该项目是由MINECO资助授予BFU201343608-P和PSI2013-49348-EXP和JCYL授予SA343U14男男性行为者和MRC核心资金ARP。 YAA举行了国家科学技术委员会（216106）和SEP奖学金。

所有试验程序都在萨拉曼卡大学与批准进行，使用符合标准的方法，萨拉曼卡动物保健委员会的大学，以及欧盟的标准（指令63分之2010/ EU）对在神经科学研究中使用动物。 1.钨电极注意:钨电极的制造是基于在美林和安斯沃思27和安斯沃思等人 28所述的原技术和使用布洛克等人 17所述的工作站设置进行。 <ol><li>以记录的IC神经元的单单元外活性，使用电极1.5的尖端阻抗 - 2.5兆欧。这里，所涉及的钨电极的制造步骤仅简要地描述的，由于一个详细描述在上述参考文献中找到。 </li><li>将钨丝在定制校准工具（ 图1A），以协助它们切割成所要求的长度。对准工具包括以2毫米的间隔在一端胶合并联，止损30针（25克）来限制电线〜40毫米的长度。认真重视用胶带的电线有始有终，砍电线的其余部分具有较强的剪刀。 </li><li>从磁带轻轻拉动以从对准工具移除钨丝，并确保所有的导线保持附着到磁带上。滚动磁带到抛光黄铜锭（ 图1B，C），抱着电线坚决反对主轴所以有良好的电气连接。 </li><li>主轴连接到工作站5的转速电动机，浸入突出导线提示到蚀刻液（KNO 2，每80毫升90克）。角主轴轴线相对于蚀刻液的表面45°。浸入线材提示，使得导线的〜1/3接触的溶液。 </li><li> IMMERSE碳棒电极浸入蚀刻浴以闭合电路。使用弹簧铜编织刷而主轴旋转的蚀刻供给适用于主轴。调节是通过在电极和蚀刻溶液250 mA的通过的电流。停止尖端蚀刻时，电流下降到200毫安。该线提示将被蚀刻成很细的点。 </li><li>传递一个削尖线通过火焰，以消除任何油脂和残胶。放置电线（钝端在前）到高硼硅玻璃毛细管（1.5 mm外径，0.86毫米内径） 与它的下端封闭橡皮泥。垂直夹住吸管在顶部和底部。拉使用加热线圈（直径为5毫米，深度5毫米）和悬浮柱塞吸管。当导线被柱塞的重量拉下，熔融玻璃形成围绕它非常精细涂层。 </li><li>除去覆盖尖端在电极的尖锐端与钠的熔融珠的帮助下在玻璃四硼酸。以形成胎圈，以水（约0.5毫升）少量混合的四硼酸钠（〜0.25g）和缓慢将其置于一个加热元件上，直到它融化成珠〜2毫米的直径。加热元件的温度是由一个电位器控制。放置在固定于表一个操纵臂胎圈和加热元件，并移动，直到胎圈是在低放大倍数的显微镜下聚焦。 </li><li>固定玻璃包线到幻灯片，并把它放在显微镜下。移动滑板与阶段旋钮直到尖端和四硼酸珠处于焦点。热火珠，直到它稍微融化，然后将丝尖端〜10 - 15微米。关闭供暖电位器了。作为珠子冷却下来时，它收缩并从电极的前端去掉玻璃，暴露下面的钨。钨电极就可以使用了。 </li></ol> 2.多管玻璃吸管制造<ol><li>保障多的两端桶玻璃毛细管（以H-配置五桶）用热缩管，让更好的抓地力，车夫夹具和防止破损，并放置一个在垂直拉拔。 </li><li>要获取〜15毫米尖的长度，设置起拔器以下参数:热火:84分磁铁力:49，主磁铁力:38微调这些参数，根据特定的设置，变更以及后加热元件。 </li><li>拉毛细管获得两个移液器闭塞的提示。安装在使用橡皮泥滑动吸管和在显微镜下打破枪头直到外径为约20 - 30微米，用细剪刀或镊子或手术刀的扁平侧。如果破碎的边缘过于粗糙，使用步骤1.7中所述的四硼酸珠技术，完善它。 </li><li>放置一个钨电极（从第1部分）在一个3轴微型微定位器的端部与一个20G的针制成的支持器安装在显微镜雄鹿即使用镊子，弯曲电极5的端部 - 10°，〜从末端30毫米。 </li><li>在显微镜下，小心地将在多管尖钨电极。一旦对准，降低电极直到它接触到多管，在两个上部桶之间的槽嵌合。 20微米从多管的前端远 - 直到它突出〜15滑动电极的尖端。使在电极和多管尽可能小，以获得更好的粘合和更薄的合奏之间的角度。 </li><li>从技巧应用的光固化胶粘剂〜5mm的小降了。