首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Topical Treatment with Xiaozheng Zhitong Paste (XZP) Alleviates Bone Destruction and Bone Cancer Pain in a Rat Model of Prostate Cancer-Induced Bone Pain by Modulating the RANKL/RANK/OPG Signaling
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Topical Treatment with Xiaozheng Zhitong Paste (XZP) Alleviates Bone Destruction and Bone Cancer Pain in a Rat Model of Prostate Cancer-Induced Bone Pain by Modulating the RANKL/RANK/OPG Signaling

机译:消症止痛膏(XZP)的局部治疗通过调节RANKL / RANK / OPG信号传导减轻前列腺癌诱导的骨痛大鼠模型的骨破坏和骨癌痛。

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To explore the effects and mechanisms of Xiaozheng Zhitong Paste (XZP) on bone cancer pain, Wistar rats were inoculated with vehicle or prostate cancer PC-3 into the tibia bone and treated topically with inert paste, XZP at 15.75, 31.5, or 63 g/kg twice per day for 21 days. Their bone structural damage, nociceptive behaviors, bone osteoclast and osteoblast activity, and the levels of OPG, RANL, RNAK, PTHrP, IGF-1, M-CSF, IL-8, and TNF-αwere examined. In comparison with that in the placebo group, significantly reduced numbers of invaded cancer cells, decreased levels of bone damage and mechanical threshold and paw withdrawal latency, lower levels of serum TRACP5b, ICTP, PINP, and BAP, and less levels of bone osteoblast and osteoclast activity were detected in the XZP-treated rats (P<0.05). Moreover, significantly increased levels of bone OPG but significantly decreased levels of RANL, RNAK, PTHrP, IGF-1, M-CSF, IL-8, and TNF-αwere detected in the XZP-treated rats (P<0.05for all). Together, XZP treatment significantly mitigated the cancer-induced bone damage and bone osteoclast and osteoblast activity and alleviated prostate cancer-induced bone pain by modulating the RANKL/RANK/OPG pathway and bone cancer-related inflammation in rats.
机译:为了研究消症止痛膏(XZP)对骨癌疼痛的影响和机制,将Wistar大鼠用媒介物或前列腺癌PC-3接种到胫骨中,并用惰性糊剂XZP分别以15.75、31.5或63μg的剂量进行治疗。 / kg,每天两次,共21天。检查了它们的骨结构损伤,伤害行为,破骨细胞和成骨细胞活性,以及​​OPG,RANL,RNAK,PTHrP,IGF-1,M-CSF,IL-8和TNF-α的水平。与安慰剂组相比,显着减少了侵袭癌细胞的数量,降低了骨损伤和机械阈值以及爪退缩潜伏期,降低了血清TRACP5b,ICTP,PINP和BAP的水平,降低了成骨细胞和成骨细胞的水平。在XZP处理的大鼠中检测到破骨细胞活性(P <0.05)。此外,在用XZP治疗的大鼠中检测到骨OPG的水平显着升高,但RANL,RNAK,PTHrP,IGF-1,M-CSF,IL-8和TNF-α的水平显着降低(所有P均<0.05)。总之,XZP治疗通过调节RANKL / RANK / OPG途径和大鼠与骨癌相关的炎症,显着减轻了癌症引起的骨损伤,破骨细胞和成骨细胞的活性,减轻了前列腺癌引起的骨痛。

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