44: Renal Function and Anesthesia

CHAPTER 44 Renal Function and Anesthesia




1 Describe the anatomy of the kidney


The kidneys are paired organs lying retroperitoneally against the posterior abdominal wall. Although their combined weight is only 300 g (about 0.5% of total body weight), they receive 20% to 25% of the total cardiac output. The renal arteries are branches of the aorta, originating below the superior mesenteric artery. The renal veins drain into the inferior vena cava. Nerve supply is abundant; sympathetic constrictor fibers are distributed via celiac and renal plexuses. There is no sympathetic dilator or parasympathetic innervation. Pain fibers, mainly from the renal pelvis and upper ureter, enter the spinal cord via splanchnic nerves.


On cross section of the kidney, three zones are apparent: cortex, outer medulla, and inner medulla (Figure 44-1). Eighty percent of renal blood flow is distributed to cortical structures. Each kidney contains about 1 million nephrons. Nephrons are classified as superficial (about 85%) or juxtamedullary, depending on location and length of the tubules. The origin of all nephrons is within the cortex.



The glomerulus and capsule are known collectively as the renal corpuscle. Each Bowman’s capsule is connected to a proximal tubule that is convoluted within its cortical extent but becomes straight limbed within the outer cortex; at this point the tubule is known as the loop of Henle. The loop of Henle of superficial nephrons descends only to the intermedullary junction, where it makes a hairpin turn, becomes thick limbed, and ascends back into the cortex, where it approaches and touches the glomerulus with a group of cells known as the juxtaglomerular apparatus. The superficial nephrons form distal convoluted tubules that merge to form collecting tubules within the cortex. The renal corpuscles of juxtamedullary nephrons are located at juxtamedullary cortical tissue. They have long loops of Henle that descend deep into the medullary tissue; the loops also reascend into cortical tissue, where they form distal convoluted tubules and collecting tubules. These nephrons (15% of the total) are responsible for conservation of water.


About 5000 tubules join to form collecting ducts. Ducts merge at minor calyces, which in turn merge to form major calyces. The major calyces join and form the renal pelvis, the most cephalic aspect of the ureter.





4 Review the site of action and significant effects of commonly used diuretics


See Table 44-1.


TABLE 44-1 Diuretics*



























Drug (Example) Site of Action Action and Side Effects
Carbonic anhydrase inhibitors (acetazolamide) Proximal convoluted tubule Inhibits sodium resorption; interferes with H excretion; hyperchloremic, hypokalemic acidosis
Thiazides (hydrochlorothiazide) Cortical diluting segment (between ascending limb and aldosterone-responsive DCT) Inhibits sodium resorption; accelerates sodium-potassium exchange (hypokalemia); decreases GFR in volume-contracted states
Potassium-sparing diuretics (spironolactone, triamterene) Competitive inhibition of aldosterone in DCT Inhibiting aldosterone prevents sodium resorption and sodium-potassium exchange
Loop diuretics (furosemide, bumetanide, ethacrynic acid) Inhibit Cl resorption at thick ascending loop of Henle Potent diuretic; acts on critical urine-concentrating process; renal vasodilator; hypokalemia; can produce hypovolemia
Osmotic diuretics (mannitol, urea) Filtered at glomerulus but not resorbed; creates osmotic gradient in tubules; excretion of water and some sodium Hyperosmolality reduces cellular water; limited ability to excrete sodium; renal vasodilator

DCT, Distal convoluted tubule; GFR, glomerular filtration rate.


* With the exception of osmotic diuretics, all diuretics interfere with sodium conservation.



5 Describe the unique aspects of renal blood flow and control


Renal blood flow (RBF) of about 1200 ml/min is well maintained (autoregulated) at blood pressures of 80 to 180 mm Hg. The cortex requires about 80% of blood flow to achieve its excretory and regulatory functions, and the outer medulla receives 15%. The inner medulla receives a small percent of blood flow; a higher flow would wash out solutes responsible for the high tonicity (1200 mOsm/kg) of the inner medulla. Without this hypertonicity, urinary concentration would not be possible.


Control of RBF is through extrinsic and intrinsic neural and hormonal influences; a principal goal of blood flow regulation is to maintain GFR. The euvolemic, nonstressed state has little baseline sympathetic tone. Under mild-to-moderate stress RBF decreases slightly; but efferent arterioles constrict, maintaining GFR. During periods of severe stress (e.g., hemorrhage, hypoxia, major surgical procedures) both RBF and GFR decrease secondary to sympathetic stimulation.


The renin-angiotensin-aldosterone axis also has an effect on RBF. A proteolytic enzyme formed at the macula densa of the juxtaglomerular apparatus, renin acts on angiotensinogen within the circulation to produce angiotensin I. Enzymes within lung and plasma convert angiotensin I to angiotensin II, which is a potent renal vasoconstricting agent (especially of the efferent arteriole) and a factor in the release of aldosterone. During periods of stress levels of angiotensin are elevated and contribute (along with sympathetic stimulation and catecholamines) to decreased RBF.


Prostaglandins (PGs) are also found within the kidney. PGE2 and PGE3 are intrinsic mediators of blood flow, producing vasodilation.


May 31, 2016 | Posted by in ANESTHESIA | Comments Off on 44: Renal Function and Anesthesia

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