Neuropathic Pain Causes Memory Deficits and Dendrite Tree Morphology Changes in Mouse Hippocampus

References

• Abdallah CG, Geha P. Chronic pain and chronic stress: two sides of the same coin? Chronic Stress. 2017;1:2470547017704763. doi:10.1177/2470547017704763
   Google Scholar
• Alfarez DN, Joëls M, Krugers HJ. Chronic unpredictable stress impairs long‐term potentiation in rat hippocampal CA1 area and dentate gyrus in vitro. Eur J Neurosci. 2003;17(9):1928–1934. doi:10.1046/j.1460-9568.2003.02622.x
   Web of Science ®Google Scholar
• Allen JW, Yaksh TL. Assessment of acute thermal nociception in laboratory animals. In: Luo DZ, editor. Pain Research: methods and protocols. Humana Press; 2004:11–23. doi:10.1385/1-59259-770-X:011
   Google Scholar
• Barylko B, Wilkerson JR, Cavalier SH, et al. Palmitoylation and membrane binding of Arc/Arg3. 1: a potential role in synaptic depression. Biochemistry. 2017;57(5):520–524. doi:10.1021/acs.biochem.7b00959
   Web of Science ®Google Scholar
• Bastian TW, Duck KA, Michalopoulos GC, et al. Eltrombopag, a thrombopoietin mimetic, crosses the blood–brain barrier and impairs iron‐dependent hippocampal neuron dendrite development. J Thromb. 2017;15(3):565–574. doi:10.1111/jth.13602
   PubMed Web of Science ®Google Scholar
• Bennett GJ, Xie YK. A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man. Pain. 1988;33(1):87–107. doi:10.1016/0304-3959(88)90209-6
   PubMed Web of Science ®Google Scholar
• Bourne J, Harris KM. Do thin spines learn to be mushroom spines that remember? Curr Opin Neurobiol. 2007;17(3):381–387. doi:10.1016/j.conb.2007.04.009
   PubMed Web of Science ®Google Scholar
• Cardoso-Cruz H, Paiva P, Monteiro C, Galhardo V. Selective optogenetic inhibition of medial prefrontal glutamatergic neurons reverses working memory deficits induced by neuropathic pain. Pain. 2019;160(4):805–823. doi:10.1097/j.pain.0000000000001457
   Web of Science ®Google Scholar
• Célérier E, González JR, Maldonado R, Cabañero D, Puig MM. Opioid-induced hyperalgesia in a murine model of postoperative painrole of nitric oxide generated from the inducible nitric oxide synthase. Anesthesiology. 2006;104(3):546–555. doi:10.1097/00000542-200603000-00023
   PubMed Web of Science ®Google Scholar
• Chater TE, Goda Y. The role of AMPA receptors in postsynaptic mechanisms of synaptic plasticity. Front Cell Neurosci. 2014;8:401. doi:10.3389/fncel.2014.00401
   PubMed Web of Science ®Google Scholar
• Chowdhury S, Shepherd JD, Okuno H, et al. Arc/Arg3. 1 interacts with the endocytic machinery to regulate AMPA receptor trafficking. Neuron. 2006;52(3):445–459. doi:10.1016/j.neuron.2006.08.033
   PubMed Web of Science ®Google Scholar
• Kodama D, Ono H, Tanabe M. Increased hippocampal glycine uptake and cognitive dysfunction after peripheral nerve injury. Pain. 2011;152(4):809–817. doi:10.1016/j.pain.2010.12.029
   Web of Science ®Google Scholar
• Dees RL, Kesner RP. The role of the dorsal dentate gyrus in object and object-context recognition. Neurobiol Learn Mem. 2013;106:112–119. doi:10.1016/j.nlm.2013.07.013
   Web of Science ®Google Scholar
• Dick BD, Rashiq S. Disruption of attention and working memory traces in individuals with chronic pain. Anesth Analg. 2007;104(5):1223–1229. doi:10.1213/01.ane.0000263280.49786.f5
   PubMed Web of Science ®Google Scholar
• Dioli C, Patrício P, Sousa N, et al. Chronic stress triggers divergent dendritic alterations in immature neurons of the adult hippocampus, depending on their ultimate terminal fields. Transl Psychiatry. 2019;9(1):143. doi:10.1038/s41398-019-0477-7
   Web of Science ®Google Scholar
• Finnerup NB, Søren HS, Troels SJ. Chronic neuropathic pain: mechanisms, drug targets and measurement. Fundam Clin Pharmacol. 2007;21:129–136. doi:10.1111/j.1472-8206.2007.00474.x
