lec 2 Flashcards
defect in the intestinal A.A transport system are seen in inborn errors of metabolism
- HARTNUP DS
2. Cystinuria + slide 25
Peptide Absorption
More rapid than absorption of free A.A
• Active transport
Metabolized into free A.A in enterocyte
• Only free A.A absorbed into blood
Free Amino Acid Absorption
active transport Carrier systems • Neutral AA • Basic AA • Acidic AA • Imino acids
Absorption of Intact Proteins Newborns
– First 24 hours after birth
– Immunoglobulins
• Passive immunity
Absorption of Intact Proteins Adults
– Paracellular routes • Tight junctions between cells – Intracellular routes • Endocytosis • Pinocytosis
Enterokinase or enteropeptidase)
- Trypsinogen trypsin
* Trypsin then activates all the other enzymes
Dipeptidases
Cleave dipeptides into Aas
Aminopeptidases
Cleave at N-terminal AA
In the Enterocytes
• First cells that can use the amino acids –Transport into portal blood –Protein synthesis •Digestive enzymes • Structure and growth –Energy
Abnormalities in the protein digestion
and amino acid absorption
Defect in the pancreatic secreation.
Defective carrier system
Defect in the pancreatic secreation
Cystic fibrosis,
Cystic fibrosis,
,incomplete digestion of fat and protein,results in abnormal appearance of lipids (steatorrhea) and proteins in fece
Glycerol absorption short and medium chain fatty acids
directly absorbed from the intestinal lumen → portal vein → liver for further utilization
free cholesterol and βacyl glycerol absorption
Long chain fatty acids,
bile salts form mixed micelles.
Mixed micelles are
soluble in the aqueous environment of the intestinal lumen