Changes of AT1 receptor expression in rat adipose tissue with respect to adiposity

Author(s):  
Katarína Tybitanclová ◽  
Štefan Zorad
1995 ◽  
Vol 13 (11) ◽  
pp. 1241-1246 ◽  
Author(s):  
Riccardo Sarzani ◽  
Vittoria M. Paci ◽  
Cristina M. Zingaretti ◽  
Claudia Pierleoni ◽  
Saverio Cinti ◽  
...  

1997 ◽  
Vol 323 (2) ◽  
pp. 359-364 ◽  
Author(s):  
Khadija El HADRI ◽  
Christine CHARON ◽  
Jacques PAIRAULT ◽  
Sylvie HAUGUEL-DE MOUZON ◽  
Annie QUIGNARD-BOULANGÉ ◽  
...  

The β3-adrenergic receptor (β3-AR) exerts a central role in the transduction of catecholamine effects in white and brown adipose tissue (WAT and BAT). A recent report has documented that insulin strongly down-regulates β3-AR expression and catecholamine responsiveness in 3T3-F442A adipocytes [Fève, El Hadri, Quignard-Boulangé and Pairault (1994) Proc. Natl. Acad. Sci. U.S.A. 91, 5677–5681]. In the present report we show that the rise in plasma insulin levels elicited by the fasted/fed transition is associated with a reduction in β3-AR mRNA levels and β-adrenergic responsiveness in WAT and BAT. β3-AR transcripts are also decreased in adipose tissue from animals subjected for 6 h to euglycaemic hyperinsulinaemic glucose clamps. Moreover, insulin acts directly on cultured rat white and brown adipocytes to decrease β3-AR gene expression and adenylate cyclase activity in response to β3-AR-selective agonists. These results suggest that there is a close relationship between food intake, plasma insulin levels and β3-AR expression.


2005 ◽  
Vol 288 (1) ◽  
pp. E200-E207 ◽  
Author(s):  
S. Rodriguez-Cuenca ◽  
M. Monjo ◽  
A. M. Proenza ◽  
P. Roca

Sex hormones play an important role in adipose tissue metabolism by activating specific receptors that alter several steps of the lipolytic and lipogenic signal cascade in depot- and sex-dependent manners. However, studies focusing on steroid receptor status in adipose tissue are scarce. In the present study, we analyzed steroid content [testosterone (T), 17β-estradiol (17β-E2), and progesterone (P4)] and steroid receptor mRNA levels in different rat adipose tissue depots. As expected, T levels were higher in males than in females ( P = 0.031), whereas the reverse trend was observed for P4 ( P < 0.001). It is noteworthy that 17β-E2 adipose tissue levels were higher in inguinal than in the rest of adipose tissues for both sexes, where no sex differences in 17β-E2 tissue levels were noted ( P = 0.010 for retroperitoneal, P = 0.005 for gonadal, P = 0.018 for mesenteric). Regarding steroid receptor levels, androgen (AR) and estrogen receptor (ER)α and ERβ densities were more clearly dependent on adipose depot location than on sex, with visceral depots showing overall higher mRNA densities than their subcutaneous counterparts. Besides, expression of ERα predominated over ERβ expression, and progesterone receptor (PR-B form and PR-A+B form) mRNAs were identically expressed regardless of anatomic depot and sex. In vitro studies in 3T3-L1 cells showed that 17β-E2 increased ERα ( P = 0.001) and AR expression ( P = 0.001), indicating that estrogen can alter estrogenic and androgenic signaling in adipose tissue. The results highlighted in this study demonstrate important depot-dependent differences in the sensitivity of adipose tissues to sex hormones between visceral and subcutaneous depots that could be related to metabolic situations observed in response to sex hormones.


1983 ◽  
Vol 24 (5) ◽  
pp. 522-532
Author(s):  
G J Hausman ◽  
R L Richardson

1975 ◽  
Vol 16 (6) ◽  
pp. 461-464 ◽  
Author(s):  
G Holm ◽  
B Jacobsson ◽  
P Björntorp ◽  
U Smith

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