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- Title
The efficacy of combination treatment of gabapentin and electro-acupuncture on paclitaxel-induced neuropathic pain.
- Authors
Min Joon Kim; Ji Hwan Lee; Jo Ung Jang; Fu Shi Quan; Sun Kwang Kim; Woojin Kim
- Abstract
Paclitaxel, a chemotherapeutic drug, induces severe peripheral neuropathy. Gabapentin (GBT) is a first line agent used to treat neuropathic pain, and its effect is mediated by spinal noradrenergic and muscarinic cholinergic receptors. Electro- acupuncture (EA) is used for treating various types of pain via its action through spinal opioidergic and noradrenergic receptors. Here, we investigated whether combined treatment of these two agents could exert a synergistic effect on paclitaxelinduced cold and mechanical allodynia, which were assessed by the acetone drop test and von Frey filament assay, respectively. Significant signs of allodynia were observed after four paclitaxel injections (a cumulative dose of 8 mg/kg, i.p.). GBT (3, 30, and 100 mg/kg, i.p.) or EA (ST36, Zusanli) alone produced dose-dependent anti-allodynic effects. The medium and highest doses of GBT (30 and 100 mg/kg) provided a strong analgesic effect, but they induced motor dysfunction in Rota-rod tests. On the contrary, the lowest dose of GBT (3 mg/kg) did not induce motor weakness, but it provided a brief analgesic effect. The combination of the lowest dose of GBT and EA resulted in a greater and longer effect, without inducing motor dysfunction. This effect on mechanical allodynia was blocked by spinal opioidergic (naloxone, 20 mg), or noradrenergic (idazoxan, 10 mg) receptor antagonist, whereas on cold allodynia, only opioidergic receptor antagonist blocked the effect. In conclusion, the combination of the lowest dose of GBT and EA has a robust and enduring analgesic action against paclitaxel-induced neuropathic pain, and it should be considered as an alternative treatment method.
- Subjects
GABAPENTIN; PACLITAXEL; TREATMENT of peripheral neuropathy; ALLODYNIA; ANALGESICS; THERAPEUTICS
- Publication
Korean Journal of Physiology & Pharmacology, 2017, Vol 21, Issue 6, p657
- ISSN
1226-4512
- Publication type
Article
- DOI
10.4196/kjpp.2017.21.6.657