Diese Studie wurde unterstützt durch das National Institute for Nursing Research (K99/R00NR014369).

<ol>
	<li>Mancia, G., Grassi, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+autonomic+nervous+system+and+hypertension.">The autonomic nervous system and hypertension.</a> Circulation Research. 114 (11), 1804-1814 (2014).</li><li>Kannan, A., Medina, R. I., Nagajothi, N., Balamuthusamy, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Renal+sympathetic+nervous+system+and+the+effects+of+denervation+on+renal+arteries.">Renal sympathetic nervous system and the effects of denervation on renal arteries.</a> World Journal of Cardiology. 6 (8), 814-823 (2014).</li><li>Johns, E. J., Kopp, U. C., DiBona, G. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neural+control+of+renal+function.">Neural control of renal function.</a> Comprehensive Physiology. 1 (2), 767 (2011).</li><li>Fink, A. M., Dean, C., Piano, M. R., Carley, D. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+pedunculopontine+tegmentum+controls+renal+sympathetic+nerve+activity+and+cardiorespiratory+activities+in+Nembutal-anesthetized+rats.">The pedunculopontine tegmentum controls renal sympathetic nerve activity and cardiorespiratory activities in Nembutal-anesthetized rats.</a> PLoS One. 12 (11), e0187956 (2017).</li><li>Dean, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Endocannabinoid+modulation+of+sympathetic+and+cardiovascular+responses+to+acute+stress+in+the+periaqueductal+gray+of+the+rat.">Endocannabinoid modulation of sympathetic and cardiovascular responses to acute stress in the periaqueductal gray of the rat.</a> American Journal of Physiology, Regulatory, Integrative and Comparative Physiology. 300 (3), R771-R779 (2011).</li><li>Seagard, J. L., 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=Anandamide+content+and+interaction+of+endocannabinoid/GABA+modulatory+effects+in+the+NTS+on+baroreflex-evoked+sympathoinhibition.">Anandamide content and interaction of endocannabinoid/GABA modulatory effects in the NTS on baroreflex-evoked sympathoinhibition.</a> American Journal of Physiology-Heart and Circulatory Physiology. 286 (3), H992-H1000 (2004).</li><li>Ferreira, C. B., Cravo, S. L., Stocker, S. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Airway+obstruction+produces+widespread+sympathoexcitation:+Role+of+hypoxia,+carotid+chemoreceptors,+and+NTS+neurotransmission.">Airway obstruction produces widespread sympathoexcitation: Role of hypoxia, carotid chemoreceptors, and NTS neurotransmission.</a> Physiological Reports. 6 (3), (2018).</li><li>Stocker, S. D., Muntzel, M. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Recording+sympathetic+nerve+activity+chronically+in+rats:+Surgery+techniques,+assessment+of+nerve+activity,+and+quantification.">Recording sympathetic nerve activity chronically in rats: Surgery techniques, assessment of nerve activity, and quantification.</a> American Journal of Physiology-Heart and Circulatory Physiology. 305 (10), H1407-H1416 (2013).</li><li>Miki, K., Kosho, A., Hayashida, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Method+for+continuous+measurements+of+renal+sympathetic+nerve+activity+and+cardiovascular+function+during+exercise+in+rats.">Method for continuous measurements of renal sympathetic nerve activity and cardiovascular function during exercise in rats.</a> Experimental Physiology. 87 (1), 33-39 (2002).</li><li>Huetteman, D. A., Bogie, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Direct+blood+pressure+monitoring+in+laboratory+rodents+via+implantable+radio+telemetry.">Direct blood pressure monitoring in laboratory rodents via implantable radio telemetry.</a> Methods in Molecular Biology. 573, 57-73 (2009).</li><li>Jespersen, B., Knupp, L., Northcott, C. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Femoral+arterial+and+venous+catheterization+for+blood+sampling,+drug+administration+and+conscious+blood+pressure+and+heart+rate+measurements.">Femoral arterial and venous catheterization for blood sampling, drug administration and conscious blood pressure and heart rate measurements.</a> Journal of Visualized Experiments. (59), 3496 (2012).</li><li>Paxinos, G., Watson, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> The rat brain in stereotaxic coordinates. , (2014).</li><li>Scislo, T. J., Augustyniak, R. A., O'Leary, D. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Differential+arterial+baroreflex+regulation+of+renal,+lumbar,+and+adrenal+sympathetic+nerve+activity+in+the+rat.">Differential arterial baroreflex regulation of renal, lumbar, and adrenal sympathetic nerve activity in the rat.</a> American Journal of Physiology. 275, R995-R1002 (1998).</li><li>Kopp, U. C., Jones, S. Y., DiBona, G. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Afferent+renal+denervation+impairs+baroreflex+control+of+efferent+renal+sympathetic+nerve+activity.">Afferent renal denervation impairs baroreflex control of efferent renal sympathetic nerve activity.</a> American Journal of Physiology, Regulatory, Integrative and Comparative Physiology. 295 (6), R1882-R1890 (2008).</li><li>Guild, S. J., 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=Quantifying+sympathetic+nerve+activity:+problems,+pitfalls+and+the+need+for+standardization.">Quantifying sympathetic nerve activity: problems, pitfalls and the need for standardization.</a> Experimental Physiology. 95 (1), 41-50 (2010).</li><li>Stocker, S. D., Hunwick, K. J., Toney, G. