Abstract | BACKGROUND AND OBJECTIVE:
Obesity is highly complicated by hypertension and hyperglycemia. In particular, it has been proposed that obesity-related hypertension is caused by adipocyte-derived factors that are recognized as undetermined proteins secreted from adipocytes. Adipocyte-derived factors have been known to be related to aldosterone secretion in the adrenal gland. So far, Wnt proteins, CTRP-1, VLDL, LDL, HDL and leptin have been demonstrated to stimulate aldosterone secretion. In contrast, it has not yet been clarified whether adipocyte-derived factors also affect adrenal cortisol secretion. METHODS AND RESULTS: In the present study, we investigated the effect of adipocyte-derived factors on cortisol synthase gene CYP11B1 mRNA expression in vitro study using adrenocortical carcinoma H295R cells and mouse fibroblast 3T3-L1cells. Interestingly, adipocyte-derived factors were demonstrated to have the ability to stimulate CYP11B1 mRNA expression. CONCLUSION:
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Authors | Hiroki Shimada, Erika Noro, Susumu Suzuki, Jun Sakamoto, Ikuko Sato, Rehana Parvin, Atsushi Yokoyama, Akira Sugawara |
Journal | Current molecular pharmacology
(Curr Mol Pharmacol)
Vol. 13
Issue 1
Pg. 2-6
( 2020)
ISSN: 1874-4702 [Electronic] United Arab Emirates |
PMID | 31613736
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Copyright | Copyright© Bentham Science Publishers; For any queries, please email at [email protected]. |
Chemical References |
- C1QTNF1 protein, human
- Leptin
- Lipoproteins, LDL
- Proteins
- RNA, Messenger
- Wnt Proteins
- Cytochrome P-450 CYP11B2
- Steroid 11-beta-Hydroxylase
- Hydrocortisone
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Topics |
- Adipocytes
(chemistry)
- Adrenal Cortex
(drug effects, metabolism)
- Adrenal Cortex Neoplasms
(metabolism, pathology)
- Animals
- Carcinoma
(metabolism, pathology)
- Cell Line
- Cell Line, Tumor
- Cytochrome P-450 CYP11B2
(biosynthesis, genetics)
- Fibroblasts
- Gene Expression Regulation
(drug effects)
- Humans
- Hydrocortisone
(metabolism)
- Leptin
(metabolism, pharmacology)
- Lipoproteins, LDL
(metabolism, pharmacology)
- Mice
- Proteins
(genetics, physiology)
- RNA, Messenger
(biosynthesis, genetics)
- Steroid 11-beta-Hydroxylase
(biosynthesis, genetics)
- Wnt Proteins
(metabolism, pharmacology)
- Zona Fasciculata
(drug effects, metabolism)
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