小心胶水没有达到尖端避免阻塞多管通道。 </li><li>治用蓝光LED灯的胶水。如果需要重复上胶/固化，获得更好的粘接。 </li><li>轻轻移动显微镜载物台，直到钨电极的端部从其架上释放。取下幻灯片背驮式合奏。 </li><li>第裹在长度较短的背驮式电极电子中段热收缩管和用于玻璃的钨电极，以进一步固定到多管应用快速固化环氧树脂为宜。 </li></ol> 3.药物对微电泳注意:在水中溶解时使用的微电泳的药物必须具有的电荷。检查文献以查看是否感兴趣的药物是适合此过程。这里，对于gabazine的程序，GABA A受体的拮抗剂，进行说明。 <ol><li>使用0.2微米的注射器过滤器进行消毒的水并固定不含有溶质过滤蒸馏水。准备〜1000微升20毫米的使用这种蒸馏水gabazine。 </li><li>使用细尖pH电极调节稀释的PH值至4以0.2微米过滤的NaOH。 </li><li>在-20ºC200微升等分 - 存储100个。除霜在记录的那天。这天，在此之前的动物是克制版，填充桶 - 的多管电极（3 5微升）用的药物，使用装配有柔性塑料针100微升微量。 </li></ol> 4.手术和Headpost植入<ol><li>在两名男性CBA / J小鼠（ 小家鼠 ）为27和30克的重量进行实验。按照科比和他的同事29的手术和登记程序，Portfors和合作者30-32，和杜克和马尔米耶卡26。 </li><li>在手术前的日子里，处理动物，让他们自由地探索他们habituate到录音室。执行每天三节，每一个至少持续30分钟。这样，录音过程中，动物会平静和舒适。 </li><li>麻醉用氯胺酮（50毫克/千克）和赛拉嗪（10毫克/千克）的混合鼠标肌内注射。与该剂量的动物为约1小时深度麻醉。提供补充剂量的1锡尔的根据需要初始剂量d的。 </li><li>放置动物上的加热毯设定为保持38±1℃的高温和通过使用两个耳棒和咬的酒吧在立体定位框架稳定动物的头。要小心，不要刺穿与耳棒鼓膜。 </li><li>通过应用眼用凝胶一滴保护眼睛。 </li><li>用剪刀刮头皮，并应用碘伏消毒皮肤。 </li><li>使用手术刀，做一个切口沿中线，露出头骨和缩回覆盖顶和枕部的骨头更延髓部分骨膜。 </li><li>胶水一个轻量级的杜拉铝headpost（重量〜0.65克，长30毫米， 图2A）与颅骨圆平底（直径为5毫米）。胶银线到headpost离开其端部自由的中间。银线将被用作用于电生理记录的参比电极。 </li><li>应用的LIG一薄层在头骨HT固化性粘合剂和headpost的基础。等待10秒，然后将headpost在顶骨的喙区域，沿中线。 </li><li>为一个有效的接合强度，光使用蓝色光源20秒固化粘合剂。 </li><li>钻三个孔周围使用电钻和小钻头headpost的基地后面。 </li><li>放置在钻孔两位制表螺钉（〜2毫米长），以服务于头骨和探头之间的附加的接触点。螺丝需要1.5变为实现紧密贴合。测试用钳子螺丝，以确保他们没有松动。 </li><li>将银接地线的尖端插入第三孔，确保它接触硬脑膜。申请耐水氰基丙烯酸酯胶的一小滴的导线的头骨结合。 </li><li>应用光固化复合材料加强与颅骨headpost的债券。覆盖headpost的基础上，所述银线的低部分，和螺钉，小心不要延长背后的lambda，允许在录制过程中访问。固化使用蓝色光源。 </li><li>缩回肌肉在颈部的其插入邻近于头骨后部。用一个小环钻（直径2.35毫米），钻一个圆窗下方的lambda缝合和横向的中线，暴露下丘（IC）。当边界松动，拉起覆盖骨细镊子。如果发生出血，用冷无菌生理盐水冲洗，以阻止它。 </li><li>使窗口周围的小（约1毫米宽，约1毫米高）墙复合光固化它。 </li><li>覆盖暴露的头骨和肌肉用抗生素软膏。然后，弄湿了IC的暴露表面用无菌盐水并用凡士林覆盖它，填充使记录窗口周围的壁之后阱产生的。 </li><li>注入丁丙诺啡皮下（0.03毫克/公斤，在无菌盐水中1:10稀释）作为镇痛剂。 </li><li>保持T上的动物他电热毯加热，直到它醒来，并返回到其房屋笼从手术中恢复了之前的记录会话三天。