Calcium channel modulation as a target in chronic pain control

R Patel, C Montagut‐Bordas… - British Journal of …, 2018 - Wiley Online Library
Neuropathic pain remains poorly treated for large numbers of patients, and little progress
has been made in developing novel classes of analgesics. To redress this issue, ziconotide …

Targeting voltage‐gated calcium channels: developments in peptide and small‐molecule inhibitors for the treatment of neuropathic pain

S Vink, PF Alewood - British journal of pharmacology, 2012 - Wiley Online Library
Chronic pain affects approximately 20% of people worldwide and places a large economic
and social burden on society. Despite the availability of a range of analgesics, this condition …

The physiology, pathology, and pharmacology of voltage-gated calcium channels and their future therapeutic potential

GW Zamponi, J Striessnig, A Koschak… - Pharmacological …, 2015 - ASPET
Voltage-gated calcium channels are required for many key functions in the body. In this
review, the different subtypes of voltage-gated calcium channels are described and their …

T‐type voltage‐gated calcium channels as targets for the development of novel pain therapies

SM Todorovic… - British journal of …, 2011 - Wiley Online Library
It is well recognized that voltage‐gated calcium (Ca2+) channels modulate the function of
peripheral and central pain pathways by influencing fast synaptic transmission and neuronal …

[HTML][HTML] Recent advances in targeting ion channels to treat chronic pain

EB Stevens, GJ Stephens - British journal of pharmacology, 2018 - ncbi.nlm.nih.gov
Pain represents a complex heterogeneous sensory experience, almost uniquely influenced
by emotional condition and experience. This broad description alludes to the fact that pain is …

Ziconotide: neuronal calcium channel blocker for treating severe chronic pain

GP Miljanich - Current medicinal chemistry, 2004 - ingentaconnect.com
Ziconotide (PRIALT®) is a neuroactive peptide in the final stages of clinical development as
a novel non-opioid treatment for severe chronic pain. It is the synthetic equivalent of ω …

Recent updates of N-type calcium channel blockers with therapeutic potential for neuropathic pain and stroke

T Yamamoto, A Takahara - Current topics in medicinal …, 2009 - ingentaconnect.com
The voltage-dependent N-type calcium channel (Cav2. 2), which is distributed in the nerve
endings of the central and peripheral nerves, is known to be strongly associated with the …

Analgesic effects of a substituted N-triazole oxindole (TROX-1), a state-dependent, voltage-gated calcium channel 2 blocker

C Abbadie, OB McManus, SY Sun, RM Bugianesi… - … of Pharmacology and …, 2010 - ASPET
Voltage-gated calcium channel (Cav) 2.2 (N-type calcium channels) are key components in
nociceptive transmission pathways. Ziconotide, a state-independent peptide inhibitor of …

Ziconotide-a novel neuron-specific calcium channel blocker for the intrathecal treatment of severe chronic pain-a short review.

U Klotz - International Journal of Clinical Pharmacology & …, 2006 - search.ebscohost.com
Worldwide a large number of patients suffer from severe chronic pain even after treatment
with opioids following the 3-step analgesic ladder developed by the WHO. Intraspinal …

[HTML][HTML] Targeting voltage-gated calcium channels for neuropathic pain management

D Perret, ZD Luo - Neurotherapeutics, 2009 - Elsevier
Voltage-gated calcium channels (VGCC) play obligatory roles in diverse physiological
functions. Pathological conditions leading to changes in their biophysical properties and …