1399: Expression of Luteinizing Hormone and its Receptor in the RAT Epididymis and Seminal Vesicle

2004 ◽  
Vol 171 (4S) ◽  
pp. 368-369
Author(s):  
Sung Ho Lee ◽  
Soo Woong Kim ◽  
Jae-Seung Paick
1983 ◽  
Vol 61 (11) ◽  
pp. 2405-2410 ◽  
Author(s):  
H. M. Charlton ◽  
S. A. Chiappa ◽  
G. Fink ◽  
C. A. Grocock ◽  
E. Versi

Pituitary luteinizing hormone (LH) and hypothalamic gonadotropin-releasing hormone (GnRH) contents were measured in male voles trapped in the field over a period of 5 years. Pituitary LH contents were positively correlated with testicular and seminal vesicle weights but hypothalamic GnRH contents showed no correlation with pituitary LH contents or organ weights. Pituitary LH contents and testicular and seminal vesicle weights increased between January to April, reached peak values during May to July, and fell from August to December. Hypothalamic GnRH contents were high for most of the year with low values during December and January. During July, August, and September two populations of males were studied; a group with large active testes and high pituitary LH levels and a group with small testes and low pituitary LH levels. With the exception of the group in July of animals with small testes, all males, both sexually active and inhibited, had high hypothalamic GnRH levels.


Author(s):  
V. F. Allison ◽  
G. C. Fink ◽  
G. W. Cearley

It is well known that epithelial hyperplasia (benign hypertrophy) is common in the aging prostate of dogs and man. In contrast, little evidence is available for abnormal epithelial cell growth in seminal vesicles of aging animals. Recently, enlarged seminal vesicles were reported in senescent mice, however, that enlargement resulted from increased storage of secretion in the lumen and occurred concomitant to epithelial hypoplasia in that species.The present study is concerned with electron microscopic observations of changes occurring in the pseudostratified epithelium of the seminal vescles of aging rats. Special attention is given to certain non-epithelial cells which have entered the epithelial layer.


Author(s):  
Venita F. Allison

In 1930, Moore, Hughes and Gallager reported that after castration seminal vesicle epithelial cell atrophy occurred and that cell regeneration could be achieved with daily injections of testis extract. Electron microscopic studies have confirmed those observations and have shown that testosterone injections restore the epithelium of the seminal vesicle in adult castrated male rats. Studies concerned with the metabolism of androgens point out that dihydrotestosterone stimulates cell proliferation and that other metabolites of testosterone probably influence secretory function in certain target cells.Although the influence of androgens on adult seminal vesicle epithelial cytology is well documented, little is known of the effect of androgen depletion and replacement on those cells in aging animals. The present study is concerned with the effect of castration and testosterone injection on the epithelium of the seminal vesicle of aging rats.


Author(s):  
Alan N. Hodgson

The hermaphrodite duct of pulmonate snails connects the ovotestis to the fertilization pouch. The duct is typically divided into three zones; aproximal duct which leaves the ovotestis, the middle duct (seminal vesicle) and the distal ovotestis duct. The seminal vesicle forms the major portion of the duct and is thought to store sperm prior to copulation. In addition the duct may also play a role in sperm maturation and degredation. Although the structure of the seminal vesicle has been described for a number of snails at the light microscope level there appear to be only two descriptions of the ultrastructure of this tissue. Clearly if the role of the hermaphrodite duct in the reproductive biology of pulmonatesis to be understood, knowledge of its fine structure is required.Hermaphrodite ducts, both containing and lacking sperm, of species of the terrestrial pulmonate genera Sphincterochila, Levantina, and Helix and the marine pulmonate genus Siphonaria were prepared for transmission electron microscopy by standard techniques.


2001 ◽  
Vol 32 (1) ◽  
pp. 50-50
Author(s):  
S. F. Ge ◽  
M. N. Romanov ◽  
P. J. Sharp ◽  
D. W. Burt ◽  
I. R. Paton ◽  
...  

2000 ◽  
Vol 35 (3-4) ◽  
pp. 129-133
Author(s):  
B Gawronska ◽  
A Stepien ◽  
AJ Ziecik
Keyword(s):  

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