHATIC SYSTEM
LYMPHATIC CAPILLARIES
• Found in most places that contain capillaries .
• Exception :
bonemarrow,cartilage,cns,cornea,nail,spleen .
• More permeable than blood capillaries.
• Nature of lymphatic capillaries allow WBC s ,
pathogens & cancer cells to enter easily .
Lymphatic collecting vessels
• Capillaries join together to form lymphatic
collecting vessels
• Morphologically similar to veins, except
contain more valves
 3 coats
Valves give beaded appearance
• Pass through lymph nodes
• Can be superficial or deep.
LYMPH NODES
• b/w two lymphatic collecting vessels
• Capture foreign material
• Site of lymphocyte production
• Become inflamed/engorged with infectious
material
• Can be found in large clusters in
inguinal,cervical & axillary region.
Lymphatic ducts
• Collecting vessels end up as either right or left
lymphatic duct.
Functions of lymph flow
• Return proteins from tissue spaces to blood.
• Absorption of nutrients
• Act as a transport mechanism
• Supplies nutrients & oxygen
• Role in defense mechanism
• Large enzymes like lipases reach circulation
thru lymphatics
MECHANISM OF LYMPH FLOW
• INTRINSIC LYMPHATIC PUMP
• PUMPING BY EXTERNAL COMPRESSION OF
LYMPHATICS
• NEGATIVE INTRATHORACIC PRESSURE
• SUCTION EFFECT OF HIGH VELOCITY BLOOD
FLOW
• INTERSTITIAL FLUID PRESSURE
• INCREASE IN CAPILLAY SURFACE AREA
• INCREASE IN CAPILLARY PERMEABILITY
• INCREASE IN FUNCTIONAL ACTIVITY OF TISSUE
LYMPHAGOUGES
• Substances that increases the flow of lymph.
• Eg:
Sunlight
Warmth
Histamine
Dionin
SL0 5
APPLIED PHYSIOLOGY
1. LYMPHADENOPATHY
2. OEDEMA
3. CHYLURIA
4. CHYLOTHORAX
1.Enlarged lymph nodes
Lymphadenopathy
 Lymphadenopathy refers to one or more enlarged lymph
nodes.
 Small groups or individually enlarged lymph nodes are
generally reactive in response to infection or inflammation.
This is called local lymphadenopathy.
 When many lymph nodes in different areas of the body are
involved, this is called generalised lymphadenopathy.
Generalised lymphadenopathy may be caused by c/c
infns,connective tissue diseases,malignancies
2.Edema
• In certain pathological conditions there is
Accumulation of free fluid in excess in
interstitial tissue spaces
• Accumulate in dependent parts of body
• Intracellular edema- due to increased ICF
• Extracellular edema- due to increased fluid in
interstitial spaces.
Intracellular edema
• Depression of metabolic systems of tissues
• Lack of adequate nutrition to cells
• Inflammation
Extracellular edema due to
* increased filtration of fluid into
interstitial tissue space
* decreased removal of fluid
from interstitial tissue space
INCREASED FILTRATION
1.Increased capillary hydrostatic pressure
 Raisedvenous pressure –
• heartfailure
• failure of venous pumps.
• venous obstrn
Venular constriction
IncreasedECF volume – renal failure
Decreasedarteriolar resistance – excessive heat, vasodilator drugs
2. Decreased oncotic pressure
• Protein loss in urine– nephrotic syndrome
• Protein loss fromdenuded skin areas- burns, wounds
• Failure to produce protein- liver cirrhosis, malnutrition
• Applied aspect – edema in malnutrition, liver disease, renal
disease
3. Increased capillary permeability
• Action of chemical substances
• Bacterial toxins
• Vitamin deficiency
• Prolonged ischemia
DECREASED REMOVAL
Decreased lymph drainage
• Lymphedema
• Due to:
• Lymphangitis
• Surgery – radical
mastectomy
• Infection – filariasis/
elephantiasis
Classificn OF EDEMA
• Localised-commonly inflammatory
• Generalised-malnutrition, renal diseases
• Pitting –inflmmn,ccf,renal disease
• Non pitting-late filariasis,myxedema
• UNILATERAL-
DVT,CELLULITIS,LYMPHOEDEMA,MALIGNANCY
• BILATERAL –MEDICATIONS,SYSTEMIC
DISEASES(cardiac,renal,hepatic,pulmonary)
Safety factors that px edema
• Low compliance of the interstitium when the
interstitial fluid pressure is in the neg press.
