Chinese Medical Sciences Journal ›› 2023, Vol. 38 ›› Issue (1): 29-37.doi: 10.24920/004087
• Original Article • Previous Articles Next Articles
Kaveh Shahveisi1, Seyedeh Marziyeh Hadi2, Hamed Ghazvini3, 4, Mehdi Khodamoradi5, *()
Received:
2022-03-21
Accepted:
2022-09-06
Published:
2023-03-31
Online:
2023-02-28
Contact:
Mehdi Khodamoradi
E-mail:mehdi0khodamoradi@gmail.com
Kaveh Shahveisi, Seyedeh Marziyeh Hadi, Hamed Ghazvini, Mehdi Khodamoradi. Role of Cannabinoid CB1 Receptor in Object Recognition Memory Impairment in Chronically Rapid Eye Movement Sleep-deprived Rats[J].Chinese Medical Sciences Journal, 2023, 38(1): 29-37.
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Figure 1.
Timeline of the experimental protocols used in the present study. (A) Rimonabant was administered either at one hour prior to the sample phase for learning/acquisition, or immediately after the sample phase for consolidation, or at one hour before the test phase for retrieval of object recognition memory. (B) For the reconsolidation task, rimonabant was administered immediately after the second sample phase to examine reconsolidation of object recognition memory. A1-A5 represent familiar objects and B is a novel object. RSD: rapid eye movement sleep deprivation."
Table 1.
Time spent during the sample and test phases and also time spent exploring the familiar and novel objects during the test phase in the acquisition experiment"
Groups | Time spent exploring objects during the sample phase (s) | Time spent exploring both objects during the test phase (s) | Time spent exploring familiar object during the test phase (s) | Time spent exploring novel object during the test phase (s) |
---|---|---|---|---|
WP | 27.54 ± 2.64 | 21.52 ± 3.03 | 10.64 ± 1.33 | 32.40 ± 3.38*** |
RSD | 24.80 ± 2.50 | 19.41 ± 2.16 | 18.19 ± 3.07 | 20.63 ± 2.99 |
RSD-Veh | 23.45 ± 2.52 | 17.96 ± 2.21 | 17.08 ± 3.53 | 18.85 ± 2.62 |
RSD-R 1 mg/kg | 24.27 ± 2.49 | 19.18 ± 2.14 | 18.69 ± 2.99 | 19.67 ± 3.06 |
RSD-R 3 mg/kg | 23.18 ± 2.56 | 20.23 ± 2.21 | 17.60 ± 1.88 | 22.85 ± 3.83 |
Table 2.
Time spent during the sample and test phases and also time spent exploring the familiar and novel objects during the test phase in the consolidation experiment"
Groups | Time spent exploring objects during the sample phase (s) | Time spent exploring both objects during the test phase (s) | Time spent exploring familiar object during the test phase (s) | Time spent exploring novel object during the test phase (s) |
---|---|---|---|---|
WP | 26.98 ± 2.36 | 21.34 ± 3.05 | 10.27 ± 1.85 | 32.40 ± 3.07*** |
RSD | 23.26 ± 2.38 | 20.32 ± 2.02 | 16.78 ± 1.74 | 23.86 ± 3.25 |
RSD-Veh | 25.21 ± 2.72 | 18.49 ± 2.26 | 15.96 ± 2.50 | 21.02 ± 3.58 |
RSD-R 1 mg/kg | 24.01 ± 2.22 | 20.61 ± 2.02 | 16.94 ± 1.80 | 24.27 ± 3.23 |
RSD-R 3 mg/kg | 24.61 ± 2.43 | 19.40 ± 1.87 | 16.25 ± 1.69 | 22.54 ± 3.04* |
Table 3.
