Role of astroglia in cocaine-induced neurotoxicity

描述（由申请人提供）：本提案的重点是开发一种新的原型光学扩散荧光（ODF）探针的技术，用于体内研究星形胶质细胞在可卡因诱导的血流动力学，代谢和大脑功能中的作用。所讨论的光学探针是独特的，因为它使用多个波长在体内以高时间分辨率同时跟踪脑血容量（CBV），血红蛋白（HbO2），脱氧血红蛋白（HbR）和细胞内钙（[Ca++]）i。我们已经在活体啮齿动物中建立了新探针设计的原理证明，最近获得的结果表明，静脉注射可卡因和局部麻醉剂利多卡因后，皮质[ca++]i显著增加，而哌甲酯没有，这表明可卡因的局部麻醉特性而不是其儿茶酚胺能作用是这种效果的基础。我们假设可卡因诱导的[Ca++]i增加是潜在有害的，因为[Ca++]i增加会使组织更容易受到继发于脑血流量的潜在减少的缺血，否则不会引起缺血和/或细胞损伤。我们建议进一步发展ODF技术，以分离可卡因诱导的[Ca++]i增加的细胞来源。我们的主要假设是，可卡因诱导的[ca++]I反应来自星形胶质细胞，而不是神经元。我们进一步假设谷氨酸在一定程度上介导了在皮层中观察到的星形细胞[Ca++]的增加。为了验证我们的假设，我们提出了以下具体目标：i)证明ODF探针与钙敏感荧光染料Rhod-2 （AM）和细胞特异性组织加载技术相结合，可以在体内用于区分神经元和星形胶质细胞网络中的[Ca++]i动态，同时跟踪CBV， HbO2和HbR的变化；ii)证明ODF探针测量的可卡因诱导的[ca++]i反应部分源自星形胶质细胞；iii)可卡因诱导的[Ca++]i升高可被选择性代谢代谢谷氨酸受体1 （mGluR1）拮抗剂阻断。这个研究领域的重要性毒瘾将是1)首次实现一个新的实验方法,能够跟踪(Ca + +)我从特定的瞬变,大细胞种群(星形神经胶质细胞)在体内中枢神经系统,2)直接解决cocaine-induced星形神经胶质细胞的作用的大脑功能的变化生活动物和3)首次获得信息(Ca + +)我cb v动力同时,都未正常和可卡因暴露大脑中HbO2和HbR的变化。我们的长期目标是进一步巩固和简化ODF探针技术，以评估大脑功能和氧含量，从而使广泛的神经科学界进入药物成瘾研究领域的进一步研究。关于星形胶质细胞在成瘾过程和/或滥用药物的神经毒性中的作用的新信息将有可能导致确定新的治疗靶点和新的治疗策略，这将有利于公共卫生。本研究的重点是开发一种用于药物成瘾研究的新型光学扩散荧光探针的原型技术。这项研究与公共卫生的相关性在于，与目前的技术（共聚焦和双光子显微镜）相比，新的探针价格低廉，因此研究人员可以广泛使用，从而有助于加强我们对导致吸毒成瘾的过程的理解，并最终对其进行治疗和预防。

DESCRIPTION (provided by applicant): This proposal focuses on developing technology for a new prototype optical diffusion fluorescence (ODF) probe to be used in vivo to study the role of astroglia cells in cocaine-induced effects on hemodynamics, metabolism and function in the brain. The optical probe in question is unique because it uses multiple wave- lengths to track cerebral blood volume (CBV), oxyhemoglobin (HbO2), deoxyhemoglobin (HbR) and intracellular calcium ([Ca++])i simultaneously at high temporal resolution in vivo. We have established proof-of- principle of the new probe design in the living rodent and recently obtained results demonstrating significant increases in cortical [Ca++]i following intravenous administration of cocaine and the local anesthetic lidocaine but not with methylphenidate indicating that cocaine's local anesthetic properties but not its catecholaminergic actions underlie this effect. We hypothesized that the cocaine-induced [Ca++]i increases are potentially harmful because the [Ca++]i increases would make the tissue more vulnerable to ischemia secondary to potential decreases in cerebral blood flow which would otherwise not induce ischemia and/or cell damage. We are proposing to further develop the ODF technology to isolate the cellular origin of the [Ca++]i increases induced by cocaine. Our main hypothesis states that the cocaine-induced [Ca++]I response originates from astroglia cells and not from neurons. We further hypothesize that glutamate in part mediates the increases in astrocytic [Ca++]i observed in cortex. To test our hypothesis we propose the following specific aims: i) To demonstrate that the ODF probe in combination with the calcium-sensitive fluorescence dye Rhod-2 (AM) and cell-specific tissue loading technology can be used to differentiate [Ca++]i dynamics in neuronal and astroglia cellular networks in vivo while simultaneously tracking changes in CBV, HbO2 and HbR; ii) To demonstrate that the cocaine-induced [Ca++]i response measured by the ODF probe originate in part from astroglia cells; iii) that the cocaine-induced [Ca++]i increases can be blocked by a selective metabotrobic glutamate receptor 1 (mGluR1) antagonist. The significance of this research to the field of drug addiction will be to 1) implement for the first time a new experimental methodology which is capable of tracking [Ca++]i transients from specific and large cell populations (astroglia cells) in the central nervous system in vivo, 2) directly address the role of astroglia cells in cocaine-induced changes in brain function in the living animal and 3) for the first time obtain information on [Ca++]i dynamics simultaneously with CBV, HbO2 and HbR in the normal and cocaine-exposed brain in vivo. Our long-term goal is to further solidify and simplify the ODF probe technology to assess brain function and oxygen content, thereby, allowing broad neuroscience community access to further studies in the area of drug addiction research. New information on the role of astroglia cells in the addiction process and/or neurotoxicity of drugs of abuse will potentially lead to identification of new treatment targets and new therapeutic strategies which will benefit public health. This proposal focuses on developing technology for a new prototype optical diffusion fluorescence (ODF) probe to be used in drug addiction research. The relevance of this research to public health is that the new probe in comparison to current technology (confocal and two-photon microscopes) is affordable and therefore can become widely accessible to researchers and thus help enhance our understanding of processes leading to addiction to drugs of abuse and ultimately to its treatment and prevention.