This work was supported by NIH grants 5R01NS051305-14 and 5R01NS076980-08 to PJS.

1. Experimental preparation
<ol>
	<li>Collect flies as they eclose into vials, separating male and female flies. 
	NOTE: Sleep experiments are commonly conducted with female flies. It is important to collect virgin females. Mated females will lay eggs that hatch into larvae complicating the analysis of the data.</li>
	<li>House flies of a single sex in groups of &#60;20. 
	NOTE: Housing flies in a socially enriched environment (groups of &#62;50) modulates sleep drive6,<sup ...

<ol>
	<li>Nath, R. 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=The+Jellyfish+Cassiopea+Exhibits+a+Sleep-like+State.">The Jellyfish Cassiopea Exhibits a Sleep-like State.</a> Current Biology. 27 (19), 2984-2990 (2017).</li><li>Vorster, A. P., Krishnan, H. C., Cirelli, C., Lyons, L. C. <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+Aplysia+californica.">Characterization of sleep in Aplysia californica.</a> Sleep. 37 (9), 1453-1463 (2014).</li><li>Zhdanova, I. V., Wang, S. Y., Leclair, O. U., Danilova, N. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Melatonin+promotes+sleep-like+state+in+zebrafish.">Melatonin promotes sleep-like state in zebrafish.</a> Brain Research. 903 (1-2), 263-268 (2001).</li><li>Shaw, P. J., Cirelli, C., Greenspan, R. J., Tononi, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Correlates+of+sleep+and+waking+in+Drosophila+melanogaster.">Correlates of sleep and waking in Drosophila melanogaster.</a> Science. 287 (5459), 1834-1837 (2000).</li><li>Hendricks, J. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Rest+in+Drosophila+is+a+sleep-like+state.">Rest in Drosophila is a sleep-like state.</a> Neuron. 25 (1), 129-138 (2000).</li><li>Ganguly-Fitzgerald, I., Donlea, J., Shaw, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Waking+experience+affects+sleep+need+in+Drosophila.">Waking experience affects sleep need in Drosophila.</a> Science. 313 (5794), 1775-1781 (2006).</li><li>Seugnet, L., Suzuki, Y., Vine, L., Gottschalk, L., Shaw, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=D1+receptor+activation+in+the+mushroom+bodies+rescues+sleep-loss-induced+learning+impairments+in+Drosophila.">D1 receptor activation in the mushroom bodies rescues sleep-loss-induced learning impairments in Drosophila.</a> Current Biology. 18 (15), 1110-1117 (2008).</li><li>Donlea, J. M., Thimgan, M. S., Suzuki, Y., Gottschalk, L., Shaw, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inducing+sleep+by+remote+control+facilitates+memory+consolidation+in+Drosophila.">Inducing sleep by remote control facilitates memory consolidation in Drosophila.</a> Science. 332 (6037), 1571-1576 (2011).</li><li>Seidner, G., 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=Identification+of+Neurons+with+a+Privileged+Role+in+Sleep+Homeostasis+in+Drosophila+melanogaster.">Identification of Neurons with a Privileged Role in Sleep Homeostasis in Drosophila melanogaster.</a> Current Biology. 25 (22), 2928-2938 (2015).</li><li>Li, X., Yu, F., Guo, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sleep+deprivation+specifically+impairs+short-term+olfactory+memory+in+Drosophila.">Sleep deprivation specifically impairs short-term olfactory memory in Drosophila.</a> Sleep. 32 (11), 1417-1424 (2009).</li><li>Melnattur, 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=A+conserved+role+for+sleep+in+supporting+Spatial+Learning+in+Drosophila.">A conserved role for sleep in supporting Spatial Learning in Drosophila.</a> Sleep. , 197 (2020).</li><li>Seugnet, L., Suzuki, Y., Donlea, J. M., Gottschalk, L., Shaw, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sleep+deprivation+during+early-adult+development+results+in+long-lasting+learning+deficits+in+adult+Drosophila.">Sleep deprivation during early-adult development results in long-lasting learning deficits in adult Drosophila.</a> Sleep. 34 (2), 137-146 (2011).</li><li>Donlea, J. M., Ramanan, N., Shaw, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Use-dependent+plasticity+in+clock+neurons+regulates+sleep+need+in+Drosophila.">Use-dependent plasticity in clock neurons regulates sleep need in Drosophila.</a> Science. 324 (5923), 105-108 (2009).</li><li>Bushey, D., Tononi, G., 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=Sleep+and+synaptic+homeostasis:+structural+evidence+in+Drosophila.">Sleep and synaptic homeostasis: structural evidence in Drosophila.</a> Science. 