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Journal articles on the topic 'AIA interneurons'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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1

Shinkai, Y., Y. Yamamoto, M. Fujiwara, et al. "Behavioral Choice between Conflicting Alternatives Is Regulated by a Receptor Guanylyl Cyclase, GCY-28, and a Receptor Tyrosine Kinase, SCD-2, in AIA Interneurons of Caenorhabditis elegans." Journal of Neuroscience 31, no. 8 (2011): 3007–15. http://dx.doi.org/10.1523/jneurosci.4691-10.2011.

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2

D’Angelo, Vincenza, Mauro Giorgi, Emanuela Paldino, et al. "A2A Receptor Dysregulation in Dystonia DYT1 Knock-Out Mice." International Journal of Molecular Sciences 22, no. 5 (2021): 2691. http://dx.doi.org/10.3390/ijms22052691.

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We aimed to investigate A2A receptors in the basal ganglia of a DYT1 mouse model of dystonia. A2A was studied in control Tor1a+/+ and Tor1a+/− knock-out mice. A2A expression was assessed by anti-A2A antibody immunofluorescence and Western blotting. The co-localization of A2A was studied in striatal cholinergic interneurons identified by anti-choline-acetyltransferase (ChAT) antibody. A2A mRNA and cyclic adenosine monophosphate (cAMP) contents were also assessed. In Tor1a+/+, Western blotting detected an A2A 45 kDa band, which was stronger in the striatum and the globus pallidus than in the entopeduncular nucleus. Moreover, in Tor1a+/+, immunofluorescence showed A2A roundish aggregates, 0.3–0.4 μm in diameter, denser in the neuropil of the striatum and the globus pallidus than in the entopeduncular nucleus. In Tor1a+/−, A2A Western blotting expression and immunofluorescence aggregates appeared either increased in the striatum and the globus pallidus, or reduced in the entopeduncular nucleus. Moreover, in Tor1a+/−, A2A aggregates appeared increased in number on ChAT positive interneurons compared to Tor1a+/+. Finally, in Tor1a+/−, an increased content of cAMP signal was detected in the striatum, while significant levels of A2A mRNA were neo-expressed in the globus pallidus. In Tor1a+/−, opposite changes of A2A receptors’ expression in the striatal-pallidal complex and the entopeduncular nucleus suggest that the pathophysiology of dystonia is critically dependent on a composite functional imbalance of the indirect over the direct pathway in basal ganglia.

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3

Song, Wen-Jie, Tatiana Tkatch, and D. James Surmeier. "Adenosine Receptor Expression and Modulation of Ca2+Channels in Rat Striatal Cholinergic Interneurons." Journal of Neurophysiology 83, no. 1 (2000): 322–32. http://dx.doi.org/10.1152/jn.2000.83.1.322.

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Adenosine is a potent regulator of acetylcholine release in the striatum, yet the mechanisms mediating this regulation are largely undefined. To begin to fill this gap, adenosine receptor expression and coupling to voltage-dependent Ca2+ channels were studied in cholinergic interneurons by combined whole cell voltage-clamp recording and single-cell reverse transcription–polymerase chain reaction. Cholinergic interneurons were identified by the presence of choline acetyltransferase mRNA. Nearly all of these interneurons (90%, n = 28) expressed detectable levels of A1 adenosine receptor mRNA. A2a and A2b receptor mRNAs were less frequently detected. A3 receptor mRNA was undetectable. Adenosine rapidly and reversibly reduced N-type Ca2+ currents in cholinergic interneurons. The A1 receptor antagonist 8-cyclopentyl-1,3-dimethylxanthine completely blocked the effect of adenosine. The IC50 of the A1 receptor selective agonist 2-chloro-N6-cyclopentyladenosine was 45 nM, whereas it was near 30 μM for the A2a receptor agonist CGS-21680. Dialysis with GDPβS or brief exposure to the G protein (Gi/o) alkylating agent N-ethylmaleimide also blocked the adenosine modulation. The reduction in N-type currents was partially reversed by depolarizing prepulses. A membrane-delimited pathway mediated the modulation, because it was not seen in cell-attached patches when agonist was applied to the bath. Activation of protein kinase C attenuated the adenosine modulation. Taken together, our results argue that activation of A1 adenosine receptors in cholinergic interneurons reduces N-type Ca2+currents via a membrane-delimited, Gi/o class G-protein pathway that is regulated by protein kinase C. These observations establish a cellular mechanism by which adenosine may serve to reduce acetylcholine release.

