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Perineuronal nets provide a polyanionic, glia‐associated form of microenvironment around certain neurons in many parts of the rat brain
Abstract
The nature and function of previously described perineuronal nets are still obscure. In the present study their polyanionic components were demonstrated in the rat brain using colloidal iron hydroxide (CIH) staining. In subcortical regions, such as the red nucleus, cerebellar, and vestibular nuclei, most neurons were ensheathed by CIH‐binding material. In the cerebral cortex perineuronal nets were seen around numerous nonpyramidal neurons. Biotinylated hyaluronectin revealed that hyaluronan occurs in perineuronal nets. Two plant lectins [ Wisteria floribunda agglutinin (WFA) and Vicia villosa agglutinin (VVA)] with affinity for N‐acetylgalactosamine visualized perineuronal nets similar to those rich in anionic components. Glutamic acid decarboxylase (GAD)‐immunoreactive synaptic boutons were shown to occupy numerous meshes of perineuronal VVA‐positive nets. Electron microscopically, VVA binding sites were scattered throughout perisynaptic profiles, but accumulated at membranes and in the extra‐cellular space except not in synaptic clefts. To investigate the spatial relationship between glial cell processes and perineuronal nets, two astrocytic markers (S100‐protein and glutamine synthetase) were visualized at the light and electron microscopic level. Two methods to detect microglia by the use of Griffonia simplicifolia agglutinin (GSA I‐B 4 ) and the monoclonal antibody, OX‐42, were also applied. Labelled structures forming perineuronal nets were observed with both astrocytic, but not with microglial, markers. It is concluded that perineuronal nets are composed of a specialized type of glia‐associated extracellular matrix rich in polyanionic groups and N‐acetylgalactosamine. The net‐like appearance is due to perisynaptic arrangement of the astrocytic processes and these extracellular components. Similar to the ensheathment of nodes of Ranvier, perineuronal nets may provide a special ion buffering capacity required around various, perhaps highly active, types of neurons. © 1993 Wiley‐Liss, Inc.
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In the citing paper
“Sulphate groups attached to these GAGs in concert with the negatively charged hyaluronic acid generate a highly polyanionic microenvironment around PN-ensheathed neurons.20, 21”
From Aggrecan, link protein and tenascin-R are essential components of the perineuronal net to protect neurons against iron-induced oxidative stress (2014) · cites this paper as [20]
In the citing paper
“the polyanionic components might also interact with ions of potential pathophysiological relevance such as iron ions involved in generating oxidative stress.20, 22, 26, 27”
From Aggrecan, link protein and tenascin-R are essential components of the perineuronal net to protect neurons against iron-induced oxidative stress (2014) · cites this paper as [20]
In the citing paper
“Astrocytes extend their processes into PNNs localized near the synapse (Brückner et al., 1993; Blümcke et al., 1995), suggesting a tetrapartite synaptic organization involving ECM, pre/post synaptic sites and astrocytes (Dityatev and Rusakov, 2011; Smith et al., 2015) whose synergistic functions remain unexplored.”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Brückner et al., 1993
In the citing paper
“First, PNNs carry a high degree of negative charge and may function as cation sinks (Bruckner et al, 1993).”
From Reduced Labeling of Parvalbumin Neurons and Perineuronal Nets in the Dorsolateral Prefrontal Cortex of Subjects with Schizophrenia (2016) · cites this paper as Bruckner et al, 1993
In the citing paper
“As part of the extracellular matrix (ECM), perineuronal nets (PNs) are polyanionic, chondroitin sulfate proteoglycan (CSPG)-rich coatings of certain neurons, known to be affected in various neural diseases.”
From Damaged Neocortical Perineuronal Nets Due to Experimental Focal Cerebral Ischemia in Mice, Rats and Sheep (2017) · cites this paper as Brückner et al., 1993
In the citing paper
“They are composed of chondroitin sulfate proteoglycans (CSPGs) and their glycosaminoglycans, hyaluronic acid and tenascins, produced by various neural cell types (Brückner et al., 1993).”
