Finansman: Bu çalışma Vakfı Bertarelli hibe (DJL), bir MED-EL hibe (DJL) ve Sağlık Hibeler DC01089 bir National Institutes (MCB) tarafından desteklenmiştir.

NOT: Bütün deneysel prosedürler Halk Sağlığı Servisi İnsanca Bakım Politikası ve laboratuvar Hayvanların Kullanımı, dahil olmak üzere ulusal hayvan bakımı yönergeleri izleyin Massachusetts Göz Hayvan Bakımı ve Kullanımı Komitesi ve Kulak Revir ve Harvard Tıp Okulu, uygun yapılmaktadır Ilar Kılavuzu ve Hayvan Refahı Yasası. Deneysel işlemler sol DCN detay maruz aşağıda listelenen. Sağkalım ameliyat yaparken steril aletler kullanın. 1. İlköğretim Kraniyotomi ve Dorsal Cochlear Nucleus Pozlama <ol><li> Anestezi <ol><li> Bir intraperitonal uygulama yoluyla ksilazin 20 mg / kg ve ketamin 100 mg / kg ile 18-24 g ağırlığında 8-12 haftalık, yaşlı bir fare, anestezisi. Izleme kalp hızı, solunum hızı, yanı sıra ayak tutam çekilme refleksi ile uygun anestezi onaylayın. Gözleri yerleştirin veteriner merhem anestezi altında iken kuruluğu önlemek için. Bir kez yeterli anestezi altında, tıraş saç örten tO cerrahi siteye engelsiz erişim sağlamak için kafa derisi. </li></ol></li><li> Cerrahi konumlandırma <ol><li> Bir burun kelepçe ile yerinde tutulan küçük bir hayvan steryotaksik tutucu, güvenli bir şekilde fare yerleştirin. </li><li> Burun kelepçe tamamen fare kafasını hareketsiz yeterli solunum ama yeterince sıkı sağlamak için yeterli gevşek olduğundan emin olun. Fare kafası gevşek ise, hayvan prosedürünün kraniotomi bölümü sırasında baş yuvasından dışarı düşmesi muhtemeldir. </li><li> Kalp hızı izleme sağlar standart moda, işitsel beyinsapı implantı elektrotları yerleştirin. Solunum hızı görselleştirme tarafından takip edilmelidir. Normal kalp hızı ve solunum hızı fare yaşına bağlı olarak değişecektir unutmayın. </li><li> Bir homotermik ısıtma battaniye yerleştirme yoluyla bir termometre yerleştirilir ve euthermia sağlanır. </li></ol></li><li> Cilt kesi ve kafatası interparietal ve oksipital kemikler maruz <ol><li> Bir Microsc altındaope, deri yoluyla dikey kesi doğrudan kepçesi arasında, orta hatta başlayan ve oksiputa kaudal kısmına uzanan yapmak. Orta hat cilt kesi ardından, yanal cildi yerinden. Kafatasının sol arka yönünü kapsayan kasları gözünüzde canlandırın. </li><li> Bir neşter veya iris makas ile kendi kemiklere, kas ekleri dezartikülasyon ile kas sol parietal, interparietal örten ve kafatasının oksipital kemikleri çıkarın. Kesme kas kenarları boyunca kanama küçük bir derecede dikkat edin. 10-15 saniye için bir pamuk uçlu bir aplikatör ile hafif basınç ile bu en aza indirin. </li></ol></li><li> Kranyotomi üstteki Cochlear Nucleus <ol><li> Sagital ve lambda sütür hatları (Şekil 1, Sol Panel) dahil olmak üzere ilgili dikiş hatları, tanımlayın. </li><li> Rongeurs kullanarak, lambda dikiş hattına orta hat sol interparietal kemik üzerinde opera, ~ 2 mm kaudal yapmak. Bu bölge DCN üzerler. </li><li> Following kraniotomi, beyincik üzerinde uzanan dura ince bir tabaka gözlemlemek. Bir neşter bıçak kullanarak, dura çıkarın. (Şekil 1, Orta Panel). Not: dura çıkarılması kanama küçük olmasına neden olabilir. Dura kaldırmak için neşter bıçak kullanarak Bu süreç beyin yüzeyinin ve DCN ve karanlık tanımlanmasına havuz olacak beyincik aspirasyon sırasında kan kaybı miktarını azaltmak için tasarlanmıştır. Fare toplam kan hacmi% 15 daha&gt; ~ 1.5 ml geçmemelidir değildir. Kanama, bu miktarı aşarsa, fare sıvı takviyesi ile birlikte sağlanmalıdır. </li><li> Pamuk uçlu aplikatör ile beyincik kaplayan pıhtılaşmış kan çıkarın. İsteğe bağlı olarak, yavaşça kan kanı temizlemek için beyincik üzerine bir diş noktası kullanarak tuzlu damla. </li></ol></li><li> Serebellar Aspirasyon <ol><li> DCN karşısında olduğu kadar 5 Fransız emme kullanarak, DCN örten sol beyincik lateral-en bölümünü aspireual (Şekil 1, Sağ Panel). Sol beyincik yaklaşık 1/4 1/3 çıkarın. DCN bitişik ana dönüm superior semisirküler kanalın ampulla olduğunu. NOT: beyincik Aspirasyon protokolünün önemli bir adımdır. O kanamaya neden olur, bu gibi emme birden paslar ile bir tek denemede oluşur ve eğer beyinciğin