The Role of Statins in Cutaneous Wound Healing
The Role of Statins in Cutaneous Wound Healing
批准号:
8324546
负责人:
Marjana Tomic-Canic
金额:
$20.66万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-08-25 至 2015-03-31
关键词:
AcuteAgonistAnti-Inflammatory AgentsAnti-inflammatoryAntimicrobial EffectBacterial InfectionsCholesterolClinicalCoenzyme ACollagenCommunitiesCutaneousDataDepositionDiseaseDoseElderlyEnzyme-Linked Immunosorbent AssayExperimental ModelsFamily suidaeGlucocorticoid ReceptorGoalsGranulation TissueHealedHydroxyl RadicalHyperlipidemiaImpairmentIn VitroIncidenceIndividualInfiltrationInflammatoryInflammatory ResponseKnowledgeLeadLearningMeasuresMediatingModelingMolecularMorbidity - disease rateNuclearObesityOxidoreductasePainPathway interactionsPatientsPharmaceutical PreparationsPhosphorylationProcessRegulationResearchRoleSiteSkinSpecimenSterolsTestingTherapeutic UsesThickTopical applicationWound HealingWound Infectionangiogenesisantimicrobialbasecytokinediabeticexperiencefarnesyl pyrophosphatehealinghigh riskimprovedin vivoin vivo Modelinhibitor/antagonistinsightkeratinocytemacrophagemethicillin resistant Staphylococcus aureusmevalonatemigrationneutrophilnovel therapeutic interventionnovel therapeuticspre-clinicaltissue repairwound
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Hyperlipidemia and obesity are well known factors that inhibit wound healing. Conversely, statins, the 3- hydroxyl-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors that lower circulating cholesterol levels improve tissue repair. Recently, we have identified molecular mechanism by which statins accelerate wound healing. We found that statins promote wound healing, via blocking the synthesis of Farnesyl pyrophosphate (FPP), an important branch-point intermediate in the mevalonate pathway, essential for synthesis of sterols and isoprenylated cellular metabolites leading to cholesterol synthesis. FPP inhibits keratinocyte migration in vitro and wound healing ex vivo by acting as an anti-inflammatory agent, i.e. a bona fide agonist for glucocorticoid receptor (GR), whereas statins reverse this effect. Therefore, we hypothesize that statins may accelerate wound healing by modulating the inflammatory response. This hypothesis will be tested using topical statins on hyperlipidemic and healthy (normolipidemic) porcine wound healing model in vivo. Once an optimal topical dose of statins is determined (Aim 1) we will determine the effects of statins on the inflammatory response by measuring levels of pro- and anti-inflammatory cytokines, GR- phosphorylation as well as neutrophil and macrophage infiltration in hyperlipidemic and normolipidemic porcine wound model (Aim 2A). Recently, statins were found to have anti-microbial effect. Bacterial infection is one of the most common complications of wound healing, known to inhibit this process. Thus, we will also test if topical statins alone or in combination with systemic statins, accelerate wound healing of bacterially-infected wounds (Aim 2B). The high impact of proposed study is multi-factorial: 1) it will provide a validated in vivo experimental models to study cutaneous wound healing and infection related to obesity and high cholesterol levels; 2) develop pre- clinical evidence for potential topical use of statins to treat wound healing disorders and 3) provide new insights into the mechanism by which statins may impact healing ability of wounds in patients who are using them systemically.
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会议论文
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