From Damaged Neocortical Perineuronal Nets Due to Experimental Focal Cerebral Ischemia in Mice, Rats and Sheep (2017) · cites this paper as Brückner et al., 1993
In the citing paper
“More recent evidence indicates that WFA-labeled PNNs are associated with more heterogeneous neuronal phenotypes than previously thought, including several subgroups of interneurons, a small subset of cortico-cortical pyramidal cells, spinal cord motor neurons and cerebellum Purkinje cells (Ajmo et al., 2008; Brauer et al., 1995; Bruckner et al., 1993; Gati and Lendvai, 2013; Hartig et al., 1995;”
From Losing the sugar coating: Potential impact of perineuronal net abnormalities on interneurons in schizophrenia (2015) · cites this paper as Bruckner et al., 1993
In the citing paper
“PNNs have been implicated in ion homeostasis around highly active neurons”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Bruckner et al., 1993
In the citing paper
“They can thus potentially act as a buffering system for physiologically relevant ions such as calcium, potassium, and sodium around highly active types of neurons”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Bruckner et al., 1993
In the citing paper
“The PNN is a unique ECM structure that is most prominently displayed around GABAergic interneurons, with parvalbumin expressing cells having the highest level of colocalization (Brückner et al., 1993;Celio and Chiquet-Ehrismann, 1993;Morris and Henderson, 2000).”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Brückner et al., 1993
In the citing paper
“Perineuronal nets are extracellular matrix structures which surround synapses of highly active neuronal subtypes and are associated with microglia [156].”
From Apolipoprotein E4, inhibitory network dysfunction, and Alzheimer’s disease (2019) · cites this paper as [156]
Citations
Cites
Handbook of Chemical Neuroanatomy
Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,160
Fine structural localization of glutamine synthetase in astrocytes of rat brain
Norenberg, M. D., & Martinez-Hernandez, A. (1979) · Brain Research · doi:10.1016/0006-8993(79)90071-4 · Cited by 1,349
Parvalbumin in Most γ-Aminobutyric Acid-Containing Neurons of the Rat Cerebral Cortex
Celio, M. R. (1986) · Science · doi:10.1126/science.3945815 · Cited by 740
A simple, non-chromatographic procedure to purify immunoglobulins from serum and ascites fluid
McKinney, M. M., & Parkinson, A. (1987) · Journal of Immunological Methods · doi:10.1016/0022-1759(87)90324-3 · Cited by 618
Wisteria floribunda agglutinin-labelled nets surround parvalbumin-containing neurons
Härtig, W., Brauer, K., & Brückner, G. (1992) · NeuroReport · doi:10.1097/00001756-199210000-00012 · Cited by 440
Self-citationOertel, W., Schmechel, D. E., Tappaz, M., & Kopin, I. J. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90113-5 · Cited by 419
Self-citationStreit, W. J. (1990) · Journal of Histochemistry & Cytochemistry · doi:10.1177/38.11.2212623 · Cited by 372
Expression of tenascin in the developing and adult cerebellar cortex
Bartsch, S., Bartsch, U., Dörries, U., Faissner, A., Weller, A., Ekblom, P., & Schachner, M. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-03-00736.1992 · Cited by 271
GABA Neurons in the Cerebral Cortex
Houser, C. R., Vaughn, J. E., Hendry, S. H. C., Jones, E. G., & Peters, A. (1984) · Cerebral cortex · doi:10.1007/978-1-4615-6610-6_3 · Cited by 261
Organization of radial glial cells during the development of the rat dentate gyrus
Rickmann, M., Amaral, D. G., & Cowan, W. M. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902640403 · Cited by 243
Self-citation
Flagged first, then by citations
Research works printed but not linked: 13
- Delpech B., 1989, The Biology of Hyaluronan. CIBA Foundation Symposion, 143
- Faissner A., 1989, Dynamics and Plasticity in Neuronal Systems. Proc. 17th Göttingen Neurobiology Conference, 1
- Golgi C., 1891, La réseau diffus des centres du système nerveux, Arch. Ital. Biol., 15, 314
- Graumann W., 1958, Weitere Untersuchungen zur Spezifität der histochemischen Polysaccharid‐Eisenreaktion, Acta Histochem., 6, 1
- Hockfield S., 1989, Neuroimmune Networks, 57
- Kettenmann H., 1988, In: Glial Cell Receptors, 95
- Kimelberg H. K., 1988, Glial Cell Receptors
- McGeer P. L., 1986, In: Neurohistochemistry: Modern Methods and Applications P. Panula, 355
- Raff M. C., 1990, In: Differentiation and Functions of Glial Cells, 17
- Ramon y Cajal S., 1906, Studien über die Hirnrinde des Menschen
- Schweizer M. Müller C. M. andStreit J. W.(1991)Perisynaptic lectin‐binding sites in cat visual cortex: an electron microscopical investigation. In: Synapse‐Transmission‐Moduluation. Proc. 19th Göttingen Neurobiology Conference. Elsner N. and eds. Thieme Stuttgart p.226.
