Long-term activation of spinal opioid analgesia after inflammation

炎症后脊髓阿片类药物镇痛的长期激活

• 批准号: 9751233
• 负责人: BRADLEY K. TAYLOR
• 金额: $ 58.65万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2018
• 资助国家: 美国
• 起止时间: 2018-08-01 至 2022-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9751233
• 关键词: Absence of pain sensation; Acute; Address; Adenylate Cyclase; Affect; Affective; Agonist; American; Analgesics; Behavior; Behavioral; Binding; Brain; Burn injury; Cutaneous; Cyclic AMP; Cyclic AMP Receptors; Cyclic AMP-Dependent Protein Kinases; Data; Disease remission; Dynorphins; Electrophysiology (science); Enkephalins; Equilibrium; Event; Excitatory Postsynaptic Potentials; Feedback; Goals; Hernia; Homeostasis; Human; Hyperalgesia; Inflammation; Inguinal region; Injury; Knockout Mice; Knowledge; Masks; Mediating; Messenger RNA; Modeling; Molecular; Mus; N-Methyl-D-Aspartate Receptors; N-Methylaspartate; NR1 gene; Naloxone; Naltrexone; Nature; Neurons; Nociception; Nociceptors; Operative Surgical Procedures; Opioid; Opioid Analgesics; Opioid Antagonist; Opioid Peptide; Opioid Receptor; Pain; Pain management; Pathologic; Phase; Phosphorylation; Physical Function; Physiologic pulse; Posterior Horn Cells; Postoperative Pain; Presynaptic Terminals; Process; Productivity; Protein Isoforms; Proteins; Public Health; Publishing; Quality of life; Receptor Activation; Relapse; Resolution; Science; Secondary Hyperalgesias; Site; Slice; Spinal; Spinal Cord; Stress; Synapses; Synaptosomes; Syndrome; System; Testing; Tissues; Translating; Traumatic injury; Vision; Work; adenylyl cyclase 1; allostasis; central sensitization; chronic pain; cost; delta opioid receptor; dorsal horn; endogenous opioids; healing; heat injury; inhibitor/antagonist; innovation; kappa opioid receptors; mental function; mouse model; mu opioid receptors; naltrexol; neurobiological mechanism; pain behavior; pain relief; patch clamp; peripheral pain; prevent; public health relevance; receptor; relating to nervous system; repaired; response; spinal nerve posterior root; spontaneous pain; trafficking

DESCRIPTION (provided by applicant): Severe tissue injury generates central sensitization (increased responsiveness of CNS nociceptive neurons to normal or sub-threshold afferent input) that contributes to hyperalgesia. Latent sensitization (LS) is a silent form of central sensitization that persists after tissue has healed and overt signs of hyperalgesia have resolved. LS can be revealed with opioid receptor antagonists or inverse agonists that "rekindle" or reinstate hyperalgesia. Thus, pain remission during LS is likely maintained by tonic opioid receptor activity that masks the pronociceptive components of LS. LS is important because it primes nociceptive systems such that, when inhibitory systems fail, a pain episode ensues. A key first step in understanding LS is to demonstrate the translational significance, and we now show that the opioid receptor inverse agonist, naloxone, can reinstate experimental pain when delivered 1 wk after the resolution of secondary hyperalgesia following first degree thermal injury. Specific Aim 1 tests the hypothesis that burn or surgery triggers LS and long-term opioid analgesia in humans. To further study the neurobiological mechanisms of LS, we will also use a mouse model that is long-lasting, powerful, broad range, repeatable, and translates to human studies. We found that mu opioid receptor (MOR) inverse agonists reinstated behavioral and molecular signs of hyperalgesia, even when administered months after tissue injury, and this required NMDA receptor activation of adenylyl cyclase type 1 (AC1). Our results are important because they suggest that any event, such as stress, that interferes with MOR analgesia during LS will lead to relapse of hyperalgesia in chronic pain syndromes in humans. Specific Aim 2 tests the hypothesis that MOR constitutive activity (MORCA) and/or activation of MOR, delta (DOR), or kappa (KOR) receptors by opioid peptides in the DH or rostroventromedial medulla maintains endogenous analgesia and thereby restricts LS to a state of pain remission. Specific Aim 3 determines the extent to which MORs inhibit spatially coordinated neural activity in the DH (using an innovative 64-channel field recording system) and synaptic strength in presynaptic terminals of primary afferent nociceptors or on DH neurons (using patch clamp electrophysiology) during LS. Specific Aim 4 then tests whether MORs specifically inhibit spinal NMDA receptor subunits (GluN2A or GluN2B) and/or Epac1 (exchange protein directly activated by cAMP, recently found to contribute to peripheral pain senstization) to block pain during LS. Completion of this project will bring us closer to our long-term goal of alleviating chronic pain b either: a) facilitating endogenous opioid analgesia, thus restricting LS within a state of remission; or b) extinguishing LS altogether, for example with a selective AC1 or Epac1 inhibitor. Our general model and hypothesis shares similarities with the concept of allostasis: a pathologically-elevated balance between opposing processes (MOR and LS) that facilitate each other by mutual feedback. Our long-term vision is a new conceptual strategy for chronic pain therapy, to restore homeostasis, where there is neither central sensitization nor MOR compensatory responses.

