作者感谢朱蒂丝兰格, 玛丽亚 Karg, Grégoire Friz, 雷切尔哈伯历和玛丽克莱尔 Pflimlin 从罗氏和 Tifany 马丁·舍尔和黛博拉保卢奇从 HiQScreen 为他们出色的技术援助。

爪蟾被安置和处理根据日内瓦小行政区动物指南。
1. 放射配基装订
<ol><li>
测定板的制备
	<ol>
<li>用5毫米氯化钾、1.25 毫米 CaCl2、1.25 毫米氯化镁2、120毫米氯化钠和15毫米三种方法制备 1.5 L 的测定缓冲器;用 HCl 调整 pH 值为7.4。</li>
		<li>准备在50.76 µM (例如, 5 µL 化合物10毫米到980µL 化验缓冲区在离心管) 测试的化合物。用涡流机在高速2–5的情况下混合。</li>
		<li>吹打1µL 的化合物 (10 毫米) 到1970µL 的检测缓冲剂, 制备参考化合物马西尼的预稀释。用涡流机在高速2–5的情况下混合。</li>
		<li>稀释 [3H] 马西尼股票溶液与化验缓冲器在4°c 到4毫微米在50毫升聚丙烯管。</li>
		<li>吸管50µL/井的化验缓冲区进入1和3–11的96井微板块, 如图 2所示的板块布局显示。</li>
		<li>吸管73.2 µL 的化合物稀释在50.76 µM (见步骤 1.1.2) 到12栏的板块。</li>
		<li>稀释每个化合物, 使用几何级数超过9步 (1E-10 -1E-06米), 23.12 µL 传输量和填充柱3–11。彻底混合稀释。每次稀释后都要改变笔尖。</li>
	</ol>
</li>
	<li>
稀释细胞膜
	<ol>
<li>解冻先前从 HEK293 overexpressing 人 GABAA受体 (0.025–0.15 毫克/毫升) 中分离出来的细胞膜, 在室温下获得80毫升, 并将悬浮液转移至4摄氏度的化验缓冲器。</li>
		<li>并用重悬膜溶液仍然在4°c 与组织均质体为 30–40 s 在 10,000–12,000 rpm。</li>
	</ol>
</li>
	<li>
稀安定用于非特定结合 (NSB) 控制
	<ol>
<li>将4毫米安定的溶液稀释成5毫升的浓度为40µM 的测定缓冲液。</li>
	</ol>
</li>
	<li>
开始反应
	<ol>
<li>吸管50µL 4 毫微米 [3H] 马西尼入96井板材的每个井并且保持它在一个冰水容器。</li>
		<li>添加100µL 的 GABAa受体亚型膜制备有 0.5mg/毫升的蛋白质浓度。</li>
		<li>吸管50µL 40 µM 安定入专栏2。</li>
		<li>在冰上孵化1小时的盘子。</li>
		<li>在96井滤板的每个井中添加50µL, 用于后续膜分离和放射性测量, 随后停止反应。</li>
	</ol>
</li>
	<li>
停止反应
	<ol>
<li>准备一个洗涤缓冲器与50毫米三 HCl, pH 值7.4。</li>
		<li>使用96井细胞收割机过滤解决方案。用300µL 的冷水洗涤缓冲液将板材洗净3x。</li>
		<li>用塑料薄膜封住盘子的底部, 并添加40µL 的闪烁鸡尾酒, 用于每个井中的液体闪烁计数, 并用乙醇70% 擦拭。</li>
		<li>在 RT 中轻轻摇动盘子至少1小时。让它至少在 RT 上再坚持一个小时。</li>
		<li>通过将盘子放在闪烁计数器上测量放射性 (在 CPM 中)。允许测量每井3分钟。</li>
	</ol>
</li>
	<li>
数据分析
	<ol>
<li>确定8复制非特定绑定 (NSB) 和总绑定 (TB) 以及样本的重复或 triplicates 的平均值。根据以下公式计算每个样本的平均值的% 特定绑定 (SB): <img alt="Equation 1" src="/files/ftp_upload/57842/57842eq1.jpg"> 这里 总某人= 平均 TB 减去平均 NSB。</li>
		<li>在横坐标中, 在调节抑制剂浓度时, 将其与对照。使用单一站点竞争分析公式拟合数据: <img alt="Equation 2" src="/files/ftp_upload/57842/57842eq2.jpg"> 这里 y = 某人的%, 最小的y, B = 最大y, C = IC50, X = 竞争化合物浓度的对数10 , D = 曲线的斜率 (一个小山系数)。</li>
		<li>用半最大抑制浓度 (IC50) 计算结合亲和性 (基), [3h] 马西尼在各自膜9上的离解常数 (Kd) 和 [3h] 的浓度马西尼在化验中根据以下数据使用等式: <img alt="Equation 3" src="/files/ftp_upload/57842/57842eq3.jpg">
</li>
	</ol>
</li>
</ol>2.爪蟾卵母细胞的受体表达和记录
<ol><li>卵巢采集与卵母细胞的制备
	<ol>
<li>制备无菌 Barth 溶液, 88 毫米氯化钠, 1 毫米氯化钾, 2.4 毫米 NaHCO3, 10 毫米 HEPES, 0.82 毫米 MgSO4. 7H2o, 0.33 毫米钙 (NO3)2. 4H2o, 0.41 毫米 CaCl2. 6H2o, pH 值7。4, 辅以100单位/毫升青霉素, 100 µg/毫升链霉素和0.25 µg/毫升两性霉素 B。</li>
		<li>准备 1x OR2 培养基 (no CaCl2) 与88.5 毫米氯化钠, 2.5 毫米氯化钾, 5 毫米 HEPES, 1 毫米氯化镁2. 6H2O, pH 值7.4。</li>
		<li>在冷却的 Tricaine 甲磺酸 (浓度为150毫克/升, 调整在 pH 7.4) 和碳酸氢钠 (300 毫克/升) 后, 以20分钟的深度麻醉, 牺牲一只爪蟾女性, 然后斩首。</li>
		<li>用干净的剪刀和镊子迅速收获卵巢, 并将其放置在2培养皿 (10 厘米), 填充40毫升 1x Barth 溶液和抗生素/防霉。</li>
		<li>将非游离卵巢存放在 Barth 溶液中长达2周, 达到4摄氏度。</li>
		<li>为离解, 切开卵巢与干净剃刀刀片在小组分 (3) 并且孵化他们在50毫升 OR2 培养基没有 CaCl2 (OR2-noCaCl2) 包含0.2% 个胶原酶 (I 型) 在17–19°c 在100毫升整流罩瓶与缓慢的搅拌第4-5 h. 验证磁条是否放置在微调瓶底部约3–5厘米, 以避免粉碎卵母细胞。</li>
		<li>在第4-5 h 之后, 验证大多数卵母细胞是从卵泡中释放出来的 (也就是说, 它们单独游动)。用200毫升的 OR2 1.8 毫米 CaCl2洗净他们的5x。</li>
		<li>将 defolliculated 卵母细胞转移到培养皿 (10 厘米), 填充 Barth 溶液和抗生素/antimycotics, 并使它们至少在17摄氏度前一夜间在 cDNA 或 mRNA 注射之前。</li>
		<li>第二天, 在双目下选择一个健康的卵母细胞, 它呈现出一种清晰而独特的动物与植物极 (用于植物极的暗褐色与淡黄色)。使用干净的巴斯德吸管, 并将卵母细胞一个一个地处理成无菌的锥形96注入井板。 注: 在放置卵母细胞时, 不需要特别注意注射;而对于 cDNA 注射来说, 将卵母细胞定向到向上的动物极是必不可少的。</li>
	</ol></li>
	<li>mRNA 或 cDNA 自动注射
	<ol>
<li>根据推荐的说明, 使用商业上可用的工具包合成基因。用 RNase 清洁仪器和桌子, 戴上适当的防护手套。 注意: mrna 的质量是决定表达良好的决定性因素, 在注射过程中防止 mrna 降解是必不可少的。</li>
		<li>使用商用套件准备基因, 并在 bidistilled 水中溶解所需量, 浓度为0.2 µg/µL。</li>
