This work was supported by NIGMS award GM127872 ACK, NINDS award 105072 to ERD and ACK, and NSF award 1656574 to ACK.

NOTE: Set up systems for behavioral tracking in larvae and adults.
1. Constructing a Sleep System for Larvae
NOTE: The monitoring system for tracking larval through juvenile fish aged 4 days post fertilization (dpf) through 30 dpf A. mexicanus requires multiple pieces of equipment including infrared (IR) lighting, acrylic IR light diffusers, automated light controls (timers), computers, cameras, and secondary materials such as wiring and powe...

<ol>
	<li>Keene, A. C., Duboue, E. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+origins+and+evolution+of+sleep.">The origins and evolution of sleep.</a> The Journal of Experimental Biology. , (2018).</li><li>Joiner, 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=Unraveling+the+Evolutionary+Determinants+of+Sleep.">Unraveling the Evolutionary Determinants of Sleep.</a> Current Biology. 26 (20), R1073-R1087 (2016).</li><li>Allada, R., Siegel, J. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Unearthing+the+phylogenetic+roots+of+sleep.">Unearthing the phylogenetic roots of sleep.</a> Current biology. 18, R670-R679 (2008).</li><li>Sehgal, A., Mignot, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Genetics+of+sleep+and+sleep+disorders.">Genetics of sleep and sleep disorders.</a> Cell. 146, 194-207 (2011).</li><li>Campbell, S. S., Tobler, I. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Animal+sleep:+a+review+of+sleep+duration+across+phylogeny.">Animal sleep: a review of sleep duration across phylogeny.</a> Neuroscience and Biobehavioral Reviews. 8, 269-300 (1984).</li><li>Raizen, D. 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=Lethargus+is+a+Caenorhabditis+elegans+sleep-like+state.">Lethargus is a Caenorhabditis elegans sleep-like state.</a> Nature. 451, 569-572 (2008).</li><li>Geissmann, Q., Rodriguez, L. G., Beckwith, E. J., French, A. S., Jamasb, A. R., Gilestro, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ethoscopes:+An+Open+Platform+For+High-Throughput+Ethomics.">Ethoscopes: An Open Platform For High-Throughput Ethomics.</a> bioRxiv. , 113647 (2017).</li><li>Garbe, D. S., 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=Context-specific+comparison+of+sleep+acquisition+systems+in+Drosophila.">Context-specific comparison of sleep acquisition systems in Drosophila.</a> Biology Open. 4 (11), (2015).</li><li>Branson, K., Robie, A. A., Bender, J., Perona, P., Dickinson, M. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High-throughput+ethomics+in+large+groups+of+Drosophila.">High-throughput ethomics in large groups of Drosophila.</a> Nature Methods. 6 (6), 451-457 (2009).</li><li>Gilestro, G. F., Cirelli, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=PySolo:+A+complete+suite+for+sleep+analysis+in+Drosophila.">PySolo: A complete suite for sleep analysis in Drosophila.</a> Bioinformatics. 25, 1466-1467 (2009).</li><li>Swierczek, N. A., Giles, A. C., Rankin, C. H., Kerr, R. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High-throughput+behavioral+analysis+in+C.+elegans.">High-throughput behavioral analysis in C. elegans.</a> Nature Methods. 8 (7), 592-598 (2011).</li><li>Branson, K., Robie, A. A., Bender, J., Perona, P., Dickinson, M. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High-throughput+ethomics+in+large+groups+of+Drosophila.">High-throughput ethomics in large groups of Drosophila.</a> Nature Methods. 6, 451-457 (2009).</li><li>Rihel, 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=Zebrafish+behavioral+profiling+links+drugs+to+biological+targets+and+rest/wake+regulation.">Zebrafish behavioral profiling links drugs to biological targets and rest/wake regulation.</a> Science (New York, N.Y.). 327, 348-351 (2010).</li><li>Yoshizawa, 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=Distinct+genetic+architecture+underlies+the+emergence+of+sleep+loss+and+prey-seeking+behavior+in+the+Mexican+cavefish.">Distinct genetic architecture underlies the emergence of sleep loss and prey-seeking behavior in the Mexican cavefish.</a> BMC Biology. 13, (2015).</li><li>Chiu, C. N., Prober, D. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Regulation+of+zebrafish+sleep+and+arousal+states:+current+and+prospective+approaches.">Regulation of zebrafish sleep and arousal states: current and prospective approaches.</a> Frontiers in Neural Circuits. 7 (April), 58 (2013).</li><li>Elbaz, I., Foulkes, N. S., Gothilf, Y., Appelbaum, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Circadian+clocks,+rhythmic+synaptic+plasticity+and+the+sleep-wake+cycle+in+zebrafish.">Circadian clocks, rhythmic synaptic plasticity and the sleep-wake cycle in zebrafish.