房子动物个体rat&#39;s住房笼笼防止队友清理出果冻和headpost触摸金属网罩。放置一些富集在笼子里时，动物的单装。此外，每日更换木屑，防止感染，并仔细检查动物的正常恢复并没有显示不舒服的迹象。还要检查是否凡士林是在记录窗口保护暴露大脑。 </li></ol> 5.电生理记录和微电泳<ol><li>恢复后，给动物的时间来适应环境的录音环境，并具有其头部约束。通过在鼠标坐在雕花其机身尺寸（ 图2B）定制的缓冲泡沫阻挡器headpost固定到支架驯化动物。这将LIM它鼠标的移动，将有助于它的宁静。 </li><li>开始10分钟的会议，并逐步增加持续时间长达120分钟。在会议期间，在给定的时间间隔33奖励甜液体动物（炼乳，用水稀释30:70）。后来，记录会话期间，给予同样的奖励在启动，并在会议结束时或者在没有神经元被隔离。 </li><li>如果动物是非常之前记录激发，注入轻度镇静乙酰丙嗪（2mg / kg的，腹膜内）。根据感兴趣的神经系统，镇静会影响你的成绩。 </li><li>让动物自由探索录音室5 - 10分钟。 </li><li>将动物的尸体进入泡沫定制的缓冲阻挡（ 图2B）。 </li><li>固定headpost到附着到立体定位框架（ 图2C）的保持器。这是给动物液体奖励的好时机。 </li><li>有限公司版本的动物的身体用棉毯和松散耦合固定使用塑料hemicylinder及胶粘带它。 </li><li>从记录窗口中删除凡士林用温无菌生理盐水冲洗。 </li><li>记录神经活动和gabazine离子电渗应用。 <ol><li>放置在其支架上的多管电极，由一个微驱动控制，并连接到一个显微。 </li><li>连接线记录，用小鳄鱼夹。连接正极端子连接到钨电极的端，和接地端子的银导线接触硬脑膜。 </li><li>放置一个未涂覆的银线每个桶的内部，所以一端接触溶液，而另一端是可访问的。这些目的连接到微电泳装置中，按照制造商的说明书。 </li><li>移动多管电极直到尖端接触大脑的表面上。套用温暖无菌生理盐水，以防止日的干燥Ë脑组织。在这一点上施加保持电流（-10 nA的用于gabazine，检查文献对于特定的药物），以避免从筒体前端的药物漏出，同时寻找单个单位活动。 </li><li>使用标准技术分离单个神经元细胞外的活动。获得神经元的频率响应区域（FRA）， 即 ，频率和能够因神经元是这些声音34-36敏感唤起的响应的强度的组合。 </li><li>选择两个频率（F1和F2），该唤起一个类似的燃烧速率和图案。目前古怪范式下的各频率的稀有和重复的刺激。 注意:简单地说，在古怪范例，一个频率（F1）是作为与发生的概率高的重复刺激，而第二（F2）是很少发生的异常刺激，重复那些中无规地散布。在第二古怪序列，相对两个刺激概率逆转。刺激范式的细节先前已经描述22,37。 </li><li> （ - 20 nA的10）当前转向正值释放gabazine。再次获得FRA和gabazine应用下重复古怪的范例。保持的喷射，直到在被观察到的燃烧率的可见效果;通常需要5 - 20分钟，这取决于具体的药物，其浓度，和喷射电流的幅度。重复记录协议，以获得药物的作用下的值。 </li><li>通过返回电流到保留值停止注射。等待药物的作用通​​过监测的FRA或响应于古怪范例返回到控制值，以洗去。 注意:记录会话可以持续2 - 每天3小时，而如果动物显示不适或挣扎的任何迹象应提前结束。给予奖励液体并覆盖录音通道凡士林琥珀色。 </li></ol></li></ol> 6.数据分析<ol><li>测量前后gabazine注入以及SSA水平期间FRA。 </li><li>由共SSA指数（CSI），并如先前19,22,23,38,39所描述的特定频率的SSA指数（SI）量化SSA响应的强度。的CSI和SI反映到罕见刺激神经元响应，并重复一个响应之间的归一化。正CSI和SI值表明神经反应（每穗刺激）较反复的音调更高罕见。 </li><li>比较从控制和药物喷射条件数据。 </li></ol>