Yönetmen aspirasyon en başarılı yapılır. Aspirasyon yardımcı olmak için, beyincik yüzeyine biraz uzak olacak CN, beklenen derinlikte mikroskop odak düzlemi ayarlanır. CN odak düzlemi ayarlanması görselleştirme geliştirmek ve keskin bir görüntü sağlayacaktır. </li><li> DCN aşağıdaki aspirasyon, daha kanama, beyin omurilik sıvısı (BOS) birikmesi ve beyincik deplasman bekleniyor. Kan pıhtılaşmasını önlemek için hızla Kraniotomi içine steril serum fizyolojik 0.5 cc aşılamak. Bir diş alanına ve emme ile hafifçe vurma bir kombinasyonu daha sonra olabilirDCN doğrudan görüntülenmesi için bir yol temizlemek için kullanılır. Doğrudan DCN yüzeyine temas etmeyin. </li></ol></li></ol> Virüs-aracılı Gen Transferi ve Cerrahi Kurtarma 2. Basınç Mikroenjeksiyon <ol><li> DCN örten kan ve CSF serbest olan ve net bir şekilde görülebilir sonra, 2 dakikalık bir süre boyunca, 10 ul Hamilton şırıngası kullanılarak DCN içine basınç microinjections olun. </li><li> Ucu artık DCN yüzeyinin altında görünür oluncaya kadar bir micromanipulator ile iğne tanıtın. </li><li> En iyi performans için, künt travma en aza indirmek ve bir ince DCN içinde enjeksiyon hacmi, lokalize, 45 ° olarak, sığ konik böyle bir 33 veya 34 gauge iğne (34 gauge iğne ile bir gaz geçirmez şırınga kullanın) kullanın ve sığ beyin yapısı (&lt;300 mikron kalınlığında). NOT: Diğer mikroenjeksiyon aletleri kullanılan dayalı olabilir. İdeal olarak, enjeksiyon enstrüman bazı hafif ben izin vermek için esnek olmalıdırd eğer doğrudan DCN hedef için gerekli. Fare nedeniyle solunum prosedür boyunca hafifçe hareket gibi Ayrıca, enstrüman hareketinin küçük miktarlarda dayanacak kadar sağlam olmalıdır. </li></ol> 3. Cerrahi Kurtarma <ol><li> Hemen ardından enjeksiyon, cilt yeniden yaklaştığı ve fare standart kurtarma prosedürüne göre kurtarmak için izin verir. Kalan beyincik ve skar dokusu beyincik aspirasyonu nedeniyle boşluğunda dolduracaktır. Yeterli bilinç sternum yatma korumak için sağlanıncaya kadar sürekli hayvanları izlemek. Kalp hızı, solunum sayısı, hem de besleme becerisi izleyin. NOT: Tamamen iyileşene kadar hiçbir hayvan ameliyatı geçirmiş diğer hayvanlarla bir kafese geri döner. </li><li> Bir fare operasyon sonrası çevrelerinde yürümeye başlarsa büyük olasılıkla zor bir zaman besleme olurdu gibi (&lt;olguların% 5), cilt kesi kapatılması sonra genellikle 2-4 saat, hemen, fare kurban. TOnun yan etkisi nedeniyle beyincik aspirasyon muhtemeldir. Hayvan postoperatif ağrı için izlenmelidir, ve uygun uyuşturucu kurumsal standartlara dayalı hayvan konfor sağlamak için verilmelidir. Antibiyotikler, gerekli enfeksiyon durumunda kanıtı olabilir. </li></ol> 4. İkincil Kraniyotomi ve Cochlear Nucleus Pozlama <ol><li> Şifa ve virüs aracılı gen transferi inkübasyon 2-4 hafta sonra, önceden enjekte fare ve adımı tekrarlayın 1,1-1,5 Optimal inkübasyon süresi aktarılan genin tipine göre değişir yeniden uyutmak. </li><li> Cımbız, neşter ve rongeurs bir kombinasyonu ile Kraniotomi sitesi üzerinden skar dokusu çıkarın. </li><li> Kraniotomiye görselleştirmek sonra, DCN örten beyincik ve skar dokusu kalan bir arada tanımlamak. Örten beyincik / (önceki serebellar aspirasyon benzer) skar dokusu aspire 5 Fransız emiş kullanın. </li><li> Aspirasyon ardından, daha kanama, BOS b bekliyoruzuild-up ve beyincik kalan bitleri. Hızla kan pıhtılaşmasını önlemek için Kraniotomi içine tuzlu tanıtmak. DCN doğrudan görselleştirme yolunu temizlemek için yumuşak diş nokta dabbing ve emme bir arada kullanın. </li><li> DCN yüzeyini gözlemlemek. DCN artık erişilebilir olduğu gibi Optogenetik-tabanlı fizyolojisi deneyleri. Bir Optogenetik tabanlı deney sürmek için, bir fiber optik (Şekil 2), örneğin, hafif bir uyarıcı, tanıtılması. </li></ol> 5. Histoloji <ol><li> Deneylerin sonucu takiben, ketamin dozu ile fare euthanize. % 4 paraformaldehid tarafından takip normal tuzlu su ile fare serpmek. </li><li> 2 saat kafatası ve post-fix gelen beyin sapı ayıklayın. 24-48 saat süreyle% 30 sukroz içinde beyin sapı cryoprotect. Bölüm 60 mikron bölümleri kullanarak standart bir kriyostat kullanarak beyin sapı. </li></ol>