</a> Frontiers in Neural Circuits. 7, (2013).</li><li>Dubou&#233;, E. R., Keene, A. C., Borowsky, R. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Evolutionary+convergence+on+sleep+loss+in+cavefish+populations.">Evolutionary convergence on sleep loss in cavefish populations.</a> Current Biology. 21, 671-676 (2011).</li><li>Beale, 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=Circadian+rhythms+in+Mexican+blind+cavefish+Astyanax+mexicanus+in+the+lab+and+in+the+field.">Circadian rhythms in Mexican blind cavefish Astyanax mexicanus in the lab and in the field.</a> Nature Communications. 4, 2769 (2013).</li><li>Keene, A. C., Yoshizawa, M., McGaugh, S. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Biology and Evolution of the Mexican Cavefish. , (2015).</li><li>Jeffery, W. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Regressive+evolution+in+Astyanax+cavefish.">Regressive evolution in Astyanax cavefish.</a> Annual Review of Genetics. 43, 25-47 (2009).</li><li>Gross, J. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+complex+origin+of+Astyanax+cavefish.">The complex origin of Astyanax cavefish.</a> BMC Evolutionary Biology. 12, 105 (2012).</li><li>Aspiras, A., Rohner, N., Marineau, B., Borowsky, R., Tabin, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Melanocortin+4+receptor+mutations+contribute+to+the+adaptation+of+cavefish+to+nutrient-poor+conditions.">Melanocortin 4 receptor mutations contribute to the adaptation of cavefish to nutrient-poor conditions.</a> Proceedings of the National Academy of Sciences. 112 (31), 9688 (2015).</li><li>Jaggard, 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=The+lateral+line+confers+evolutionarily+derived+sleep+loss+in+the+Mexican+cavefish.">The lateral line confers evolutionarily derived sleep loss in the Mexican cavefish.</a> Journal of Experimental Biology. 220 (2), (2017).</li><li>Jaggard, J. B., Stahl, B. A., Lloyd, E., Prober, D. A., Duboue, E. R., Keene, A. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hypocretin+underlies+the+evolution+of+sleep+loss+in+the+Mexican+cavefish.">Hypocretin underlies the evolution of sleep loss in the Mexican cavefish.</a> eLife. , e32637 (2018).</li><li>Hinaux, 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=A+Developmental+Staging+Table+for+Astyanax+mexicanus+Surface+Fish+and+Pacho+&#180;n+Cavefish.">A Developmental Staging Table for Astyanax mexicanus Surface Fish and Pacho &#180;n Cavefish.</a> Zebrafish. 8 (4), 155-165 (2011).</li><li>Bill, B. R., Petzold, A. M., Clark, K. J., La Schimmenti, ., Ekker, 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=A+primer+for+morpholino+use+in+zebrafish.">A primer for morpholino use in zebrafish.</a> Zebrafish. 6 (1), 69-77 (2009).</li><li>Bilandzija, H., Ma, L., Parkhurst, A., Jeffery, W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+potential+benefit+of+albinism+in+Astyanax+cavefish:+downregulation+of+the+oca2+gene+increases+tyrosine+and+catecholamine+levels+as+an+alternative+to+melanin+synthesis.">A potential benefit of albinism in Astyanax cavefish: downregulation of the oca2 gene increases tyrosine and catecholamine levels as an alternative to melanin synthesis.</a> Plos One. 8 (11), e80823 (2013).</li><li>Yokogawa, 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=Characterization+of+sleep+in+zebrafish+and+insomnia+in+hypocretin+receptor+mutants.">Characterization of sleep in zebrafish and insomnia in hypocretin receptor mutants.</a> PLoS Biology. 5, 2379-2397 (2007).</li><li>Appelbaum, 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=Sleep-wake+regulation+and+hypocretin-melatonin+interaction+in+zebrafish.">Sleep-wake regulation and hypocretin-melatonin interaction in zebrafish.</a> Proceedings of the National Academy of Sciences of the United States of America. 106, 21942-21947 (2009).</li><li>Singh, C., Oikonomou, G., Prober, D. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Norepinephrine+is+required+to+promote+wakefulness+and+for+hypocretin-induced+arousal+in+zebrafish.">Norepinephrine is required to promote wakefulness and for hypocretin-induced arousal in zebrafish.</a> eLife. 4 (September), (2015).</li><li>Elipot, Y., Hinaux, H., Callebert, J., R&#233;taux, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Evolutionary+shift+from+fighting+to+foraging+in+blind+cavefish+through+changes+in+the+serotonin+network.">Evolutionary shift from fighting to foraging in blind cavefish through changes in the serotonin network.</a> Current Biology. 23 (1), 1-10 (2013).</li><li>Bell, M. A., Foster, S. 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The authors declare they have no competing interests.