332 (6037), 1576-1581 (2011).</li><li>Huang, S., Piao, C., Beuschel, C. B., G&#246;tz, T., Sigrist, S. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Presynaptic+Active+Zone+Plasticity+Encodes+Sleep+Need+in+Drosophila.">Presynaptic Active Zone Plasticity Encodes Sleep Need in Drosophila.</a> Current Biology. 30 (6), 1077-1091 (2020).</li><li>Kirszenblat, 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+regulates+visual+selective+attention+in+Drosophila.">Sleep regulates visual selective attention in Drosophila.</a> Journal of Experimental Biology. 221, (2018).</li><li>Singh, P., Donlea, 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=Bidirectional+Regulation+of+Sleep+and+Synapse+Pruning+after+Neural+Injury.">Bidirectional Regulation of Sleep and Synapse Pruning after Neural Injury.</a> Current Biology. 30 (6), 1063-1076 (2020).</li><li>Stanhope, B. A., Jaggard, J. B., Gratton, M., Brown, E. B., 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=Sleep+Regulates+Glial+Plasticity+and+Expression+of+the+Engulfment+Receptor+Draper+Following+Neural+Injury.">Sleep Regulates Glial Plasticity and Expression of the Engulfment Receptor Draper Following Neural Injury.</a> Current Biology. 30 (6), 1092-1101 (2020).</li><li>Kayser, M. S., Yue, Z., Sehgal, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+critical+period+of+sleep+for+development+of+courtship+circuitry+and+behavior+in+Drosophila.">A critical period of sleep for development of courtship circuitry and behavior in Drosophila.</a> Science. 344 (6181), 269-274 (2014).</li><li>Kayser, M. S., Mainwaring, B., Yue, Z., Sehgal, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sleep+deprivation+suppresses+aggression+in+Drosophila.">Sleep deprivation suppresses aggression in Drosophila.</a> Elife. 4, 07643 (2015).</li><li>Szuperak, 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=A+sleep+state+in+Drosophila+larvae+required+for+neural+stem+cell+proliferation.">A sleep state in Drosophila larvae required for neural stem cell proliferation.</a> Elife. 7, (2018).</li><li>Vaccaro, 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=Sleep+Loss+Can+Cause+Death+through+Accumulation+of+Reactive+Oxygen+Species+in+the+Gut.">Sleep Loss Can Cause Death through Accumulation of Reactive Oxygen Species in the Gut.</a> Cell. 181 (6), 1307-1328 (2020).</li><li>Kempf, A., Song, S. M., Talbot, C. B., Miesenb&#246;ck, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+potassium+channel+&#946;-subunit+couples+mitochondrial+electron+transport+to+sleep.">A potassium channel &#946;-subunit couples mitochondrial electron transport to sleep.</a> Nature. 568 (7751), 230-234 (2019).</li><li>Donlea, J. M., Pimentel, D., Miesenb&#246;ck, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neuronal+machinery+of+sleep+homeostasis+in+Drosophila.">Neuronal machinery of sleep homeostasis in Drosophila.</a> Neuron. 81 (4), 860-872 (2014).</li><li>Liu, S., Liu, Q., Tabuchi, M., Wu, M. N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sleep+Drive+Is+Encoded+by+Neural+Plastic+Changes+in+a+Dedicated+Circuit.">Sleep Drive Is Encoded by Neural Plastic Changes in a Dedicated Circuit.</a> Cell. 165 (6), 1347-1360 (2016).</li><li>Pimentel, 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=Operation+of+a+homeostatic+sleep+switch.">Operation of a homeostatic sleep switch.</a> Nature. 536 (7616), 333-337 (2016).</li><li>Sitaraman, 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=Propagation+of+Homeostatic+Sleep+Signals+by+Segregated+Synaptic+Microcircuits+of+the+Drosophila+Mushroom+Body.">Propagation of Homeostatic Sleep Signals by Segregated Synaptic Microcircuits of the Drosophila Mushroom Body.</a> Current Biology. 25 (22), 2915-2927 (2015).</li><li>Foltenyi, K., Greenspan, R. J., Newport, J. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Activation+of+EGFR+and+ERK+by+rhomboid+signaling+regulates+the+consolidation+and+maintenance+of+sleep+in+Drosophila.">Activation of EGFR and ERK by rhomboid signaling regulates the consolidation and maintenance of sleep in Drosophila.</a> Nature Neuroscience. 10 (9), 1160-1167 (2007).</li><li>Seugnet, 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=Notch+signaling+modulates+sleep+homeostasis+and+learning+after+sleep+deprivation+in+Drosophila.">Notch signaling modulates sleep homeostasis and learning after sleep deprivation in Drosophila.</a> Current Biology. 21 (10), 835-840 (2011).