- Szentagothai J., 1975, In: Golgi Centennial Symposium, 1
- Wolff J. R., 1970, Proc. 6th Intern. Congr. Neuropathology, 327
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Angelov, D. N., Walther, M. R., Streppel, M., Guntinas‐Lichius, O., Neiss, W. F., Probstmeier, R., & Pesheva, P. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-16-06218.1998 · Cited by 77
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Brauer, K., Ha¨rtig, W., Bigl, V., & Bru¨ckner, G. (1993) · Brain Research · doi:10.1016/0006-8993(93)91205-7 · Cited by 75
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Roßner, S., Härtig, W., Schliebs, R., Brückner, G., Brauer, K., Perez-Polo, J. R., Wiley, R. G., & Bigl, V. (1995) · Journal of Neuroscience Research · doi:10.1002/jnr.490410306 · Cited by 68
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Uliana, D. L., Lisboa, J. R., Gomes, F. V., & Grace, A. A. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116298 · Cited by 71
Vitellaro‐Zuccarello, L., Mazzetti, S., Bosisio, P., Monti, C., & Biasi, S. D. (2005) · Glia · doi:10.1002/glia.20196 · Cited by 64
Härtig, W., Singer, A., Grosche, J., Brauer, K., Ottersen, O. P., & Brückner, G. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02211-9 · Cited by 62
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Blosa, M., Sonntag, M., Brückner, G., Jäger, C., Seeger, G., Matthews, R. T., Rübsamen, R., Arendt, T., & Morawski, M. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.10.003 · Cited by 60
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Slaker, M. L., Barnes, J., Sorg, B. A., & Grimm, J. W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168256 · Cited by 57
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Nakamura, M., Nakano, K., Morita, S., Nakashima, T., Oohira, A., & Miyata, S. (2009) · Brain Research · doi:10.1016/j.brainres.2008.11.022 · Cited by 54
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Blümcke, I., Eggli, P., & Celio, M. R. (1995) · Glia · doi:10.1002/glia.440150205 · Cited by 53
Härtig, W., Mages, B., Aleithe, S., Nitzsche, B., Altmann, S., Barthel, H., Krueger, M., & Michalski, D. (2017) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2017.00015 · Cited by 53
Self-citationStevens, S. R., Longley, C. M., Ogawa, Y., Teliska, L. H., Arumanayagam, A. S., Nair, S., Oses-Prieto, J. A., Burlingame, A. L., Cykowski, M. D., Xue, M., et al. (2021) · eLife · doi:10.7554/elife.66491 · Cited by 53
Perisynaptic barrier of proteoglycans in the mature brain and spinal cord
MURAKAMI, T., & Ohtsuka, A. (2003) · Archivum histologicum japonicum · doi:10.1679/aohc.66.195 · Cited by 54
Eberhorn, A. C., Ardeleanu, P., Büttner‐Ennever, J. A., & Horn, A. K. E. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20715 · Cited by 52
Kritzer, M. F., & Kohama, S. G. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990705)409:3 · Cited by 126
Mendis, D. B., Malaval, L., & Brown, I. R. (1995) · Brain Research · doi:10.1016/0006-8993(95)00101-u · Cited by 52
Turley, E. A., Hossain, M. Z., Sorokan, T., Jordan, L. M., & Nagy, J. I. (1994) · Glia · doi:10.1002/glia.440120109 · Cited by 52
Gray, E., Thomas, T. L., Betmouni, S., Scolding, N., & Love, S. (2008) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e318183d003 · Cited by 51
McRae, P. A., Baranov, E., Sarode, S., Brooks-Kayal, A. R., & Porter, B. E. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.05.015 · Cited by 49
Grosche, J., & Br�ckner, G. (2001) · Experimental Brain Research · doi:10.1007/s002210000617 · Cited by 55
