Edward C. Hurlbut

Pineal, retinal and harderian gland melatonin in a diurnal species, the richardson's ground squirrel (Spermophilus richardsonii)

Abstract Melatonin levels were estimated over a 24 h period in the pineal glands, retinas and Harderian glands of a diurnal rodent, the Richardsons ground squirrel ( Spermophilus richardsonii ). Animals were kept in light:dark cycles of 14:10 (lights on at 06.00 h) and killed at the following time points: 20.00, 24.00, 02.00, 04.00 and 08.00 h. Pineal levels of melatonin were low (

The Influence of Various Irradiances of Artificial Light, Twilight, and Moonlight on the Suppression of Pineal Melatonin Content in the Syrian Hamster

The purpose of the present studies using artificial light was to determine how the timing and duration of exposure influence the light‐induced suppression of pineal melatonin levels in hamsters. An 8‐min exposure to 0.186 μW/cm2 of cool white fluorescent light caused a continued depression of pineal melatonin even when animals were returned to darkness. In addition, the pineal gland does not appear to change its sensitivity to light throughout the night. A 20‐min exposure to 0.019 μW/cm2 of cool white fluorescent light did not significantly suppress pineal melatonin during any time of the melatonin peak, whereas a 20‐min exposure to 0.186 μW/cm2was capable of always suppressing melatonin. Furthermore, increasing the duration of 0.019‐μW/cm2 exposure to 30, 60, 120, or 180 min does not increase the capacity of this irradiance to depress melatonin.

Influence of light irradiance on hydroxyindole-O-methyltransferase activity, serotonin-N-acetyltranferase activity, and radioimmunoassayable melatonin levels in the pineal gland of the diurnally active Richardson's ground squirrel

When Richardsons ground squirrels were kept under light:dark cycles of 14:10 h there was no nocturnal rise in pineal hydroxyindole-O-methyltransferase (HIOMT) activity. Conversely, the 10 h dark period was associated with large nocturnal rises in both pineal serotonin-N-acetyltransferase (NAT) activity and radioimmunoassayable melatonin levels. The nighttime rises in pineal NAT and melatonin were not suppressed by the exposure of the animals to a light irradiance of 925 mu W/cm2 during the normal dark period. On the other hand, when the light irradiance was increased to 1850 mu W/cm2 the rise in pineal NAT activity was eliminated while the melatonin rise was greatly reduced. When ground squirrels were acutely exposed to a light irradiance of 1850 mu W/cm2 for 30 min beginning at 5.5 h after lights out, pineal NAT activity and melatonin levels were reduced to daytime values within 30 min. The half-time (t 1/2) for each constituent was less than 10 min. Exposure to a light irradiance of either 5 s or 5 min (beginning at 5.5 h into dark period) was equally as effective as 30 min light exposure in inhibiting pineal NAT activity and melatonin levels. When animals were returned to darkness after a 30 min exposure to a light irradiance of 1850 mu W/cm2 at night, both pineal NAT activity and melatonin levels were restored to high nighttime levels within 2 h of their return to darkness. The results indicate that the pineal gland of the wild-captured, diurnal Richardsons ground squirrel is 9000 X less sensitive to light at night than is the pineal gland of the laboratory raised, nocturnal Syrian hamster.

Studies on pineal melatonin levels in a diurnal species, the Eastern chipmunk (Tamias striatus): Effects of light at night, propranolol administration or superior cervical ganglionectomy

