Loose ligation of the rat sciatic nerve elicits early accumulation of Shank1 protein in the post-synaptic density of spinal dorsal horn neurons

Pain

Volumn 149, Issue 1, 2010, Pages 152-159

  Miletic, Gordana ^a   Dumitrascu, Catalina I ^a   Honstad, Christopher E ^a   Micic, Daniela ^a   Miletic, Vjekoslav ^a  

^a UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

Chronic constriction injury; Glutamate receptors; Neuropathic pain; Nociception; Structural proteins; Synaptic plasticity

Indexed keywords

1,4 DIAMINO 1,4 BIS(2 AMINOPHENYLTHIO) 2,3 DICYANOBUTADIENE; ANISOMYCIN; DIZOCILPINE; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR 2B; POSTSYNAPTIC DENSITY PROTEIN 95; PROTEIN SH3; PROTEIN SHANK 1; SMALL INTERFERING RNA; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BEHAVIOR; CONTROLLED STUDY; CROSS LINKING; HYPERALGESIA; MALE; NERVE CELL PLASTICITY; NERVE LIGATION; NEUROPATHIC PAIN; NOCICEPTION; NONHUMAN; POSTSYNAPTIC MEMBRANE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BLOOD LEVEL; PROTEIN FUNCTION; RAT; SCIATIC NERVE; SHAM PROCEDURE; SPINAL CORD DORSAL HORN; THERMAL STIMULATION;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANIMALS; HYPERALGESIA; LIGATION; MALE; POSTERIOR HORN CELLS; RATS; RATS, SPRAGUE-DAWLEY; SCIATIC NEUROPATHY; SYNAPTIC POTENTIALS;

EID: 77349102941     PISSN: 03043959     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pain.2010.02.001     Document Type: Article

References (24)

1. Bennett G.J., and Xie Y.K. A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man. Pain 33 (1988) 87-107
2. Boeckers T.M., Kreutz M.R., Winter C., Zuschratter W., Smalla K.H., Sanmarti-Vila L., Wex H., Langnaese K., Bockmann J., Garner C.C., and Gundelfinger E.D. Proline-rich synapse-associated protein-1/cortactin binding protein 1 (ProSAP1/CortBP1) is a PDZ-domain protein highly enriched in the postsynaptic density. J Neurosci 15 (1999) 6506-6518
3. Boeckers T.M., Segger-Junius M., Iglauer P., Bockmann J., Gundelfinger E.D., Kreutz M.R., Richter D., Kindler S., and Kreienkamp H.J. Differential expression and dendritic transcript localization of Shank family members: identification of a dendritic targeting element in the 3′ untranslated region of Shank1 mRNA. Mol Cell Neurosci 26 (2004) 182-190
4. de Bartolomeis A., and Iasevoli F. The homer family and the signal transduction system at glutamatergic postsynaptic density: potential role in behavior and pharmacotherapy. Psychopharmacol Bull 37 (2003) 51-83
5. Durand C.M., Betancur C., Boeckers T.M., Bockmann J., Chaste P., Fauchereau F., Nygren G., Rastam M., Gillberg I.C., Anckarsater H., Sponheim E., Goubran-Botros H., Delorme R., Chabane N., Mouren-Simeoni M.C., de Mas P., Bieth E., Roge B., Heron D., Burglen L., Gillberg C., Leboyer M., and Bourgeron T. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet 39 (2007) 25-27
6. Guo W., Wei F., Zou S., Robbins M.T., Sugiyo S., Ikeda T., Tu J.C., Worley P.F., Dubner R., and Ren K. Group I metabotropic glutamate receptor NMDA receptor coupling and signaling cascade mediate spinal dorsal horn NMDA receptor 2B tyrosine phosphorylation associated with inflammatory hyperalgesia. J Neurosci 24 (2004) 9161-9173
7. Hargreaves K., Dubner R., Brown F., Flores C., and Joris J.A. A new and sensitive method for measuring thermal nociception in cutaneous hyperalgesia. Pain 32 (1988) 77-88
8. Hung A.Y., Futai K., Sala C., Valtschanoff J.G., Ryu J., Woodworth M.A., Kidd F.L., Sung C.C., Miyakawa T., Bear M.F., Weinberg R.J., and Sheng M. Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1. J Neurosci 28 (2008) 1697-1708
9. Kreienkamp H.J. Scaffolding proteins at the postsynaptic density: Shank as the architectural framework. Handb Exp Pharmacol 186 (2008) 365-380
10. Lim S., Naisbitt S., Yoon J., Hwang J.I., Suh P.G., Sheng M., and Kim E. Characterization of the Shank family of synaptic proteins. Multiple genes, alternative splicing, and differential expression in brain and development. J Biol Chem 274 (1999) 29510-29518
11. Malenka R.C., and Bear M.F. LTP and LTD: an embarrassment of riches. Neuron 44 (2004) 5-21
12. Mestre C., Pelissier T., Fialip J., Wilcox G., and Eschalier A.J. A method to perform direct transcutaneous intrathecal injection in rats. J Pharmacol Toxicol Methods 32 (1994) 197-200
13. Miletic G., Miyabe T., Gebhardt K.J., and Miletic V. Increased levels of Homer1b/c and Shank1a in the post-synaptic density of spinal dorsal horn neurons are associated with neuropathic pain in rats. Neurosci Lett 386 (2005) 189-193
14. Miletic G., and Miletic V. Loose ligation of the sciatic nerve is associated with TrkB receptor-dependent decreases in KCC2 protein levels in the ipsilateral spinal dorsal horn. Pain 137 (2008) 532-539
15. Millan M. The induction of pain: an integrative review. Prog Neurobiol 57 (1999) 1-164
16. Miyabe T., Miletic G., and Miletic V. Loose ligation of the sciatic nerve in rats elicits transient up-regulation of Homer1a gene expression in the spinal dorsal horn. Neurosci Lett 398 (2006) 296-299
17. Naisbitt S., Kim E., Tu J.C., Xiao B., Sala C., Valtschanoff J., Weinberg R.J., Worley P.F., and Sheng M. Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin. Neuron 23 (1999) 569-582
18. Rosenblum K., Meiri N., and Dudai Y. Taste memory: the role of protein synthesis in gustatory cortex. Behav Neural Biol 59 (1993) 49-56
19. Roussignol G., Ango F., Romorini S., Tu J.C., Sala C., Worley P.F., Bockaert J., and Fagni L. Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons. J Neurosci 25 (2005) 3560-3570
20. Sala C., Piech V., Wilson N.R., Passafaro M., Liu G., and Sheng M. Regulation of dendritic spine morphology and synaptic function by Shank and Homer. Neuron 31 (2001) 115-130
21. Sandkuhler J. Models and mechanisms of hyperalgesia and allodynia. Prog Brain Res 89 (2009) 707-758
22. Sheng M., and Kim E. The Shank family of scaffold proteins. J Cell Science 113 (2000) 1851-1856
23. Valtschanoff J.G., and Weinberg R.J. Laminar organization of the NMDA receptor complex within the postsynaptic density. J Neurosci 21 (2001) 1211-1217
24. Zimmermann M. Ethical guidelines for investigations of experimental pain in conscious animals. Pain 16 (1983) 109-110