Mechanism of prostatic acid phosphatase-mediated analgesia

前列腺酸性磷酸酶介导的镇痛机制

• 批准号: 7541147
• 负责人: Nathaniel A Sowa
• 金额: $ 2.85万
• 依托单位: UNIV OF NORTH CAROLINA CHAPEL HILL
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-09-01 至 2013-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7541147
• 关键词: Absence of pain sensation; Address; Adenosine; Adenosine Monophosphate; Adult; Adverse effects; Agonist; Analgesics; Animals; Behavioral; Biochemical; Biological Assay; Calcium; Cannabinoids; Cells; Chronic inflammatory pain; Condition; Economic Burden; Event; Fibroblasts; G-Protein-Coupled Receptors; Generations; Genes; Genetic; In Vitro; Incubated; Injection of therapeutic agent; Intrathecal Injections; Knowledge; Lead; Life; Ligands; Lysophospholipids; Measures; Mediating; Medical; Modeling; Molecular Biology; Mus; Nervous system structure; Neurons; Nociception; Numbers; Pain; Pathologic; Pharmacology; Phosphoric Monoester Hydrolases; Production; Productivity; Property; Protein Dephosphorylation; Protein Overexpression; Proteins; Public Health; Purinergic P1 Receptors; Quality of life; Reporting; Role; Signal Pathway; Signal Transduction; Societies; Spinal Cord; Spinal Ganglia; Tactile; Testing; Thermal Hyperalgesias; Time; United States; Work; allodynia; base; chronic pain; day; in vivo; inflammatory pain; lost work time; lysophosphatidic acid; neuronal excitability; neurotransmission; novel strategies; novel therapeutics; prostatic fraction Acid phosphatase isoenzyme; receptor; receptor coupling; response; transmission process

DESCRIPTION (provided by applicant): Chronic pain is a common medical complaint in the United States, reported by over 25% of adults. It is also very costly to treat, and results in additional economic burdens to society through lost work-time and productivity. Current treatments for chronic pain are often ineffective and have dangerous side-effects. Further understanding of pain transmission is needed to allow for new therapeutic strategies to treat this debilitating condition. My long term objectives are to increase our understanding of pain transmission within the nervous system and to provide a potentially novel therapeutic approach for treating pain. We have recently identified that a phosphatase called Prostatic Acid Phosphatase (PAP) is present in pain-sensing neurons. Injection of a soluble form of this protein into the spinal cord results in long-lasting analgesia, while genetic elimination of the protein results in enhanced inflammatory pain responses. The mechanisms of PAPmediated analgesia are unknown, although PAP can produce the analgesic compounds adenosine and cannabinoids in biochemical assays. The specific aims of this proposal are to: first, test if PAP reduces cell signaling in vitro by producing analgesic molecules; second, to test if PAP suppresses pain in vivo by producing analgesic molecules; and third, test if PAP-mediated analgesia is due to decreased neuronal excitability in pain-sensing neurons. I will use a combination of molecular biology and pharmacology to study the activity of PAP in vitro and in live animals. PUBLIC HEALTH RELEVANCE: Understanding the mechanism of PAP-mediated analgesia will provide opportunities to develop novel approaches to treat chronic pain.

描述（由申请人提供）： 慢性疼痛在美国是一种常见的医疗投诉，超过25%的成年人报告。治疗费用也很高，并因工作时间和生产力的损失而给社会造成额外的经济负担。目前对慢性疼痛的治疗往往无效，并有危险的副作用。需要进一步了解疼痛传递，以允许新的治疗策略来治疗这种使人衰弱的疾病。我的长期目标是增加我们对神经系统内疼痛传递的理解，并为治疗疼痛提供一种潜在的新治疗方法。我们最近发现，一个磷酸酶称为前列腺酸性磷酸酶（PAP）存在于痛觉神经元。将这种蛋白质的可溶性形式注射到脊髓中导致持久的镇痛，而基因消除该蛋白质导致增强的炎性疼痛反应。PAP介导的镇痛机制尚不清楚，尽管PAP在生化测定中可以产生镇痛化合物腺苷和大麻素。该提案的具体目标是：首先，测试PAP是否通过产生镇痛分子来减少体外细胞信号传导;第二，测试PAP是否通过产生镇痛分子来抑制体内疼痛;第三，测试PAP介导的镇痛是否是由于疼痛感测神经元中神经元兴奋性降低。我将使用分子生物学和药理学相结合的方法来研究PAP在体外和活体动物中的活性。 公共卫生相关性：了解PAP介导的镇痛机制将为开发治疗慢性疼痛的新方法提供机会。