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hypothalamic+paraventricular+nucleus+differentially+supports+lumbar+and+renal+sympathetic+outflow+in+water-deprived+rats.">Hypothalamic paraventricular nucleus differentially supports lumbar and renal sympathetic outflow in water-deprived rats.</a> Journal of Physiology. 15 (563 Pt 1), 249-263 (2005).</li><li>Stocker, S. D., Gordon, K. W. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Glutamate+receptors+in+the+hypothalamic+paraventricular+nucleus+contribute+to+insulin-induced+sympathoexcitation.">Glutamate receptors in the hypothalamic paraventricular nucleus contribute to insulin-induced sympathoexcitation.</a> Neurophysiology. 113 (5), 1302-1309 (2015).</li><li>Saponjic, J., Radulovacki, M., Carley, D. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Injection+of+glutamate+into+the+pedunculopontine+tegmental+nuclei+of+anesthetized+rat+causes+respiratory+dysrhythmia+and+alters+EEG+and+EMG+power.">Injection of glutamate into the pedunculopontine tegmental nuclei of anesthetized rat causes respiratory dysrhythmia and alters EEG and EMG power.</a> Sleep and Breathing. 9 (2), 82-91 (2005).</li><li>DiBona, G. F., Jones, S. Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dynamic+analysis+of+renal+nerve+activity+responses+to+baroreceptor+denervation+in+hypertensive+rats.">Dynamic analysis of renal nerve activity responses to baroreceptor denervation in hypertensive rats.</a> Hypertension. 37 (4), 1153-1163 (2001).</li><li>Kunitake, T., Kannan, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Discharge+pattern+of+renal+sympathetic+nerve+activity+in+the+conscious+rat:+spectral+analysis+of+integrated+activity.">Discharge pattern of renal sympathetic nerve activity in the conscious rat: spectral analysis of integrated activity.</a> Journal of Neurophysiology. 84 (6), 2859-2867 (2000).</li><li>Machado, B. H., Bonagamba, L. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Microinjection+of+L-glutamate+into+the+nucleus+tractus+solitarii+increases+arterial+pressure+in+conscious+rats.">Microinjection of L-glutamate into the nucleus tractus solitarii increases arterial pressure in conscious rats.</a> Brain Research. 576 (1), 131-138 (1992).</li><li>Murakami, 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=Inhalation+anesthesia+is+preferable+for+recording+rat+cardiac+function+using+an+electrocardiogram.">Inhalation anesthesia is preferable for recording rat cardiac function using an electrocardiogram.</a> Biological and Pharmaceutical Bulletin. 37 (5), 834-839 (2014).</li><li>Nakamura, T., Tanida, M., Niijima, A., Hibino, H., Shen, J., Nagai, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Auditory+stimulation+affects+renal+sympathetic+nerve+activity+and+blood+pressure+in+rats.">Auditory stimulation affects renal sympathetic nerve activity and blood pressure in rats.</a> Neuroscience Letters. 416 (2), 107-112 (2007).</li><li>Bardgett, M. E., McCarthy, J. J., Stocker, S. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Glutamatergic+receptor+activation+in+the+rostral+ventrolateral+medulla+mediates+the+sympathoexcitatory+response+to+hyperinsulinemia.">Glutamatergic receptor activation in the rostral ventrolateral medulla mediates the sympathoexcitatory response to hyperinsulinemia.</a> Hypertension. 55 (2), 284-290 (2010).</li><li>Brozoski, D. T., Dean, C., Hopp, F. A., Seagard, J. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Uptake+blockade+of+endocannabinoids+in+the+NTS+modulates+baroreflex-evoked+sympathoinhibition.">Uptake blockade of endocannabinoids in the NTS modulates baroreflex-evoked sympathoinhibition.</a> Brain Research. 1059 (2), 197-202 (2005).</li><li>Barman, S. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=What+can+we+learn+about+neural+control+of+the+cardiovascular+system+by+studying+rhythms+in+sympathetic+nerve+activity?.">What can we learn about neural control of the cardiovascular system by studying rhythms in sympathetic nerve activity?.</a> International Journal of Psychophysiology. 103, 69-78 (2016).</li><li>Charkoudian, N., Wallin, B. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sympathetic+neural+activity+to+the+cardiovascular+system:+integrator+of+systemic+physiology+and+interindividual+characteristics.">Sympathetic neural activity to the cardiovascular system: integrator of systemic physiology and interindividual characteristics.</a> Comprehensive Physiology. 4 (2), 825-850 (2014).</li><li>Malpas, S. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sympathetic+nervous+system+overactivity+and+its+role+in+the+development+of+cardiovascular+disease.">Sympathetic nervous system overactivity and its role in the development of cardiovascular disease.</a> Physiological Reviews. 90 (2), 513-557 (2010).</li><li>Chen, W. W., Xiong, X. Q., Chen, Q., Li, Y. H., Kang, Y. M., Zhu, G. Q. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cardiac+sympathetic+afferent+reflex+and+its+implications+for+sympathetic+activation+in+chronic+heart+failure+and+hypertension.">Cardiac sympathetic afferent reflex and its implications for sympathetic activation in chronic heart failure and hypertension.</a> Acta Physiologica. 213 (4), 778-794 (2015).</li><li>Linz, D., 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=Modulation+of+renal+sympathetic+innervation:+Recent+insights+beyond+blood+pressure+control.">Modulation of renal sympathetic innervation: Recent insights beyond blood pressure control.</a> Clinical Autonomic Research. , (2018).</li></ol>

