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The flower pot method of REM sleep deprivation causes apoptotic cell death in the hepatocytes of rat

https://doi.org/10.1101/375717
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/hep.20437openalex-snapshot
Mitochondrial permeability transition in acetaminophen-induced necrosis and apoptosis of cultured mouse hepatocytes
inferredcites →https://doi.org/10.1002/hep.21062openalex-snapshot
Apoptosis and Necrosis in the Liver: A Tale of Two Deaths?
inferredcites →https://doi.org/10.1002/jnr.21987openalex-snapshot
BCL‐2 and BAX proteins expression throughout the light–dark cycle and modifications induced by sleep deprivation and rebound in adult rat brain
inferredcites →https://doi.org/10.1006/bbrc.1998.0139openalex-snapshot
A Comparative Study of Apoptosis and Necrosis in HepG2 Cells: Oxidant-Induced Caspase Inactivation Leads to Necrosis
inferredcites →https://doi.org/10.1007/978-1-4939-6578-6_11openalex-snapshot
Physiological Changes of Sleep
inferredcites →https://doi.org/10.1007/s00125-015-3669-6openalex-snapshot
Cytokines induce endoplasmic reticulum stress in human, rat and mouse beta cells via different mechanisms
inferredcites →https://doi.org/10.1007/s00415-005-0614-5openalex-snapshot
Parkinsonism with excessive daytime sleepiness
inferredcites →https://doi.org/10.1016/0014-5793(94)01161-3openalex-snapshot
p53 expression in nitric oxide‐induced apoptosis
inferredcites →https://doi.org/10.1016/0031-9384(81)90250-xopenalex-snapshot
Paradoxical sleep deprivation and locomotor activity in rats
inferredcites →https://doi.org/10.1016/0306-9877(93)90121-6openalex-snapshot
Is Alzheimer's disease related to a deficit or malfunction of rapid eye movement (REM) sleep?
inferredcites →https://doi.org/10.1016/0925-4439(95)00104-2openalex-snapshot
Increased p53 mRNA expression in liver and kidney apoptosis
inferredcites →https://doi.org/10.1016/j.bbr.2004.08.004openalex-snapshot
Role of alpha and beta adrenoceptors in locus coeruleus stimulation-induced reduction in rapid eye movement sleep in freely moving rats
inferredcites →https://doi.org/10.1016/j.bbrc.2011.05.123openalex-snapshot
REM sleep deprivation of rats induces acute phase response in liver
inferredcites →https://doi.org/10.1016/j.cub.2011.10.052openalex-snapshot
REM Sleep Depotentiates Amygdala Activity to Previous Emotional Experiences
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2005.10.056openalex-snapshot
JNK signaling pathway is a key modulator in cell death mediated by reactive oxygen and nitrogen species
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.12.011openalex-snapshot
Carbon monoxide blocks oxidative stress-induced hepatocyte apoptosis via inhibition of the p54 JNK isoform
inferredcites →https://doi.org/10.1016/j.jhep.2005.07.034openalex-snapshot
Superoxide anions and hydrogen peroxide induce hepatocyte death by different mechanisms: Involvement of JNK and ERK MAP kinases
inferredcites →https://doi.org/10.1016/j.mehy.2004.01.014openalex-snapshot
Active sleep and its role in the prevention of apoptosis in the developing brain
inferredcites →https://doi.org/10.1016/j.neuron.2012.08.015openalex-snapshot
REM Sleep Reorganizes Hippocampal Excitability
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.06.026openalex-snapshot
Increased apoptosis in rat brain after rapid eye movement sleep loss