This protocol describes a custom system for quantifying sleep and locomotor activity in larval and adult cavefish. Cavefish have emerged as a leading model for studying the evolution of sleep that can be used to investigate the genetic and neural basis of sleep regulation1. The critical steps in this protocol include optimization of lighting and video quality in order to assure accurate tracking that is necessary to quantify sleep. The system for acquisition and analysis described here are fully f...

Sleep is highly conserved throughout the animal kingdom at the physiological, functional, and behavioral levels1,2,3. While sleep in mammalian laboratory animals is typically assessed using electroencephalograms, electrophysiological recordings are less practical in small genetically amenable model systems and thus sleep is typically measured based on behavior3,4. Behavioral characteristics associated with sleep are highly conserved throughout the animal kingdom and include increased arousal threshold, reversibility with stimulation, and prolonged behavioral quiescence5. These measures can be used to characterize sleep in animals ranging from the nematode worm, C. elegans, through humans6.
The use of behavioral quiescence to characterize sleep requires automated tracking software. With tracking software, periods of activity and immobility are determined over a number of days, and long periods of inactivity are classified as sleep7,8. In recent years, multiple tracking systems have been developed for acquiring activity data among a diversity of small genetically-amenable model systems; including worms, fruit flies and fish9,10,11. These programs are accompanied by software that allows for automated tracking of animal behavior, including both open source freeware and commercially available software7,12,13,14. These systems differ in their flexibility and allow for efficient screening and characterization of sleep phenotypes in numerous genetically amendable models.
Genetic investigation of sleep in the zebrafish, Danio rerio, has led to the identification of numerous genes and neural circuits that regulate sleep15,16. While this has provided a powerful system for investigating the neural basis of sleep in a vertebrate laboratory animal, much less is known about how sleep evolves and how natural variation contributes to sleep regulation. The Mexican cavefish, Astyanax mexicanus (A. mexicanus), have evolved dramatic differences in sleep, locomotor activity and circadian rhythms17,18. These fish exist as eyed surface fish that inhabit the rivers of Mexico and Southern Texas and at least 29 cave populations around the Sierra Del Abra region of Northeast Mexico19,20,21. Remarkably, many behavioral differences, including sleep loss, appear to have emerged independently in multiple cavefish populations14,22. Therefore, cavefish provide a model for investigating the convergent evolution of sleep, circadian, and social behaviors.
This protocol describes a system for measuring sleep and locomotor behavior in A. mexicanus larvae and adults. A custom-built infrared-based recording system allows for video recording of animals under light and dark conditions. Commercially available software can be used to measure activity and custom macros are used to quantify several aspects of inactivity and determine periods of sleep. This protocol also describes experimental modifications for tracking the activity of multiple animals within a tank, providing the ability to examine interactions between sleep and social behaviors. These systems can be applied to measure sleep, circadian behavior, and locomotor activity in additional fish species including zebrafish and sticklebacks.

