The effects of short pulses of light at night on numbers of pineal ?synaptic? ribbons and serotonin N-acetyltransferase activity in male Sprague-Dawley rats (original) (raw)
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Cell and Tissue Research, 1985
Previous studies have shown that the "synaptic" ribbons (SR) and spherules (SS) of the mammalian pineal gland may respond differently under physiological and various experimental conditions. The aim of the present study was to gain insight into the mechanisms that may be responsible for the numerical changes of these organelles during a 24-h cycle. As the possibility exists that the structures are influenced by substances synthesized within the pinealocyte, rat pineal glands were cultured with and without added melatonin or serotonin, using an experimental protocol such that the addition of melatonin and serotonin mimicks the circadian changes of the respective substances within the pineal. The tissue was processed for electron microscopy and the numbers of SR and SS were counted in a unit area of pineal tissue. The results obtained indicate that melatonin added to the incubation medium increases the number of SR in the first half of the night; serotonin decreases SR numbers in the morning. SS numbers, by contrast, decrease following melatonin administration in the afternoon, and increase in the morning following serotonin administration. It thus appears that the numbers of SR and SS are influenced by melatonin and serotonin and that the two structures are regulated by differential, but nevertheless biochemically closely related mechanisms. -Melatonin (effect of) -Serotonin (effect of) A functionally important feature of the mammalian pineal gland is the formation of melatonin (5-methoxy-N-acetyltryptamine), which undergoes a prominent circadian rhythm. During daytime, serotonin, the substrate for melatonin, increases strikingly; at night, one of the melatoninforming enzymes, serotonin-N-acetyltransferase (NAT), in-Send offprint requests to."
“Synaptic” ribbons and spherules of the rat pineal gland: Day/night changes in vitro?
Experimental Brain Research, 1982
In the present study pineal glands of rats aged 69-71 days were studied in vivo and in vitro with respect to day/night changes of "synaptic" ribbons and spherules. It was found that ribbons outnumber spherules by a factor of 3. In vivo, both ribbons and spherules show a roughly 3-fold increase in number at 1 a.m. when compared to 1 p.m. Up to 39 h in vitro, the two structures in question did not reveal day/night differences in amount, suggesting that diurnal rhythmicity of the gland did apparently not persist in organ culture. After 3 h in organ culture, the spherules, but not the ribbons, showed a striking increase in number, showing that ribbons and spherules may be governed by different mechanisms.
Journal of Neural Transmission, 1988
Serotonin N-acetyltransferase (NAT), which is crucial for the formation of melatonin, undergoes a typical day/night rhythm in the pineal gland with low levels during daytime and high levels at night. Short pulses of light given at night have been shown to rapidly depress NAT activity in some species, but not in others, the reasons for this difference being unclear. As diurnality and nocturnality of the experimental animals may play a role and since diurnally active animals have been little investigated in this respect, in the present study the diurnally active guinea pig was investigated. Male guinea pigs kept under a lighting regimen of LD 12:12 (lights off at 1700 hrs) were killed between 1200 or 1300 hrs and between 0000 and 0200 hrs, at night in the dark or after exposure to 10 or 45 rain of light. The results obtained show that the day/night difference of NAT activity is about 2-fold. 10min or 45 min of light given at night significantly depress pineal NAT activity. Re-exposure to darkness for 1 hr of animals previously given light for 10 min leads to restoration of NAT activity. These findings together with data from the literature suggest that it does not appear to be the activity pattern (diurnality versus nocturnality) of an animal nor the amplitude of the day/night difference of pineal NAT activity that account for the suppressibility or non-suppressibility of pineal NAT activity by light at night.
Journal of Pineal Research, 1985
In three separate experiments, the effect of acute exposure to either artificial o r natural light during darkness of pineal N-acetyltransferase (NAT) activity and melatonin content was studied in the cotton rat (Szgmodon hispidus). The exposure of animals to an artificial-light irradiance of 160,000 pW/cm2 during darkness for either 1 s, 5 s, or 30 min was followed by a precipitous decline in pineal NAT activity and melatonin content when measured at either 15 or 30 min after light onset. When cotton rats were acutely exposed to light at night for 5 s, irradiances of either 3.2, 32, 320, and 3,200 did not suppress either pineal NAT or melatonin 30 min later; however, if the 5-s exposure had an irradiance of either 32,000 or 160,000 pWlcm2, the pineal enzyme activity and indole content were depressed. Moonlight, which had a maximal irradiance of 0.32 pW/cm2, was unable to suppress pineal NAT activity and melatonin content even when the animals were exposed to the moonlight for 30 min. The treatment of cotton rats with either norepinephrine or its agonist, isoproterenol, before their exposure to light at night retarded slightly the suppressive effect of light on the pineal constituents measured. Also, these drug treatments suppressed the pre-exposure levels of both NAT activity and melatonin content in the cotton rat pineal gland.