		<li>注射10–50的 mRNA 溶液浓度为0.2 µg/µL, 或 10 nL 的 cDNA 溶液在浓度范围从0.02–0.2 µg/µL, 最好是分批95卵母细胞。</li>
		<li>对于需要多个亚基的膜蛋白 (即异型缝隙连接α1β2γ2氨基丁酸A受体), 将相应的基因或基因混合在所需比例 (即1:1: 1 或 1:10:1)。</li>
		<li>将卵母细胞保持在17摄氏度, 以防止卵母细胞对热休克蛋白的表达;将微板块存储在一个温度控制的存储区域中。</li>
		<li>在0.1–1,000 µM OR2 的结合试验中, 溶解测试的化合物, 用于电生理记录, 并在96井平底聚丙烯板上处理。</li>
	</ol></li>
	<li>表达的质粒
	<ol>
<li>遵循商业可用的试剂盒的指导手册, 为 mRNA 合成与细菌 T7 或 T6 助剂, 并使20µL 的解决方案在0.2 µg/µL 在 RNase 无水。</li>
		<li>准备至少20µL 的溶液, 其中含有真核细胞表达载体的 cDNA 表达, 通常在 bidistilled 水中溶解的0.2 µg/µL。</li>
	</ol></li>
	<li>卵母细胞显微注射及其质量的可视化
	<ol>
<li>注射含有质粒的溶液的 10–50 nL (见步骤2.3.1 或 2.3.2), 使用玻璃微注射针, 顶端直径可达100µm 安装在机器人装有压力弹射系统或自动注射系统。 注: 在这里讨论的例子中, 卵母细胞由95批次注射, 其自动化系统适合用于 cDNA 或 mRNA。</li>
		<li>用1µL 的染料 (如亚甲基蓝) 填充注射针 1%, 并使用标准程序 (无论是在细胞核中的 cDNA 或细胞质中的 mRNA) 注射卵母细胞。</li>
		<li>将注射卵母细胞在沸水中释放约1分钟。在双目下用剃刀刀片将卵母细胞切成两半。 注: 染料保持本地化, 如图 3E所示, 允许对注射进行精确观察。</li>
	</ol></li>
	<li>双电极电压钳记录
	<ol>
<li>将含有卵母细胞的井板放在自动系统上, 使用图 4所示的原理。 注: 与图 5所示的膜片钳系统相比, 该电池的真实膜电位是由电压电极读取的。</li>
		<li>使用基于图标的界面编程自动记录系统, 例如,图 6所示的方案确定浓度活动关系。</li>
	</ol></li>
	<li>曲线拟合
	<ol>
<li>使用适当的软件分析结果, 使用图示的浓度活化曲线, 将电流振幅绘制为激动剂浓度对数的函数。</li>
		<li>观察 sigmoidal 曲线, 随后可以在形式上与经验性的希尔方程配合使用: <img alt="Equation 4" src="/files/ftp_upload/57842/57842eq4.jpg"> 这里 Y= 诱发电流的分数, 欧共体50 = 集中为50% 激活, x = 化合物的浓度, nH = 小山系数或明显的协同。</li>
		<li>通过将每个响应的振幅除以最高浓度记录的值来分析从一系列单元获得的数据, 将电流正常化为统一。</li>
		<li>通过标准可用软件, 确定平均误差和标准偏差, 实现曲线拟合。</li>
	</ol></li>
</ol>3. 脑切片的电生理记录
注: 海马大鼠切片是根据国家和机构指南编写的。
<ol><li>
海马切片的制备
	<ol>
<li>准备解剖人工脑脊髓液 (dACSF) 与124毫米氯化钠 124, 2.5 毫米氯化钾, 1.25 毫米的 CaCl 2PO4, 2 毫米 MgSO4. 7H2o, 2.5 毫米2 2H2o, 26 毫米 NaHCO3, 10 毫米葡萄糖和4毫米蔗糖在瓶子里掺入 95% O2和 5% CO2的混合物。</li>
		<li>准备记录人工脑脊髓液 (rACSF), 124 毫米氯化钠, 5 毫米氯化钾, 1.25 毫米的2PO4, 2 毫米 MgSO4. 7H2o, 2.5 毫米 CaCl2 2H2o, 25 毫米 NaHCO3, 10 毫米葡萄糖在瓶子里掺入 95% O2和 5% CO2的混合物。</li>
		<li>麻醉大鼠使用2.5% 异氟醚和纯氧的混合物, 并斩首它们。</li>
		<li>用一把细剪刀剪下中线的头皮。沿中线切开头骨, 不损害底层组织。用镊子取出头骨, 用细铲铲出大脑。</li>
		<li>将大脑放在 RT 的毒气 dACSF 溶液中, 用细铲解剖左海马的形成。</li>
		<li>将横片 (400 µm 厚) 从海马体的中等部位切割成组织斩波器, 并用画笔将其转移到录音室。保持45分钟的 RT 切片。</li>
		<li>灌注的切片与毒气 rACSF 在35摄氏度和以1.5 毫升/分钟的速度. 气泡溶液与 95% O2和 5% CO2的混合物。 注意: 在这一步之后, 切片已经准备好进行电生理实验。</li>
	</ol>
</li>
	<li>
单种群穗记录
	<ol>
<li>将脑切片放入显微镜下的腔室。</li>
		<li>灌注的速度为3毫升/分钟与 rACSF。</li>
		<li>拉一杯硼硅酸盐玻璃微与具有 2 MΩ电阻的吸管拉出器。 注: 此微用作记录电极, 并与放大器电连接。</li>
		<li>用含有2米氯化钠的溶液填充微, 将其放入放大器的吸管支架中。</li>
		<li>用右机器人将记录微定位在海马片 CA1 区 pyramidale 地层中。 注意:图 7中的位置以示意图表示。</li>
		<li>将绝缘双极铂/铱电极置于左侧机器人的支架上。 注: 此电极用作刺激电极, 并与刺激发生器电连接。</li>
		<li>用右机器人将刺激电极定位在海马片 CA1 区的谢弗络中。 注意:图 7中的位置以示意图表示。</li>
		<li>每三十年代使用刺激发生器将电流脉冲传递给刺激电极 (100 µs 持续时间, 从10µA 开始), 并逐渐增加刺激强度直到出现人口峰值 (PS)。</li>
		<li>调整刺激强度以唤起与可获得的最大振幅的45% 对应的 PS。PSs 被过滤在2.4 赫和数字化在20赫使用信号放大器。</li>
	</ol>
</li>
	<li>
配对脉冲抑制
	<ol>
<li>准备脑切片 (步骤 3.1) 并按照前面的描述进行 (步骤 3.2. 1–3.2 7)。</li>
		<li>使用刺激发生器, 每三十年代交付两个电流脉冲 (100 µs 持续时间在20毫秒间隔) 到刺激电极。设置刺激强度来唤起一个对应于最大振幅的45% 的 PS。</li>
	</ol>
</li>
	<li>
复合测试
	<ol>
<li>使稀释的化合物在毒气 ACSF 中进行测试, 使亚砜的最终浓度不高于0.1%。</li>
		<li>在与复合溶液相同浓度的控制溶液中添加亚砜。</li>
		<li>记录单个 (步骤 3.2) 或配对脉冲 (步骤 3.3) PS 诱发的谢弗间接刺激每三十年代至少30分钟。PS 形状在这个基线期间应该是稳定的。</li>
		<li>准备一个装有含毒气 rACSF 的烧杯, 以测试该化合物的固定浓度。</li>
		<li>灌注海马切片与这个解决方案, 而仍然记录单或配对脉冲 PS。</li>
		<li>通过灌注片与无化合物的加毒气 rACSF 来评价复合效应的恢复。 注: 对于可逆效果, PS 还原为在复合应用程序之前的基线期间观察到的初始形状。</li>
	</ol>
</li>
	<li>
数据分析
	<ol>
<li>使用数据分析软件在4块实验过程中记录的 PS 痕迹平均值。</li>
		<li>测量平均迹线的 PS 振幅。</li>
		<li>将振幅正常化为在灌注化合物之前记录10分钟的基线值的百分比。</li>
		<li>将数据表示为平均值。</li>
	</ol>
</li>
</ol>