Self-citationHorn, A. K. E., Brückner, G., Härtig, W., & Messoudi, A. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10495 · Cited by 49
Self-citationSubpopulations of neurons expressing parvalbumin in the human amygdala
Pantazopoulos, H., Lange, N., Hassinger, L., & Berretta, S. (2006) · Journal of Comparative Neurology · doi:10.1002/cne.20961 · Cited by 45
Mix, A., Hoppenrath, K., & Funke, K. (2015) · Developmental Neurobiology · doi:10.1002/dneu.22205 · Cited by 48
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Adams, I., Brauer, K., Arélin, C., Härtig, W., Fine, A., Mäder, M., Arendt, T., & Brückner, G. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00419-5 · Cited by 48
Self-citationPerineuronal nets in the auditory system
Sonntag, M., Blosa, M., Schmidt, S., Rübsamen, R., & Morawski, M. (2015) · Hearing Research · doi:10.1016/j.heares.2014.12.012 · Cited by 50
Wicht, H., Derouiche, A., & Korf, H. (1994) · Journal of Neurocytology · doi:10.1007/bf01262057 · Cited by 48
Self-citationHyaluronan synthesis by developing cortical neurons in vitro
Fowke, T. M., Karunasinghe, R. N., Bai, J.-Z., Jordan, S., Gunn, A. J., & Dean, J. M. (2017) · Scientific Reports · doi:10.1038/srep44135 · Cited by 47
Perineuronal and perisynaptic extracellular matrix in the human spinal cord
Jäger, C., Lendvai, D., Seeger, G., Brückner, G., Matthews, R. T., Arendt, T., Alpár, A., & Morawski, M. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.02.014 · Cited by 48
Self-citationRollenhagen, A., Klook, K., Sätzler, K., Qi, G., Anstötz, M., Feldmeyer, D., & Lübke, J. H. R. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0850-5 · Cited by 54
Expression of aggrecan components in perineuronal nets in the mouse cerebral cortex
Ueno, H., Fujii, K., Suemitsu, S., Murakami, S., Kitamura, N., Wani, K., Aoki, S., Okamoto, M., Ishihara, T., & Takao, K. (2018) · IBRO Reports · doi:10.1016/j.ibror.2018.01.002 · Cited by 49
Schüppel, K., Brauer, K., Härtig, W., Grosche, J., Earley, B., Leonard, B. E., & Brückner, G. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03569-2 · Cited by 47
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Olson, J. E., & Li, G. (1997) · Glia · doi:10.1002/(sici)1098-1136(199707)20:3 · Cited by 46
Wintergerst, E. S., Faissner, A., & Celio, M. R. (1996) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(96)00011-1 · Cited by 46
Karetko-Sysa, M., Skangiel-Kramska, J., & Nowicka, D. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.05.022 · Cited by 45
Ueno, H., Suemitsu, S., Okamoto, M., Matsumoto, Y., & Ishihara, T. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.04.041 · Cited by 49
Härtig, W. (2001) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00179-2 · Cited by 46
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Jang, D. G., Sim, H. J., Song, E. K., Kwon, T., & Park, T. J. (2020) · BMB Reports · doi:10.5483/bmbrep.2020.53.10.156 · Cited by 45
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Gabryel, B., & Trzeciak, H. I. (2001) · Neurotoxicity Research · doi:10.1007/bf03033192 · Cited by 42
Hobohm, C., Härtig, W., Brauer, K., & Brückner, G. (1998) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(98)00044-1 · Cited by 41
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Fiedler, A., Reinert, T., Morawski, M., Brückner, G., Arendt, T., & Butz, T. (2007) · Nuclear Instruments and Methods in Physics Research Section B Beam Interactions with Materials and Atoms · doi:10.1016/j.nimb.2007.02.069 · Cited by 40
