The role of voltage-gated sodium channels in pain signaling

DL Bennett, AJ Clark, J Huang… - Physiological …, 2019 - journals.physiology.org
Acute pain signaling has a key protective role and is highly evolutionarily conserved.
Chronic pain, however, is maladaptive, occurring as a consequence of injury and disease …

Methods used to evaluate pain behaviors in rodents

JR Deuis, LS Dvorakova, I Vetter - Frontiers in molecular …, 2017 - frontiersin.org
Rodents are commonly used to study the pathophysiological mechanisms of pain as studies
in humans may be difficult to perform and ethically limited. As pain cannot be directly …

Etiology and pharmacology of neuropathic pain

SRA Alles, PA Smith, LL Isom - Pharmacological reviews, 2018 - Elsevier
Injury to or disease of the nervous system can invoke chronic and sometimes intractable
neuropathic pain. Many parallel, interdependent, and time-dependent processes, including …

[HTML][HTML] Peptide therapeutics from venom: Current status and potential

MW Pennington, A Czerwinski, RS Norton - Bioorganic & medicinal …, 2018 - Elsevier
Peptides are recognized as being highly selective, potent and relatively safe as potential
therapeutics. Peptides isolated from the venom of different animals satisfy most of these …

Structural basis for the modulation of voltage-gated sodium channels by animal toxins

H Shen, Z Li, Y Jiang, X Pan, J Wu… - Science, 2018 - science.org
INTRODUCTION Almost all venoms contain toxins that modulate the activity of voltage-gated
sodium (Nav) channels in order to incapacitate prey or predators. The single-chain …

Antibodies and venom peptides: new modalities for ion channels

H Wulff, P Christophersen, P Colussi… - Nature Reviews Drug …, 2019 - nature.com
Ion channels play fundamental roles in both excitable and non-excitable tissues and
therefore constitute attractive drug targets for myriad neurological, cardiovascular and …

Peripheral voltage-gated cation channels in neuropathic pain and their potential as therapeutic targets

SRA Alles, PA Smith - Frontiers in Pain Research, 2021 - frontiersin.org
The persistence of increased excitability and spontaneous activity in injured peripheral
neurons is imperative for the development and persistence of many forms of neuropathic …

A central mechanism of analgesia in mice and humans lacking the sodium channel NaV1. 7

DI MacDonald, S Sikandar, J Weiss, M Pyrski, AP Luiz… - Neuron, 2021 - cell.com
Deletion of SCN9A encoding the voltage-gated sodium channel Na V 1.7 in humans leads
to profound pain insensitivity and anosmia. Conditional deletion of Na V 1.7 in sensory …

Ion channels as therapeutic antibody targets

CJ Hutchings, P Colussi, TG Clark - MAbs, 2019 - Taylor & Francis
It is now well established that antibodies have numerous potential benefits when developed
as therapeutics. Here, we evaluate the technical challenges of raising antibodies to …

Fifteen years of NaV1.7 channels as an analgesic target: Why has excellent in vitro pharmacology not translated into in vivo analgesic efficacy?

DA Eagles, CY Chow, GF King - British journal of pharmacology, 2022 - Wiley Online Library
In 2006, humans with a congenital insensitivity to pain (CIP) were found to lack functional
NaV1. 7 channels. In the subsequent 15 years there was a rush to develop selective …