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作者弗雷德里克·帕西 Knoflach 和玛丽亚-克莱门的雇员是霍夫曼-罗氏股份公司, 4070 瑞士巴塞尔, 一家制药公司。作者丹尼尔. HiQScreen Sàrl 6, Compois, 1222 Vésenaz 瑞士日内瓦, 为制药公司提供甄别设施的雇员。

在配体-门控离子通道上活性的新型化合物的开发, 如 GABA 受体需要使用多种方法。通常, 第一步通常是使用结合分析进行的;然而, 这种测量不足以描述化合物的生理活动或其精确的药理学。特别是, 与受体结合的化合物可以增强或抑制其功能, 甚至不产生功能性影响 (即, 在不改变其功能的情况下绑定到受体)。因此, 一个完整的复合特性需要一个功能测试。
装订化验: 结合试验的主要优点是, 它可以有效地进行大量的样品, 范围达数以千计, 它为活性分子提供了具有约束力的亲和力。如本文所述, 第一步包括建立一个评估所需受体亚型的方法。也就是说, 虽然结合可以对本地受体从分数或整个大脑, 这样的方法将防止确定的亲和力在特定的受体亚型。因此, 有必要使用重组系统在所需目标上筛选分子。目前, 在细胞系中对所需受体亚单位基因的瞬态或稳定转染提供了一种有效而可靠的方法来表达感兴趣的受体亚型 (如GABAa α5β3γ2)。传统的结合检测利用 radioligands, 但现在的技术可以避免处理放射性的不便 (例如, 定量荧光基配体结合)。
主机系统中的函数表达式: 为了表达宿主系统中的基因, 必须将感兴趣的编码序列插入包含适当助剂的质粒中。通常, 对于体外mRNA 合成, 使用细菌 T7 或 T6 助剂。对于 cDNA 表达, 感兴趣基因的转录必须由真核细胞助剂 (巨细胞病毒) 或等效物来调节。现在, 有几个质粒, 包括两个助剂 (即pUNIV, pCMV-6AC, psf-CMV/T7, pCI-新, pcDNA), 可以允许在体外合成 mRNA 或 cDNA 表达式, 如图 15所示。氨基丁酸受体的表达可以忠实地获得在细胞系或爪蟾卵母细胞。后者的主要优点是缺乏内源性受体表达、操作的简单性以及用于微注射和录音的自动化系统的有效性。本协议中描述的程序说明了自动系统的效率, 允许在大约7分钟内注射96只卵母细胞, 不需要微操作系统技能。记住, 在10,000–30,000 卵母细胞之间的一个单一的卵巢从爪蟾包含, 很明显, 大量的细胞测量可以进行一个单一的准备。此外, 作为一个表达可以使用 cDNA 注射, 相同的质粒含有的基因, 为结合实验开发的兴趣, 可以用于功能表征, 而无需进一步的分子生物学操作。
由于它的大面积和高表面表达, 一个单一的卵母细胞产生了一些受体, 大约相当于35毫米培养皿中的汇合细胞。然而, 卵母细胞的制备和注射是细胞系成本的一小部分, 因为实验不需要特定的培养基和无菌操作。一个单一的 GABA 的激活通道产生一些 picoamperes (10-12) 和电流范围高达十 microampere (10-6) 很容易记录在一个单一的卵母细胞, 这证实了伴随的活动, 数以百万计的受体在一个单一的反应。
在配体-门控离子通道的表征中, 第一步通常是受体的明显亲和性的测定。需要进行的实验包括应用一系列短暂的激动剂测试脉冲和绘制诱发电流的振幅, 或者在某些情况下, 将曲线下的区域作为激动剂浓度对数的函数。由于在同一批卵母细胞中 microinject 不同质粒浓度和比值是很容易的, 这种表达系统特别适合于这种特征。此外, 批对批次的比较显示, 在不同的 EC50s 的高度稳定性。亚单位组成对受体的明显亲和性的影响是容易形象化使用蜘蛛情节, 如图 10所示。
在爪蟾卵母细胞中获得的双电极电压钳的结果往往与使用膜片钳电极的录音进行比较。虽然它将超出这项工作的范围, 深入到这两个系统之间的详细比较, 有几个点可以审查。虽然细胞中的膜片钳为生物物理特性的快速药物应用提供了优势, 但它的要求比爪蟾卵母细胞的双电极记录更复杂。第一个和不可忽略的困难是一个特定的蛋白质的表达与细胞培养的必要性, 瞬变或稳定的转染, 以及表达所需结构的细胞的标识。此外, 研究细胞内源表达的可能贡献也是必不可少的。此外, 膜片钳记录要求有技能的人在高放大显微镜下进行微操作系统, 而该人也需要在实验期间进行充分的分析, 以评估, 例如, 密封的质量,接触电阻等, 双电极电压钳记录, 特别是使用自动电生理系统, 不需要任何具体技能, 可以由实验室技术员进行。
在获得电生理设置时, 成本考虑无疑是需要仔细分析的一个重要因素。例如, 虽然自动化系统的成本相对较高, 但更接近的比较表明, 安装完整的电生理平台包括购买设备, 如良好的并联, 双目透镜, 放大器, 灌注系统, 以及一个反振动表, 同时也获取数据和执行分析。两电极电压钳设置与膜片钳设置之间的成本比较显示出更大的差异。此外, 自动化系统还提供了全自动设备的优点, 日夜无人值守。
化合物的药理性质由受体的作用方式决定。例如, 竞争性抑制剂是分子, 可以进入相同的捆绑口袋, 或 orthosteric 网站, 因为激动剂本身导致竞争。非竞争性抑制剂是抑制受体的化合物, 在另一地点相互作用, 在配体-门控离子通道的情况下, 可以进入和阻断离子孔隙, 例如。这将超出这项工作的范围, 以审查不同的互动机制, 但进一步的信息可以获得从药理教科书和/或其他工作, 如22。
在构调制器的情况下, 化合物绑定在一个与 orthosteric 站点不同的站点上, 但分子的存在改变了活动状态和其他状态之间的能量屏障。正构调制器 (PAMs) 是一种能将能量屏障从静止状态减少到活性态的化合物, 因此增强了激动剂的作用。为了描述可能的 PAM 效应, 因此, 有必要确定接触到化合物是否增强了对激动剂的反应, 如果是这样, 那么浓度。图 11和图 14所示的实验说明了可以成功用于 PAMs 在 GABAA受体上的特性的协议。
在某些情况下, 单独接触 PAM 可能足以激活受体。此类活动可以通过对此处提出的实验协议稍加修改来确定。即, 在接触氨基丁酸的过程中, 不使用调制器的联合应用, 可以对该协议进行修改, 以单独使用该化合物, 然后在 gaba 的存在下进行。直接激动剂活动的特征将由化合物本身诱发的反应幅度的测定和与 GABA 诱发电流的比较来进行。
在脑切片中进行的实验, 如图 7所示, 用于确定抑制回路中的原生受体的复合活动, 然后再进一步的动物模型和沿路径的临床试验。相对简单的数据记录和分析协议, 通过评估其对 PS 振幅的差分调节效应, 可以对多个化合物进行排序。也可以检测与 GABA 系统无关的化合物的非特异效应 (例如, 当观察到 PS 形状的变化时)。直接, GABAergic 神经传递可以评估这些情况下, 通过测量化合物对抑制性突触后电流 (IPSCs) 使用全细胞膜片钳技术8。

