scholarly journals Daidzein impairs Leydig cell testosterone production and Sertoli cell function in neonatal mouse testes: An in vitro study

2016 ◽  
Vol 14 (6) ◽  
pp. 5325-5333 ◽  
Author(s):  
Yanfeng Zhu ◽  
Hua Xu ◽  
Min Li ◽  
Zhibin Gao ◽  
Jie Huang ◽  
...  
1985 ◽  
Vol 132 (2) ◽  
pp. 729-734 ◽  
Author(s):  
M. Benahmed ◽  
C. Grenot ◽  
E. Tabone ◽  
P. Sanchez ◽  
A.M. Morera

1984 ◽  
Vol 438 (1 Hormonal Cont) ◽  
pp. 684-687 ◽  
Author(s):  
M. BENAHMED ◽  
J. REVENTOS ◽  
E. TABONE ◽  
J. M. SAEZ

Metabolism ◽  
1994 ◽  
Vol 43 (5) ◽  
pp. 533-537 ◽  
Author(s):  
Joseph Tai ◽  
Wah Jun Tze ◽  
Noriko Murase ◽  
Thomas E. Starzl

2015 ◽  
Vol 24 (2) ◽  
pp. 276-284 ◽  
Author(s):  
Daniela Fanigliulo ◽  
Pietro Enea Lazzerini ◽  
Pier Leopoldo Capecchi ◽  
Cristina Ulivieri ◽  
Cosima Tatiana Baldari ◽  
...  

Endocrinology ◽  
2014 ◽  
Vol 156 (2) ◽  
pp. 680-693 ◽  
Author(s):  
Elizabeth I. Tang ◽  
Ka-Wai Mok ◽  
Will M. Lee ◽  
C. Yan Cheng

2008 ◽  
Vol 140 ◽  
pp. 119-126
Author(s):  
Jing Lu ◽  
Thomas J. Webster

Atherosclerosis, which is caused by endothelial dysfunction, vascular inflammation, and the build-up of lipids, cholesterol, calcium, and cellular debris within the intima of the vessel wall, is one of the most important complications of health. Vascular stenting is the procedure of implanting a thin tube into the site of a narrow or blocked artery due to atherosclerosis. However, the application of vascular stents using conventional metals is limited because the implantation process will cause significant injury to the vascular wall and endothelium, which functions as a protective biocompatible barrier between the tissue and the circulating blood, resulting in neointima hyperplasia followed by the development of long-term restenosis. The objective of this in vitro study was to investigate the endothelial cell function, especially their adhesion behaviour, on highly controllable features on nanostructured surface. Considering the importance of the endothelium and its properties, highly controllable nanostructured surface features of titanium, a popular vascular stent metal, were created using E-beam evaporation to promote endothelialization and to control the direction of endothelial cells on vascular stents. Endothelial cells are naturally aligned with the blood flow in the body. In this manner, the present in vitro study provides much promise for the use of nanotechnology for improving metallic materials for vascular stent applications.


1986 ◽  
Vol 24 (1) ◽  
pp. 311-315 ◽  
Author(s):  
M. Benahmed ◽  
E. Tabone ◽  
C. Grenot ◽  
P. Sanchez ◽  
M.A. Chauvin ◽  
...  

Endocrinology ◽  
2003 ◽  
Vol 144 (8) ◽  
pp. 3279-3284 ◽  
Author(s):  
P. J. O’Shaughnessy ◽  
L. M. Fleming ◽  
G. Jackson ◽  
U. Hochgeschwender ◽  
P. Reed ◽  
...  

Abstract Adult Leydig cell steroidogenesis is dependent on LH but fetal Leydig cells can function independently of gonadotropin stimulation. To identify factors that may be involved in regulation of fetal Leydig cells expressed sequence tag libraries from fetal and adult testes were compared, and fetal-specific genes identified. The ACTH receptor [melanocortin type 2 receptor (Mc2r)] was identified within this fetal-specific group. Subsequent real-time PCR studies confirmed that Mc2r was expressed in the fetal testis at 100-fold higher levels than in the adult testis. Incubation of fetal or neonatal testes with ACTH in vitro stimulated testosterone production more than 10-fold, although ACTH had no effect on testes from animals aged 20 d or older. The steroidogenic response of fetal and neonatal testes to a maximally stimulating dose of human chorionic gonadotropin was similar to the response shown to ACTH. The ED50 for ACTH, measured in isolated fetal and neonatal testicular cells, was 5 × 10−10m and the lowest dose of ACTH eliciting a response was 2 × 10−11m. Circulating ACTH levels in fetal mice were around 8 × 10−11m. Neither α-MSH nor γ-MSH had any effect on androgen production in vitro at any age. Fetal testosterone levels were normal in mice that lack circulating ACTH (proopiomelanocortin-null) indicating that ACTH is not essential for fetal Leydig cell function. Results show that both LH and ACTH can regulate testicular steroidogenesis during fetal development in the mouse and suggest that fetal Leydig cells, but not adult Leydig cells, are sensitive to ACTH stimulation.


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