Bee Venom Acupuncture Attenuates Oxaliplatin-Induced Neuropathic Pain by Modulating Action Potential Threshold in A-Fiber Dorsal Root Ganglia Neurons

被引:20
|
作者
Lee, Ji Hwan [1 ,2 ]
Gang, Juan [3 ]
Yang, Eunhee [4 ]
Kim, Woojin [1 ,2 ,3 ]
Jin, Young-Ho [4 ]
机构
[1] Kyung Hee Univ, Coll Korean Med, Dept Physiol, Seoul 02453, South Korea
[2] Kyung Hee Univ, Grad Sch, Dept Sci Korean Med, Seoul 02453, South Korea
[3] Kyung Hee Univ, Grad Sch, Dept East West Med, Seoul 02453, South Korea
[4] Kyung Hee Univ, Coll Med, Dept Physiol, Seoul 02453, South Korea
基金
新加坡国家研究基金会;
关键词
action potential; allodynia; bee venom acupuncture; oxaliplatin; voltage-gated sodium channel; SODIUM-CHANNELS; PERIPHERAL NEUROPATHY; ANTICANCER DRUG; NEUROTOXICITY; MECHANISMS; PREVENTION; MANAGEMENT; CISPLATIN; MODEL; NA+;
D O I
10.3390/toxins12120737
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Oxaliplatin is a third-generation platinum-based chemotherapeutic drug widely used in colorectal cancer treatment. Although potent against this tumor, it can induce cold and mechanical allodynia even after a single injection. The currently used drugs to attenuate this allodynia can also cause unwanted effects, which limit their use. Bee venom acupuncture (BVA) is widely used in Korean medicine to treat pain. Although the effect of BVA on oxaliplatin-induced neuropathic pain has been addressed in many studies, its action on dorsal root ganglia (DRG) neurons has never been investigated. A single oxaliplatin injection (6 mg/kg, intraperitoneally) induced cold and mechanical allodynia, and BVA (0.1 and 1 mg/kg, subcutaneous, ST36) dose-dependently decreased allodynia in rats. On acutely dissociated lumbar 4-6 DRG neurons, 10 min application of oxaliplatin (100 mu M) shifted the voltage-dependence of sodium conductance toward negative membrane potentials in A- but not C-fibers. The resting membrane potential remained unchanged, but the action potential threshold decreased significantly compared to that of the control (p < 0.05). However, 0.1 mu g/mL of BVA administration increased the lowered action potential threshold. In conclusion, these results suggest that BVA may attenuate oxaliplatin-induced neuropathic pain by altering the action potential threshold in A-fiber DRG neurons.
引用
收藏
页数:13
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