Question:medium

Receptor for absorption of glucose in intestine when a person is given ORS is:

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ORS efficacy depends on sodium-glucose co-transport at the apical surface of small intestinal enterocytes.
Updated On: Jun 23, 2026
  • SGLT-1
  • SGLT-2
  • GLP-1
  • GLUT-1
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The Correct Option is A

Solution and Explanation

ORS and intestinal glucose transport:

The scientific basis of ORS is the glucose-sodium co-transport system in the gut, discovered in the 1960s. Even during active secretory diarrhea, the absorptive mechanism of the enterocyte remains intact.

Glucose transporters comparison:
  • SGLT-1: Apical membrane of small intestinal enterocytes; co-transports 1 glucose + 2 Na+ (secondary active); the key transporter for ORS absorption -- CORRECT
  • SGLT-2: Kidney proximal tubule (S1 segment); reabsorbs ~90% of filtered glucose; target of gliflozin drugs; NOT in intestine
  • GLUT-2: Basolateral membrane of enterocytes; exports glucose from enterocyte into blood (facilitative, not sodium-linked)
  • GLP-1: An incretin hormone from intestinal L-cells -- not a transporter at all
  • GLUT-1: RBCs, blood-brain barrier -- not relevant to intestinal ORS absorption

The sodium gradient driving SGLT-1 is maintained by the basolateral $Na^+/K^+$-ATPase, making this an example of secondary active transport.
\[\boxed{\text{SGLT-1}}\]
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