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蜂毒针刺疗法与吗啡对奥沙利铂诱导的小鼠神经性疼痛的联合作用

Combined Effects of Bee Venom Acupuncture and Morphine on Oxaliplatin-Induced Neuropathic Pain in Mice.

作者信息

Kim Woojin, Kim Min Joon, Go Donghyun, Min Byung-Il, Na Heung Sik, Kim Sun Kwang

机构信息

Department of Physiology, College of Korean Medicine, Kyung Hee University, 26 Kyungheedae-ro, Dongdamoon-gu, Seoul 02447, Korea.

Department of East-West Medicine, Graduate School, Kyung Hee University, 26 Kyungheedae-ro, Dongdamoon-gu, Seoul 02447, Korea.

出版信息

Toxins (Basel). 2016 Jan 22;8(2):33. doi: 10.3390/toxins8020033.

Abstract

Oxaliplatin, a chemotherapeutic drug for colorectal cancer, induces severe peripheral neuropathy. Bee venom acupuncture (BVA) has been used to attenuate pain, and its effect is known to be mediated by spinal noradrenergic and serotonergic receptors. Morphine is a well-known opioid used to treat different types of pain. Here, we investigated whether treatment with a combination of these two agents has an additive effect on oxaliplatin-induced neuropathic pain in mice. To assess cold and mechanical allodynia, acetone and von Frey filament tests were used, respectively. Significant allodynia signs were observed three days after an oxaliplatin injection (6 mg/kg, i.p.). BVA (0.25, 1, and 2.5 mg/kg, s.c., ST36) or morphine (0.5, 2, and 5 mg/kg, i.p.) alone showed dose-dependent anti-allodynic effects. The combination of BVA and morphine at intermediate doses showed a greater and longer effect than either BVA or morphine alone at the highest dose. Intrathecal pretreatment with the opioidergic (naloxone, 20 μg) or 5-HT3 (MDL-72222, 15 μg) receptor antagonist, but not with α2 adrenergic (idazoxan, 10 μg) receptor antagonist, blocked this additive effect. Therefore, we suggest that the combination effect of BVA and morphine is mediated by spinal opioidergic and 5-HT3 receptors and this combination has a robust and enduring analgesic action against oxaliplatin-induced neuropathic pain.

摘要

奥沙利铂是一种用于治疗结直肠癌的化疗药物,可引发严重的周围神经病变。蜂毒针刺疗法(BVA)已被用于减轻疼痛,其作用已知是由脊髓去甲肾上腺素能和5-羟色胺能受体介导的。吗啡是一种众所周知的用于治疗不同类型疼痛的阿片类药物。在此,我们研究了这两种药物联合治疗对小鼠奥沙利铂诱导的神经性疼痛是否具有相加作用。为了评估冷觉和机械性异常性疼痛,分别使用了丙酮和von Frey细丝试验。在注射奥沙利铂(6 mg/kg,腹腔注射)三天后观察到明显的异常性疼痛体征。单独使用BVA(0.25、1和2.5 mg/kg,皮下注射,足三里)或吗啡(0.5、2和5 mg/kg,腹腔注射)均显示出剂量依赖性的抗异常性疼痛作用。中等剂量的BVA和吗啡联合使用比单独使用最高剂量的BVA或吗啡显示出更大且更持久的效果。鞘内预先注射阿片类药物(纳洛酮,20 μg)或5-HT3(MDL-72222,15 μg)受体拮抗剂,但不注射α2肾上腺素能(咪唑克生,10 μg)受体拮抗剂,可阻断这种相加作用。因此,我们认为BVA和吗啡的联合作用是由脊髓阿片类药物和5-HT3受体介导的,并且这种联合对奥沙利铂诱导的神经性疼痛具有强大而持久的镇痛作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c74c/4773786/bf2dde1285a4/toxins-08-00033-g001.jpg

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