Guest guest Posted March 20, 2005 Report Share Posted March 20, 2005 " Misty L. Trepke " <mistytrepke Sun, 20 Mar 2005 15:18:10 -0000 Subject:[s-A] The Liver & Anatomy/Physiology of Digestion http://www..com The Role of the Liver in Normal Digestion Article 6/21/2004 Through the process of digestion, carbohydrates, fats, and proteins are reduced into substances that can be used by the body for energy, physiologic regulation and tissue maintenance. This article reviews those processes, with special attention paid to the role of the liver in the digestive cycle. Normal Carbohydrate Digestion Carbohydrates are molecules that are fundamentally composed of simple sugars. Carbohydrate metabolism begins in the mouth, where enzymes in saliva begin breaking down complex carbohydrates into disaccharides (2- sugar molecules) and trisaccharides (3-sugar molecules). Stomach acids inactivate these enzymes, but carbohydrate processing resumes in the small intestine through the action of enzymes secreted by the pancreas and intestinal mucosa. Eventually, digestive enzymes convert all digestible carbohydrates into simple sugars: glucose, galactose, fructose, and maltose. These simple sugars are absorbed through the intestinal wall, and are transported to the liver by the portal vein. Galactose, fructose and maltose are converted to glucose by the liver. The liver uses some glucose immediately to power its many metabolic processes. The liver also buffers and regulates the fluctuating absorption of glucose (and other sugars) from the intestinal mucosa, keeping the level of serum glucose (blood sugar) within range of 90 to 150 mg/dL. When surplus glucose is available in serum, the pancreas is stimulated to release insulin. Insulin is a hormone that decreases the level of glucose in the blood by increasing the uptake of glucose by the cells of the body, and causing the liver to convert glucose to glycogen. Glycogen is then stored in the liver and skeletal muscle. When the quantity of glycogen stored in the liver exceeds roughly 5% of the liver's weight, the liver converts surplus glucose to triglyceride, a lipid (fatty) substance that binds with proteins in the blood to form lipoprotein. Although small quantities of lipids are stored in the liver, most of the lipoproteins are circulated in the blood and then stored in fatty tissues of the body. When serum glucose levels decline below 80 mg/dL, the pancreas is stimulated to release glucagon. This hormone causes the liver to break down stored glycogen into glucose, increasing levels of blood glucose and ensuring a relatively steady level of serum glucose for the body's metabolic needs. If glycogen reserves become depleted and serum glucose levels decrease to roughly 70 mg/dL, the liver can synthesize glucose from smaller carbon fragments. Normal Protein Metabolism Proteins form components of many body structures, such as muscle and connective tissue. Proteins also are components of hemoglobin, enzymes, hormones, neurotransmitters and antibodies. Proteins contribute to the regulation and distribution of fluid in the body, and act as " carrier " molecules for other substances, assisting in the transportation of these substances throughout the body. Proteins can be used to generate energy, but not as easily as carbohydrates or fats. In total, there are roughly 100,000 different types of proteins in the body. Proteins are tightly coiled molecules composed of amino acids held together by peptide bonds, and must be reduced to amino acids by the digestive process before they can be used by the body. The digestion of protein begins when powerful acids in the stomach denature (uncoil) proteins, allowing digestive enzymes to break the protein's peptide bonds. Digestion continues in the small intestine, where enzymes reduce protein into amino acids. Eventually, amino acids are transported through the intestinal wall and are carried to the liver in the blood by the portal vein. Once amino acids reach the liver, they can be: Reassembled to form new proteins Converted into other, nonessential amino acids Converted to glucose for energy Converted to fat for energy storage Released into circulation for use by other cells. Normal Fat Metabolism Fats belong to a class of substances known as lipids. Fats differ from carbohydrates and proteins in that they are not water-soluble. Although there are various types of fats, fundamentally they are all composed of one to three fatty acid chains attached to a " backbone " molecule of glycerol. Monoglycerides are composed of a single fatty acid and a glycerol molecule Diglycerides are composed of two fatty acids and a glycerol molecule Triglycerides are composed of three fatty acids and a glycerol molecule. Triglycerides, in the form of dairy products, meats, oils, butter, and margarine, are the most common type of dietary fat and represent a major source of energy. Fats have a number of important roles in the body. Fats are the most concentrated form of stored energy, containing 9 calories per gram. In contrast, proteins and carbohydrates yield 4 calories per gram each. Fats carry linoleic acid, which is essential to the maintenance of cellular membranes and normal growth. Fats provide a medium for the fat-soluble vitamins A, D, E and K, and fat-based components of cell membranes regulate the movement of substances into and out of cells. Fat provides a layer of insulation to maintain body temperature and also provides a cushion layer for the kidneys, heart and pancreas. As you may have noticed, many Americans have more insulation than they need. While not technically a fat, cholesterol is a fat-like substance that is critical to a number of physical processes, including the maintenance of cell membranes, the production of the sex hormones testosterone and estrogen, and steroid hormones. Steroid hormones influence the formation of glucose, control serum electrolytes (sodium and potassium), and promote wound healing. Interestingly, there is no dietary requirement for cholesterol. The liver is capable of building as much cholesterol as the body needs from other fatty acids. Fat digestion begins in the mouth as salivary enzymes begin to break apart fats into fatty acids. The process continues in the stomach, but most of the digestion of fat occurs in the small intestine. Once in the small intestine, fats are exposed to bile, which emulsifies the fat. Bile is produced in the liver, stored and concentrated in the gallbladder, and released into the small intestine in response to eating. Bile emulsification increases fat's exposure to other digestive enzymes, facilitating the reduction of fat into fatty acids of varying lengths. The other products of fat digestion in the small intestine are glycerol, phospholipids, monoglycerides and cholesterol. Long-chain fatty acids, monoglycerides, phospholipids and cholesterol are absorbed by the lining of the small intestine and combined to form chylomicrons, which are water-soluble molecules. Chylomicrons are absorbed by the lymphatic system and then routed to the blood, where they circulate to adipose (fat) tissue, liver and muscle cells. During circulation, chylomicrons are broken apart into monoglycerides and fatty acids, which are absorbed by muscle and fat tissues. The residual cholesterol circulates and is eventually taken up by the liver. Short and medium length fatty acids are absorbed by the intestinal lining and combined with a protein to form lipoprotein, and are then transported to the liver by the portal vein. Glycerol is water-soluble, and so is absorbed directly into the blood from the intestine and is transported to the liver. Once fatty acids, glycerol and cholesterol arrive at the liver, they can be processed in several different ways. They can be stored in the liver in the form of fat droplets They can be used to produce cholesterol and other fat-like substances, which are secreted back into blood and delivered to other cells in the body Triglycerides can be assembled from fatty acids and glycerol, and used as an energy source. Summary The liver is central to the process of digestion, the regulation of physical processes and appropriate utilization of nutrients. Clinical symptoms can develop as liver disease decreases the organs functional ability. Source Brown E. The Science of Human Nutrition. Harcort Brace Jovanovich, New York, 1990. McCance K, Huether S. Pathophysiology: The Biologic Basis for Diseases in Adults and Children, 2nd ed. Mosby, St. Louis, 1994. Jacob S, Francone C. Structure and Function in Man, 3rd ed. W. B. Saunders, Philadelphia, 1974. Martini F. Fundamentals of Anatomy and Physiology, 2nd ed. Prentice Hall, New Jersey, 1992. Quote Link to comment Share on other sites More sharing options...
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