</li><li>Seugnet, L., Galvin, J. E., Suzuki, Y., Gottschalk, L., Shaw, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Persistent+short-term+memory+defects+following+sleep+deprivation+in+a+Drosophila+model+of+Parkinson+disease.">Persistent short-term memory defects following sleep deprivation in a Drosophila model of Parkinson disease.</a> Sleep. 32 (8), 984-992 (2009).</li><li>Tabuchi, 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=Sleep+interacts+with+a&#946;+to+modulate+intrinsic+neuronal+excitability.">Sleep interacts with a&#946; to modulate intrinsic neuronal excitability.</a> Current Biology. 25 (6), 702-712 (2015).</li><li>Melnattur, K., Zhang, B., Shaw, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Disrupting+flight+increases+sleep+and+identifies+a+novel+sleep-promoting+pathway+in+Drosophila.">Disrupting flight increases sleep and identifies a novel sleep-promoting pathway in Drosophila.</a> Science Advances. 6 (19), 2166 (2020).</li><li>Thimgan, M. S., Suzuki, Y., Seugnet, L., Gottschalk, L., Shaw, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+perilipin+homologue,+lipid+storage+droplet+2,+regulates+sleep+homeostasis+and+prevents+learning+impairments+following+sleep+loss.">The perilipin homologue, lipid storage droplet 2, regulates sleep homeostasis and prevents learning impairments following sleep loss.</a> PLOS Biology. 8 (8), (2010).</li><li>Keene, A. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Clock+and+cycle+limit+starvation-induced+sleep+loss+in+Drosophila.">Clock and cycle limit starvation-induced sleep loss in Drosophila.</a> Current Biology. 20 (13), 1209-1215 (2010).</li><li>Shaw, P. J., Tononi, G., Greenspan, R. J., Robinson, D. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Stress+response+genes+protect+against+lethal+effects+of+sleep+deprivation+in+Drosophila.">Stress response genes protect against lethal effects of sleep deprivation in Drosophila.</a> Nature. 417 (6886), 287-291 (2002).</li><li>Andretic, R., Shaw, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Essentials+of+sleep+recordings+in+Drosophila:+moving+beyond+sleep+time.">Essentials of sleep recordings in Drosophila: moving beyond sleep time.</a> Methods Enzymol. 393, 759-772 (2005).</li><li>Seugnet, 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=Identifying+sleep+regulatory+genes+using+a+Drosophila+model+of+insomnia.">Identifying sleep regulatory genes using a Drosophila model of insomnia.</a> Journal of Neuroscience. 29 (22), 7148-7157 (2009).</li><li>Bushey, D., Huber, R., Tononi, G., 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=Drosophila+Hyperkinetic+mutants+have+reduced+sleep+and+impaired+memory.">Drosophila Hyperkinetic mutants have reduced sleep and impaired memory.</a> Journal of Neuroscience. 27 (20), 5384-5393 (2007).</li><li>Geissmann, Q., 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=Ethoscopes:+An+open+platform+for+high-throughput+ethomics.">Ethoscopes: An open platform for high-throughput ethomics.</a> PLOS Biology. 15 (10), 2003026 (2017).</li><li>Faville, R., Kottler, B., Goodhill, G. J., Shaw, P. J., van Swinderen, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=How+deeply+does+your+mutant+sleep?+Probing+arousal+to+better+understand+sleep+defects+in+Drosophila.">How deeply does your mutant sleep? Probing arousal to better understand sleep defects in Drosophila.</a> Scientific Reports. 5, 8454 (2015).</li><li>Huber, 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=Sleep+homeostasis+in+Drosophila+melanogaster.">Sleep homeostasis in Drosophila melanogaster.</a> Sleep. 27 (4), 628-639 (2004).</li><li>Klose, M., Shaw, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sleep-drive+reprograms+clock+neuronal+identity+through+CREB-binding+protein+induced+PDFR+expression.">Sleep-drive reprograms clock neuronal identity through CREB-binding protein induced PDFR expression.</a> bioRxiv. , (2019).</li><li>Dissel, 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=Sleep+restores+behavioral+plasticity+to+Drosophila+mutants.">Sleep restores behavioral plasticity to Drosophila mutants.</a> Current Biology. 25 (10), 1270-1281 (2015).</li><li>Gerstner, J. R., Vanderheyden, W. M., Shaw, P. J., Landry, C. F., Yin, J. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fatty-acid+binding+proteins+modulate+sleep+and+enhance+long-term+memory+consolidation+in+Drosophila.">Fatty-acid binding proteins modulate sleep and enhance long-term memory consolidation in Drosophila.</a> PLoS One. 6 (1), 15890 (2011).</li></ol>

