Article(id=1304388203419558492, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388108988997783, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.12.017, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1770048000000, receivedDateStr=2026-02-03, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788919982056, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788919982056, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788919982056, creator=13701087609, updateTime=1788919982056, updator=13701087609, issue=Issue{id=1304388108988997783, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='12', pageStart='4509', pageEnd='4948', issueExtLink='null', onlineDate='null', pubDate='1782576000000', pubDateStr='2026-06-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788919959542, creator='13701087609', updateTime=1788923461082, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304402795579330582, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388108988997783, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304402795579330583, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388108988997783, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=4721, endPage=4733, ext={EN=ArticleExt(id=1304388205726425695, articleId=1304388203419558492, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Citronellol promotes wound healing in methicillin-resistant Staphylococcus aureus-infected mice by inhibiting NLRP3 inflammasome pathway, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To explore the therapeutic effect and related mechanism of citronellol on methicillin-resistant Staphylococcus aureus (MRSA)-induced skin infections in mice via NOD-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome pathway. Methods The minimum inhibitory concentration (MIC) of citronellol against standard MRSA strains was determined using the microbroth dilution method. A full-thickness skin MRSA infection model was established in female C57BL/6 mice, control group, model group, positive control (2% mupirocin) group, citronellol low-, medium- and high-dose (0.75%, 1.50%, 3.00% citronellol gel) groups were set up. Local administration was performed for 7 d. Wound healing rates were dynamically monitored, hematoxylin-eosin (HE) staining was used to observe histopathological changes in skin tissues, and ELISA was used to detect levels of interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), superoxide dismutase (SOD) and malondialdehyde (MDA) in skin tissues. Masson staining was used to observe collagen fiber deposition in skin tissues. RNA-seq transcriptome sequencing, qRT-PCR and Western blotting were employed to analyze the expressions of NLRP3 inflammasome pathway-related genes and proteins in skin tissues, while molecular docking was used to predict the binding affinity of citronellol to relevant inflammatory targets. The lactate dehydrogenase (LDH) release assay was used to evaluate the effect of citronellol on pyroptosis in MRSA-infected immortalized keratinocytes. Results Citronellol exhibited significant antibacterial activity against MRSA, with an MIC ranging from 0.312 5—0.625 0 mg/mL. In vivo experiments revealed that compared with model group, citronellol significantly accelerated wound healing, reduced inflammatory cell infiltration and tissue edema, decreased IL-1β and TNF-α levels in skin tissues (P < 0.05, 0.01, 0.001), markedly increased collagen