Slow Transit Constipation (STC) Model

Huateng Bio offers validated slow transit constipation models in C57BL/6 mice. Features loperamide-induced hypomotility, mosapride responsiveness, and carmine red transit testing.

Model Name
Slow Transit Constipation (STC) Model
Animal Strains
Male C57BL/6 Mice (6-8 weeks old, 20-24g)

Model Description

Slow transit constipation (STC) is a functional gastrointestinal disorder characterized by delayed colonic motility, reduced bowel movements, and hardened stools due to excessive water absorption. Our loperamide-induced STC model replicates human pathophysiology through:

  • Opioid receptor-mediated gut hypomotility
  • Reduced fecal output (≥50% decrease vs controls)
  • Increased colonic transit time (≥2x baseline)

Clinical Relevance:
✓ Mimics refractory STC: Poor response to conventional laxatives
✓ Drug development utility: Validated with prokinetic agents (e.g., mosapride)


 

Applications

• Prokinetic drug efficacy evaluation
• Enteric nervous system (ENS) function studies
• Gut microbiome-motility interaction research
• Novel laxative mechanism exploration


 

Modeling Protocol —— 14-Day Loperamide Induction

1. Group Design:

  • Normal Group: 0.5% CMC-Na solution (oral gavage)
  • Model Group: Loperamide HCl 5 mg/kg (oral gavage)
  • Treatment Group: Loperamide + mosapride (post 3h administration)

 

2. Procedure:

  • Days 1-14: Daily dosing (9:00 AM)
  • Fecal monitoring: Collect 24h output on Days 7/14

 

3. Terminal assessment: Intestinal transit rate via carmine red dye


 

Validation & Testing

Category

Parameters

Fecal Analysis

• 24h fecal pellet count ∙ Fecal water content (%)

Intestinal Motility

Carmine red transit rate: Distance traveled (%) / Total intestinal length

Histopathology

H&E staining: Colonic mucosal thickness ∙ Goblet cell density

Molecular Analysis

qPCR: 5-HT4 receptor ∙ Aquaporin-3 expression

 


Technical Advantages

Feature

Our Model

Alternative Models

Disease Specificity

Targeted μ-opioid receptor inhibition

Non-specific obstruction models

Intervention Window

14-day reversible phase

Acute models (≤7 days)

Translational Value

Validated with mosapride (5-HT4 agonist)

Limited drug correlation

Data

Figure 1 Comparison of 24-hour feces output, fecal water content (%), and intestinal propulsion rate (%) among mice in various groups

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