Cited by 336Neuroendocrine regulation and behaviorNeuropeptides and Animal PhysiologyPain Mechanisms and Treatments

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The distribution of oxytocin‐ and neurophysin‐stained fibers in the spinal cord of the rat and monkey

Swanson, L. W., McKellar, S.·1979·Journal of Comparative Neurology

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Abstract

Immunohistochemical methods have been used to describe the distribution of neurophysin I‐ and oxytocin‐stained fibers in the spinal cord. In albino rats of either sex, such fibers descend through the dorsal part of the lateral funiculus to the caudal end of the cord. Fibers leave the lateral funiculus to innervate the marginal zone of the dorsal horn at all levels, and the intermediolateral column at thoracic, lumbar and sacral levels. Some fibers course medially through the intermediate gray to end in the central gray, which is innervated at all levels, and also appears to be innervated by fibers descending in the central gray itself. A semiquantitative analysis shows that the density of terminal fields in the intermediolateral column, marginal zone, and central gray varies significantly at different levels. The intermediolateral column is preferentially innervated between T 1 ‐T 3 , T 9 ‐T 11 , and T 13 ‐L 2 . The nucleus intercalatus spinalis and the dorsal commissural nucleus (between T 13 and L 2 ), both of which contain preganglionic neurons, are densely innervated. In the monkey ( Macaca fascicularis ), neurophysin I‐ and oxytocin‐stained fibers descend through the lateral funiculus to the filum terminale, where some of them enter the pia‐arachnoid surrounding the filum. The intermediolateral column is not innervated between T 1 ‐T 3 , is sparsely innervated at sacral levels, and is moderately innervated between T 4 and L 3 ; the greatest density of fibers occurs at L 3 . At most levels, few if any fibers are found in the central gray and marginal zone; the central gray is sparsely innervated between T 8 and L 2 , at S 2 , and between Co 3 ‐Co 6 , and the marginal zone contains a small number of fibers in the region of S 2 and Co 6 . Neurophysin I‐ and oxytocin‐stained fibers were also found in the intermediolateral column, marginal zone, and central gray of homozygous Brattleboro, spontaneously hypertensive, and Egyptian sand rats. The results suggest that the paraventriculo‐spinal pathway is particularly related to specific groups of sympathetic and parasympathetic preganglionic neurons, and to the marginal zone, which is involved in the relay of ascending nociceptive information through the spinothalamic tract.

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Ricardo, J. A., & Koh, E. T. (1978) · Brain Research · doi:10.1016/0006-8993(78)91125-3 · Cited by 1,362
A cytoarchitectonic atlas of the spinal coed in the cat
Rexed, B. (1954) · The Journal of Comparative Neurology · doi:10.1002/cne.901000205 · Cited by 1,258
Direct hypothalamo-autonomic connections
Saper, C. B., Loewy, A. D., Swanson, L. W., & Cowan, W. M. (1976) · Brain Research · doi:10.1016/0006-8993(76)90738-1 · Cited by 1,199
Self-citation
The connections of the septal region in the rat
Swanson, L. W., & Cowan, W. M. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901860408 · Cited by 1,136
Self-citation
Croonian Lecture - The antidiuretic hormone and the factors which determine its release
Verney, E. B. (1947) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1947.0037 · Cited by 1,099
Intra- and extrahypothalamic vasopressin and oxytocin pathways in the rat
Buijs, R. M., Swaab, D. F., Dogterom, J., & van Leeuwen, F. W. (1978) · Cell and Tissue Research · doi:10.1007/bf00224932 · Cited by 1,029
HIPPOCAMPAL PROJECTIONS AND RELATED NEURAL PATHWAYS TO THE MID-BRAIN IN THE CAT
Nauta, W. J. H. (1958) · Brain · doi:10.1093/brain/81.3.319 · Cited by 990
Ascending projections of the locus coeruleus in the rat. II. Autoradiographic study
Jones, B. E., & Moore, R. Y. (1977) · Brain Research · doi:10.1016/0006-8993(77)90378-x · Cited by 865
Intra- and extrahypothalamic vasopressin and oxytocin pathways in the rat
Buijs, R. M. (1978) · Cell and Tissue Research · doi:10.1007/bf00212323 · Cited by 830
Efferents from medial basal forebrain and hypothalamus in the rat. II. An autoradiographic study of the anterior hypothalamus
Conrad, L. C. A., & Pfaff, D. W. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901690206 · Cited by 633

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Research works printed but not linked: 9