<ol>
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H., 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=Optogenetic+stimulation+of+the+auditory+pathway.">Optogenetic stimulation of the auditory pathway.</a> J Clin Invest. 124 (3), 1114-1129 (2014).</li><li>Adamantidis, 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=Optogenetic+interrogation+of+dopaminergic+modulation+of+the+multiple+phases+of+reward-seeking+behavior.">Optogenetic interrogation of dopaminergic modulation of the multiple phases of reward-seeking behavior.</a> J Neurosci. 30 (31), 10829-10835 (2011).</li><li>Kim, 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=Optogenetic+mimicry+of+the+transient+activation+of+dopamine+neurons+by+natural+reward+is+sufficient+for+operant+reinforcement.">Optogenetic mimicry of the transient activation of dopamine neurons by natural reward is sufficient for operant reinforcement.</a> PloS One. 7 (4), e33612 (2012).</li><li>Britt, J., Bonci, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optogenetic+interrogations+of+the+neural+circuits+underlying+addiction.">Optogenetic interrogations of the neural circuits underlying addiction.</a> Curr Opin Neurobiol. 23 (4), 539-545 (2013).</li><li>Abbott, S., Coates, M., Stornetta, R., Guyenet, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optogenetic+stimulation+of+c1+and+retrotrapezoid+nucleus+neurons+causes+sleep+state-dependent+cardiorespiratory+stimulation+and+arousal+in+rats.">Optogenetic stimulation of c1 and retrotrapezoid nucleus neurons causes sleep state-dependent cardiorespiratory stimulation and arousal in rats.</a> Hypertension. 61 (4), 835-841 (2013).</li><li>Carter, M., 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=Tuning+arousal+with+optogenetic+modulation+of+locus+coeruleus+neurons.">Tuning arousal with optogenetic modulation of locus coeruleus neurons.</a> Nat Neurosci. 13 (12), 1526-1533 (2010).</li><li>Darrow, 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=Optogenetic+control+of+central+auditory+neurons.">Optogenetic control of central auditory neurons.</a> Assoc. 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(695), (2012).</li><li>Shimano, 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=Assessment+of+the+AAV-mediated+expression+of+channelrhodopsin-2+and+halorhodopsin+in+brainstem+neurons+mediating+auditory+signaling.">Assessment of the AAV-mediated expression of channelrhodopsin-2 and halorhodopsin in brainstem neurons mediating auditory signaling.</a> Brain Res. 1511, 138-152 (2013).</li><li>Doucet, J., Ryugo, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Projections+from+the+ventral+cochlear+nucleus+to+the+dorsal+cochlear+nucleus+in+rats.">Projections from the ventral cochlear nucleus to the dorsal cochlear nucleus in rats.</a> J Comp Neurol. 385, 245-264 (1997).</li><li>Brown, M., Drottar, M., Benson, T., Darrow, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Commissural+axons+of+the+mouse+cochlear+nucleus.">Commissural axons of the mouse cochlear nucleus.</a> J Comp Neurol. 521, 1683-1696 (2013).</li><li>Verma, R., 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=Auditory+responses+to+electric+and+infrared+neural+stimulation+of+the+rat+cochlear+nucleus.">Auditory responses to electric and infrared neural stimulation of the rat cochlear nucleus.</a> Hear Res. 310, 69-75 (2014).</li><li>Taberner, A. 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C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Response+properties+of+single+auditory+nerve+fibers+in+the+mouse.">Response properties of single auditory nerve fibers in the mouse.</a> J Neurophysiol. 93 (1), 557-569 (2005).</li><li>Rolls, 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=Optogenetic+disruption+of+sleep+continuity+impairs+memory+consolidation.">Optogenetic disruption of sleep continuity impairs memory consolidation.</a> Proc Natl Acad Sci. 108 (32), 13305-13310 (2011).</li><li>Huff, M., Miller, R., Deisseroth, K., Moorman, D., LaLumiere, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Posttraining+optogenetic+manipulations+of+basolateral+amygdala+activity+modulate+consolidation+of+inhibitory+avoidance+memory+in+rats.">Posttraining optogenetic manipulations of basolateral amygdala activity modulate consolidation of inhibitory avoidance memory in rats.</a> Proc Natl Acad Sci. 110 (9), 3597-3602 (2013).</li><li>Stortkuhl, K., Fiala, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+Smell+of+Blue+Light:+A+New+Approach+toward+Understanding+an+Olfactory+Neuronal+Network.">The Smell of Blue Light: A New Approach toward Understanding an Olfactory Neuronal Network.</a> Front Neurosci. 5 (72), (2011).</li><li>Hira, R., 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=Transcranial+optogenetic+stimulation+for+functional+mapping+of+the+motor+cortex.">Transcranial optogenetic stimulation for functional mapping of the motor cortex.</a> J Neurosci Methods. 179 (2), 258-263 (2009).</li><li>Ayling, O., Harrison, T., Boyd, J., Foroshkov, A., Murphy, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Automated+light-based+mapping+of+motor+cortex+by+photoactivation+of+channelrhodopsin-2+transgenic+mice.">Automated light-based mapping of motor cortex by photoactivation of channelrhodopsin-2 transgenic mice.</a> Nat Methods. 6 (3), 219-224 (2009).</li><li>Boyden, E., Zhang, F., Bamberg, E., Nagel, G., Deisseroth, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Millisecond-timescale,+genetically+targeted+optical+control+of+neural+activity.">Millisecond-timescale, genetically targeted optical control of neural activity.</a> Nat. 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Yazarlar ifşa hiçbir şey yok.