fiber deposition at wound sites (P < 0.05, 0.01), and inhibited the activation of NLRP3 inflammasome-cell pyroptosis pathway (P < 0.05, 0.01, 0.001). Molecular docking results indicated that citronellol could bind to target proteins such as IL-1β. In vitro experiments demonstrated that citronellol significantly suppressed LDH release in MRSA-infected HaCaT cells (P < 0.05, 0.01). Conclusion Citronellol exerts significant antibacterial, anti-inflammatory and wound repair-promoting effects on MRSA-induced skin infections in mice. Its mechanism may be related to inhibiting NLRP3 inflammasome-cell pyroptosis pathway, reducing the release of pro-inflammatory cytokines, improving the local immune microenvironment, and promoting collagen deposition., authors=NING Yixiao, PU Zhonghui, LIAO Xinyun, WANG Yuzhen, JIANG Zhuoting, DAI Min, authorsList=NING Yixiao, PU Zhonghui, LIAO Xinyun, WANG Yuzhen, JIANG Zhuoting, DAI Min, authorCompany=null, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1304388205529293406, articleId=1304388203419558492, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=香茅醇通过抑制NLRP3炎症小体通路促进耐甲氧西林金黄色葡萄球菌感染小鼠伤口愈合, columnId=1304140191707456168, journalTitle=中草药, columnName=药理与临床, runingTitle=null, highlight=null, articleAbstract=目的 基于NOD样受体热蛋白结构域3(NOD like receptor family pyrin domain containing 3,NLRP3)炎症小体通路探讨香茅醇对耐甲氧西林金黄色葡萄球菌(methicillin-resistant Staphylococcus aureus,MRSA)诱导小鼠皮肤感染的治疗作用及相关机制。方法 采用微量肉汤稀释法测定香茅醇对标准MRSA菌株的最低抑菌浓度(minimum inhibitory concentration,MIC);建立C57BL/6雌性小鼠背部全层皮肤MRSA感染模型,设置对照组、模型组、阳性对照(2%莫匹罗星)组和香茅醇低、中、高剂量(0.75%、1.50%、3.00%香茅醇凝胶)组,局部给药7 d。动态检测伤口愈合率,苏木素-伊红(hematoxylin-eosin,HE)染色观察皮肤组织病理变化,ELISA法检测皮肤组织中白细胞介素-1β(interleukin-1β,IL-1β)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)、超氧化物歧化酶(superoxide dismutase,SOD)和丙二醛(malondialdehyde,MDA)水平,Masson染色观察皮肤组织胶原纤维沉积;通过RNA-seq转录组测序、qRT-PCR及Western blotting检测皮肤组织中NLRP3炎症小体通路相关基因及蛋白表达,分子对接预测香茅醇与相关炎症靶点的结合能力。乳酸脱氢酶(lactate dehydrogenase,LDH)释放实验检测香茅醇对MRSA感染的人永生化角质形成细胞焦亡的影响。结果 香茅醇对MRSA具有显著的抗菌活性,MIC为0.312 5~0.625 0 mg/mL。体内实验中,与模型组比较,香茅醇能显著加快伤口愈合,减轻炎症细胞浸润及组织水肿,降低皮肤组织IL-1β、TNF-α水平(P<0.05、0.01、0.001),显著增加伤口部位胶原纤维沉积(P<0.05、0.01),并抑制NLRP3炎症小体-细胞焦亡通路激活(P<0.05、0.01、0.001)。分子对接结果显示,香茅醇可与IL-1β等靶蛋白结合。体外实验中,香茅醇显著抑制MRSA感染的HaCaT细胞LDH释放(P<0.05、0.01)。结论 香茅醇对MRSA诱导的小鼠皮肤感染具有显著的抗菌、抗炎及促修复作用,其机制可能与抑制NLRP3炎症小体-细胞焦亡通路、减少促炎细胞因子释放、改善局部免疫微环境及促进胶原沉积相关。, authors=宁溢潇1, 蒲忠慧1,2,3, 廖新云1, 王雨珍1, 蒋卓廷1, 代敏1,2,3, authorsList=宁溢潇, 蒲忠慧, 廖新云, 王雨珍, 蒋卓廷, 代敏, authorCompany=1 成都医学院检验医学院,四川 成都 610500;
2 成都医学院 四川省动物源性食品兽药残留防控技术工程实验室,四川成都 610500;
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Staphylococcus aureus-associated skin and soft tissue infections: Anatomical localization, epidemiology, therapy and potential prophylaxis [J]. Curr Top Microbiol Immunol, 2017, 409: 199-227.
Blake K J, Baral P, Voisin T, et al. Staphylococcus aureus produces pain through pore-forming toxins and neuronal TRPV1 that is silenced by QX-314[J]. Nat Commun, 2018, 9: 37.
Zhang X L, Liu J, Fu P, et al. Epidemiological profile and antimicrobial resistance trends of Staphylococcus aureus in Chinese pediatric intensive care units from 2016 to 2022: A multi-center retrospective study [J]. BMC Infect Dis, 2025, 25(1): 298.
张悦, 姜孟伶, 曹金丹, 等. 枸杞多糖通过TLR4/Src通路促进巨噬细胞吞噬金黄色葡萄球菌[J]. 中草药, 2023, 54(22): 7466-7473.
Lin J Y, Lai J K, Chen J Y, et al. Global insights into MRSA bacteremia: A bibliometric analysis and future outlook [J]. Front Microbiol, 2024, 15: 1516584.