<table>
	<tbody>
		<tr>
			<td>12V power adaptor</td>
			<td>Environmental Lights</td>
			<td>24 Watt 12 VDC Power Supply</td>
			<td></td>
		</tr>
		<tr>
			<td>Acrylic dividers (adults)</td>
			<td>TAP Plastic</td>
			<td></td>
			<td>Order sheets in sizes as needed</td>
		</tr>
		<tr>
			<td>Adult infrared light power source</td>
			<td>Environmnental Lights 24 Watt 12 VDC Power Supply</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Battery pack</td>
			<td>CyberPower</td>
			<td>CP850PFCLCD</td>
			<td></td>
		</tr>
		<tr>
			<td>Camera lens (adult)</td>
			<td>Navitar Zoom 7000</td>
			<td>Zoom 7000</td>
			<td></td>
		</tr>
		<tr>
			<td>Camera lens (larval)</td>
			<td>Fujian 35mm f/1.7</td>
			<td>B01CHX7668</td>
			<td>Purchase on Amazon</td>
		</tr>
		<tr>
			<td>Camera lens adapter</td>
			<td>d</td>
			<td>1524219</td>
			<td></td>
		</tr>
		<tr>
			<td>Camera mount</td>
			<td>CowboyStudio Super Clamp</td>
			<td>B002LV7X1K</td>
			<td>Purchase on Amazon</td>
		</tr>
		<tr>
			<td>Fish tank</td>
			<td>Deep Blue Professional</td>
			<td>ADB11006</td>
			<td></td>
		</tr>
		<tr>
			<td>Heat sink (adult)</td>
			<td>M-D Building products</td>
			<td>SKU: 61085</td>
			<td>Cut to fit</td>
		</tr>
		<tr>
			<td>Heat sink (larval)</td>
			<td>M-D Building products</td>
			<td>SKU: 57000</td>
			<td>Cut to fit</td>
		</tr>
		<tr>
			<td>Infrared lights (adults)</td>
			<td>Environmental Lights Infrared 850 nm 5050 LED strip</td>
			<td>irrf850-5050-60-reel</td>
			<td>Cut to fit</td>
		</tr>
		<tr>
			<td>Infrared lights (larval)</td>
			<td>LED World</td>
			<td>B00MO9H7H4</td>
			<td>Purchase on Amazon</td>
		</tr>
		<tr>
			<td>IR-diffusing acrylic</td>
			<td>TAP Plastic</td>
			<td></td>
			<td>Order sheets in sizes as needed</td>
		</tr>
		<tr>
			<td>Laptop/computer</td>
			<td>N/A</td>
			<td>N/A</td>
			<td>Any laptop will work.</td>
		</tr>
		<tr>
			<td>LED light</td>
			<td>Chanzon 10 High Power Led Chip 3W White (6000K-6500K/600mA-700mA/DC 3V-3.4V/3 Watt)</td>
			<td>B06XKTRSP7</td>
			<td>Use with Chanzon 25pcs 1W 3W 5W LED Heat Sink (2 pin Black) Aluminum Base Plate Panel</td>
		</tr>
		<tr>
			<td>light timer</td>
			<td>Century 24 Hour Plug-in Mechanical Timer Grounded</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Plastic wall mount for IR</td>
			<td>Everbilt Plastic pegboard</td>
			<td>Model # 17961</td>
			<td></td>
		</tr>
		<tr>
			<td>Power cable</td>
			<td>BNTECHGO 22 Gauge Silicone Wire</td>
			<td>B01K4RPE0Y</td>
			<td></td>
		</tr>
		<tr>
			<td>Power source</td>
			<td>Rapid LED</td>
			<td>MOONLIGHT DRIVER (350MA)</td>
			<td></td>
		</tr>
		<tr>
			<td>Tissue culture plates</td>
			<td>Fisherbrand</td>
			<td colspan="2">12-well (FB012928) 24-well (FB012929)</td>
		</tr>
		<tr>
			<td>Tripod Ball head</td>
			<td>Demon DB-44</td>
			<td>B00TQ54CZO</td>
			<td>Purchase on Amazon</td>
		</tr>
		<tr>
			<td>USB Hardrive</td>
			<td>Seagate 3TB backup</td>
			<td>STDT3000100</td>
			<td></td>
		</tr>
		<tr>
			<td>USB Webcam</td>
			<td>Microsoft LifeCam</td>
			<td>Q2F-00014</td>
			<td>Purchase on Amazon</td>
		</tr>
		<tr>
			<td>Wall mount for camera</td>
			<td>LDR Industries 1/2&#34; Steel pipe</td>
			<td>307 12X36</td>
			<td>Mounted on wall with Flange and 90 degree pipe elbow. Could also use a tripod to hold camera.</td>
		</tr>
	</tbody>
</table>