The authors have nothing to disclose.

Sleep in Drosophila was independently characterized in 2000, by two groups4,5. In these pioneering studies, flies were deprived of sleep by gentle handling (i.e., hand deprivation) and shown to exhibit a robust homeostatic response to overnight sleep deprivation. Importantly, with any sleep deprivation experiment it is crucial to control for potential confounding effects of the method used to keep the animal awake. Hand deprivation studies set the benchm...

Sleep is near universal in animals, yet its function remains unclear. Sleep homeostasis, the compensatory increase in sleep following sleep deprivation, is a defining property of sleep, that has been used to characterize sleep states in a number of animals1,2,3,4,5.
Sleep in the fly has many similarities with human sleep, including a robust homeostatic response to sleep loss4,5. Numerous studies of sleep in the fly have used sleep deprivation both to infer sleep function by examining the adverse consequences that accrue from extended waking, and to understand sleep regulation by determining the neurobiological mechanisms controlling the homeostatic regulation of sleep. Thus sleep deprived flies were shown to exhibit impairments in learning and memory6,7,8,9,10,11,12, structural plasticity13,14,15, visual attention16, recovery from neuronal injury17,18, mating and aggressive behaviors19,20, cell proliferation21, and responses to oxidative stress22,23 to name a few. Further, investigations into the neurobiological mechanisms controlling rebound sleep have yielded critical insights into the neuronal machinery that constitutes the sleep homeostat8,9,23,24,25,26,27,28,29. Finally, in addition to revealing fundamental insights into sleep function in healthy animals, sleep deprivation studies have also informed insights into sleep function in diseased states30,31.
While sleep deprivation is undeniably a powerful tool, with any sleep deprivation experiment, it is important to distinguish phenotypes that result from extended waking, from those induced by the stimulus used to keep the animal awake. Sleep deprivation by hand deprivation or gentle handling, is generally regarded as setting the standard for minimally disruptive sleep deprivation. Here we describe a protocol for sleep depriving flies using the Sleep Nullifying Apparatus (SNAP). The SNAP is a device that delivers a mechanical stimulus to flies every 10s, keeping flies awake by inducing negative geotaxis (Figure 1). The SNAP efficiently deprives flies of &#62;98% of night-time sleep, even in flies with high sleep drive8,32. The SNAP has been calibrated on bang sensitive flies, agitation of flies in the SNAP does not harm flies; sleep deprivation with the SNAP induces a rebound comparable with that obtained by hand deprivation7. The SNAP is thus a robust method to sleep deprive flies while controlling for the effects of the arousing stimulus.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Locomotor activity tubes</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Fisher Tissue Prep Wax</td>
			<td>Thermo Fisher</td>
			<td>13404-122</td>
			<td>Wax used for sealing tubes</td>
		</tr>
		<tr>
			<td>Glass tubes</td>
			<td>Wale Apparatus</td>
			<td>244050</td>
			<td>We cut 5mm diameter Pyrex glass&#160;tubes into 65mm long tubes&#160;to record sleep. Pre-cut tubes&#160;can also be purchased.</td>
		</tr>
		<tr>
			<td>Nutri Fly Bloomington Formulation fly food</td>
			<td>Genesee Scientific</td>
			<td>66-113</td>
			<td>Labs might use their own fly food recipe. It is important that sleep be recorded on the same food that flies were reared in.</td>
		</tr>
		<tr>
			<td>Rotary glass cutting tool</td>
			<td>Dremel Multi Pro</td>
			<td>395</td>
			<td>Used to cut 65mm long glass tubes&#160;</td>
		</tr>
		<tr>
			<td>Monitoring Sleep</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>DAM System and DAMFileScan software</td>
			<td>Trikinetics</td>
			<td></td>
			<td>Software used to acquire data from DAM monitors and save the acquired data in an appropriate format</td>
		</tr>
		<tr>
			<td>Data acquisition computer</td>
			<td>Lenovo</td>
			<td>Idea Centre AIO3</td>
			<td>A equivalent computer from any manufacturer can substitute</td>
		</tr>
		<tr>
			<td>Drosophila Activity Monitors</td>
			<td>Trikinetics</td>
			<td>DAM2</td>
			<td>These monitors are used to record flies&#39; locomotor activity</td>
		</tr>
		<tr>
			<td>Environment Monitor</td>
			<td>Trikinetics</td>
			<td>DEnM</td>
			<td>Not essential, but an easy way to monitor environmental conditions in the chamber where sleep is recorded</td>
		</tr>
		<tr>
			<td>Light Controller</td>
			<td>Trikinetics</td>
			<td>LC4</td>
			<td>A convenient way to control the timing of when the SNAP is turned on and off</td>
		</tr>
		<tr>
			<td>Power Supply Interface Unit for DAM</td>
			<td>Trikinetics</td>
			<td>PSIU-9</td>
			<td>Required for data acquisition computers to record Trikinetics locomotor acitvity data</td>
		</tr>
		<tr>
			<td>RJ11 connector</td>
			<td>7001-64PC</td>
			<td>Multicomp</td>
			<td>DAM monitors accept RJ11 jacks</td>
		</tr>
		<tr>
			<td>Splitters</td>
			<td>Trikinetics</td>
			<td>SPLT5</td>
			<td>Used to connect upto 5 DAM monitors</td>
		</tr>
		<tr>
			<td>Telephone cable wire</td>
			<td>Radioshack</td>
			<td>278-367</td>
			<td>Phone cables to acquire data from DAM monitors</td>
		</tr>
		<tr>
			<td>Sleep Deprivation</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Power supply</td>
			<td>Gw INSTEK</td>
			<td>GPS-30300</td>
			<td>Power supply for the SNAP</td>
		</tr>
		<tr>
			<td>Sleep Nullifying Apparatus</td>
			<td>Washington University School of Medicine machine shop</td>
			<td></td>
			<td></td>
		</tr>
	</tbody>
</table>

