Gastrointestinal Pathophysiology II Pancreas and Liver

1. Gastrointestinal Pathophysiology IIPancreas and Liver Nancy Long Sieber Ph.D. December 13, 2010

2. Brief Historical Interlude… Dr. William Beaumont with Alexis St. Martin http://sportsci.org/news/history/beaumont/Wbeaumont.jpg

3. The Pancreas

4. Pancreatic enzymes are usually released in an inactive form.

5. Cystic Fibrosis (CF) and the pancreas • Pancreatic enzyme secretion uses the same CFTR chloride channel we heard about with cholera • This channel is defective in people with CF, and causes them to have problems with the digestion of food and absorption of nutrients.

6. Regulation of Pancreatic Function • Secretin – Stimulates release of bicarbonate • Bicarb release also stimulated by smell and taste of food, distension of stomach, acid in duodenum, and gastrin. • CCK - Stimulates release of enzymes • Enzyme release also stimulated by smell and taste of food, distension of stomach, and presence of peptides and fatty acids.

7. The Liver

8. http://www.niaaa.nih.gov/Resources/GraphicsGallery/Liver/214c.htmhttp://www.niaaa.nih.gov/Resources/GraphicsGallery/Liver/214c.htm

9. The openings (fenestrations) in the capillaries mean that the hepatocytes are essentially in direct contact with the blood. http://www.siumed.edu/~dking2/erg/liver.htm

11. Bile duct and sphincter of Oddi

15. Bile Pigments When bilirubin metabolism is insufficient, then bile pigments accumulate in the tissues, giving the skin and eyes a jaundiced (yellowish) appearance. http://www.mfi.ku.dk/ppaulev/chapter23/images/23-1.jpg

16. Cirrhosis of the Liver

17. Cirrhosis occurs when scarring and fibrosis lead to the death of hepatocytes.

18. Portal hypertension can cause bleeding into the GI tract, as well as congestion of blood in the spleen, leading to destruction of platelets http://www.clevelandclinic.org/health/health-info/pictures/tipspre.gif

19. The yellow coloring of the eye in a patient with jaundice reflects the accumulation of bile pigments in the connective tissues. Skin also becomes yellowish.

20. Consequences of Liver Failure • Portal Hypertension – blood backs up into the GI tract • Blood does not pass through liver, so nutrients are not absorbed, also loss of immune surveillance • Varices • Promotes development of ascites • Congestion of blood in spleen, leads to RBC destruction

21. Consequences of Liver Failure, (cont.) • Ascites formation – watery fluid in the abdominal cavity • Infection • Generalized edema • Neurologic disorders (from accumulation of ammonia and other toxins)

22. Consequences of Liver Failure, (cont.) • Increased bleeding from • lack of liver-produced clotting factors, • lack of absorption of vitamin K, • hyperactivity of the spleen • Endocrine disorders • Lack of liver-produced hormone carriers • Inability to degrade estrogen

23. Consequences of Liver Failure, (cont.) • Manifestations of decreased bile production • Jaundice (build-up of bile pigments leading to yellowish color of eyes and skin) • Decreased fat absorption (diarrhea, steatorrhea, deficiencies of fat-soluble vitamins)

24. Consequences of Liver Failure, (cont.) • Problems with glucose metabolism – sometimes hypoglycemia (since liver is site of gluconeogenesis, sometimes hyperglycemia (since blood bypasses liver, glucose is not absorbed from it) Problems with lipid metabolism – liver is the only place where fatty acid can be converted to ketones, which provide energy during fasting.

25. Consequences of Liver Failure, (cont.) • Increased plasma levels of liver enzymes (aminotransferase and alkaline phosphatase) are indicators of liver damage • Problems with salt and water balance – due to lack of albumin and angiotensinogen.