Up-regulation of vasopressin and angiotensin II receptors in the thalamus and brainstem of inbred polydipsic mice
Abstract
Vasopressin (AVP), angiotensin II (Ang II) and oxytocin (OT) receptors were mapped in the brain of inbred polydipsic mice of the STR/N strain by quantitative in vitro autoradiography and receptor binding levels, compared with those found in control non-polydipsic mice of the ICR strain. A remarkable difference was evidenced in the thalamic paraventricular nucleus where AVP receptor binding was 7- to 10-fold higher in polydipsic mice than in control mice. Another disparity was observed in the hypothalamic paraventricular nucleus, which contained AVP binding sites in the control mice, but was unlabelled in the polydipsic animals. Ang II receptor binding was reduced in the hypothalamic paraventricular nucleus of the polydipsic mice, whereas it was abundant in the brainstem region, encompassing area postrema and the nucleus of the solitary tract. The distribution and amount of OT receptor binding were similar in the polydipsic and control mice. Strain-related differences of AVP and Ang II receptor binding were observed both in male and female animals. A sex-related difference was seen only for OT receptor binding in the hypothalamic ventromedial nucleus, where labelling was less intense in males than in females of both strains. Altogether, our results support the view that central AVP and Ang II systems are involved in the mechanisms responsible for polydipsia in STR/N mice.
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ICR mice showed no sex differences in V1aR binding in all regions analyzed.
“In ICR mice, using the 125I linear V1aR antagonist, males (n=6) and females (n=6) showed a lack of sex differences in all regions analyzed”
From Vasopressin and oxytocin receptor systems in the brain: Sex differences and sex-specific regulation of social behavior (2016) · cites this paper as Tribollet et al., 2002
Other rodent studies that did not find sex differences in OTR binding analyzed only a few brain regions.
“other rodent studies that did not find sex differences in OTR binding analyzed only a few brain regions”
From Vasopressin and oxytocin receptor systems in the brain: Sex differences and sex-specific regulation of social behavior (2016) · cites this paper as Tribollet et al., 2002
Cites
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859 · see citing works
Autoradiographic localization of angiotensin II receptors in rat brain.
Mendelsohn, F. A. O., Quirion, R., Saavedra, J. M., Aguilera, G., & Catt, K. J. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.5.1575 · Cited by 570 · see citing works
Single base deletion in the vasopressin gene is the cause of diabetes insipidus in Brattleboro rats
Schmale, H., & Richter, D. (1984) · Nature · doi:10.1038/308705a0 · Cited by 405 · see citing works
Efferent projections of the paraventricular thalamic nucleus in the rat
Moga, M. M., Weis, R. P., & Moore, R. Y. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903590204 · Cited by 402 · see citing works
Vasopressin and oxytocin receptors in the central nervous system
Tribollet, E., & Barberis, C. (1996) · Critical Reviews™ in Neurobiology · doi:10.1615/critrevneurobiol.v10.i1.60 · Cited by 399 · see citing works
Saper, C. B., & Stornetta, R. L. (2004) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00023-1 · Cited by 321 · see citing works
Vaccari, C., Lolait, S. J., & Ostrowski, N. L. (1998) · Endocrinology · doi:10.1210/endo.139.12.6382 · Cited by 308 · see citing works
Hernando, F., Schoots, O., Lolait, S. J., & Burbach, J. P. H. (2001) · Endocrinology · doi:10.1210/endo.142.4.8067 · Cited by 275 · see citing works
125I-labelled d(CH2)5[Tyr(Me)2,Thr4,Tyr-NH29]OVT: a selective oxytocin receptor ligand
Elands, J., Barberis, C., Jard, S., Tribollet, E., Dreifuss, J.-J., Bankowski, K., Manning, M., & Sawyer, W. H. (1988) · European Journal of Pharmacology · doi:10.1016/0014-2999(88)90778-9 · Cited by 245 · see citing works
Johnson, A. K., Cunningham, J. T., & Thunhorst, R. L. (1996) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.1996.tb02594.x · Cited by 166 · see citing works
Bhatnagar, S., & Dallman, M. F. (1999) · Brain Research · doi:10.1016/s0006-8993(99)02108-3 · Cited by 122 · see citing works
Barberis, C., Balestre, M., Jard, S., Tribollet, E., Arsenijévic, Y., Dreifuss, J. J., Bańkowski, K., Manning, M., Chan, W. Y., Schlosser, S. S., et al. (2008) · Neuroendocrinology · doi:10.1159/000126998 · Cited by 95 · see citing works
Verbalis, J. G., Blackburn, R. E., Hoffman, G. E., & Stricker, E. M. (1995) · PubMed · Cited by 85 · see citing works
Jöhren, O., Imboden, H., Häuser, W., Maye, I., Sanvitto, G. L., & Saavedra, J. M. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00220-5 · Cited by 84 · see citing works
Characterization and distribution of angiotensin II receptor subtypes in the mouse brain
Häuser, W., Jöhren, O., & Saavedra, J. M. (1998) · European Journal of Pharmacology · doi:10.1016/s0014-2999(98)00134-4 · Cited by 75 · see citing works
Primary Polydipsia and Hydronephrosis in an Inbred Strain of Mice.