the sleep nullifying apparatus: a highly efficient method of sleep depriving drosophila

Sleep homeostasis, the increase in sleep observed following sleep loss, is one of the defining criteria used to identify sleep throughout the animal kingdom. As a consequence, sleep deprivation and sleep restriction are powerful tools that are commonly used to provide insight into sleep function. Nonetheless, sleep deprivation experiments are inherently problematic in that the deprivation stimulus itself may be the cause of observed changes in physiology and behavior. Accordingly, successful sleep deprivation techniques should keep animals awake and, ideally, result in a robust sleep rebound without also inducing a large number of unintended consequences. Here, we describe a sleep deprivation technique for Drosophila melanogaster. The Sleep Nullifying Apparatus (SNAP) administers a stimulus every 10s to induce negative geotaxis. Although the stimulus is predictable, the SNAP effectively prevents &#62;95% of nighttime sleep even in flies with high sleep drive. Importantly, the subsequent homeostatic response is very similar to that achieved using hand-deprivation. The timing and spacing of the stimuli can be modified to minimize sleep loss and thus examine non-specific effects of the stimulus on physiology and behavior. The SNAP can also be used for sleep restriction and to assess arousal thresholds. The SNAP is a powerful sleep disruption technique that can be used to better understand sleep function.

Canton S (Cs) was used as a wild-type strain. Flies were maintained on a 12 h light: 12 h dark schedule, and sleep deprived for 12 hours overnight. Inspection of the sleep profiles of Cs flies on the baseline day (bs), sleep deprivation day (sd), and two recovery days (rec1 and rec2) (Figure 2A) suggests that flies were effectively sleep deprived in the SNAP, and recovered sleep during the day consistent with observed reports in the literature<sup class="xref...

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The Sleep Nullifying Apparatus: A Highly Efficient Method of Sleep Depriving Drosophila

Sleep deprivation is a powerful tool to investigate sleep function and regulation. We describe a protocol to sleep deprive Drosophila using the Sleep Nullifying Apparatus, and to determine the extent of rebound sleep induced by deprivation.

The Sleep Nullifying Apparatus: A Highly Efficient Method of Sleep Depriving Drosophila

Sleep homeostasis, the increase in sleep observed following sleep loss, is one of the defining criteria used to identify sleep throughout the animal ...