在这里, 我们提出的协议, 发现化合物活性在 GABAA受体, 从绑定到生理学和药理学。在寻找特定于氨基丁酸受体的新分子时, 至关重要的是, 尽可能精确地定义感兴趣的亚型和新确定化合物的特异性评估 (例如, 为审查, 见鲁道夫和Knoflach1或 Sieghart2)。图 1说明了药物发现的典型路径和需要实现的步骤。
有约束力的化验已经和仍然是主要用于药物发现的第一步。在氨基丁酸受体的情况下, 它们被优化, 以确定绑定到受体苯二氮结合部位的化合物, 治疗有用和安全的药物绑定。其他技术, 使用荧光成像板阅读器 (FLIPR) 膜电位的红色染料为基础的化验3, 检测化合物, 如巴比妥, 绑定到其他网站, 是不太可取的, 因为他们不需要的副作用的轮廓。此外, 使用的染料可以直接激活 GABA 的受体, 从而质疑这些化验的效用4药物发现。结合化验只能提供证据表明, 某一化合物可以绑定到特定的受体类。用细胞膜进行体外检测, 鉴定选择性人 GABA α5β3γ2受体配位。瞬时转染的 HEK293 细胞表达人 GABAA α5β3γ2, α1β3γ2, α2β3γ2和α3β3γ2受体被用来为这些化验准备膜。对配体的影响通过测量马西尼的 [3h] 的闪烁 (抑制 [3h] 马西尼结合) 来检测。这项技术的主要优点是, 在感兴趣的受体中, 快速有效地测定复合结合的亲和性。
功能性研究对评价化合物的功能活性是至关重要的, 并对化合物与受体的结合所引起的机制提出生理和药理解释。今天, 它是公认的功能 GABAA感受器起因于五个亚基的汇编在由离子孔形成的 pseudosymmetry 的轴附近和结果从五个相同亚基的汇编。大多数 GABAA受体由两个或多个不同的亚基组成。主要大脑 GABAa受体, 例如, 由α1, β2和γ2亚基组成的化学计量学 2, 2 和1分别5,6。在诸如爪蟾卵母细胞或 HEK293 的宿主系统中进行重组, 可以快速探索受体的药理特性。
然后用脑切片7中的胞外记录探讨这些化合物的药理性质。这种方法可以探索化合物对神经传递的影响, 并提供了一个有效的方法来确认在异源表达系统中确定的化合物在本机受体水平上的功能效应, 在整个神经元环境。GABAergic 神经传递还可以通过测量化合物对抑制突触后电流 (IPSCs)8的影响, 在分子水平上进行评估。但是在这里使用的协议和基于全细胞补丁钳录音的脑切片更详细, 并产生较低的吞吐量。
最后, 从不同的技术及其内在的局限性出发, 探讨了体外筛选α5β3γ2的优缺点。这项工作应提供专家和非专家在氨基丁酸受体领域的一个有用的审查结合不同的体外方法, 用于解决新的调制器, 这些配体门控离子通道的发现。