Lin C C, Lin F Q, Wang J, et al. Mupirocin-piperine microemulsion hydrogels accelerate healing of infected wounds through deep penetration and biofilm disruption [J]. Mol Pharm, 2025, 22(7): 4230-4244.
Morguette A E B, Bartolomeu-Gonçalves G, Andriani G M, et al. The antibacterial and wound healing properties of natural products: A review on plant species with therapeutic potential against Staphylococcus aureus wound infections [J]. Plants, 2023, 12(11): 2147.
Sharafutdinov I S, Trizna E Y, Baidamshina D R, et al. Antimicrobial effects of sulfonyl derivative of 2(5H)-furanone against planktonic and biofilm associated methicillin-resistant and-susceptible Staphylococcus aureus [J]. Front Microbiol, 2017, 8: 2246.
Xu Y S, Wang L, Guo D B, et al. Baohuoside I targets SaeR as an antivirulence strategy to disrupt MRSA biofilm formation and pathogenicity [J]. NPJ Biofilms Microbiomes, 2025, 11: 45.
Alexpandi R, Abirami G, Balaji M, et al. Proteomic insights into the multi-target mechanism and therapeutic application of citronellol-loaded carboxymethyl chitosan-based hydrogel for wound infection treatment [J]. Int J Biol Macromol, 2025, 323: 147179.
杨佳佳, 韦世权, 张科, 等. 香茅醇自乳化递送系统的制备及其体外抗肿瘤活性评价[J]. 中草药, 2020, 51(5): 1196-1204.
Tall A R, Bornfeldt K E. Inflammasomes and atherosclerosis: A mixed picture [J]. Circ Res, 2023, 132(11): 1505-1520.
Zhang W F, Li G C, Luo R J, et al. Cytosolic escape of mitochondrial DNA triggers cGAS-STING-NLRP3 axis-dependent nucleus pulposus cell pyroptosis [J]. Exp Mol Med, 2022, 54(2): 129-142.
Cai J J, Shi J R, Chen C, et al. Structural-activity relationship-inspired the discovery of saturated fatty acids as novel colistin enhancers [J]. Adv Sci, 2023, 10(29): 2302182.
Li Y M, Sun R Y, Kong Y J, et al. Antibacterial effect of ultrasound and β-citronellol against Listeria monocytogenes and its application in carrot preservation [J]. Ultrason Sonochem, 2024, 102: 106752.
梁小雪, 高鸣乡, 邱敏, 等. 丁香挥发油联合喹诺酮类抗生素抗耐甲氧西林金黄色葡萄球菌作用研究[J]. 中草药, 2020, 51(23): 5998-6005.
邱敏, 龙娜娜, 高鸣乡, 等. 丁香油联用β-内酰胺类抗生素体外抗耐甲氧西林金黄色葡萄球菌作用研究[J]. 中草药, 2019, 50(7): 1629-1635.
Khadour F A, Khadour Y A, Xu T. NLRP3 overexpression exacerbated synovium tissue degeneration in juvenile collagen-induced arthritis [J]. Sci Rep, 2025, 15: 7024.
Wang D, Zhan X, Wu R, et al. Assessment of pyroptosis-related indicators as potential biomarkers and their association with severity in patients with liver cirrhosis [J]. J Inflamm Res, 2021, 14: 3185-3196.
Choi J Q, Zheng M, Kim J L, et al. Inhibition of Nrf2/HO-1 signaling leads to increased activation of the NLRP3 inflammasome in osteoarthritis [J]. J Inflamm Res, 2021, 14: 4749-4764.
De Santis S, Martini C, Ferraro E, et al. ER-mitochondria association negatively affects wound healing by regulating NLRP3 activation [J]. Cell Death Dis, 2024, 15(6): 462.
Chen Y H, Li Y, Guo L M, et al. Bibliometric analysis of the inflammasome and pyroptosis in brain [J]. Front Pharmacol, 2020, 11: 626502.
