Fluid and Electrolyte Balance
Human Anatomy & Physiology
Chapter 25 - Fluid and Electrolyte Balance
Part 1
Body Water Content
Varies with age and tissue type.
Skeletal muscle > adipose tissue.
Infants have a higher total body water content compared to the elderly.
Fluid Compartments
Intracellular Fluid (ICF): Represents 2/3 of total body fluids.
Extracellular Fluid (ECF): Comprises 1/3 of total body fluids and is subdivided into:
Interstitial Fluid: Forms 2/3 of the ECF.
Blood Plasma: Makes up 1/3 of the ECF.
Transcellular Fluid: A small portion of ECF, which includes several compartments such as:
Cerebrospinal Fluid.
Aqueous Humor.
Synovial Fluid (not directly involved in fluid balance).
Composition of Fluid Compartments
Intracellular Fluid:
Higher concentrations of:
Potassium ions [K+].
Magnesium ions [Mg+].
Proteins.
Phosphate ions [HPO4^2-].
Extracellular Fluid (Interstitial Fluid & Plasma):
Higher concentrations of:
Chloride ions [Cl-].
Sodium ions [Na+].
Bicarbonate ions [HCO3-].
Fluid Movement
Fluid movement occurs primarily due to osmosis of water.
Fluid Balance
Fluid Intake
Sources of fluid intake include:
Ingested water (H₂O).
Metabolic water produced by cellular respiration.
Fluid Output
Methods of fluid output include:
Breathing.
Sweating (cutaneous).
Defecation.
Urination.
Fluid output can be categorized as:
Sensible loss: Includes urine, defecation, and sweating.
Insensible loss.
Obligatory loss.
Facultative loss (variable).
Fluid Imbalance
Fluid imbalance can occur when:
Fluid intake does not equal fluid output.
Fluid is incorrectly distributed in compartments.
Changes in Osmolarity:
Dehydration: Water loss exceeds electrolyte loss, leading to hypertonic fluids.
Hypotonic hydration: Excessive water consumption without electrolytes.
Fluid Sequestration:
Accumulation of fluid in a specific area (e.g., edema).
Types of edema:
Systemic Edema.
Pulmonary Edema.
Regulation of Fluid Balance
Volume and concentration are indirectly monitored through:
Blood volume and pressure.
Blood osmolarity.
Regulation of Fluid Intake:
When fluid intake exceeds output:
Results in increased blood pressure and blood volume, possibly decreasing blood osmolarity.
Leads to decreased renin release (and subsequent RAA pathway activation).
Results in decreased aldosterone secretion and decreased thirst activation.
When fluid intake is less than output:
Results in decreased blood pressure and blood volume, possibly increasing blood osmolarity.
Stimulates increased renin release (and subsequent RAA pathway activation).
Leads to increased aldosterone secretion and increased thirst activation.
Thirst Center (Hypothalamus):
Stimulated by:
The RAA pathway (specifically angiotensin II).
Antidiuretic Hormone (ADH).
Decreased salivation.
Inhibited by:
The reversal of previous stimuli and stomach distention.
Regulation of Fluid Output
Controlled primarily through urine formation regulated by hormones, which include:
Renin.
Angiotensin II.
Antidiuretic Hormone (ADH).
Atrial Natriuretic Peptide (ANP).
Electrolyte Homeostasis
Electrolytes: Substances that dissociate into ions in solution, examples include:
Sodium ions [Na+].
Potassium ions [K+].
Chloride ions [Cl-].
Calcium ions [Ca2+].
Phosphate ions [PO4^3-].
Magnesium ions [Mg2+].
Hydrogen ions [H+] and bicarbonate ions [HCO3-].
Sodium Homeostasis
Sodium [Na+] is predominantly found in the ECF (99%).
Daily requirement: approximately 2 g/day; the average American consumes 3-7 g/day through table salt and processed foods.
Losses occur through urine, feces, and sweat, regulated by:
ADH.
Aldosterone.
ANP.
Importance of Sodium:
It is the most significant osmotic particle affecting blood pressure and volume.
Conditions Related to Sodium Levels:
Hypernatremia: Elevated blood sodium.
Hyponatremia: Low blood sodium.
Potassium Homeostasis
Potassium [K+] is primarily found in the ICF (98%) and is the principal cation involved in membrane potentials.
Losses occur mainly through urine.
K+ Imbalance: Potentially Lethal
Hyperkalemia: High plasma [K+] can lead to an irregular heartbeat.
Hypokalemia: Low plasma [K+] can cause paralysis of skeletal muscles.
K+ Shifts:
As blood pH changes, H+ ions move from ICF to ECF (or vice versa), prompting K+ ions to move in the opposite direction.
Insulin stimulates Na+/K+ pumps, influencing K+ levels in the bloodstream.
Chloride Homeostasis
Chloride [Cl-] is the most abundant anion found in ECF and is closely associated with Na+.
Functions include:
Contributing to hydrochloric acid (HCl) in the stomach.
Participating in ion shifts in red blood cells (RBCs).
Loss of chloride occurs through sweat, urine, and stomach secretions.
Calcium Homeostasis
Calcium [Ca2+] is 99% present in bone and teeth, playing crucial roles in:
Maintaining membrane potentials.
Neurotransmitter release.
Serving in second messenger systems.
Blood clotting and muscle contraction.
Losses of calcium occur through urine, feces, and sweat.
