Spinal Cord Transplants of GABAergic Precursor Cells to Treat Chronic Pain

GABA能前体细胞脊髓移植治疗慢性疼痛

• 批准号: 9084660
• 负责人: Allan I. Basbaum
• 金额: $ 33.91万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-09-28 至 2017-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9084660
• 关键词: Acetylcholine; Adult; Adverse effects; Animals; Behavior; Cell Therapy; Cell Transplantation; Cell Transplants; Cells; Characteristics; Clinical; Clozapine; Development; Disease; Dose; Electrons; Electrophysiology (science); Elements; Embryo; Freund' s Adjuvant; G-Protein-Coupled Receptors; GABA transporter; Genetic Engineering; Human; Hyperalgesia; Hypersensitivity; Immunoelectron Microscopy; In Vitro; Injury; Interneurons; Label; Mechanics; Medial; Mediating; Microscopic; Modeling; Mus; Muscarinic Acetylcholine Receptor; Nerve; Nerve Tissue; Neurodegenerative Disorders; Neurons; Nociceptors; Oxides; Paclitaxel; Pain; Patients; Peripheral; Peripheral nerve injury; Persistent pain; Pharmaceutical Preparations; Phenotype; Preparation; Process; Property; Recovery; Regulation; Resolution; Slice; Specificity; Spinal Cord; Spinal cord posterior horn; Synapses; TRPV1 gene; Testing; Therapeutic; Thermal Hyperalgesias; Tissues; Tracer; Transgenic Organisms; Transplantation; Variant; allodynia; chemical genetics; chemotherapeutic agent; chemotherapy; chronic constriction injury; chronic pain; design; designer receptors exclusively activated by designer drugs; experience; functional improvement; gamma-Aminobutyric Acid; genetic approach; in vivo; inhibitory neuron; mechanical allodynia; nerve injury; neuronal circuitry; novel; novel therapeutic intervention; painful neuropathy; postsynaptic; precursor cell; spontaneous pain; success; symptom management

DESCRIPTION (provided by applicant): Loss of inhibitory circuits in the spinal cord dorsal horn is one of the major contributors to persistent pain following nerve injury (neuropathic pain). The loss of inhibition contributes not only to the development of spontaneous pain, but also to the hyperexcitability that underlies the allodynia and hyperalgesia that are characteristic of thes clinical conditions. Pharmacological management of nerve injury-induced neuropathic pain is directed at enhancing inhibitory controls, but unfortunately, not all patients are responsive to such therapies. Furthermore, adverse side effects, which arise because treatments typically involve systemic drug administration, often limit the use of effective doses. We propose to develop a novel therapeutic approach (transplantation of precursor inhibitory neurons) that is designed to restore the inhibitory controls in the spinal cord. The treatment regime differs from traditional pharmacological therapies that are directed at symptom management; transplantation to replace missing interneuronal control is a disease modifying approach. Transplantation of embryonic precursor cells has, in fact, resulted in functional improvement in various neurodegenerative diseases, but still very little is known about the underlying therapeutic mechanisms and the extent to which connectivity exists between grafted cells and host tissue. We propose to transplant cells derived from the mouse embryonic medial ganglionic eminence (MGE). In Specific Aim 1, we will continue our analysis of the circuits in which the transplants participate and will use electrophysiology to assess the extent to which inhibitory controls derive from the transplants. In Specific Aim 2, we will assess the ability of the transplants to alleviate the persistent pain produced by peripheral nerve injury, including those produced by chemotherapeutic agents. Using selective antagonists to counter the effects of the transplants, we will determine whether GABA is indeed the major contributor to recovery. Finally, in Specific Aim 3, we will use a novel chemical-genetic approach to achieve in vivo spatio-temporal control of the activity of the transplants. These studies will establish that MGE-derived cells have the essential properties for a cell-based therapy, particularly when loss of inhibitory control is a major contributor to the clinical condition. Success in this endeavor will establish the proof of concept necessary for eventual studies of cell transplantation for persistent pain in humans.

描述(申请人提供)：脊髓后角抑制回路的丧失是神经损伤后持续性疼痛(神经病理性疼痛)的主要因素之一。 抑制的丧失不仅导致自发性疼痛的发展，而且还导致以这些临床情况为特征的超常痛觉和痛觉过敏的过度兴奋性。神经损伤引起的神经病理性疼痛的药物治疗旨在加强抑制控制，但不幸的是，并不是所有的患者对这种治疗都有反应。此外，由于治疗通常涉及全身给药而产生的不良副作用往往会限制有效剂量的使用。我们建议开发一种新的治疗方法(前体抑制神经元移植)，旨在恢复脊髓的抑制控制。治疗方案不同于针对症状管理的传统药物治疗；移植取代缺失的神经元间控制是一种改善疾病的方法。事实上，胚胎前体细胞移植已经导致了各种神经退行性疾病的功能改善，但对其潜在的治疗机制以及移植细胞与宿主组织之间的连接程度仍知之甚少。我们建议移植来自小鼠胚胎内侧神经节隆起(MGE)的细胞。在具体目标1中，我们将继续分析移植物参与的回路，并将使用电生理学来评估抑制控制产生的程度。 从移植来的。在具体目标2，我们将评估移植的能力，以缓解 周围神经损伤引起的持续性疼痛，包括化疗药物引起的疼痛。使用选择性拮抗剂来对抗移植的影响，我们将确定GABA是否确实是恢复的主要贡献者。最后，在具体目标3中，我们将使用一种新的化学遗传方法来实现体内移植活动的时空控制。这些研究将确定MGE来源的细胞具有以细胞为基础的治疗的基本特性，特别是当抑制控制的丧失是导致临床状况的主要因素时。这一努力的成功将为细胞移植治疗人类持续性疼痛的最终研究奠定必要的概念证据。