   PubMed Web of Science ®Google Scholar
• Fishbain DA, Cutler R, Rosomoff HL, Rosomoff RS. Chronic pain-associated depression: antecedent or consequence of chronic pain? A review. Clin J Pain. 1997;13:116–137. doi:10.1097/00002508-199706000-00006
   PubMed Web of Science ®Google Scholar
• Ge S, Goh EL, Sailor KA, Kitabatake Y, Ming GL, Song H. GABA regulates synaptic integration of newly generated neurons in the adult brain. Nature. 2006;439(7076):589–593. doi:10.1038/nature04404
   PubMed Web of Science ®Google Scholar
• Holtmaat A, Wilbrecht L, Knott GW, Welker E, Svoboda K. Experience-dependent and cell-type-specific spine growth in the neocortex. Nature. 2006;441(7096):979. doi:10.1038/nature04783
   PubMed Web of Science ®Google Scholar
• Hu Y, Liao HB, Dai-Hong G, et al. Antidepressant-like effects of 3, 6′-disinapoyl sucrose on hippocampal neuronal plasticity and neurotrophic signal pathway in chronically mild stressed rats. Neurochem Int. 2010;56(3):461–465. doi:10.1016/j.neuint.2009.12.004
   PubMed Web of Science ®Google Scholar
• Ishiyama T, Tokuda K, Ishibashi T, et al. Lurasidone (SM-13496), a novel atypical antipsychotic drug, reverses MK-801-induced impairment of learning and memory in the rat passive-avoidance test. Eur J Pharmacol. 2007;572(2–3):160–170. doi:10.1016/j.ejphar.2007.06.058
   PubMed Web of Science ®Google Scholar
• Kallarackal AJ, Kvarta MD, Cammarata E, et al. (2013) Chronic stress induces a selective decrease in AMPA receptor-mediated synaptic excitation at hippocampal temporoammonic-CA1 synapses J. Neurosci. 2007;33(40):15669–15674. doi:10.1523/JNEUROSCI.2588-13.2013
   Web of Science ®Google Scholar
• Kitamura T, Macdonald CJ, Tonegawa S. Entorhinal–hippocampal neuronal circuits bridge temporally discontiguous events. Learn Mem. 2015;22(9):438–443. doi:10.1101/lm.038687.115
   PubMed Web of Science ®Google Scholar
• Kodama D, Ono H, Tanabe M. Altered hippocampal long-term potentiation after peripheral nerve injury in mice. Eur J Pharmacol. 2007;574(2–3):127–132. doi:10.1016/j.ejphar.2007.07.054
   Web of Science ®Google Scholar
• Ling B, Coudoré-Civiale MA, Balayssac D, Eschalier A, Coudoré F, Authier N. Behavioral and immunohistological assessment of painful neuropathy induced by a single oxaliplatin injection in the rat. Toxicol. 2007;234(3):176–184. doi:10.1016/j.tox.2007.02.013
   PubMed Web of Science ®Google Scholar
• Liu MG, Chen J. Roles of the hippocampal formation in pain information processing. Neurosci Bull. 2009;25(5):237. doi:10.1007/s12264-009-0905-4
   Web of Science ®Google Scholar
• McLaughlin KJ, Wilson JO, Harman J, et al. Chronic 17β‐estradiol or cholesterol prevents stress‐induced hippocampal CA3 dendritic retraction in ovariectomized female rats: possible correspondence between CA1 spine properties and spatial acquisition. Hippocampus. 2010;20(6):768–786. doi:10.1002/hipo.20678
   Web of Science ®Google Scholar
• Morris AM, Weeden CS, Churchwell JC, Kesner RP. The role of the dentate gyrus in the formation of contextual representations. Hippocampus. 2013;23(2):162–168. doi:10.1002/hipo.22078
   Web of Science ®Google Scholar
• Mutso AA, Radzicki D, Baliki MN, et al. Abnormalities in hippocampal functioning with persistent pain. J Neurosci. 2012;32(17):5747–5756. doi:10.1523/JNEUROSCI.0587-12.2012
   PubMed Web of Science ®Google Scholar
• Narita M, Kaneko C, Miyoshi K, et al. Chronic pain induces anxiety with concomitant changes in opioidergic function in the amygdala. Neuropsychopharmacol. 2006;31:739–750. doi:10.1038/sj.npp.1300858
   PubMed Web of Science ®Google Scholar