Calcium Imbalances:
Hypercalcemia: High calcium levels.
Hypocalcemia: Low calcium levels.
Phosphate Homeostasis
Phosphate [PO4^3-] is the most abundant anion found in ICF and is involved in:
Forming nucleotides and phospholipids.
99% of phosphate is found in bone in the form of calcium phosphate (CaPO4).
Acts as an intracellular pH buffer through forms like HPO4^2- and H2PO4-.
Regulated by the same mechanisms applicable to calcium.
Magnesium Homeostasis
Magnesium [Mg2+] is the second most abundant cation in ICF and is essential for many enzymatic reactions, notably in:
ATP synthesis and protein synthesis.
Hormonal Regulation of Fluid and Electrolyte Balance
Key Hormones Involved in Fluid and Electrolyte Regulation:
Angiotensin I, Antidiuretic Hormone (ADH), Aldosterone, Atrial Natriuretic Peptide (ANP).
Angiotensin II:
Produced by the activation of the Renin-Angiotensin-Aldosterone (RAA) pathway.
Functions include:
Stimulating vasoconstriction of systemic blood vessels, thus increasing blood pressure.
Decreasing glomerular filtration rate (GFR) and urine formation.
Stimulating thirst center and the release of ADH and aldosterone.
Antidiuretic Hormone (ADH):
Released from the posterior pituitary gland in responses to low blood pressure or volume, high blood osmolarity, or angiotensin II presence.
Functions include:
Stimulating thirst center.
Increasing water reabsorption in the kidneys (via aquaporins in the collecting duct).
At high levels, can cause vasoconstriction of systemic blood vessels.
Aldosterone:
Secreted by the adrenal cortex in response to low blood pressure, low blood sodium, high blood potassium, or angiotensin II.
Stimulates:
Sodium and water reabsorption.
Excretion of potassium or hydrogen ions.
Atrial Natriuretic Peptide (ANP):
Released by atrial heart cells in response to high blood pressure or volume.
Stimulates:
Dilation of systemic blood vessels.
Dilation of the afferent arteriole and glomerulus, reducing reabsorption of sodium and water.
Inhibition of ADH, angiotensin II, and aldosterone.
Part 2 - pH Balance
pH Balance Overview
H+ concentration of arterial blood is approximately 7.4.
Influenced by:
Acids and bases entering or leaving the body.
Output through kidneys and respiration.
Buffers present in the body.
Types of Acids
Fixed Acids:
Produced from metabolic waste.
Volatile Acids:
Including carbonic acid (H2CO3).
Excess H+ Ions
Sources include dietary intake or metabolic processes.
Loss of bicarbonate ions (HCO3-) due to diarrhea leads to increased H+.
Kidneys respond by secreting H+ (into urine) or producing HCO3- to be reabsorbed.
Alkaline Conditions
Conditions characterized by low H+ ion concentration.
More common from:
Vegetarian diets.
Excessive antacid intake.
Vomiting leading to loss of H+.
Kidneys reabsorb H+ (back into blood) or produce HCO3- (that is secreted into urine).
Role of Respiration
Respiratory regulation helps remove excess carbon dioxide (CO2).
Increased CO2 leads to H+ concentration increase, lowering pH, which subsequently stimulates increased respiration.
Buffer Systems
Protein Buffers:
Located in plasma and ICF, accounting for roughly 3/4 of the buffering capacity.
Amine groups act as weak bases, while carboxylic groups act as weak acids.
Phosphate Buffering:
Primarily occurs in ICF.
Composed of HPO4²- (weak base) and H2PO4- (weak acid).
Bicarbonate Buffering:
Occurs in plasma.
Comprises HCO3- (weak base) and H2CO3 (weak acid).
Acid-Base Imbalance
Acidosis (Acidemia):
Blood pH falls below 7.35.
Alkalosis (Alkalemia):
Blood pH rises above 7.45, with levels beyond 7.0 or lower than 7.7 being life-threatening.
Indicates that buffering capacity has been exceeded.
Types of Acid-Base Imbalance
Respiratory Acidosis:
Caused by hypoventilation and decreased alveolar gas exchange.
The reaction: CO2 + H2O ⇌ H2CO3 ⇌ H+ + HCO3-.
Respiratory Alkalosis:
Caused by hyperventilation, which can result from anxiety, hypoxia, or aspirin overdose.
Diagnosis is based on low CO2 levels.
Metabolic Acidosis:
Due to increased lactic acid, ketoacidosis, or acetic acid or reduced kidney function leading to bicarbonate loss (HCO3-), often from diarrhea.
Metabolic Alkalosis:
Results from loss of H+ ions such as from vomiting or increased urine production (diuretics) and excessive intake of antacids.
K+ Shifts due to pH Changes
Increased blood H+ causes K+ to shift out of ICF into ECF (opposite movement of H+).
Decreased blood H+ causes K+ to shift into ICF, potentially leading to:
Hyperkalemia: High blood K+ levels.
Hypokalemia: Low blood K+ levels.
Compensation Mechanisms
Renal Compensation
In response to acidosis:
Increased H+ secretion.
Increased production and reabsorption of HCO3-.
In response to alkalosis:
Increased H+ reabsorption.
Increased secretion of HCO3-.
Respiratory Compensation
Adjustments made in respiration to compensate for acidosis or alkalosis, maintaining homeostasis of blood pH.