Silverstein, E., Sokoloff, L., Mickelsen, O., & Jay, G. E. (1961) · PubMed Central · Cited by 69 · see citing works
Novak, C. M., Harris, J. A., Smale, L., & Núñez, A. A. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02572-5 · Cited by 59 · see citing works
Dubois-Dauphin, M., Barberis, C., & de Bilbao, F. (1996) · Brain Research · doi:10.1016/s0006-8993(96)01019-0 · Cited by 57 · see citing works
Angiotensin II type 1 receptor-modulated signaling pathways in neurons
Richards, E. M., Raizada, M. K., Gelband, C. H., & Sumners, C. (1999) · Molecular Neurobiology · doi:10.1007/bf02741376 · Cited by 43 · see citing works
Ueta, Y., Yamashita, H., Kawata, M., & Koizumi, K. (1995) · Brain Research · doi:10.1016/0006-8993(95)00142-d · Cited by 37 · see citing works
Vasopressin- and oxytocin-immunoreactive hypothalamic neurones of inbred polydipsic mice
Ison, A. J., Yuri, K., Ueta, Y., Leng, G., Koizumi, K., Yamashita, H., & Kawata, M. (1993) · Brain Research Bulletin · doi:10.1016/0361-9230(93)90234-3 · Cited by 31 · see citing works
κ-Opioid antagonist strongly attenuates drinking of genetically polydipsic mice
Katafuchi, T., Hattori, Y., Nagatomo, I., & Koizumi, K. (1991) · Brain Research · doi:10.1016/0006-8993(91)91152-q · Cited by 22 · see citing works
Region-specific effect of testosterone on oxytocin receptor binding in the brain of the aged rat
Arsenijévic, Y., & Tribollet, E. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01429-7 · Cited by 20 · see citing works
Sensitivity to angiotensin II of neurons in the circumventricular organs of polydipsic inbred mice
Hattori, Y., & Koizumi, K. (1990) · Brain Research · doi:10.1016/0006-8993(90)90688-8 · Cited by 19 · see citing works
Involvement of angiotensin II in water intake of genetically polydipsic mice
Katafuchi, T., Hattori, Y., Nagatomo, I., Koizumi, K., & Silverstein, E. (1991) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1991.260.6.r1152 · Cited by 16 · see citing works
Effect of Hybridization on the Primary Polydipsic Trait of an Inbred Strain of Mice
Silverstein, E. (1961) · Nature · doi:10.1038/191523a0 · Cited by 15 · see citing works
Increase of vasopressin mRNA in the hypothalamus of inbred polydipsic mice
Nishi, R., Ueta, Y., Serino, R., Nomura, M. J., Yamamoto, Y., Shibuya, I., Koizumi, K., & Yamashita, H. (1999) · Brain Research Bulletin · doi:10.1016/s0361-9230(99)00082-9 · Cited by 8 · see citing works
The Hypothalamic Vasopressinergic Neurons of the Inbred Polydipsic Mouse
Koizumi, K., Zeballos, M., Kawata, M., Kannan, H., & Yamashita, H. (1993) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1993.tb55607.x · Cited by 6 · see citing works
Analysis of the vasopressin system and water regulation in genetically polydipsic mice
Yambe, Y., Watanabe-Tomita, Y., Kakiya, S., Yokoi, H., Nagasaki, H., Arima, H., Murase, T., Yuasa, H., Kondo, K., Yamashita, H., et al. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.278.2.e189 · Cited by 5 · see citing works
Hyperalgesic response to noxious stimulation in genetically polydipsic mice
Kamikawa, H., Katafuchi, T., Hosoi, M., Yamamoto, T., & Hori, T. (1999) · Brain Research · doi:10.1016/s0006-8993(99)02006-5 · Cited by 2 · see citing works
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Dumais, K. M., & Veenema, A. H. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2015.04.003 · Cited by 520 · see citing works
“In ICR mice, using the 125I linear V1aR antagonist, males (n=6) and females (n=6) showed a lack of sex differences in all regions analyzed (subfornical organ, LS, PVN, paraventricular thalamus, mammillary complex, parabrachial nucleus, area postrema-nucleus of the solitary tract, and hypoglossal nucleus; Tribollet et…”
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Schorscher-Petcu, A., Sotocinal, S., Ciura, S., Dupre, A., Ritchie, J., Sorge, R. E., Crawley, J. N., Hu, S.-B., Nishimori, K., Young, L. J., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1594-10.2010 · Cited by 189 · see citing works