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			<td height="53" style="height:53px;width:465px;">General equipment</td>
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			<td height="53" style="height:53px;">96 well cell harvester -(Filtermate 196)&#160;</td>
			<td style="width:169px;">Packard</td>
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			<td>To filter membranes with bound radioligand</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Microtiter plate liquid scintillation counter (Top Count NXT)</td>
			<td>Packard</td>
			<td></td>
			<td style="width:253px;">Microplate Scintillation and Luminescence counter</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Vial liquid scintillation counter (Beta-Couter 2500 TR)</td>
			<td>Packard</td>
			<td></td>
			<td style="width:253px;">Vial Scintillation and Luminescence counter</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Liquid&#160; handler (Biomek 2000)</td>
			<td style="width:169px;">Beckman coulter</td>
			<td style="width:136px;"></td>
			<td style="width:253px;">To prepare compound dilutions</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;width:465px;">Vortex (Vortex Genie 2)</td>
			<td>Scientific industries Inc.</td>
			<td style="width:136px;"></td>
			<td style="width:253px;">To mix compound stock solutions</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Tissue homogenizer (Polytron PT1200E)</td>
			<td>Kinematica AG</td>
			<td style="width:136px;"></td>
			<td style="width:253px;">To resuspend the membrane preparations</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">XLfit5 software</td>
			<td style="width:169px;">Microsoft Excel 
			&#160;add-on by IDBS</td>
			<td style="width:136px;"></td>
			<td style="width:253px;">Curve fitting software</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Smart Pull</td>
			<td>UniPix</td>
			<td style="width:136px;">-</td>
			<td>Electrode Puller</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">RoboInject</td>
			<td>MultiChannel Systems</td>
			<td style="width:136px;">-</td>
			<td>Automated Injection (Xenopus Oocytes)</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">HiClamp</td>
			<td>MultiChannel Systems</td>
			<td style="width:136px;">-</td>
			<td>Automated Voltage Clamp (Xenopus Ooocytes)</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">DataMining</td>
			<td>MultiChannel Systems</td>
			<td style="width:136px;">-</td>
			<td>Data Analysis Software</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">DataMerger</td>
			<td>MultiChannel Systems</td>
			<td style="width:136px;">-</td>
			<td>Data Processing Software</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Digidata 1550</td>
			<td>Molecular Devices</td>
			<td></td>
			<td>Low noise data acquisition system</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">CyberAmp 380 or equivalent</td>
			<td style="width:169px;">Axon Instruments</td>
			<td style="width:136px;"></td>
			<td style="width:253px;">Programmable Signal Conditioner</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">pClamp program suite</td>
			<td>Molecular Devices</td>
			<td style="width:136px;"></td>
			<td style="width:253px;">Software for data acquisition and analysis software</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Antivibraton table&#160;</td>
			<td style="width:169px;">TMC</td>
			<td style="width:136px;"></td>
			<td style="width:253px;">To avoid microelectrode vibrations&#160;</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Patchstar Micromanipulators</td>
			<td style="width:169px;">Scientifica</td>
			<td style="width:136px;"></td>
			<td style="width:253px;">To accurately position microelectrodes in brain slices</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Faraday Cage&#160;</td>
			<td style="width:169px;">Sutter Instruments</td>
			<td style="width:136px;"></td>
			<td style="width:253px;">To isolate recordings from noise</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">McIlwain Tissue Chopper</td>
			<td style="width:169px;">Campden Instruments LTD&#160;</td>
			<td></td>
			<td>To prepare brain slices</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Borosilicate glass micropipette&#160;</td>
			<td style="width:169px;">Warner Instruments</td>
			<td>GC150TF-10</td>
			<td style="width:253px;">To record extracellular potentials in brain slices</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Twisted pair, platinum iridium wires stimulation electrode</td>
			<td style="width:169px;">World Precision Instruments</td>
			<td></td>
			<td style="width:253px;">To stimulate the brain slices with current</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Stimulus generator for current and voltage driven stimulation</td>
			<td>MultiChannel Systems</td>
			<td>STG4000</td>
			<td style="width:253px;">Delivers the current to the stimulation electrode</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Plasticware</td>
			<td style="width:169px;"></td>
			<td style="width:136px;"></td>
			<td style="width:253px;"></td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Microtiter plate round bottom</td>
			<td style="width:169px;">Corning</td>
			<td style="width:136px;">#3365</td>
			<td>Used for the binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">GF/C glassfibre filter-bottom 96-well microplate with 1.2&#181;m poresize, for cell harvesting assays using a vacuum manifoldwell filter&#160;</td>
			<td style="width:169px;">Packard&#160;</td>
			<td>#6005174</td>
			<td style="width:253px;">used for the binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">50 mL Tubes</td>
			<td style="width:169px;">Falcon&#160;</td>
			<td>#352070</td>
			<td style="width:253px;">used for the binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Safe-lock tubes 1.5 mL</td>
			<td style="width:169px;">Eppendorf</td>
			<td>#0030 120086</td>
			<td style="width:253px;">used for the binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Safe-lock tubes 2 mL</td>
			<td style="width:169px;">Eppendorf</td>
			<td>#0030 120094</td>
			<td style="width:253px;">used for the binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Shipping tubes 180ml&#160;</td>
			<td style="width:169px;">Semadeni Europe AG&#160;</td>
			<td>#3722</td>
			<td style="width:253px;">used for the binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Pony vial Polyethylene 6ml&#160;</td>
			<td style="width:169px;">Perkin Elmer&#160;</td>
			<td>#6013329</td>
			<td style="width:253px;">used for the binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Top Seal&#160;</td>
			<td>Perkin Elmer&#160;</td>
			<td>#60051859</td>
			<td style="width:253px;">used for the binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Spinner Flask</td>
			<td>Bellco</td>
			<td>BELLCO # 1965-00100</td>
			<td>Spinner Flask</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">96&#160; Well Plate (Conical)</td>
			<td style="width:169px;">Thermo Scientific Milian</td>
			<td>56368</td>
			<td style="width:253px;">Injection plate for the oocytes</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">96&#160; Well Plate (Flat bottom)</td>
			<td style="width:169px;">Corning (Vitaris Switzerland)</td>
			<td>3364-cor</td>
			<td style="width:253px;">Compound Plate for the HiClamp</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Glass capillary&#160;</td>
			<td style="width:169px;">Hilgenberg (Germany)</td>
			<td style="width:136px;">-</td>
			<td style="width:253px;">borosilicate glass 1.2 O.D. 0.76 I.D. with filament</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">RNA preparation</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Ambion mMessage mMachine</td>
			<td>Thermo Fisher Scientific</td>
			<td></td>
			<td>for the in vitro synthesis</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Chemicals</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Assay buffer: KCl 5 mM; CaCl2 1.25 mM; MgCl2 1.25 mM; NaCl 120 mM; Tris 15 mM pH adjust with HCl to 7.4; store up to 3 months at 4&#176;C.</td>
			<td></td>
			<td></td>
			<td>Used for binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Washing buffer: Tris 50mM -HCl pH 7.4; store at 4&#176;C.</td>
			<td></td>
			<td></td>
			<td>Used for binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Stock solution of test compounds 10mM in DMSO</td>
			<td></td>
			<td></td>
			<td>Used for binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Flumazenil (RO0151788) 10mM in DMSO</td>
			<td></td>
			<td></td>
			<td>Used for binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Diazepam 4mM in DMSO</td>
			<td></td>
			<td></td>
			<td>Used for binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">[3H]-Flumazenil 60-85 Ci/mmol in Ethanol; store at -20&#176;C</td>
			<td></td>
			<td></td>
			<td>Used for binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Microscint 40&#160;</td>
			<td>Packard&#160;</td>
			<td>#6013641</td>
			<td>Used for binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Ultima Gold&#160;</td>
			<td style="width:169px;">Perkin Elmer&#160;</td>
			<td style="width:136px;">#6013329</td>
			<td>Used for binding assay</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">MS-222</td>
			<td style="width:169px;">Sigma</td>
			<td>Sigma # A5040</td>
			<td>MS-222</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">AB/AM</td>
			<td style="width:169px;">Sigma</td>
			<td>Sigma # A5955</td>
			<td>antibiotics / antimycotics</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Collagenase</td>
			<td style="width:169px;">Sigma</td>
			<td>Sigma # C1030</td>
			<td>Collagenase Type I</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Rnase</td>
			<td style="width:169px;">Sigma</td>
			<td>Sigma # R2020-250 mL</td>
			<td>RNaseZAP</td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">EndoFree Plasmid maxi Kit</td>
			<td style="width:169px;">Qiagen</td>
			<td>Qiagen # 12362</td>
			<td></td>
		</tr>
		<tr height="53">
			<td height="53" style="height:53px;">Salts for artificial cerebrospinal fluid (NaCl, KCl, etc.)</td>
			<td style="width:169px;">Sigma</td>
			<td></td>
			<td></td>
		</tr>
		<tr height="37">
			<td height="37" style="height:37px;">Membranes</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="89">
			<td height="89" style="height:89px;">Frozen membrane preparations from transient or stably transfected HEK293 overexpressing different human GABAA receptor subtypes: &#945;1&#946;3&#947;2, &#945;2&#946;3&#947;2, &#945;3&#946;3&#947;2, &#945;5&#946;3&#947;2. See Ballard et al 2009 for detailed methods.</td>
			<td></td>
			<td></td>
			<td>Used for binding assay</td>
		</tr>
	</tbody>
</table>

methods for the discovery of novel compounds modulating a gamma-aminobutyric acid receptor type a neurotransmission