Bu kağıt, merkezi işitme sisteminin manipülasyonu için fare modelinde DCN doğrudan görselleştirme tekniği anlatılmaktadır. Doğrudan görselleştirme özetlenen yaklaşım stereotaksik yaklaşımlar ana alternatif üzerinde önemli avantajlar sağlar. Stereotaksik yaklaşımlar doğrudan görselleştirme göze değil oysa Öncelikle, DCN doğrudan görselleştirme, beyin sapı sitenin hemen onay veriyor. Virüs-aracılı gen transferi durumunda olduğu gibi, inkübasyon sürelerini uzun süreli gerektirecek d...

Virus-mediated gene transfer to reverse hearing loss has largely been focused on the peripheral auditory system.1 Targeting the cochlea, investigators have examined a host of delivery routes, including osmotic minipump infusion2, vector-transgene complex-soaked Gelfoam&#174;2 or gelatin sponge3, direct microinjection4; numerous gene transfer vectors, including adeno-associated viral vectors5,6, lentiviral vectors7, and cationic liposomes2; and the dissemination of gene transfer vectors beyond the target tissue2. Most recently, adeno-associated virus (AAV)-1 has been introduced in the cochlea in order to treat deafness in mice due to loss of vesicular glutamate transporter-3.8 Further, the application of optogenetics in peripheral auditory system has recently been described.9
Few studies, however, have examined gene transfer to the central auditory system. The dorsal cochlear nucleus (DCN) of the brainstem contain second order neurons of the auditory pathway. While gene transfer techniques in the cochlear nucleus (CN) may be utilized for a host of investigations, gene transfer of opsins, light-sensitive proteins, to the DCN may also be utilized to enable optogenetics-based experimental techniques. Following virus-mediated gene transfer delivery of an opsin, such as channelrhodopsin-2 (ChR2), the neurons of the DCN becomes sensitive to light stimuli. Optogenetic gene transfer has been previously attempted in several brainstem regions, including the rat retrotrapezoid nucleus, mouse locus coeruleus, monkey superior colliculus, and mouse ventral tegmental area.10-14
Recently, investigators have examined the use of optogenetics in the DCN.15,16 The DCN is the location of placement of auditory brainstem implants in humans, making it an attractive part of the auditory system to study for translational studies on auditory neuroprostheses. However, given the location of the DCN, surgical exposure is challenging. The technique described herein provides a protocol for maximal exposure of the DCN via posterior fossa approach to enable viral vector gene transfer and optogenetics-based experiments in a murine model. Previous studies used stereotactic microinjection into the DCN with channelrhodopsin-2.16 Stereotaxic injections, however, are potentially less accurate than injections made by direct visualization, especially in a nucleus as small and deep along the brainstem as the DCN. Transgenic mice expressing tissue specific proteins in the CN are also an attractive option and would obviate the need for gene transfer. Our protocol for exposure of the DCN would also work in transgenic mice as the DCN would need to be directly exposed for optical stimulation. This technique for surgical exposure of the DCN is adapted from previous protocols involving recordings from the auditory nerve and cochlear nucleus in mice and rat models.15,17-20
The overall goal of the protocol is to provide direct exposure to the CN to allow for gene transfer techniques. More specifically, the approach is compatible with both acute and survival surgery and the preparation can be repeated in the same animal for subsequent neurophysiological testing. The direct exposure of the DCN protocol has implications for optogenetics- and virus-mediated gene transfer-based experimentation in other nuclei of the brainstem.

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			<td height="21" style="height:21px;width:197px;">Scalpel blade #11</td>
			<td style="width:227px;">Fine Surgical Tools</td>
			<td>10011-00</td>
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			<td height="21" style="height:21px;width:197px;">Iris scissor</td>
			<td style="width:227px;">Fine Surgical Tools</td>
			<td>14084-08</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:197px;">5 French suction</td>
			<td style="width:227px;">Symmetry Surgical</td>
			<td>2777914</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:197px;">Dental Points</td>
			<td style="width:227px;">Henry Schein</td>
			<td>100-8170</td>
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		<tr height="25">
			<td height="46" rowspan="2" style="height:46px;width:197px;">Bone rongeur</td>
			<td rowspan="2" style="width:227px;">Fine Surgical Tools</td>
			<td rowspan="2">16020-14</td>
		</tr>
		<tr height="21">
		</tr>
		<tr height="30">
			<td height="51" rowspan="2" style="height:52px;width:197px;">10 &#181;l Hamilton syringe</td>
			<td rowspan="2" style="width:227px;">Hamilton&#160;</td>
			<td rowspan="2">7633-01</td>
		</tr>
		<tr height="21">
		</tr>
		<tr height="21">
			<td height="42" rowspan="2" style="height:42px;width:197px;">34 gauge, needle</td>
			<td rowspan="2" style="width:227px;">Hamilton&#160;</td>
			<td rowspan="2">207434</td>
		</tr>
		<tr height="21">
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Rongeurs</td>
			<td>Fine Surgical Tools</td>
			<td>16021-14</td>
		</tr>
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</table>

direct visualization of the murine dorsal cochlear nucleus for optogenetic stimulation of the auditory pathway