• Obata K, Yamanaka H, Dai Y, et al. Differential activation of extracellular signal-regulated protein kinase in primary afferent neurons regulates brain-derived neurotrophic factor expression after peripheral inflammation and nerve injury. J Neurosci. 2003;23(10):4117–4126. doi:10.1523/JNEUROSCI.23-10-04117.2003
   PubMed Web of Science ®Google Scholar
• Peebles CL, Yoo J, Thwin MT, et al. Arc regulates spine morphology and maintains network stability in vivo. PNAS Proc Natl Acad Sci. 2010;107(42):18173–18178. doi:10.1073/pnas.1006546107
   Web of Science ®Google Scholar
• Radwanska K, Medvedev NI, Pereira GS, et al. Mechanism for long-term memory formation when synaptic strengthening is impaired. PNAS Proc Natl Acad Sci. 2011;108(45):18471–18475. doi:10.1073/pnas.1109680108
   Web of Science ®Google Scholar
• Ren WJ, Liu Y, Zhou LJ, et al. Peripheral nerve injury leads to working memory deficits and dysfunction of the hippocampus by upregulation of TNF-α in rodents. Neuropsychopharmacol. 2011;36(5):979–992. doi:10.1038/npp.2010.236
   Web of Science ®Google Scholar
• Romero-Grimaldi C, Berrocoso E, Alba-Delgado C, et al. Stress increases the negative effects of chronic pain on hippocampal neurogenesis. Anesth Analg. 2015;121(4):1078–1088. doi:10.1213/ANE.0000000000000838
   Web of Science ®Google Scholar
• Saffarpour S, Shaabani M, Naghdi N, Farahmandfar M, Janzadeh A, Nasirinezhad F. In vivo evaluation of the hippocampal glutamate, GABA and the BDNF levels associated with spatial memory performance in a rodent model of neuropathic pain. Physiol Behav. 2017;175:97–103. doi:10.1016/j.physbeh.2017.03.025
   PubMed Web of Science ®Google Scholar
• Schmidt MV, Scharf SH, Liebl C, et al. A novel chronic social stress paradigm in female mice. Horm Behav. 2010;57(4–5):415–420. doi:10.1016/j.yhbeh.2010.01.010
   PubMed Web of Science ®Google Scholar
• Sholl DA. Dendritic organization in the neurons of the visual and motor cortices of the cat. J Anat. 1953;87(Pt 4):387–406.
   PubMed Web of Science ®Google Scholar
• Sousa N, Lukoyanov NV, Madeira MD, Almeida OF, Paula-Barbosa MM. Reorganization of the morphology of hippocampal neurites and synapses after stress-induced damage correlates with behavioral improvement. Neuroscience. 2000;97(2):253–266. doi:10.1016/s0306-4522(00)00050-6
   PubMed Web of Science ®Google Scholar
• Stone DJ, Walsh JP, Sebro R, Stevens R, Pantazopolous H, Benes FM. Effects of pre‐and postnatal corticosterone exposure on the rat hippocampal GABA system. Hippocampus. 2001;11(5):492–507. doi:10.1002/hipo.1066
   Web of Science ®Google Scholar
• Suh J, Rivest AJ, Nakashiba T, Tominaga T, Tonegawa S. Entorhinal cortex layer III input to the hippocampus is crucial for temporal association memory. Science. 2011;334(6061):1415–1420. doi:10.1126/science.1210125
   Web of Science ®Google Scholar
• Kaizuka T, Takumi T. Postsynaptic density proteins and their involvement in neurodevelopmental disorders. J Biochem. 2018;163(6):447–455. doi:10.1093/jb/mvy022
   PubMed Web of Science ®Google Scholar
• Tyrtyshnaia AA, Manzhulo IV, Sultanov RM, Ermolenko EV. Adult hippocampal neurogenesis in neuropathic pain and alkyl glycerol ethers treatment. Acta Histochem. 2017;119:812–821. doi:10.1016/j.acthis.2017.10.007
   Web of Science ®Google Scholar
• Verde EM, Lee-Osbourne J, Worley PF, Malinow R, Cline HT. Increased expression of the immediate-early gene arc/arg3. 1 reduces AMPA receptor-mediated synaptic transmission. Neuron. 2006;52(3):461–474. doi:10.1016/j.neuron.2006.09.031
   Web of Science ®Google Scholar
• Waung MW, Pfeiffer BE, Nosyreva ED, Ronesi JA, Huber KM. Rapid translation of Arc/Arg3. 1 selectively mediates mGluR-dependent LTD through persistent increases in AMPAR endocytosis rate. Neuron. 2008;59(1):84–97. doi:10.1016/j.neuron.2008.05.014
   PubMed Web of Science ®Google Scholar