Biliary Tract Obstruction
Summary: Bile Salts
- Synthesis: Bile salts are steroid molecules synthesized by hepatocytes.
- Primary Bile Salts:
- Cholic acid and chenodeoxycholic acid are the primary bile salts in humans.
- These account for approximately 80% of the bile salts produced.
- Conjugation:
- Primary bile salts are conjugated with either taurine or glycine.
- Secondary Bile Salts:
- In the intestine, primary bile salts can undergo bacterial alteration to form secondary bile salts:
- Deoxycholate
- Lithocholate
- In the intestine, primary bile salts can undergo bacterial alteration to form secondary bile salts:
- Function:
- The primary purpose of bile salts is to solubilize lipids and facilitate their absorption in the intestine.
Summary: Bile Acid Synthesis
- Origin: Bile acids are synthesized from cholesterol.
- Pathways:
- Classic Pathway:
- Leads to the formation of cholic acid.
- This is the predominant pathway of bile acid synthesis in humans.
- Alternative Pathway:
- Results in the synthesis of chenodeoxycholic acid.
- Classic Pathway:
- Bile Acid Pool:
- 60% to 70% of the bile acid pool consists of cholic acid and its metabolite deoxycholic acid.
- Chenodeoxycholic acid is less commonly found in human bile compared to cholic acid.
(Source: Blumgart, 6th edition, page 124)



MCQ: Lesions Commonly Associated with Type I Biliary Tract Obstruction
Question: Which of the following lesions is not commonly associated with Type I biliary tract obstruction?
Options: a) Choledocholithiasis
b) Carcinoma of gallbladder
c) Cholangiocarcinoma
d) Common bile duct ligation
Answer: a) Choledocholithiasis
Explanation:
- Type I Biliary Tract Obstruction is typically caused by conditions leading to complete obstruction of the bile duct. Common lesions include:
- Carcinoma of the gallbladder (Option B)
- Cholangiocarcinoma (Option C)
- Common bile duct ligation (Option D)
- Choledocholithiasis (Option A), which refers to the presence of stones in the common bile duct, is more commonly associated with Type II: Intermittent Obstruction, rather than complete obstruction.
Correct Answer: A) Choledocholithiasis

MCQ: Pathophysiological Alterations in Obstructive Jaundice
Question: Which of the following is not a pathophysiological alteration associated with obstructive jaundice?
Options: a) Decrease synthesis of albumin and clotting factors
b) Decrease capacity to excrete drugs through bile
c) Increase Kupffer function clearance
d) Decrease renal function
Answer: c) Increase Kupffer function clearance
Explanation:
- Option A (Decrease synthesis of albumin and clotting factors): Obstructive jaundice leads to a decrease in the synthetic function of hepatocytes, including the production of albumin and clotting factors.
- Option B (Decrease capacity to excrete drugs through bile): In obstructive jaundice, there is a reduced capacity to excrete drugs that are normally secreted into bile, such as antibiotics.
- Option C (Increase Kupffer function clearance): This statement is not true. Obstructive jaundice actually decreases the function of Kupffer cells, reducing their ability to clear bacteria and endotoxins, and impairing immune function.
- Option D (Decrease renal function): Renal function can be compromised in obstructive jaundice due to factors like hypovolemia, bile salt effects, and endotoxemia.
Correct Answer: C) Increase Kupffer function clearance
Immune System Changes in Obstructive Jaundice
- Impaired T-cell proliferation
- Decreased neutrophil chemotaxis
- Defective bacterial phagocytosis
- Suppressed natural killer-cell activity
- Reduced T-lymphocyte proliferation
- Decreased adhesion molecule expression
- Altered monocyte functions
These changes weaken immune defense, increasing susceptibility to infections.
(Source: Blumgart, 6th edition, page 129)