The authors have nothing to disclose.

的神经活性物质在清醒的动物的微电泳是一个功能强大的技术来探测并解剖上单个神经元40,41的活性的特定的突触输入的作用。更重要的是，这个过程可以对神经回路的神经递质和调质无麻醉剂的潜在干扰的影响的决心。这里，我们表明，在清醒小鼠的集成电路gabazine的应用鲁棒改变频率调谐（ 图4A），时间的反应模式（ 图4B）和SSA（ 图5）。 <p cla...

神经兴奋和抑制的相互作用是感觉信息1的处理的基础。它也已知麻醉对皮层激活和突触输入2,3的时间模式的动态的强烈冲击。例如，已经观察到，麻醉剂改变的视觉诱发反应在皮质神经元3,4的持续时间。此外，兴奋性和抑制性突触输入之间的比例是在麻醉和清醒动物4,5-不同，改变既诱发和自发活动率6,7。通过测量突触电导，海德尔和他的同事发现4在振幅抑制匹配激励麻醉下而清醒时，抑制作用大于激发更强。这些发现提示的实验程序的开发，研究具体的突触输入感官处理在清醒动物的影响。 &lt;P类="jove_content"&gt;通过施加小电流注射的（NA的数量级上）带电神经活性物质的受控喷射已被广泛用于研究的突触输入的贡献，并推定细胞受体的感觉处理8-13的作用。这种技术被称为微电泳，允许药物在记录神经元，这有助于快速和密闭效果附近的应用。这个过程是更适合于学习的神经活性物质局部作用，相比于其它实验操作如全身注射，微透析或使用光遗传学技术引起了广泛的影响。通常，一个背驮式电极结构14,15被用于同时记录所述目标神经元，并提供所关注的神经活性物质。它由附接到承载神经活性物质的多管吸移管的记录电极。邻的修改通过Havey和Caspary 14描述riginal程序已付诸实施。例如，钨电极，而不是玻璃之一，可以用来记录神经活动16。对钨电极17,18的制造先前公布的方法包括三个基本步骤:钨丝提示，玻璃绝缘，并且末端曝光调整电解蚀刻，以满足记录的要求。 听觉神经科学的一个有趣的和紧急字段是特定刺激的适应（SSA 19）的研究。 SSA是在给不推广到其他，很少呈现声音重复声音的神经反应的特定下降。 SSA的重要性在于它在听觉大脑神经机制底层偏差检测，以及对听觉的后期失匹配负成分的可能相关的神经元的潜在作用诱发电位20,21。 ØSSA从IC ccurs到听觉皮层19,22-24。 GABA A介导的抑制已被证实作为对SSA 7,16,25的增益控制机制，这也被证明是由麻醉26的影响。这里，我们提出，结合先前描述的方法之前和清醒小鼠的GABA A -受体的选择性拮抗物的应用过程中记录的IC神经元的单单元活动的协议。首先，我们描述背驮式电极和下，手术和记录方法中的用途。为了测试药物释放的功效，我们比较了感受域以及集成电路神经元SSA之前和gabazine的微电泳喷射期间的水平。