inferredcites →https://doi.org/10.1016/j.pnpbp.2009.02.014openalex-snapshot
Distinct effects of acute and chronic sleep loss on DNA damage in rats
inferredcites →https://doi.org/10.1016/j.tox.2005.05.028openalex-snapshot
Soman-induced convulsions: The neuropathology revisited
inferredcites →https://doi.org/10.1016/s0006-8993(02)02448-4openalex-snapshot
Increases in amino-cupric-silver staining of the supraoptic nucleus after sleep deprivation
inferredcites →https://doi.org/10.1016/s0006-8993(99)01768-0openalex-snapshot
No evidence of brain cell degeneration after long-term sleep deprivation in rats1Published on the World Wide Web on 8 July 1999.1
inferredcites →https://doi.org/10.1016/s0016-5085(03)00907-7openalex-snapshot
Hepatocyte apoptosis and fas expression are prominent features of human nonalcoholic steatohepatitis
inferredcites →https://doi.org/10.1016/s0031-9384(96)00363-0openalex-snapshot
Sleep Deprivation by the “Flower Pot” Technique and Spatial Reference Memory
inferredcites →https://doi.org/10.1016/s0168-8278(00)00089-1openalex-snapshot
Hepatocyte apoptosis is a pathologic feature of human alcoholic hepatitis
inferredcites →https://doi.org/10.1023/a:1014472430976openalex-snapshot
Apoptosis and apoptosis related proteins in chronic viral liver disease
inferredcites →https://doi.org/10.1038/20959openalex-snapshot
Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC
inferredcites →https://doi.org/10.1038/cddis.2011.55openalex-snapshot
Role of TRAIL and the pro-apoptotic Bcl-2 homolog Bim in acetaminophen-induced liver damage
inferredcites →https://doi.org/10.1038/nature04285openalex-snapshot
Clues to the functions of mammalian sleep
inferredcites →https://doi.org/10.1038/nn.4479openalex-snapshot
REM sleep selectively prunes and maintains new synapses in development and learning
inferredcites →https://doi.org/10.1053/jhep.2002.32534openalex-snapshot
NF-κB inhibition sensitizes hepatocytes to TNF-induced apoptosis through a sustained activation of JNK and c-Jun
inferredcites →https://doi.org/10.1073/pnas.0909781107openalex-snapshot
Disruption of TAK1 in hepatocytes causes hepatic injury, inflammation, fibrosis, and carcinogenesis
inferredcites →https://doi.org/10.1073/pnas.93.6.2442openalex-snapshot
Nitric oxide-induced p53 accumulation and regulation of inducible nitric oxide synthase expression by wild-type p53.
inferredcites →https://doi.org/10.1074/jbc.271.33.20192openalex-snapshot
Bcl-2 Protects Macrophages from Nitric Oxide-induced Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m407659200openalex-snapshot
Inhibition of Transcription Factor Activity by Nuclear Compartment-associated Bcl-2
inferredcites →https://doi.org/10.1080/00207450212022openalex-snapshot
SLEEP DEPRIVATION DOES NOT AFFECT INDICES OF NECROSIS OR APOPTOSIS IN RAT BRAIN
inferredcites →https://doi.org/10.1080/01926230490260673openalex-snapshot
Immunohistochemical Detection of Activated Caspases in Apoptotic Hepatocytes in Rat Liver
inferredcites →https://doi.org/10.1080/01926230701481956openalex-snapshot
An Immunohistochemical Approach to Differentiate Hepatic Lipidosis from Hepatic Phospholipidosis in Rats
inferredcites →https://doi.org/10.1080/08977194.2017.1314277openalex-snapshot
REM sleep deprivation impairs muscle regeneration in rats
inferredcites →https://doi.org/10.1083/jcb.119.3.493openalex-snapshot
Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation.
