The DOI matches its Crossref record.
Rat oxytocin receptor in brain, pituitary, mammary gland, and uterus: partial sequence and immunocytochemical localization.
Abstract
Partial complementary DNAs of an oxytocin (OT) receptor were cloned from rat brain and uterus. The complementary DNAs encoded for the same amino acid sequence, which showed a high degree of homology with the human and porcine uterine OT receptors, except for a region in the third intracellular loop. Antibodies were raised against nonoverlapping sequences of the third intracellular loop of this rat OT receptor. Using these antisera, OT receptor expression was demonstrated in the brain, pituitary, mammary gland, and uterus by immunocytochemistry. In the brain, several areas including the ventromedial hypothalamus, the bed nucleus of the stria terminalis, the ventral pallidum, the paraventricular nucleus, and the dorsal part of the supraoptic nucleus, demonstrated OT-receptor immunoreactivity. However, no immunoreactivity was detected in two areas of the brain known to contain dense OT-binding sites by receptor autoradiography studies: the ventral hippocampus and the central nucleus of the amygdala. In the pituitary, both the anterior and posterior lobes were positive for OT receptor immunoreactivity, whereas the intermediate lobe was negative. These results demonstrate that the same receptor type is expressed in both peripheral OT target tissues and the brain, and also suggest the possibility that a different OT receptor subtype may be present in some areas of the brain.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Seminal animal work using histochemistry and immunohistochemistry revealed high concentrations of OXTR mRNA in the hypothalamus, amygdala, olfactory bulb, ventral pallidum, and the dorsal vagal nucleus in rodents7,8.”
From Oxytocin pathway gene networks in the human brain (2019) · cites this paper as [8]
Citations
Cited by
Sorted by citations
Items 101–143 of 143
Grieb, Z. A., & Lonstein, J. S. (2021) · Journal of Neuroendocrinology · doi:10.1111/jne.12926 · Cited by 12
Oxytocin regulation of maternal behavior
Pedersen, C. A. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139017855.012 · Cited by 11
Jin, H. S., Umemura, S., Iwasaka, T., et al. (2000) · Pathology International · doi:10.1046/j.1440-1827.2000.01064.x · Cited by 11
Effect of oxytocin on growth hormone release in vitro
Hulting, A., Grenbäck, E., Pineda, J., Coya, R., Hökfelt, T. G. M., Meister, B., & Uvnäs‐Moberg, K. (1996) · Regulatory Peptides · doi:10.1016/s0167-0115(96)00112-7 · Cited by 11
Endogenous oxytocin excites phasic contraction of gallbladder in rabbits through oxytocin receptor.
Liu, C., Liu, J.-Z., Xie, D., Liu, P., & Wang, P. S. (2003) · PubMed · Cited by 11
Młynarczyk, M., Imamura, T., Umezaki, H., et al. (2003) · Biology of Reproduction · doi:10.1095/biolreprod.103.018556 · Cited by 11
Mirnaghizadeh, S. V., Zendehdel, M., & Babapour, V. (2016) · Veterinary Research Communications · doi:10.1007/s11259-016-9672-7 · Cited by 9
Comprehensive gene expression analyses of the rat prefrontal cortex after oxysterol treatment
Loke, S. Y., Tanaka, K., & Ong, W. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12142 · Cited by 9
Vasopressin and oxytocin receptors (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database
Bichet, D. G., Bouvier, M., Chini, B., Gimpl, G., Guillon, G., Kimura, T., Knepper, M. A., Lolait, S. J., Manning, M., Mouillac, B., et al. (2019) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f66/2019.4 · Cited by 8
Self-citationSchoots, O., Hernando, F., Knoers, N. V. A. M., & Burbach, J. P. H. (1999) · Results and problems in cell differentiation · doi:10.1007/978-3-540-49421-8_6 · Cited by 8
Self-citationTranscriptional Regulation of the Oxytocin Receptor Gene
Bale, T. L., & Dorsa, D. M. (1998) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4871-3_38 · Cited by 7
Morel, G., Péchoux, C., Raccurt, M., & Zingg, H. H. (2001) · Cell and Tissue Research · doi:10.1007/s004410100382 · Cited by 7
Neuropeptides affecting social behavior in mammals: Oxytocin
Zhou, H., Zhu, R., Xia, Y., Zhang, X., Wang, Z., Lorimer, G. H., Ghiladi, R. A., Bayram, H., & Wang, J. (2024) · Peptides · doi:10.1016/j.peptides.2024.171223 · Cited by 6
Górski, K., Hasiec, M., Zielińska-Górska, M. K., Fülöp, F., & Misztal, T. (2017) · Czech Journal of Animal Science · doi:10.17221/30/2016-cjas · Cited by 6
Zingg, H. H. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50059-7 · Cited by 6
Kheradkhah, G., Sheibani, M., Kianfar, T., Toreyhi, Z., & Azizi, Y. (2024) · Cardio-Oncology · doi:10.1186/s40959-024-00293-3 · Cited by 5
DelaCuesta-Barrutia, J., Hidema, S., Caldwell, H. K., Nishimori, K., Erdozain, A. M., & Peñagarikano, O. (2024) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2024.03.028 · Cited by 4
Correlation of Histamine Receptors and Adrenergic Receptor in Broilers Appetite.
