Synergistic and Toxicity-reducing Effects of Periplaneta americana Extract CⅡ-3 Combined with CTX on H22 Tumor Bearing Mice

IF 0.8 4区 医学 Q3 EDUCATION, SCIENTIFIC DISCIPLINES
Rui Yuan, Guangming Liu, Meixian Guo, Xiaobo Liu
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引用次数: 0

Abstract

Abstract: Background: Cyclophosphamide (CTX) is widely used in tumor treatment, but its clinical therapeutic effect is not ideal due to many side effects. Materials and Methods: In the present study, we researched the synergistic and attenuating effects of CⅡ-3 combined with CTX and their underlying mechanism in H22 tumor-bearing mice. Firstly, we established an H22 tumor-bearing mice model, and the body weight, tumor weight, and survival time were recorded. Secondly, HE staining of tumor tissue was performed, and the related organ index, NK cell killing activity, peripheral blood cells, and bone marrow nucleated cells were measured. Moreover, the changes in IL-6 and IFN-1β in serum were detected by ELISA. Finally, RT-qPCR and Western Blot were performed to detect the expressions of TLR4, TLR9 and NF-κB in tumor tissue. Results: The treatment of CⅡ-3 combined with CTX could increase life extension rate of H22 tumor-bearing mice, reduce tumor weight. Additionally, it could inhibit tumor cell proliferation, increase thymus and spleen index, enhance the activity of T cells in spleen, promote the killing activity of NK cells, and had a certain ameliorate effect on the reduction of WBC, Neut, LYM and bone marrow nucleated cells caused by CTX. And the expression of mRNA and the protein of TLR4, TLR9 and NF-κB in tumor mass of H22 tumor-bearing mice were down-regulated. Conclusion: There were synergistic and attenuating effects of CTX combined with CⅡ-3 in the treatment of tumor and the effects might be mediated by the TLR4/NF-κB and TLR9/NF-κB signaling pathways. Keywords Anti-tumor, Cyclophosphamide, Immune depression, Periplaneta americana, Synergism and attenuation.
美洲大蠊提取物CⅡ-3联合CTX对H22荷瘤小鼠的增效及减毒作用
摘要:背景:环磷酰胺(Cyclophosphamide, CTX)广泛应用于肿瘤治疗,但其副作用多,临床治疗效果不理想。材料与方法:本实验研究CⅡ-3联合CTX对H22荷瘤小鼠的增效、减毒作用及其机制。首先建立H22荷瘤小鼠模型,记录体重、肿瘤重量、生存时间。其次,对肿瘤组织进行HE染色,测定相关脏器指数、NK细胞杀伤活性、外周血细胞、骨髓有核细胞。ELISA法检测血清中IL-6、IFN-1β的变化。最后采用RT-qPCR和Western Blot检测肿瘤组织中TLR4、TLR9和NF-κB的表达。结果:CⅡ-3联合CTX治疗可提高H22荷瘤小鼠的寿命延长率,减轻肿瘤重量。抑制肿瘤细胞增殖,提高胸腺和脾脏指数,增强脾脏T细胞活性,促进NK细胞杀伤活性,对CTX所致WBC、Neut、LYM及骨髓有核细胞减少有一定改善作用。H22荷瘤小鼠肿瘤组织中TLR4、TLR9、NF-κB mRNA及蛋白表达下调。结论:CTX联合CⅡ-3治疗肿瘤具有增效和减毒作用,其作用可能通过TLR4/NF-κB和TLR9/NF-κB信号通路介导。关键词抗肿瘤,环磷酰胺,免疫抑制,美洲大蠊,协同衰减。
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
227
审稿时长
>12 weeks
期刊介绍: The official journal of Association of Pharmaceutical Teachers of India (APTI) and is being published since 1967. IJPER, a quarterly publication devoted to publish reviews and research articles in pharmacy and the related disciplines of Pharmaceutical education. It mainly covers the articles of special interest, covering the areas of Pharmaceutical research, teaching and learning, laboratory innovations, education technology, curriculum design, examination reforms, training and other related issues. It encourages debates and discussions on the issues of vital importance to Pharmaceutical education and research. The goal of the journal is to provide the quality publications and publish most important research and review articles in the field of drug development and pharmaceutical education. It is circulated and referred by more than 6000 teachers, 40,000 students and over 1000 professionals working in Pharmaceutical industries, Regulatory departments, hospitals etc.
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