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Chapter 13<br />

Hepatic Function<br />

Bud C. Tennant<br />

Department <strong>of</strong> <strong>Clinical</strong> Sciences<br />

New York State College <strong>of</strong> Veterinary Medicine<br />

Cornell University<br />

Ithaca, New York<br />

Sharon A. Center<br />

Department <strong>of</strong> <strong>Clinical</strong> Sciences<br />

New York State College <strong>of</strong> Veterinary Medicine<br />

Cornell University<br />

Ithaca, New York<br />

I. INTRODUCTION<br />

II. FUNCTIONAL ANATOMY<br />

III. CLINICAL MANIFESTATIONS OF HEPATIC<br />

INSUFFICIENCY<br />

A. Icterus<br />

B. Hepatic Encephalopathy<br />

C. Hepatic Photosensitivity<br />

D. Ascites<br />

IV. LABORATORY ASSESSMENT OF HEPATIC<br />

FUNCTION<br />

A. Hepatic Enzymes<br />

B. Serum Bilirubin<br />

C. Serum Bile Acids<br />

D. Serum Proteins<br />

E. Dye Excretion<br />

V. OVERVIEW AND CONCLUSIONS<br />

REFERENCES<br />

advances have been made in our understanding <strong>of</strong> the<br />

pathophysiological, biochemical, and molecular mechanisms<br />

responsible for hepatic disease. Our current knowledge<br />

<strong>of</strong> veterinary hepatology is the result <strong>of</strong> the collective<br />

work <strong>of</strong> individuals from a variety <strong>of</strong> disciplines, including<br />

practicing veterinarians, biomedical scientists, and,<br />

more recently, molecular and cell biologists and molecular<br />

geneticists. No one individual had a more important or<br />

sustained impact than Dr. Cornelius, and no one was more<br />

active in maintaining a comparative perspective on the subject<br />

( Cornelius, 1993 ). In this chapter, we describe the biochemical<br />

mechanisms responsible for the cardinal clinical<br />

manifestations <strong>of</strong> hepatic insufficiency and the biochemical<br />

tests used in the clinical diagnosis <strong>of</strong> liver disease and<br />

to assess hepatic function. As in previous editions, the goal<br />

is to provide students <strong>of</strong> veterinary medicine at all stages<br />

<strong>of</strong> career development with information useful for managing<br />

the diseases <strong>of</strong> animal patients.<br />

I . INTRODUCTION<br />

The liver has an essential role in nutrient metabolism<br />

including the control and maintenance <strong>of</strong> the blood glucose<br />

level; in detoxification and excretion <strong>of</strong> hydrophobic<br />

metabolites and xenobiotics; in the synthesis <strong>of</strong> most<br />

plasma proteins; and in digestion through synthesis, biliary<br />

secretion, and conservation <strong>of</strong> bile acids that are essential<br />

both for digestion and intestinal absorption <strong>of</strong> fats and<br />

other lipids including fat soluble vitamins. The clinical<br />

manifestations <strong>of</strong> hepatic disease are directly attributable<br />

to alterations in the metabolic, excretory, synthetic, and<br />

digestive functions <strong>of</strong> the liver. The liver has great reserve,<br />

and signs <strong>of</strong> hepatic failure <strong>of</strong>ten do not develop until 70%<br />

or more <strong>of</strong> functional capacity is lost. Importantly, even<br />

when a major fraction <strong>of</strong> the hepatocellular mass has been<br />

lost following acute injury, recovery is possible because <strong>of</strong><br />

the unique regenerative capacity <strong>of</strong> the liver.<br />

Since Dr. Charles E. Cornelius wrote this chapter for earlier<br />

editions <strong>of</strong> this textbook (Cornelius, 1970), remarkable<br />

II . FUNCTIONAL ANATOMY<br />

During embryological development, the liver arises as an<br />

outgrowth <strong>of</strong> the primitive gut and is located cranial to the<br />

abdominal viscera and other abdominal organs between<br />

the splanchnic and the peripheral (systemic) circulatory<br />

systems. Unlike other mammalian organs, afferent blood to<br />

the liver is derived from two sources, the hepatic artery and<br />

the hepatic portal vein. Efferent blood leaves the liver by<br />

the hepatic vein and enters the systemic circulation via the<br />

caudal vena cava. Twenty to 30% <strong>of</strong> afferent blood comes<br />

from the hepatic artery, and the remainder from the hepatic<br />

portal vein, which drains the pancreas, spleen, stomach,<br />

small intestine, and all but the most terminal portion <strong>of</strong> the<br />

large intestine.<br />

The peripheral border <strong>of</strong> the classical liver lobule is<br />

formed by the most peripheral row <strong>of</strong> hepatocytes (the<br />

terminal plate) and by two, three, or more portal tracks<br />

(portal triads) that contain preterminal branches <strong>of</strong> the<br />

hepatic artery, the hepatic portal vein, and bile ductules.<br />

<strong>Clinical</strong> <strong>Biochemistry</strong> <strong>of</strong> <strong>Domestic</strong> <strong>Animals</strong>, 6th <strong>Edition</strong> 379<br />

Copyright © 2008, Elsevier Inc.<br />

All rights reserved.

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