描述（由申请方提供）：重度组织损伤产生中枢致敏（CNS伤害感受神经元对正常或阈下传入输入的反应性增加），导致痛觉过敏。潜伏性敏化（Latent sensitization，LS）是一种沉默的中枢敏化形式，在组织愈合和明显的痛觉过敏症状消失后持续存在。LS可以用阿片受体拮抗剂或反向激动剂“重新点燃”或恢复痛觉过敏来揭示。因此，LS期间的疼痛缓解可能是通过掩蔽LS的原伤害感受成分的强直性阿片受体活性来维持的。LS是重要的，因为它启动伤害感受系统，使得当抑制系统失败时，疼痛发作会发生。理解LS的关键第一步是证明其翻译意义，我们现在表明，阿片受体反向激动剂纳洛酮在一级热损伤后继发性痛觉过敏消退后1周给予可以恢复实验性疼痛。具体目标1测试烧伤或手术触发LS和人类长期阿片类镇痛的假设。为了进一步研究LS的神经生物学机制，我们还将使用一种持久，强大，广泛，可重复的小鼠模型，并将其转化为人类研究。我们发现，μ阿片受体（莫尔）反向激动剂恢复痛觉过敏的行为和分子体征，即使在组织损伤后数月给药，这需要腺苷酸环化酶1型（AC 1）的NMDA受体激活。我们的研究结果是重要的，因为他们表明，任何事件，如压力，干扰莫尔镇痛在LS将导致复发的慢性疼痛综合征的人类痛觉过敏。特定目的2检验了以下假设：莫尔组成性活性（MORCA）和/或DH或头腹内侧髓质中阿片肽对莫尔、δ（DOR）或κ（KOR）受体的激活维持内源性镇痛，从而将LS限制在疼痛缓解状态。具体目标3确定MORs抑制DH中空间协调的神经活动（使用创新的64通道场记录系统）和初级传入伤害感受器或DH神经元（使用膜片钳电生理学）的突触前末梢中的突触强度的程度。特异性目的4然后测试MORs是否特异性抑制脊髓NMDA受体亚基（GluN 2A或GluN 2B）和/或Epac 1（由cAMP直接激活的交换蛋白，最近发现有助于外周疼痛敏化）以阻断LS期间的疼痛。该项目的完成将使我们更接近缓解慢性疼痛的长期目标B：a）促进内源性阿片镇痛，从而将LS限制在缓解状态;或B）完全消除LS，例如使用选择性AC 1或Epac 1抑制剂。我们的一般模型和假设与变稳态的概念有相似之处：通过相互反馈相互促进的对立过程（莫尔和LS）之间的病理性升高的平衡。我们的长期愿景是慢性疼痛治疗的新概念策略，以恢复稳态，其中既没有中枢致敏也没有莫尔代偿反应。