Analysis of sleep-wakefulness rhythms in male rats after suprachiasmatic nucleus lesions and ocular enucleation

1977 ◽  
Vol 122 (1) ◽  
pp. 33-47 ◽  
Author(s):  
Nobuo Ibuka ◽  
Shin-ichi T. Inouye ◽  
Hiroshi Kawamura
1999 ◽  
Vol 73 (7) ◽  
pp. 367-372 ◽  
Author(s):  
Tadashi Furukawa ◽  
Sunao Manabe ◽  
Toshiyuki Watanabe ◽  
Shinya Sehata ◽  
Satoru Sharyo ◽  
...  

Author(s):  
Somaye Mesgar ◽  
Seyed Behnamedin Jameie ◽  
Abbas Aliaghaei ◽  
Siavash Parvardeh ◽  
Abolfazl Torabi ◽  
...  

1998 ◽  
Vol 792 (2) ◽  
pp. 343-347 ◽  
Author(s):  
Mario Engelmann ◽  
Karl Ebner ◽  
Rainer Landgraf ◽  
Carsten T Wotjak

Endocrinology ◽  
2014 ◽  
Vol 155 (2) ◽  
pp. 525-535 ◽  
Author(s):  
M. Guzmán-Ruiz ◽  
N. Saderi ◽  
F. Cazarez-Márquez ◽  
N. N. Guerrero-Vargas ◽  
M. C. Basualdo ◽  
...  

2014 ◽  
Vol 307 (7) ◽  
pp. C611-C621 ◽  
Author(s):  
Julie A. Highland ◽  
Michael J. Weiser ◽  
Laura R. Hinds ◽  
Robert L. Spencer

Entrainment of the intrinsic suprachiasmatic nucleus (SCN) molecular clock to the light-dark cycle depends on photic-driven intracellular signal transduction responses of SCN neurons that converge on cAMP response element-binding protein (CREB)-mediated regulation of gene transcription. Characterization of the CREB coactivator proteins CREB-regulated transcriptional coactivators (CRTCs) has revealed a greater degree of differential activity-dependent modulation of CREB transactivational function than previously appreciated. In confirmation of recent reports, we found an enrichment of crtc2 mRNA and prominent CRTC2 protein expression within the SCN of adult male rats. With use of a hypothalamic organotypic culture preparation for initial CRTC2-reactive antibody characterization, we found that CRTC2 immunoreactivity in hypothalamic neurons shifted from a predominantly cytoplasmic profile under basal culture conditions to a primarily nuclear localization (CRTC2 activation) 30 min after adenylate cyclase stimulation. In adult rat SCN, we found a diurnal variation in CRTC2 activation (peak at zeitgeber time of 4 h and trough at zeitgeber time of 16–20 h) but no variation in the total number of CRTC2-immunoreactive cells. There was no diurnal variation of CRTC2 activation in the hypothalamic paraventricular nucleus, another site of enriched CRTC2 expression. Exposure of rats to light (50 lux) for 30 min during the second half of their dark (nighttime) phase produced CRTC2 activation. We observed in the SCN a parallel change in the expression of a CREB-regulated gene (FOS). In contrast, nighttime light exposure had no effect on CRTC2 activation or FOS expression in the paraventricular nucleus, nor did it affect corticosterone hormone levels. These results suggest that CRTC2 participates in CREB-dependent photic entrainment of SCN function.


1982 ◽  
Vol 94 (2) ◽  
pp. 157-166 ◽  
Author(s):  
M. Héry ◽  
M. Faudon ◽  
G. Dusticier ◽  
F. Héry

In order to determine the temporal relationships between variations in 5-hydroxy-tryptamine (5-HT, serotonin) metabolism in the suprachiasmatic nucleus (SCN) and the cyclic LH surge, and also to check whether implantation of oestradiol capsules might modulate 5-HT metabolism in the SCN, we carried out a parallel study of 5-HT content in the SCN and median eminence, and 5-HT metabolism in the SCN and supraoptic region in vitro. These experiments were performed on intact male rats, ovariectomized females and ovariectomized females implanted with oestradiol. It was only in ovariectomized rats implanted with oestradiol, in which we have described the existence of a clear-cut circadian rhythm of LH secretion, that we found fluctuations in the content, synthesis and utilization of 5-HT. The content and synthesis were characterized by a peak between 12.00 and 15.00 h, whereas utilization was 50% higher at 09.00 and 19.00 h than at 15.00 h. These fluctuations in 5-HT content and metabolism were specific to the SCN; the median eminence and the supraoptic region did not show such variations. They were also specific to ovariectomized rats implanted with oestradiol, since the patterns of 5-HT content and metabolism in the SCN were the same in males and ovariectomized females and did not differ from those in the median eminence, the supraoptic region or the whole hypothalamus. These results suggest that 5-HT terminals in the SCN play an important role in the control of cyclic LH secretion at a critical period. Moreover, oestradiol seems to be partly responsible for the fluctuations of 5-HT metabolism in the SCN of ovariectomized rats implanted with oestradiol.


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