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8/3/2019 Body Fluids (2)
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Body fluid
The maintenance of a relatively constantvolume and a stable composition of the body
fluids are essential for homeostasis.
[Most important problems in clinical medicinearise because of abnormalities in the controlsystems that maintain this constancy of thebody fluids] .
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During steady-state conditions intake and outputmust be balanced, despite the continuous exchange of
fluid and solutes with the external environment as wellas within the different compartments of the body
Intake 2.3 L/day : Output 2.3 L/day :
-Ingested water 2.1 L/d - Insensible loss 700water, food evaporation, diffusion
-Synthesis 200 - Sweat 100 , hot moreoxydation- Feces 100 ml/d
- Urine 1.4 , 0.5-20L
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Table 14-3, p. 451
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Table 14-2, p. 447
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Body fluid compartments 60% of body weight
IntravascularExtravascular
a. Plasmaa. Extracellular 20% b. Interstitial
c. Transcellular : in
synovial, peritoneal, pericardial , CSF.
b. Intracellular 40%
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Body fluid compartments
Percentage of fluids determines by age.Gender, and degree of obesity.
ICF : 28 L, around 40% of body weight.
ECF : 14 L around 20% of body weight.Interstitial is 75%, plasma is 25%.
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• contains both ICF (RBCs) & ECF (plasma)
• considered as a separate compartment because it’s
contained in the circulatory system.
7% of body weight: 5 L, 60% plasma, 40% blood cells.
• hematocrit :(packed red cell volume) the fraction of blood
composed of RBCs (in men: 0.4 , in women: 0.36).
in anemic patients the hematocrit is lower. patients with polycythemia have higher hematocrit
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C a p i l l a
r y w a l l
P l a s m a m
e m b r a n e
PlasmaInterstitialfluid
Intracellularfluid(skeletal muscle)
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Composition of ECF
Donnan effect: Plasma proteinsnegatively charged, so attract morecations in plasma, and repel negatively
charged out. 2% cations more iside. ICF: small quantities of sodium, chloride,
almost no calcium, but large amount of
potassium, phosphate, sulfate ions, andlarge amount of proteins (4 times morethan plasma)
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Measurement of fluidvolumes
Indicator-diluting-principle:
indicator: - evenly distributed in targetedcompartment. - not metabolized, or
excreted. - not toxic -easy to use.
Analyze concentration of indicator:
- chemically - photo electrically
-radioactivity.
Injected mass = mass after dispersion
Vi . Ci =Vf . Cf
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Measurement of fluid volumes :
- Indicator-dilution principle Vi Ci = Vf Cf
a. Total body water: tritium H2O, deuterium H2O,Antipyrine
b. ECF : Labeled Na , Cl, thiosolfate , iothalmate, and
inuline
c. ICF = TBW - ECF (calculated)
d. Plasma : I - serum albumin, Evans blue dye
e. Interstitial = ECF - plasma (calculated)
f. Blood vol. = plasma vol. g. RBC: chromium1 - Hct
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Regulation of fluid exchange
b/w intra-and extracellular fluid
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egu a on o uexchange
Distribution b/w plasma & interstitial isdetermined by balance of hydrostatic &colloid forces across capillary.
Distribution b/w IC and ECF isdetermined by osmotic effect of thesmaller solutes acting across cell
membrane.
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egu a on o uexchange
Relation b/w moles and osmoles: waterconcentration in a solution depends onthe # of solute particles in solution, so a
concentration term is needed todescribe the total concentration of soluteparticles, regardless of their exact
composition. Total # of particles in solution is
measured in osmoles.
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egu a on o uexchange
Osmotic pressure: Precise amount ofpressure required to prevent theosmosis.
The higher the osmotic pressure of asolution, the lower the waterconcentration and the higher the solute
concentration of the solution.
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1 osmole = 1 mole of solute particles (6.02 x10).
1 mole glucose = 1 osm.
1 mole NaCl = 2 osm.1 mole Na2SO3 = 3 osm.
Relation between moles andosmoles
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•Osmotic pressure : pressure thatprevents the osmosis .
•The higher the osmotic pressure of asolution, the lower its [H2O] but the higherits [solute].
•According to Van’t hoff’s law: π = CRTπ= 19300 mm Hg for 1 osmole/liter at
body temp.
π(osmotic pr.) C(solute con. In osmole/liter)
R (ideal gas const.) T(absolute temp.)
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Osmolarity of body fluids
In ECF more than 80-90% related tosodium chloride concentration.
In ICF 50% related to potassium
concentration.
ECF & ICF osmolarity almost 300mOsm/L.
Plasma has one mOsm/L more becauseof plasma proteins effect.
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Osmolarity of body fluids
If particles exert interionic &intermolecular attraction, that causingslight decrease of osmotic activity.
