Behavioral/neuroendocrine regulation of wound healing

伤口愈合的行为/神经内分泌调节

• 批准号: 6491385
• 负责人: John F Sheridan
• 金额: $ 14.5万
• 依托单位: OHIO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-09-25 至 2004-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6491385
• 关键词: androgens; chemokine; corticosterone; cytokine; gene expression; growth factor; hairless mouse; immunogenetics; inflammation; mifepristone; neuroendocrine system; nuclear factor kappa beta; psychoneuroimmunology; restricted physical activity; stress; stressor; wound healing

DESCRIPTION (adapted from investigator's abstract): The hypothesis of this proposal is that physiologic changes associated with stress, down-regulate pro-inflammatory cytokine, chemokine and growth factor gene expression resulting in alterations in cellular trafficking and activation, thus impairing wound healing. The long term goal of these studies is to understand the mechanisms underlying stress-related changes between the neuroendocrine and inflammatory responses that are responsible for altered wound healing. The aims of the proposal are 1) to determine the influence of stress on the pattern and kinetics of chemokine, pro-inflammatory cytokine and growth factor gene expression during the early stages of wound healing, 2) to determine the stress-induced, neuro-endocrine mechanisms that regulate pro-inflammatory cytokine, chemokine and growth factor gene expression during wound healing and 3) to determine the mechanism of the anti-glucocorticoid actions of androstenediol (a metabolite of DHEA) and delineate its ability to regulate pro-inflammatory cytokines (IL-1 alpha and beta and TNF alpha), chemokines (KC, IP10, MCP-1 and MIP 1 alpha) and growth factor (KGF, VEGF and TGF beta )gene expression as a therapeutic strategy to improve wound healing in stressed individuals. The proposal makes use of histological, molecular biology and pharmacological approaches to address the specific aims. The in vivo study of wound healing is accompanied by in vitro studies of the direct effect of glucocorticoids and AED (a metabolite of dihydroxyepiandrosterone) on cellular expression of transcription factors and cytokines. Restraint stress repeated over several days is to be used as a stress paradigm, skin wounding will be used to determine the rate of healing and the profile of cytokines and chemokines during the healing period. Subsequent studies will use an in vitro approach in which neutrophils and macrophages isolated from female mice will be incubated with corticosterone to determine the effect of LPS induced stimulation of cytokine and chemokine release and on changes in NF-kappa beta. In addition, the influence of AED on wound healing, cytokine and chemokine production and transcription factor NF-kappa beta will also be addressed in vivo.

描述（改编自研究者摘要）：该提案的假设是，与应激相关的生理变化下调促炎细胞因子、趋化因子和生长因子基因表达，导致细胞运输和活化的改变，从而损害伤口愈合。这些研究的长期目标是了解神经内分泌和炎症反应之间的应激相关变化的机制，这些变化是导致伤口愈合改变的原因。该提案的目的是1）确定在伤口愈合的早期阶段应激对趋化因子、促炎细胞因子和生长因子基因表达的模式和动力学的影响，2）确定调节促炎细胞因子的应激诱导的神经内分泌机制，创伤愈合过程中趋化因子和生长因子基因表达的研究; 3）确定雄烯二醇抗糖皮质激素作用的机制（DHEA的代谢物），并描述其调节促炎细胞因子（IL-1 α和β以及TNF α）、趋化因子（KC、IP 10、MCP-1和MIP 1 α）和生长因子（KGF、VEGF和TGF β）基因表达的能力，作为改善应激个体中伤口愈合的治疗策略。该提案利用组织学、分子生物学和药理学方法来实现具体目标。伤口愈合的体内研究伴随着糖皮质激素和AED（二羟基表雄酮的代谢物）对转录因子和细胞因子的细胞表达的直接作用的体外研究。重复数天的束缚应激将用作应激范例，皮肤创伤将用于确定愈合速率以及愈合期间细胞因子和趋化因子的概况。随后的研究将使用体外方法，其中将从雌性小鼠分离的中性粒细胞和巨噬细胞与皮质酮一起孵育，以确定LPS诱导的细胞因子和趋化因子释放刺激以及对NF-κ β变化的影响。此外，AED对伤口愈合、细胞因子和趋化因子产生以及转录因子NF-κ β的影响也将在体内得到解决。