Anne M. Fink ist Mitglied des Kundenbeirats für Data Sciences International.

Wichtige Schritte zur Messung der RSNA gehören: (1) Vermeidung von dehnen der Nierenarterie und Nerven, wenn die Niere die Trennung von der paraspinalen Muskulatur und beim Platzieren der Nerv-Segment auf den Aufnahme-Elektroden (2) sorgfältig seziert die renale Nervenfasern aus dem umliegenden Gewebe/Schiff (3) zu gewährleisten, die die Elektrode Leitungen sind frei von Gewebe, Blut oder Lymphflüssigkeit und die Nerven vor dem Austrocknen durch die Anwendung von Mineralöl auf die renale Nerven und Silica-Gel auf die Nerv-Elektroden-Einheit (4) zu verhindern. Für die Fehlersuche ist es wichtig, sicherzustellen, dass das Aufnahmesystem ausreichend geerdet ist. Um ein klares Signal der RSNA zu erhalten, kann die Position der Elektrode sorgfältig eingestellt werden, während der Visualisierung und hören das Rohsignal RSNA, vor dem Einbetten in Silica-Gel. Erfolgreicher Abschluss der Operation resultiert ein RSNA-Signal, das durch CNS Manipulationen für die Experimente mehrstündigen moduliert werden kann.
Bei der Interpretation der Ergebnisse sollten die Ermittler den Einfluss der Anästhesie auf arterielle Mitteldruck und RSNA. Dieses Protokoll verwendet Barbiturat-Narkose (Pentobarbital-Natrium), die mittleren arteriellen Druck reduzieren und autonome Reaktionen21ändern kann. Je nach dem Experiment kann Ziele, anderen injizierbaren Formulierungen oder Inhalation Anästhesie (via Nase-Kegel oder Tracheostoma) verwendeten22sein. Forscher sollten die Alternativen wie Urethan23 und Alpha-Chloralose24. Diese Agenten haben weniger Auswirkungen auf die Herz-Kreislauf-Reflexe Abstumpfung aber mögliche gesundheitliche Gefahren auf die Ermittler darstellen können.
Zusätzlich zu den in diesem Protokoll beschriebenen Methoden sind alternative Ansätze von anderen Labors für die Erfassung und die Herstellung von Elektroden eingesetzt worden. RSNA kann mit Edelstahl4,9, silberne25oder Platin26 Draht aufgezeichnet werden. Neben der Aufhebung der freigelegten Nerv-Segment auf der Elektrode Draht, haben Wissenschaftler erfolgreich monophasisch erfasst, RSNA an den zentralen Enden der renalen sympathischen Nerven26geschnitten. Flexibilität unterscheidet sich basierend auf die Zugfestigkeit des Drahtes (gemessen mit kPSI Einheiten). Höheren kPSI Draht ist eher spröde, aber behält seine Form; niedrige kPSI Draht ist flexibler und weniger wahrscheinlich zu brechen, wenn wiederholt gebogen. Für RSNA Aufnahmen ist es wichtig, einen Draht zu wählen, der leicht gebogen und bei Aufnahmen neu positioniert. Der Draht sollte nicht allzu flexibel, so dass es schwierig, Haken, um position unter den Nerv zu erstellen, aber nicht zu steif sein. Letzteres erhöht das Risiko von Strecken und die Nerven zu beschädigen. Unser Labor wird Draht aus nichtrostendem Stahl mit 155-185 kPSI verwendet.
Viele Ansätze für die Analyse der RSNA stehen zur Verfügung. Anstatt die Durchschnittswerte für 10 s Aufzeichnung Segmente Quantifizierung und Berechnung der Unterschiede als die Prozent Änderung, RSNA ermittelt werden, durch Quantifizierung platzen Frequenz4,26,27. Dieser Ansatz kann bevorzugt sein, wenn die Ausgangswerte und Größen der RSNA Antworten unter Ratten in einer Studie15,26unterscheiden. Ein weiterer Ansatz beinhaltet die Berichtigung und die Integration des RSNA Signals; die RSNA Amplitude (gemessen in mV) wird über einen ausgewählten Zeitraum hinweg summiert (zB., 20 ms)15,26. Integrator wendet einen Filter Low-Phase und bietet die durchschnittliche Entladung Amplitude während Aktivitätsspitzen überschreiten die Zeitkonstante (zB., > 20 s)15,27. Integrierte Signale eignen sich für die Prüfung der Amplitude und Phase der RSNA, aber dieser Ansatz liefert keine Informationen über oszillierenden Änderungen. Frequenz-Domäne und Zeit Domäne-Methoden wurden angewendet, wenn Forscher RSNA Schwingungen untersuchen. Der Ansatz häufig für RSNA ist die schnelle Fourier-Transformation (FFT), die ein Signal in die sinusförmigen Schwingungen kategorisiert, jeweils mit einer eindeutigen Amplitude und Phase20,26. FFT ist ein sinnvoller Ansatz für die Prüfung der nieder- und hochfrequente platzt in der RSNA und für das Studium Atem- und Herzstillstand Modulation des Signals RSNA.
Die Methoden in diesem Protokoll sind wichtig für den Umgang mit Hypothesen über die funktionale Bedeutung von CNS-Kernen. Renalen sympathische Nerven direkte neuronale Kommunikation zwischen dem ZNS und Nieren und akute Veränderungen im RSNA stellen daher eine wichtige Variable in der Herz-Kreislauf-Forschung. CNS-Mechanismen, die Regulierung der sympathischen Abfluss zu definieren ist ein Schwerpunktbereich Forschung, wenn man bedenkt, dass renale Sympathoexcitation trägt zur Pathophysiologie und klinische Präsentation vieler Krankheiten (zB., chronische Nierenerkrankungen, Herz Ausfall, Herzrhythmusstörungen, Diabetes Mellitus und Obstruktive Schlafapnoe)28,29. Indirekte Maßnahmen der sympathischen Nerven-Aktivität (zB., BP, Herzfrequenz-Variabilität, Katecholamin-Ebenen) eignen sich nicht immer für die Studien über die funktionale Bedeutung von CNS-Kernen. Daher stellt die direkte Messung der RSNA und arterielle Mitteldruck bei anästhesierten Ratten eine wertvolle Methode zur funktional, anatomisch Definition der Quellen der aberranten sympathischen Nierenfunktion.

Prä-klinischen Entdeckungen über autonome Kontrolle des Herz-Kreislauf-Systems informieren Sie Strategien für die Verwaltung von Erkrankungen wie Bluthochdruck, Herzinsuffizienz und Niereninsuffizienz. Überaktivität des sympathischen Nervensystems und reduzierte kardiale vagotonus tragen zu erhöhter Blutdruck (BP)1. Chronisch erhöhten renalen sympathischen Abfluss Katecholamin-Sekretion erhöht und verringert renale Durchblutung mit schädlichen Folgen für das Herz-Kreislauf-/ renal Systeme2,3. Um die neurobiologischen Wege zu einer autonomen Dysfunktion zu definieren, sind Studien an Nagern wichtig für die Bestimmung, wie Neuronen des zentralen Nervensystems (ZNS) sympathischen Parameter regulieren. Der Zweck dieses Protokolls ist es, technische Auskunft über Messung der renalen sympathischen Nerven Aktivität (RSNA) und BP und die Techniken zur Quantifizierung der akuten sympathischer Änderungen als Reaktion auf CNS Manipulationen bei anästhesierten Ratten zu skizzieren.
Akute (Überleben) RSNA Messungen (dauerhafte min bis h) sind nützlich, wenn Wissenschaftler die CNS, pharmakologisch, elektrisch Sonde werden, oder Optogenetically in Ratten betäubt, die die Funktionen von bestimmten Kernen zu bestimmen. Mit diesen Methoden, Strukturen wie der einsame Kern, Periaquäduktales grau, wurden Pedunculopontine Tegmentum und rostral ventrolateralen Medulla untersucht um neurobiologische Wege Regulierung der sympathischen Parameter4zu definieren, 5,6,7. Dieser Ansatz ist wichtig für die Identifizierung von CNS Zielen zu untersuchenden in chronischen Modelle der autonomen Dysfunktion8,9weiter. Um diese Experimente zu vervollständigen, benötigt das Labor einen Lötkolben, Operationsmikroskop, stereotaktischen Rahmen, Mikroelektrode Verstärker und Audio-Monitor. Abhängig von den Faktoren im Labor vorhanden, die elektrische Störungen beitragen, erfordern chirurgische/Aufnahmebereich ein Faraday-Käfig/Erdung Riemen, elektrische Störungen in der RSNA Aufnahme zu reduzieren. Wenn Gehirn Analysen Gewebe Fixierung benötigen, eine Perfusion Pumpe und Dunst Haube sind erforderlich. Daten können digitalisiert und mit mehreren physiologischen Softwaredaten Erwerb (analog-Digital-Wandler) Einheiten4,5, mit verschiedenen Auswertungsmöglichkeiten und Kompatibilitäten für die Einbeziehung der telemetrischen Signale aufgezeichnet .