inferredcites →https://doi.org/10.1089/152308602760598918openalex-snapshot
Role of Mitochondrial Inner Membrane Permeabilization in Necrotic Cell Death, Apoptosis, and Autophagy
inferredcites →https://doi.org/10.1097/00007890-199904270-00003openalex-snapshot
ENDOTHELIAL CELL AND HEPATOCYTE DEATHS OCCUR BY APOPTOSIS AFTER ISCHEMIA-REPERFUSION INJURY IN THE RAT LIVER1,2
inferredcites →https://doi.org/10.1097/00007890-199907150-00018openalex-snapshot
APOPTOSIS OF SINUSOIDAL ENDOTHELIAL CELLS OCCURS DURING LIVER PRESERVATION INJURY BY A CASPASE-DEPENDENT MECHANISM1
inferredcites →https://doi.org/10.1101/lm.48803openalex-snapshot
Sleep Deprivation Selectively Impairs Memory Consolidation for Contextual Fear Conditioning
inferredcites →https://doi.org/10.1111/j.1365-2362.1992.tb01438.xopenalex-snapshot
Prolonged sleep‐deprivation induced disturbed liver functions serum lipid levels, and hyperphosphatemia
inferredcites →https://doi.org/10.1126/science.275.5303.1132openalex-snapshot
The Release of Cytochrome c from Mitochondria: A Primary Site for Bcl-2 Regulation of Apoptosis
inferredcites →https://doi.org/10.1126/science.aad5252openalex-snapshot
Causal evidence for the role of REM sleep theta rhythm in contextual memory consolidation
inferredcites →https://doi.org/10.1146/annurev.cellbio.15.1.269openalex-snapshot
Biochemical Pathways of Caspase Activation During Apoptosis
inferredcites →https://doi.org/10.1152/ajpgi.2000.278.5.g693openalex-snapshot
Role of caspases and NF-κB signaling in hydrogen peroxide- and superoxide-induced hepatocyte apoptosis
inferredcites →https://doi.org/10.1152/physrev.00061.2009openalex-snapshot
Hepatocyte Death: A Clear and Present Danger
inferredcites →https://doi.org/10.1242/jcs.03293openalex-snapshot
Outcomes of p53 activation - spoilt for choice
inferredcites →https://doi.org/10.1371/journal.pbio.0060216openalex-snapshot
Is Sleep Essential?
inferredcites →https://doi.org/10.1371/journal.pone.0047042openalex-snapshot
Sleep Deprivation Impairs Consolidation of Cued Fear Memory in Rats
inferredcites →https://doi.org/10.1523/jneurosci.18-04-01363.1998openalex-snapshot
Bax Involvement in p53-Mediated Neuronal Cell Death
inferredcites →https://doi.org/10.18203/issn.2454-2156.intjscirep20182728openalex-snapshot
Effect of sleep deprivation on the liver, kidney and heart: histological and immunohistochemical study
inferredcites →https://doi.org/10.2174/15672026113109990002openalex-snapshot
REM Sleep Loss and Recovery Regulates Blood-Brain Barrier Function
inferredcites →https://doi.org/10.2307/1421644openalex-snapshot
Depriving Rats of REM Sleep: The Identification of a Methodological Problem
inferredcites →https://doi.org/10.23736/s0022-4707.16.06159-4openalex-snapshot
One night of partial sleep deprivation increased biomarkers of muscle and cardiac injuries during acute intermittent exercise
inferredcites →https://doi.org/10.3389/fneur.2016.00025openalex-snapshot
Rapid Eye Movement Sleep Deprivation Induces Neuronal Apoptosis by Noradrenaline Acting on Alpha1 Adrenoceptor and by Triggering Mitochondrial Intrinsic Pathway
inferredcites →https://doi.org/10.3785/j.issn.1008-9292.2006.05.013openalex-snapshot
[Cannabinoid receptor 1 expression and pathological changes in rat hippocampus after deprivation of rapid eye movement sleep].
inferredcites →https://doi.org/10.5665/sleep.4244openalex-snapshot
Cell Injury and Repair Resulting from Sleep Loss and Sleep Recovery in Laboratory Rats
inferredcites →https://doi.org/10.5935/1984-0063.20180039openalex-snapshot
Rapid Eye Movement sleep deprivation of rat generates ROS in the hepatocytes and makes them more susceptible to oxidative stress

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/978-3-031-74744-1_4openalex-snapshot
Sleep and Circadian Rhythm in Peripheral Inflammation: Realm of Interconnected Frontiers
inferred← citeshttps://doi.org/10.1101/515379openalex-snapshot
Differential gene expression in brain and liver tissue of Wistar rats after rapid eye movement sleep deprivation
inferred← citeshttps://doi.org/10.3390/clockssleep2040033openalex-snapshot
Differential Gene Expression in Brain and Liver Tissue of Wistar Rats after Rapid Eye Movement Sleep Deprivation
inferred← citeshttps://doi.org/10.5935/1984-0063.20180039openalex-snapshot
Rapid Eye Movement sleep deprivation of rat generates ROS in the hepatocytes and makes them more susceptible to oxidative stress
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