这篇手稿提出了一个分步的协议, 筛选化合物在伽玛-丁酸 a (GABAa) 受体和它的用途, 以鉴定新分子活性的临床前化验方法从体外重组受体对他们的药理作用在本机受体在啮齿动物脑切片。对于受体的苯二氮部位的化合物结合, 第一步是建立一个主要的屏幕, 其中包括发展放射配基结合化验的细胞膜表达主要 GABAa亚型。然后, 利用鼠和人 GABA 的异种表达, 在 爪蟾卵母细胞或 HEK 293 胞内的受体, 可以在电生理检测中探讨不同受体的生理特性亚型和所鉴定化合物的药理性质。爪蟾卵母细胞系统将在这里提出, 从分离的卵母细胞和他们的显微注射与不同的基因, 由药理学表征使用双电极电压钳。最后, 在啮齿类动物脑切片中进行的录音将被描述为一种二次生理试验, 用于评估在定义良好的神经元回路中的分子在其本机受体中的活性。利用多神经元的种群反应进行细胞外记录, 并与药物应用相结合。

Watch this Scientific Journal Video about Methods for the Discovery of Novel Compounds Modulating a Gamma-Aminobutyric Acid Receptor Type A Neurotransmission at JoVE.com

Methods for the Discovery of Novel Compounds Modulating a Gamma-Aminobutyric Acid Receptor Type A Neurotransmission

在这里, 我们提出的协议, 以发现活性化合物在 GABAA受体, 从绑定到生理学和药理学。

新化合物调制伽玛-丁酸受体 a 型神经传递的发现方法

This manuscript presents a step-by-step protocol for screening compounds at gamma-aminobutyric acid type A (GABAA) receptors and its use towards the ...

methods-for-discovery-novel-compounds-modulating-gamma-aminobutyric

Research

Education

JoVE Core

JoVE Journal

Pharmacology

Neuroscience

Unit 1

Anxiolytics, Sedatives and Hypnotics

SCIENTISTS IN ACTION

13.4K 次观看.  Roche Innovation Center Basel. 在这里, 我们提出的协议, 以发现活性化合物在 GABAA受体, 从绑定到生理学和药理学。

视频: Methods for the Discovery of Novel Compounds Modulating a Gamma-Aminobutyric Acid Receptor Type A Neurotransmission

Novel Apparatus and Method for Drug Reinforcement

Animal models of reinforcement have proven to be useful for understanding the neurobiological mechanisms underlying drug addiction. Operant drug self-administration and conditioned place preference (CPP) procedures are expansively used in animal research to model various components of drug reinforcement, consumption, and addiction in humans. For this study, we used a novel approach to studying drug reinforcement in rats by combining traditional CPP and self-administration methodologies. We assembled an apparatus using two Med Associate operant chambers, sensory stimuli, and a Plexiglas-constructed neutral zone. These modifications allowed our experiments to encompass motivational aspects of drug intake through self-administration and drug-free assessment of drug/cue conditioning strength with the CPP test. In our experiments, rats self-administered cocaine (0.75 mg/kg/inj, i.v.) during either four (e.g., the "short-term") or eight (e.g., the "long-term") alternating-day sessions in an operant environment containing distinctive sensory cues (e.g., olfactory and visual). On the alternate days, in the other (differently-cued) operant environment, saline was available for self-infusion (0.1 ml, i.v.). Twenty-four hours after the last self-administration/cue-pairing session, a CPP test was conducted. Consistent with typical CPP findings, there was a significant preference for the chamber associated with cocaine self-administration. In addition, in animals undergoing the long-term experiment, a significant positive correlation between CPP magnitude and the number of cocaine-reinforced lever responses. In conclusion, this apparatus and approach is time and cost effective, can be used to examine a wide array of topics pertaining to drug abuse, and provides more flexibility in experimental design than CPP or self-administration methods alone.

Operant drug self-administration and conditioned place preference (CPP) procedures are expansively used in research to model various components of drug reinforcement, consumption, and addiction in humans. In this report, we combined traditional CPP and self-administration methods as a novel approach to studying drug reinforcement and addiction in rats.

新型仪器和药物加固方法

Animal models of reinforcement have proven to be useful for understanding the neurobiological mechanisms underlying drug addiction.  Operant drug ...

科研

神经科学

Application of a NMDA Receptor Conductance in Rat Midbrain Dopaminergic Neurons Using the Dynamic Clamp Technique

Neuroscientists study the function of the brain by investigating how neurons in the brain communicate. Many investigators look at changes in the electrical activity of one or more neurons in response to an experimentally-controlled input. The electrical activity of neurons can be recorded in isolated brain slices using patch clamp techniques with glass micropipettes. Traditionally, experimenters can mimic neuronal input by direct injection of current through the pipette, electrical stimulation of the other cells or remaining axonal connections in the slice, or pharmacological manipulation by receptors located on the neuronal membrane of the recorded cell.
Direct current injection has the advantages of passing a predetermined current waveform with high temporal precision at the site of the recording (usually the soma). However, it does not change the resistance of the neuronal membrane as no ion channels are physically opened. Current injection usually employs rectangular pulses and thus does not model the kinetics of ion channels. Finally, current injection cannot mimic the chemical changes in the cell that occurs with the opening of ion channels.
Receptors can be physically activated by electrical or pharmacological stimulation. The experimenter has good temporal precision of receptor activation with electrical stimulation of the slice. However, there is limited spatial precision of receptor activation and the exact nature of what is activated upon stimulation is unknown. This latter problem can be partially alleviated by specific pharmacological agents. Unfortunately, the time course of activation of pharmacological agents is typically slow and the spatial precision of inputs onto the recorded cell is unknown.
The dynamic clamp technique allows an experimenter to change the current passed directly into the cell based on real-time feedback of the membrane potential of the cell (Robinson and Kawai 1993, Sharp et al., 1993a,b; for review, see Prinz et al. 2004). This allows an experimenter to mimic the electrical changes that occur at the site of the recording in response to activation of a receptor. Real-time changes in applied current are determined by a mathematical equation implemented in hardware.
We have recently used the dynamic clamp technique to investigate the generation of bursts of action potentials by phasic activation of NMDA receptors in dopaminergic neurons of the substantia nigra pars compacta (Deister et al., 2009; Lobb et al., 2010). In this video, we demonstrate the procedures needed to apply a NMDA receptor conductance into a dopaminergic neuron.

In this video, we demonstrate how to apply a conductance into a dopaminergic neuron recorded in the whole cell configuration in rat brain slices. This technique is called the dynamic clamp.

一个NMDA受体电导的大鼠中脑多巴胺能神经元的动态钳技术中的应用

Neuroscientists study the function of the brain by investigating how neurons in the brain communicate. Many investigators look at changes in the ...