<table>
	<tbody>
		<tr>
			<td>Stainless steel wire</td>
			<td>A-M Systems; Sequim, WA</td>
			<td>791000</td>
			<td>RSNA electrode</td>
		</tr>
		<tr>
			<td>Polyethylene (PE-50) tubing</td>
			<td>VWR; Radnor, PA</td>
			<td>63019-048</td>
			<td>RSNA electrode; vessel cannulation</td>
		</tr>
		<tr>
			<td>Miniature pin connector</td>
			<td>A-M Systems; Sequim, WA</td>
			<td>520200</td>
			<td>RSNA electrode</td>
		</tr>
		<tr>
			<td>Crimping tool</td>
			<td>Daniels Manufacturing Corp.; Orlando, FL</td>
			<td>M22520</td>
			<td>RSNA electrode</td>
		</tr>
		<tr>
			<td>Connector strip</td>
			<td>Amphenol; Clinton Township, MI</td>
			<td>221-2653</td>
			<td>RSNA electrode</td>
		</tr>
		<tr>
			<td>J-B Kwik Epoxy</td>
			<td>J-B Weld, Sulphur Springs, TX</td>
			<td>8270</td>
			<td>RSNA electrode</td>
		</tr>
		<tr>
			<td>Silicone</td>
			<td>Permatex; Hartford, CT</td>
			<td>2222</td>
			<td>RSNA electrode</td>
		</tr>
		<tr>
			<td>Heparin sodium; Injectable (10 mL vial, 1000 U/mL)</td>
			<td>KV Veterinary Supply; David City, NE</td>
			<td>P03466</td>
			<td>Venous line patency</td>
		</tr>
		<tr>
			<td>Phenylephrine HCl; Injectable (1 mL vial; 10 mg/mL)</td>
			<td>ACE Surgical Supply; Brockton, MA</td>
			<td>950-6312</td>
			<td>Testing renal sympathoinhibition</td>
		</tr>
		<tr>
			<td>Single-hook elastic surgical stays</td>
			<td>Harvard Apparatus; Holliston, MA</td>
			<td>72-2595</td>
			<td>Incision</td>
		</tr>
		<tr>
			<td>Silk surgical tape</td>
			<td>3M, Minneapolis, MN</td>
			<td>1538-0</td>
			<td>Secure surgical stays</td>
		</tr>
		<tr>
			<td>Needles, 20 G</td>
			<td>Sigma-Aldrich; St. Louis, MO</td>
			<td>Z192554-100EA</td>
			<td>Vessel cannulation</td>
		</tr>
		<tr>
			<td>Dumont #7 curved forceps</td>
			<td>Fine Science Tools; Foster City, CA</td>
			<td>11274-20</td>
			<td>Vessel cannulation</td>
		</tr>
		<tr>
			<td>5-0 silk suture ties</td>
			<td>Braintree Scientific; Braintree, MA</td>
			<td>SUT-S 106</td>
			<td>Vessel cannulation</td>
		</tr>
		<tr>
			<td>Delicate hemostatic forceps</td>
			<td>Roboz Surgical Instrument Co.; Gaithersburg, MD</td>
			<td>RS-7117</td>
			<td>Vessel cannulation and RSNA surgery</td>
		</tr>
		<tr>
			<td>Crile Hemostatic forceps</td>
			<td>Fine Science Tools; Foster City, CA</td>
			<td>13004-14</td>
			<td>Needle bending</td>
		</tr>
		<tr>
			<td>Telemetry transmitter</td>
			<td>Data Sciences International; Minneapolis, MN</td>
			<td>PA-10</td>
			<td>Mean arterial pressure monitoring (telemetry)</td>
		</tr>
		<tr>
			<td>Re-gel syringe</td>
			<td>Data Sciences International; Minneapolis, MN</td>
			<td>276-0038-001</td>
			<td>Transmitter reuse (telemetry)</td>
		</tr>
		<tr>
			<td>Disposable pressure transducer</td>
			<td>Transpac; San Clemente, CA</td>
			<td>MI-1224</td>
			<td>Mean arterial pressure monitoring</td>
		</tr>
		<tr>
			<td>Clear-Cuff pressure infuser</td>
			<td>MILA International Inc.; Florence, KY</td>
			<td>2281339</td>
			<td>Mean arterial pressure monitoring</td>
		</tr>
		<tr>
			<td>Vessel cannulation forceps</td>
			<td>Fine Science Tools; Foster City, CA</td>
			<td>00574-11</td>
			<td>Catheter insertion</td>
		</tr>
		<tr>
			<td>Black monofilament nylon 4-0 suture on reverse cutting needle</td>
			<td>McKesson Medical-Surgical; San Francisco, CA</td>
			<td>S661GX</td>
			<td>Secure telemetry transmitter</td>
		</tr>
		<tr>
			<td>Telemetry receiver</td>
			<td>Data Sciences International; Minneapolis, MN</td>
			<td>RPC-1</td>
			<td>Mean arterial pressure monitoring (telemetry)</td>
		</tr>
		<tr>
			<td>LabChart Pro (software), PowerLab (acquisition hardware)</td>
			<td>AD Instruments; Colorado Springs, CO</td>
			<td>ML846, MX2 matrix 2.0 (Compatible with Data Science International telemetry)</td>
			<td>3 options for software/acquisition hardware</td>
		</tr>
		<tr>
			<td>SciWorks (software), DataWave (acquisition hardware)</td>
			<td>DataWave Technologies, Loveland, CO</td>
			<td>N/A</td>
			<td></td>
		</tr>
		<tr>
			<td>Spike 2 (software), Micro1401-3</td>
			<td>Cambridge Electronic Design Ltd., London UK</td>
			<td>1401-3</td>
			<td></td>
		</tr>
		<tr>
			<td>Micro-drill</td>
			<td>Roboz Surgical Instrument Co.; Gaithersburg, MD</td>
			<td>RS-6300</td>
			<td>CNS surgery</td>
		</tr>
		<tr>
			<td>Stereotaxic surgery frame</td>
			<td>Stoelting; Wood Dale, IL</td>
			<td>51600</td>
			<td>CNS surgery</td>
		</tr>
		<tr>
			<td>Microelectrode amplifier with 10X pre-amplifier</td>
			<td>A-M Systems; Sequim, WA</td>
			<td>1800-2</td>
			<td>RSNA recording</td>
		</tr>
		<tr>
			<td>Retractors</td>
			<td>Fine Science Tools; Foster City, CA</td>
			<td>17009-07</td>
			<td>RSNA surgery</td>
		</tr>
		<tr>
			<td>Micro-dissecting tweezers</td>
			<td>Fine Science Tools; Foster City, CA</td>
			<td>11251-10</td>
			<td>RSNA surgery</td>
		</tr>
		<tr>
			<td>Micro-hook</td>
			<td>Fine Science Tools; Foster City, CA</td>
			<td>10064-14</td>
			<td>RSNA surgery</td>
		</tr>
		<tr>
			<td>Mineral oil</td>
			<td>Fisher Scientific; Waltham, MA</td>
			<td>8042-47-5</td>
			<td>RSNA surgery</td>
		</tr>
		<tr>
			<td>Audio monitor</td>
			<td>A-M Systems; Sequim, WA</td>
			<td>3300</td>
			<td>RSNA surgery</td>
		</tr>
		<tr>
			<td>Silica gel</td>
			<td>Wacker, Munchen; Germany</td>
			<td>RT601A-B</td>
			<td>RSNA surgery</td>
		</tr>
		<tr>
			<td>Electrical clips</td>
			<td>Tyco Electronics; Schaffhausen, Switzerland</td>
			<td>EB0283-000</td>
			<td>Grounding or securing perfusion needle</td>
		</tr>
		<tr>
			<td>Bonn scissors, straight/sharp points</td>
			<td>Roboz Surgical Instrument Co; Gaithersburg, MD</td>
			<td>RS-5840</td>
			<td>Perfusion</td>
		</tr>
		<tr>
			<td>Gavage needle</td>
			<td>Harvard Apparatus; Holliston, MA</td>
			<td>75-0286</td>
			<td>Perfusion</td>
		</tr>
		<tr>
			<td>Masterflex perfusion pump</td>
			<td>Cole-Parmer; Vernon Hills, IL</td>
			<td>7524-10</td>
			<td>Perfusion</td>
		</tr>
		<tr>
			<td>Masterflex platinum-cured silicone tubing</td>
			<td>Cole-Parmer; Vernon Hills, IL</td>
			<td>96410-15</td>
			<td>Perfusion</td>
		</tr>
		<tr>
			<td>Formalin (10% buffered solution; 4 L)</td>
			<td>Sigma-Aldrich; St. Louis, MO</td>
			<td>HT501128</td>
			<td>Perfusion</td>
		</tr>
		<tr>
			<td>Sucrose</td>
			<td>Sigma-Aldrich; St. Louis, MO</td>
			<td>S0389</td>
			<td>Cryoprotection</td>
		</tr>
	</tbody>
</table>