Time spent during the sample and test phases and also time spent exploring the familiar and novel objects during the test phase in the retrieval experiment"
Groups | Time spent exploring objects during the sample phase (s) | Time spent exploring both objects during the test phase (s) | Time spent exploring familiar object during the test phase (s) | Time spent exploring novel object during the test phase (s) |
---|---|---|---|---|
WP | 28.37 ± 2.58 | 22.77 ± 3.58 | 10.97 ± 1.77 | 34.56 ± 3.67** |
RSD | 24.12 ± 2.91 | 18.58 ± 2.01 | 15.98 ± 1.72 | 21.17 ± 3.42 |
RSD-Veh | 24.41 ± 2.52 | 19.33 ± 1.92 | 17.10 ± 2.00 | 21.57 ± 3.12 |
RSD-R 1 mg/kg | 23.05 ± 2.70 | 20.28 ± 2.17 | 15.96 ± 1.90 | 24.61 ± 3.39* |
RSD-R 3 mg/kg | 22.91 ± 2.32 | 20.57 ± 2.20 | 16.07 ± 2.07 | 25.07 ± 3.32** |
Table 4.
Time spent during the sample and test phases and also time spent exploring the familiar and novel objects during the test phase in the reconsolidation experiment"
Groups | Time spent exploring objects during the 1st sample phase (s) | Time spent exploring objects during the 2nd sample phase (s) | Time spent exploring both objects during the test phase (s) | Time spent exploring familiar object during the test phase (s) | Time spent exploring novel object during the test phase (s) |
---|---|---|---|---|---|
WP | 26.61 ± 2.72 | 22.94 ± 2.41 | 24.34 ± 3.24 | 12.23 ± 1.93 | 36.45 ± 2.99 |
RSD | 24.99 ± 2.23 | 23.38 ± 2.31 | 22.36 ± 2.78 | 15.61 ± 2.60 | 29.11 ± 3.75 |
RSD-Veh | 24.86 ± 2.69 | 23.22 ± 2.18 | 22.18 ± 2.47 | 16.91 ± 2.68 | 27.44 ± 3.33 |
RSD-R 1 mg/kg | 25.05 ± 2.37 | 23.67 ± 2.38 | 23.51 ± 2.77 | 17.88 ± 2.38 | 29.14 ± 4.33 |
RSD-R 3 mg/kg | 25.44 ± 2.37 | 22.65 ± 1.90 | 23.82 ± 2.79 | 17.88 ± 3.18 | 29.76 ± 3.74 |
[1] |
Antony JW, Schonauer M, Staresina BP, et al. Sleep spindles and memory reprocessing. Trends Neurosci 2019; 42(1): 1-3. doi: 10.1016/j.tins.2018.09.012.
doi: S0166-2236(18)30258-3 pmid: 30340875 |
[2] |
Chambers AM. The role of sleep in cognitive processing: focusing on memory consolidation. Wiley Interdiscip Rev Cogn Sci 2017; 8(3). doi: 10.1002/wcs.1433.
doi: 10.1002/wcs.1433 |
[3] |
Dahl RE. Sleep and the developing brain. Sleep 2007; 30(9): 1079-80. doi: 10.1093/sleep/30.9.1079.
doi: 10.1093/sleep/30.9.1079 pmid: 17910377 |
[4] |
Peterson MJ, Benca RM. Sleep in mood disorders. Psychiatr Clin North Am 2006; 29(4): 1009-32. doi: 10.1016/j.psc.2006.09.003.
doi: 10.1016/j.psc.2006.09.003 |
[5] |
Walker MP. The role of sleep in cognition and emotion. Ann N Y Acad Sci 2009; 1156: 168-97. doi: 10.1111/j.1749-6632.2009.04416.x.
doi: 10.1111/j.1749-6632.2009.04416.x |
[6] |
Bendor D, Wilson MA. Biasing the content of hippocampal replay during sleep. Nat Neurosci 2012; 15(10): 1439-44. doi: 10.1038/nn.3203.
doi: 10.1038/nn.3203 pmid: 22941111 |
[7] |
Sara SJ. Retrieval and reconsolidation: toward a neurobiology of remembering. Learn Mem 2000; 7(2): 73-84. doi: 10.1101/lm.7.2.73.