Barry J., 1954, De l'existence de voies neurosécrétoires hypothalamo‐télencéphalique chez la chauve souris (Rhinolophus ferrum equinum) en état d'hibernation, Bull. Soc. Sci. Nancy, 13, 126
Barry J., 1956, Les voies extra‐hypophysaires de la neurosécrétion diencephalique, Bull. Ass. Anat., 89, 264
Barry J., 1961, Recherches morphlogiques et expérimentales sur la glande diencephalique et l'appariel hypothalamo‐hypophysaire, Ann. Sci. Univ. Besancon. Zool. Physiol. Sci., 2, 3
Ciriello J., 1978, Paraventricular and supraoptic hypothalamic nuclei: What are their roles in central regulation of heart rate?, Soc. Neurosci. Abs., 4, 18
Legait H., 1956, Les voies efférentes des noyaux neurosécrétoires hypothalamiques chez les oiseaux, C.R. Soc. Biol., 150, 996
Nilaver G., 1978, Oxytocin‐neurophysin pathways to the lower brainstem and spinal cord of the rat, Soc. Neurosci. Abs., 4, 351
Smith O. A., 1965, Nervous Control of the Heart, 34
Swanson L. W., 1978, Extra‐hypophysial oxytocin‐containing pathways in the brain and spinal cord of the rat and monkey, Soc. Neurosci. Abst., 4, 415
Waibl H., 1973, Zur topographic der Medulla spinalis der Albinoratte (Rattus norvegicus), Adv. Anat. Embryol. Cell Biol., 47, 1

