A single day of constant light (L/L) provides immunity to behavioral despair in female rats maintained on an L/D cycle

2004 ◽  
Vol 28 (8) ◽  
pp. 1261-1265 ◽  
Author(s):  
Ajda Yilmaz ◽  
Ayla Aksoy ◽  
Resit Canbeyli
1961 ◽  
Vol 36 (4) ◽  
pp. 617-624 ◽  
Author(s):  
Richard Jay Wurtman ◽  
Willard Roth ◽  
Mark D. Altschule ◽  
Judith J. Wurtman

ABSTRACT Either exposure to constant light for 80 days or pinealectomy produced similar changes in the weights of the ovaries and adrenals of female rats. These were not additive when both procedures were employed. Pinealectomy did not share with light-exposure the capacity to induce uterine hypertrophy. Rats exposed to constant light for 56 days had lighter pineals than animals kept in darkness; this decrease was not affected by administration of bovine pineal extracts. The increase in ovarian weight produced in rats by exposure to light for 56 days was prevented by bovine pineal extracts, but these extracts were without effect on the uterine hypertrophy produced under the same conditions. These data suggest that the effect of light upon the weight of the ovary is mediated via the pineal.


1972 ◽  
Vol 54 (2) ◽  
pp. 263-NP ◽  
Author(s):  
R. RELKIN ◽  
M. ADACHI ◽  
S. A. KAHAN

SUMMARY The effects of constant light, constant darkness and diurnal lighting, in combination with pinealectomy or sham-pinealectomy, on pituitary and plasma concentrations of radioimmunoassayable prolactin were investigated in 8-week-old male and virgin female rats. Two to three days after operation random groups of pinealectomized and sham-pinealectomized animals of the same sex were placed together in either continous light, continuous darkness or diurnal light, and killed 21 days later. Compared with sham-operated diurnally-illuminated controls, constant darkness caused a decrease in pituitary prolactin content and a rise in plasma prolactin levels. Pinealectomy or constant illumination reversed the effect of constant darkness, resulting in an increase in pituitary prolactin content and a fall in plasma prolactin levels when compared with sham-operated diurnally-illuminated controls. Electron microscopy of lactotrophic cells of the sham-pinealectomized animals exposed to constant darkness revealed few cytoplasmic granules, whereas these cells in the sham-pinealectomized animals exposed to constant light contained abundant granules; compared with the former groups, lactotrophic cells of sham-pinealectomized rats exposed to diurnal lighting revealed an intermediate degree of granulation.


2004 ◽  
Vol 114 (12) ◽  
pp. 1513-1520 ◽  
Author(s):  
A. AKSOY ◽  
D. SCHULZ ◽  
A. YILMAZ ◽  
R. CANBEYLI

Author(s):  
K. B. Singh ◽  
F. K. Khosho

It is now well established that exposure of cyclic female rats to continuous light induces persistent estrus (PE), a syndrome which in many respects resembles the human polycystic ovary (PCO) syndrome. As in the human PCO, light microscopic studies of cystic ovaries of the constant light rat show numerous atretic follicles, and the surface epithelium grossly appears smooth and white. In the present study, we have utilized scanning (SEM) and transmission electron microscopy (TEM) to study changes on the surface epithelium of PCO in the constant light rat model.


Author(s):  
K. B. Singh ◽  
F. K. Khosho

Exposure of female rats to continuous light eventually induces persistent estrus (PE), a syndrome which in many respects resembles the human polycystic ovary syndrome. Light microscopic studies on the polycystic ovaries of constant light PE rats have been previously reported. In the present study, we have utilized scanning electron microscopy (SEM) to provide information regarding three-dimensional changes occurring on the surface of the polycystic ovary.Following exposure to continuous light for 50 days, PE was induced in a group of Sprague-Dawley female rats according to the procedure described elsewhere (2). Polycystic ovaries from constant light PE rats and ovaries from controls were fixed in 2.5% glutaraldehyde in 0.1M Na cacodylate buffer, pH 7.3 at room temperature for 24 hours. They were then cut into two equal halves along their long axis and fixed for an additional 3-4 hours. The specimens were processed for SEM studies by a modified OTOTO technique, dehydrated and critical point dried with CO2.


Author(s):  
Khosho Francis K. ◽  
Kaufmann Robert C. ◽  
Amankwah Kofi S.

Adult female rats exposed to constant light will develop anovulatory acyclicity characterized by persistent vaginal cornification (PE) and formation of multiple large cystic follicles on the ovaries. The purpose of the present communication is to describe the ultrastructural changes in vaginal epithelia in PE rats as compared to that in normal estrous rats.Persistent vaginal estrous with PCO was induced in a group of Sprague-Dawely rats by exposure to constant light for 50-150 days. Rats in normal estrous, as determined by vaginal smears, were used as controls. Nembutal- anethesized rats were perfused through the aorta with 2.5% gluteraldehyde in 1M sodium cacodylate buffer (pH 7.3). The mucosa of the vaginal folds just inferior to the cervix were dissected by microsurgery, postfixed, stained with 0.5% ruthenium red in 1% osmium tetroxide, dehydrated, and embedded in polybed. Thick sections (1μ) were stained with toludine blue for light microscopy studies. Thin sections were stained with uranyl acetate and lead citrate.


Author(s):  
Khosho Francis K. ◽  
Kaufmann Robert C. ◽  
Amankwah Kofi S.

Light exerts a major influence on the reproductive functions of the female rat, and the presence of constant light results in an aberrant vaginal cycle, leading to infertility associated with polycystic ovary (PCO) syndrome. In the present communication, we have utilized scanning electron microscopy (SEM) to study changes on the surface epithelium of persistent estrous (PE) rats with PCO.Sprague-Dawely female rats were exposed to constant light for 50-150 days according to protocol that has been previously described. Rats in normal estrous, as determined by vaginal smears, were used as controls. Nembutal- anesthesized rats were perfused through the aorta with 2.5% gluteraldehyde in 0.1M sodium cacodylate buffer (pH 7.3). The mucosa of the upper third of the vagina from PE and control rats were microdissected, processed for SEM studies by a modified 0T0T0 technique, dehydrated, and critical point dried with C02- The specimens were examined in a Hitachi scanning electron microscope Model S-500.


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