Five experiments were carried out on the control of melatonin levels in the pineal gland of a diurnal species, the Eastern chipmunk (Tamias striatus). We confirmed that the exposure of chipmunks to fluorescent white light of 3,981–4,304 lux during the normal dark period does not prevent the rise in pineal melatonin levels normally associated with darkness. Also, the administration of propranolol (20mg/kg) at 8 p.m. did not block the rise in pineal melatonin in animals exposed to either dark or light at night. Similarly, if chipmunks received propranolol 4 hours into the dark phase, pineal melatonin levels were not depressed 2 hours later. When animals were superior cervical ganglionectomized, however, the pineal content of melatonin remained low regardless of whether the animals were exposed to darkness or light at night. The exposure of chipmunks acutely to light at midnight (4 hours after darkness onset) had only a slight depressive effect on pineal melatonin 30 min later; by comparison, when chipmunks were acutely exposed to light at 3 a.m. (7 hours after darkness onset) daytime pineal melatonin levels were reached within 15 min after light onset. These findings in a diurnal species, the Eastern chipmunk, differ markedly when compared to previously reported observations on nocturnal laboratory rodents.

Day-night differences in the number of pineal “synaptic” ribbons in two diurnal rodents, the chipmunk (Tamias striatus) and the ground squirrel (Spermophilus richardsonii)

SummaryDaytime numbers of pineal “synaptic” ribbons higher than reported in the pineal gland of any other mammalian species were observed in two diurnal rodents, the eastern chipmunk and Richardsons ground squirrel. The number of “synaptic” ribbons was lower during the daytime and higher at night in both of these species.

Changes in serotonin levels, N-acetyltransferase activity, hydroxyindole-O-methyltransferase activity, and melatonin levels in the pineal gland of the Richardson's ground squirrel in relation to the light-dark cycle

Pineal serotonin and melatonin levels and the activities of hydroxyindole-O-methyltransferase (HIOMT) and N-acetyltransferase (NAT) were studied over a 24-hour period in the pineal gland of the diurnally active Richardsons ground squirrel (Spermophilus richardsonii). Under alternating light-dark conditions (light:dark hours 14:10), pineal serotonin and melatonin levels exhibited a rhythm with high values occurring either during the day (serotonin) or during the night (melatonin). NAT activity was also markedly increased during darkness. HIOMT activity exhibited no 24-hour variation. Exposure of squirrels to constant light for 7 days exaggerated the serotonin rhythm, but obliterated the cycles of NAT and melatonin. Under constant darkness (for 7 days), the rhythms in serotonin, melatonin and NAT persisted, each having a period of about 24 h. In the second study, ground squirrels were exposed to light-dark cycles of either 8:16, 10:14 or 14:10. Under each of these photoperiodic environments, rhythms in pineal NAT and melatonin were apparent. Increasing the daily dark period from 10 to 14 h caused a prolongation of the elevated NAT and melatonin levels. However, a further prolongation of the daily dark period (to 16 h) did not further increase the duration of the rise in NAT and melatonin. The results show that continual light exposure (irradiance of 200 microW/cm2) for 7 days suppresses the pineal rhythms in both NAT activity and melatonin level in the Richardsons ground squirrel. Conversely, light exposure, rather than depressing the serotonin rhythm, actually exaggerates it. Constant darkness for 7 days has little influence on the 24-hour rhythms of either NAT or melatonin.(ABSTRACT TRUNCATED AT 250 WORDS)

Comparative studies on the retinal dopamine response to altered magnetic fields in rodents

Previously it was demonstrated that experimental alteration of the ambient magnetic field at night significantly reduced catecholamine levels in the retinae of Sprague-Dawley rats. As this effect appeared to depend on intact photoreceptors, it seemed of interest to examine whether the dopamine response to altered magnetic fields (MFs) differed between rod-dominant retinae and cone-dominant retinae. Furthermore, the effect of MFs on daytime dopamine content was explored. As in previous nocturnal investigations, dopamine levels in light-adapted (i.e. daytime) retinae from albino rats were significantly reduced by MFs. In the cone-dominant retina of the pigment ground squirrel, a similar MF effect was observed. However, in the rod-dominant retina of the golden hamster, dopamine levels increased significantly following daytime MF exposure. These results indicate that the retinal dopaminergic system is differentially responsive to MFs in various rodent species. Hence, the retina may play an important role in the perception of MFs by mammals.

