NaV1.7 Channel Blocker [Ala5, Phe6, Leu26, Arg28]GpTx-1 Attenuates CFA-induced Inflammatory Hypersensitivity in Rats via Endogenous Enkephalin Mechanism-Reference-Cited by-同舟云学术

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NaV1.7 Channel Blocker [Ala5, Phe6, Leu26, Arg28]GpTx-1 Attenuates CFA-induced Inflammatory Hypersensitivity in Rats via Endogenous Enkephalin Mechanism

Published:2023-05 Issue:5 Volume:24 Page:840-859
ISSN:1526-5900
Container-title:The Journal of Pain
language:en
Short-container-title:The Journal of Pain

Author:

Xu Biao,Zhang Run,Zhang Mengna,Chen Dan,Zhang Qinqin,Zhang Nan,Shi Yonghang,Hu Xuanran,Li Ning,Fang Quan^ORCID

Publisher

Elsevier BV

Subject

Anesthesiology and Pain Medicine,Neurology (clinical),Neurology

Reference57 articles.

1. The delta opioid receptor in pain control;Abdallah;Handb Exp Pharmacol,2018

2. Lengths of the C-terminus and interconnecting loops impact stability of spider-derived gating modifier toxins;Agwa;Toxins (Basel),2017

3. Subtype-selective small molecule inhibitors reveal a fundamental role for nav1.7 in nociceptor electrogenesis, axonal conduction and presynaptic release;Alexandrou;PLoS One,2016

4. Sensory neuron-derived NaV1.7 contributes to dorsal horn neuron excitability;Alles;Sci Adv,2020

5. Met-enkephalin is preferentially transported into the peripheral processes of primary afferent fibres in both control and HSV1-driven proenkephalin A overexpressing rats;Antunes bras;Neuroscience,2001

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Spider and scorpion knottins targeting voltage-gated sodium ion channels in pain signaling;Biochemical Pharmacology;2024-09

2. Endogenous opiates and behavior: 2023;Peptides;2024-09

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