In animal tests, dermorphin had greater antinociceptive potency than its N-terminal tetrapeptide metabolite.
In plain wordsIn animal tests, dermorphin reduced pain responses more potently than its N-terminal tetrapeptide metabolite.
- Peptide
- Dermorphin
- Outcome
- IncreaseAntinociceptive potency
- Study
n: not reported in source
- Comparator
- N-terminal tetrapeptide
- Outcome group
- Pain · Nervous system and cognition
- Studied dose
- Dose not stated · intracerebroventricularAs given in this study.
Measurements
- Relative potency of tetrapeptide
- 84 times less potent
- than parent heptapeptide
Source sentences
Moreover, the N-terminal tetrapeptide was 84 times less potent than its parent heptapeptide when administered intracerebroventricularly.
1 context sentence(design, population, supporting numbers)
In addition, the potency of dermorphin was compared with that of one of its metabolites, N-terminal tetrapeptide (Tyr-D-Ala-Phe-Gly), by using the tail pressure test.