The action potential (AP) conduction in nerve fibers plays a crucial role in transmitting nociceptive information from the periphery to the cerebral cortex. Nerve AP conduction inhibition possibly results in analgesia. It is well-known that many analgesics suppress nerve AP conduction and voltage-dependent sodium and potassium channels that are involved in producing APs. The compound action potential (CAP) recorded from a bundle of nerve fibers is a guide for knowing if analgesics affect nerve AP conduction. This entry mentions the inhibitory effects of clinically used analgesics, analgesic adjuvants, and plant-derived analgesics on fast-conducting CAPs and voltage-dependent sodium and potassium channels. The efficacies of their effects wer...
The mechanism of acetaminophen (APAP) analgesia is at least partially unknown. Previously, we showed...
International audienceOral amitriptyline hydrochloride (amitriptyline) is ineffective against some f...
Transient receptor potential subfamily V, member 1 (TRPV1) channels are important integrators of nox...
Antiepileptics used for treating neuropathic pain have various actions including voltage-gated Na+ a...
Copyright © 2014 Yuhei Uemura et al. This is an open access article distributed under the Creative C...
Chinese herbal medicines may be sources of pain relief that many are using as alternative therapies....
AbstractBecause local anesthetics are known to inhibit both sodium and potassium channels, and anest...
Chronic pain is very difficult to treat. Thus, novel analgesics are a critical area of research. Str...
Previous studies have demonstrated that QX-314, an intracellular sodium channel blocker, can enter i...
International audienceMenthol is a natural compound of plant origin known to produce cool sensation ...
While genetic evidence shows that the Nav1.7 voltage-gated sodium ion channel is a key regulator of ...
It is apparent that the ‘pain pathway’ is not a static, hard-wired component of the nervous system, ...
Local anaesthetic agents suppress action potentials in excitable tissues by blocking voltage-gated N...
The mechanism of acetaminophen (APAP) analgesia is at least partially unknown. Previously, we showed...
International audienceOral amitriptyline hydrochloride (amitriptyline) is ineffective against some f...
Transient receptor potential subfamily V, member 1 (TRPV1) channels are important integrators of nox...
Antiepileptics used for treating neuropathic pain have various actions including voltage-gated Na+ a...
Copyright © 2014 Yuhei Uemura et al. This is an open access article distributed under the Creative C...
Chinese herbal medicines may be sources of pain relief that many are using as alternative therapies....
AbstractBecause local anesthetics are known to inhibit both sodium and potassium channels, and anest...
Chronic pain is very difficult to treat. Thus, novel analgesics are a critical area of research. Str...
Previous studies have demonstrated that QX-314, an intracellular sodium channel blocker, can enter i...
International audienceMenthol is a natural compound of plant origin known to produce cool sensation ...
While genetic evidence shows that the Nav1.7 voltage-gated sodium ion channel is a key regulator of ...
It is apparent that the ‘pain pathway’ is not a static, hard-wired component of the nervous system, ...
Local anaesthetic agents suppress action potentials in excitable tissues by blocking voltage-gated N...
The mechanism of acetaminophen (APAP) analgesia is at least partially unknown. Previously, we showed...
International audienceOral amitriptyline hydrochloride (amitriptyline) is ineffective against some f...
Transient receptor potential subfamily V, member 1 (TRPV1) channels are important integrators of nox...