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Anti-Inflammation of Spirocyclopiperazinium Salt Compound LXM-10 Targeting α7 nAChR and M4 mAChR and Inhibiting JAK2/STAT3 Pathway in Rats

机译:靶向α7nAChR和M4 mAChR并抑制JAK2 / STAT3通路的螺环哌嗪盐化合物LXM-10的抗炎作用

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摘要

The present study aims to investigate the therapeutic effects of LXM-10 by intragastric administration in both acute and chronic inflammatory models, and to explore the underlying molecular mechanisms. The results showed that LXM-10 produced significant anti-inflammatory effects on carrageenan induced paw edema and complete Freund's adjuvant (CFA) induced arthritis, in which LXM-10 inhibited paw swelling in a dose- and time-dependent manner. ELISA analysis showed the production of pro-inflammatory cytokines including TNF-α and IL-6 was decreased by LXM-10. Western blot analysis showed that LXM-10 significantly reduced phosphorylation of Janus kinase 2 (JAK2) and further blunted phosphorylation of signal transducer and activator of transcription-3 (STAT3). The effects that LXM-10 had shown were attenuated by methyllycaconitine citrate (an α7 nicotinic acetylcholine receptor antagonist) or tropicamide (an M4 muscarinic acetylcholine receptor antagonist) in vivo. In conclusion, the studies showed that intragastric administration of LXM-10 exerted significant anti-inflammation effects in acute and chronic models, which may be attribute to the activation of α7 nicotinic acetylcholine receptor and M4 muscarinic acetylcholine receptor, thereby inhibiting the JAK2/STAT3 signal pathway, and ultimately reducing the production of pro-inflammatory cytokines of TNF-α and IL-6.
机译:本研究旨在研究在急性和慢性炎症模型中通过胃内给药对LXM-10的治疗作用,并探讨其潜在的分子机制。结果表明,LXM-10对角叉菜胶诱发的足爪水肿和完全弗氏佐剂(CFA)诱发的关节炎具有显着的抗炎作用,其中LXM-10以剂量和时间依赖性的方式抑制足爪肿胀。 ELISA分析表明,LXM-10可减少促炎细胞因子包括TNF-α和IL-6的产生。蛋白质印迹分析表明,LXM-10显着降低了Janus激酶2(JAK2)的磷酸化,并进一步减弱了信号转导子和转录激活子3(STAT3)的磷酸化。在体内,柠檬酸甲基卡卡尼碱(α7烟碱乙酰胆碱受体拮抗剂)或tropicamide(M4毒蕈碱型乙酰胆碱受体拮抗剂)减弱了LXM-10所显示的作用。总之,研究表明,胃内给药LXM-10在急性和慢性模型中均具有明显的抗炎作用,这可能归因于α7烟碱型乙酰胆碱受体和M4毒蕈碱型乙酰胆碱受体的激活,从而抑制了JAK2 / STAT3信号。途径,最终减少促炎细胞因子TNF-α和IL-6的产生。

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