Tutuklama veya işitme kaybı ters virüs aracılı gen transferi kullanımı soruşturma büyük ölçüde çevresel işitme sisteminin küme olmuştur. Birkaç çalışma, merkezi işitme sistemine gen transferi inceledik. işitsel yolun ikinci dereceden nöronları içeren beyin sapı dorsal koklear nükleus (DCN), gen transferi için potansiyel bir sitedir. Bu protokol, posterior fossa yaklaşımı ile kemirgen DCN doğrudan ve maksimal maruz kalma bir tekniktir gösterilmiştir. Bu yaklaşım, akut ya da hayatta kalma cerrahi sağlar. DCN doğrudan görselleştirme sonra, deney bir ana bilgisayar, bir mavi ışık lazer bağlanmış bir fiber optik ile koklear nükleus ve daha sonra stimülasyon içine opsins püskürtülmesi de dahil olmak üzere uygulanabilir. Böyle elektrik stimülasyonu ve nöral enjektör iz gibi diğer nörofizyoloji deneyler de mümkün bulunmaktadır. Visualiza düzeyiyon ve uyarılma süresi elde deneyler geniş bu yaklaşım uygulanamaz hale.

Kısmi Serebellar Aspirasyon Koklear Nucleus Erişim gösterir Kafatası örten deri ve kas gibi koronal ve lamda sütür hatları gibi, kafatası yüzey işaretlerini, kaldırıldıktan sonra, Kraniotomi yaklaşık lokalizasyonu göstermektedir. Rongeurs ile kraniyotomi ardından, beyincik görüntülenmiştir. Serebellumun küçük bir kısmı dikkatlice aspire enjekte edilebilir CN, (Şekil 1) görselleştirme gösterir. Mavi Iş?...

Watch this Scientific Journal Video about Direct Visualization of the Murine Dorsal Cochlear Nucleus for Optogenetic Stimulation of the Auditory Pathway at JoVE.com

Direct Visualization of the Murine Dorsal Cochlear Nucleus for Optogenetic Stimulation of the Auditory Pathway

The goal of this protocol is to outline a surgical approach to provide direct access to the dorsal cochlear nucleus in a murine model.

İşitsel Yolu ve optogenetic Stimülasyon için Murin Dorsal Koklear Çekirdek Doğrudan Görselleştirme

Investigation into the use of virus-mediated gene transfer to arrest or reverse hearing loss has largely been relegated to the peripheral auditory system. ...

direct-visualization-murine-dorsal-cochlear-nucleus-for-optogenetic

Research

JoVE Journal

Neuroscience

9.1K Görüntüleme.  Harvard Medical School. The goal of this protocol is to outline a surgical approach to provide direct access to the dorsal cochlear nucleus in a murine model. 

Video: Direct Visualization of the Murine Dorsal Cochlear Nucleus for Optogenetic Stimulation of the Auditory Pathway

TMS: Using the Theta-Burst Protocol to Explore Mechanism of Plasticity in Individuals with Fragile X Syndrome and Autism

Fragile X Syndrome (FXS), also known as Martin-Bell Syndrome, is a genetic abnormality found on the X chromosome.1,2 Individuals suffering from FXS display abnormalities in the expression of FMR1 - a protein required for typical, healthy neural development.3 Recent data has suggested that the loss of this protein can cause the cortex to be hyperexcitable thereby affecting overall patterns of neural plasticity.4,5
In addition, Fragile X shows a strong comorbidity with autism: in fact, 30% of children with FXS are diagnosed with autism, and 2 - 5% of autistic children suffer from FXS.6
Transcranial Magnetic Stimulation (a non-invasive neurostimulatory and neuromodulatory technique that can transiently or lastingly modulate cortical excitability via the application of localized magnetic field pulses 7,8) represents a unique method of exploring plasticity and the manifestations of FXS within affected individuals. More specifically, Theta-Burst Stimulation (TBS), a specific stimulatory protocol shown to modulate cortical plasticity for a duration up to 30 minutes after stimulation cessation in healthy populations, has already proven an efficacious tool in the exploration of abnormal plasticity.9,10 
Recent studies have shown the effects of TBS last considerably longer in individuals on the autistic spectrum - up to 90 minutes.11 This extended effect-duration suggests an underlying abnormality in the brain's natural plasticity state in autistic individuals - similar to the hyperexcitability induced by Fragile X Syndrome.
In this experiment, utilizing single-pulse motor-evoked potentials (MEPs) as our benchmark, we will explore the effects of both intermittent and continuous TBS on cortical plasticity in individuals suffering from FXS and individuals on the Autistic Spectrum.

In this article, we examine the effects of Theta-Burst TMS stimulation on cortical plasticity in individuals suffering from Fragile X syndrome and individuals on the autistic spectrum.

TMS: Fragile X Sendromu ve Otizm Bireylerde Plastisite, Mechasnism keşfedin Theta-Burst Protokolü kullanma

Fragile X Syndrome (FXS), also known as Martin-Bell Syndrome, is a genetic abnormality found on the X chromosome.1,2 Individuals suffering from FXS ...