If particles repel each other, that causesa slight increase in osmotic activity.
Plasma = 282 mOsm/L
ECF & ICF = 281 mOsm/L
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-Frequent problem in the treatment ofseriously ill patients is the difficulty of
maintaining adequate fluids in one orboth of the intra- and extracellularcompartments.
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- Osmotic effect of electrolytes (NaCl)determines the distribution of fluidsb/w intra- and extracell. comp.
(because the membrane is permeablefor H2O but not for Na and Cl)
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- Osmolality and osmolarity inhuman fluids are equal.
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• osmotic pr. = osmolarity(mOsm/L) X 19.3 mmHg
• the calculated value is not 100% correct due to intraionic
and intermolecular interactions between the particles andit has to be multiplied by the “osmotic coefficient” of the
particles to reach the true value.
• the osmolarity of the body fluids is around 300 mOsm/L,
the plasma being 1mOsm/L higher because of the osmotic
effect of plasma proteins
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Osmotic equilibrium
Small changes in concentration of impermeantsolutes in the ECF can cause tremendous
changes in cell volume .
Isotonic Hypertonic HypoticIsosmotic Hyperosmotic Hypoosmotic
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Osmotic Equilibrium
Isotonic, hypotonic and hypertonicsolutions depend on how cells behavein the solution, whether they swell or
shrink or do not change their volume.
Iso-smotic, hyper-osmotic, and hypo-
osmotic : determine the level ofosmolarity regardless of weather solutecan penetrate cell membrane.
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Osmotic equilibrium
Transfer of fluid across membraneoccurs rapidly, so osmolariteis b/w IC &ECF are corrected w/in seconds, or at
the most, minutes. After drinking water we need only 30
min. to reach equilibrium everywhere in
the body.
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1. Osmolarity of ECF and ICF remain
almost exactly equal, except for a fewminute after a change in onecompartment.
2. Cell membrane almost impermeable tomany solutes so # of osmoles is constantunless solutes are aded to or lost from the
ECF.
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1. Calculation of H2O deficit in
dehydration
- 70 Kg pt. dehydrated unconscious.Plasma osm. 320 mOsm.
- How much water needed to restoreplasma osmolarity to 280 mOsm/L .
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First step: assuming ECF 20% of body wt.
ICF 40% ____
ECF ICF Total
Vol. 14 L 28 L 42 LOsmoles 4480 896 13440
(because osm. = 320)
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Second step: determine the volume
needed to reduce osmol. to 280 mOsm/L.Knowing that # of mosmoles is constantthen volume = # mosmoles
osmolarity
ECF ICF Total
Vol. 16 32 48 LOsm. 280 280 280# osm. 4480 8960 13440
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Third step : Calculate the fluid volume
needed.
48 L - 42 L = 6 L water
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Volume & osmolarity inabnormal states
-Ingestion of water
- Dehydration
-I.V infusion
-Loss of fluids:
From GI : diarrhea, vomiting.
Sweating : during hot weather, or heavyexercise.
From kidneys: diabetes insipidus, andneprogenic.
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What is the effect of infusing 2 liters of ahypertonic 3.0 per cent sodium chlorideinto the ECF compartment of a 70Kgpatient whose initial plasma osmolarity is
280mOsm/L?
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Table 14-4, p. 453
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Glucose and other solutionsadministered for nutritive purposes
• given to patients who can not otherwise take
adequate amounts of nutrition.
• the osmotic ally active substances’concentrations are adjusted nearly to isotonicity,or they are given slowly enough in order not todisturb the osmotic eq. of the body.
• after they are metabolized what is left is only
water that is excreted by the kidneys in the formof very dilute urine.
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2- Hyponatremia :
(a). Water excess in ECF :(hypoosmotic overhydration)- Excess secretion of ADH
(b). Loss of NaCl ( hypoosmoticdehydration)
-Excessive sweating, diarrhea, vomiting- Overuse of diuretics- Addison’s disease hypoaldosterone dedcreases Na reabsorption in kidneys
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3. Hypernatremia :
a. Loss of water from ECF hyperosmotic dehydration.
-No ADH (diabetes insipidus,nephrogenic diabetes insipidus)- Heavy sweating.
b. Excessive NaCladdedhyperosmoticoverhydration. Hyperaldosterone.
St li ill
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Starling capillarycirculation
-Balance of hydrostatic and colloidosmotic forces across the capillarymembrane determines the
distribution of ECF b/w plasma andinterstitial fluids.