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4

Freund, T. F., and G. Buzsáki. "Interneurons of the hippocampus." Hippocampus 6, no. 4 (1998): 347–470. http://dx.doi.org/10.1002/(sici)1098-1063(1996)6:4<347::aid-hipo1>3.0.co;2-i.

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5

Kharazia, V. N., R. J. Wenthold, and R. J. Weinberg. "GluR1-immunopositive interneurons in rat neocortex." Journal of Comparative Neurology 368, no. 3 (1996): 399–412. http://dx.doi.org/10.1002/(sici)1096-9861(19960506)368:3<399::aid-cne6>3.0.co;2-0.

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6

Arcangeli, Sara, Alessandro Tozzi, Michela Tantucci, et al. "Ischemic-LTP in Striatal Spiny Neurons of both Direct and Indirect Pathway Requires the Activation of D1-Like Receptors and NO/Soluble Guanylate Cyclase/cGMP Transmission." Journal of Cerebral Blood Flow & Metabolism 33, no. 2 (2012): 278–86. http://dx.doi.org/10.1038/jcbfm.2012.167.

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Striatal medium-sized spiny neurons (MSNs) are highly vulnerable to ischemia. A brief ischemic insult, produced by oxygen and glucose deprivation (OGD), can induce ischemic long-term potentiation (i-LTP) of corticostriatal excitatory postsynaptic response. Since nitric oxide (NO) is involved in the pathophysiology of brain ischemia and the dopamine D1/D5-receptors (D1-like-R) are expressed in striatal NOS-positive interneurons, we hypothesized a relation between NOS-positive interneurons and striatal i-LTP, involving D1R activation and NO production. We investigated the mechanisms involved in i-LTP induced by OGD in corticostriatal slices and found that the D1-like-R antagonist SCH-23390 prevented i-LTP in all recorded MSNs. Immunofluorescence analysis confirmed the induction of i-LTP in both substance P-positive, (putative D1R-expressing) and adenosine A2A-receptor-positive (putative D2R-expressing) MSNs. Furthermore, i-LTP was dependent on a NOS/cGMP pathway since pharmacological blockade of NOS, guanylate-cyclase, or PKG prevented i-LTP. However, these compounds failed to prevent i-LTP in the presence of a NO donor or cGMP analog, respectively. Interestingly, the D1-like-R antagonism failed to prevent i-LTP when intracellular cGMP was pharmacologically increased. We propose that NO, produced by striatal NOS-positive interneurons via the stimulation of D1-like-R located on these cells, is critical for i-LTP induction in the entire population of MSNs involving a cGMP-dependent pathway.

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7

Buckmaster, Paul S., and Ivan Soltesz. "Neurobiology of hippocampal interneurons: A workshop review." Hippocampus 6, no. 3 (1996): 330–39. http://dx.doi.org/10.1002/(sici)1098-1063(1996)6:3<330::aid-hipo9>3.0.co;2-q.

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8

Maxwell, D. J., R. Kerr, E. Jankowska, and J. S. Riddell. "Synaptic connections of dorsal horn group II spinal interneurons: Synapses formed with the interneurons and by their axon collaterals." Journal of Comparative Neurology 380, no. 1 (1997): 51–69. http://dx.doi.org/10.1002/(sici)1096-9861(19970331)380:1<51::aid-cne4>3.0.co;2-s.

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9

Cicchetti, Francesca, Thomas G. Beach, and Andr� Parent. "Chemical phenotype of calretinin interneurons in the human striatum." Synapse 30, no. 3 (1998): 284–97. http://dx.doi.org/10.1002/(sici)1098-2396(199811)30:3<284::aid-syn6>3.0.co;2-7.

