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Journal of Experimental Pharmacology Volume 7, 2015 - Issue
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Original Research

Antihyperalgesic effects of ProTx-II, a Nav1.7 antagonist, and A803467, a Nav1.8 antagonist, in diabetic mice

Ken-ichiro Tanaka1 Department of Pathophysiology and Therapeutics, School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan;2 Department of Endocrinology and Metabolism, Graduate School of Medicine, Yokohama City University, Yokohama, Japan
,
Shota Sekino1 Department of Pathophysiology and Therapeutics, School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
,
Megumi Ikegami1 Department of Pathophysiology and Therapeutics, School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
,
Hiroko Ikeda1 Department of Pathophysiology and Therapeutics, School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan
&
Junzo Kamei1 Department of Pathophysiology and Therapeutics, School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, JapanCorrespondence[email protected]
Pages 11-16 | Published online: 24 Jun 2015

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Jessica A. I. Muller, Lai Y. Chan, Monica C. Toffoli-Kadri, Marcia R. Mortari, David J. Craik & Johannes Koehbach. (2023) Antinociceptive peptides from venomous arthropods. Toxin Reviews 42:1, pages 362-381.
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Articles from other publishers (6)

David A. Eagles, Chun Yuen Chow & Glenn F. King. (2020) Fifteen years of Na V 1.7 channels as an analgesic target: Why has excellent in vitro pharmacology not translated into in vivo analgesic efficacy? . British Journal of Pharmacology 179:14, pages 3592-3611.
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Yashad Dongol, Phil M. Choi, David T. Wilson, Norelle L. Daly, Fernanda C. Cardoso & Richard J. Lewis. (2021) Voltage-Gated Sodium Channel Modulation by a New Spider Toxin Ssp1a Isolated From an Australian Theraphosid. Frontiers in Pharmacology 12.
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H. Hu, S. E. Mawlawi, T. Zhao, J. R. Deuis, S. Jami, I. Vetter, R. J. Lewis & F. C. Cardoso. (2021) Engineering of a Spider Peptide via Conserved Structure-Function Traits Optimizes Sodium Channel Inhibition In Vitro and Anti-Nociception In Vivo. Frontiers in Molecular Biosciences 8.
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Fernanda C. Cardoso & Richard J. Lewis. (2019) Structure–Function and Therapeutic Potential of Spider Venom-Derived Cysteine Knot Peptides Targeting Sodium Channels. Frontiers in Pharmacology 10.
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Xiao-Long Zhang, Xian-Ying Cao, Ren-Chun Lai, Man-Xiu Xie & Wei-An Zeng. (2019) Puerarin Relieves Paclitaxel-Induced Neuropathic Pain: The Role of Nav1.8 β1 Subunit of Sensory Neurons. Frontiers in Pharmacology 9.
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Tânia C. Gonçalves, Evelyne Benoit, Michel Partiseti & Denis Servent. (2018) The NaV1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons. Frontiers in Pharmacology 9.
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