首页> 外文期刊>Anesthesia and Analgesia: Journal of the International Anesthesia Research Society >The effects of electroacupuncture at the ST36 (Zusanli) acupoint on cancer pain and transient receptor potential vanilloid subfamily 1 expression in walker 256 tumor-bearing rats
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The effects of electroacupuncture at the ST36 (Zusanli) acupoint on cancer pain and transient receptor potential vanilloid subfamily 1 expression in walker 256 tumor-bearing rats

机译:针刺ST36(祖三里)穴对沃克256荷瘤大鼠癌痛和瞬时受体电位类香草素亚家族1表达的影响

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BACKGROUND: Several studies have addressed the expression of transient receptor potential vanilloid subfamily 1(TRPV1) playing an important role in the generation of cancer pain. Electroacupuncture (EA) is an effective method of acupuncture shown to attenuate different kinds of pain such as inflammatory, neuropathic, and cancer. In this study, we investigated the effect of EA on cancer pain caused by intraplantar injection of Walker 256 carcinoma cells and cancer-driven TRPV1 expression in the dorsal root ganglions (DRGs). METHODS: Rats were randomly divided into 4 groups: the nontumor cell inoculation group (normal control, n = 8); Walker 256 carcinoma cell inoculation group (tumor control, n = 8); sham point electrical stimulation treatment with Walker 256 carcinoma cell inoculation group (SES, n = 8); EA treatment with Walker 256 carcinoma cell inoculation group (EA, n = 8). The time courses of thermal, mechanical sensitivity, and spontaneous nocifensive behavior were determined. In addition, TRPV1 expression in DRGs was observed by quantitative real-time polymerase chain reaction and Western blotting. RESULTS: Injection of cancer cells decreased the paw withdrawal threshold, increased spontaneous nocifensive behavior, and induced significant thermal hyperalgesia that was attenuated by EA at the ST36 acupoint (2 Hz, 0.3 ms, ≤1 mA). TRPV1 mRNA and protein in DRGs were upregulated in the cancer pain model, and EA at ST36 acupoint counteracted the cancer-driven upregulation of TRPV1 expression in the corresponding DRGs. CONCLUSIONS: EA at ST36 could attenuate cancer-induced pain, at least in part, through suppressing TRPV1 mRNA and protein upregulation in the DRGs.
机译:背景:一些研究已经解决了短暂性受体电位香草样亚家族1(TRPV1)的表达在癌症疼痛的产生中起重要作用。电针(EA)是一种有效的针灸方法,可减轻各种疼痛,例如炎症性,神经性和癌症。在这项研究中,我们调查了EA对足底注射Walker 256癌细胞和背根神经节(DRGs)中癌症驱动的TRPV1表达引起的癌痛的影响。方法:将大鼠随机分为4组:非肿瘤细胞接种组(正常对照组,n = 8);非肿瘤细胞接种组(n = 8)。 Walker 256癌细胞接种组(肿瘤对照组,n = 8); Walker 256癌细胞接种组假点电刺激治疗(SES,n = 8);用Walker 256癌细胞接种组进行EA治疗(EA,n = 8)。确定了热,机械敏感性和自发伤害行为的时间过程。另外,通过定量实时聚合酶链反应和蛋白质印迹观察到DRG中TRPV1的表达。结果:注射癌细胞降低了爪退缩阈值,增加了自发的伤害行为,并诱导了显着的热痛觉过敏,在ST36穴位(2 Hz,0.3 ms,≤1mA),EA减弱了痛觉过敏。在癌症疼痛模型中,DRGs中的TRPV1 mRNA和蛋白上调,而ST36穴位的EA抵消了癌症驱动的相应DRGs中TRPV1表达的上调。结论:ST36的EA至少可以通过抑制DRGs中TRPV1 mRNA和蛋白上调来减轻癌症引起的疼痛。

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