Paired Nanoinjection and Electrophysiology Assay to Screen for Bioactivity of Compounds using the Drosophila melanogaster Giant Fiber System

Screening compounds for in vivo activity can be used as a first step to identify candidates that may be developed into pharmacological agents1,2. We developed a novel nanoinjection/electrophysiology assay that allows the detection of bioactive modulatory effects of compounds on the function of a neuronal circuit that mediates the escape response in Drosophila melanogaster3,4. Our in vivo assay, which uses the Drosophila Giant Fiber System (GFS, Figure 1) allows screening of different types of compounds, such as small molecules or peptides, and requires only minimal quantities to elicit an effect. In addition, the Drosophila GFS offers a large variety of potential molecular targets on neurons or muscles. The Giant Fibers (GFs) synapse electrically (Gap Junctions) as well as chemically (cholinergic) onto a Peripheral Synapsing Interneuron (PSI) and the Tergo Trochanteral Muscle neuron (TTMn)5. The PSI to DLMn (Dorsal Longitudinal Muscle neuron) connection is dependent on D&alpha;7 nicotinic acetylcholine receptors (nAChRs)6. Finally, the neuromuscular junctions (NMJ) of the TTMn and the DLMn with the jump (TTM) and flight muscles (DLM) are glutamatergic7-12. Here, we demonstrate how to inject nanoliter quantities of a compound, while obtaining electrophysiological intracellular recordings from the Giant Fiber System13 and how to monitor the effects of the compound on the function of this circuit. We show specificity of the assay with methyllycaconitine citrate (MLA), a nAChR antagonist, which disrupts the PSI to DLMn connection but not the GF to TTMn connection or the function of the NMJ at the jump or flight muscles.
Before beginning this video it is critical that you carefully watch and become familiar with the JoVE video titled "Electrophysiological Recordings from the Giant Fiber Pathway of D. melanogaster " from Augustin et al7, as the video presented here is intended as an expansion to this existing technique. Here we use the electrophysiological recordings method and focus in detail only on the addition of the paired nanoinjections and monitoring technique.

Paired Nanoinjection and Electrophysiology Assay to Screen for Bioactivity of Compounds using the Drosophila melanogaster Giant Fiber System

A rapid in vivo assay to test for neuromodulatory compounds using the Giant Fiber System (GFS) of Drosophila melanogaster is described. Nanoinjections in the head of the animal along with electrophysiological recordings of the GFS can reveal bioactivity of compounds on neurons or muscles.

电检测屏幕的配对Nanoinjection和生物活性化合物的使用果蝇巨人纤维系统

Screening compounds for in vivo activity can be used as a first step to identify candidates that may be developed into pharmacological agents1,2. We ...

Methods for Intravenous Self Administration in a Mouse Model

Animal models have been developed to study the reinforcing effects of drugs, including the intravenous self-administration (IVSA) paradigm. The advantages of using an IVSA paradigm to study the reinforcing properties of drugs of abuse such as cocaine include the fact that the drug is self-administered instead of experimenter-administered, the schedule of reinforcement can be altered, and accurate measurement of the quantities of drug consumed as well as the timing and pattern of IV injections can be obtained. Furthermore, the intravenous route of administration avoids potential confounds related to first pass metabolism or taste, and produces rapid increases in blood and brain drug levels. As outlined in this video, intravenous self-administration can be obtained without prior food restriction or prior drug training following careful catheter placement during surgery and meticulous daily catheter flushing and maintenance. Experimental procedures outlined in this paper include a description of animal housing and acclimation methods, operant training using sweetened milk solutions, and catheter implantation surgery.

The intravenous self-administration (IVSA) paradigm is considered to be the gold standard in examining the reinforcing properties of drugs of abuse in rodents. This manuscript outlines the experimental procedures and surgical techniques necessary to obtain reliable IVSA data. In particular, meticulous catheter implantation and maintenance are highlighted.

在小鼠模型中静脉自我管理的方法

Animal models have been developed to study the reinforcing effects of drugs, including the intravenous self-administration (IVSA) paradigm. The advantages ...

High-resolution Functional Magnetic Resonance Imaging Methods for Human Midbrain

Functional MRI (fMRI) is a widely used tool for non-invasively measuring correlates of human brain activity. However, its use has mostly been focused upon measuring activity on the surface of cerebral cortex rather than in subcortical regions such as midbrain and brainstem. Subcortical fMRI must overcome two challenges: spatial resolution and physiological noise. Here we describe an optimized set of techniques developed to perform high-resolution fMRI in human SC, a structure on the dorsal surface of the midbrain; the methods can also be used to image other brainstem and subcortical structures.
High-resolution (1.2 mm voxels) fMRI of the SC requires a non-conventional approach. The desired spatial sampling is obtained using a multi-shot (interleaved) spiral acquisition1. Since, T2* of SC tissue is longer than in cortex, a correspondingly longer echo time (TE ~ 40 msec) is used to maximize functional contrast. To cover the full extent of the SC, 8-10 slices are obtained. For each session a structural anatomy with the same slice prescription as the fMRI is also obtained, which is used to align the functional data to a high-resolution reference volume.
In a separate session, for each subject, we create a high-resolution (0.7 mm sampling) reference volume using a T1-weighted sequence that gives good tissue contrast. In the reference volume, the midbrain region is segmented using the ITK-SNAP software application2. This segmentation is used to create a 3D surface representation of the midbrain that is both smooth and accurate3. The surface vertices and normals are used to create a map of depth from the midbrain surface within the tissue4.
Functional data is transformed into the coordinate system of the segmented reference volume. Depth associations of the voxels enable the averaging of fMRI time series data within specified depth ranges to improve signal quality. Data is rendered on the 3D surface for visualization.
In our lab we use this technique for measuring topographic maps of visual stimulation and covert and overt visual attention within the SC1. As an example, we demonstrate the topographic representation of polar angle to visual stimulation in SC.

This article describes techniques to perform high-resolution functional magnetic resonance imaging with 1.2 mm sampling in human midbrain and subcortical structures using a 3T scanner. Use of these techniques to resolve topographic maps of visual stimulation in the human superior colliculus (SC) is given as an example.

高分辨率人类中脑功能磁共振成像方法

Functional MRI (fMRI) is a widely used tool for non-invasively measuring correlates of human brain activity. However, its use has mostly been focused upon ...

Methods for Studying the Mechanisms of Action of Antipsychotic Drugs in Caenorhabditis elegans

Caenorhabditis elegans is a simple genetic organism amenable to large-scale forward and reverse genetic screens and chemical genetic screens. The C. elegans genome includes potential antipsychotic drug (APD) targets conserved in humans, including genes encoding proteins required for neurotransmitter synthesis and for synaptic structure and function. APD exposure produces developmental delay and/or lethality in nematodes in a concentration-dependent manner. These phenotypes are caused, in part, by APD-induced inhibition of pharyngeal pumping1,2. Thus, the developmental phenotype has a neuromuscular basis, making it useful for pharmacogenetic studies of neuroleptics. Here we demonstrate detailed procedures for testing APD effects on nematode development and pharyngeal pumping. For the developmental assay, synchronized embryos are placed on nematode growth medium (NGM) plates containing APDs, and the stages of developing animals are then scored daily. For the pharyngeal pumping rate assay, staged young adult animals are tested on NGM plates containing APDs. The number of pharyngeal pumps per unit time is recorded, and the pumping rate is calculated. These assays can be used for studying many other types of small molecules or even large molecules.

Methods for Studying the Mechanisms of Action of Antipsychotic Drugs in Caenorhabditis elegans

Approaches for testing the effects of antipsychotic drugs (APDs) in Caenorhabditis elegans are demonstrated. Assays are described for testing drug effects on development and viability and on pharyngeal pumping rate. These methods are also applicable for pharmacogenetic experiments with drug classes other than APDs.

方法研究抗精神病药物的作用机制在<em&gt;秀丽隐杆线虫</em

Caenorhabditis elegans is a simple genetic organism amenable to  large-scale forward and reverse genetic screens and chemical genetic screens. The C.  ...

