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Analgesic Effect of Chinese Herbal Formula Hua-Jian-Ba-Du Ointment on Visceral Pain in Mice Induced by Acetic Acid

机译:中药配方华健巴渡膏对醋酸致小鼠内脏痛的镇痛作用

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Introduction. Visceral pain is one of the most important pains caused by cancer or other diseases, and most of the medications may lead to tolerance, addiction, and toxic side effects. Hua-Jian-Ba-Du Ointment (HJBDO), which is a commonly used conjugate based on traditional Chinese medicine theory, has been effective against visceral pain. Here, we verify the efficacy and underlying mechanism of HJBDO in an acetic-acid induced visceral pain model. Methods. Mice were subjected to acetic acid with or without HJBDO. Hua-Jian-Ba-Du Ointment at low (7.5 mL/kg center dot d), moderate (15 mL/kg center dot d), and high (30 mL/kg center dot d) dosages was applied on the abdomen, 3 times per day for 3 days. The acetic acid writhing test was used to evaluate antinociception. Interleukin-2 (IL-2) in serum, tumor necrosis factor- (TNF-), interleukin-6 (IL-6), and prostaglandin E-2 (PGE(2)) in peritoneal fluid were detected by ELISA. 5-hydroxytryptamine (5-HT), norepinephrine (NE), dopamine (DA), and -endorphin (-EP) were examined by high performance liquid chromatography and radioimmunoassay, respectively. N-methyl-D-aspartic acid receptor (NMDAR1) and c-fos expressions in both rostral ventromedial medulla (RVM) and spinal dorsal horn were determined by western blot. Results. Hua-Jian-Ba-Du Ointment at 3 dosage levels produced dose-dependent antinociception and shortened the latent time. Hua-Jian-Ba-Du Ointment at high or moderate dosage inhibited the release of TNF-, IL-6, and PGE(2), as well as increased the release of IL-2. Hua-Jian-Ba-Du Ointment could also increase NE and 5-HT contents and decrease the NE content. No effect of HJBDO at 3 dosages on the DA system was detected. Furthermore, HJBDO could suppress the expressions of NMDAR and c-fos in both RVM and spinal dorsal horn. Conclusion. Our results exhibited the analgesic effect of HJBDO on visceral pain in mice, and this effect might be mediated by the regulation of inflammation and neurotransmitters.
机译:介绍。内脏疼痛是由癌症或其他疾病引起的最重要的疼痛之一,大多数药物可能导致耐受性,成瘾性和毒性副作用。华健巴杜软膏(HJBDO)是一种基于传统中药理论的常用结合物,对内脏痛有效。在这里,我们验证了HJBDO在乙酸诱发的内脏痛模型中的功效和潜在机制。方法。在有或没有HJBDO的情况下使小鼠经受乙酸。在腹部上以低剂量(7.5 mL / kg中心点d),中度(15 mL / kg中心点d)和高剂量(30 mL / kg中心点d)施用华健霸都软膏3每天3次。乙酸扭体试验用于评估抗伤害感受。 ELISA检测血清中的白细胞介素2(IL-2),腹膜液中的肿瘤坏死因子-(TNF-),白细胞介素6(IL-6)和前列腺素E-2(PGE(2))。通过高效液相色谱和放射免疫分析法分别检测了5-羟色胺(5-HT),去甲肾上腺素(NE),多巴胺(DA)和-内啡肽(-EP)。通过蛋白质印迹法测定了鼻侧腹膜延髓(RVM)和脊髓背角中的N-甲基-D-天冬氨酸受体(NMDAR1)和c-fos表达。结果。 3种剂量的华健巴杜软膏产生剂量依赖性抗伤害感受,并缩短了潜伏期。高剂量或中等剂量的华健巴杜软膏可抑制TNF-,IL-6和PGE(2)的释放,并增加IL-2的释放。华健霸都软膏还可以增加NE和5-HT含量并降低NE含量。未检测到3种剂量的HJBDO对DA系统的影响。此外,HJBDO可以抑制RVM和脊髓背角中NMDAR和c-fos的表达。结论。我们的研究结果显示了HJBDO对小鼠内脏痛的镇痛作用,并且这种作用可能是由炎症和神经递质的调节介导的。

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