Sorted by citations

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Petty, M. A., Lang, R. E., Unger, T., & Ganten, D. (1985) · European Journal of Pharmacology · doi:10.1016/0014-2999(85)90497-2 · Cited by 65
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Kita, I., Yoshida, Y., & Nishino, S. (2006) · Neuroscience Research · doi:10.1016/j.neures.2005.12.005 · Cited by 55
Hypothalamus
Saper, C. B. (1990) · Elsevier eBooks · doi:10.1016/b978-0-12-547625-6.50020-9 · Cited by 53
Immunohistochemical evidence for cholecystokinin-like peptides in neuronal cell bodies of the rat spinal cord
Vanderhaeghen, J., Deschepper, C. F., Lotstra, F., Vierendeels, G., & Schoenen, J. E. (1982) · Cell and Tissue Research · doi:10.1007/bf01258503 · Cited by 52
Oxytocin acts at V1 receptors to excite sympathetic preganglionic neurones in neonate rat spinal cord in vitro
Sermasi, E., & Coote, J. H. (1994) · Brain Research · doi:10.1016/0006-8993(94)91331-5 · Cited by 51
Neuroanatomical Pathways Related to Vasopressin
Weindl, A., & Sofroniew, M. V. (1985) · Current topics in neuroendocrinology · doi:10.1007/978-3-642-68493-7_5 · Cited by 51
Biochemical and electrophysiological evidence of functional vasopressin receptors in the rat superior cervical ganglion.
Kiraly, M., Audigier, S., Tribollet, E., Barberis, C., Dolivo, M., & Dreifuss, J.-J. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.14.5335 · Cited by 50
Distribution and identity of neurons expressing the oxytocin receptor in the mouse spinal cord
Wrobel, L. J., Schorscher-Petcu, A., Dupré, A., Yoshida, M., Nishimori, K., & Tribollet, E. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.03.033 · Cited by 49
Role of paraventricular nucleus (PVH) in baroreflex-mediated changes in lumbar sympathetic nerve activity and heart rate
Patel, K. P., & Schmid, P. G. (1988) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(88)90109-9 · Cited by 49
Noradrenergic axon terminals in the substantia gelatinosa of the rat spinal cord
Satoh, K., Kashiba, A., Kimura, H., & Maeda, T. (1982) · Cell and Tissue Research · doi:10.1007/bf00213218 · Cited by 49
The distribution of thyrotropin-releasing hormone (TRH) in the Rhesus monkey spinal cord
Lechan, R. M., Snapper, S. B., Jacobson, S., & JACKSON, I. M. D. (1984) · Peptides · doi:10.1016/0196-9781(84)90276-6 · Cited by 48
Kainic acid lesions of paraventricular nucleus neurons reverse the elevated arterial pressure after aortic baroreceptor denervation in the rat
Zhang, T., & Ciriello, J. (1985) · Brain Research · doi:10.1016/0006-8993(85)90979-5 · Cited by 47
Branched oxytocinergic innervations from the paraventricular hypothalamic nuclei to superficial layers in the spinal cord
Condés‐Lara, M., Martı́nez-Lorenzana, G., Rojas‐Piloni, G., & Rodríguez-Jiménez, J. (2007) · Brain Research · doi:10.1016/j.brainres.2007.05.031 · Cited by 44
Oxytocinergic innervation to the upper thoracic sympathetic preganglionic neurons in the rat
Hosoya, Y., Matsukawa, M., Okado, N., Sugiura, Y., & Kohno, K. (1995) · Experimental Brain Research · doi:10.1007/bf00228011 · Cited by 44
Direct Link From the Suprachiasmatic Nucleus to Hypothalamic Neurons Projecting to the Spinal Cord: A Combined Tracing Study Using Cholera Toxin Subunit B and Phaseolus vulgaris-Leucoagglutinin
Vrang, N., Mikkelsen, J. D., & Larsen, P. J. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00138-x · Cited by 44
Expression of c-fos protein in lumbosacral spinal cord in response to vaginocervical stimulation in rats
Chinapen, S., Swann, J. M., Steinman, J. L., & Komisaruk, B. R. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90211-o · Cited by 44
Effect of paraventricular nucleus lesions on arterial pressure and heart rate after aortic baroreceptor denervation in the rat
Zhang, T., & Ciriello, J. (1985) · Brain Research · doi:10.1016/0006-8993(85)91477-5 · Cited by 44
The intermediolateral nucleus: an ‘open’ or ‘closed’ nucleus?
Vera, P. L., Ellenberger, H. H., Haselton, J. R., Haselton, C. L., & Schneiderman, N. (1986) · Brain Research · doi:10.1016/0006-8993(86)90144-7 · Cited by 44
Oxytocin, but not vassopressin, modulates nociceptive responses in dorsal horn neurons
Rojas‐Piloni, G., Mejía-Rodríguez, R., Martı́nez-Lorenzana, G., & Condés‐Lara, M. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.03.076 · Cited by 43
Paraventricular nucleus of the hypothalamus: an electrophysiological investigation of neurons projecting directly to intermediolateral nucleus in the cat
Caverson, M. M., Ciriello, J., & Calaresu, F. R. (1984) · Brain Research · doi:10.1016/0006-8993(84)90447-5 · Cited by 43
Oxytocin administered intrathecally preferentially increases heart rate rather than arterial pressure in the rat
Yashpal, K., Gauthier, S. G., & Henry, J. L. (1987) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(87)90114-7 · Cited by 42
Synaptic structure of the monoamine and peptide nerve terminals in the intermediolateral nucleus of the guinea pig thoracic spinal cord
Chiba, T., & Masuko, S. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902620206 · Cited by 42
Paraventricular hypothalamic oxytocinergic cells responding to noxious stimulation and projecting to the spinal dorsal horn represent a homeostatic analgesic mechanism
Condés‐Lara, M., Rojas‐Piloni, G., Martı́nez-Lorenzana, G., & Rodríguez‐Jiménez, J. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06899.x · Cited by 41
Evidence for a direct projection from the paraventricular nucleus of the hypothalamus to putative serotoninergic neurons of the nucleus paragigantocellularis involved in the control of erection in rats
Bancila, M., Giuliano, F., Rampin, O., Mailly, P., Brisorgueil, M., Calas, A., & Vergé, D. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02184.x · Cited by 38
An electrophysiological analysis of caudally-projecting neurones from the hypothalamic paraventricular nucleus in the rat
Zerihun, L., & Harris, M. C. (1983) · Brain Research · doi:10.1016/0006-8993(83)91278-7 · Cited by 41
Oxytocin and mothering behavior in the rat
Pedersen, C. A., & Prange, A. J. (1985) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(85)90056-7 · Cited by 40
Cytoarchitecture of the Spinal Cord
Heise, C. E., & Kayalıoğlu, G. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374247-6.50010-9 · Cited by 40
Lamina x of primate spinal cord: Distribution of five neuropeptides and serotonin
LaMotte, C. C. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90265-5 · Cited by 40
Peptide neuroregulators in invertebrates
HAYNES, L. (1980) · Progress in Neurobiology · doi:10.1016/0301-0082(80)90023-4 · Cited by 40
Neural mechanisms of female sexual behavior in the rat; comparison with male ejaculatory control
