Activity of monoamine oxidase in the medial preoptic area and median eminence of female rats of different ages

2008 ◽  
Vol 2 (3) ◽  
pp. 193-196
Author(s):  
A. V. Razygraev ◽  
A. V. Arutjunyan ◽  
M. G. Stepanov ◽  
Yu. P. Milyutina ◽  
T. A. Mazur
Endocrinology ◽  
2016 ◽  
Vol 157 (1) ◽  
pp. 323-335 ◽  
Author(s):  
Bruna Kalil ◽  
Aline B. Ribeiro ◽  
Cristiane M. Leite ◽  
Ernane T. Uchôa ◽  
Ruither O. Carolino ◽  
...  

Abstract In rodents, kisspeptin neurons in the rostral periventricular area of the third ventricle (RP3V) of the preoptic area are considered to provide a major stimulatory input to the GnRH neuronal network that is responsible for triggering the preovulatory LH surge. Noradrenaline (NA) is one of the main modulators of GnRH release, and NA fibers are found in close apposition to kisspeptin neurons in the RP3V. Our objective was to interrogate the role of NA signaling in the kisspeptin control of GnRH secretion during the estradiol induced LH surge in ovariectomized rats, using prazosin, an α1-adrenergic receptor antagonist. In control rats, the estradiol-induced LH surge at 17 hours was associated with a significant increase in GnRH and kisspeptin content in the median eminence with the increase in kisspeptin preceding that of GnRH and LH. Prazosin, administered 5 and 3 hours prior to the predicted time of the LH surge truncated the LH surge and abolished the rise in GnRH and kisspeptin in the median eminence. In the preoptic area, prazosin blocked the increases in Kiss1 gene expression and kisspeptin content in association with a disruption in the expression of the clock genes, Per1 and Bmal1. Together these findings demonstrate for the first time that NA modulates kisspeptin synthesis in the RP3V through the activation of α1-adrenergic receptors prior to the initiation of the LH surge and indicate a potential role of α1-adrenergic signaling in the circadian-controlled pathway timing of the preovulatory LH surge.


2015 ◽  
Vol 42 (12) ◽  
pp. 3138-3148 ◽  
Author(s):  
M. Dean Graham ◽  
James Gardner Gregory ◽  
Dema Hussain ◽  
Wayne G. Brake ◽  
James G. Pfaus

1979 ◽  
Vol 28 (4) ◽  
pp. 234-240 ◽  
Author(s):  
R.L. Cooper ◽  
S.J. Brandt ◽  
M. Linnoila ◽  
R.F. Walker

2014 ◽  
Vol 1578 ◽  
pp. 23-29 ◽  
Author(s):  
Fernanda Barbosa Lima ◽  
Fábio Honda Ota ◽  
Fernanda Jankur Cabral ◽  
Bruno Del Bianco Borges ◽  
Celso Rodrigues Franci

1984 ◽  
Vol 39 (1) ◽  
pp. 74-80 ◽  
Author(s):  
Friedemann Döcke ◽  
Wolfgang Rohde ◽  
Peter Gerber ◽  
Gerold Kreuz

1977 ◽  
Vol 24 (5) ◽  
pp. 497-502 ◽  
Author(s):  
YASUHIKO IBATA ◽  
YOSHIAKI NOJYO ◽  
KIMINAO MIZUKAWA ◽  
YUTAKA SANO

Endocrinology ◽  
2011 ◽  
Vol 152 (5) ◽  
pp. 1979-1988 ◽  
Author(s):  
Annika Sjoeholm ◽  
Robert S. Bridges ◽  
David R. Grattan ◽  
Greg M. Anderson

Pregnancy and lactation cause long-lasting enhancements in maternal behavior and other physiological functions, along with increased hypothalamic prolactin receptor expression. To directly test whether reproductive experience increases prolactin responsiveness in the arcuate, paraventricular, and supraoptic nuclei and the medial preoptic area, female rats experienced a full pregnancy and lactation or remained as age-matched virgin controls. At 5 wk after weaning, rats received 2.5, 100, or 4000 ng ovine prolactin or vehicle intracerebroventricularly. The brains underwent immunohistochemistry for the phosphorylated forms of signal transducer and activator of transcription 5 (pSTAT5) or ERK1/2 (pERK1/2). There was a marked increase in pSTAT5 and pERK1/2 in response to prolactin in the regions examined in both virgin and primiparous rats. Primiparous rats exhibited approximately double the number of prolactin-induced pSTAT5-immunoreactive cells as virgins, this effect being most apparent at the higher prolactin doses in the medial preoptic area and paraventricular and supraoptic nuclei and at the lowest prolactin dose in the arcuate nucleus. Dual-label immunohistochemistry showed that arcuate kisspeptin (but not oxytocin or dopamine) neurons displayed increased sensitivity to prolactin in reproductively experienced animals; these neurons may contribute to the reduction in prolactin concentration observed after reproductive experience. There was no effect of reproductive experience on prolactin-induced pERK1/2, indicating a selective effect on the STAT5 pathway. These data show that STAT5 responsiveness to prolactin is enhanced by reproductive experience in multiple hypothalamic regions. The findings may have significant implications for understanding postpartum disorders affecting maternal care and other prolactin-associated pathologies.


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