Name: a surgical procedure for the administration of drugs to the inner ear in a non-human primate common marmoset (callithrix jacchus)
Uploaded: 2018-02-27T12:30:00.000+00:00
Duration: 6 min 55 s
Description: Watch this Scientific Journal Video about A Surgical Procedure for the Administration of Drugs to the Inner Ear in a Non-Human Primate Common Marmoset Callithrix jacchus at JoVE.com

这项工作得到了日本政府下个 KAKENHI (24592560、15H04991 和 15K15624) 和武田科学基金会中频和 Jikei 大学战略优先研究基金中频的资助, 以 H.J.O。

所有实验程序都是在日本东京的 Jikei 大学进行的。动物处理和实验程序经 Jikei 大学机构动物保育和使用委员会批准 (批准号: 26-060), 并按照《 Jikei 实验室动物使用机构指南》执行。大学, 同意由日本科学理事会正确进行动物实验的指南 (2006)。动物护理是按照《护理和使用实验动物指南》 (1996 实验室动物资源研究所) 的建议进行的。
1. 术前检查
<ol><li>采取颅内计算机断层扫描 (CT) 对动物 (常见的猴) 进行检查, 以方便在手术前至少一个月内鉴定个别解剖结构。</li>
	<li>在手术前至少一个月进行听力测试。 注意: 在这里, 我们使用 ABR 来评估听力状态。简要地, 一个正极被皮下放置在顶点和一个参考负极在被刺激的耳朵的背底。地面电极被皮下放置在颈部的背部。17,18 ABRs 以音调爆裂 (1.0 毫秒音爆发持续时间0.1 毫秒上升和下降) 诱发。然后从其最大振幅的10分贝步骤中降低了声音电平。在每个声音水平 , 512 反应是平均的 ( 以刺激极替 ) 。ABR 阈值被定义为最低的声压级 (SPL), 在那里可以检测到任何波。</li>
</ol>2. 麻醉
<ol><li>快速动物从夜间手术前全身麻醉。</li>
	<li>管理4% 异氟醚和环境空气在 5-6 毫升/分钟与掩模到面通风或在感应室为慢感应 (图 1A)。确认动物不响应疼痛刺激, 如脚趾捏。</li>
	<li>Anesthestize 常见的猴肌肉注射 (入股肌) 的组合 medetomidine (0.04 毫克/千克), 咪达唑仑 (0.4 毫克/千克), 和布托啡诺 (0.4 毫克/千克)。</li>
	<li>注射氨苄西林 (0.08 毫克/克) 皮下30分钟或以上皮肤切口前抗生素。</li>
	<li>将狨放在仰卧位, 头部朝向顶部, 伸展头部和颈部。用尼龙线固定上颌骨, 拉起舌头以获得良好的视野, 或者使用喉镜可视化会厌和喉的进入 (图 1B)。</li>
	<li>在会厌的喉表面插入气管导管。 注: 有可能使用16口径静脉注射导管, 或 6-法国标准喂养管, 作为气管插管 (图 1C)。</li>
	<li>检查 EtCO2 , 从气管插管, 以确认它已正确放置到气管。在导管定位和呼吸气体运动检查后, 用胶带将气管插管固定在狨的脸上。</li>
	<li>在手术期间保持1-3% 异氟醚之间的麻醉。</li>
	<li>在操作期间监视 EtCO2、2、体温和直肠温度。在加热垫上执行所有步骤, 防止体温降低。</li>
</ol>3. 术前准备
<ol><li>在仰卧位置准备狨, 并将头部倾斜至 30-45 度角至非手术侧 (图 2A)。</li>
	<li>剃须后耳区的手术侧。</li>
	<li>对手术部位进行酒精和聚维酮碘的消毒, 无论是在耳后区还是外耳道。</li>
	<li>在狨上放置一个带圆孔的外科悬垂板 (图 2B)。</li>
</ol>4. 手术程序
<ol><li>注射1% 盐酸利多卡因 (1:100,000 肾上腺素, 0.1-0.2 毫升) 皮下进入皮肤切口部位。用15号圆形刀片在耳后皮肤上做切口。</li>
	<li>止血时, 用纱布浸泡在 1:5, 000 稀释肾上腺素中, 对出血区施加压力。双极性灼烧也是有效的 (图 2C)。</li>
	<li>打开后耳区软组织, 使耳软骨 (c) 和耳后肌 (m) 可以识别。暴露出应在软骨深处可见的外部听觉管骨 (图 3A)。</li>
	<li>为确定鼓膜的深度, 暴露鼓膜边缘的骨部, 可识别为后耳道最深部的皮肤和骨粘连。 注意: 这一步允许我们认识到中耳腔的侧部有多深 (图 3A)。</li>
	<li>将耳后肌 (胸锁乳突肌、splenius 头癣肌、二腹肌肌后腹部) 剥离至尾部, 与颞骨分离。然后暴露颞骨的侧向表面 (星号在图 3B中)。</li>
	<li>用1.0 毫米的钻石 (图 3C) 在外部听觉管道后面打一个洞, 大约5毫米。使用 1000-8000 rpm 的钻速取决于钻孔位置。 注意: 一个缓慢的速度是足够的微妙操作附近的半圆形运河或面神经。适当滴盐水在钻孔部位, 防止热损伤。</li>
	<li>通过钻孔和确认水平半圆管 (HSC) 的位置来扩大孔, 向乳突腔 (图 3D) 凸出。</li>
	<li>确定垂直部位的面神经在 HSC 前的位置。如果他们存在, 钻和删除所有的骨间隔, 以获得一个清晰的看法, 面部凹进处, 这是位于三角区中心的面神经和鼓索。</li>
	<li>在脸部神经的垂直部分和鼓膜边缘 (图 4A中的星号) 之间钻孔, 并在1000转每分钟0.6 毫米直径的钻石, 使一个小孔。</li>
	<li>将其与后管壁平行移动, 以防止面部神经受损, 通过瘦骨可以看到粉红色线。在将神经暴露为白色线结构之前, 立即停止钻孔 (图 4B)。</li>
	<li>确保圆形窗口利基可以通过孔可视化 (图 4C)。然后, 用25口径或更薄的针头将药物注入利基。为了保留在圆形窗口利基的药物, 在利基 (图 4D) 上放置粘性解决方案。</li>
	<li>在确认止血是安全控制后, 用6-0 根吸收线闭合简单的间断缝合层 (表皮层和真皮层)。</li>
	<li>把纱布固定在手术伤口上, 贴上绷带。</li>
</ol>5. 术后护理
<ol><li>管理盐酸 atipamezole (0.15 毫克/千克) 肌肉入股肌拮抗 medetomidine。</li>
	<li>当自发呼吸开始时, 取出气管导管。</li>
	<li>保持在 30% O2, 29 ℃的重症监护病房的共同狨, 直到麻醉结束, 以完成唤醒。</li>
	<li>确认没有发现提示前庭功能障碍, 如眼球震颤, 并返回动物的饲养笼。</li>
</ol>