<table><tbody><tr><td>Tungsten wire</td><td>Harvard Apparatus LTD</td><td>33-0099</td><td>0.005 inches x 3 inches</td></tr><tr><td>Borosilicate glass capillary&amp;nbsp;</td><td>Harvard Apparatus LTD</td><td>30-0053</td><td>Borosilicate standard wall without filament, 1.5 mm OD, 0.86 mm ID, 100 mm long</td></tr><tr><td>Multibarrel glass capillaries&amp;nbsp;</td><td>World Precision Instruments</td><td>5B120F-4&amp;nbsp;</td><td>5-barrel capillary, 4 inches long, 1.2 mm OD, with filament</td></tr><tr><td>Diaplus</td><td>DiaDent</td><td>2001-2101</td><td>Light-curing adhesive, used to attach the tungsten electrode to the glas multibarrel pipette</td></tr><tr><td>G-Bond</td><td>GC Corporation</td><td>2277</td><td>Light-curing adhesive, used to attach the headpost to the animal&#039;s skull</td></tr><tr><td>Charisma</td><td>Heraeus Kulzer</td><td>66000087</td><td>Light-curing composite, used to reinforce the bond of the headpost with the skull</td></tr><tr><td>Araldit Cristal</td><td>Ceys</td><td></td><td>2-component expoxy, used to further secure the attachment of the tungsten electrode to the glass multibarrel pipette</td></tr><tr><td>Heating blanket</td><td>Cibertec</td><td>RTC1</td><td></td></tr><tr><td>Stereotactic frame</td><td>Narishige</td><td>SR-6N</td><td>Modified for mice</td></tr><tr><td>Microiontophoretic device</td><td>Harvard Apparatus LTD</td><td>Neurophore BH-2</td><td>Including IP-2 iontophoresis pumps (one for each drug delivery channel) and a balance module</td></tr><tr><td>Multibarrel glass pipette puller</td><td>Narishige</td><td>Model PE-21</td><td></td></tr><tr><td>LED lamp</td><td>Technoflux</td><td>CV-215</td><td>5 W, 430-485 nm</td></tr><tr><td>MicroFil</td><td>World Precision Instruments</td><td>MF34G-5</td><td>Flexible plastic needle, 34 AWG</td></tr><tr><td>Imalgene</td><td>Merial</td><td></td><td>Ketamine, 100 mg/mL</td></tr><tr><td>Rompun</td><td>Bayer</td><td></td><td>Xylazine, 20 mg/mL</td></tr><tr><td>Gabazine / SR-95531</td><td>Sigma</td><td>S106</td><td>Prepare ~ 1000&amp;micro;l of 20 mM gabazine in distilled water and adjust the pH to 4</td></tr></tbody></table>

extracellular recording of neuronal activity combined with microiontophoretic application of neuroactive substances in awake mice

神经递质和调质，因此不同的神经反应的活性差异，可以麻醉和清醒的动物之间找到。因此，允许突触系统的清醒动物的操作方法，需要在以确定的突触输入的神经元处理由麻醉剂的影响的贡献。这里，我们提出的方法用于电极的结构，以同时记录细胞外神经活动和在清醒小鼠的记录点的附近释放多个神经活性物质。通过结合这些过程，我们进行了gabazine的微电泳注射，以选择性阻断GABA A受体头抑制小鼠的下丘神经元。 Gabazine成功修改神经反应性能如频率响应区域和特定刺激的适应。因此，我们证明我们的方法适用于recordin克单单元活动和解剖在听觉处理特定神经递质受体的作用。 所描述的过程的主要限制是在相对较短的记录时间（〜3小时），这是由动物到记录会话的习惯的水平来确定。另一方面，多个记录会话可以在相同的动物中进行。这种技术在用于操纵神经传递或神经调节（如全身注射或使用光遗传学模型）的水平的其他实验程序的优点是，药物的效果被限制在本地突触输入到目标神经元。此外，电极的定制制造允许根据神经结构和感兴趣（如用于提高记录的信噪比的尖端电阻）神经元的类型的具体参数的调整。

我们记录4以及隔离IC的神经元的单单元的活动。期间在清醒小鼠外记录获得的典型的信号-噪声比示于图3B。 图4A示出每个神经元的频率响应区域（FRA）之前和期间的GABA A的封锁与gabazine受体拮抗剂。未观察到响应强度（峰值/刺激）以及光谱调谐的扩大的增量。在诱发反应的增加也很明显在从显示（ 图4B）对所有的频率和强度?...

Watch this Scientific Journal Video about Extracellular Recording of Neuronal Activity Combined with Microiontophoretic Application of Neuroactive Substances in Awake Mice at JoVE.com

Extracellular Recording of Neuronal Activity Combined with Microiontophoretic Application of Neuroactive Substances in Awake Mice

We present methods for the construction of electrodes to simultaneously record extracellular neural activity and release multiple neuroactive substances at the vicinity of the recording sites in awake mice. This technique allows the detailed analysis of putative local synaptic inputs to the neuron of interest.

神经元电活动外记录与神经活性物质在清醒小鼠微电泳应用相结合

Differences in the activity of neurotransmitters and neuromodulators, and consequently different neural responses, can be found between anesthetized and ...

extracellular-recording-neuronal-activity-combined-with

Research

JoVE Journal

Neuroscience

10.0K 次观看.  University of Salamanca. We present methods for the construction of electrodes to simultaneously record extracellular neural activity and release multiple neuroactive substances at the vicinity of the recording sites in awake mice. This technique allows the detailed analysis of putative local synaptic inputs to the neuron of interest.

