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Clinical Chemistry In Medicine Essay Research Paper

Clinical Chemistry In Medicine Essay, Research Paper


Of the diagnostic methods available to veterinarians, the clinical


chemistry test has developed into a valuable aid for localizing pathologic


conditions. This test is actually a collection of specially selected individual


tests. With just a small amount of whole blood or serum, many body


systems can be analyzed. Some of the more common screenings give


information about the function of the kidneys, liver, and pancreas and


about muscle and bone disease. There are many blood chemistry tests


available to doctors. This paper covers the some of the more common


tests.


Blood urea nitrogen (BUN) is an end-product of protein metabolism. Like


most of the other molecules in the body, amino acids are constantly


renewed. In the course of this turnover, they may undergo deamination,


the removal of the amino group. Deamination, which takes place


principally in the liver, results in the formation of ammonia. In the liver,


the ammonia is quickly converted to urea, which is relatively nontoxic,


and is then released into the bloodstream. In the blood, it is readily


removed through the kidneys and excreted in the urine. Any disease or


condition that reduces glomerular filtration or increases protein


catabolism results in elevated BUN levels.


Creatinine is another indicator of kidney function. Creatinine is a waste


product derived from creatine. It is freely filtered by the glomerulus and


blood levels are useful for estimating glomerular filtration rate. Muscle


tissue contains phosphocreatinine which is converted to creatinine by a


nonenzymatic process. This spontaneous degradation occurs at a rather


consistent rate (Merck, 1991).


Causes of increases of both BUN and creatinine can be divided into three


major categories: prerenal, renal, and postrenal. Prerenal causes include


heart disease, hypoadrenocorticism and shock. Postrenal causes include


urethral obstruction or lacerations of the ureter, bladder, or urethra. True


renal disease from glomerular, tubular, or interstitial dysfunction raises


BUN and creatinine levels when over 70% of the nephrons become


nonfunctional (Sodikoff, 1995).


Glucose is a primary energy source for living organisms. The glucose


level in blood is normally controlled to within narrow limits. Inadequate


or excessive amounts of glucose or the inability to metabolize glucose


can affect nearly every system in the body. Low blood glucose levels


(hypoglycemia) may be caused by pancreatic tumors (over-production of


insulin), starvation, hypoadrenocorticism, hypopituitarism, and severe


exertion. Elevated blood glucose levels (hyperglycemia) can occur in


diabetes mellitus, hyperthyroidism, hyperadrenocorticism,


hyperpituitarism, anoxia (because of the instability of liver glycogen in


oxygen deficiency), certain physiologic conditions (exposure to cold,


digestion) and pancreatic necrosis (because the pancreas produces insulin


which controls blood glucose levels).


Diabetes mellitus is caused by a deficiency in the secretion


or action of insulin. During periods of low blood glucose, glucagon


stimulates the breakdown of liver glycogen and inhibits glucose


breakdown by glycolysis in the liver and stimulates glucose synthesis by


gluconeogenesis. This increases blood glucose. When glucose enters the


bloodstream from the intestine after a carbohydrate-rich meal, the


resulting increase in blood glucose causes increased insulin secretion and


decreased glucagon secretion. Insulin stimulates glucose uptake by


muscle tissue where glucose is converted to glucose-6-phosphate. Insulin


also activates glycogen synthase so that much of the


glucose-6-phosphate is converted to glycogen. It also stimulates the


storage of excess fuels as fat (Lehninger, 1993).


With insufficient insulin, glucose is not used by the tissues and


accumulates in the blood. The accumulated glucose then spills into the


urine. Additional amounts of water are retained in urine because of the


accumulation of glucose and polyuria (excessive urination) results. In


order to prevent dehydration, more water than normal is consumed


(polydipsia). In the absence of insulin, fatty acids released form adipose


tissue are converted to ketone bodies (acetoacetic acid, B-hydroxybutyric


acid, and acetone). Although ketone bodies can be used a energy


sources, insulin deficiency impairs the ability of tissues to use ketone


bodies, which accumulate in the blood. Because they are acids, ketones


may exhaust the ability of the body to maintain normal pH. Ketones are


excreted by the kidneys, drawing water with them into the urine. Ketones


are also negatively charged and draw positively charged ions (sodium,


potassium, calcium) with them into urine. Some other results of diabetes


mellitus are cataracts (because of abnormal glucose metabolism in the


lens which results in the accumulation of water), abnormal neutrophil


function (resulting in greater susceptibility to infection), and an enlarged


liver (due to fat accumulation) (Fraser, 1991).


