Non-synaptic and dendritic exocytosis from dense-cored vesicles in the suprachiasmatic nucleus
Abstract
The sites of exocytosis by dense-cored vesicles (DCVs) from neurones in the rat suprachiasmatic nucleus (SCN) were studied at the ultrastructural level. The tannic acid procedure, which stabilizes extruded proteinaceous substances, was used to demonstrate exocytosis of DCV cores. Fresh brian slices containing the SCN were incubated in media containing high levels of potassium (56 mM) or glutamate (10 mM) in the presence of tannic acid. Long-term slice explant cultures of the SCN were similarly treated. Exocytosis from DCVs occurred from axonal terminals, from dendrites, and occasionally from somata. The sites of DCV exocytosis were generally nonsynaptic or para-synaptic, including release immediately adjacent to axo-spinous synaptic densities. These observations show that, in the suprachiasmatic nucleus, neuroactive substances contained in DCVs do not necessarily function at synaptic contract zones, but could also act as neuromodulators at non-synaptic sites.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
A major source of non-synaptically released OT and AVP is the magnocellular neurons in the hypothalamus, although there is also evidence that hypothalamic parvocellular neurons can release neuropeptides from dense core vesicles non-synaptically.
“A major source of non-synaptically released OT and AVP is the magnocellular neurons in the hypothalamus, although there is also evidence that hypothalamic parvocellular neurons can also release neuropeptides from dense core vesicles non-synaptically [111].”
From Cross-talk among oxytocin and arginine-vasopressin receptors: Relevance for basic and clinical studies of the brain and periphery (2018) · cites this paper as [111]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Still being checked.
Cited by
Sorted by citations
GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits
Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033 · see citing works
Dendritic peptide release and peptide-dependent behaviours
Ludwig, M., & Leng, G. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1845 · Cited by 945 · see citing works
Activity-Dependent Regulation of Synapses by Retrograde Messengers
Regehr, W., Carey, M. R., & Best, A. R. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.021 · Cited by 294 · see citing works
Song, Z., & Albers, H. E. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.10.004 · Cited by 244 · see citing works
Talking back: dendritic neurotransmitter release
Ludwig, M., & Pittman, Q. J. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00072-9 · Cited by 210 · see citing works
Albers, H. E. (2015) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.07.001 · Cited by 200 · see citing works
Vasopressin and the Output of the Hypothalamic Biological Clock
Kalsbeek, A., Fliers, E., Hofman, M. A., Swaab, D. F., & Buijs, R. M. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.01956.x · Cited by 192 · see citing works
A genetically encoded sensor measures temporal oxytocin release from different neuronal compartments
Qian, T., Wang, H., Wang, P., Geng, L., Mei, L., Osakada, T., Wang, L. A., Tang, Y., Kania, A., Grinevich, V., et al. (2023) · Nature Biotechnology · doi:10.1038/s41587-022-01561-2 · Cited by 145 · see citing works
Entrainment of Circadian Rhythms Depends on Firing Rates and Neuropeptide Release of VIP SCN Neurons
Mazuski, C. N., Abel, J. H., Chen, S. P., Hermanstyne, T. O., Jones, J. R., Simon, T., Doyle, F. J., & Herzog, E. D. (2018) · Neuron · doi:10.1016/j.neuron.2018.06.029 · Cited by 122 · see citing works