<ol>
	<li>Liberman, M. C., Kujawa, S. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cochlear+synaptopathy+in+acquired+sensorineural+hearing+loss:+Manifestations+and+mechanisms.">Cochlear synaptopathy in acquired sensorineural hearing loss: Manifestations and mechanisms.</a> Hear Res. 349, 138-147 (2017).</li><li>World Health Organization. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Deafness and hearing loss (Fact sheet N8300). , (2015).</li><li>Thompson, D. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Universal+newborn+hearing+screening:+summary+of+evidence.">Universal newborn hearing screening: summary of evidence.</a> JAMA. 286 (16), 2000-2010 (2001).</li><li>Wang, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neural+coding+strategies+in+auditory+cortex.">Neural coding strategies in auditory cortex.</a> Hear Res. 229 (1-2), 81-93 (2007).</li><li>Wang, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=On+cortical+coding+of+vocal+communication+sounds+in+primates.">On cortical coding of vocal communication sounds in primates.</a> Proc Natl Acad Sci U S A. 97 (22), 11843-11849 (2000).</li><li>Bendor, D., Wang, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+neuronal+representation+of+pitch+in+primate+auditory+cortex.">The neuronal representation of pitch in primate auditory cortex.</a> Nature. 436 (7054), 1161-1165 (2005).</li><li>Bendor, D., Wang, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neural+coding+of+periodicity+in+marmoset+auditory+cortex.">Neural coding of periodicity in marmoset auditory cortex.</a> J Neurophysiol. 103 (4), 1809-1822 (2010).</li><li>Eliades, S. J., Wang, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sensory-motor+interaction+in+the+primate+auditory+cortex+during+self-initiated+vocalizations.">Sensory-motor interaction in the primate auditory cortex during self-initiated vocalizations.</a> J Neurophysiol. 89 (4), 2194-2207 (2003).</li><li>Eliades, S. J., Wang, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dynamics+of+auditory-vocal+interaction+in+monkey+auditory+cortex.">Dynamics of auditory-vocal interaction in monkey auditory cortex.</a> Cereb Cortex. 15 (10), 1510-1523 (2005).</li><li>Eliades, S. J., Wang, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neural+substrates+of+vocalization+feedback+monitoring+in+primate+auditory+cortex.">Neural substrates of vocalization feedback monitoring in primate auditory cortex.</a> Nature. 453 (7198), 1102-1106 (2008).</li><li>Hosoya, M., Fujioka, M., Ogawa, K., Okano, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Distinct+Expression+Patterns+Of+Causative+Genes+Responsible+For+Hereditary+Progressive+Hearing+Loss+In+Non-Human+Primate+Cochlea.">Distinct Expression Patterns Of Causative Genes Responsible For Hereditary Progressive Hearing Loss In Non-Human Primate Cochlea.</a> Sci Rep. 6, 22250 (2016).</li><li>Hosoya, M., Fujioka, M., Kobayashi, R., Okano, H., Ogawa, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Overlapping+expression+of+anion+exchangers+in+the+cochlea+of+a+non-human+primate+suggests+functional+compensation.">Overlapping expression of anion exchangers in the cochlea of a non-human primate suggests functional compensation.</a> Neurosci Res. 110, 1-10 (2016).</li><li>Sasaki, E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Generation+of+transgenic+non-human+primates+with+germline+transmission.">Generation of transgenic non-human primates with germline transmission.</a> Nature. 459 (7246), 523-527 (2009).</li><li>Sato, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Generation+of+a+Nonhuman+Primate+Model+of+Severe+Combined+Immunodeficiency+Using+Highly+Efficient+Genome+Editing.">Generation of a Nonhuman Primate Model of Severe Combined Immunodeficiency Using Highly Efficient Genome Editing.</a> Cell Stem Cell. 19 (1), 127-138 (2016).</li><li>Sasaki, E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Establishment+of+novel+embryonic+stem+cell+lines+derived+from+the+common+marmoset+(Callithrix+jacchus).">Establishment of novel embryonic stem cell lines derived from the common marmoset (Callithrix jacchus).</a> Stem Cells. 23 (9), 1304-1313 (2005).</li><li>Tomioka, I., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Generating+induced+pluripotent+stem+cells+from+common+marmoset+(Callithrix+jacchus)+fetal+liver+cells+using+defined+factors,+including+Lin28.">Generating induced pluripotent stem cells from common marmoset (Callithrix jacchus) fetal liver cells using defined factors, including Lin28.</a> Genes Cells. 15 (9), 959-969 (2010).</li><li>Harada, T., Tokuriki, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effects+of+click+intensity+and+frequency+on+the+brain-stem+auditory+evoked+potentials+in+the+common+marmoset+(Callithrix+jacchus).">Effects of click intensity and frequency on the brain-stem auditory evoked potentials in the common marmoset (Callithrix jacchus).