Nörobilim

The NeuroStar TMS Device: Conducting the FDA Approved Protocol for Treatment of Depression

The Neuronetics NeuroStar Transcranial Magnetic Stimulation (TMS) System is a class II medical device that produces brief duration, pulsed magnetic fields. These rapidly alternating fields induce electrical currents within localized, targeted regions of the cortex which are associated with various physiological and functional brain changes.1,2,3
In 2007, O'Reardon et al., utilizing the NeuroStar device, published the results of an industry-sponsored, multisite, randomized, sham-stimulation controlled clinical trial in which 301 patients with major depression, who had previously failed to respond to at least one adequate antidepressant treatment trial, underwent either active or sham TMS over the left dorsolateral prefrontal cortex (DLPFC). The patients, who were medication-free at the time of the study, received TMS five times per week over 4-6 weeks.4
The results demonstrated that a sub-population of patients (those who were relatively less resistant to medication, having failed not more than two good pharmacologic trials) showed a statistically significant improvement on the Montgomery-Asberg Depression Scale (MADRS), the Hamilton Depression Rating Scale (HAMD), and various other outcome measures. In October 2008, supported by these and other similar results5,6,7, Neuronetics obtained the first and only Food and Drug Administration (FDA) approval for the clinical treatment of a specific form of medication-refractory depression using a TMS Therapy device (FDA approval K061053).
In this paper, we will explore the specified FDA approved NeuroStar depression treatment protocol (to be administered only under prescription and by a licensed medical profession in either an in- or outpatient setting).

In this article, we examine the methodology and considerations relevant to the FDA approved depression treatment protocol using the Neuronetics NeuroStar TMS device.

NeuroStar TMS Aygıt: FDA yürütülmesi Depresyon Tedavisinde Protokolü Onaylandı

The Neuronetics NeuroStar Transcranial Magnetic Stimulation (TMS) System is a class II medical device that produces brief duration, pulsed magnetic ...

Electrode Positioning and Montage in Transcranial Direct Current Stimulation

Transcranial direct current stimulation (tDCS) is a technique that has been intensively investigated in the past decade as this method offers a non-invasive and safe alternative to change cortical excitability2. The effects of one session of tDCS can last for several minutes, and its effects depend on polarity of stimulation, such as that cathodal stimulation induces a decrease in cortical excitability, and anodal stimulation induces an increase in cortical excitability that may last beyond the duration of stimulation6. These effects have been explored in cognitive neuroscience and also clinically in a variety of neuropsychiatric disorders &#x2013; especially when applied over several consecutive sessions4. One area that has been attracting attention of neuroscientists and clinicians is the use of tDCS for modulation of pain-related neural networks3,5. Modulation of two main cortical areas in pain research has been explored: primary motor cortex and dorsolateral prefrontal cortex7. Due to the critical role of electrode montage, in this article, we show different alternatives for electrode placement for tDCS clinical trials on pain; discussing advantages and disadvantages of each method of stimulation.

Transcranial direct current stimulation (tDCS) is an established technique to modulate cortical excitability1,2. It has been used as an investigative tool in neuroscience due to its effects on cortical plasticity, easy operation, and safe profile. One area that tDCS has been showing encouraging results is pain alleviation 3-5.

Transkraniyal Doğru Akım Uyarım Elektrot Konumlandırma ve Montaj

Transcranial direct current stimulation (tDCS) is a technique that has been intensively investigated in the past decade as this method offers a ...

Visualization of Proprioceptors in Drosophila Larvae and Pupae

Proprioception is the ability to sense the motion, or position, of body parts by responding to stimuli arising within the body. In fruitflies and other insects proprioception is provided by specialized sensory organs termed chordotonal organs (ChOs) 2. Like many other organs in Drosophila, ChOs develop twice during the life cycle of the fly. First, the larval ChOs develop during embryogenesis. Then, the adult ChOs start to develop in the larval imaginal discs and continue to differentiate during metamorphosis.
The development of larval ChOs during embryogenesis has been studied extensively 10,11,13,15,16. The centerpiece of each ChO is a sensory unit composed of a neuron and a scolopale cell. The sensory unit is stretched between two types of accessory cells that attach to the cuticle via specialized epidermal attachment cells 1,9,14. When a fly larva moves, the relative displacement of the epidermal attachment cells leads to stretching of the sensory unit and consequent opening of specific transient receptor potential vanilloid (TRPV) channels at the outer segment of the dendrite 8,12. The elicited signal is then transferred to the locomotor central pattern generator circuit in the central nervous system.
Multiple ChOs have been described in the adult fly 7. These are located near the joints of the adult fly appendages (legs, wings and halters) and in the thorax and abdomen. In addition, several hundreds of ChOs collectively form the Johnston's organ in the adult antenna that transduce acoustic to mechanical energy 3,5,17,4.
In contrast to the extensive knowledge about the development of ChOs in embryonic stages, very little is known about the morphology of these organs during larval stages. Moreover, with the exception of femoral ChOs 18 and Johnston's organ, our knowledge about the development and structure of ChOs in the adult fly is very fragmentary.
Here we describe a method for staining and visualizing ChOs in third instar larvae and pupae. This method can be applied together with genetic tools to better characterize the morphology and understand the development of the various ChOs in the fly.

Visualization of Proprioceptors in Drosophila Larvae and Pupae

A method to immunostain and visualize chordotonal organs in larvae and pupae of Drosophila melanogaster is described.

Içinde proprioseptörlere Görselleştirmesi<em&gt; Drosophila</em&gt; Larva ve Pupa

Proprioception is the ability to sense the motion, or position, of body parts by responding to stimuli arising within the body. In fruitflies and other ...