doi: 10.1101/lm.7.2.73 |
[8] |
Stickgold R, Walker MP. Memory consolidation and reconsolidation: what is the role of sleep? Trends Neurosci 2005; 28(8): 408-15. doi: 10.1016/j.tins.2005.06.004.
doi: 10.1016/j.tins.2005.06.004 pmid: 15979164 |
[9] |
Buzsaki G. Memory consolidation during sleep: a neurophysiological perspective. J Sleep Res 1998; 7 Suppl 1: 17-23. doi: 10.1046/j.1365-2869.7.s1.3.x.
doi: 10.1046/j.1365-2869.7.s1.3.x |
[10] |
Winters BD, Huang YH, Dong Y, et al. Sleep loss alters synaptic and intrinsic neuronal properties in mouse prefrontal cortex. Brain Res 2011; 1420: 1-7. doi: 10.1016/j.brainres.2011.08.078.
doi: 10.1016/j.brainres.2011.08.078 pmid: 21962531 |
[11] |
Babson KA, Sottile J, Morabito D. Cannabis, cannabinoids, and sleep: a review of the literature. Curr Psychiatry Rep 2017; 19(4): 23. doi: 10.1007/s11920-017-0775-9.
doi: 10.1007/s11920-017-0775-9 |
[12] |
Hampson RE, Deadwyler SA. Role of cannabinoid receptors in memory storage. Neurobiol Dis 1998; 5(6 Pt B): 474-82. doi: 10.1006/nbdi.1998.0223.
doi: 10.1006/nbdi.1998.0223 pmid: 9974179 |
[13] |
Murillo-Rodriguez E. The role of the CB1 receptor in the regulation of sleep. Prog Neuropsychopharmacol Biol Psychiatry 2008; 32(6): 1420-27. doi: 10.1016/j.pnpbp.2008.04.008.
doi: 10.1016/j.pnpbp.2008.04.008 |
[14] |
Murillo-Rodriguez E. The modulatory role of endocannabinoids in sleep. Rev Neurol 2008; 46(3): 160-6. doi: 10.33588/rn.4603.2006616.
doi: 10.33588/rn.4603.2006616 pmid: 18297624 |
[15] |
De Vries TJ, Schoffelmeer AN. Cannabinoid CB1 receptors control conditioned drug seeking. Trends Pharmacol Sci 2005; 26(8): 420-6. doi: 10.1016/j.tips.2005.06.002.
doi: 10.1016/j.tips.2005.06.002 pmid: 15992935 |
[16] |
Pertwee RG. Pharmacology of cannabinoid CB1 and CB2 receptors. Pharmacol Ther 1997; 74(2): 129-80. doi: 10.1016/S0163-7258(97)82001-3.
doi: 10.1016/S0163-7258(97)82001-3 |
[17] |
Chen L, Tian S, Ke J. Rapid eye movement sleep deprivation disrupts consolidation but not reconsolidation of novel object recognition memory in rats. Neurosci Lett 2014; 563: 12-16. doi: 10.1016/j.neulet.2014.01.024.
doi: 10.1016/j.neulet.2014.01.024 pmid: 24472565 |
[18] |
Shahveisi K, Farnia V, Khazaie H, et al. Novel object recognition memory in REM sleep-deprived rats: Role of the cannabinoid CB1 receptor. Behav Brain Res 2020; 381: 112311. doi: 10.1016/j.bbr.2019.112311.
doi: 10.1016/j.bbr.2019.112311 pmid: 31711896 |
[19] |
Akirav I, Maroun M. Ventromedial prefrontal cortex is obligatory for consolidation and reconsolidation of object recognition memory. Cereb Cortex 2006; 16(12): 1759-65. doi: 10.1093/cercor/bhj114.
doi: 10.1093/cercor/bhj114 |
[20] |
Barker GR, Bird F, Alexander V, et al. Recognition memory for objects, place, and temporal order: a disconnection analysis of the role of the medial prefrontal cortex and perirhinal cortex. J Neurosci 2007; 27(11): 2948-57. doi: 10.1523/JNEUROSCI.5289-06.2007.