</a> J Vet Med Sci. 59 (7), 561-567 (1997).</li><li>Harada, T., Tokuriki, M., Tanioka, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Age-related+changes+in+the+brainstem+auditory+evoked+potentials+of+the+marmoset.">Age-related changes in the brainstem auditory evoked potentials of the marmoset.</a> Hear Res. 128 (1-2), 119-124 (1999).</li><li>Juhn, S. K., Hunter, B. A., Odland, R. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Blood-labyrinth+barrier+and+fluid+dynamics+of+the+inner+ear.">Blood-labyrinth barrier and fluid dynamics of the inner ear.</a> Int Tinnitus J. 7 (2), 72-83 (2001).</li><li>Nakashima, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Disorders+of+cochlear+blood+flow.">Disorders of cochlear blood flow.</a> Brain Res Brain Res Rev. 43 (1), 17-28 (2003).</li><li>Akil, O., Rouse, S. L., Chan, D. K., Lustig, L. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Surgical+method+for+virally+mediated+gene+delivery+to+the+mouse+inner+ear+through+the+round+window+membrane.">Surgical method for virally mediated gene delivery to the mouse inner ear through the round window membrane.</a> J Vis Exp. (97), (2015).</li><li>Jero, J., Tseng, C. J., Mhatre, A. N., Lalwani, A. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+surgical+approach+appropriate+for+targeted+cochlear+gene+therapy+in+the+mouse.">A surgical approach appropriate for targeted cochlear gene therapy in the mouse.</a> Hear Res. 151 (1-2), 106-114 (2001).</li><li>Iizuka, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Noninvasive+in+vivo+delivery+of+transgene+via+adeno-associated+virus+into+supporting+cells+of+the+neonatal+mouse+cochlea.">Noninvasive in vivo delivery of transgene via adeno-associated virus into supporting cells of the neonatal mouse cochlea.</a> Hum Gene Ther. 19 (4), 384-390 (2008).</li><li>Kilpatrick, L. A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Adeno-associated+virus-mediated+gene+delivery+into+the+scala+media+of+the+normal+and+deafened+adult+mouse+ear.">Adeno-associated virus-mediated gene delivery into the scala media of the normal and deafened adult mouse ear.</a> Gene Ther. 18 (6), 569-578 (2011).</li><li>Yamasoba, T., Yagi, M., Roessler, B. J., Miller, J. M., Raphael, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inner+ear+transgene+expression+after+adenoviral+vector+inoculation+in+the+endolymphatic+sac.">Inner ear transgene expression after adenoviral vector inoculation in the endolymphatic sac.</a> Hum Gene Ther. 10 (5), 769-774 (1999).</li><li>Kawamoto, K., Oh, S. H., Kanzaki, S., Brown, N., Raphael, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+functional+and+structural+outcome+of+inner+ear+gene+transfer+via+the+vestibular+and+cochlear+fluids+in+mice.">The functional and structural outcome of inner ear gene transfer via the vestibular and cochlear fluids in mice.</a> Mol Ther. 4 (6), 575-585 (2001).</li><li>Praetorius, M., Baker, K., Weich, C. M., Plinkert, P. K., Staecker, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hearing+preservation+after+inner+ear+gene+therapy:+the+effect+of+vector+and+surgical+approach.">Hearing preservation after inner ear gene therapy: the effect of vector and surgical approach.</a> ORL J Otorhinolaryngol Relat Spec. 65 (4), 211-214 (2003).</li><li>Nakagawa, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Topical+insulin-like+growth+factor+1+treatment+using+gelatin+hydrogels+for+glucocorticoid-resistant+sudden+sensorineural+hearing+loss:+a+prospective+clinical+trial.">Topical insulin-like growth factor 1 treatment using gelatin hydrogels for glucocorticoid-resistant sudden sensorineural hearing loss: a prospective clinical trial.</a> BMC Med. 8, 76 (2010).</li><li>Piu, F., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=OTO-104:+a+sustained-release+dexamethasone+hydrogel+for+the+treatment+of+otic+disorders.">OTO-104: a sustained-release dexamethasone hydrogel for the treatment of otic disorders.</a> Otol Neurotol. 32 (1), 171-179 (2011).</li><li>Plontke, S. K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=double+blind,+placebo+controlled+trial+on+the+safety+and+efficacy+of+continuous+intratympanic+dexamethasone+delivered+via+a+round+window+catheter+for+severe+to+profound+sudden+idiopathic+sensorineural+hearing+loss+after+failure+of+systemic+therapy.">double blind, placebo controlled trial on the safety and efficacy of continuous intratympanic dexamethasone delivered via a round window catheter for severe to profound sudden idiopathic sensorineural hearing loss after failure of systemic therapy.</a> Laryngoscope. 119 (2), 359-369 (2009).</li><li>Wenzel, G. I., Warnecke, A., Stover, T., Lenarz, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effects+of+extracochlear+gacyclidine+perfusion+on+tinnitus+in+humans:+a+case+series.">Effects of extracochlear gacyclidine perfusion on tinnitus in humans: a case series.</a> Eur Arch Otorhinolaryngol. 267 (5), 691-699 (2010).</li></ol>