Daneshvar, M. S., Zendehdel, M., Vazir, B., et al. (2022) · PubMed · doi:10.22092/ari.2021.354450.1638 · Cited by 4
Sun, L.-H., Tzeng, W.-Y., Liao, Y., Deng, W.-T., Cherng, C. G., & Yu, L. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05290-4 · Cited by 4
Neuroendocrinology, Neurochemistry, and Molecular Neurobiology of Affiliative Behavior
Hammock, E. A. D., & Young, L. J. (2006) · Springer eBooks · doi:10.1007/978-0-387-30405-2_6 · Cited by 4
Endocrine Regulation of Maternal Behavior Postpartum
Williams, G. L. (1998) · Humana Press eBooks · doi:10.1007/978-1-4612-1804-3_20 · Cited by 3
Vecsernyés, M., Nagy, G. G., Mészáros, L., et al. (2000) · Endocrine Research · doi:10.3109/07435800009066171 · Cited by 3
Peptide-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
Single transcript level atlas of oxytocin and the oxytocin receptor in the mouse brain
Ryu, V., Gumerova, A. A., Pevnev, G., Korkmaz, F., Kannangara, H. S., Cullen, L., Sultana, F., Witztum, R., Sims, S. L., Frolinger, T., et al. (2026) · eLife · doi:10.7554/elife.95215 · Cited by 2
The Perinatal Application of Oxytocin and Its Possible Influence on the Human Psyche
Plothe, C. (2009) · Cited by 2
Sanna, F., Bratzu, J., Angioni, L., Sorighe, M. P., Cocco, C., Argiolas, A., & Melis, M. R. (2021) · Brain Research · doi:10.1016/j.brainres.2021.147705 · Cited by 2
Yu, X., Chen, Y., Zhao, M., Zhang, X., Ye, Y., Fei, W., Kong, M., Tang, M., Sun, D., & Zheng, C. (2024) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2024.106379 · Cited by 1
Regulation of oxytocin and vasopressin secretion
Higashida, H., Lopatina, O. L., & Amina, S. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139017855.005 · Cited by 1
Investigation of the oxytocin receptor gene in sheep
Feng, H. C. (2000) · Victoria University Research Repository (Victoria University) · Cited by 1
Star, B. (2005) · University Library - University of Saskatchewan (University of Saskatchewan) · Cited by 1
Hoyda, T. D. (2010) · QSpace (Queen's University Library) · Cited by 1
Oxytocin, Aggression, and Neural Activity in the Naked Mole-rat
Hathaway, G. A. (2014) · TSpace (University of Toronto) · Cited by 1
Bochini, J. C. (2008) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.10.2008.tde-18112008-153251
Characterization of short-term synaptic plasticity at excitatory synapses to the supraoptic nucleus
Quinlan, M. E. (2006) · Memorial University Research Repository (Memorial University)
REVIEW Sex, parturition and motherhood without oxytocin?
Russell, J. A., & Leng, G. (2015)
Neumann, I. D., Torner, L., Toschi, N., Veenema, A. H., Inga, D., Torner, L., Toschi, N., & Veen, A. H. (2006)
***To be considered for inclusion in the 'World Congress on Neurohypophysial Hormones Special
Grundwald, N. J., Benítez, D. P., & Brunton, P. J. (2015)
Ultrasound imaging of anatomy and milk ejection in the human lactating breast
Geddes, D. T. (2004) · UWA Profiles and Research Repository (University of Western Australia)
Pharmacological Characterisation of Novel Oxytocin and Vasopressin Receptor Ligands
Gulliver, D. W. (2021) · The Sydney eScholarship Repository (The University of Sydney)
Conséquences pharmacologiques et fonctionnelles de l'hétérodimérisation des récepteurs V1B et CRF1
Mion, J. (2013) · theses.fr (ABES) · doi:10.70675/91d47531z8447z44d1z9f7ezf39a8e060318
The oxytocinergic descending control of pain and its modulation by neonatal maternal separation
Melchior, M. (2018) · theses.fr (ABES) · doi:10.70675/368c73c0ze731z4b57zb52cz8f31049fb33c
Metadata
- Authors
- Adan, R. A., Van Leeuwen, F. W., Sonnemans, M. A., Brouns, M., Hoffman, G., Verbalis, J. G., & Burbach, J. P.
- Affiliations
- Utrecht University (NL)
- Venue
- Endocrinology
- Publisher
- The Endocrine Society
- Published
- 1995-09
- Volume
- 136
- Issue
- 9
- Pages
- 4022-4028
- ISSN
- 0013-7227 (ISSN-L)
- 1945-7170
- OpenAlex
- W1969541181
- Cited by
- 147
- References
- 0
- Citations by year
- 2026: 1 · 2024: 5 · 2023: 2 · 2022: 3 · 2021: 5 · 2020: 5 · 2019: 4 · 2018: 7 · 2017: 5 · 2016: 8 · 2015: 7 · 2014: 5 · 2013: 8 · 2012: 2
- FWCI
- 13.50
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrinology (publishedVersion)
- PubMed (publishedVersion)
- VU Research Portal (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- 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 › Reproductive Medicine › Hypothalamic control of reproductive hormones
- Keywords
- oxytocin receptor, rats, cDNA cloning, third intracellular loop, receptor homology, immunocytochemical localization, brain, pituitary gland, mammary gland, uterus, hypothalamus, bed nucleus of the stria terminalis, paraventricular nucleus, supraoptic nucleus, receptor subtypes
- MeSH terms
- Amino Acid Sequence, Amygdalin, Animals, Base Sequence, Brain Chemistry, Female, Hippocampus, Immune Sera, Immunohistochemistry, Mammary Glands, Animal, Molecular Sequence Data, Oligonucleotides, Paraventricular Hypothalamic Nucleus, Pituitary Gland, Supraoptic Nucleus, Uterus, Ventromedial Hypothalamic Nucleus, Polymerase Chain Reaction, Sequence Homology, Amino Acid, Receptors, Oxytocin, DNA, Complementary, Rats
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