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Effect of Bee Venom Acupuncture on Oxaliplatin-Induced Cold Allodynia in Rats
Author(s) -
Byeong-Hak Lim,
Hak Jin Moon,
Dong Xing Li,
Munsoo Gil,
Joon Ki Min,
Giseog Lee,
Hyunsu Bae,
Sun Kwang Kim,
Byung-Il Min
Publication year - 2013
Publication title -
evidence-based complementary and alternative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.552
H-Index - 90
eISSN - 1741-4288
pISSN - 1741-427X
DOI - 10.1155/2013/369324
Subject(s) - allodynia , medicine , antagonist , oxaliplatin , pharmacology , (+) naloxone , anesthesia , idazoxan , zusanli , neuropathic pain , phentolamine , acupuncture , hyperalgesia , nociception , propranolol , receptor , electroacupuncture , prazosin , colorectal cancer , alternative medicine , cancer , pathology
Oxaliplatin, a chemotherapy drug, often leads to neuropathic cold allodynia after a single administration. Bee venom acupuncture (BVA) has been used in Korea to relieve various pain symptoms and is shown to have a potent antiallodynic effect in nerve-injured rats. We examined whether BVA relieves oxaliplatin-induced cold allodynia and which endogenous analgesic system is implicated. The cold allodynia induced by an oxaliplatin injection (6 mg/kg, i.p.) was evaluated by immersing the rat's tail into cold water (4°C) and measuring the withdrawal latency. BVA (1.0 mg/kg, s.c.) at Yaoyangguan (GV3), Quchi (LI11), or Zusanli (ST36) acupoints significantly reduced cold allodynia with the longest effect being shown in the GV3 group. Conversely, a high dose of BVA (2.5 mg/kg) at GV3 did not show a significant antiallodynic effect. Phentolamine ( α -adrenergic antagonist, 2 mg/kg, i.p.) partially blocked the relieving effect of BVA on allodynia, whereas naloxone (opioid antagonist, 2 mg/kg, i.p.) did not. We further confirmed that an intrathecal administration of idazoxan ( α 2 -adrenergic antagonist, 50  μ g) blocked the BVA-induced anti-allodynic effect. These results indicate that BVA alleviates oxaliplatin-induced cold allodynia in rats, at least partly, through activation of the noradrenergic system. Thus, BVA might be a potential therapeutic option in oxaliplatin-induced neuropathy.

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