Document Detail


Metastin stimulates aldosterone synthesis in human adrenal cells.
MedLine Citation:
PMID:  18089602     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Kisspeptins, including metastin, are encoded by the KiSS-1 gene and play an important role in regulating the hypothalamic gonadotropin-releasing hormone (GnRH) system via G protein-coupled receptor 54 (GPR54, also called KiSS-1R). Normally, metastin (also called Kp-54) levels are quite low, except during pregnancy, when levels increase 1000-fold over those found in men and nonpregnant women. However, the potential hormonal role of metastin in the fetal and maternal circulation is unknown. In this study, the authors examine the levels of GPR54 mRNA expression in human adult and fetal adrenals using quantitative real-time reverse-transcriptase polymerase chain reaction (RT-PCR). In addition, they examine the effects of metastin on steroidogenesis and steroidogenic enzyme mRNA levels in fetal adrenal cells and in the H295R adrenocortical cell line using enzyme immunoassay and RT-PCR techniques. The authors demonstrate that GPR54 mRNA is significantly higher (50-fold) in human fetal adrenals than in adult adrenals. Immunohistochemical studies have demonstrated that the GPR54 protein is predominantly expressed in the neocortex of human fetal adrenals in the third trimester. Metastin increases aldosterone production (approximately 2-fold) in both fetal neocortex adrenal cells and H295R adrenal cells, with a maximal increase seen at 100 nM. In addition, metastin increased angiotensin II (Ang II)-stimulated aldosterone production by approximately 1.5-fold. Metastin also increased the ability of the H295R cells to metabolize exogenously added pregnenolone to aldosterone but had no effect on the expression of aldosterone synthase (CYP11B2). These results suggest that the high fetal/maternal levels of metastin seen during pregnancy may affect adrenal production of aldosterone.
Authors:
Yasuhiro Nakamura; Satoshi Aoki; Yewei Xing; Hironobu Sasano; William E Rainey
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Reproductive sciences (Thousand Oaks, Calif.)     Volume:  14     ISSN:  1933-7205     ISO Abbreviation:  Reprod Sci     Publication Date:  2007 Dec 
Date Detail:
Created Date:  2007-12-19     Completed Date:  2008-02-14     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101291249     Medline TA:  Reprod Sci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  836-45     Citation Subset:  IM    
Affiliation:
Department of Physiology, Medical College of Georgia, Augusta, Georgia 30912, USA.
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MeSH Terms
Descriptor/Qualifier:
Adrenal Glands / metabolism*
Aldosterone / biosynthesis*
Aldosterone Synthase / genetics,  metabolism
Cell Line, Tumor
Female
Fetus
Humans
Hydrocortisone / metabolism
Pregnancy
RNA, Messenger / biosynthesis,  genetics
Receptors, G-Protein-Coupled / genetics,  metabolism*
Tumor Suppressor Proteins / biosynthesis,  genetics,  metabolism*
Grant Support
ID/Acronym/Agency:
DK43140/DK/NIDDK NIH HHS; HD11149/HD/NICHD NIH HHS
Chemical
Reg. No./Substance:
0/KISS1 protein, human; 0/KISS1R protein, human; 0/RNA, Messenger; 0/Receptors, G-Protein-Coupled; 0/Tumor Suppressor Proteins; 50-23-7/Hydrocortisone; 52-39-1/Aldosterone; EC 1.14.15.4/Aldosterone Synthase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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