In rats with DNBS-induced visceral hypersensitivity, linaclotide produced pain relief comparable to A3AR agonists.
In plain wordsIn rats, linaclotide relieved visceral pain similarly to A3AR agonists.
- Peptide
- Linaclotide
- Outcome
- No significant changeVisceral pain relief
- Study
ratn: not reported in source
DNBS-induced visceral hypersensitivity- Comparator
- A3AR agonists MRS5980 and Cl-IB-MECA
- Outcome group
- Pain · Gastrointestinal
- Studied dose
- Dose not stated
Source sentences
Efficacy was comparable to effects induced by linaclotide.
2 context sentences(design, population, supporting numbers)
A3AR agonists significantly reduced DNBS-evoked visceral pain both in the postinflammatory (14 and 21 days after DNBS injection) and persistence (28 and 35 days after DNBS) phases.
The effects of A3AR agonists (MRS5980 and Cl-IB-MECA) were evaluated over time after DNBS injection and compared to that of the selective Cav2.2 blocker PD173212, and the clinically used drug linaclotide.