视频: Extracellular Recording of Neuronal Activity Combined with Microiontophoretic Application of Neuroactive Substances in Awake Mice

Flat-floored Air-lifted Platform: A New Method for Combining Behavior with Microscopy or Electrophysiology on Awake Freely Moving Rodents

It is widely acknowledged that the use of general anesthetics can undermine the relevance of electrophysiological or microscopical data obtained from a living animal&#8217;s brain. Moreover, the lengthy recovery from anesthesia limits the frequency of repeated recording/imaging episodes in longitudinal studies. Hence, new methods that would allow stable recordings from non-anesthetized behaving mice are expected to advance the fields of cellular and cognitive neurosciences. Existing solutions range from mere physical restraint to more sophisticated approaches, such as linear and spherical treadmills used in combination with computer-generated virtual reality. Here, a novel method is described where a head-fixed mouse can move around an air-lifted mobile homecage and explore its environment under stress-free conditions. This method allows researchers to perform behavioral tests (e.g., learning, habituation or novel object recognition) simultaneously with two-photon microscopic imaging and/or patch-clamp recordings, all combined in a single experiment. This video-article describes the use of the awake animal head fixation device (mobile homecage), demonstrates the procedures of animal habituation, and exemplifies a number of possible applications of the method.

This method creates a tangible, familiar environment for the mouse to navigate and explore during microscopic imaging or single-cell electrophysiological recordings, which require firm fixation of the animal&#8217;s head.

平地板的空气解禁平台:一种新方法与显微镜或电对清醒结合行为自由移动鼠害

It is widely acknowledged that the use of general anesthetics can undermine the relevance of electrophysiological or microscopical data obtained from a ...

科研

行为学

Preparation of an Awake Mouse for Recording Neural Responses and Injecting Tracers

It is well known that anesthesia alters neural response properties in various regions of the brain.13. In the auditory system, fundamental response properties of brainstem neurons including threshold, frequency specificity, and inhibitory sidebands are altered in significant ways under anesthesia1-2. These observations prompted physiologists to seek ways to record from single neurons without the contaminating effects of anesthesia. One result was a decerebrate preparation, where the brainstem was completely transected at the level of the midbrain4. The drawbacks of this preparation are a formidable surgery, the elimination of descending projections from the forebrain, and an inability to use sensory stimulation to examine structures above the midbrain. A different strategy has been to implant electrode arrays chronically to record from single neurons and multiunit clusters while the animal is awake and/or behaving5,6. These techniques however are not compatible with injecting tracer dyes after first electrophysiologically characterizing a brain structure. To avoid altering neural response properties with anesthetics while recording electrophysiological response properties from single neurons, we have adapted a head restraint technique long used in bats7-9 to mouse10-12. Using this method, we are able to conduct electrophysiological recordings over several days in the unanesthetized mouse. At the end of the recording sessions, we can then inject a dye to reconstruct electrode positions and recording sites or inject a tracer so that pathways to and from the recording loci can be determined. This method allows for well isolated single neuron recordings over multiple days without the use anesthetics.

Electrophysiological characterization of neuronal responses is important for understanding brain function and for guiding the placement of dyes for pathway tracing. However, many studies are performed in anesthetized animals. To understand brain function without anesthetics, we developed a method to record neuronal response properties and inject dyes in awake mouse.

记录神经反应和注射示踪剂一个清醒小鼠的制备

It is well known that anesthesia alters neural response properties in various regions of the brain.13.  In the auditory system, fundamental response ...

神经科学

Juxtacellular Monitoring and Localization of Single Neurons within Sub-cortical Brain Structures of Alert, Head-restrained Rats

There are a variety of techniques to monitor extracellular activity of single neuronal units. However, monitoring this activity from deep brain structures in behaving animals remains a technical challenge, especially if the structures must be targeted stereotaxically. This protocol describes convenient surgical and electrophysiological techniques that maintain the animal&#8217;s head in the stereotaxic plane and unambiguously isolate the spiking activity of single neurons. The protocol combines head restraint of alert rodents, juxtacellular monitoring with micropipette electrodes, and iontophoretic dye injection to identify the neuron location in post-hoc histology. While each of these techniques is in itself well-established, the protocol focuses on the specifics of their combined use in a single experiment. These neurophysiological and neuroanatomical techniques are combined with behavioral monitoring. In the present example, the combined techniques are used to determine how self-generated vibrissa movements are encoded in the activity of neurons within the somatosensory thalamus. More generally, it is straightforward to adapt this protocol to monitor neuronal activity in conjunction with a variety of behavioral tasks in rats, mice, and other animals. Critically, the combination of these methods allows the experimenter to directly relate anatomically-identified neurophysiological signals to behavior.