quantifying acute changes in renal sympathetic nerve activity in response to central nervous system manipulations in anesthetized rats

Renalen sympathischen Nerven-Aktivität (RSNA) und arterielle Mitteldruck sind wichtige Parameter in der Herz-Kreislauf- und autonome Forschung; Allerdings gibt es begrenzte Ressourcen leiten Wissenschaftler in den Techniken für die Messung und Analyse dieser Variablen. Dieses Protokoll beschreibt die Methoden zur Messung der RSNA und arterielle Mitteldruck bei anästhesierten Ratten. Das Protokoll enthält auch die Ansätze für den Zugriff auf das Gehirn während der RSNA Aufnahmen für Manipulationen des zentralen Nervensystems (ZNS). Die RSNA Aufnahmetechnik ist kompatibel mit pharmakologische, optogenetische oder elektrische Stimulation des ZNS. Der Ansatz ist nützlich, wenn ein Ermittler kurzfristige (min bis h) autonome Reaktionen in nicht überleben Experimente anatomisch korrelieren mit CNS Kerne gemessen wird. Der Ansatz soll nicht verwendet werden, um chronische (Überleben) Aufnahmen der RSNA in Ratten zu erhalten. Entladungen in RSNA, gemittelt korrigiert RSNA und arterielle Mitteldruck kann quantifiziert und weiter über parametrische statistische Tests analysiert. Verfahren für den Erhalt der venösen Zugang, arterielle Mitteldruck telemetrisch aufnehmen und Gehirn Fixierung für künftige histologische Analysen sind auch in dem Artikel beschrieben.

