Skip to Main Content

We have a new app!

Take the Access library with you wherever you go—easy access to books, videos, images, podcasts, personalized features, and more.

Download the Access App here: iOS and Android. Learn more here!

INTRODUCTION

The functional integrity of the mammalian kidney is vital to total body homeostasis because the kidney plays a principal role in the excretion of metabolic wastes and in the regulation of extracellular fluid volume, electrolyte composition, and acid–base balance. In addition, the kidney synthesizes and releases hormones such as renin and erythropoietin and metabolizes vitamin D3 to the active 1,25-dihydroxy vitamin D3 form. A toxic insult to the kidney therefore could disrupt any or all of these functions and could have profound effects on total body metabolism. Fortunately, the kidneys are equipped with a variety of detoxification mechanisms and have considerable functional reserve and regenerative capacities. Nonetheless, the nature and severity of the toxic insult may be such that these detoxification and compensatory mechanisms are overwhelmed, and kidney injury ensues. The outcome of renal failure can be profound; permanent renal damage may result, requiring chronic dialysis treatment or kidney transplantation.

FUNCTIONAL ANATOMY

Gross examination of a sagittal section of the kidney reveals three clearly demarcated anatomic areas: the cortex, medulla, and papilla (Figs. 14-1 and 14-2). The cortex constitutes the major portion of the kidney and receives a disproportionately higher percentage (90%) of blood flow compared to the medulla (about 6% to 10%) or papilla (1% to 2%). Thus, when a blood-borne toxicant is delivered to the kidney, a high percentage of the material will be delivered to the cortex and will have a greater opportunity to influence cortical rather than medullary or papillary functions. However, medullary and papillary tissues are exposed to higher luminal concentrations of toxicants for prolonged periods of time, a consequence of the more concentrated tubular fluid and the more sluggish flow of blood and filtrate in these regions.

Figure 14-1.

Schematic of the human kidney showing the major blood vessels and the microcirculation and tubular components of each nephron. (From Guyton and Hall [1996, p. 318], with permission from Elsevier.)

Figure 14-2.

Schematic of short- and long-looped nephrons and the collecting system. A medullary ray is delineated by a dashed line within the cortex. (1) Renal corpuscle including Bowman's capsule and the glomerulus; (2) proximal convoluted tubule; (3) proximal straight tubule; (4) descending thin limb; (5) thin ascending limb; (6) thick ascending limb; (7) macula densa, located within the final portion of the thick ascending limb; (8) distal convoluted tubule; (9) connecting tubule; (9*) connecting tubule of the juxtamedullary nephron, which forms an arcade; (10) cortical collecting duct; (11) outer medullary collecting duct; (12) inner medullary collecting duct. (From Kriz [1988], with permission.)

The functional unit of the kidney, the nephron, may be considered in three portions: the vascular element, the glomerulus, and the tubular element.

Pop-up div Successfully Displayed

This div only appears when the trigger link is hovered over. Otherwise it is hidden from view.