Craven R R, Gao X, Allen I C, et al. Staphylococcus aureus alpha-hemolysin activates the NLRP3-inflammasome in human and mouse monocytic cells [J]. PLoS One, 2009, 4(10): e7446.
Lian N, Chen Y J, Chen S H, et al. Gasdermin D-mediated keratinocyte pyroptosis as a key step in psoriasis pathogenesis [J]. Cell Death Dis, 2023, 14: 595.
Messingham K N, Cahill M P, Kilgore S H, et al. TSST-1+ Staphylococcus aureus in bullous pemphigoid [J]. J Investig Dermatol, 2022, 142(4): 1032-1039.
Hu J J, Liu X, Xia S Y, et al. FDA-approved disulfiram inhibits pyroptosis by blocking gasdermin D pore formation [J]. Nat Immunol, 2020, 21(7): 736-745.
del Mar Ferrà-Cañellas M, Garcia-Sureda L. Exploring the potential of micro-immunotherapy in the treatment of periodontitis [J]. Life, 2024, 14(5): 552.
Bora P K, Borah G, Kalita D, et al. Mushroom-mediated reductive bioconversion of aldehyde-rich essential oils for aroma alteration: A rose-like floral bioflavor from Citronella oil [J]. J Agric Food Chem, 2023, 71(3): 1690-1700.)
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香茅醇通过抑制NLRP3炎症小体通路促进耐甲氧西林金黄色葡萄球菌感染小鼠伤口愈合
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中草药 | 药理与临床 2026,57(12): 4721-4733
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中草药 |药理与临床 2026 , 57 (12) : 4721 -4733
香茅醇通过抑制NLRP3炎症小体通路促进耐甲氧西林金黄色葡萄球菌感染小鼠伤口愈合
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宁溢潇1, 蒲忠慧1,2,3, 廖新云1, 王雨珍1, 蒋卓廷1, 代敏1,2,3
作者信息
    1 成都医学院检验医学院,四川 成都 610500;
    2 成都医学院 四川省动物源性食品兽药残留防控技术工程实验室,四川成都 610500;
    3 成都医学院四川省中医药管理局血管衰老与中医药干预中医药重点实验室,四川 成都 610500
通讯作者:
代敏
作者简介:
宁溢潇: 宁溢潇(1999—),男,硕士研究生,研究方向为中药抗菌活性及作用机制。E-mail:1483554822@qq.com 蒲忠慧: 蒲忠慧(1982—),女,教授,研究方向为天然产物抗菌活性及作用机制。E-mail:zhonghui.pu@163.com
Citronellol promotes wound healing in methicillin-resistant Staphylococcus aureus-infected mice by inhibiting NLRP3 inflammasome pathway
  • NING Yixiao, PU Zhonghui, LIAO Xinyun, WANG Yuzhen, JIANG Zhuoting, DAI Min
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.12.017
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    目的 基于NOD样受体热蛋白结构域3(NOD like receptor family pyrin domain containing 3,NLRP3)炎症小体通路探讨香茅醇对耐甲氧西林金黄色葡萄球菌(methicillin-resistant Staphylococcus aureus,MRSA)诱导小鼠皮肤感染的治疗作用及相关机制。方法 采用微量肉汤稀释法测定香茅醇对标准MRSA菌株的最低抑菌浓度(minimum inhibitory concentration,MIC);建立C57BL/6雌性小鼠背部全层皮肤MRSA感染模型,设置对照组、模型组、阳性对照(2%莫匹罗星)组和香茅醇低、中、高剂量(0.75%、1.50%、3.00%香茅醇凝胶)组,局部给药7 d。动态检测伤口愈合率,苏木素-伊红(hematoxylin-eosin,HE)染色观察皮肤组织病理变化,ELISA法检测皮肤组织中白细胞介素-1β(interleukin-1β,IL-1β)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)、超氧化物歧化酶(superoxide dismutase,SOD)和丙二醛(malondialdehyde,MDA)水平,Masson染色观察皮肤组织胶原纤维沉积;通过RNA-seq转录组测序、qRT-PCR及Western blotting检测皮肤组织中NLRP3炎症小体通路相关基因及蛋白表达,分子对接预测香茅醇与相关炎症靶点的结合能力。乳酸脱氢酶(lactate dehydrogenase,LDH)释放实验检测香茅醇对MRSA感染的人永生化角质形成细胞焦亡的影响。结果 香茅醇对MRSA具有显著的抗菌活性,MIC为0.312 5~0.625 0 mg/mL。体内实验中,与模型组比较,香茅醇能显著加快伤口愈合,减轻炎症细胞浸润及组织水肿,降低皮肤组织IL-1β、TNF-α水平(P<0.05、0.01、0.001),显著增加伤口部位胶原纤维沉积(P<0.05、0.01),并抑制NLRP3炎症小体-细胞焦亡通路激活(P<0.05、0.01、0.001)。分子对接结果显示,香茅醇可与IL-1β等靶蛋白结合。体外实验中,香茅醇显著抑制MRSA感染的HaCaT细胞LDH释放(P<0.05、0.01)。结论 香茅醇对MRSA诱导的小鼠皮肤感染具有显著的抗菌、抗炎及促修复作用,其机制可能与抑制NLRP3炎症小体-细胞焦亡通路、减少促炎细胞因子释放、改善局部免疫微环境及促进胶原沉积相关。