Veening, J. G., Coolen, L. M., & Gerrits, P. O. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.11.025 · Cited by 38
Hypothalamic paraventricular axons projecting to the female rat lumbosacral spinal cord contain oxytocin immunoreactivity
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Peptidergic Activation of Locomotor Pattern Generators in the Neonatal Spinal Cord
Pearson, S. A., Mouihate, A., Pittman, Q. J., & Whelan, P. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-31-10154.2003 · Cited by 39
Electrophysiological identification of neurones of paraventricular nucleus sending axons to both the neurohypophysis and the medulla in the rat
Zerihun, L., & Harris, M. C. (1981) · Neuroscience Letters · doi:10.1016/0304-3940(81)90033-1 · Cited by 37
Cardiac sympatho-excitatory action of PVN-spinal oxytocin neurones
Yang, Z. R., Han, D., & Coote, J. H. (2009) · Autonomic Neuroscience · doi:10.1016/j.autneu.2009.01.013 · Cited by 37
Nerve cells immunoreactive for p62 in select hypothalamic and brainstem nuclei of controls and Parkinson’s disease cases
Braak, H., Thal, D. R., & Tredici, K. D. (2010) · Journal of Neural Transmission · doi:10.1007/s00702-010-0508-2 · Cited by 36
Pro-ejaculatory effect of the aqueous crude extract of cihuapatli (Montanoa tomentosa) in spinal male rats
Carro-Juárez, M., Lobatón, I., Benítez, O., & Espíritu, A. (2006) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2005.12.011 · Cited by 36
Dehydration-anorexia derives from a reduction in meal size, but not meal number
Boyle, C. N., Lorenzen, S. M., Compton, D. S., & Watts, A. G. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.08.005 · Cited by 34
Distribution of angiotensin II receptor binding in the spinal cord of the sheep
Oldfield, B. J., Allen, A. M., Hards, D. K., McKinley, M. J., Schlawe, I., & Mendelsohn, F. A. O. (1994) · Brain Research · doi:10.1016/0006-8993(94)90204-6 · Cited by 34
Chapter 10 Neuropeptides in spinal cord
Tohyama, M., & Shiotani, Y. (1986) · Progress in brain research · doi:10.1016/s0079-6123(08)64605-1 · Cited by 34
Fluorescent Visualisation of Oxytocin in the Hypothalamo‐neurohypophysial/‐spinal Pathways After Chronic Inflammation in Oxytocin‐Monomeric Red Fluorescent Protein 1 Transgenic Rats
Matsuura, T., Kawasaki, M., Hashimoto, H., Ishikura, T., Yoshimura, M., Ohkubo, J., Maruyama, T., Motojima, Y., Sabanai, K., Mori, T., et al. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12290 · Cited by 33
The Effect of Oxytocin on the Contractile Force of Human Atrial Trabeculae
Rosaeg, O. P., Cicutti, N. J., & Labow, R. S. (1998) · Anesthesia & Analgesia · doi:10.1097/00000539-199801000-00008 · Cited by 33
Possible Involvement of the Rat Hypothalamo‐Neurohypophysial/‐Spinal Oxytocinergic Pathways in Acute Nociceptive Responses
Matsuura, T., Kawasaki, M., Hashimoto, H., Yoshimura, M., Motojima, Y., Saito, R., Ueno, H., Maruyama, T., Ishikura, T., Sabanai, K., et al. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12396 · Cited by 32
Electrophysiological evidence for oxytocin receptors on sympathetic preganglionic neurones — an in vitro study on the neonatal rat
Desaulles, E., Reiter, M. K., & FELTZ, P. (1995) · Brain Research · doi:10.1016/0006-8993(95)01019-r · Cited by 31
Coincidence of ?ladder-like patterns? in distributions of monoaminergic terminals and sympathetic preganglionic neurons in the rat spinal cord
Hosoya, Y., Okado, N., Kohno, K., & Sugiura, Y. (1991) · Experimental Brain Research · doi:10.1007/bf00231058 · Cited by 31
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Godley, F. A., Meitzen, J., Nahman‐Averbuch, H., O’Neal, M. A., Yeomans, D. C., Santoro, N. F., Riggins, N., & Edvinsson, L. I. (2024) · Journal of Personalized Medicine · doi:10.3390/jpm14020184 · Cited by 30
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García-Boll, E., Martı́nez-Lorenzana, G., Condés‐Lara, M., & González‐Hernández, A. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.11.031 · Cited by 30
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Meidahl, A. C., Eisenried, A., Klukinov, M., Cao, L., Tzabazis, A., & Yeomans, D. C. (2017) · Headache The Journal of Head and Face Pain · doi:10.1111/head.13248 · Cited by 30
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Rojas‐Piloni, G., Martı́nez-Lorenzana, G., DelaTorre, S., & Condés‐Lara, M. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06366.x · Cited by 29
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Aramant, R. B., GIRONJR, L., & ZIEGLER, M. (1986) · Brain Research · doi:10.1016/s0006-8993(86)80224-4 · Cited by 29
Spinal Cord
Şengül, G., & WATSON, C. R. R. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-369497-3.10013-5 · Cited by 28
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Kubo, T., Hagiwara, Y., Sekiya, D., Chiba, S., & Fukumori, R. (2000) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00343-9 · Cited by 28
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Dubois‐Dauphin, M., & Zakarian, S. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90046-7 · Cited by 28
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Lenz, K. M., & Sengelaub, D. R. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.07.010 · Cited by 29
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Teclemariam‐Mesbah, R., Kalsbeek, A., Buijs, R. M., & Pévet, P. (1997) · Cell and Tissue Research · doi:10.1007/s004410050772 · Cited by 27
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Rønnekleiv, O. K. (1988) · Journal of Pineal Research · doi:10.1111/j.1600-079x.1988.tb00652.x · Cited by 27
Oxytocin and [1-deamino, 8-d-arginine]-vasopressin (dDAVP): intrathecal effects on blood pressure, heart rate and urine output
Riphagen, C. L., & Pittman, Q. J. (1986) · Brain Research · doi:10.1016/0006-8993(86)90432-4 · Cited by 27
Postnatal development of dopamine-β-hydroxylase-immunoreactive fibers of the spinal cord of the rat
Aramant, R. B., Giron, L. T., & Ziegler, M. G. (1986) · Developmental Brain Research · doi:10.1016/0165-3806(86)90205-1 · Cited by 27
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Fuxé, K., Ganten, D., Anderson, K., Calzà, L., Agnati, L. F., Lang, R. E., Poulsen, K., Hökfelt, T. G. M., & Bernardi, P. (1982) · Experimental brain research. Supplementum · doi:10.1007/978-3-642-46456-0_15 · Cited by 27
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Buijs, R. M. (1990) · Springer eBooks · doi:10.1007/978-3-7091-9062-3_10 · Cited by 26
Topography of chemically identified neurons in the central nervous system: progress in 1981–1983
Palkovits, M. (1984) · Elsevier eBooks · doi:10.1016/b978-0-444-90377-8.50005-3 · Cited by 26