doi: 10.1523/JNEUROSCI.5289-06.2007 pmid: 17360918 |
[21] |
Ennaceur A, Delacour J. A new one-trial test for neurobiological studies of memory in rats. 1: Behavioral data. Behav Brain Res 1988; 31(1): 47-59. doi: 10.1016/0166-4328(88)90157-x.
doi: 10.1016/0166-4328(88)90157-x pmid: 3228475 |
[22] |
Palchykova S, Winsky-Sommerer R, Meerlo P, et al. Sleep deprivation impairs object recognition in mice. Neurobiol Learn Mem 2006; 85(3): 263-71. doi: 10.1016/j.nlm.2005.11.005.
doi: 10.1016/j.nlm.2005.11.005 pmid: 16423541 |
[23] |
Salari M, Sheibani V, Saadati H, et al. The compensatory effect of regular exercise on long-term memory impairment in sleep deprived female rats. Behav Processes 2015; 119: 50-7. doi: 10.1016/j.beproc.2015.06.014.
doi: 10.1016/j.beproc.2015.06.014 |
[24] |
Shahveisi K, Abdoli N, Farnia V, et al. REM sleep deprivation before extinction or reinstatement alters methamphetamine reward memory via D1-like dopamine receptors. Pharmacol Biochem Behav 2022; 213: 173319. doi: 10.1016/j.pbb.2021.173319.
doi: 10.1016/j.pbb.2021.173319 |
[25] |
Shahveisi K, Abdoli N, Khazaie H, et al. Maternal sleep deprivation affects extinction and reinstatement of methamphetamine reward memory in male offspring: Role of the D1-like and D2-like dopamine receptors. Brain Res 2022; 1792: 148033. doi: 10.1016/j.brainres.2022.148033.
doi: 10.1016/j.brainres.2022.148033 |
[26] |
Shahveisi K, Khazaie H, Farnia V, et al. REM sleep deprivation impairs retrieval, but not reconsolidation, of methamphetamine reward memory in male rats. Pharmacol Biochem Behav 2019: 172759. doi: 10.1016/j.pbb.2019.172759.
doi: 10.1016/j.pbb.2019.172759 |
[27] |
Novati A, Roman V, Cetin T, et al. Chronically restricted sleep leads to depression-like changes in neurotransmitter receptor sensitivity and neuroendocrine stress reactivity in rats. Sleep 2008; 31(11): 1579-85. doi: 10.1093/sleep/31.11.1579.
doi: 10.1093/sleep/31.11.1579 pmid: 19014078 |
[28] |
Khodamoradi M, Tirgar F, Ghazvini H, et al. Role of the cannabinoid CB1 receptor in methamphetamine-induced social and recognition memory impairment. Neurosci Lett 2022; 779: 136634. doi: 10.1016/j.neulet.2022.136634.
doi: 10.1016/j.neulet.2022.136634 |
[29] |
Riedel G, Micheau J, Lam AG, et al. Reversible neural inactivation reveals hippocampal participation in several memory processes. Nat Neurosci 1999; 2(10): 898-905. doi: 10.1038/13202.
doi: 10.1038/13202 pmid: 10491611 |
[30] |
Steele RJ, Morris RG. Delay-dependent impairment of a matching-to-place task with chronic and intrahippocampal infusion of the NMDA-antagonist D-AP5. Hippocampus 1999; 9(2): 118-36. doi: 10.1002/(SICI)1098-1063(1999)9:2<118::AID-HIPO4>3.0.CO;2-8.
doi: 10.1002/(SICI)1098-1063(1999)9:2<118::AID-HIPO4>3.0.CO;2-8 pmid: 10226773 |
[31] |
Moser MB, Moser EI. Distributed encoding and retrieval of spatial memory in the hippocampus. J Neurosci 1998; 18(18): 7535-42. doi: 10.1523/JNEUROSCI.18-18-07535.1998.