    香茅醇  /  耐甲氧西林金黄色葡萄球菌  /  皮肤感染  /  NLRP3炎症小体  /  细胞焦亡
    Objective To explore the therapeutic effect and related mechanism of citronellol on methicillin-resistant Staphylococcus aureus (MRSA)-induced skin infections in mice via NOD-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome pathway. Methods The minimum inhibitory concentration (MIC) of citronellol against standard MRSA strains was determined using the microbroth dilution method. A full-thickness skin MRSA infection model was established in female C57BL/6 mice, control group, model group, positive control (2% mupirocin) group, citronellol low-, medium- and high-dose (0.75%, 1.50%, 3.00% citronellol gel) groups were set up. Local administration was performed for 7 d. Wound healing rates were dynamically monitored, hematoxylin-eosin (HE) staining was used to observe histopathological changes in skin tissues, and ELISA was used to detect levels of interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), superoxide dismutase (SOD) and malondialdehyde (MDA) in skin tissues. Masson staining was used to observe collagen fiber deposition in skin tissues. RNA-seq transcriptome sequencing, qRT-PCR and Western blotting were employed to analyze the expressions of NLRP3 inflammasome pathway-related genes and proteins in skin tissues, while molecular docking was used to predict the binding affinity of citronellol to relevant inflammatory targets. The lactate dehydrogenase (LDH) release assay was used to evaluate the effect of citronellol on pyroptosis in MRSA-infected immortalized keratinocytes. Results Citronellol exhibited significant antibacterial activity against MRSA, with an MIC ranging from 0.312 5—0.625 0 mg/mL. In vivo experiments revealed that compared with model group, citronellol significantly accelerated wound healing, reduced inflammatory cell infiltration and tissue edema, decreased IL-1β and TNF-α levels in skin tissues (P < 0.05, 0.01, 0.001), markedly increased collagen fiber deposition at wound sites (P < 0.05, 0.01), and inhibited the activation of NLRP3 inflammasome-cell pyroptosis pathway (P < 0.05, 0.01, 0.001). Molecular docking results indicated that citronellol could bind to target proteins such as IL-1β. In vitro experiments demonstrated that citronellol significantly suppressed LDH release in MRSA-infected HaCaT cells (P < 0.05, 0.01). Conclusion Citronellol exerts significant antibacterial, anti-inflammatory and wound repair-promoting effects on MRSA-induced skin infections in mice. Its mechanism may be related to inhibiting NLRP3 inflammasome-cell pyroptosis pathway, reducing the release of pro-inflammatory cytokines, improving the local immune microenvironment, and promoting collagen deposition.
