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Bile acid thesis

Bile acids are synthesized from cholesterol in the liver and released into the digestive tract where they function to emulsify dietary fats and facilitate lipid absorption in the small intestine. The synthesis of bile acids in the liver is regulated by a negative feedback mechanism from the bile acids reabsorbed from the intestine. The concentration of 7aC4 in serum is a surrogate for the amount of bile acid synthesis in the liver. There is some diurnal variation in 7aC4 serum concentrations, so measurement should be performed on a fasting morning sample. Patients with increased bile acid in their stool suffer from chronic diarrhea termed bile acid diarrhea BAD.
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Bile salts: structure, function, synthesis, and enterohepatic circulation

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Bile acid - Wikipedia

Bile salts and bile acids are polar cholesterol derivatives, and represent the major route for the elimination of the steroid from the body. They are molecules with similar but not identical structures, and diverse physical and biological characteristics. They are synthesized in the liver, stored in the gallbladder, secreted into the duodenum, and finally, for the most part, reabsorbed in the ileum. Because at physiological pH these molecules are present as anions, the terms bile acid and bile salts are used herein as synonyms.
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Bile acid synthesis

How are bile acid synthesis disorders diagnosed? To find out if a patient has Bile Acid Synthesis Disorder, the doctor will probably begin by taking a medical history and doing a physical exam. In addition, he or she may do :.
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Bile acids are a group of amphipathic steroids synthesized by hepatocytes from cholesterol and excreted into bile. They function to emulsify fat in intestine and facilitate nutrient absorption and are highly conserved via enterohepatic circulation as outlined below. This emulsification is possible because of their amphipathic nature and tendency to form micelles. The excretion of bile acids into the biliary canaliculi sets up an osmotic gradient, which draws water into bile and drives bile salt-dependent bile flow. In dogs, the IBAT protein is primarily expressed in the ileum, cecum and colon.

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