scholarly journals Immunohistochemical Study of Growth Hormone and Prolactin Cells in the Pituitaries of Anguilliform Leptocephali Captured in the Atlantic Sargasso Sea.

1992 ◽  
Vol 58 (9) ◽  
pp. 1723-1727 ◽  
Author(s):  
Chitose Orikasa ◽  
Susumu Hyodo ◽  
Akihisa Urano
1980 ◽  
Vol 17 (1) ◽  
pp. 2-16 ◽  
Author(s):  
M. F. El Etreby ◽  
R. Müller-Peddinghaus ◽  
A. S. Bhargava ◽  
M. R. Fath El Bab ◽  
K.-J. Gräf ◽  
...  

The morphological changes of the pituitary gland of 29 female dogs with spontaneous mammary tumours or dysplasia or both were correlated with basal serum prolactin, growth hormone, adrenocorticotrophin, thyrotrophin, cortisol, total cholesterol, thyroxine and thyroid binding index as well as with lesions in other endocrine and genital organs. Spontaneous canine mammary tumorigenesis seemed to be associated with increased secretory activity of growth hormone rather than prolactin cells. Depressed secretory activity of follicle stimulating hormone-, luteinizing hormone- and thyrotrophin-producing cells, as well as signs of inhibition of ovarian (anovulation) and thyroid function, were also consistent findings in dogs with mammary tumours. There also was disturbance in pituitary-adrenal function associated with hyperplastic and neoplastic changes of the pituitary gland and adrenal cortex.


1982 ◽  
Vol 93 (1) ◽  
pp. 117-121 ◽  
Author(s):  
Fumihiko Sasaki ◽  
Masao Sano

The number of prolactin and growth hormone cells was estimated in the mouse anterior pituitary gland. During postnatal development in females, the number of prolactin cells showed a rectilinear increase from about 0·3 × 104 at 20 days of age to about 21 × 104 in adult female mice, while growth hormone cells gradually increased from about 7 × 104 on day 20 to about 20 × 104 on days 60–70, with a plateau level of about 14 × 104 cells around puberty. Prolactin cells were more abundant in adult female (about 21 × 104) than in male (about 5 × 104) mice, while there were fewer growth hormone cells in adult females (about 20 × 104) than in males (about 25 × 104). Ovariectomy before puberty induced the male pattern of pituitary development by inhibition of the increase in the number of prolactin cells and stimulation of that of growth hormone cells. In animals ovariectomized just before puberty (30–35 days of age) or 5 days after vaginal opening (40–45 days of age) the number of prolactin cells showed no further increase after the day of operation. On the other hand, when animals were ovariectomized at 10 days of age, the number of prolactin cells increased to the level found in 30-day-old normal control females. This implies that the increase in prolactin cells between 10 and 30 days of age is not dependent on the ovary, although after puberty the increase does depend on the presence of the ovary.


1994 ◽  
Vol 276 (2) ◽  
pp. 253-261 ◽  
Author(s):  
Fredrick Van Goor ◽  
Jeffrey I. Goldberg ◽  
Anderson O.L. Wong ◽  
Richard M. Jobin ◽  
John P. Chang

1980 ◽  
Vol 85 (2) ◽  
pp. 283-289 ◽  
Author(s):  
F. SASAKI ◽  
M. SANO

To clarify the role of the ovary in the sexual differentiation of prolactin and growth hormone cells, the anterior pituitary glands of mice ovariectomized before or after puberty were studied by a stereological morphometric technique with the electron microscope. A marked sex difference was observed in the relative proportions of these two types of cells in normal adult control animals. In male mice about 52% of anterior pituitary cells were growth hormone cells and about 10% were prolactin cells, while in female mice prolactin cells represented about 39% and growth hormone cells about 37% of the anterior pituitary cell population. Ovariectomy before puberty reduced the proportion of prolactin cells to about 10% and increased growth hormone cells to about 50% of the cell population. The size of prolactin cells and the development of their cell organelles was also reduced. Ovariectomy after puberty had less marked effects. These results suggest that ovariectomy before puberty induced the male phenotype by inhibition of the differentiation of prolactin cells and stimulation of the differentiation of growth hormone cells. The significance of these results in relation to the sexual differentiation of the pituitary gland is discussed.


1995 ◽  
Vol 6 (3) ◽  
pp. 239-246 ◽  
Author(s):  
Heiji Naritaka ◽  
Toru Kameya ◽  
Yuichi Sato ◽  
Shigeru Furuhata ◽  
Junichi Okui ◽  
...  

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