This protocol describes the design and surgical implantation of a head-restraining mechanism to monitor neuronal activity in sub-cortical brain structures in alert rats. It delineates procedures to isolate single neurons in the juxtacellular configuration and to efficiently identify their anatomical locations.

警报，头抑制大鼠子皮层的大脑结构中Juxtacellular监测和本地化单神经元

There are a variety of techniques to monitor extracellular activity of single neuronal units. However, monitoring this activity from deep brain structures ...

Simultaneous Electrophysiological Recording and Micro-injections of Inhibitory Agents in the Rodent Brain

Here we describe a method for the construction of a single-use &#8220;injectrode&#8221; using commercially accessible and affordable parts. A probing system was developed that allows for the injection of a drug while recording electrophysiological signals from the affected neuronal population. This method provides a simple and economical alternative to commercial solutions. A glass pipette was modified by combining it with a hypodermic needle and a silver filament. The injectrode is attached to commercial microsyringe pump for drug delivery. This results in a technique that provides real-time pharmacodynamics feedback through multi-unit extracellular signals originating from the site of drug delivery. As a proof of concept, we recorded neuronal activity from the superior colliculus elicited by flashes of light in rats, concomitantly with delivery of drugs through the injectrode. The injectrode recording capacity permits the functional characterization of the injection site favoring precise control over the localization of drug delivery. Application of this method also extends far beyond what is demonstrated here, as the choice of chemical substance loaded into the injectrode is vast, including tracing markers for anatomic experiments.

Here, we craft a glass pipette with dual functions: inhibition of deep brain structures by microinjections of drugs and real-time monitoring of their effects through simultaneous electrophysiological recordings.

同时电生理记录和抑制剂在啮齿动物大脑微注射

Here we describe a method for the construction of a single-use &#8220;injectrode&#8221; using commercially accessible and affordable parts. A probing ...

Induction of an Isoelectric Brain State to Investigate the Impact of Endogenous Synaptic Activity on Neuronal Excitability In Vivo

The way neurons process information depends both on their intrinsic membrane properties and on the dynamics of the afferent synaptic network. In particular, endogenously-generated network activity, which strongly varies as a function of the state of vigilance, significantly modulates neuronal computation. To investigate how different spontaneous cerebral dynamics impact single neurons&#39; integrative properties, we developed a new experimental strategy in the rat consisting in suppressing in vivo all cerebral activity by means of a systemic injection of a high dose of sodium pentobarbital. Cortical activities, continuously monitored by combined electrocorticogram (ECoG) and intracellular recordings are progressively slowed down, leading to a steady isoelectric profile. This extreme brain state, putting the rat into a deep comatose, was carefully monitored by measuring the physiological constants of the animal throughout the experiments. Intracellular recordings allowed us to characterize and compare the integrative properties of the same neuron embedded into physiologically relevant cortical dynamics, such as those encountered in the sleep-wake cycle, and when the brain was fully silent.

Induction of an Isoelectric Brain State to Investigate the Impact of Endogenous Synaptic Activity on Neuronal Excitability In Vivo

This procedure performs long-lasting in vivo intracellular recordings from single neurons during physiologically relevant cerebral states and after complete abolition of ongoing electrical activities, resulting in an isoelectric brain state. The physiological constants of the animal are carefully monitored during the transition to the artificial comatose condition.

等电脑国家的诱导研究内源性突触活动对神经元兴奋性影响<em&gt;在体内</em

The way neurons process information depends both on their intrinsic membrane properties and on the dynamics of the afferent synaptic network. In ...

Acute In Vivo Electrophysiological Recordings of Local Field Potentials and Multi-unit Activity from the Hyperdirect Pathway in Anesthetized Rats

Converging evidence shows that many neuropsychiatric diseases should be understood as disorders of large-scale neuronal networks. To better understand the pathophysiological basis of these diseases, it is necessary to precisely characterize in which way the processing of information is disturbed between the different neuronal parts of the circuit. Using extracellular in vivo electrophysiological recordings, it is possible to accurately delineate neuronal activity within a neuronal network. The application of this method has several advantages over alternative techniques, e.g., functional magnetic resonance imaging and calcium imaging, as it allows a unique temporal and spatial resolution and does not rely on genetically engineered organisms. However, the use of extracellular in vivo recordings is limited since it is an invasive technique that cannot be universally applied. In this article, a simple and easy to use method is presented with which it is possible to simultaneously record extracellular potentials such as local field potentials and multiunit activity at multiple sites of a network. It is detailed how a precise targeting of subcortical nuclei can be achieved using a combination of stereotactic surgery and online analysis of multi-unit recordings. Thus, it is demonstrated, how a complete network such as the hyperdirect cortico-basal ganglia loop can be studied in anesthetized animals in vivo.

