In Vitro Uptake of Benzodiazepines by Rat Pineal Gland

1984 ◽  
Vol 1 (3) ◽  
pp. 207-213 ◽  
Author(s):  
Pedro R. Lowenstein ◽  
César González Solveyra ◽  
Daniel P. Cardinali
Endocrinology ◽  
2014 ◽  
Vol 155 (8) ◽  
pp. 2966-2975 ◽  
Author(s):  
Kristian Rohde ◽  
Louise Rovsing ◽  
Anthony K. Ho ◽  
Morten Møller ◽  
Martin F. Rath

The cone-rod homeobox (Crx) gene encodes a transcription factor in the retina and pineal gland. Crx deficiency influences the pineal transcriptome, including a reduced expression of arylalkylamine N-acetyltransferase (Aanat), a key enzyme in nocturnal pineal melatonin production. However, previous functional studies on pineal Crx have been performed in melatonin-deficient mice. In this study, we have investigated the role of Crx in the melatonin-proficient rat pineal gland. The current study shows that pineal Crx transcript levels exhibit a circadian rhythm with a peak in the middle of the night, which is transferred into daily changes in CRX protein. The study further shows that the sympathetic innervation of the pineal gland controls the Crx rhythm. By use of adenovirus-mediated short hairpin RNA gene knockdown targeting Crx mRNA in primary rat pinealocyte cell culture, we here show that intact levels of Crx mRNA are required to obtain high levels of Aanat expression, whereas overexpression of Crx induces Aanat transcription in vitro. This regulatory function of Crx is further supported by circadian analysis of Aanat in the pineal gland of the Crx-knockout mouse. Our data indicate that the rhythmic nature of pineal CRX protein may directly modulate the daily profile of Aanat expression by inducing nighttime expression of this enzyme, thus facilitating nocturnal melatonin synthesis in addition to its role in ensuring a correct tissue distribution of Aanat expression.


1992 ◽  
Vol 89 (3) ◽  
pp. 167-178 ◽  
Author(s):  
B. B. P. Gupta ◽  
A. Seidel ◽  
R. Spessert ◽  
W. B�ttner ◽  
N. Klauke ◽  
...  

1979 ◽  
Vol 91 (3) ◽  
pp. 571-576 ◽  
Author(s):  
J. L. Sartin ◽  
B. C. Bruot ◽  
R. J. Orts

ABSTRACT Studies were performed to determine the effects of neurotransmitters on arginine vasotocin (AVT) release in vitro. Rat pineal glands were incubated with 10−8m or 10−6m norepinephrine (NE), dopamine (DA), serotonin (5HT), and acetylcholine (ACH) for eight h after which the concentrations of AVT in the media were determined by radioimmunoassay. With the exception of ACH, none of the neurotransmitters had a significant effect on AVT release. ACH significantly (P < 0.05) elevated AVT release in vitro at the 10−6m concentration but not at the 10−8m concentration. The data indicate that ACH may play a role in the regulation of rat pineal gland secretion of AVT in vitro.


1989 ◽  
Vol 123 (2) ◽  
pp. 205-211 ◽  
Author(s):  
L. M. E. Finocchiaro ◽  
A. Scheucher ◽  
S. Finkielman ◽  
V. E. Nahmod ◽  
C. J. Pirola

ABSTRACT [3H]Quinuclidinyl benzylate ([3H]QNB)-binding sites, showing similar properties to cholinergic muscarinic receptors in other tissues, were disclosed in the rat pineal gland. Functionality of these receptors was demonstrated, as in-vitro muscarinic activation by pilocarpine increased the pineal metabolic production of the hydroxyindole derivatives 5-hydroxytryptophan and serotonin, with a slight effect on melatonin biosynthesis. Electric-field stimulation of pineal slices caused similar metabolic effects. These effects were inhibited by muscarinic blockade with atropine and enhanced by neostigmine inactivation of acetylcholinesterase. These results suggest that acetyl-choline is the neurotransmitter involved. Cholinergic activity may, therefore, regulate indole metabolism in the pineal gland. Journal of Endocrinology (1989) 123, 205–211


1978 ◽  
Vol 34 (9) ◽  
pp. 1232-1233 ◽  
Author(s):  
A. C. Reinharz ◽  
S. Pavel ◽  
M. B. Vallotton

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