Fiber-optic Implantation for Chronic Optogenetic Stimulation of Brain Tissue

Elucidating patterns of neuronal connectivity has been a challenge for both clinical and basic neuroscience. Electrophysiology has been the gold standard for analyzing patterns of synaptic connectivity, but paired electrophysiological recordings can be both cumbersome and experimentally limiting. The development of optogenetics has introduced an elegant method to stimulate neurons and circuits, both in vitro1 and in vivo2,3. By exploiting cell-type specific promoter activity to drive opsin expression in discrete neuronal populations, one can precisely stimulate genetically defined neuronal subtypes in distinct circuits4-6. Well described methods to stimulate neurons, including electrical stimulation and/or pharmacological manipulations, are often cell-type indiscriminate, invasive, and can damage surrounding tissues. These limitations could alter normal synaptic function and/or circuit behavior. In addition, due to the nature of the manipulation, the current methods are often acute and terminal. Optogenetics affords the ability to stimulate neurons in a relatively innocuous manner, and in genetically targeted neurons. The majority of studies involving in vivo optogenetics currently use a optical fiber guided through an implanted cannula6,7; however, limitations of this method include damaged brain tissue with repeated insertion of an optical fiber, and potential breakage of the fiber inside the cannula. Given the burgeoning field of optogenetics, a more reliable method of chronic stimulation is necessary to facilitate long-term studies with minimal collateral tissue damage. Here we provide our modified protocol as a video article to complement the method effectively and elegantly described in Sparta et al.8 for the fabrication of a fiber optic implant and its permanent fixation onto the cranium of anesthetized mice, as well as the assembly of the fiber optic coupler connecting the implant to a light source. The implant, connected with optical fibers to a solid-state laser, allows for an efficient method to chronically photostimulate functional neuronal circuitry with less tissue damage9 using small, detachable, tethers. Permanent fixation of the fiber optic implants provides consistent, long-term in vivo optogenetic studies of neuronal circuits in awake, behaving mice10 with minimal tissue damage.

The development of optogenetics now provides the means to precisely stimulate genetically defined neurons and circuits, both in vitro and in vivo. Here we describe the assembly and implantation of a fiber optic for chronic photostimulation of brain tissue.

Beyin Dokusu Kronik Optogenetic uyarılması için Fiber-optik İmplantasyon

Elucidating patterns of neuronal connectivity has been a challenge for both clinical and basic neuroscience. Electrophysiology has been the gold standard ...

Optogenetic Stimulation of Escape Behavior in Drosophila melanogaster

A growing number of genetically encoded tools are becoming available that allow non-invasive manipulation of the neural activity of specific neurons in Drosophila melanogaster1. Chief among these are optogenetic tools, which enable the activation or silencing of specific neurons in the intact and freely moving animal using bright light. Channelrhodopsin (ChR2) is a light-activated cation channel that, when activated by blue light, causes depolarization of neurons that express it. ChR2 has been effective for identifying neurons critical for specific behaviors, such as CO2 avoidance, proboscis extension and giant-fiber mediated startle response2-4. However, as the intense light sources used to stimulate ChR2 also stimulate photoreceptors, these optogenetic techniques have not previously been used in the visual system. Here, we combine an optogenetic approach with a mutation that impairs phototransduction to demonstrate that activation of a cluster of loom-sensitive neurons in the fly's optic lobe, Foma-1 neurons, can drive an escape behavior used to avoid collision. We used a null allele of a critical component of the phototransduction cascade, phospholipase C-&beta;, encoded by the norpA gene, to render the flies blind and also use the Gal4-UAS transcriptional activator system to drive expression of ChR2 in the Foma-1 neurons. Individual flies are placed on a small platform surrounded by blue LEDs. When the LEDs are illuminated, the flies quickly take-off into flight, in a manner similar to visually driven loom-escape behavior. We believe that this technique can be easily adapted to examine other behaviors in freely moving flies.

Optogenetic Stimulation of Escape Behavior in Drosophila melanogaster

Genetically encoded optogenetic tools enable noninvasive manipulation of specific neurons in the Drosophila brain. Such tools can identify neurons whose activation is sufficient to elicit or suppress particular behaviors. Here we present a method for activating Channelrhodopsin2 that is expressed in targeted neurons in freely walking flies.

Yılında Escape Davranış Optogenetic Uyarım<em&gt; Drosophila melanogaster</em

A  growing number of genetically encoded tools are becoming available that allow non-invasive  manipulation of the neural activity of specific neurons in ...

In vivo Optogenetic Stimulation of the Rodent Central Nervous System

The ability to probe defined neural circuits in awake, freely-moving animals with cell-type specificity, spatial precision, and high temporal resolution has been a long sought tool for neuroscientists in the systems-level search for the neural circuitry governing complex behavioral states. Optogenetics is a cutting-edge tool that is revolutionizing the field of neuroscience and represents one of the first systematic approaches to enable causal testing regarding the relation between neural signaling events and behavior. By combining optical and genetic approaches, neural signaling can be bi-directionally controlled through expression of light-sensitive ion channels (opsins) in mammalian cells. The current protocol describes delivery of specific wavelengths of light to opsin-expressing cells in deep brain structures of awake, freely-moving rodents for neural circuit modulation. Theoretical principles of light transmission as an experimental consideration are discussed in the context of performing in vivo optogenetic stimulation. The protocol details the design and construction of both simple and complex laser configurations and describes tethering strategies to permit simultaneous stimulation of multiple animals for high-throughput behavioral testing.

In vivo Optogenetic Stimulation of the Rodent Central Nervous System

Optogenetics has become a powerful tool for use in behavioral neuroscience experiments. This protocol offers a step-by-step guide to the design and set-up of laser systems, and provides a full protocol for carrying out multiple and simultaneous in vivo optogenetic stimulations compatible with most rodent behavioral testing paradigms.