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Fowke, T. M., Galinsky, R., Davidson, J. O., Wassink, G., Karunasinghe, R. N., Prasad, J. D., Bennet, L., Gunn, A. J., & Dean, J. M. (2018) · Scientific Reports · doi:10.1038/s41598-018-36083-y · Cited by 39
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Alonge, K. M., Logsdon, A. F., Murphree, T. A., Banks, W. A., Keene, C. D., Edgar, J. S., Whittington, D., Schwartz, M. W., & Guttman, M. (2019) · Glycobiology · doi:10.1093/glycob/cwz060 · Cited by 38
Hoppenrath, K., Härtig, W., & Funke, K. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00022 · Cited by 41
Self-citationUriarte, N., Ferreño, M., Méndez, D., & Nogueira, J. (2020) · Scientific Reports · doi:10.1038/s41598-020-62163-z · Cited by 39
Reimers, S., Hartlage‐Rübsamen, M., Brückner, G., & Roßner, S. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05514.x · Cited by 40
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Synaptophysin Staining in Normal Brain
Quinn, B. (1998) · The American Journal of Surgical Pathology · doi:10.1097/00000478-199805000-00005 · Cited by 38
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Hilbig, H., Nowack, S., Boeckler, K., Bidmon, H. J., & Zilles, K. (2007) · Journal of Anatomy · doi:10.1111/j.1469-7580.2007.00713.x · Cited by 36
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Myers, A. K., Ray, J., & Kulesza, R. J. (2012) · Brain Research · doi:10.1016/j.brainres.2012.05.024 · Cited by 34
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Dunning, K. R., Watson, L. N., Sharkey, D. J., Brown, H. M., Norman, R. J., Thompson, J. G., Robker, R. L., & Russell, D. L. (2012) · Biology of Reproduction · doi:10.1095/biolreprod.111.096271 · Cited by 32
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Donegan, J. J., & Lodge, D. J. (2016) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw095 · Cited by 35
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Derouiche, A. (2003) · Advances in molecular and cell biology · doi:10.1016/s1569-2558(03)31006-9 · Cited by 30
Self-citation
Metadata
- Authors
- Brückner, G., Brauer, K., Härtig, W., Wolff, J. R., Rickmann, M. J., Derouiche, A., Delpech, B., Girard, N., Oertel, W. H., & Reichenbach, A.
- Affiliations
- Leipzig University (DE)
- University of Göttingen (DE)
- Goethe University Frankfurt (DE)
- Centre Henri Becquerel (FR)
- Ludwig-Maximilians-Universität München (DE)
- Corresponding author
- Brückner, Gert
- Venue
- Glia
- Publisher
- Wiley
- Published
- 1993-07
- Volume
- 8
- Issue
- 3
- Pages
- 183-200
- ISSN
- 0894-1491 (ISSN-L)
- 1098-1136
- OpenAlex
- W2099040370
- Cited by
- 358
- References
- 74
- Citations by year
- 2026: 8 · 2025: 13 · 2024: 7 · 2023: 9 · 2022: 17 · 2021: 13 · 2020: 16 · 2019: 13 · 2018: 25 · 2017: 19 · 2016: 17 · 2015: 10 · 2014: 10 · 2013: 13 · 2012: 14
- FWCI
- 2.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Glia (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- perineuronal nets, N-acetylgalactosamine, hyaluronic acid, astrocytes, microglia, glutamine synthetase, S-100 protein, glutamic acid decarboxylase, synaptic boutons, red nucleus, cerebellar nuclei, vestibular nuclei, cerebral cortex, lectin binding
- MeSH terms
- Acetylgalactosamine, Animals, Anions, Brain, Brain Chemistry, Colloids, Cytoplasm, Extracellular Matrix, gamma-Aminobutyric Acid, Glutamate Decarboxylase, Glutamate-Ammonia Ligase, Hyaluronic Acid, Hydroxides, S100 Proteins, Neuroglia, Neurons, Organic Chemicals, Staining and Labeling, Synapses, Biomarkers, Rats, Sprague-Dawley, Rats, Wistar, Microglia, Lectins, Rats, Iron Compounds
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