作者没有什么可透露的。

耳蜗血流量非常小, 估计是在人类总心脏输出的 1/100万的顺序, 和访问是有限的血-耳蜗屏障的存在, 分离内耳从一般循环19 ,20。由于这些原因, 药物或病毒的媒介管理进入内耳是有利的, 不是通过系统性的管理, 而是由直接管理。在小鼠和豚鼠实验中, 报告了各种方法, 如采用耳后入路或腹侧方法的转圆窗、cochleostomy、淋巴囊传递和半圆管方法...

感音神经性听力丧失 (SNHL) 主要出现在耳蜗损伤或缺陷。SNHL 的常见原因包括老化 (例如聋)、遗传缺陷、暴露于噪音、感染和毒性药物1。世界卫生组织 (卫生组织) 估计, 占世界人口5.3% 的3.6亿多人患有听力损失2。据估计, 在900至1的2500新生儿中, 有轻度、严重和深刻的先天性永久性听力丧失, 而1/3 岁以上的成年人有一定程度的听力损失65。然而, 对于这些患者来说, 听力丧失没有有效的临床治疗方法。
听力研究一直使用啮齿动物或豚鼠模型, 并提出了许多方法, 如基因治疗和再生治疗, 被认为是一种新的治疗听力损失。然而, 人类和啮齿动物在听觉系统上有很大的区别, 很难将动物模型转化为人类的应用。狨 (jacchus) 是来自亚马逊的新一代世界猴, 由于多种原因, 它已成为各种基础研究研究的一种具有吸引力的非人类灵长类动物模型。首先, 它的解剖和生理学更类似于人类而不是啮齿动物。第二, 关于这个物种的基本生物学信息, 包括疾病、神经网络、行为和基因组, 都有很好的特点。听觉和声带处理, 周期性皮质编码, 音高的表示, 和常见的猴的听觉声音互动也被报告了4,5,6,7,8,9,10. 在最近的组织学研究中, 研究人员发现了20种耳聋基因和阴离子交换器在普通狨耳蜗中的独特表达模式, 发现五基因是渐进性耳聋的病因, 三阴离子交换器, 有不同的表达模式, 从啮齿动物11,12。这些概况使我们相信, 共同狨是听觉研究的有力工具。
作为实验动物的常见狨的最显著属性如下:
<ul><li>简单的处理与小体型相比, 一些老世界的猴子: 成年猕猴重 300-400 克, 身高约60厘米, 这是类似于大鼠。</li>
	<li>高度繁殖的灵长类动物: 在18月的年龄, 它能达到性成熟, 每年能承受两次, 每年产生4到6个子代。</li>
	<li>基因修改是可利用的: et 等人成功地创建了转基因的13和敲出14灵长类动物使用猴的基因修饰涉及神经系统疾病 (例如,帕金森的疾病和阿尔茨海默病)。</li>
	<li>胚胎干细胞和诱导的多能干细胞 (iPS) 细胞已经建立了15,16。虽然与啮齿目动物相比, 保持相同数量的绒猴是相当困难的, 但干细胞或 iPS 细胞的可用性提供了体外化验, 这将减少所需的体内化验的数量。</li>
</ul>为了促进耳聋及其潜在治疗领域的更好的翻译研究, 我们建立了一种利用听觉脑干反应 (ABRs) 进行 CT 和 MRI、全身麻醉和听力测试的成像研究协议。这些实验系统可以为我们提供更好的机会, 以获得临床前证明的概念研究, 这对于弥合啮齿类动物研究和临床试验之间的差距是必不可少的。在这里, 我们报告一个外科方法, 通过圆窗膜对普通狨的内耳进行药物管理。为了在圆形窗口周围获得清晰的视野, 在不操作可能导致传导性听力损失的鼓膜的情况下, 从乳突腔中接近是有用的。临床上, 这种方法, 称为 "后鼓膜置" 是很好的建立, 通常用于人工耳蜗植入和胆脂瘤手术。我们相信, 后鼓膜置允许我们进行准确的药物管理, 而不诱发听力损失。

