PMID- 31134844 OWN - NLM STAT- MEDLINE DCOM- 20191209 LR - 20191217 IS - 1532-2513 (Electronic) IS - 0892-3973 (Linking) VI - 41 IP - 3 DP - 2019 Jun TI - Pulegone inhibits inflammation via suppression of NLRP3 inflammasome and reducing cytokine production in mice. PG - 420-427 LID - 10.1080/08923973.2019.1588292 [doi] AB - Context: Pulegone, a key compound in Schizonepeta essential oil, has been identified as an anti-inflammatory. However, its underlying molecular mechanisms on NLR family pyrin domain containing 3 (NLRP3) inflammasome have not been elucidated. Objective: Here, the modulatory effects of pulegone on NLRP3 inflammasome were investigated. Materials and methods: The C57BL/6J mice were randomly divided into five groups: Normal, Lipopolysaccharides (LPS), Dexamethasone (DEX, 5 mg/kg), Pulegone (0.095 and 0.190 g/kg) groups. All mice were challenged by LPS except for the Normal group. Results: A reduced expression of Interleukin-18 (IL-18), Interleukin-1beta (IL-1beta), Interleukin-5 (IL-5), Tumor necrosis factor-alpha (TNF-alpha), Interferon-gamma (IFN-gamma), Monocyte chemoattratctant protein-1 (MCP-1), Macrophage inflammatory protein-1beta (MIP-1beta), Monocyte colony stimulating factor (M-CSF) and Granulocyte-macrophage colony stimulating factor (GM-CSF) in serum were detected in the pulegone groups as compared to the LPS group. In addition, a reduced mRNA and protein expression production of ASC, NLRP3, and Caspase-1 were detected in lungs after pulegone administration. Histological analysis results indicated that the histological changes of lungs caused by LPS were ameliorated by pulegone. Immunohistochemical study showed a decreased positive cell numbers of P2X7R in Pulegone (0.095 and 0.190 g/kg) groups. Conclusion: Pulegone exerts anti-inflammatory effects on LPS-induced sepsis mice via inhibition of the NLRP3 expression. FAU - Yang, Qingxin AU - Yang Q AD - a Department of Pharmacology, College of Pharmacy , Chengdu University of TCM , Chengdu , PR China. AD - b Sichuan College of Traditional Chinese Medicine , Mianyang , PR China. FAU - Luo, Jie AU - Luo J AD - a Department of Pharmacology, College of Pharmacy , Chengdu University of TCM , Chengdu , PR China. FAU - Lv, Hongjun AU - Lv H AD - a Department of Pharmacology, College of Pharmacy , Chengdu University of TCM , Chengdu , PR China. FAU - Wen, Taoqun AU - Wen T AD - a Department of Pharmacology, College of Pharmacy , Chengdu University of TCM , Chengdu , PR China. FAU - Shi, Boyu AU - Shi B AD - a Department of Pharmacology, College of Pharmacy , Chengdu University of TCM , Chengdu , PR China. FAU - Liu, Xiaobo AU - Liu X AD - a Department of Pharmacology, College of Pharmacy , Chengdu University of TCM , Chengdu , PR China. FAU - Zeng, Nan AU - Zeng N AD - a Department of Pharmacology, College of Pharmacy , Chengdu University of TCM , Chengdu , PR China. LA - eng PT - Journal Article DEP - 20190528 PL - England TA - Immunopharmacol Immunotoxicol JT - Immunopharmacology and immunotoxicology JID - 8800150 RN - 0 (Cyclohexane Monoterpenes) RN - 0 (Cytokines) RN - 0 (Inflammasomes) RN - 0 (NLR Family, Pyrin Domain-Containing 3 Protein) RN - 0 (Nlrp3 protein, mouse) RN - 4LF2673R3G (pulegone) SB - IM MH - Animals MH - Cyclohexane Monoterpenes/*pharmacology MH - Cytokines/*immunology MH - Inflammasomes/*immunology MH - Inflammation/chemically induced/drug therapy/immunology/pathology MH - Male MH - Mice MH - NLR Family, Pyrin Domain-Containing 3 Protein/*immunology OTO - NOTNLM OT - LPS OT - NLRP3 OT - Pulegone OT - inflammation OT - sepsis EDAT- 2019/05/29 06:00 MHDA- 2019/12/18 06:00 CRDT- 2019/05/29 06:00 PHST- 2019/05/29 06:00 [pubmed] PHST- 2019/12/18 06:00 [medline] PHST- 2019/05/29 06:00 [entrez] AID - 10.1080/08923973.2019.1588292 [doi] PST - ppublish SO - Immunopharmacol Immunotoxicol. 2019 Jun;41(3):420-427. doi: 10.1080/08923973.2019.1588292. Epub 2019 May 28.