Role of vasopressin in the management of septic shock
Mutlu, G., & Factor, P. H. (2004) · Intensive Care Medicine · doi:10.1007/s00134-004-2283-8 · Cited by 178 · see citing works
Schorscher-Petcu, A., Dupré, A., & Tribollet, E. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.06.016 · Cited by 111 · see citing works
Self-citationSexually dimorphic oxytocin receptor-expressing neurons in the preoptic area of the mouse brain
Sharma, K., LeBlanc, R. M., Haque, M., Nishimori, K., Reid, M. M., & Teruyama, R. (2019) · PLoS ONE · doi:10.1371/journal.pone.0219784 · Cited by 63 · see citing works
Smith, C. J. W., DiBenedictis, B. T., & Veenema, A. H. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.02.001 · Cited by 59 · see citing works
Xue, B., Gole, H., Pamidimukkala, J., & Hay, M. (2003) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00793.2002 · Cited by 30 · see citing works
Ford, M. M. (2014) · Alcohol · doi:10.1016/j.alcohol.2014.01.005 · Cited by 25 · see citing works
Dumais, K. M., & Veenema, A. H. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-802114-9.00011-1 · Cited by 11 · see citing works
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Tsumura, K., Li, X., Murdiastuti, K., Parvin, M. N., Akamatsu, T., Yao, C., Kanamori, N., Inenaga, K., Yamashita, H., & Hosoi, K. (2005) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00029.2005 · Cited by 8 · see citing works
Chu, C., Kato, K., Kunitake, T., Watanabe, S., Qiu, D., Ueta, Y., & Kannan, H. (2003) · Brain Research · doi:10.1016/s0006-8993(02)03981-1 · Cited by 3 · see citing works
Freeman, A. R., Arenas, S., Lee, D. N., Singh, B., & Ophir, A. G. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1390203 · Cited by 3 · see citing works
Teruyama, R., & Govar, A. A. (2024) · Peptides · doi:10.1016/j.peptides.2024.171283 · Cited by 1 · see citing works
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Chu, C., Cui, B., Kannan, H., & Qiu, D. (2015) · Physiological Research · doi:10.33549/physiolres.932820 · Cited by 1 · see citing works
Araujo, J. D. C. (2017) · Cited by 1 · see citing works
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Hovey, D. (2018) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Friesen, C. N., Selke, A., Vries, G. J. D., & Petrulis, A. (2026) · Hormones and Behavior · doi:10.1016/j.yhbeh.2026.105931
Weisenseel, Z., & Glasper, E. R. (2026) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2026.101328
Gould, B. R., & Zingg, H. H. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00283-5 · Cited by 138 · see citing works
- Authors
- Tribollet, E., Ueta, Y., Heitz, F., Marguerat, A., Koizumi, K., & Yamashita, H.
- Affiliations
- University of Geneva (CH)
- University of Occupational and Environmental Health Japan (JP)
- State University of New York (US)
- Venue
- Neuroendocrinology
- Publisher
- S. Karger AG
- Published
- 2002
- Volume
- 75
- Issue
- 2
- Pages
- 113-123
- ISSN
- 0028-3835 (ISSN-L)
- 1423-0194
- OpenAlex
- W2047204382
- Cited by
- 20
- References
- 30
- Citations by year
- 2026: 2 · 2024: 2 · 2020: 1 · 2019: 2 · 2018: 1 · 2017: 1 · 2015: 3 · 2014: 1
- FWCI
- 2.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroendocrinology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Renin-Angiotensin System Studies
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Electrolyte and hormonal disorders
- Keywords
- vasopressin receptor, angiotensin II receptor, oxytocin receptor, polydipsia, hypothalamic paraventricular nucleus, area postrema, nucleus tractus solitarius, brainstem, sex differences, receptor binding, strain differences
- MeSH terms
- Angiotensin II, Animals, Drinking, Female, Iodine Radioisotopes, Male, Mice, Inbred ICR, Mice, Mutant Strains, Oxytocin, Paraventricular Hypothalamic Nucleus, Polyuria, Radioligand Assay, Receptors, Angiotensin, Sex Characteristics, Ventromedial Hypothalamic Nucleus, Up-Regulation, Receptors, Vasopressin, Solitary Nucleus, Receptors, Oxytocin, Midline Thalamic Nuclei, Mice
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