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A large part of protein digestion occurs in the stomach ( [link] ). The stomach is a saclike organ that secretes gastric digestive juices.
Protein digestion is carried out by an enzyme called pepsin in the stomach chamber. The highly acidic environment kills many microorganisms in the food and, combined with the action of the enzyme pepsin, results in the catabolism of protein in the food. Chemical digestion is facilitated by the churning action of the stomach caused by contraction and relaxation of smooth muscles. The partially digested food and gastric juice mixture is called chyme . Gastric emptying occurs within two to six hours after a meal. Only a small amount of chyme is released into the small intestine at a time. The movement of chyme from the stomach into the small intestine is regulated by hormones, stomach distension and muscular reflexes that influence the pyloric sphincter. The low pH of the stomach will denature the amylase and lipase that were secreted in the mouth. Therefore, over time, chemical digestion of starches and fats will decrease in the stomach.
The stomach lining is unaffected by pepsin and the acidity because pepsin is released in an inactive form (pepsinogen) that is activated by the low pH. The stomach also has a thick mucus lining that protects the underlying tissue.
Chyme moves from the stomach to the small intestine. The small intestine is the organ where the digestion of protein, fats, and carbohydrates is completed. The small intestine is a long tube-like organ with a highly folded surface containing finger-like projections called the villi. The top surface of each villus has many microscopic projections called microvilli. The epithelial cells at the surface of these structures absorb nutrients from the digested food and release them to the bloodstream on the other side. Methods of transport previously discussed (e.g.active transport)are used during this movement. The villi and microvilli, with their many folds, increase the surface area of the small intestine and increase absorption efficiency of the nutrients.
The human small intestine is over 6 m (19.6 ft) long and is divided into three parts: the duodenum, the jejunum and the ileum. The duodenum is separated from the stomach by the pyloric sphincter. The chyme is mixed with pancreatic juices, an alkaline/basic solution rich in bicarbonate that neutralizes the acidity of chyme from the stomach. This result raises the pH and creates an environment that is appropriate for enzymes. Pancreatic juices contain several digestive enzymes (amylase, trypsin, and lipase) that break down starches, proteins, and fats, respectively. Bile is produced in the liver and stored and concentrated in the gallbladder; it enters the duodenum through the bile duct. Bile contains bile salts, which make lipids accessible to the water-soluble enzymes. This is accomplished via a process called emulsification, a type of physical digestion. Bile keeps fat droplets from coming back together again, thus increasing the surface area available to lipase. The wall of the small intestines secrete disaccharidases, which faciltate digestion of disaccharides (e.g. maltose, sucrose, and lactose) into their respective monosaccharides. The monosaccharides, amino acids, bile salts, vitamins, and other nutrients are absorbed by the cells of the intestinal lining.
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