Acute In Vivo Electrophysiological Recordings of Local Field Potentials and Multi-unit Activity from the Hyperdirect Pathway in Anesthetized Rats

In this study, the methodology is presented on how to perform multi-site in vivo electrophysiological recordings from the hyperdirect pathway under urethane anesthesia.

急性<em&gt;体内</em&gt;麻醉大鼠超导途径局部场电位和多单位活动的电生理记录

Converging evidence shows that many neuropsychiatric diseases should be understood as disorders of large-scale neuronal networks. To better understand the ...

Optogenetics Identification of a Neuronal Type with a Glass Optrode in Awake Mice

It is a major concern in neuroscience how different types of neurons work in neural circuits. Recent advances in optogenetics have enabled the identification of the neuronal type in in vivo electrophysiological experiments in broad brain regions. In optogenetics experiments, it is critical to deliver the light to the recording site. However, it is often hard to deliver the stimulation light to the deep brain regions from the brain&#39;s surface. Especially, it is difficult for the stimulation light to reach the deep brain regions when the optical transparency of the brain surface is low, as is often the case with recordings from awake animals. Here, we describe a method to record spike responses to the light from an awake mouse using a custom-made glass optrode. In this method, the light is delivered through the recording glass electrode so that it is possible to reliably stimulate the recorded neuron with light in the deep brain regions. This custom-made optrode system consists of accessible and inexpensive materials and is easy to assemble.

This work introduces a method to perform an optogenetic single-unit recording reliably from an awake mouse using a custom-made glass optrode.

光遗传学玻璃光纤化学传感在醒鼠中的神经型鉴定

It is a major concern in neuroscience how different types of neurons work in neural circuits. Recent advances in optogenetics have enabled the ...

小鼠运动皮层中的细胞外电生理记录

Multichannel Extracellular Recording in Freely Moving Mice

The protocol aims to uncover the properties of neuronal firing and network local field potentials (LFPs) in behaving mice carrying out specific tasks by correlating the electrophysiological signals with spontaneous and/or specific behavior. This technique represents a valuable tool in studying the neuronal network activity underlying these behaviors. The article provides a detailed and complete procedure for electrode implantation and consequent extracellular recording in free-moving conscious mice. The study includes a detailed method for implanting the microelectrode arrays, capturing the LFP and neuronal spiking signals in the motor cortex (MC) using a multichannel system, and the subsequent offline data analysis. The advantage of multichannel recording in conscious animals is that a greater number of spiking neurons and neuronal subtypes can be obtained and compared, which allows the evaluation of the relationship between a specific behavior and the associated electrophysiological signals. Notably, the multichannel extracellular recording technique and the data analysis procedure described in the present study can be applied to other brain areas when conducting experiments in behaving mice.

作者聚焦:用于研究自由移动小鼠神经元活动的多通道细胞外记录的进展 

The protocol describes the methodology of extracellular recording in the motor cortex (MC) to reveal extracellular electrophysiological properties in freely moving conscious mice, as well as the data analysis of local field potentials (LFPs) and spikes, which is useful for evaluating the network neural activity underlying behaviors of interest.

自由移动小鼠的多通道细胞外记录

The protocol aims to uncover the properties of neuronal firing and network local field potentials (LFPs) in behaving mice carrying out specific tasks by ...

神经元电活动外记录与神经活性物质在清醒小鼠微电泳应用相结合

摘要

探索更多视频

此视频中的章节

平地板的空气解禁平台:一种新方法与显微镜或电对清醒结合行为自由移动鼠害

记录神经反应和注射示踪剂一个清醒小鼠的制备

警报，头抑制大鼠子皮层的大脑结构中Juxtacellular监测和本地化单神经元

同时电生理记录和抑制剂在啮齿动物大脑微注射

等电脑国家的诱导研究内源性突触活动对神经元兴奋性影响

急性

光遗传学玻璃光纤化学传感在醒鼠中的神经型鉴定

自由移动小鼠的多通道细胞外记录

自由移动小鼠的多通道细胞外记录

自由移动小鼠的多通道细胞外记录