    citronellol  /  methicillin-resistant Staphylococcus aureus  /  skin infection  /  NLRP3 inflammasome  /  cell pyroptosis
    宁溢潇, 蒲忠慧, 廖新云, 王雨珍, 蒋卓廷, 代敏. 香茅醇通过抑制NLRP3炎症小体通路促进耐甲氧西林金黄色葡萄球菌感染小鼠伤口愈合. 中草药, 2026 , 57 (12) : 4721 -4733 . DOI: 10.7501/j.issn.0253-2670.2026.12.017
    NING Yixiao, PU Zhonghui, LIAO Xinyun, WANG Yuzhen, JIANG Zhuoting, DAI Min. Citronellol promotes wound healing in methicillin-resistant Staphylococcus aureus-infected mice by inhibiting NLRP3 inflammasome pathway[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (12) : 4721 -4733 . DOI: 10.7501/j.issn.0253-2670.2026.12.017

      国家自然科学基金资助项目 (82204601); 国家自然科学基金资助项目 (82472328); 四川省重点研发计划项目 (2024YFFK0090); “成医英才”登峰计划人才项目 (2024qnGzn14); 临床科学研究基金资助项目 (2024GJQY23,24LHBBYY1-04,23LHPDZYB21)

    参考文献 引证文献
    排序方式:
    Olaniyi R, Pozzi C, Grimaldi L, et al. Staphylococcus aureus-associated skin and soft tissue infections: Anatomical localization, epidemiology, therapy and potential prophylaxis [J]. Curr Top Microbiol Immunol, 2017, 409: 199-227.
    Blake K J, Baral P, Voisin T, et al. Staphylococcus aureus produces pain through pore-forming toxins and neuronal TRPV1 that is silenced by QX-314[J]. Nat Commun, 2018, 9: 37.
    Zhang X L, Liu J, Fu P, et al. Epidemiological profile and antimicrobial resistance trends of Staphylococcus aureus in Chinese pediatric intensive care units from 2016 to 2022: A multi-center retrospective study [J]. BMC Infect Dis, 2025, 25(1): 298.
    张悦, 姜孟伶, 曹金丹, 等. 枸杞多糖通过TLR4/Src通路促进巨噬细胞吞噬金黄色葡萄球菌[J]. 中草药, 2023, 54(22): 7466-7473.
    Lin J Y, Lai J K, Chen J Y, et al. Global insights into MRSA bacteremia: A bibliometric analysis and future outlook [J]. Front Microbiol, 2024, 15: 1516584.
    Lin C C, Lin F Q, Wang J, et al. Mupirocin-piperine microemulsion hydrogels accelerate healing of infected wounds through deep penetration and biofilm disruption [J]. Mol Pharm, 2025, 22(7): 4230-4244.
    Morguette A E B, Bartolomeu-Gonçalves G, Andriani G M, et al. The antibacterial and wound healing properties of natural products: A review on plant species with therapeutic potential against Staphylococcus aureus wound infections [J]. Plants, 2023, 12(11): 2147.
    Sharafutdinov I S, Trizna E Y, Baidamshina D R, et al. Antimicrobial effects of sulfonyl derivative of 2(5H)-furanone against planktonic and biofilm associated methicillin-resistant and-susceptible Staphylococcus aureus [J]. Front Microbiol, 2017, 8: 2246.
    Xu Y S, Wang L, Guo D B, et al. Baohuoside I targets SaeR as an antivirulence strategy to disrupt MRSA biofilm formation and pathogenicity [J]. NPJ Biofilms Microbiomes, 2025, 11: 45.
    Alexpandi R, Abirami G, Balaji M, et al. Proteomic insights into the multi-target mechanism and therapeutic application of citronellol-loaded carboxymethyl chitosan-based hydrogel for wound infection treatment [J]. Int J Biol Macromol, 2025, 323: 147179.
    杨佳佳, 韦世权, 张科, 等. 香茅醇自乳化递送系统的制备及其体外抗肿瘤活性评价[J]. 中草药, 2020, 51(5): 1196-1204.
    Tall A R, Bornfeldt K E. Inflammasomes and atherosclerosis: A mixed picture [J]. Circ Res, 2023, 132(11): 1505-1520.