Kemirgen Santral Sinir Sistemi vivo optogenetic Stimülasyon içinde

The ability to probe defined neural circuits in awake, freely-moving animals with cell-type specificity, spatial precision, and high temporal resolution ...

Optogenetic Stimulation of the Auditory Nerve

Direct electrical stimulation of spiral ganglion neurons (SGNs) by cochlear implants (CIs) enables open speech comprehension in the majority of implanted deaf subjects1-6. Nonetheless, sound coding with current CIs has poor frequency and intensity resolution due to broad current spread from each electrode contact activating a large number of SGNs along the tonotopic axis of the cochlea7-9. Optical stimulation is proposed as an alternative to electrical stimulation that promises spatially more confined activation of SGNs and, hence, higher frequency resolution of coding. In recent years, direct infrared illumination of&#160;the cochlea has been used to evoke responses in the auditory nerve10. Nevertheless it requires higher energies than electrical stimulation10,11 and uncertainty remains as to the underlying mechanism12. Here we describe a method based on optogenetics to stimulate SGNs with low intensity blue light, using transgenic mice with neuronal expression of channelrhodopsin 2 (ChR2)13 or virus-mediated expression of the ChR2-variant CatCh14. We used micro-light emitting diodes (&#181;LEDs) and fiber-coupled lasers to stimulate ChR2-expressing SGNs through a small artificial opening (cochleostomy) or the round window. We assayed the responses by scalp recordings of light-evoked potentials (optogenetic auditory brainstem response: oABR) or by microelectrode recordings from the auditory pathway and compared them with acoustic and electrical stimulation.

Cochlear implants (CIs) enable hearing by direct electrical stimulation of the auditory nerve. However, poor frequency and intensity resolution limits the quality of hearing with CIs. Here we describe optogenetic stimulation of the auditory nerve in mice as an alternative strategy for auditory research and developing future CIs.

İşitsel Sinir optogenetic uyarılması

Direct electrical stimulation of spiral ganglion neurons (SGNs) by cochlear implants (CIs) enables open speech comprehension in the majority of implanted ...

Analysis of Gene Expression Changes in the Rat Hippocampus After Deep Brain Stimulation of the Anterior Thalamic Nucleus

Deep brain stimulation (DBS) surgery, targeting various regions of the brain such as the basal ganglia, thalamus, and subthalamic regions, is an effective treatment for several movement disorders that have failed to respond to medication. Recent progress in the field of DBS surgery has begun to extend the application of this surgical technique to other conditions as diverse as morbid obesity, depression and obsessive compulsive disorder. Despite these expanding indications, little is known about the underlying physiological mechanisms that facilitate the beneficial effects of DBS surgery. One approach to this question is to perform gene expression analysis in neurons that receive the electrical stimulation. Previous studies have shown that neurogenesis in the rat dentate gyrus is elicited in DBS targeting of the anterior nucleus of the thalamus1. DBS surgery targeting the ATN is used widely for treatment refractory epilepsy. It is thus of much interest for us to explore the transcriptional changes induced by electrically stimulating the ATN. In this manuscript, we describe our methodologies for stereotactically-guided DBS surgery targeting the ATN in adult male Wistar rats. We also discuss the subsequent steps for tissue dissection, RNA isolation, cDNA preparation and quantitative RT-PCR for measuring gene expression changes. This method could be applied and modified for stimulating the basal ganglia and other regions of the brain commonly clinically targeted. The gene expression study described here assumes a candidate target gene approach for discovering molecular players that could be directing the mechanism for DBS.

The mechanism underlying the therapeutic effects of Deep Brain Stimulation (DBS) surgery needs investigation. The methods presented in this manuscript describe an experimental approach to examine the cellular events triggered by DBS by analyzing the gene expression profile of candidate genes that can facilitate neurogenesis post DBS surgery.

Ön Talamusun Çekirdek Derin Beyin Stimülasyon sonra Sıçan Hippocampus Gen İfade Değişim Analizi

Deep brain stimulation (DBS) surgery, targeting various regions of the brain such as the basal ganglia, thalamus, and subthalamic regions, is an effective ...

In Vitro Modeling of Cancerous Neural Invasion: The Dorsal Root Ganglion Model

One way that solid tumors disseminate is through neural invasion. This route is well-known in cancers of the head and neck, prostate, and pancreas. These neurotropic cancer cells have a unique ability to migrate unidirectionally along nerves towards the central nervous system (CNS). The dorsal root ganglia (DRG)/cancer cell model is a three dimensional (3D) in vitro model frequently used for studying the interaction between neural stroma and cancer cells. In this model, mouse or human cancer cell lines are grown in ECM adjacent to preparations of freshly dissociated cultured DRG. In this article, the DRG isolation protocol from mice, and implantation in petri dishes for co-culturing with pancreatic cancer cells are demonstrated. Five days after implantation, the cancer cells made contact with the DRG neurites. Later, these cells formed bridgeheads to facilitate more extensive polarized, neurotropic migration of cancer cells.

In Vitro Modeling of Cancerous Neural Invasion: The Dorsal Root Ganglion Model

This video article shows the use of the dorsal root ganglia (DRG)/cancer cell model in pancreatic ductal adenocarcinoma.

Sırt kök ganglion Modeli: Kanserli Sinir Invasion Vitro Modelleme

One way that solid tumors disseminate is through neural invasion. This route is well-known in cancers of the head and neck, prostate, and pancreas. These ...