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Spider Venom Peptide Pn3a Inhibition of Primary Afferent High Voltage-Activated Calcium Channels
Despite potently inhibiting the nociceptive voltage-gated sodium (Na(v)) channel, Na(v)1.7, µ-theraphotoxin Pn3a is antinociceptive only upon co-administration with sub-therapeutic opioid agonists, or by itself at doses >3,000-fold greater than its Na(v)1.7 IC (50) by a yet undefined mechanism. N...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Front Pharmacol |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Frontiers Media S.A.
2021
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7875911/ https://ncbi.nlm.nih.gov/pubmed/33584315 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2020.633679 |
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