EndothelialC ill
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Fig. 10-16a, p. 292
Endothelialcell
Pores
Capillary
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Starling capillary circulation
- 3 mmHg - 3 mmHg8 mmHg 1 8 mmHg ____________________________
130 mmHg 1 28 mmHg
1 10 mmHg
______________________________
Mean capillary pr. 17.3 mmHgNegative interstitial pr. 03.0 mmHg
Osmotic interstitial pr. 08.0 mmHgPlasma colloid pr. 28.0 mmHg
____
Net filtration 0.3 mmHg
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Fig. 10-18 (middle), p. 294
11 mm Hg
(ultrafiltration)
Interstitial fluid
From arteriole To venule
9 mm Hg
(reabsorption)
Initial lymphaticvessel
Blood capillary(See next slide)
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Fig. 10-19, p. 295
Capillarypressure
(mm Hg) Transitionpoint
Fluidmovement
Inward pressure
( pP + PIF)
Outward pressure
(PC + pIF)
Beginning Capillary length End
= Ultrafiltration = Reabsorption
Edema
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Edema
A- Intracellular : causes
1. depression of the metabolic system of thetissues.
2. Lack of adequate nutrition to the cell.
3. Ischemia, inflammation.
Na-K pump stopped - Na lacks insideH2O follows.
T j
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B- Extracellular : Two major causes
(1). Abnormal leakage of fluid from theplasma to the interstitial spaces acrossthe capillaries.
(2). Failure of the lymphatic to returnfluid from the interstitial back into theblood.
Filtration = Kf x (Pc -Pif - π c + π if )
Causes of extracellular edema
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Causes of extracellular edema
1.Increased capillary pressure :
A. Excessive kidney retention of salt and water1. Acute or chronic kidney failure2. Mineral corticoid excess
B. High venous pressure :
1. Heart failure 2. venous obstruction3. Failure of venous pumps:
- muscle paralysis - Immobilized part- Venous valve failure
C. Decreased arteriolar resistance:1. Heat 2. Insufficiency of symp. S.
3. vasodilators
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•edema caused by heart failure:
the heart fails to pump blood from the veins
to the arteries which causes:↑venous pr. ↑ capillary pr. ↑capillary
filtration.
↓arterial pr. ↓excretion of salts ↑blood
volume ↑ capillary hydrostatic pr. . ↓blood flow to the kidneys ↑aldosterone ↑salt & water retention.
2 Decreased plasma proteins:
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2. Decreased plasma proteins :
A. Nephrotic syndrome: increase proteinleakage.
B. Protein loss : Wounds , burns
C. Failure to produce proteins:
- Liver disease, cirrhosis- Malnutrition
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•edema caused by decreased plasma proteins:
Can be caused by:
1- plasma proteins’ leakage, and this can benoted in nephrotic syndrome
2- failure to produce normal amounts ofproteins such as in liver cirrhosis
cirrhosis also causes edema by compressingthe abdominal portal venous drainage beforeentering the general circulation↑ capillary
hydrostatic pr. In the GI area transudationof fluid and proteins to the abdominalcavity this is known as ascites
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•edema caused by decreased kidney
excretion:Diseased kidney fails to excrete water andsalts accumulation of water and salts in
the blood and the interstitial space thiscauses:
1- extracellular edema
2- hypertension
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3.Increased capillary permeability :
A. Immune rxnshistamine releaseB. Bacterial infiction.C. Toxins
D. Vitamin C deficiencyE. BurnsF. Prolong ischemia
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4.Blockage of lymph Return :
A. Cancer
B.Infections (filari)C.SurgeryD. Congenital abnormality of lymphatic
vessels
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C-Safety factors that prevent edema :
1.Low tissue compliance of the
interstitium when pres. is (-). 3mmHg
2.Ability of lymphatic flow to increase 10-
50 times. 7mmHg
3.Washout proteins from interstitium.7mmHG
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Interstitial low compliance
Large change in pressure will causesmall change in volume. This is onlywhen interstitial space has negative
pressure. Compliance increases markedly, once
interstitial pressure rises above zero.
Protoglycan creates gel form of fluidprevents flowing “no free fluid spaces”.
When + pressure pitting edema.
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Lymphatic flow
Lymphatic vessels able to increase theirflow ten to fifty folds.
This increase will be significant whenthe interstitial pressure is zero andabove.
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Fluid pressure on the outside of the vessel
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Fig. 10-20b, p. 296
Fluid pressure on the outside of the vesselpushes the endothelial cell’s free edge inward, permitting entrance of interstitial fluid(now lymph).
Fluid pressure on the inside of the vesselforces the overlapping edges together sothat lymph cannot escape.
Interstitialfluid
Overlapping
endothelial cell
Lymph
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Edema in potential spaces
These type of edema called “Effusion”
Accumulation of fluids in transcellularspaces.
Ascites: collection of fluids in theabdominal cavity, huge 20 liters.
All transcellular spaces have negative
pressure: - pleural=7-8mm Hg- synovial=3-5mm Hg
- pericardial=5-6mm Hg.