Ultrastructure of pinealocytes of the kangaroo rat (Dipodomys ordi)

SummaryThe ultrastructure of the pinealocytes of the wild-captured ord kangaroo rat (Dipodomys ordi) was examined. A homogeneous population of pinealocytes was present in the pineal gland of the kangaroo rat. The Golgi apparatus, granular endoplasmic reticulum, mitochondria, lysosomes, dense-core vesicles, vacuoles containing a flocculent material and lipid droplets were consistent components of the pinealocyte cytoplasm, whereas infrequently-observed organelles included centrioles, multivesicular bodies, subsurface cisternae, “synaptic” ribbons and cilia. The number of dense-core vesicles was relatively high and dense-core vesicles and vacuoles containing a flocculent material were present in the same cell.Although it has been recently suggested that two different secretory processes, i.e., neurosecretory-like (Golgi apparatus — dense-core vesicles) and ependymal-like (granular endoplasmic reticulum — vacuoles containing a flocculent material) may be involved in different regulatory mechanisms in the pinealocytes, the definitive answer to this is still far from clear. Therefore, the pineal gland of the kangaroo rat appears to be a good model for the study of the potential relationship between these two secretory processes, especially in respect to seasonal changes.

Melatonin synthesis in the pineal gland of the Richardson's ground squirrel (Spermophilus richardsonii): Influence of age and insulin-induced hypoglycemia

The nocturnal rises in pineal N-acetyltransferase (NAT) activity and melatonin levels were compared in young (25–35 days old) and adult (at least 1 year old) Richardsons ground squirrels. When expressed as NAT activity per pineal gland, the nighttime rise in the activity of this enzyme was less in young than in the adult animals; conversely, the melatonin content of the pineal glands of young animals was higher at one point (4 a.m., 8 hours after darkness onset) when compared to that in adult squirrels. When data were expressed relative to total protein, the NAT and melatonin rhythms in the pineals of young and adult animals were very similar. The effect of insulin-induced hypoglycemia on both daytime and nighttime NAT and melatonin levels in the pineal gland of the Richardsons ground squirrel was also assessed. Low daytime levels of these constituents were not influenced by the administration of 10 units insulin, a treatment which caused a marked drop in circulating glucose levels. At night, when pineal NAT and melatonin levels were high insulin injection had a very modest stimulatory effect on NAT activity (one point was elevated above saline injected controls) while melatonin levels remained unchanged by the treatment. These findings in the ground squirrel in reference to insulin-induced hypoglycemia, and Stressors in general, appear to differ from those in the rat where stress can have a substantial influence or both low daytime and high nighttime levels of pineal NAT and melatonin.

A 15-minute light pulse during darkness prevents the antigonadotrophic action of afternoon melatonin injections in male hamsters

When adult male Syrian hamsters were maintained under 14 h light and 10 h darkness daily (lights on from 0600-2000 h), peak pineal melatonin levels (705 pg/gland) were attained at 0500 h. When the dark phase of the light:dark cycle was interrupted with a 15 min pulse of light from 2300–2315 h (3 h after lights out), the highest melatonin levels achieved was roughly 400 pg/gland. Finally, if the 15 min pulse of light was given at 0200–0215 h (6 h after lights out) the nocturnal rise in pineal melatonin was completely abolished. Having made these observations, a second experiment was designed to determine the ability of afternoon melatonin injections to inhibit reproduction in hamsters kept under an uninterrupted 14∶10 cycle or under the same lighting regimen where the dark phase was interrupted with a 15 min pulse of light (0200–0215 h). In the uninterrupted light:dark schedule the daily afternoon injection of 25 μg melatonin caused the testes and the accessory sex organs to atrophy within 11 weeks. Conversely, if the dark phase was interrupted with light between 0200–0215 h, afternoon melatonin injections were incapable of inhibiting the growth of the reproductive organs. The findings suggest that exogenously administered melatonin normally synergizes with endogenously produced melatonin to cause gonadal involution in hamsters.