Neurotransmitters of the suprachiasmatic nuclei
Reghunandanan, V., & Reghunandanan, R. (2006) · Journal of Circadian Rhythms · doi:10.1186/1740-3391-4-2 · Cited by 118 · see citing works
Sex-dependent regulation of social reward by oxytocin: an inverted U hypothesis
Borland, J. M., Rilling, J. K., Frantz, K. J., & Albers, H. E. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-018-0129-2 · Cited by 116 · see citing works
Albers, H. E., Walton, J. C., Gamble, K. L., McNeill, J. K., & Hummer, D. L. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.11.003 · Cited by 113 · see citing works
Pennartz, C. M. A., de Jeu, M. T. G., Geurtsen, A. M. S., Sluiter, A. A., & Hermes, M. L. H. J. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.775bv.x · Cited by 114 · see citing works
Vasopressin, oxytocin, and social odor recognition
Wacker, D. W., & Ludwig, M. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.08.014 · Cited by 112 · see citing works
Castel, M., & Morris, J. F. (2000) · Journal of Anatomy · doi:10.1046/j.1469-7580.2000.19610001.x · Cited by 100 · see citing works
Self-citationSherry, D. M., Mitchell, R., Standifer, K. M., & du Plessis, B. (2006) · BMC Neuroscience · doi:10.1186/1471-2202-7-54 · Cited by 87 · see citing works
Wotjak, C. T., Naruo, T., Muraoka, S., Simchen, R., Landgraf, R., & Engelmann, M. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01613.x · Cited by 85 · see citing works
Functional Morphology of the Suprachiasmatic Nucleus
Ibata, Y., Okamura, H., Tanaka, M., Tamada, Y., Hayashi, S., Iijima, N., Matsuda, T., Munekawa, K., Takamatsu, T., Hisa, Y., et al. (1999) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1999.0180 · Cited by 85 · see citing works
Ulrich‐Lai, Y. M., Flores, C. M., Harding-Rose, C., Goodis, H. E., & Hargreaves, K. (2001) · Pain · doi:10.1016/s0304-3959(00)00439-5 · Cited by 80 · see citing works
The essential role of cAMP/Ca2+ signalling in mammalian circadian timekeeping
O'Neill, J. S., & Reddy, A. B. (2012) · Biochemical Society Transactions · doi:10.1042/bst20110691 · Cited by 72 · see citing works
Collective timekeeping among cells of the master circadian clock
Evans, J. A. (2016) · Journal of Endocrinology · doi:10.1530/joe-16-0054 · Cited by 77 · see citing works
Invited Review: A neural clockwork for encoding circadian time
Herzog, E. D., & Schwartz, W. J. (2002) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00836.2001 · Cited by 71 · see citing works
Wagner, S., Sagiv, N., & Yarom, Y. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.00853.x · Cited by 70 · see citing works
Oxytocin: Parallel Processing in the Social Brain?
Dölen, G. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12284 · Cited by 65 · see citing works
Release of vasopressin within the brain contributes to neuroendocrine and behavioral regulation
Landgraf, R., Wotjak, C. T., Neumann, I. D., & Engelmann, M. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)61571-x · Cited by 66 · see citing works
Oxytocin Influences Male Sexual Activity via Non-synaptic Axonal Release in the Spinal Cord
Oti, T., Satoh, K., Uta, D., Nagafuchi, J., Tateishi, S., Ueda, R., Takanami, K., Young, L. J., Galione, A., Morris, J. F., et al. (2021) · Current Biology · doi:10.1016/j.cub.2020.09.089 · Cited by 63 · see citing works
Self-citationGlanowska, K. M., & Moenter, S. M. (2014) · Endocrinology · doi:10.1210/en.2014-1458 · Cited by 63 · see citing works
Cellular Mechanisms of Circadian Pacemaking: Beyond Transcriptional Loops
O'Neill, J. S., Maywood, E. S., & Hastings, M. H. (2013) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-25950-0_4 · Cited by 62 · see citing works