Range
• Ability of lymph flow to increase 10- 50 fold
• Wash down of interstitial fluid prtn concn
which reduces interstitial fluid colloid osmotic
pressure as capillary filtration increases.
• Effusion – edema fluid collecting in the
potential spaces like pleural, pericardial,
peritoneal cavities
3.Chyluria
• Excretion of milky urine
• Lymph from small intestine is excreted into
urine
4.Chylothorax
• Lymph from small intestine accumulates in
pleural cavity
Thank you

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Lymph definition ,formation and factors affecting lymph flow including applied aspects.

  • 1. LYMPH Dr . LEKSHMI PRIYA J S JR
  • 2. SPECIFIC LEARNING OBJECTIVES • LYMPH FORMATION • COMPOSITION OF LYMPH • LYMPHATIC SYSTEM • LYMPH FLOW • APPLIED ASPECTS- PATHOLOGY
  • 3. SLO – 1 LYMPH FORMATION • CAPILLARY FILTRATION  major route of transport of fluid b/w intravascular fluid( blood) and extra vascular fluid ( fluid in interstitial space ) Occurs because of the difference in various pressures
  • 4. • 2 pressures promote filtration & 2 pressures oppose filtration 1. Hydrostatic pressure of blood  ( + ) 2. Osmotic pressure of interstitial fluid ( + ) 3. Oncotic pressure (osmotic press of blood due to pl.prtns)( -- ) 4. Tissue hydrostatic pressure  ( -- ) Balance b/w these pressures determine net filtration.
  • 5. STARLING FORCES 1. Capillary hydrostatic pressure(Pc)- forces fluid outward through capillary membrane 2. Interstitial fluid pressure(Pif)- force fluid inwardthroughthe capillary membrane 3. Plasma colloid osmotic pressure(∏p)- osmosis of fluid inward through capillary membrane 4. Interstitial fluidcolloidosmotic pressure(∏if)- osmosis of fluid outward
  • 6.
  • 7. NET FILTRATION Pressure diff : At arteriole end = [(37-1)-25] = 11 mmHg;OUTWARD At venule = [(17-1)-25] =- 9 mmHg; INWARD
  • 8. • Net filtration pressure(NFP)= k[(Pc-Pif)-(∏p-∏if)] • If NFP +ve, fluid filtration occurs across the capillary membrane • If NFP –ve, fluid absorption into capillaries • Usually NFP +ve • Pc-capillary pressure • Pif-interstitial fluid pressure • ∏p-plasma colloid osmotic pressure • ∏if-interstitial fluid colloid osmotic pressure • k= capillary filtration coefficient, proportional to permeability of capillary wall and area available for filtration; varies in different tissues
  • 9. • About 2 units of fluid are left in the interstitial tissue space as the outward filtration at arteriolar end is 2mmhg more than the inward filtration at venular end. • Usually taken up by lymphatics in interstitial space,which is again brought back to circulation as lymphatics finally drain to veins.
  • 10. LYMPH • Most of the fluid filtered at the arterial end of capillary is reabsorbed at its venous end . • Remaining 10% enters circulation through lymphatics and is called LYMPH . • LYMPH IS A TRANSUDATE FORMED FROM BLOOD IN TISSUE SPACES . • Ie, it is derived from interstitial fluid .
  • 11. LYMPH PLASMA Flows thru lymph vessels Flows thru blood vessels Protein content 2-6 g% 6-8g% Less coagulation factors,clots slowly Clots rapidly Wbc count 1000-2000/cu mm 4000-11000/cu.mm Fat content more Less
  • 12. SLO 2 COMPOSITION OF LYMPH • 94% WATER • 6% SOLIDS • Composition similar to that of plasma • Protein content lower than plasma and depends on area it drains • Fat content is more • Cells chiefly lymphocytes • Carbohydrates less than that of plasma • Clotting factors • Ions :Na+,k+,ca2+,Cl-,po4.
  • 14. LYMPH FLOW FROM THE TISSUE
  • 16.
  • 17. LYMPHATIC CAPILLARIES • Found in most places that contain capillaries . • Exception : bonemarrow,cartilage,cns,cornea,nail,spleen . • More permeable than blood capillaries. • Nature of lymphatic capillaries allow WBC s , pathogens & cancer cells to enter easily .
  • 18.
  • 19.
  • 20. Lymphatic collecting vessels • Capillaries join together to form lymphatic collecting vessels • Morphologically similar to veins, except contain more valves  3 coats Valves give beaded appearance • Pass through lymph nodes • Can be superficial or deep.
