Extracellular fluid and its proteins : dehydration, shock, and recovery

• Published in: Pediatric nephrology (Berlin, West) West), 1999-11, Vol.13 (9), p.989-995
• Main Author: HOLLIDAY, M. A
• Format: Article
• Language: English
• Subjects: Adults; Biological and medical sciences; Blood Proteins - metabolism; Burns; Collagen; Connective tissue; Dehydration - drug therapy; Dehydration - metabolism; Extracellular Space - metabolism; Glomerulonephritis; Humans; Hypovolemia - drug therapy; Hypovolemia - metabolism; Kidney - physiopathology; Lymph - metabolism; Medical sciences; Metabolism; Nephrology. Urinary tract diseases; Nephropathies. Renovascular diseases. Renal failure; Permeability; Plasma; Proteins; Serum Albumin - deficiency; Serum Albumin - therapeutic use; Shock - drug therapy; Shock - metabolism; Skin; Space life sciences; Traumas. Diseases due to physical agents
• ISSN: 0931-041X; 1432-198X
• DOI: 10.1007/s004670050741

This review highlights characteristics of extracellular fluid (ECF) that are often overlooked. ECF has, in addition to plasma and interstitial fluid (ISF) surrounding cells, a third large compartment, the ISF of skin and connective tissue. This acts as a reservoir that gives up ECF to plasma volume (PV) in order to sustain circulation in the event of either shock or dehydration. While Starling forces drive filtration, ECF is returned to PV more by lymph and less by Starling forces than previously appreciated. Lymph return to PV is dependent on physical activity and muscle contraction to overcome gravity. Regional change in metabolic rate alters the need for oxygen and nutrients that is met by a regional increase in capillary blood flow. Blood flow is controlled by vasoactive compounds released in response to a drop in PO(2); these relax capillary smooth muscle to increase blood flow and delivery of oxygen and nutrients. Plasma proteins, including albumin, are filtered into the interstitium through larger pores than those filtering ECF. The rate of protein filtration is set by size and charge of these larger endothelial pores and by size and charge of proteins. Charge of these pores, hence albumin permeability, is regulated by many of the same vasoactive compounds that control capillary flow. As a consequence, in response to gravitational stress and other forms of shock that reduce effective circulation, albumin as well as ECF is rapidly shifted from plasma and sequestered in ISF. When this has occurred, as in burn shock, restoration is better effected by generous expansion of ECF with Ringer's solution alone, rather than with Ringer's solution supplemented with human serum albumin or other colloid. Restoring both PV and ISF volume restores lymph circulation and returns sequestered albumin to PV.