automated measurements of sleep and locomotor activity in mexican cavefish

Across phyla, sleep is characterized by highly conserved behavioral characteristics that include elevated arousal threshold, rebound following sleep deprivation, and consolidated periods of behavioral immobility. The Mexican cavefish, Astyanax mexicanus (A. mexicanus), is a model for studying trait evolution in response to environmental perturbation. A. mexicanus exist as in eyed surface-dwelling forms and multiple blind cave-dwelling populations that have robust morphological and behavioral differences. Sleep loss has occurred in multiple, independently-evolved cavefish populations. This protocol describes a methodology for quantifying sleep and locomotor activity in A. mexicanus cave and surface fish. A cost-effective video monitoring system allows for behavioral imaging of individually-housed larval or adult fish for periods of a week or longer. The system can be applied to fish aged 4 days post fertilization through adulthood. The approach can also be adapted for measuring the effects of social interactions on sleep by recording multiple fish in a single arena. Following behavioral recordings, data is analyzed using automated tracking software and sleep analysis is processed using customized scripts that quantify multiple sleep variables including duration, bout length, and bout number. This system can be applied to measure sleep, circadian behavior, and locomotor activity in almost any fish species including zebrafish and sticklebacks.

Larvae ages 4-30 dpf can be reliably recorded in the custom-build closed system described in Figure 1. The system includes both IR and visible lighting to allow for recordings under light and dark conditions, under various visible light conditions (Figure 1A). The videos are then analyzed using tracking software (Figure 1B,C) and post-processed using a custom sleep macro (See <strong...

Watch this Scientific Journal Video about Automated Measurements of Sleep and Locomotor Activity in Mexican Cavefish at JoVE.com

Automated Measurements of Sleep and Locomotor Activity in Mexican Cavefish

This protocol details the methodology for quantifying locomotor behavior and sleep in the Mexican cavefish. Previous analyses are extended to measure these behaviors in socially-housed fish. This system can be widely applied to study sleep and activity in other fish species.

Across phyla, sleep is characterized by highly conserved behavioral characteristics that include elevated arousal threshold, rebound following sleep ...