    Zhang W F, Li G C, Luo R J, et al. Cytosolic escape of mitochondrial DNA triggers cGAS-STING-NLRP3 axis-dependent nucleus pulposus cell pyroptosis [J]. Exp Mol Med, 2022, 54(2): 129-142.
    Cai J J, Shi J R, Chen C, et al. Structural-activity relationship-inspired the discovery of saturated fatty acids as novel colistin enhancers [J]. Adv Sci, 2023, 10(29): 2302182.
    Li Y M, Sun R Y, Kong Y J, et al. Antibacterial effect of ultrasound and β-citronellol against Listeria monocytogenes and its application in carrot preservation [J]. Ultrason Sonochem, 2024, 102: 106752.
    梁小雪, 高鸣乡, 邱敏, 等. 丁香挥发油联合喹诺酮类抗生素抗耐甲氧西林金黄色葡萄球菌作用研究[J]. 中草药, 2020, 51(23): 5998-6005.
    邱敏, 龙娜娜, 高鸣乡, 等. 丁香油联用β-内酰胺类抗生素体外抗耐甲氧西林金黄色葡萄球菌作用研究[J]. 中草药, 2019, 50(7): 1629-1635.
    Khadour F A, Khadour Y A, Xu T. NLRP3 overexpression exacerbated synovium tissue degeneration in juvenile collagen-induced arthritis [J]. Sci Rep, 2025, 15: 7024.
    Wang D, Zhan X, Wu R, et al. Assessment of pyroptosis-related indicators as potential biomarkers and their association with severity in patients with liver cirrhosis [J]. J Inflamm Res, 2021, 14: 3185-3196.
    Choi J Q, Zheng M, Kim J L, et al. Inhibition of Nrf2/HO-1 signaling leads to increased activation of the NLRP3 inflammasome in osteoarthritis [J]. J Inflamm Res, 2021, 14: 4749-4764.
    De Santis S, Martini C, Ferraro E, et al. ER-mitochondria association negatively affects wound healing by regulating NLRP3 activation [J]. Cell Death Dis, 2024, 15(6): 462.
    Chen Y H, Li Y, Guo L M, et al. Bibliometric analysis of the inflammasome and pyroptosis in brain [J]. Front Pharmacol, 2020, 11: 626502.
    Craven R R, Gao X, Allen I C, et al. Staphylococcus aureus alpha-hemolysin activates the NLRP3-inflammasome in human and mouse monocytic cells [J]. PLoS One, 2009, 4(10): e7446.
    Lian N, Chen Y J, Chen S H, et al. Gasdermin D-mediated keratinocyte pyroptosis as a key step in psoriasis pathogenesis [J]. Cell Death Dis, 2023, 14: 595.
    Messingham K N, Cahill M P, Kilgore S H, et al. TSST-1+ Staphylococcus aureus in bullous pemphigoid [J]. J Investig Dermatol, 2022, 142(4): 1032-1039.
    Hu J J, Liu X, Xia S Y, et al. FDA-approved disulfiram inhibits pyroptosis by blocking gasdermin D pore formation [J]. Nat Immunol, 2020, 21(7): 736-745.
    del Mar Ferrà-Cañellas M, Garcia-Sureda L. Exploring the potential of micro-immunotherapy in the treatment of periodontitis [J]. Life, 2024, 14(5): 552.
    Bora P K, Borah G, Kalita D, et al. Mushroom-mediated reductive bioconversion of aldehyde-rich essential oils for aroma alteration: A rose-like floral bioflavor from Citronella oil [J]. J Agric Food Chem, 2023, 71(3): 1690-1700.
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    doi: 10.7501/j.issn.0253-2670.2026.12.017
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    2种不同金属材料的力学参数

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    鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
    小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
    多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
    红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
    小菇属 Mycena 11 5.26
    光柄菇属 Pluteus 5 2.39
    红菇属 Russula 17 8.13
    栓菌属 Trametes 5 2.39
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