Snap-25 is polarized to axons and abundant along the axolemma: an immunogold study of intact neurons
Tao-Cheng, J.-H., Du, J., & McBain, C. J. (2000) · Journal of Neurocytology · doi:10.1023/a:1007168231323 · Cited by 56 · see citing works
Vasopressin and social odor processing in the olfactory bulb and anterior olfactory nucleus
Wacker, D. W., Engelmann, M., Tobin, V. A., Meddle, S., & Ludwig, M. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05885.x · Cited by 51 · see citing works
Vasopressin casts light on the suprachiasmatic nucleus
Tsuji, T., Allchorne, A. J., Zhang, M., Tsuji, C., Tobin, V. A., Pineda, R., Raftogianni, A., Stern, J. E., Grinevich, V., Leng, G., et al. (2017) · The Journal of Physiology · doi:10.1113/jp274025 · Cited by 42 · see citing works
Swim stress triggers the release of vasopressin within the suprachiasmatic nucleus of male rats
Engelmann, M., Ebner, K., Landgraf, R., & Wotjak, C. T. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00243-1 · Cited by 39 · see citing works
Circuit development in the master clock network of mammals
Carmona‐Alcocer, V., Rohr, K. E., Joye, D. A. M., & Evans, J. A. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14259 · Cited by 37 · see citing works
Histamine‐immunoreactive neurons in the mouse and rat suprachiasmatic nucleus
Michelsen, K. A., Lozada, A. F., Kaslin, J., Karlstedt, K. A., Kukko‐Lukjanov, T., Holopainen, I. E., Ohtsu, H., & Panula, P. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04387.x · Cited by 35 · see citing works
Jacomy, H., Burlet, A. J., & Bosler, O. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00259-0 · Cited by 34 · see citing works
The SCN is Comprised of a Population of Coupled Oscillators
Miller, J. D. (1998) · Chronobiology International · doi:10.3109/07420529808998704 · Cited by 33 · see citing works
Keun-young Kim, A., Rios, L. C., Le, H. D., Perez, A. J., Phan, S., Bushong, E. A., Deerinck, T. J., Liu, Y. H., Ellisman, M., Lev‐Ram, V., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.006 · Cited by 32 · see citing works
Zhang, L., Volknandt, W., Gundelfinger, E. D., & Zimmermann, H. (2000) · Journal of Neurocytology · doi:10.1023/a:1007108012667 · Cited by 31 · see citing works
Membrane Properties and Morphology of Vasopressin Neurons in Slices of Rat Suprachiasmatic Nucleus
Pennartz, C. M. A., Bos, N. P. A., de Jeu, M. T. G., Geurtsen, A. M. S., Mirmiran, M., Sluiter, A. A., & Buijs, R. M. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.5.2710 · Cited by 30 · see citing works
Satoh, K., Oti, T., Katoh, A., Ueta, Y., Morris, J. F., Sakamoto, T., & Sakamoto, H. (2015) · FEBS Journal · doi:10.1111/febs.13291 · Cited by 21 · see citing works
Self-citationDehkordi, O., Kc, P., Balan, K. V., & Haxhiu, M. A. (2006) · Autonomic Neuroscience · doi:10.1016/j.autneu.2006.02.023 · Cited by 20 · see citing works
TGFα and AVP in the mouse suprachiasmatic nucleus: Anatomical relationship and daily profiles
van der Zee, E. A., Román, V., ten Brinke, O., & Meerlo, P. (2005) · Brain Research · doi:10.1016/j.brainres.2005.06.075 · Cited by 19 · see citing works
Cheng, P.-C., Wang, Y.-C., Chen, Y.-S., Cheng, R.-C., Yang, J.-J., & Huang, R.-C. (2018) · Journal of Biomedical Sciences · doi:10.1186/s12929-018-0447-z · Cited by 11 · see citing works
Salsolinol Up‐Regulates Oxytocin Expression and Release During Lactation in Sheep
Górski, K., Marciniak, E., Zielińska-Górska, M. K., & Misztal, T. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12362 · Cited by 13 · see citing works