This protocol can be used to quantify sleep and activity in any fish population and has the potential to expand the number of model systems used to study sleep regulation. The advantage of this technique is its flexibility. For example, fish can be tracked in a variety of arena sizes or in singly-housed or group-housed experiments.A strength of measuring sleep in this system is the amenability of the method for high throughput drug or genetic screening. We have applied this method to the study of the evolution of sleep in two different populations of cavefish that demonstrate dramatically different sleep phenotypes. Although it can be difficult to establish a system for behavioral imaging, our system provides a cost-effective method for studying larval and adult fish.To build the system to accurately track locomotor behavior for studying sleep and circadian rhythms in larval A.mexicanus, use 0.33-centimeter-thick white sign acrylic to construct a platform for the larval tracking system. Place the recording platform on top of the lighted square heat sink upon which fish-containing arenas will reside during the behavioral tracking experiments, and place a second acrylic inside the box between the lights in the animal housing to diffuse the infrared for optimal lighting and contrast. Place the entire larval tracking stage and lighting set up within an enclosed plastic tube.Use a rotary tool to remove the lens from an experimentally-suitable webcam. Remove the small screws on the back of the camera to remove the inner housing, and remove the small screws inside the body of the camera to loosen the remainder of the lens. Use a small screwdriver to remove any portions of the lens housing that are left after cutting the lens.And remove the blue light-emitting diode on the top part of the charge-coupled device or CCD housing. Next, return the inner housing to its original orientation before screwing the two outer screws back into their original positions. Use a small saw to route the inside of the camera to allow the camera to be fitted with a rounded plastic routing bit smoothing down the extra plastic until it can accompany a lens adapter.Install an infrared pass filter inside the camera as close to the CCD as possible without making direct contact with the camera, and screw the adapter of a 35-millimeter fixed lens in the front of the camera into the back of the lens. Then place the camera and lens into the hole drilled into the lid at the top of the tube that houses the stage and lights, and attach the USB to the computer on which the animals will be recorded. To construct a sleep system for adult fish, first cut infrared strips at approximately 46-centimeter intervals.And place a 46 by five by 0.32-centimeter 9%light pass white sign acrylic sheet directly in front of each infrared light strip to diffuse the infrared light. Then place all of the tanks on a rack that supports rear-mounted infrared lighting, and use opaque plastic dividers and 10-liter glass tanks to create individual arenas. To record the locomotor activity of the Mexican tetra fish place day four to six post-fertilization fish into individual wells of a 24-well tissue plate, and days 20 to 30 post-fertilization in individual wells of a six-well tissue plate.To record adult tetra sleep and activity in a social setting house up to five adults per 10-liter tank with or without the dividers. In this representative experiment larval fish from three independent cave fish populations displayed a significant reduction in sleep compared to surface fish. This sleep production is consistent across all of the ages tested as sleep was also significantly reduced in adult Pachon, Molino, and Tinaja cave fish compared to surface fish.Notably, social housing robustly reduced sleep in surface fish without affecting sleep in Pacho cave fish likely due to a basement effect in the cave fish populations. When recording the fish care should be taken to ensure that the camera lighting is optimal to enhance the signal of the fish relative to the background. Some basic command line coding is required for this protocol that is fully described in the text and should be amenable to any lab setting.This protocol has led to numerous questions about sleep evolution and is currently being used for drug screens, track sleep behavior, and understand how social behavior affects sleep.

automated-measurements-sleep-locomotor-activity-mexican

Research

JoVE Journal

Behavior

6.7K visualizações.  Florida Atlantic University. Este protocolo pode ser usado para quantificar o sono e a atividade em qualquer população de peixes e tem o potencial de expandir o número de sistemas de modelos usados para estudar a regulação do sono. A vantagem dessa técnica é sua flexibilidade. Por exemplo, os peixes podem ser rastreados em uma variedade de tamanhos de arena ou em experimentos de casas e agrupadas.Uma força de medir o sono neste sistema é a comodidade do método para medicamentos de alta produtividade ou t...