Abbildung 1 zeigt eine Probe RSNA und BP-Aufnahme aus einer Ratte Nembutal betäubt. Eine intravenöse Injektion von Phenylephrin wurde verwendet, um eine Zunahme der mittleren arteriellen Druckes induzieren und zu evozieren die Baroreflex und transiente Sympathoinhibition4,6. Quantifizierung der RSNA war die rohe RSNA gleichgerichtet und gemittelt für 10 s-Segmente nicht überlappende; die Lärm-Schätzung wurde von jedem Segment abgezogen.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/58205/58205fig1.jpg"> Abbildung 1: RSNA und BP in Reaktion auf Phenylephrin Injektion IV. Die rohen RSNA (A) war Vollweg-korrigiert (B); zerkleinerte "Null" behoben RSNA ist im Einschub Cgezeigt. Nicht-überlappende 10 s Durchschnitte (minus Rauschen) wurden berechnet (D). Um die Baroreflex hervorrufen, wurde intravenös (beim Pfeil) 0,1 mL Phenylephrin (1 µg/mL) injiziert. Die Bolus-Infusion löste einen abrupten Anstieg der BP und vorübergehende Hemmung der RSNA. Diese Zahl wurde von Fink AM, Dean C, Klavier Herr, Carley DW angepasst. Die Pedunculopontine Tegmentum steuert renalen sympathischen Nerven-Aktivität und Kardiorespiratorische Aktivitäten bei Ratten Nembutal betäubt. PLoS One. 2017; 12 (11): e01879564. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/58205/58205fig1large.jpg" target="_blank">Bitte klicken Sie hier für eine größere Version dieser Figur.</a>

Watch this Scientific Journal Video about Quantifying Acute Changes in Renal Sympathetic Nerve Activity in Response to Central Nervous System Manipulations in Anesthetized Rats at JoVE.com

Quantifying Acute Changes in Renal Sympathetic Nerve Activity in Response to Central Nervous System Manipulations in Anesthetized Rats

Quantifizierung der akute Veränderungen im renalen sympathischen Nerven Aktivität als Reaktion auf Zentralnervensystem Manipulationen bei anästhesierten Ratten

Methoden zur Messung der sympathischer und Herz-Kreislauf-Antworten auf zentrale Nervensystem (ZNS) Manipulationen sind wichtig für die Förderung der Neurowissenschaften. Dieses Protokoll wurde entwickelt, um Wissenschaftler mit Messung und Quantifizierung der akute Veränderungen im renalen sympathischen Nerven-Aktivität (RSNA) bei anästhesierten Ratten (Überleben) zu unterstützen.

Renal sympathetic nerve activity (RSNA) and mean arterial pressure are important parameters in cardiovascular and autonomic research; however, there are ...

quantifying-acute-changes-renal-sympathetic-nerve-activity-response

Nanyang Technological University

Research

JoVE Journal

Neuroscience

7.7K Aufrufe.  University of Illinois at Chicago. Methoden zur Messung der sympathischer und Herz-Kreislauf-Antworten auf zentrale Nervensystem (ZNS) Manipulationen sind wichtig für die Förderung der Neurowissenschaften. Dieses Protokoll wurde entwickelt, um Wissenschaftler mit Messung und Quantifizierung der akute Veränderungen im renalen sympathischen Nerven-Aktivität (RSNA) bei anästhesierten Ratten (Überleben) zu unterstützen.

Serie: Quantifying Acute Changes in Renal Sympathetic Nerve Activity in Response to Central Nervous System Manipulations in Anesthetized Rats

Optic Nerve Transection: A Model of Adult Neuron Apoptosis in the Central Nervous System

Retinal ganglion cells (RGCs) are CNS neurons that output visual information from the retina to the brain, via the optic nerve. 
The optic nerve can be accessed within the orbit of the eye and completely transected (axotomized), cutting the axons of the entire RGC population. Optic nerve 
transection is a reproducible model of apoptotic neuronal cell death in the adult CNS 1-4. This model is particularly attractive because the vitreous
 chamber of the eye acts as a capsule for drug delivery to the retina, permitting experimental manipulations via intraocular injections. The diffusion of chemicals 
through the vitreous fluid ensures that they act upon the entire RGC population. Moreover, RGCs can be selectively transfected by applying short interfering RNAs 
(siRNAs), plasmids, or viral vectors to the cut end of the optic nerve 5-7 or injecting vectors into their target, the superior colliculus 8. 
This allows researchers to study apoptotic mechanisms in the desired neuronal population without confounding effects on other bystander neurons or surrounding glia. 
An additional benefit is the ease and accuracy with which cell survival can be quantified after injury. The retina is a flat, layered tissue and RGCs are localized in 
the innermost layer, the ganglion cell layer. The survival of RGCs can be tracked over time by applying a fluorescent tracer (3% Fluorogold) to the cut end of the 
optic nerve at the time of axotomy, or by injecting the tracer into the superior colliculus (RGC target) one week prior to axotomy. The tracer is retrogradely transported, labeling 
the entire RGC population. Because the ganglion cell layer is a monolayer (one cell thick), RGC densities can be quantified in flat-mounted tissue, without the need 
for stereology. Optic nerve transection leads to the apoptotic death of 90% of injured RGCs within 14 days postaxotomy 9-11. RGC apoptosis has a 
characteristic time-course whereby cell death is delayed 3-4 days postaxotomy, after which the cells rapidly degenerate. This provides a time window for 
experimental manipulations directed against pathways involved in apoptosis.

Optic Nerve transection is a widely used model of adult CNS injury. Ninety percent of retinal ganglion cells (RGCs) whose axons are completely transected (axotomy) die within 14 days after axotomy. This model is easily amenable to experimental manipulations and highly reproducible.

Optic Nerve Durchtrennung: Ein Modell des Adult Neuron Apoptose in das zentrale Nervensystem

Retinal ganglion cells (RGCs) are CNS neurons that output visual information from the retina to the brain, via the optic nerve. 
The optic nerve can be ...