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10

Ratt�, St�phanie, and Ronald Chase. "Morphology of interneurons in the procerebrum of the snailHelix aspersa." Journal of Comparative Neurology 384, no. 3 (1997): 359–72. http://dx.doi.org/10.1002/(sici)1096-9861(19970804)384:3<359::aid-cne4>3.0.co;2-2.

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11

Mart�nez-Guijarro, Francisco J., Jes�s G. Bri��n, Jos� M. Blasco-Ib��ez, Katsuo Okazaki, Hiroyoshi Hidaka, and Jos� R. Alonso. "Neurocalcin-immunoreactive cells in the rat hippocampus are GABAergic interneurons." Hippocampus 8, no. 1 (1998): 2–23. http://dx.doi.org/10.1002/(sici)1098-1063(1998)8:1<2::aid-hipo2>3.0.co;2-p.

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12

Thomas, Traci M., Yol Smith, Allan I. Levey, and Steven M. Hersch. "Cortical inputs to m2-immunoreactive striatal interneurons in rat and monkey." Synapse 37, no. 4 (2000): 252–61. http://dx.doi.org/10.1002/1098-2396(20000915)37:4<252::aid-syn2>3.0.co;2-a.

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13

Tozzi, A., A. de Iure, M. Di Filippo, et al. "The Distinct Role of Medium Spiny Neurons and Cholinergic Interneurons in the D2/A2A Receptor Interaction in the Striatum: Implications for Parkinson's Disease." Journal of Neuroscience 31, no. 5 (2011): 1850–62. http://dx.doi.org/10.1523/jneurosci.4082-10.2011.

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14

Datskovskaia, Aygul, W. Breckinridge Carden, and Martha E. Bickford. "Y retinal terminals contact interneurons in the cat dorsal lateral geniculate nucleus." Journal of Comparative Neurology 430, no. 1 (2000): 85–100. http://dx.doi.org/10.1002/1096-9861(20010129)430:1<85::aid-cne1016>3.0.co;2-k.

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15

Van Vulpen, E. H. S., and D. Van Der Kooy. "Differential maturation of cholinergic interneurons in the striatal patch versus matrix compartments." Journal of Comparative Neurology 365, no. 4 (1996): 683–91. http://dx.doi.org/10.1002/(sici)1096-9861(19960219)365:4<683::aid-cne12>3.0.co;2-i.

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16

Sadikot, Abbas F., and Rachel Sasseville. "Neurogenesis in the mammalian neostriatum and nucleus accumbens: Parvalbumin-immunoreactive GABAergic interneurons." Journal of Comparative Neurology 389, no. 2 (1997): 193–211. http://dx.doi.org/10.1002/(sici)1096-9861(19971215)389:2<193::aid-cne1>3.0.co;2-x.

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17

Ratt�, St�phanie, and Ronald Chase. "Synapse distribution of olfactory interneurons in the procerebrum of the snailHelix aspersa." Journal of Comparative Neurology 417, no. 3 (2000): 366–84. http://dx.doi.org/10.1002/(sici)1096-9861(20000214)417:3<366::aid-cne9>3.0.co;2-i.

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18

Stocker, Reinhard F., Gertrud Heimbeck, Nana� Gendre, and J. Steven de Belle. "Neuroblast ablation in Drosophila P[GAL4] lines reveals origins of olfactory interneurons." Journal of Neurobiology 32, no. 5 (1997): 443–56. http://dx.doi.org/10.1002/(sici)1097-4695(199705)32:5<443::aid-neu1>3.0.co;2-5.

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19

Hu, Huaiyu. "Polysialic acid regulates chain formation by migrating olfactory interneuron precursors." Journal of Neuroscience Research 61, no. 5 (2000): 480–92. http://dx.doi.org/10.1002/1097-4547(20000901)61:5<480::aid-jnr2>3.0.co;2-m.