The American journal of anatomy, 1983
The present study deals with the functionally enigmatic "synaptic" ribbons and spherules of guinea pig pinealocytes. Whereas the ribbons have been shown to exhibit a 24-hr rhythmicity with low numbers during the day and high numbers at night, very little of a definitive nature is known about the spherules. Sixteen male guinea pigs of the Hartley strain were perfusion fixed, 8 between 0900-1100 hr, and 8 between 2100-2300 hr. The ribbons and spherules were counted in the pineal parenchyma of the proximal, intermediate, and distal regions. In confirmation of earlier studies, it was found that "synaptic" ribbons are equally abundant in the proximal, intermediate, and distal regions of the gland, during both the day and the night, and that they increase significantly in number at night when compared with daytime values. The spherules, by contrast, are more abundant proximally and are present in greater numbers during the day than at night. As ribbons and spherules ar...
Anatomy and Embryology, 1989
Melatonin metabolism in the mammalian pineal gland is under the clear influence of sympathetic fibers originating in the superior cervical ganglia (SCG). Previous studies suggested that pineal "synaptic" ribbons (SR) as well are regulated by the gland's sympathetic innervation. To gain more insight into the mechanisms involved, we examined the effects of sympathetic stimulation on SR number and on the activity of melatonin forming enzymes, serotonin N-acetyltransferase (NAT) and hydoxyindole-Omethyltransferase (HIOMT). The SCG in adult male rats were stimulated electrically during daytime for either 15 or 120 rain. Immediately following stimulation, the glands were removed and processed for electron microscopy and for the determination of NAT and HIOMT activities. No differences in pineal SR number, size or location were found in rats stimulated with either parameters when compared with sham-stimulated or control animals. While the activity of HIOMT remained unchanged, the activity of NAT was also unaltered following 15 min of stimulation, but was augmented approximately three-fold in animals stimulated for 120 min. It is concluded that if SR in the rat pineal gland are under sympathetic control, the regulation is different from that involved in melatonin formation.
Circadian variations of ?synaptic? bodies in the pineal glands of Brattleboro rats
Cell and Tissue Research, 1990
The function of the mammalian pineal gland is regulated primarily by the sympathetic system. Arginine-vasopressin (AVP) may also be involved in the regulation of pineal melatonin synthesis under experimental conditions. The present study was conducted in the AVP-deficient rat strain, the Brattleboro rat, to investigate whether the numbers and rhythms of pineal "synaptic" bodies in this strain are different from those found in intact rats. AVP or its non-vasoconstrictive analog, deamino-D-AVP, was also injected intra-arterially in Brattleboro or Sprague-Dawley rats to test whether this procedure influences "synaptic" body numbers. Brattleboro rats were killed at different timepoints throughout the 24 h-cycle in March, June and September. "Synaptic" ribbons, spherules and intermediate structures were quantified and examined with regard to their intracellular location, with or without nocturnal AVP or D-AVP treatment. Numbers of ribbons were low during the day and high during the night (as in genetically intact rats), whereas spherules and intermediate structures numbers exhibited inconstant daily patterns. Night levels of "synaptic" ribbons were highest in June, lowest in March, whereas day levels did not differ significantly. No significant alterations in pineal "synaptic" body numbers were found following administration of AVP or D-AVP. Our results therefore indicate that AVP does not play a crucial role in the regulation of pineal "synaptic" body numbers in rats.
Journal of Pineal Research, 1984
The size of synaptic ribbons (SR) in photoreceptor cells of the goldfish pineal organ was quantified over 24-h 1ight:dark cycles of long (16:8) and short (10:14) photoperiods during summer and winter months, respectively. The amplitude of both rhythms was similar with peak values occurring toward the latter part of the photophase or early dark. When fish were entrained to the long photoperiod and exposed to continual light, SR size continued to increase during the expected dark time. The effect of extending the photoperiod into the expected dark time was diminished when fish were entrained to a short photoperiod and presented with 6 h of darkness at the end of the 24-h period. The size increase in response to environmental lighting is believed to reflect a greater demand for either vesicle attachment sites or neurotransmitter storage sites since vesicles (neurotransmitter) have been hypothesized to accumulate in the synaptic pedicles during inhibition by light. From a comparative standpoint it is noteworthy that synaptic ribbons (vesicle-crowned rods) in mammals react in a similar manner to both normal and experimental lighting conditions.