<table><tbody><tr><td>common marmoset</td><td>CLEA Japan</td><td>EDM:C.Marmoset(Jic)</td><td></td></tr><tr><td>isoflurane</td><td>Phizer</td><td></td><td></td></tr><tr><td>medetomidine</td><td>ZENOAQ</td><td></td><td></td></tr><tr><td>midazolam</td><td>astellas</td><td></td><td></td></tr><tr><td>butorphanol</td><td>Meiji Seika</td><td></td><td></td></tr><tr><td>ampicillin</td><td>Meiji Seika</td><td></td><td></td></tr><tr><td>lidocaine hydrochloride</td><td>AstraZeneca</td><td></td><td></td></tr><tr><td>&amp;nbsp;6-0 absorbent thread</td><td>ETHICON</td><td>RD-1</td><td></td></tr><tr><td>atipamezole hydrochloride</td><td>ZENOAQ</td><td></td><td></td></tr><tr><td>phosphate buffered saline</td><td>Wako</td><td>045-29795</td><td></td></tr><tr><td>Surge Wave</td><td>Morita</td><td>TR-900-OR</td><td></td></tr><tr><td>Diamond Bar 006</td><td>Morita</td><td>14070057</td><td></td></tr><tr><td>Diamond Bar 010</td><td>Morita</td><td>14070081</td><td></td></tr><tr><td>intensive care unit</td><td>Menix</td><td>P-100</td><td></td></tr></tbody></table>

a surgical procedure for the administration of drugs to the inner ear in a non-human primate common marmoset (callithrix jacchus)

虽然在某些疾病中, 人类的症状不能概括, 但长期以来, 啮齿类动物模型已经促进了听觉研究。常见的狨 (Callithrix jacchus) 是一种小型的、易于处理的新世界猴, 它具有类似于颞骨的解剖, 包括中耳听骨链和内耳对人类, 比与啮齿动物的比较。在这里, 我们报告一个可重现的, 安全的, 合理的手术方法的耳蜗圆形窗口的利基为药物传递到内耳的共同狨。我们采用后鼓膜置, 这是一个在人体外科临床应用的程序, 以避免对鼓膜的操纵, 可能导致传导性听力丧失。这个手术过程并没有导致任何重大的听力损失。这种方法是可能的, 由于共同狨的大泡结构, 虽然侧半圆管和面神经的垂直部分应仔细考虑。这种手术方法使我们能够在无听力损失的情况下对药物进行安全、准确的管理, 这对于获得临床翻译研究概念的前期证明具有重要意义。

术后鼓膜置无并发症, 如手术部位感染, 血管损伤出血, 前庭功能障碍, 有时发生中耳操纵。我们在7岁的普通狨的右耳上进行后鼓膜置, 并将1µL 磷酸盐缓冲盐水用于圆窗利基。ABRs 在手术前和两个月后进行测量 (图 5A-B)。ABRs 的波形和阈值与以前的研究17、18相同, 在手术前后这些参数没有变化 (<st...

