A&P Kai

I. Osmoregulation & Fluid Balance
  • Osmolarity Maintenance: ECF/ICF osmolarity is 300 mOsm\approx 300 \text{ mOsm}, maintained by sodium (Na+\text{Na}^+).

  • Kidney Function: Nephrons filter blood, reabsorb useful substances (e.g., >99\% of filtered sodium), and secrete unwanted substances.

  • Na+\text{Na}^+ & Water Reabsorption: When Na+\text{Na}^+ is reabsorbed, water follows by osmosis, increasing blood volume and pressure but not osmolarity.

  • Hormonal Regulation:

    • Aldosterone: Increases Na+\text{Na}^+ and water reabsorption; primarily controls blood volume/pressure in response to low BP/volume.

    • Antidiuretic Hormone (ADH): Increases water reabsorption independently; controls blood osmolarity (high osmolarity triggers release).

    • Atrial Natriuretic Peptide (ANP): Decreases Na+\text{Na}^+ and water reabsorption, reducing blood volume.

II. Capillary Fluid Exchange
  • Capillaries & Interstitial Fluid: Capillaries have gaps, allowing fluid and nutrients to move into interstitial fluid.

  • Normal Exchange (Starling Forces):

    • Filtration: Fluid moves out of capillaries due to capillary hydrostatic pressure (arterial end).

    • Reabsorption: Fluid moves into capillaries due to capillary colloidal osmotic pressure (proteins in blood).

  • Lymphatic System: Returns excess interstitial fluid and proteins to circulation, preventing fluid loss.

III. Disorders of Fluid Balance
  • Edema: Accumulation of interstitial fluid due to:

    • Increased capillary hydrostatic pressure (e.g., heart failure).

    • Decreased capillary colloidal osmotic pressure (e.g., liver/kidney disease).

    • Increased capillary permeability (e.g., inflammation).

    • Lymphatic obstruction.

    • Pulmonary edema is life-threatening as it impairs gas exchange.

  • Isotonic Hypovolemia (Fluid Volume Deficit): Proportionate loss of Na+\text{Na}^+ and water, decreasing ECF volume (osmolarity unchanged).

    • Causes: Inadequate intake, excessive GI/renal/skin losses, third-space losses.

    • Manifestations: Thirst, weight loss, decreased urine, postural hypotension, tachycardia, dry membranes, decreased tissue turgor.

  • Isotonic Hypervolemia (Fluid Volume Excess): Proportionate increase in ECF Na+\text{Na}^+ and water.

    • Etiology: Increased total body sodium, decreased renal elimination, excessive intake.

    • Manifestations: Weight gain, edema, distended neck veins, full pulse, pulmonary edema.

IV. Disorders of Electrolyte Balance

A. Sodium Balance

  • Overview: Main ECF cation; vital for osmolarity, ECF volume, acid-base, nerve function.

1. Hyponatremia (plasma \text{Na}^+ < 135 \text{ mEq/L} )

  • Types: Hypertonic (water shift from ICF), Hypotonic (dilutional due to water retention - hypovolemic, euvolemic, hypervolemic).

  • Manifestations: Cell swelling (especially brain), muscle cramps, GI issues, CNS symptoms (lethargy, confusion, seizures, coma).

2. Hypernatremia (plasma \text{Na}^+ > 145 \text{ mEq/L} )

  • Characterized by: ECF hypertonicity and cellular dehydration.

  • Causes: Net water loss (DI), sodium gain, impaired thirst.

  • Manifestations: Thirst, decreased urine, dry skin/mucous membranes, ECF loss signs (tachycardia, low BP), CNS symptoms (agitation, seizures, coma) due to brain cell shrinkage.

B. Potassium Balance

  • Overview: Major ICF cation (140-150 mEq/L140 \text{-} 150 \text{ mEq/L}), ECF (3.5-5.0 mEq/L3.5 \text{-} 5.0 \text{ mEq/L}); critical for cell integrity, acid-base, nerve/muscle excitability.

  • Regulation: Renal elimination, transcellular shifts (insulin, acid-base).

1. Hypokalemia (plasma \text{K}^+ < 3.5 \text{ mEq/L} )

  • Etiology: Inadequate intake, excessive losses (renal, GI), transcellular shifts.

  • Manifestations: Renal (impaired concentration), GI (constipation, ileus), CV (dysrhythmias, digitalis toxicity), Neuromuscular (weakness, paralysis).

2. Hyperkalemia (plasma \text{K}^+ > 5 \text{ mEq/L} )

  • Etiology: Decreased renal elimination (renal failure), rapid administration, movement from ICF to ECF (tissue trauma).

  • Manifestations: Decreased neuromuscular excitability (paresthesias, muscle weakness), serious cardiac conduction issues (peaked T waves, wide QRS, arrest).

C. Calcium Balance

  • Overview: 99%99\% in bone; ionized (Ca2+\text{Ca}^{2+}) is vital for neuromuscular/cardiac excitability, muscle contraction, clotting.

  • Regulation: Vitamin D (absorption), Parathyroid Hormone (PTH - raises Ca2+\text{Ca}^{2+} from bone, kidney, activates Vit D), Calcitonin (lowers Ca2+\text{Ca}^{2+}).

1. Hypocalcemia (plasma \text{Ca}^{2+} < 8.5 \text{ mg/dL} )

  • Etiology: Impaired bone mobilization (hypoparathyroidism, Vit D deficiency), abnormal renal losses, increased protein binding.

  • Manifestations: Increased neuromuscular excitability (paresthesias, cramps, tetany, positive Chvostek/Trousseau signs, prolonged QT interval), cardiac insufficiency.

2. Hypercalcemia (plasma \text{Ca}^{2+} > 10.5 \text{ mg/dL} )

  • Etiology: Increased bone resorption (neoplasms, hyperparathyroidism), increased intestinal absorption, decreased elimination.

  • Manifestations: Decreased neural excitability (dulling, weakness, coma), GI (constipation, nausea), Kidney (polyuria, stones), CV (hypertension, shortened QT).