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- Publisher Website: 10.1096/fj.10-165399
- Scopus: eid_2-s2.0-78649747023
- PMID: 20739612
- WOS: WOS:000284824400040
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Article: An indispensable role of secretin in mediating the osmoregulatory functions of angiotensin II
Title | An indispensable role of secretin in mediating the osmoregulatory functions of angiotensin II |
---|---|
Authors | |
Keywords | Circumventricular organs Fluid homeostasis Secretin receptor-deficient mice Vasopressin |
Issue Date | 2010 |
Publisher | Federation of American Societies for Experimental Biology. The Journal's web site is located at http://www.fasebj.org/ |
Citation | Faseb Journal, 2010, v. 24 n. 12, p. 5024-5032 How to Cite? |
Abstract | Fluid balance is critical to life and hence is tightly controlled in the body. Angiotensin II (ANGII), one of the most important components of this regulatory system, is recognized as a dipsogenic hormone that stimulates vasopressin (VP) expression and release. However, detailed mechanisms regarding how ANGII brings about these changes are not fully understood. In the present study, we show initially that the osmoregulatory functions of secretin (SCT) in the brain are similar to those of ANGII in mice and, more important, we discovered the role of SCT as the link between ANGII and its downstream effects. This was substantiated by the use of two knockout mice, SCTR -/- and SCT -/-, in which we show the absence of an intact SCT/secretin receptor (SCTR) axis resulted in an abolishment or much reduced ANGII osmoregulatory functions. By immunohistochemical staining and in situ hybridization, the proteins and transcripts of SCT and its receptor are found in the paraventricular nucleus (PVN) and lamina terminalis. We propose that SCT produced in the circumventricular organs is transported and released in the PVN to stimulate vasopressin expression and release. In summary, our findings identify SCT and SCTR as novel elements of the ANGII osmoregulatory pathway in maintaining fluid balance in the body. © FASEB. |
Persistent Identifier | http://hdl.handle.net/10722/179215 |
ISSN | 2023 Impact Factor: 4.4 2023 SCImago Journal Rankings: 1.412 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, VHY | en_US |
dc.contributor.author | Lee, LTO | en_US |
dc.contributor.author | Chu, JYS | en_US |
dc.contributor.author | Lam, IPY | en_US |
dc.contributor.author | Siu, FKY | en_US |
dc.contributor.author | Vaudry, H | en_US |
dc.contributor.author | Chow, BKC | en_US |
dc.date.accessioned | 2012-12-19T09:53:00Z | - |
dc.date.available | 2012-12-19T09:53:00Z | - |
dc.date.issued | 2010 | en_US |
dc.identifier.citation | Faseb Journal, 2010, v. 24 n. 12, p. 5024-5032 | en_US |
dc.identifier.issn | 0892-6638 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/179215 | - |
dc.description.abstract | Fluid balance is critical to life and hence is tightly controlled in the body. Angiotensin II (ANGII), one of the most important components of this regulatory system, is recognized as a dipsogenic hormone that stimulates vasopressin (VP) expression and release. However, detailed mechanisms regarding how ANGII brings about these changes are not fully understood. In the present study, we show initially that the osmoregulatory functions of secretin (SCT) in the brain are similar to those of ANGII in mice and, more important, we discovered the role of SCT as the link between ANGII and its downstream effects. This was substantiated by the use of two knockout mice, SCTR -/- and SCT -/-, in which we show the absence of an intact SCT/secretin receptor (SCTR) axis resulted in an abolishment or much reduced ANGII osmoregulatory functions. By immunohistochemical staining and in situ hybridization, the proteins and transcripts of SCT and its receptor are found in the paraventricular nucleus (PVN) and lamina terminalis. We propose that SCT produced in the circumventricular organs is transported and released in the PVN to stimulate vasopressin expression and release. In summary, our findings identify SCT and SCTR as novel elements of the ANGII osmoregulatory pathway in maintaining fluid balance in the body. © FASEB. | en_US |
dc.language | eng | en_US |
dc.publisher | Federation of American Societies for Experimental Biology. The Journal's web site is located at http://www.fasebj.org/ | en_US |
dc.relation.ispartof | FASEB Journal | en_US |
dc.subject | Circumventricular organs | - |
dc.subject | Fluid homeostasis | - |
dc.subject | Secretin receptor-deficient mice | - |
dc.subject | Vasopressin | - |
dc.subject.mesh | Angiotensin Ii - Pharmacology | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Drinking - Drug Effects | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Hypothalamus - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Immunohistochemistry | en_US |
dc.subject.mesh | In Situ Hybridization | en_US |
dc.subject.mesh | Mice | en_US |
dc.subject.mesh | Mice, Knockout | en_US |
dc.subject.mesh | Paraventricular Hypothalamic Nucleus - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Pituitary Gland - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Polymerase Chain Reaction | en_US |
dc.subject.mesh | Receptors, G-Protein-Coupled - Genetics - Metabolism | en_US |
dc.subject.mesh | Receptors, Gastrointestinal Hormone - Genetics - Metabolism | en_US |
dc.subject.mesh | Secretin - Genetics - Metabolism - Pharmacology | en_US |
dc.subject.mesh | Vasopressins - Metabolism | en_US |
dc.subject.mesh | Water-Electrolyte Balance - Drug Effects | en_US |
dc.title | An indispensable role of secretin in mediating the osmoregulatory functions of angiotensin II | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lee, LTO: ltolee2@hkucc.hku.hk | en_US |
dc.identifier.email | Chu, JYS: hitan@graduate.hku.hk | en_US |
dc.identifier.email | Chow, BKC: bkcc@hku.hk | en_US |
dc.identifier.authority | Lee, LTO=rp00727 | en_US |
dc.identifier.authority | Chu, JYS=rp00684 | en_US |
dc.identifier.authority | Chow, BKC=rp00681 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1096/fj.10-165399 | en_US |
dc.identifier.pmid | 20739612 | - |
dc.identifier.scopus | eid_2-s2.0-78649747023 | en_US |
dc.identifier.hkuros | 185541 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-78649747023&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 24 | en_US |
dc.identifier.issue | 12 | en_US |
dc.identifier.spage | 5024 | en_US |
dc.identifier.epage | 5032 | en_US |
dc.identifier.eissn | 1530-6860 | - |
dc.identifier.isi | WOS:000284824400040 | - |
dc.publisher.place | United States | en_US |
dc.identifier.f1000 | 10505956 | - |
dc.identifier.scopusauthorid | Lee, VHY=14050662700 | en_US |
dc.identifier.scopusauthorid | Lee, LTO=8367269000 | en_US |
dc.identifier.scopusauthorid | Chu, JYS=34975209300 | en_US |
dc.identifier.scopusauthorid | Lam, IPY=14050702700 | en_US |
dc.identifier.scopusauthorid | Siu, FKY=6701518484 | en_US |
dc.identifier.scopusauthorid | Vaudry, H=35446602600 | en_US |
dc.identifier.scopusauthorid | Chow, BKC=7102826193 | en_US |
dc.identifier.issnl | 0892-6638 | - |