Watch this Scientific Journal Video about A Surgical Procedure for the Administration of Drugs to the Inner Ear in a Non-Human Primate Common Marmoset Callithrix jacchus at JoVE.com

A Surgical Procedure for the Administration of Drugs to the Inner Ear in a Non-Human Primate Common Marmoset Callithrix jacchus

我们报告一种外科方法, 以管理药物的内耳的非人类灵长类, 常见的狨 (Callithrix jacchus), 通过圆窗膜。

一种非人类灵长类常见狨中内耳药物的外科手术方法 (Callithrix jacchus)

Hearing research has long been facilitated by rodent models, although in some diseases, human symptoms cannot be recapitulated. The common marmoset ...

a-surgical-procedure-for-administration-drugs-to-inner-ear-non-human

Research

JoVE Journal

Medicine

A Surgical Procedure for the Administration of Drugs to the Inner Ear in a Non-Human Primate Common Marmoset (Callithrix jacchus)

8.6K 次观看.  Jikei University School of Medicine. 我们报告一种外科方法, 以管理药物的内耳的非人类灵长类, 常见的狨 (Callithrix jacchus), 通过圆窗膜。

视频: A Surgical Procedure for the Administration of Drugs to the Inner Ear in a Non-Human Primate Common Marmoset Callithrix jacchus

Canalostomy As a Surgical Approach to Local Drug Delivery into the Inner Ears of Adult and Neonatal Mice

Local delivery of therapeutic drugs into the inner ear is a promising therapy for inner ear diseases. Injection through semicircular canals (canalostomy) has been shown to be a useful approach to local drug delivery into the inner ear. The goal of this article is to describe, in detail, the surgical techniques involved in canalostomy in both adult and neonatal mice. As indicated by fast-green dye and adeno-associated virus serotype 8 with the green fluorescent protein gene, the canalostomy facilitated broad distribution of injected reagents in the cochlea and vestibular end-organs with minimal damage to hearing and vestibular function. The surgery was successfully implemented in both adult and neonatal mice; indeed, multiple surgeries could be performed if required. In conclusion, canalostomy is an effective and safe approach to drug delivery into the inner ears of adult and neonatal mice and may be used to treat human inner ear diseases in the future.

Here we describe canalostomy procedure which allows local drug delivery into the inner ears of adult and neonatal mice through the semicircular canal with minimum damage to hearing and vestibular function. This method can be used to inoculate viral vectors, pharmaceuticals, and small molecules into the mouse inner ear.

Canalostomy 为成人和新生小鼠内耳局部药物传递的外科治疗方法

Local delivery of therapeutic drugs into the inner ear is a promising therapy for inner ear diseases. Injection through semicircular canals (canalostomy) ...

科研

遗传学

Surgical Method for Virally Mediated Gene Delivery to the Mouse Inner Ear through the Round Window Membrane

Gene therapy, used to achieve functional recovery from sensorineural deafness, promises to grant better understanding of the underlying molecular and genetic mechanisms that contribute to hearing loss. Introduction of vectors into the inner ear must be done in a way that widely distributes the agent throughout the cochlea while minimizing injury to the existing structures. This manuscript describes a post-auricular surgical approach that can be used for mouse cochlear therapy using molecular, pharmacologic, and viral delivery to mice postnatal day 10 and older via the round window membrane (RWM). This surgical approach enables rapid and direct delivery into the scala tympani while minimizing blood loss and avoiding animal mortality. This technique involves negligible or no damage to essential structures of the inner and middle ear as well as neck muscles while wholly preserving hearing. To demonstrate the efficacy of this surgical technique, the vesicular glutamate transporter 3 knockout (VGLUT3 KO) mice will be used as an example of a mouse model of congenital deafness that recovers hearing after delivery of VGLUT3 to the inner ear using an adeno-associated virus (AAV-1).

The described post-auricular surgical approach allows rapid and direct delivery into the mouse cochlear scala tympani while minimizing blood loss and animal mortality. This method can be used for cochlear therapy using molecular, pharmacologic and viral delivery to postnatal mice through the round window membrane.

通过圆窗膜病毒介导的基因传递给鼠标内耳手术方法

Gene therapy, used to achieve functional recovery from sensorineural deafness, promises to grant better understanding of the underlying molecular and ...

神经科学

The Mouse Round-window Approach for Ototoxic Agent Delivery: A Rapid and Reliable Technique for Inducing Cochlear Cell Degeneration

Investigators have utilized a wide array of animal models and investigative techniques to study the mammalian auditory system. Much of the basic research involving the cochlea and its associated neural pathways entails exposure of model cochleae to a variety of ototoxic agents. This allows investigators to study the effects of targeted damage to cochlear structures, and in some cases, the self-repair or regeneration of those structures. Various techniques exist for delivery of ototoxic agents to the cochlea. When selecting a particular technique, investigators must consider a number of factors, including the induction of inadvertent systemic toxicity, the amount of cochlear damage produced by the surgical procedure itself, the type of lesion desired, animal survivability, and reproducibility/reliability of results. Currently established techniques include parenteral injection, intra-peritoneal injection, trans-tympanic injection, endolymphatic sac injection, and cochleostomy with perilymphatic perfusion. Each of these methods has been successfully utilized and is well described in the literature; yet, each has various shortcomings. Here, we present a technique for topical application of ototoxic agents directly to the round window niche. This technique is non-invasive to inner ear structures, produces rapid onset of reliably targeted lesions, avoids systemic toxicity, and allows for an intra-animal control (the contra-lateral ear). Results stemming from this approach have helped deeper understanding of auditory pathophysiology, cochlear cell degeneration, and regenerative capacity in response to an acute injury. Future investigations may use this method to conduct interventional studies involving gene therapy and stem cell transplantation to combat hearing loss.