  • 21. LYMPH NODES • b/w two lymphatic collecting vessels • Capture foreign material • Site of lymphocyte production • Become inflamed/engorged with infectious material • Can be found in large clusters in inguinal,cervical & axillary region.
  • 22. Lymphatic ducts • Collecting vessels end up as either right or left lymphatic duct.
  • 23. Functions of lymph flow • Return proteins from tissue spaces to blood. • Absorption of nutrients • Act as a transport mechanism • Supplies nutrients & oxygen • Role in defense mechanism • Large enzymes like lipases reach circulation thru lymphatics
  • 24. MECHANISM OF LYMPH FLOW • INTRINSIC LYMPHATIC PUMP • PUMPING BY EXTERNAL COMPRESSION OF LYMPHATICS • NEGATIVE INTRATHORACIC PRESSURE • SUCTION EFFECT OF HIGH VELOCITY BLOOD FLOW • INTERSTITIAL FLUID PRESSURE • INCREASE IN CAPILLAY SURFACE AREA • INCREASE IN CAPILLARY PERMEABILITY • INCREASE IN FUNCTIONAL ACTIVITY OF TISSUE
  • 25.
  • 26. LYMPHAGOUGES • Substances that increases the flow of lymph. • Eg: Sunlight Warmth Histamine Dionin
  • 27.
  • 28. SL0 5 APPLIED PHYSIOLOGY 1. LYMPHADENOPATHY 2. OEDEMA 3. CHYLURIA 4. CHYLOTHORAX
  • 29. 1.Enlarged lymph nodes Lymphadenopathy  Lymphadenopathy refers to one or more enlarged lymph nodes.  Small groups or individually enlarged lymph nodes are generally reactive in response to infection or inflammation. This is called local lymphadenopathy.  When many lymph nodes in different areas of the body are involved, this is called generalised lymphadenopathy. Generalised lymphadenopathy may be caused by c/c infns,connective tissue diseases,malignancies
  • 30. 2.Edema • In certain pathological conditions there is Accumulation of free fluid in excess in interstitial tissue spaces • Accumulate in dependent parts of body • Intracellular edema- due to increased ICF • Extracellular edema- due to increased fluid in interstitial spaces.
  • 31. Intracellular edema • Depression of metabolic systems of tissues • Lack of adequate nutrition to cells • Inflammation
  • 32. Extracellular edema due to * increased filtration of fluid into interstitial tissue space * decreased removal of fluid from interstitial tissue space
  • 34. 1.Increased capillary hydrostatic pressure  Raisedvenous pressure – • heartfailure • failure of venous pumps. • venous obstrn Venular constriction IncreasedECF volume – renal failure Decreasedarteriolar resistance – excessive heat, vasodilator drugs
  • 35. 2. Decreased oncotic pressure • Protein loss in urine– nephrotic syndrome • Protein loss fromdenuded skin areas- burns, wounds • Failure to produce protein- liver cirrhosis, malnutrition • Applied aspect – edema in malnutrition, liver disease, renal disease
  • 36. 3. Increased capillary permeability • Action of chemical substances • Bacterial toxins • Vitamin deficiency • Prolonged ischemia
  • 38. Decreased lymph drainage • Lymphedema • Due to: • Lymphangitis • Surgery – radical mastectomy • Infection – filariasis/ elephantiasis
  • 39. Classificn OF EDEMA • Localised-commonly inflammatory • Generalised-malnutrition, renal diseases
  • 40. • Pitting –inflmmn,ccf,renal disease • Non pitting-late filariasis,myxedema
  • 41. • UNILATERAL- DVT,CELLULITIS,LYMPHOEDEMA,MALIGNANCY • BILATERAL –MEDICATIONS,SYSTEMIC DISEASES(cardiac,renal,hepatic,pulmonary)
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  • 44. Safety factors that px edema • Low compliance of the interstitium when the interstitial fluid pressure is in the neg press. Range • Ability of lymph flow to increase 10- 50 fold • Wash down of interstitial fluid prtn concn which reduces interstitial fluid colloid osmotic pressure as capillary filtration increases.
  • 45. • Effusion – edema fluid collecting in the potential spaces like pleural, pericardial, peritoneal cavities
  • 46. 3.Chyluria • Excretion of milky urine • Lymph from small intestine is excreted into urine
  • 47. 4.Chylothorax • Lymph from small intestine accumulates in pleural cavity