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20

Christie, Brian R., Kevin M. Franks, Jeremy K. Seamans, Karin Saga, and Terrence J. Sejnowski. "Synaptic plasticity in morphologically identified CA1 stratum radiatum interneurons and giant projection cells." Hippocampus 10, no. 6 (2000): 673–83. http://dx.doi.org/10.1002/1098-1063(2000)10:6<673::aid-hipo1005>3.0.co;2-o.

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21

Puskár, Zita, and Miklós Antal. "Localization of last-order premotor interneurons in the lumbar spinal cord of rats." Journal of Comparative Neurology 389, no. 3 (1997): 377–89. http://dx.doi.org/10.1002/(sici)1096-9861(19971222)389:3<377::aid-cne2>3.0.co;2-y.

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22

Insausti, Teresita C., and Claudio R. Lazzari. "Central projections of first-order ocellar interneurons in the bugTriatoma infestans (Heteroptera: Reduviidae)." Journal of Morphology 229, no. 2 (1996): 161–69. http://dx.doi.org/10.1002/(sici)1097-4687(199608)229:2<161::aid-jmor2>3.0.co;2-4.

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23

Ogawa, Hiroto, Yoshichika Baba, and Kotaro Oka. "Spike-dependent calcium influx in dendrites of the cricket giant interneuron." Journal of Neurobiology 44, no. 1 (2000): 45–56. http://dx.doi.org/10.1002/1097-4695(200007)44:1<45::aid-neu5>3.0.co;2-#.

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24

Nebeling, Bernd. "Morphology and physiology of auditory and vibratory ascending interneurones in bushcrickets." Journal of Experimental Zoology 286, no. 3 (2000): 219–30. http://dx.doi.org/10.1002/(sici)1097-010x(20000215)286:3<219::aid-jez1>3.0.co;2-j.

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25

Benton, Jeanne L., and Barbara S. Beltz. "Effects of serotonin depletion on local interneurons in the developing olfactory pathway of lobsters." Journal of Neurobiology 46, no. 3 (2001): 193–205. http://dx.doi.org/10.1002/1097-4695(20010215)46:3<193::aid-neu1002>3.0.co;2-8.

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26

Spruston, Nelson, Joachim L�bke, and Michael Frotscher. "Interneurons in the stratum lucidum of the rat hippocampus: An anatomical and electrophysiological characterization." Journal of Comparative Neurology 385, no. 3 (1997): 427–40. http://dx.doi.org/10.1002/(sici)1096-9861(19970901)385:3<427::aid-cne7>3.0.co;2-5.

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27

Sultan, Fahad, and James M. Bower. "Quantitative Golgi study of the rat cerebellar molecular layer interneurons using principal component analysis." Journal of Comparative Neurology 393, no. 3 (1998): 353–73. http://dx.doi.org/10.1002/(sici)1096-9861(19980413)393:3<353::aid-cne7>3.0.co;2-0.

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28

Eide, Anne-Lill, Joel Glover, Ole Kjaerulff, and Ole Kiehn. "Characterization of commissural interneurons in the lumbar region of the neonatal rat spinal cord." Journal of Comparative Neurology 403, no. 3 (1999): 332–45. http://dx.doi.org/10.1002/(sici)1096-9861(19990118)403:3<332::aid-cne4>3.0.co;2-r.

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29

Bizon, Jennifer L., Julie C. Lauterborn, and Christine M. Gall. "Subpopulations of striatal interneurons can be distinguished on the basis of neurotrophic factor expression." Journal of Comparative Neurology 408, no. 2 (1999): 283–98. http://dx.doi.org/10.1002/(sici)1096-9861(19990531)408:2<283::aid-cne9>3.0.co;2-2.

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30

Kittmann, Rolf, Josef Schmitz, and Ansgar B�schges. "Premotor interneurons in generation of adaptive leg reflexes and voluntary movements in stick insects." Journal of Neurobiology 31, no. 4 (1996): 512–31. http://dx.doi.org/10.1002/(sici)1097-4695(199612)31:4<512::aid-neu10>3.0.co;2-f.

