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Article: Adrenomedullin peptide: Gene expression of adrenomedullin, its receptors and receptor activity modifying proteins, and receptor binding in rat testis - Actions on testosterone secretion
Title | Adrenomedullin peptide: Gene expression of adrenomedullin, its receptors and receptor activity modifying proteins, and receptor binding in rat testis - Actions on testosterone secretion |
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Authors | |
Keywords | Aging Human chorionic gonadotropin Testis Testosterone |
Issue Date | 2006 |
Publisher | Society for the Study of Reproduction. The Journal's web site is located at http://www.biolreprod.org/ |
Citation | Biology Of Reproduction, 2006, v. 75 n. 2, p. 183-188 How to Cite? |
Abstract | Adrenomedullin (ADM) has been shown to be present in the human and rat male reproductive systems. This study demonstrates the expression of ADM in the rat testis and its effect on the secretion of testosterone. Whole testicular extracts had 5.43 ± 0.42 fmol of immunoreactive ADM per milligram of protein and 84 ± 8 fg of ADM mRNA per picogram of Actb (β-actin) mRNA. Immunocytochemical studies showed positive ADM immunostaining in the Leydig cells and in the Sertoli cells. Gel filtration chromatography of testicular extracts showed two peaks, with the predominant one eluting at the position of the ADM precursor. Furthermore, the testis was shown to coexpress mRNAs encoding the calcitonin receptor-like receptor and receptor activity modifying protein 1 (Ramp1), Ramp2, and Ramp3. These account for the specific binding of ADM to the testis, which was partially inhibited by human ADM (22-52) and by human calcitonin gene-related peptide (8-37), the ADM and calcitonin gene-related peptide receptor antagonists, respectively. Administration of ADM to testicular blocks in vitro resulted in a dose-dependent inhibition of hCG-stimulated release of testosterone, which was abolished by the administration of ADM (22-52). Our results suggest a paracrine effect of ADM on testicular steroidogenesis. © 2006 by the Society for the Study of Reproduction, Inc. |
Persistent Identifier | http://hdl.handle.net/10722/149657 |
ISSN | 2023 Impact Factor: 3.1 2023 SCImago Journal Rankings: 1.022 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, YY | en_HK |
dc.contributor.author | Hwang, ISS | en_HK |
dc.contributor.author | O, WS | en_HK |
dc.contributor.author | Tang, F | en_HK |
dc.date.accessioned | 2012-06-26T05:56:39Z | - |
dc.date.available | 2012-06-26T05:56:39Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | Biology Of Reproduction, 2006, v. 75 n. 2, p. 183-188 | en_HK |
dc.identifier.issn | 0006-3363 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/149657 | - |
dc.description.abstract | Adrenomedullin (ADM) has been shown to be present in the human and rat male reproductive systems. This study demonstrates the expression of ADM in the rat testis and its effect on the secretion of testosterone. Whole testicular extracts had 5.43 ± 0.42 fmol of immunoreactive ADM per milligram of protein and 84 ± 8 fg of ADM mRNA per picogram of Actb (β-actin) mRNA. Immunocytochemical studies showed positive ADM immunostaining in the Leydig cells and in the Sertoli cells. Gel filtration chromatography of testicular extracts showed two peaks, with the predominant one eluting at the position of the ADM precursor. Furthermore, the testis was shown to coexpress mRNAs encoding the calcitonin receptor-like receptor and receptor activity modifying protein 1 (Ramp1), Ramp2, and Ramp3. These account for the specific binding of ADM to the testis, which was partially inhibited by human ADM (22-52) and by human calcitonin gene-related peptide (8-37), the ADM and calcitonin gene-related peptide receptor antagonists, respectively. Administration of ADM to testicular blocks in vitro resulted in a dose-dependent inhibition of hCG-stimulated release of testosterone, which was abolished by the administration of ADM (22-52). Our results suggest a paracrine effect of ADM on testicular steroidogenesis. © 2006 by the Society for the Study of Reproduction, Inc. | en_HK |
dc.language | eng | en_US |
dc.publisher | Society for the Study of Reproduction. The Journal's web site is located at http://www.biolreprod.org/ | en_HK |
dc.relation.ispartof | Biology of Reproduction | en_HK |
dc.subject | Aging | en_HK |
dc.subject | Human chorionic gonadotropin | en_HK |
dc.subject | Testis | en_HK |
dc.subject | Testosterone | en_HK |
dc.subject.mesh | Adrenomedullin - Genetics - Metabolism - Pharmacology | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Binding Sites | en_US |
dc.subject.mesh | Calcitonin Receptor-Like Protein | en_US |
dc.subject.mesh | Chorionic Gonadotropin - Pharmacology | en_US |
dc.subject.mesh | Chromatography, Gel | en_US |
dc.subject.mesh | Dose-Response Relationship, Drug | en_US |
dc.subject.mesh | Gene Expression Regulation | en_US |
dc.subject.mesh | Intracellular Signaling Peptides And Proteins - Genetics | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Membrane Proteins - Genetics | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Rats, Sprague-Dawley | en_US |
dc.subject.mesh | Receptor Activity-Modifying Protein 1 | en_US |
dc.subject.mesh | Receptor Activity-Modifying Protein 2 | en_US |
dc.subject.mesh | Receptor Activity-Modifying Protein 3 | en_US |
dc.subject.mesh | Receptor Activity-Modifying Proteins | en_US |
dc.subject.mesh | Receptors, Adrenomedullin | en_US |
dc.subject.mesh | Receptors, Calcitonin - Genetics - Metabolism | en_US |
dc.subject.mesh | Receptors, G-Protein-Coupled - Genetics - Metabolism | en_US |
dc.subject.mesh | Testis - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Testosterone - Secretion | en_US |
dc.title | Adrenomedullin peptide: Gene expression of adrenomedullin, its receptors and receptor activity modifying proteins, and receptor binding in rat testis - Actions on testosterone secretion | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | O, WS: owaisum@hkucc.hku.hk | en_HK |
dc.identifier.email | Tang, F: ftang@hkucc.hku.hk | en_HK |
dc.identifier.email | Li, YY: cyyli@graduate.hku.hk | - |
dc.identifier.email | Hwang, ISS: isabelbelbel@hotmail.com | - |
dc.identifier.authority | O, WS=rp00315 | en_HK |
dc.identifier.authority | Tang, F=rp00327 | en_HK |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1095/biolreprod.106.052274 | en_HK |
dc.identifier.pmid | 16672720 | - |
dc.identifier.scopus | eid_2-s2.0-33746318355 | en_HK |
dc.identifier.hkuros | 117233 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33746318355&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 75 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 183 | en_HK |
dc.identifier.epage | 188 | en_HK |
dc.identifier.isi | WOS:000239199500004 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Li, YY=49763596700 | en_HK |
dc.identifier.scopusauthorid | Hwang, ISS=7201615103 | en_HK |
dc.identifier.scopusauthorid | O, WS=6701729369 | en_HK |
dc.identifier.scopusauthorid | Tang, F=7201979770 | en_HK |
dc.identifier.issnl | 0006-3363 | - |