doi: 10.1523/JNEUROSCI.18-18-07535.1998 pmid: 9736671 |
[32] |
Zhang J, Zhang L, Chang Y, et al. The endocannabinoid system contributes to memory deficits induced by rapid-eye-movement sleep deprivation in adolescent mice. Neuroscience 2020; 433: 174-83. doi: 10.1016/j.neuroscience.2020.03.016.
doi: S0306-4522(20)30166-4 pmid: 32198011 |
[33] |
McCoy JG, Christie MA, Kim Y, et al. Chronic sleep restriction impairs spatial memory in rats. Neuroreport 2013; 24(2): 91-5. doi: 10.1097/WNR.0b013e32835cd97a.
doi: 10.1097/WNR.0b013e32835cd97a pmid: 23238166 |
[34] |
Andersen ML, Ribeiro DA, Bergamaschi CT, et al. Distinct effects of acute and chronic sleep loss on DNA damage in rats. Prog Neuropsychopharmacol Biol Psychiatry 2009; 33(3): 562-7. doi: 10.1016/j.pnpbp.2009.02.014.
doi: 10.1016/j.pnpbp.2009.02.014 |
[35] |
Reibaud M, Obinu MC, Ledent C, et al. Enhancement of memory in cannabinoid CB1 receptor knock-out mice. Eur J Pharmacol 1999; 379(1): R1-2. doi: 10.1016/S0014-2999(99)00496-3.
doi: 10.1016/s0014-2999(99)00496-3 pmid: 10499380 |
[36] |
Ishikawa A, Kanayama Y, Matsumura H, et al. Selective rapid eye movement sleep deprivation impairs the maintenance of long-term potentiation in the rat hippocampus. Eur J Neurosci 2006; 24(1): 243-8. doi: 10.1111/j.1460-9568.2006.04874.x.
doi: 10.1111/j.1460-9568.2006.04874.x pmid: 16882020 |
[37] |
Bliss TV, Collingridge GL. A synaptic model of memory: long-term potentiation in the hippocampus. Nature 1993; 361(6407): 31-9. doi: 10.1038/361031a0.
doi: 10.1038/361031a0 |
[38] |
Misner DL, Sullivan JM. Mechanism of cannabinoid effects on long-term potentiation and depression in hippocampal CA1 neurons. J Neurosci 1999; 19(16): 6795-805. doi: 10.1523/JNEUROSCI.19-16-06795.1999.
doi: 10.1523/JNEUROSCI.19-16-06795.1999 pmid: 10436037 |
[39] |
Paton GS, Pertwee RG, Davies SN. Correlation between cannabinoid mediated effects on paired pulse depression and induction of long term potentiation in the rat hippocampal slice. Neuropharmacology 1998; 37(9): 1123-30. doi: 10.1016/S0028-3908(98)00096-3.
doi: 10.1016/s0028-3908(98)00096-3 pmid: 9833642 |
[40] |
Bohme GA, Laville M, Ledent C, et al. Enhanced long-term potentiation in mice lacking cannabinoid CB1 receptors. Neuroscience 2000; 95(1): 5-7. doi: 10.1016/S0306-4522(99)00483-2.
doi: 10.1016/S0306-4522(99)00483-2 pmid: 10619457 |
[41] |
de Oliveira Alvares L, Do-Monte FH. Understanding the dynamic and destiny of memories. Neurosci Biobehav Rev 2021; 125: 592-607. doi: 10.1016/j.neubiorev.2021.03.009.
doi: 10.1016/j.neubiorev.2021.03.009 pmid: 33722616 |
[42] |
Iordanova MD, Good M, Honey RC. Retrieval-mediated learning involving episodes requires synaptic plasticity in the hippocampus. J Neurosci 2011; 31(19): 7156-62. doi: 10.1523/JNEUROSCI.0295-11.2011.
doi: 10.1523/JNEUROSCI.0295-11.2011 pmid: 21562278 |
[43] |
Nader K, Einarsson EO. Memory reconsolidation: an update. Ann N Y Acad Sci 2010; 1191: 27-41. doi: 10.1111/j.1749-6632.2010.05443.x.
doi: 10.1111/j.1749-6632.2010.05443.x |
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