Bilirubin is a bile pigment derived from the breakdown of heme by the


reticuloendothelial system. The reticuloendothelial system filters out and


destroys spent red blood cells yielding a free iron molecule and


ultimately, bilirubin. Bilirubin binds to serum albumin, which restricts it


from urinary excretion, and is transported to the liver. In the liver,


bilirubin is changed into bilirubin diglucuronide, which is sufficiently


water soluble to be secreted with other components of bile into the small


intestine. Impaired liver function or blocked bile secretion causes


bilirubin to leak into the blood, resulting in a yellowing of the skin and


eyeballs (jaundice). Determination of bilirubin concentration in the blood


is useful in diagnosing liver disease (Lehninger, 1993). Increased


bilirubin can also be caused by hemolysis, bile duct obstruction, fever,


and starvation (Bistner, 1995).


Two important serum lipids are cholesterol and triglycerides. Cholesterol


is a precursor to bile salts and steroid hormones. The principle bile salts,


taurocholic acid and glycocholic acid, are important in the digestion of


food and the solubilization of ingested fats. The desmolase reaction


converts cholesterol, in mitochondria, to pregnenolone which is


transported to the endoplasmic reticulum and converted to progesterone.


This is the precursor to all other steroid hormones (Garrett, 1995).


Triglycerides are the main form in which lipids are stored and are the


predominant type of dietary lipid. They are stored in specialized cells


called adipocytes (fat cells) under the skin, in the abdominal cavity, and


in the mammary glands. As stored fuels, triglycerides have an advantage


over polysaccharides because they are unhydrated and lack the extra


water weight of polysaccharides. Also, because the carbon atoms are


more reduced than those of sugars, oxidation of triglycerides yields more


than twice as much energy, gram for gram, as that of carbohydrates


(Lehninger, 1993).


Hyperlipidemia refers to an abnormally high concentration of triglyceride


and/or cholesterol in the blood. Primary hyperlipidemia is an inherited


disorder of lipid metabolism. Secondary hyperlipidemias are usually


associated with pancreatitis, diabetes mellitus, hypothyroidism, protein


losing glomerulonephropathies, glucocorticosteroid administration, and a


variety of liver abnormalities. Hypolipidemia is almost always a result of


malnutrition (Barrie, 1995).


Alkaline phosphatase is present in high concentration in bone and liver.


Bone remodeling (disease or repair) results in moderate elevations of


serum alkaline phosphatase levels, and cholestasis (stagnation of bile


flow) and bile duct obstruction result in dramatically increased serum


alkaline phosphatase levels. The obstruction is usually intrahepatic,


associated with swelling of hepatocytes and bile stasis. Elevated serum


alkaline phosphatase and bilirubin levels suggest bile duct obstruction.


Elevated serum alkaline phosphatase and normal bilirubin levels suggest


hepatic congestion or swelling. Elevations also occur in rapidly growing


young animals and in conditions causing bone formation (Bistner, 1995).


Aspartate aminotransferase (AST) is an enzyme normally found in the


mitochondria of liver, heart, and skeletal muscle cells. In the event of


heart or liver damage, AST leaks into the blood stream and


concentrations become elevated (Bistner, 1995). AST, along with alkaline


phosphatase, are used to differentiate between liver and muscle damage


in birds.


Alanine aminotransferase (ALT) is considered a liver-specific enzyme,


although small amounts are present in the heart. ALT is generally located


in the cytosol. Liver disease results in the releasing of the enzyme into


the serum. Measurements of this enzyme are used in the diagnosis of


certain types of liver diseases such as viral hepatitis and hepatic necrosis,


and heart diseases. The ALT level remains elevated for more than a week


after hepatic injury (Sodikoff, 1995).


Fibrinogen, albumin, and globulins constitute the major proteins of the


blood plasma. Fibrinogen, which makes up about 0.3 percent of the total


protein volume, is a soluble protein involved in the clotting process. The


formation of blood clots is the result of a series of zymogen activations.


Factors released by injured tissues or abnormal surfaces caused by injury


initiate the clotting process. To create the clot, thrombin removes


negatively charged peptides from fibrinogen, converting it to fibrin. The


fibrin monomer has a different surface charge distribution than


fibrinogen. These monomers readily aggregates into ordered fibrous


arrays. Platelets and plasma globulins release a fibrin-stabilizing factor


which creates cross-links in the fibrin net to stabilize the clot. The clot


binds the wound until new tissue can be built (Garrett, 1995).


The alpha-, beta-, and gamma-globulins compose the globulins.