Various methods exist for introducing ototoxic agents to the cochleae of animal models. Presented is a surgical protocol for delivery of ototoxic agents to the round window niche. The procedure is reliable, creates targeted intra-cochlear lesions, and avoids mechanical damage to the microarchitecture. Examination of cochlear self-repair/regeneration is possible.

老鼠圆窗途径耳毒性剂递送:一个快速和可靠的技术诱导耳蜗细胞变性

Investigators have utilized a wide array of animal models and investigative techniques to study the mammalian auditory system. Much of the basic research ...

医学

Posterior Semicircular Canal Approach for Inner Ear Gene Delivery in Neonatal Mouse

Inner ear gene therapy offers great promise as a potential treatment for hearing loss and dizziness. One of the critical determinants of the success of inner ear gene therapy is to find a delivery method which results in consistent transduction efficiency of targeted cell types while minimizing hearing loss. In this study, we describe the posterior semicircular canal approach as a viable method for inner ear gene delivery in neonatal mice. We show that gene delivery through the posterior semicircular canal is able to perfuse the entire inner ear. The easy anatomic identification of the posterior semicircular canal, as well as minimal manipulation of the temporal bone required, make this surgical approach an attractive option for inner ear gene delivery.

In this study, we describe the posterior semicircular canal approach as a reliable method for inner ear gene delivery in neonatal mice. We show that gene delivery through the posterior semicircular canal is able to perfuse the entire inner ear.

后半圆管法在新生小鼠内耳基因传递中的研究

Inner ear gene therapy offers great promise as a potential treatment for hearing loss and dizziness. One of the critical determinants of the success of ...

Chronic Implantation of Whole-cortical Electrocorticographic Array in the Common Marmoset

Electrocorticography (ECoG) allows the monitoring of electrical field potentials from the cerebral cortex with high spatiotemporal resolution. Recent development of thin, flexible ECoG electrodes has enabled conduction of stable recordings of large-scale cortical activity. We have developed a whole-cortical ECoG array for the common marmoset. The array continuously covers almost the entire lateral surface of cortical hemisphere, from the occipital pole to the temporal and frontal poles, and it captures whole-cortical neural activity in one shot. This protocol describes a chronic implantation procedure of the array in the epidural space of the marmoset brain. Marmosets have two advantages regarding ECoG recordings, one being the homologous organization of anatomical structures in humans and macaques, including frontal, parietal, and temporal complexes. The other advantage is that the marmoset brain is lissencephalic and contains a large number of complexes, which are more difficult to access in macaques with ECoG, that are exposed to the brain surface.These features allow direct access to most cortical areas beneath the surface of the brain. This system provides an opportunity to investigate global cortical information processing with high resolutions at a sub-millisecond order in time and millimeter order in space.

We have developed a whole-cortical electrocorticographic array for the common marmoset that continuously covers almost the entire lateral surface of cortex, from the occipital pole to the temporal and frontal poles. This protocol describes a chronic implantation procedure of the array in the epidural space of the marmoset brain.

常见马莫塞的全皮质电皮质阵列的慢性植入

Electrocorticography (ECoG) allows the monitoring of electrical field potentials from the cerebral cortex with high spatiotemporal resolution. Recent ...

Stereotaxic Surgery for Implantation of Microelectrode Arrays in the Common Marmoset (Callithrix jacchus)

Marmosets (Callithrix jacchus) are small non-human primates that are gaining popularity in biomedical and preclinical research, including the neurosciences. Phylogenetically, these animals are much closer to humans than rodents. They also display complex behaviors, including a wide range of vocalizations and social interactions. Here, an effective stereotaxic neurosurgical procedure for implantation of recording electrode arrays in the common marmoset is described. This protocol also details the pre- and postoperative steps of animal care that are required to successfully perform such a surgery. Finally, this protocol shows an example of local field potential and spike activity recordings in a freely behaving marmoset 1 week after the surgical procedure. Overall, this method provides an opportunity to study the brain function in awake and freely behaving marmosets. The same protocol can be readily used by researchers working with other small primates. In addition, it can be easily modified to allow other studies requiring implants, such as stimulating electrodes, microinjections, implantation of optrodes or guide cannulas, or ablation of discrete tissue regions.

Stereotaxic Surgery for Implantation of Microelectrode Arrays in the Common Marmoset Callithrix jacchus

This work presents a protocol to perform a stereotaxic, neurosurgical implantation of&#160;microelectrode arrays in the common marmoset. This method specifically enables electrophysiological recordings in freely behaving animals but can be easily adapted to any other similar neurosurgical intervention in this species (e.g., cannula for drug administration or electrodes for brain stimulation).