Forschung

Neurowissenschaften

Multimodal Imaging of Stem Cell Implantation in the Central Nervous System of Mice

During the past decade, stem cell transplantation has gained increasing interest as primary or secondary therapeutic modality for a variety of diseases, both in preclinical and clinical studies. However, to date results regarding functional outcome and/or tissue regeneration following stem cell transplantation are quite diverse. Generally, a clinical benefit is observed without profound understanding of the underlying mechanism(s)1. Therefore, multiple efforts have led to the development of different molecular imaging modalities to monitor stem cell grafting with the ultimate aim to accurately evaluate survival, fate and physiology of grafted stem cells and/or their micro-environment. Changes observed in one or more parameters determined by molecular imaging might be related to the observed clinical effect. In this context, our studies focus on the combined use of bioluminescence imaging (BLI), magnetic resonance imaging (MRI) and histological analysis to evaluate stem cell grafting.
BLI is commonly used to non-invasively perform cell tracking and monitor cell survival in time following transplantation2-7, based on a biochemical reaction where cells expressing the Luciferase-reporter gene are able to emit light following interaction with its substrate (e.g. D-luciferin)8, 9. MRI on the other hand is a non-invasive technique which is clinically applicable10 and can be used to precisely locate cellular grafts with very high resolution11-15, although its sensitivity highly depends on the contrast generated after cell labeling with an MRI contrast agent. Finally, post-mortem histological analysis is the method of choice to validate research results obtained with non-invasive techniques with highest resolution and sensitivity. Moreover end-point histological analysis allows us to perform detailed phenotypic analysis of grafted cells and/or the surrounding tissue, based on the use of fluorescent reporter proteins and/or direct cell labeling with specific antibodies.
In summary, we here visually demonstrate the complementarities of BLI, MRI and histology to unravel different stem cell- and/or environment-associated characteristics following stem cell grafting in the CNS of mice. As an example, bone marrow-derived stromal cells, genetically engineered to express the enhanced Green Fluorescent Protein (eGFP) and firefly Luciferase (fLuc), and labeled with blue fluorescent micron-sized iron oxide particles (MPIOs), will be grafted in the CNS of immune-competent mice and outcome will be monitored by BLI, MRI and histology (Figure 1).

This article describes an optimized sequence of events for multimodal imaging of cellular grafts in rodent brain using: (i) in vivo bioluminescence and magnetic resonance imaging, and (ii) post mortem histological analysis. Combining these imaging modalities on a single animal allows cellular graft evaluation with high resolution, sensitivity and specificity.

Multimodale Bildgebung von Stem Cell Implantation in das zentrale Nervensystem der Mäuse

During the past decade, stem cell transplantation has gained increasing interest as primary or secondary therapeutic modality for a variety of diseases, ...

Dual Electrophysiological Recordings of Synaptically-evoked Astroglial and Neuronal Responses in Acute Hippocampal Slices

Astrocytes form together with neurons tripartite synapses, where they integrate and modulate neuronal activity. Indeed, astrocytes sense neuronal inputs through activation of their ion channels and neurotransmitter receptors, and process information in part through activity-dependent release of gliotransmitters. Furthermore, astrocytes constitute the main uptake system for glutamate, contribute to potassium spatial buffering, as well as to GABA clearance. These cells therefore constantly monitor synaptic activity, and are thereby sensitive indicators for alterations in synaptically-released glutamate, GABA and extracellular potassium levels. Additionally, alterations in astroglial uptake activity or buffering capacity can have severe effects on neuronal functions, and might be overlooked when characterizing physiopathological situations or knockout mice. Dual recording of neuronal and astroglial activities is therefore an important method to study alterations in synaptic strength associated to concomitant changes in astroglial uptake and buffering capacities. Here we describe how to prepare hippocampal slices, how to identify stratum radiatum astrocytes, and how to record simultaneously neuronal and astroglial electrophysiological responses. Furthermore, we describe how to isolate pharmacologically the synaptically-evoked astroglial currents.

The preparation of acute brain slices from isolated hippocampi, as well as the simultaneous electrophysiological recordings of astrocytes and neurons in stratum radiatum during stimulation of schaffer collaterals is described. The pharmacological isolation of astroglial potassium and glutamate transporter currents is demonstrated.

Dual-Elektrophysiologische Recordings synaptisch-evozierte astrogliale und neuronale Antworten in Acute Hippocampusschnitte

Astrocytes form together with neurons tripartite synapses, where they integrate and modulate neuronal activity. Indeed, astrocytes sense neuronal inputs ...

Labeling of Single Cells in the Central Nervous System of Drosophila melanogaster

In this article we describe how to individually label neurons in the embryonic CNS of Drosophila melanogaster by juxtacellular injection of the lipophilic fluorescent membrane marker DiI. This method allows the visualization of neuronal cell morphology in great detail. It is possible to label any cell in the CNS: cell bodies of target neurons are visualized under DIC optics or by expression of a fluorescent genetic marker such as GFP. After labeling, the DiI can be transformed into a permanent brown stain by photoconversion to allow visualization of cell morphology with transmitted light and DIC optics. Alternatively, the DiI-labeled cells can be observed directly with confocal microscopy, enabling genetically introduced fluorescent reporter proteins to be colocalised. The technique can be used in any animal, irrespective of genotype, making it possible to analyze mutant phenotypes at single cell resolution.

Labeling of Single Cells in the Central Nervous System of Drosophila melanogaster

We present a technique for labeling single neurons in the central nervous system (CNS) of Drosophila embryos, which allows the analysis of neuronal morphology by either transmitted light or confocal microscopy.

Beschriften einzelner Zellen im zentralen Nervensystem<em&gt; Drosophila melanogaster</em

In this  article we describe how to individually label neurons in the embryonic CNS of Drosophila melanogaster by juxtacellular injection of the ...

An Injury Paradigm to Investigate Central Nervous System Repair in Drosophila

An experimental method has been developed to investigate the cellular responses to central nervous system (CNS) injury using the fruit-fly Drosophila. Understanding repair and regeneration in animals is a key question in biology. The damaged human CNS does not regenerate, and understanding how to promote the regeneration is one of main goals of medical neuroscience. The powerful genetic toolkit of Drosophila can be used to tackle the problem of CNS regeneration.
A lesion to the CNS ventral nerve cord (VNC, equivalent to the vertebrate spinal cord) is applied manually with a tungsten needle. The VNC can subsequently be filmed in time-lapse using laser scanning confocal microscopy for up to 24 hr to follow the development of the lesion over time. Alternatively, it can be cultured, then fixed and stained using immunofluorescence to visualize neuron and glial cells with confocal microscopy. Using appropriate markers, changes in cell morphology and cell state as a result of injury can be visualized. With ImageJ and purposely developed plug-ins, quantitative and statistical analyses can be carried out to measure changes in wound size over time and the effects of injury in cell proliferation and cell death. These methods allow the analysis of large sample sizes. They can be combined with the powerful genetics of Drosophila to investigate the molecular mechanisms underlying CNS regeneration and repair.

