Polychlorinated biphenyl (Aroclor 1254) inhibits testosterone biosynthesis and antioxidant enzymes in cultured rat Leydig cells

2008 ◽  
Vol 25 (4) ◽  
pp. 447-454 ◽  
Author(s):  
Palaniappan Murugesan ◽  
Thirupathi Muthusamy ◽  
Karundevi Balasubramanian ◽  
Jagadeesan Arunakaran
Toxicology ◽  
2007 ◽  
Vol 232 (3) ◽  
pp. 170-182 ◽  
Author(s):  
Palaniappan Murugesan ◽  
Thirupathi Muthusamy ◽  
Karundevi Balasubramanian ◽  
Jagadeesan Arunakaran

2005 ◽  
Vol 39 (11) ◽  
pp. 1259-1272 ◽  
Author(s):  
Palaniappan Murugesan ◽  
Thirupathi Muthusamy ◽  
Karundevi Balasubramanian ◽  
Jagadeesan Arunakaran

2005 ◽  
Vol 20 (1) ◽  
pp. 117-126 ◽  
Author(s):  
Palaniappan Murugesan ◽  
Palaniyandi Kanagaraj ◽  
Sambandam Yuvaraj ◽  
Karundevi Balasubramanian ◽  
Maria Michael Aruldhas ◽  
...  

1993 ◽  
Vol 20 (3) ◽  
pp. 288-294 ◽  
Author(s):  
L. EARL GRAY ◽  
J. OSTBY ◽  
R. MARSHALL ◽  
J. ANDREWS

1980 ◽  
Vol 93 (2) ◽  
pp. 250-256 ◽  
Author(s):  
M. P. de la Llosa-Hermier ◽  
C. Tertrin-Clary ◽  
M. Evrard-Herouard ◽  
Y. Colleaux ◽  
C. Hermier ◽  
...  

Abstract. Rat intestinal cells prepared from testes were incubated in the presence of different lutropin derivatives obtained by chemical modification of the amino groups. The cAMP accumulation and the testosterone biosynthesis were determined in the cell homogenates. Binding determinations were carried out by a radioligand receptor assay using tritiated methylated lutropin. The binding activities — relative to native LH — of three different derivatives obtained by reductive alkylation (methylated, ethylated and isopropylated LH) were in good agreement with the relative potencies assessed by their capacity to stimulate cAMP and testosterone production. Guanidinated LH (11 — NH2 groups modified) exhibited a binding activity and a relative potency relatively high with regard to cAMP accumulation (as compared with that of native LH). Its steroidogenic potency, however, was very low. When Leydig cells were incubated in the presence of native and guanidinated LH, the testosterone production was similar to that induced by the derivative alone, indicating that the derivative exerted a competitive inhibitory action preventing the stimulation of steroidogenesis by native LH. These results suggest that a guanidinated derivative is able to bind to the LH receptor and the complex so formed is able to be coupled with an adenylate cyclase pool (or cAMP compartment) which is not connected with the steroidogenic pathway.


1999 ◽  
Vol 13 (6) ◽  
pp. 451-462 ◽  
Author(s):  
Eisuke P Murono ◽  
Raymond C Derk ◽  
Jesús H de León

2020 ◽  
Vol 154 ◽  
pp. 31-42
Author(s):  
Jie Zhao ◽  
Hua Yang ◽  
Mingtian Deng ◽  
Jianyu Ma ◽  
Zhibo Wang ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document