Sleep homeostasis, the increase in sleep following sleep loss, is a defining characteristic of sleep. Sleep deprivation and sleep restriction are thus powerful tools to study sleep regulation and function. This protocol efficiently sleep deprives and sleep restricts flies while minimizing potential confounds.SNAP deprives flies of greater than 95%of sleep even in flies with high sleep drive. Importantly, agitation of flies with the SNAP does not harm flies and induce a rebound comparable to that obtained with hand deprivation, which is a standard for minimally disruptive sleep deprivation. Visualizing how the SNAP keeps flies awake will help investigators use and optimize this protocol.Begin by collecting eclosing flies into vials, separating males and females. House the flies in groups of less than 20 and keep them for three to five days in a light and humidity-controlled environment. Prepare an appropriate number of tubes with fly food at one end and seal the end with wax.Individually place awake behaving flies into the tubes using an aspirator and plug the tubes with a foam stopper. Load the tubes into activity monitors to monitor sleep, making sure that the tubes are placed in the correct orientation. The end of the tube of food should be at the top of the SNAP to ensure that flies do not get pushed into the food.Place activity monitors in the recording chamber and monitor sleep for at least two full days to estimate baseline sleep. Save locomotor activity counts of flies in one-minute bins from the time of lights on a given day to lights on the previous day using activity recording software. Estimate sleep from the locomotor activity data with custom macros using five minutes of inactivity as the threshold for a bout of sleep.If sleep is stable over the two baseline days, place activity monitors into the SNAP for overnight sleep deprivation on the third day. Make sure activity monitors are secured in place with monitor holder pins. The monitor cords are plugged in and the monitors oriented correctly.Once the lights go on after overnight sleep deprivation, unplug activity monitors and take them out of the SNAP immediately. Place the flies in a recording chamber where they will be undisturbed for two days to monitor recovery sleep. For each individual fly, calculate the hourly difference between sleep obtained during sleep deprivation and the corresponding hour during baseline, then sum the hourly differences to calculate total sleep lost.Next, calculate the hourly difference between sleep obtained during recovery and the corresponding hour during baseline, then sum the hourly differences to calculate total sleep gained. Calculate the average percentage of sleep recovered over 12, 24, and 48 hours of the recovery period for each genotype. Finally, compute the average and maximum daytime sleep bout length on baseline and recovery days for each genotype.Flies were sleep deprived in the SNAP and recovered sleep during the day. The effectiveness of SNAP in keeping flies awake was demonstrated with the high activity exhibited by flies during sleep deprivation. To quantitatively estimate the effectiveness of sleep deprivation and of recovery, sleep lost during deprivation and then regained in the recovery days was calculated for each individual fly.Importantly, there was no significant change in baseline sleep between the deprivation day and the baseline day, indicating that sleep is stable in these flies. The SNAP effectively deprived flies of over 98%of their nighttime sleep. Flies recovered approximately 20%of their sleep in the first 12 hours and did not recover additional sleep during the night.They began to recover sleep the following day and recovered 36%of their sleep over 48 hours. Sleep homeostasis is characterized by both increased sleep duration and by increased sleep depth during the recovery period. Daytime sleep consolidation is commonly used as a readout of sleep depth.Sleep consolidation can be assessed as the average sleep bout duration over the entire day. However, as sleep pressure is dissipated during recovery, the average sleep bout duration is reduced. Changes in the maximum sleep bout duration can provide a more sensitive metric.This procedure can be easily modified to minimize sleep loss, thus control for non-specific effects of the stimulus. SNAP can be configured to restrict sleep, thus mimicking chronic sleep loss in humans. It can also be used to measure arousal thresholds.Sleep deprivation using the SNAP has yielded important insights into sleep function through studies that examine the negative consequences of sleep loss. By identifying manipulations that interfere with the expression of rebound sleep, sleep deprivation with the SNAP has also helped to elucidate homeostatic mechanisms that regulate sleep.

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3.2K vistas.  Washington University School of Medicine. Sleep homeostasis, the increase in sleep following sleep loss, is a defining characteristic of sleep. Sleep deprivation and sleep restriction are thus powerful tools to study sleep regulation and function. This protocol efficiently sleep deprives and sleep restricts flies while minimizing potential confounds.SNAP deprives flies of greater than 95%of sleep even in flies with high sleep drive. Importantly, agitation of flies with the SNAP does not harm flies and induce a rebound comparab...