Authors: Swanson, L. W., & McKellar, S.
Affiliations: Washington University in St. Louis (US)
ORCID: Swanson, L. W.
Venue: Journal of Comparative Neurology
Publisher: Wiley
Published: 1979-11
Volume: 188
Issue: 1
Pages: 87-106
ISSN: 0021-9967 (ISSN-L)
1096-9861
DOI: 10.1002/cne.901880108
OpenAlex: W2088007298
Cited by: 336
References: 51
Citations by year: 2026: 3 · 2025: 1 · 2024: 1 · 2023: 3 · 2022: 5 · 2021: 3 · 2020: 3 · 2019: 2 · 2018: 6 · 2017: 5 · 2016: 5 · 2015: 4 · 2014: 8 · 2013: 9 · 2012: 6
FWCI: 24.28
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 9109 d)
Locations: The Journal of Comparative Neurology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Health Sciences › Medicine › Physiology (medical) › Pain Mechanisms and Treatments
Keywords: oxytocin, neurophysin I, spinal cord, intermediolateral cell column, periaqueductal gray, marginal zone, lateral funiculus, preganglionic neurons, sympathetic innervation, parasympathetic innervation, filum terminale, spinothalamic tract, nociception, Brattleboro rats, spontaneously hypertensive rats, rats, monkeys
MeSH terms: Animals, Haplorhini, Arachnoid, Autonomic Fibers, Preganglionic, Cauda Equina, Efferent Pathways, Female, Fluorescent Antibody Technique, Ganglia, Parasympathetic, Ganglia, Sympathetic, Macaca fascicularis, Male, Neurophysins, Oxytocin, Paraventricular Hypothalamic Nucleus, Pia Mater, Species Specificity, Spinal Cord, Rats

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The distribution of oxytocin‐ and neurophysin‐stained fibers in the spinal cord of the rat and monkey

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