Alpha-globulins transport lipids, hormones, and vitamins. Also included


is a glycoprotein, ceruloplasmin, which carries copper and


haptoglobulins

, which bind hemoglobin. Iron transport is related to


beta-globulins. The glycoprotein that binds the iron is transferrin


(Lehninger, 1993). Gamma-globulins (immunoglobulins) are associated


with antibody formation. There are five different classes of


immunoglobulins. IgG is the major circulating antibody. It gives immune


protection within the body and is small enough to cross the placenta,


giving newborns temporary protection against infection. IgM also gives


protection within the body but is too large to cross the placenta. IgA is


normally found in mucous membranes, saliva, and milk. It provides


external protection. IgD is thought to function during the development


and maturation of the immune response. IgE makes of the smallest


fraction of the immunoglobulins. It is responsible for allergic and


hypersensitivity reactions.


Altered levels of alpha- and beta- globulins are rare, but immunoglobulin


levels change in various conditions. Serum immunoglobulin levels can


increase with viral or bacterial infection, parasitism, lymphosarcoma, and


liver disease. Levels are decreased in immunodeficiency.


Albumin is a serum protein that affects osmotic pressure, binds many


drugs, and transports fatty acids. Albumin is produced in the liver and is


the most prevalent serum protein, making up 40 to 60 percent of the


total protein. Serum albumin levels are decreased (hypoalbuminemia) by


starvation, parasitism, chronic liver disease, and acute glomerulonephritis


(Sodikoff, 1995). Albumin is a weak acid and hypoalbuminemia will tend


to cause nonrespiratory alkalosis (de Morais, 1995). Serum albumin


levels are often elevated in shock or severe dehydration.


Creatine Kinase (CK) is an enzyme that is most abundant in skeletal


muscle, heart muscle, and nervous tissue. CK splits creatine phosphate in


the presence of adenosine diphosphate (ADP) to yield creatine and


adenosine triphosphate (ATP). During periods of active muscular


contraction and glycolysis, this reaction proceeds predominantly in the


direction of ATP synthesis. During recovery from exertion, CK is used to


resynthesize creatine phosphate from creatine at the expense of ATP.


After a heart attack, CK is the first enzyme to appear in the blood


(Lehninger, 1993). CK values become elevated from muscle damage


(from trauma), infarction, muscular dystrophies, or inflammation.


Elevated CK values can also be seen following intramuscular injections of


irritating substances. Muscle diseases may be associated with direct


damage to muscle fibers or neurogenic diseases that result in secondary


damage to muscle fibers. Greatly increased CK values are usually


associated with heart muscle disease because of the large number of


mitochondria in heart muscle cells (Bistner, 1995).


When active muscle tissue cannot be supplied with sufficient oxygen, it


becomes anaerobic and produces pyruvate from glucose by glycolysis.


Lactate dehydrogenase (LDH) catalyzes the regeneration of NAD+ from


NADH so glycolysis can continue. The lactate produced is released into


the blood. Heart tissue is aerobic and uses lactate as a fuel, converting it


to pyruvate via LDH and using the pyruvate to fuel the citric acid cycle to


obtain energy (Lehninger, 1993). Because of the ubiquitous origins of


LDH, the total serum level is not reliable for diagnosis; but in normal


serum, there are five isoenzymes of LDH which give more specific


information. These isoenzymes can help differentiate between increases


in LDH due to liver, muscle, kidney, or heart damage or hemolysis


(Bistner, 1995).


Calcium is involved in many processes of the body, including


neuromuscular excitability, muscle contraction, enzyme activity, hormone


release, and blood coagulation. Calcium is also an important ion in that it


affects the permeability of the nerve cell membrane to sodium. Without


sufficient calcium, muscle spasms can occur due to erratic, spontaneous


nervous impulses.


The majority of the calcium in the body is found in bone as phosphate


and carbonate. In blood, calcium is available in two forms. The


nondiffusible form is bound to protein (mainly albumin) and makes up


about 45 percent of the measurable calcium. This bound form is inactive.


The ionized forms of calcium are biologically active. If the circulating


level falls, the bones are used as a source of calcium.


Primary control of blood calcium is dependent on parathyroid hormone,


calcitonin, and the presence of vitamin D. Parathyroid hormone


maintains blood calcium level by increasing its absorption in the


intestines from food and reducing its excretion by the kidneys.


Parathyroid hormone also stimulates the release of calcium into the


blood stream from the bones. Hyperparathyroidism, caused by tumors of


the parathyroid, causes the bones to lose too much calcium and become


soft and fragile. Calcitonin produces a hypocalcemic effect by inhibiting


the effect of parathyroid hormone and preventing calcium from leaving


bones. Vitamin D stimulates calcium and phosphate absorption in the


small intestine and increases calcium and phosphate utilization from


bone. Hypercalcemia may be caused by abnormal calcium/phosphorus


ratio, hyperparathyroidism, hypervitaminosis D, and hyperproteinemia.


