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BPC-157 Crohn's Disease Research Mechanism: Study Comparison

World J Gastroenterol (2017) TNBS-induced colitis (rats) 10 μg/kg IP Histological damage score 58% reduction in inflammation VEGF upregulation, mucosal healing Strong evidence for tissue repair without immunosuppression. Dose-response curve established J Physi

This comparison does not assign a generated winner or score.

  • World J Gastroenterol (2017)
  • TNBS-induced colitis (rats)
  • 10 μg/kg IP
  • Histological damage score
  • 58% reduction in inflammation
  • VEGF upregulation, mucosal healing
  • Strong evidence for tissue repair without immunosuppression. Dose-response curve established
  • J Physiol Pharmacol (2020)
  • DSS chronic colitis (mice)
  • Fecal calprotectin, crypt architecture
  • 40% lower calprotectin, improved histology
  • Tight junction protein expression, reduced permeability
  • Chronic model more relevant to human Crohn's. Results sustained over 21 days
  • Eur J Pharmacol (2018)
  • TNBS colitis (rats)
  • 10 μg/kg IP + oral
  • Microvessel density, ulcer size
  • 47% higher capillary density, 63% ulcer reduction
  • VEGFR2 activation, angiogenesis
  • Dual administration route tested. Oral showed partial efficacy, IP superior
  • Dig Dis Sci (2016)
  • Acetic acid colitis (rats)
  • 10 μg/kg gastric
  • Macroscopic damage score
  • 54% reduction in lesion area
  • Nitric oxide modulation, reduced oxidative stress
  • Early-stage evidence. Acetic acid model less clinically relevant than TNBS/DSS
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