Zhang, B.-J., Yamashita, M., Fields, R., Kusano, K., & Gainer, H. (2005) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-005-3970-x · Cited by 13 · see citing works
Role of Na+/Ca2+exchanger in Ca2+homeostasis in rat suprachiasmatic nucleus neurons
Wang, Y., Chen, Y.-S., Cheng, R.-C., & Huang, R. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00404.2014 · Cited by 12 · see citing works
Altrup, U., & Wiemann, M. (2003) · Brain Research · doi:10.1016/s0006-8993(03)02532-0 · Cited by 12 · see citing works
Kawai, T., Abe, H., & Oka, Y. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.258343 · Cited by 12 · see citing works
Herzog, E. D., & Schwartz, W. J. (2002) · Cited by 9 · see citing works
Retrograde suppression of GABAergic currents in a subset of SCN neurons
Gompf, H. S., Irwin, R. P., & Allen, C. N. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04850.x · Cited by 8 · see citing works
Synaptic exocytosis of dense-core vesicles in blue crab ( Callinectes sapidus ) stomach muscles
Patel, V., & Govind, C. K. (1997) · Cell and Tissue Research · doi:10.1007/s004410050897 · Cited by 8 · see citing works
Klett, N. J., Cravetchi, O., & Allen, C. N. (2022) · Journal of Biological Rhythms · doi:10.1177/07487304211059770 · Cited by 7 · see citing works
Extensive soma‐soma plate‐like contact sites (ephapses) connect suprachiasmatic nucleus neurons
Czeisler, M. É., Shan, Y., Schalek, R. L., Berger, D. R., Suissa‐Peleg, A., Takahashi, J. S., & Lichtman, J. W. (2024) · The Journal of Comparative Neurology · doi:10.1002/cne.25624 · Cited by 6 · see citing works
Wu, M., Kc, P., Mack, S. O., & Haxhiu, M. A. (2005) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2005.07.002 · Cited by 6 · see citing works
Zhang, X., Leng, G., & Feng, J. (2010) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2010.01.003 · Cited by 5 · see citing works
Fujioka, A., Nagano, M., Ikegami, K., Masumoto, K., Yoshikawa, T., Koinuma, S., Nakahama, K., & Shigeyoshi, Y. (2022) · Brain Research · doi:10.1016/j.brainres.2022.148129 · Cited by 3 · see citing works
Morphological Studies of Dendrites and Dendritic Secretion
Morris, J. F. (2007) · Springer eBooks · doi:10.1007/0-387-23696-1_2 · Cited by 3 · see citing works
Self-citationPeptide-Secreting Dendrites: New Controls for Neuroendocrine Neurons
Morris, J. F., Ma, D., Pow, D. V., Wang, H., & Ward, A. (1997) · Springer eBooks · doi:10.1007/978-3-642-60915-2_6 · Cited by 3 · see citing works
Self-citationInyushkin, A. N., Tkacheva, M. А., Karyan, S. D., & Михайловна, И. Е. (2018) · Izvestiya of Saratov University Chemistry Biology Ecology · doi:10.18500/1816-9775-2018-18-1-86-90
- Authors
- Castel, M., Morris, J., & Belenky, M.
- Affiliations
- University of Oxford (GB)
- Hebrew University of Jerusalem (IL)
- ORCID
- Morris, John
- Venue
- NeuroReport
- Published
- 1996-01
- Volume
- 7
- Issue
- 2
- Pages
- 543-547
- ISSN
- 0959-4965 (ISSN-L)
- OpenAlex
- W1977561781
- Cited by
- 61
- References
- 0
- Citations by year
- 2024: 1 · 2023: 1 · 2022: 2 · 2020: 2 · 2019: 1 · 2018: 5 · 2017: 2 · 2016: 4 · 2015: 3 · 2014: 3 · 2013: 2 · 2012: 1
- FWCI
- 1.20
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroreport (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Keywords
- suprachiasmatic nucleus, dense core vesicles, exocytosis, dendritic release, axonal terminals, neuromodulation, tannic acid, ultrastructure, neurosecretion
- MeSH terms
- Animals, Dendrites, Exocytosis, Extracellular Space, Male, Microscopy, Electron, Suprachiasmatic Nucleus, Synapses, Presynaptic Terminals, Rats, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review