Optical Control of a Neuronal Protein Using a Genetically Encoded Unnatural Amino Acid in Neurons

Photostimulation is a noninvasive way to control biological events with excellent spatial and temporal resolution. New methods are desired to photo-regulate endogenous proteins expressed in their native environment. Here, we present an approach to optically control the function of a neuronal protein directly in neurons using a genetically encoded unnatural amino acid (Uaa). By using an orthogonal tRNA/aminoacyl-tRNA synthetase pair to suppress the amber codon, a photo-reactive Uaa 4,5-dimethoxy-2-nitrobenzyl-cysteine (Cmn) is site-specifically incorporated in the pore of a neuronal protein Kir2.1, an inwardly rectifying potassium channel. The bulky Cmn physically blocks the channel pore, rendering Kir2.1 non-conducting. Light illumination instantaneously converts Cmn into a smaller natural amino acid Cys, activating Kir2.1 channel function. We express these photo-inducible inwardly rectifying potassium (PIRK) channels in rat hippocampal primary neurons, and demonstrate that light-activation of PIRK ceases the neuronal firing due to the outflux of K+ current through the activated Kir2.1 channels. Using in utero electroporation, we also express PIRK in the embryonic mouse neocortex in vivo, showing the light-activation of PIRK in neocortical neurons. Genetically encoding Uaa imposes no restrictions on target protein type or cellular location, and a family of photoreactive Uaas is available for modulating different natural amino acid residues. This technique thus has the potential to be generally applied to many neuronal proteins to achieve optical regulation of different processes in brains. The current protocol presents an accessible procedure for intricate Uaa incorporation in neurons in vitro and in vivo to achieve photo control of neuronal protein activity on the molecular level.

Here, a procedure to selectively activate a neuronal protein with a short pulse of light by genetically encoding a photo-reactive unnatural amino acid into a target neuronal protein expressed in neurons in culture or in vivo is presented.

一个神经元蛋白在神经元使用遗传编码的非天然氨基酸的光控制

Photostimulation is a noninvasive way to control biological events with excellent spatial and temporal resolution. New methods are desired to ...

Recording Synaptic Plasticity in Acute Hippocampal Slices Maintained in a Small-volume Recycling-, Perfusion-, and Submersion-type Chamber System

Even though experiments on brain slices have been in use since 1951, problems remain that reduce the probability of achieving a stable and successful analysis of synaptic transmission modulation when performing field potential or intracellular recordings. This manuscript describes methodological aspects that might be helpful in improving experimental conditions for the maintenance of acute brain slices and for recording field excitatory postsynaptic potentials in a commercially available submersion chamber with an outflow-carbogenation unit. The outflow-carbogenation helps to stabilize the oxygen level in experiments that rely on the recycling of a small buffer reservoir to enhance the cost-efficiency of drug experiments. In addition, the manuscript presents representative experiments that examine the effects of different carbogenation modes and stimulation paradigms on the activity-dependent synaptic plasticity of synaptic transmission.

This protocol describes the stabilization of the oxygen level in a small volume of recycled buffer and methodological aspects of recording activity-dependent synaptic plasticity in submerged acute hippocampal slices.

小容积回收-灌注-浸没式室系统中维持的急性海马切片的突触可塑性记录

Even though experiments on brain slices have been in use since 1951, problems remain that reduce the probability of achieving a stable and successful ...

Establishing a Mouse Model of a Pure Small Fiber Neuropathy with the Ultrapotent Agonist of Transient Receptor Potential Vanilloid Type 1

Patients with diabetes mellitus (DM) or those experiencing the neurotoxic effects of chemotherapeutic agents may develop sensation disorders due to degeneration and injury of small-diameter sensory neurons, referred to as small fiber neuropathy. Present animal models of small fiber neuropathy affect both large- and small-diameter sensory fibers and thus create a neuropathology too complex to properly assess the effects of injured small-diameter sensory fibers. Therefore, it is necessary to develop an experimental model of pure small fiber neuropathy to adequately examine these issues. This protocol describes an experimental model of small fiber neuropathy specifically affecting small-diameter sensory nerves with resiniferatoxin (RTX), an ultrapotent agonist of transient receptor potential vanilloid type 1 (TRPV1), through a single dose of intraperitoneal injection, referred to as RTX neuropathy. This RTX neuropathy showed pathological manifestations and behavioral abnormalities that mimic the clinical characteristics of patients with small fiber neuropathy, including intraepidermal nerve fiber (IENF) degeneration, specifically injury in small-diameter neurons, and induction of thermal hypoalgesia and mechanical allodynia. This protocol tested three doses of RTX (200, 50, and 10 &#181;g/kg, respectively) and concluded that a critical dose of RTX (50 &#181;g/kg) is required for the development of typical small fiber neuropathy manifestations, and prepared a modified immunostaining procedure to investigate IENF degeneration and neuronal soma injury. The modified procedure is fast, systematic, and economic. Behavioral evaluation of neuropathic pain is critical to reveal the function of small-diameter sensory nerves. The evaluation of mechanical thresholds in experimental rodents is particularly challenging and this protocol describes a customized metal mesh that is suitable for this type of assessment in rodents. In summary, RTX neuropathy is a new and easily established experimental model to evaluate the molecular significance and intervention underlying neuropathic pain for the development of therapeutic agents.

This study establishes an experimental model of pure small fiber neuropathy with resiniferatoxin (RTX). A unique dose of RTX (50 &#181;g/kg) is optimal for developing a small fiber neuropathy model that mimics patient characteristics and could help investigate the nociceptive molecular significance underlying neuropathic pain.

利用瞬态受体电位辣椒1型 Ultrapotent 激动剂建立单纯小纤维神经病变的小鼠模型

Patients with diabetes mellitus (DM) or those experiencing the neurotoxic effects of chemotherapeutic agents may develop sensation disorders due to ...

Novel Passive Clearing Methods for the Rapid Production of Optical Transparency in Whole CNS Tissue

Since the development of CLARITY, a bioelectrochemical clearing technique that allows for three-dimensional phenotype mapping within transparent tissues, a multitude of novel clearing methodologies including CUBIC (clear, unobstructed brain imaging cocktails and computational analysis), SWITCH (system-wide control of interaction time and kinetics of chemicals), MAP (magnified analysis of the proteome), and PACT (passive clarity technique), have been established to further expand the existing toolkit for the microscopic analysis of biological tissues. The present study aims to improve upon and optimize the original PACT procedure for an array of intact rodent tissues, including the whole central nervous system (CNS), kidneys, spleen, and whole mouse embryos. Termed psPACT (process-separate PACT) and mPACT (modified PACT), these novel techniques provide highly efficacious means of mapping cell circuitry and visualizing subcellular structures in intact normal and pathological tissues. In the following protocol, we provide a detailed, step-by-step outline on how to achieve maximal tissue clearance with minimal invasion of their structural integrity via psPACT and mPACT.

Here, we present two novel methodologies, psPACT and mPACT, for achieving maximal optical transparency and subsequent microscopic analysis of tissue vasculature in the intact rodent whole CNS.

一种新的用于全中枢神经系统光透明快速生成的无源清除方法

Since the development of CLARITY, a bioelectrochemical clearing technique that allows for three-dimensional phenotype mapping within transparent tissues, ...