在普通马莫塞特中植入微电极阵列的立体外科（Callithrix jacchus）

Marmosets (Callithrix jacchus) are small non-human primates that are gaining popularity in biomedical and preclinical research, including the ...

开发用于狨猴精确神经记录的 x-y 电极台

Electrophysiology of Laminar Cortical Activity in the Common Marmoset

The marmoset monkey provides an ideal model for examining laminar cortical circuits due to its smooth cortical surface, which facilitates recordings with linear arrays. The marmoset has recently grown in popularity due to its similar neural functional organization to other primates and its technical advantages for recording and imaging. However, neurophysiology in this model poses some unique challenges due to the small size and lack of gyri as anatomical landmarks. Using custom-built micro-drives, researchers can manipulate linear array placement to sub-millimeter precision and reliably record at the same retinotopically targeted location across recording days. This protocol describes the step-by-step construction of the micro-drive positioning system and the neurophysiological recording technique with silicon linear electrode arrays. With precise control of electrode placement across recording sessions, researchers can easily traverse the cortex to identify areas of interest based on their retinotopic organization and the tuning properties of the recorded neurons. Further, using this laminar array electrode system, it is possible to apply a current source density analysis (CSD) to determine the recording depth of individual neurons. This protocol also demonstrates examples of laminar recordings, including spike waveforms isolated in Kilosort, which span multiple channels on the arrays.

作者聚焦:优化 Micro-Drive Systems 以实现 Marmoset 中的精确电极定位

Custom-built micro-drives enable the sub-millimeter targeting of cortical recording sites with linear silicon arrays.

普通狨猴层流皮层活动的电生理学

The marmoset monkey provides an ideal model for examining laminar cortical circuits due to its smooth cortical surface, which facilitates recordings with ...

A Comparative Study of Drug Delivery Methods Targeted to the Mouse Inner Ear: Bullostomy Versus Transtympanic Injection

We present two minimally invasive microsurgical techniques in rodents for specific drug delivery into the middle ear so that it may reach the inner ear. The first procedure consists of perforation of the tympanic bulla, termed bullostomy; the second one is a transtympanic injection. Both emulate human clinical intratympanic procedures.
Chitosan-glycerophosphate (CGP) and Ringer&#180;s Lactate buffer (RL) were used as biocompatible vehicles for local drug delivery. CGP is a nontoxic biodegradable polymer widely used in pharmaceutical applications. It is a viscous liquid at RT&#160;but it congeals to a semi solid phase at body temperature. RL is an isotonic solution used for intravenous administrations in humans. A small volume of this vehicle is precisely placed on the Round Window (RW) niche by means of a bullostomy. A transtympanic injection fills the middle ear and allows less control but broader access to the inner ear.
The safety profiles of both techniques were studied and compared by using functional and morphological tests. Hearing was evaluated by registering the Auditory Brainstem Response (ABR) before and several times after microsurgery. The cytoarchitecture and preservation level of cochlear structures were studied by conventional histological techniques in paraformaldehyde-fixed and decalcified cochlear samples. In parallel, unfixed cochlear samples were taken and immediately frozen to analyze gene expression profiles of inflammatory markers by quantitative Reverse Transcriptase Polymerase Chain Reaction (qRT-PCR).
Both procedures are suitable as drug delivery methods into the mouse middle ear, although transtympanic injection proved to be less invasive compared to bullostomy.

A Comparative Study of Drug Delivery Methods Targeted to the Mouse Inner Ear: Bullostomy Versus Transtympanic Injection

Two microsurgery approaches for local drug delivery to the inner ear are described here and compared in terms of impact on hearing parameters, cochlear cytoarchitecture and expression of inflammatory markers.

针对鼠标内耳给药方法的比较研究:Bullostomy<em&gt;对战</em&gt;鼓室注射

We present two minimally invasive microsurgical techniques in rodents for specific drug delivery into the middle ear so that it may reach the inner ear. ...

一种非人类灵长类常见狨中内耳药物的外科手术方法 (Callithrix jacchus)

摘要

探索更多视频

此视频中的章节

Canalostomy 为成人和新生小鼠内耳局部药物传递的外科治疗方法

通过圆窗膜病毒介导的基因传递给鼠标内耳手术方法

老鼠圆窗途径耳毒性剂递送:一个快速和可靠的技术诱导耳蜗细胞变性

后半圆管法在新生小鼠内耳基因传递中的研究

常见马莫塞的全皮质电皮质阵列的慢性植入

在普通马莫塞特中植入微电极阵列的立体外科（Callithrix jacchus）

普通狨猴层流皮层活动的电生理学

普通狨猴层流皮层活动的电生理学

普通狨猴层流皮层活动的电生理学

针对鼠标内耳给药方法的比较研究:Bullostomy