Analgesic effects of mambalgin peptide inhibitors of acid-sensing ion channels in inflammatory and neuropathic pain
Autor: | Alain Eschalier, Sylvie Diochot, Abdelkrim Alloui, Mélodie Dauvois, Youssef Aissouni, Anne Baron, Eric Lingueglia, Valérie Friend, Précillia Rodrigues |
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Přispěvatelé: | Institut de pharmacologie moléculaire et cellulaire (IPMC), Centre National de la Recherche Scientifique (CNRS)-Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Université Côte d'Azur (UCA), Pharmacologie fondamentale et clinique de la douleur, Neuro-Dol (Neuro-Dol), Université d'Auvergne - Clermont-Ferrand I (UdA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université d'Auvergne - Clermont-Ferrand I (UdA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université d'Auvergne - Clermont-Ferrand I (UdA)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre de génétique moléculaire (CGM), Centre National de la Recherche Scientifique (CNRS), BARON, Anne, Université Nice Sophia Antipolis (1965 - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA) |
Jazyk: | angličtina |
Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Male [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology Analgesic Inflammation Pharmacology 03 medical and health sciences Route of administration Mice Xenopus laevis 0302 clinical medicine medicine Animals Ion channel Acid-sensing ion channel Elapid Venoms Mice Knockout Analgesics business.industry [SDV.NEU.NB] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology medicine.disease 3. Good health Mambalgins Rats Mice Inbred C57BL 030104 developmental biology Anesthesiology and Pain Medicine Treatment Outcome Neurology Acid Sensing Ion Channel Blockers [SDV.SP.PHARMA] Life Sciences [q-bio]/Pharmaceutical sciences/Pharmacology Neuropathic pain Neuralgia [SDV.SP.PHARMA]Life Sciences [q-bio]/Pharmaceutical sciences/Pharmacology Female Neurology (clinical) medicine.symptom business Peptides 030217 neurology & neurosurgery |
Zdroj: | PAIN PAIN, Elsevier, 2016, 157 (3), pp.552-559. ⟨10.1097/j.pain.0000000000000397⟩ PAIN, 2016, 157 (3), pp.552-559. ⟨10.1097/j.pain.0000000000000397⟩ Pain Pain, 2016, 157 (3), pp.552-559. ⟨10.1097/j.pain.0000000000000397⟩ |
ISSN: | 0304-3959 1872-6623 |
DOI: | 10.1097/j.pain.0000000000000397⟩ |
Popis: | International audience; Mambalgins are 57-amino acid peptides isolated from snake venom that evoke naloxone-resistant analgesia after local (intraplantar) and central (intrathecal) injections through inhibition of particular subtypes of acid-sensing ion channels (ASICs). We now show that mambalgins also have an opioid-independent effect on both thermal and mechanical inflammatory pain after systemic intravenous (i.v.) administration and are effective against neuropathic pain. By combining the use of knockdown and knockout animals, we show the critical involvement of peripheral ASIC1b-containing channels, along with a contribution of ASIC1a-containing channels, in the i.v. effects of these peptides against inflammatory pain. The potent analgesic effect on neuropathic pain involves 2 different mechanisms depending on the route of administration, a naloxone-insensitive and ASIC1a-independent effect associated with i.v. injection and an ASIC1a-dependent and partially naloxone-sensitive effect associated with intrathecal injection. These data further support the role of peripheral and central ASIC1-containing channels in pain, demonstrate their participation in neuropathic pain, and highlight differences in the repertoire of channels involved in different pain conditions. They also strengthen the therapeutic potential of mambalgin peptides that are active in a broader range of experimental pain models and through i.v. systemic delivery. |
Databáze: | OpenAIRE |
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