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31

Ritzmann, Roy E., and Alan J. Pollack. "Characterization of tactile-sensitive interneurons in the abdominal ganglia of the cockroach,Periplaneta americana." Journal of Neurobiology 34, no. 3 (1998): 227–41. http://dx.doi.org/10.1002/(sici)1097-4695(19980215)34:3<227::aid-neu3>3.0.co;2-4.

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32

Commons, Kathryn G., and Teresa A. Milner. "Localization of delta opioid receptor immunoreactivity in interneurons and pyramidal cells in the rat hippocampus." Journal of Comparative Neurology 381, no. 3 (1997): 373–87. http://dx.doi.org/10.1002/(sici)1096-9861(19970512)381:3<373::aid-cne8>3.0.co;2-#.

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33

Hikosaka, Ryou, and Masakazu Takahata. "Quantitative analyses of anatomical and electrotonic structures of crayfish nonspiking interneurons by three-dimensional morphometry." Journal of Comparative Neurology 392, no. 3 (1998): 373–89. http://dx.doi.org/10.1002/(sici)1096-9861(19980316)392:3<373::aid-cne7>3.0.co;2-z.

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34

McDonagh, Jennifer C., Robert B. Gorman, Edwin E. Gilliam, T. George Hornby, Robert M. Reinking, and Douglas G. Stuart. "Properties of spinal motoneurons and interneurons in the adult turtle: Provisional classification by cluster analysis." Journal of Comparative Neurology 400, no. 4 (1998): 544–70. http://dx.doi.org/10.1002/(sici)1096-9861(19981102)400:4<544::aid-cne8>3.0.co;2-a.

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35

Schl�sser, Beate, Gaby Klausa, Graham Prime, and Gerrit Ten Bruggencate. "Postnatal development of calretinin- and parvalbumin-positive interneurons in the rat neostriatum: An immunohistochemical study." Journal of Comparative Neurology 405, no. 2 (1999): 185–98. http://dx.doi.org/10.1002/(sici)1096-9861(19990308)405:2<185::aid-cne4>3.0.co;2-b.

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36

Van Vulpen, Eileen H. S., and Derek Van Der Kooy. "NGF facilitates the developmental maturation of the previously committed cholinergic interneurons in the striatal matrix." Journal of Comparative Neurology 411, no. 1 (1999): 87–96. http://dx.doi.org/10.1002/(sici)1096-9861(19990816)411:1<87::aid-cne7>3.0.co;2-s.

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37

Willins, David L., Ariel Y. Deutch, and Bryan L. Roth. "Serotonin 5-HT2A receptors are expressed on pyramidal cells and interneurons in the rat cortex." Synapse 27, no. 1 (1997): 79–82. http://dx.doi.org/10.1002/(sici)1098-2396(199709)27:1<79::aid-syn8>3.0.co;2-a.

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38

Stiedl, Oliver, Andreas Stumpner, David N. Mbungu, Gordon Atkins, and John F. Stout. "Morphology and physiology of local auditory interneurons in the prothoracic ganglion of the cricketAcheta domesticus." Journal of Experimental Zoology 279, no. 1 (1997): 43–53. http://dx.doi.org/10.1002/(sici)1097-010x(19970901)279:1<43::aid-jez4>3.0.co;2-1.

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39

Guly�s, Attila I., and Tam�s F. Freund. "Pyramidal cell dendrites are the primary targets of calbindin D28k-immunoreactive interneurons in the hippocampus." Hippocampus 6, no. 5 (1996): 525–34. http://dx.doi.org/10.1002/(sici)1098-1063(1996)6:5<525::aid-hipo5>3.0.co;2-h.

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40

Woodson, Walter, Claudia R. Farb, and Joseph E. Ledoux. "Afferents from the auditory thalamus synapse on inhibitory interneurons in the lateral nucleus of the amygdala." Synapse 38, no. 2 (2000): 124–37. http://dx.doi.org/10.1002/1098-2396(200011)38:2<124::aid-syn3>3.0.co;2-n.