An Injury Paradigm to Investigate Central Nervous System Repair in Drosophila

An injury paradigm using the Drosophila larval ventral nerve cord to investigate central nervous system regeneration and repair is described. Stabbing followed by laser scanning confocal microscopy in time-lapse and fixed specimens, combined with quantitative analysis with purposefully developed software and genetics, are used to investigate the molecular mechanisms of CNS regeneration and repair.

Eine Verletzung Paradigm Central Nervous System Repair in Untersuchen<em&gt; Drosophila</em

An experimental method has been developed to investigate the cellular responses to central nervous system (CNS) injury using the fruit-fly Drosophila. ...

Direct Intraventricular Delivery of Drugs to the Rodent Central Nervous System

Due to an inability to cross the blood brain barrier, certain drugs need to be directly delivered into the central nervous system (CNS). Our lab focuses specifically on antisense oligonucleotides (ASOs), though the techniques shown in the video here can also be used to deliver a plethora of other drugs to the CNS. Antisense oligonucleotides (ASOs) have the capability to knockdown sequence-specific targets 1 as well as shift isoform ratios of specific genes 2. To achieve widespread gene knockdown or splicing in the CNS of mice, the ASOs can be delivered into the brain using two separate routes of administration, both of which we demonstrate in the video.
The first uses Alzet osmotic pumps, connected to a catheter that is surgically implanted into the lateral ventricle. This allows the ASOs to be continuously infused into the CNS for a designated period of time. The second involves a single bolus injection of a high concentration of ASO into the right lateral ventricle. Both methods use the mouse cerebral ventricular system to deliver the ASO to the entire brain and spinal cord, though depending on the needs of the study, one method may be preferred over the other.

We describe a method to target drugs to the central nervous system by either implanting a catheter or performing a bolus injection into the right lateral ventricle in mice. We focus specifically on the delivery of antisense oligonucleotides. This technique is readily adaptable to other drugs and to rats.

Direkt Intraventrikuläre Abgabe von Arzneimitteln an die Nager Central Nervous System

Due to an inability to cross the blood brain barrier, certain drugs need to be directly delivered into the central nervous system (CNS). Our lab focuses ...

In vivo Interrogation of Central Nervous System Translatome by Polyribosome Fractionation

Multiple processes are involved in gene expression including transcription, translation and stability of mRNAs and proteins. Each of these steps are tightly regulated, affecting the final dynamics of protein abundance. Various regulatory mechanisms exist at the translation step, rendering mRNA levels alone an unreliable indicator of gene expression. In addition, local regulation of mRNA translation has been particularly implicated in neuronal functions, shifting &#39;translatomics&#39; to the focus of attention in neurobiology. The presented method can be used to bridge transcriptomics and proteomics.
Here we describe essential modifications to the technique of polyribosome fractionation, which interrogates the translatome based on the association of actively translated mRNAs to multiple ribosomes and their differential sedimentation in sucrose gradients. Traditionally, working with in vivo samples, particularly of the central nervous system (CNS), has proven challenging due to the restricted amounts of material and the presence of fatty tissue components. In order to address this, the described protocol is specifically optimized for use with minimal amount of CNS material, as demonstrated by the use of single mouse spinal cord and brain. Briefly, CNS tissues are extracted and translating ribosomes are immobilized on mRNAs with cycloheximide. Myelin flotation is then performed to remove lipid rich components. Fractionation is performed on a sucrose gradient where mRNAs are separated according to their ribosomal loading. Isolated fractions are suitable for a range of downstream assays, including new genome wide assay technologies.

In vivo Interrogation of Central Nervous System Translatome by Polyribosome Fractionation

This protocol illustrates essential modifications of polyribosome fractionation in order to study the translatome of in vivo CNS samples. It allows global assessment of translation and transcription regulation through the isolation and comparison of total RNA to ribosome bound RNA fractions.

In-vivo-Abfrage des Zentralen Nervensystems durch Translatome Polyribosom Fraktionierung

Multiple processes are involved in gene expression including transcription, translation and stability of mRNAs and proteins. Each of these steps are ...

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.

In vivo optogenetische Stimulation des Nager 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 ...

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.

Akut<em&gt; In vivo</em&gt; Elektrophysiologische Aufzeichnungen von lokalen Feldpotentialen und Multi-Unit-Aktivitäten von der Hyperdirect-Pathway in anästhesierten Ratten

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

Electrophysiological Recording of The Central Nervous System Activity of Third-Instar Drosophila Melanogaster

The majority of the currently available insecticides target the nervous system and genetic mutations of invertebrate neural proteins oftentimes yield deleterious consequences, yet the current methods for recording nervous system activity of an individual animal is costly and laborious. This suction electrode preparation of the third-instar larval central nervous system of Drosophila melanogaster, is a tractable system for testing the physiological effects of neuroactive agents, determining the physiological role of various neural pathways to CNS activity, as well as the influence of genetic mutations to neural function. This ex vivo preparation requires only moderate dissecting skill and electrophysiological expertise to generate reproducible recordings of insect neuronal activity. A wide variety of chemical modulators, including peptides, can then be applied directly to the nervous system in solution with the physiological saline to measure the influence on the CNS activity. Further, genetic technologies, such as the GAL4/UAS system, can be applied independently or in tandem with pharmacological agents to determine the role of specific ion channels, transporters, or receptors to arthropod CNS function. In this context, the assays described herein are of significant interest to insecticide toxicologists, insect physiologists, and developmental biologists for which D. melanogaster is an established model organism. The goal of this protocol is to describe an electrophysiological method to enable the measurement of electrogenesis of the central nervous system in the model insect, Drosophila melanogaster, which is useful for testing a diversity of scientific hypotheses.

Electrophysiological Recording of The Central Nervous System Activity of Third-Instar  Drosophila Melanogaster

This protocol describes a method to record the descending electrical activity of the Drosophila melanogaster central nervous system to enable the cost-efficient and convenient testing of pharmacological agents, genetic mutations of neural proteins, and/or the role of unexplored physiological pathways.

Elektrophysiologische Aufnahme der zentralen Nervensystems Tätigkeit der dritte Instar Drosophila Melanogaster

The majority of the currently available insecticides target the nervous system and genetic mutations of invertebrate neural proteins oftentimes yield ...