Peptide inhibitor of morphine- and beta-endorphin-induced analgesia.
The synthetic beta-endorphin analogs with the omission of the NH2-terminal [Met]enkephalin segment [beta-endorphin-(6-31) and beta-endorphin-(20-31)] are shown to inhibit morphine- or beta-endorphin-induced analgesia in mice by the tail-flick test, whereas the synthetic NH2-terminal pentadecapeptide...
Сохранить в:
| Опубликовано в:: | Proc Natl Acad Sci U S A |
|---|---|
| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
National Academy of Sciences
1980
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC350094/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6254086/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.77.9.5525 |
| Метки: |
Нет меток, Требуется 1-ая метка записи!
|