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41

Teicher, Martin H., Nathalie L. Dumont, and Susan L. Andersen. "The developing prefrontal cortex: Is there a transient interneuron that stimulates catecholamine terminals?" Synapse 29, no. 1 (1998): 89–91. http://dx.doi.org/10.1002/(sici)1098-2396(199805)29:1<89::aid-syn9>3.0.co;2-7.

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42

Meek, J., K. Grant, Y. Sugawara, T. G. M. Hafmans, M. Veron, and J. P. Denizot. "Interneurons of the ganglionic layer in the mormyrid electrosensory lateral line lobe: Morphology, immunohistochemistry, and synaptology." Journal of Comparative Neurology 375, no. 1 (1996): 43–65. http://dx.doi.org/10.1002/(sici)1096-9861(19961104)375:1<43::aid-cne3>3.0.co;2-o.

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43

Smith, Yoland, Jean-Fran�ois Par�, and Denis Par�. "Differential innervation of parvalbumin-immunoreactive interneurons of the basolateral amygdaloid complex by cortical and intrinsic inputs." Journal of Comparative Neurology 416, no. 4 (2000): 496–508. http://dx.doi.org/10.1002/(sici)1096-9861(20000124)416:4<496::aid-cne6>3.0.co;2-n.

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44

K�ppenbender, Karsten D., David G. Standaert, Thomas J. Feuerstein, John B. Penney, Anne B. Young, and G. Bernhard Landwehrmeyer. "Expression of NMDA receptor subunit mRNAs in neurochemically identified projection and interneurons in the human striatum." Journal of Comparative Neurology 419, no. 4 (2000): 407–21. http://dx.doi.org/10.1002/(sici)1096-9861(20000417)419:4<407::aid-cne1>3.0.co;2-i.

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45

Tomasulo, Richard A., and Oswald Steward. "Homosynaptic and heterosynaptic changes in driving of dentate gyrus interneurons after brief tetanic stimulation in vivo." Hippocampus 6, no. 1 (1996): 62–71. http://dx.doi.org/10.1002/(sici)1098-1063(1996)6:1<62::aid-hipo11>3.0.co;2-i.

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46

D�rr, Volker, Rafael Kurtz, and Martin Egelhaaf. "Two classes of visual motion sensitive interneurons differ in direction and velocity dependency ofin vivo calcium dynamics." Journal of Neurobiology 46, no. 4 (2001): 289–300. http://dx.doi.org/10.1002/1097-4695(200103)46:4<289::aid-neu1009>3.0.co;2-w.

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47

Smith, G. Troy, Ying Lu, and Harold H. Zakon. "Parvocells: A novel interneuron type in the pacemaker nucleus of a weakly electric fish." Journal of Comparative Neurology 423, no. 3 (2000): 427–39. http://dx.doi.org/10.1002/1096-9861(20000731)423:3<427::aid-cne6>3.0.co;2-s.

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48

Nagayama, Toshiki. "Organization of exteroceptive inputs onto nonspiking local interneurones in the crayfish terminal abdominal ganglion." Journal of Experimental Zoology 279, no. 1 (1997): 29–42. http://dx.doi.org/10.1002/(sici)1097-010x(19970901)279:1<29::aid-jez3>3.0.co;2-3.

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49

Shetty, Ashok K., and Dennis A. Turner. "Hippocampal interneurons expressing glutamic acid decarboxylase and calcium-binding proteins decrease with aging in Fischer 344 rats." Journal of Comparative Neurology 394, no. 2 (1998): 252–69. http://dx.doi.org/10.1002/(sici)1096-9861(19980504)394:2<252::aid-cne9>3.0.co;2-1.

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50

Wicklein, Martina, and Deszo Varj�. "Visual system of the european hummingbird hawkmothMacroglossum stellatarum (sphingidae, lepidoptera): Motion-sensitive interneurons of the lobula plate." Journal of Comparative Neurology 408, no. 2 (1999): 272–82. http://dx.doi.org/10.1002/(sici)1096-9861(19990531)408:2<272::aid-cne8>3.0.co;2-9.

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