Hypocalcemia may be caused by hypoproteinemia, renal failure, or


pancreatitis (Bistner, 1995).


Because approximately 98 percent of the total body potassium is found at


the intracellular level, potassium is the major intracellular cation. This


cation is filtered by the glomeruli in the kidneys and nearly completely


reabsorbed by the proximal tubules. It is then excreted by the distal


tubules. There is no renal threshold for potassium and it continues to be


excreted in the urine even in low potassium states. Therefore, the body


has no mechanism to prevent excessive loss of potassium


(Schmidt-Nielsen, 1995).


Potassium plays a critical role in maintaining the normal cellular and


muscular function. Any imbalance of the body’s potassium level,


increased or decreased, may result in neuromuscular dysfunction,


especially in the heart muscle. Serious, and sometimes fatal, arrythmias


may develop. A low serum potassium level, hypokalemia, occurs with


major fluid loss in gastrointestinal disorders (i.e., vomiting, diarrhea),


renal disease, diuretic therapy, diabetes mellitus, or mineralocorticoid


dysfunction (i.e., Cushing’s disease). An increased serum potassium


level, hyperkalemia, occurs most often in urinary obstruction, anuria, or


acute renal disease (Bistner, 1995).


Sodium and its related anions (i.e., chloride and bicarbonate) are


primarily responsible for the osmotic attraction and retention of water in


the extracellular fluid compartments. The endothelial membrane is freely


permeable to these small electrolytes. Sodium is the most abundant


extracellular cation, however, very little is present intracellularly. The


main functions of sodium in the body include maintenance of membrane


potentials and initiation of action potentials in excitable membranes. The


sodium concentration also largely determines the extracellular osmolarity


and volume. The differential concentration of sodium is the principal


force for the movement of water across cellular membranes. In addition,


sodium is involved in the absorption of glucose and some amino acids


from the gastrointestinal tract (Lehninger, 1993). Sodium is ingested


with food and water, and is lost from the body in urine, feces, and sweat.


Most sodium secreted into the GI tract is reabsorbed. The excretion of


sodium is regulated by the renin-angiotensin-aldosterone system


(Schmidt-Nielsen, 1995).


Decreased serum sodium levels, hyponatremia, can be seen in adrenal


insufficiency, inadequate sodium intake, renal insufficiency, vomiting or


diarrhea, and uncontrolled diabetes mellitus. Hypernatremia may occur in


dehydration, water deficit, hyperadrenocorticism, and central nervous


system trauma or disease (Bistner, 1995).


Chloride is the major extracellular anion. Chloride and bicarbonate ions


are important in the maintenance of acid-base balance. When chloride in


the form of hydrochloric acid or ammonium chloride is lost, alkalosis


follows; when chloride is retained or ingested, acidosis follows. Elevated


serum chloride levels, hyperchloremia, can be seen in renal disease,


dehydration, overtreatment with saline solution, and carbon dioxide


deficit (as occurs from hyperventilation). Decreased serum chloride


levels, hypochloremia, can be seen in diarrhea and vomiting, renal


disease, overtreatment with certain diuretics, diabetic acidosis,


hypoventilation (as occurs in pneumonia or emphysema), and adrenal


insufficiency (de Morais, 1995).


As seen above, one to two milliliters of blood can give a clinician a great


insight to the way an animals’ systems are functioning. With many more


tests available and being developed every day, diagnosis becomes less


invasive to the patient. The more information that is made available to


the doctor allows a faster diagnosis and recovery for the patient.


7b9


Barrie, Joan and Timothy D. G. Watson. ?Hyperlipidemia.?


Current Veterinary Therapy XII. Ed. John Bonagura.


Philadelphia: W. B. Saunders, 1995.


Bistner, Stephen l. Kirk and Bistner?s Handbook of Veterinary


Procedures and Emergency Treatment. Philadelphia: W. B.


Saunders, 1995.


de Morais, HSA and William W. Muir. ?Strong Ions and Acid-Base


Disorders.? Current Veterinary Therapy XII. Ed. John


Bonagura. Philadelphia: W. B. Saunders, 1995.


Fraser, Clarence M., ed. The Merck Veterinary Manual, Seventh


Edition. Rahway, N. J.: Merck & Co., 1991.


Garrett, Reginald H. and Charles Grisham. Biochemistry. Fort


Worth: Saunders College Publishing, 1995.


Lehninger, Albert, David Nelson and Michael Cox. Principles of


Biochemistry. New York: Worth Publishers, 1993.


Schmidt-Nielsen, Knut. Animal Physiology: Adaptation and


environment. New York: Cambridge University Press, 1995.


Sodikoff, Charles. Labratory Profiles of Small Animal Diseases.


Santa Barbara: American Veterinary Publications, 1995.

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