Role of prostaglandins in rat pineal neuroeffector junction. changes in melatonin and norepinephrine release in vitro
The effects of prostaglandins (PGs) on melatonin secretion and norepinephrine (NE) release in rat pineal gland were examined in vitro. To study melatonin secretion, pineal explants were incubated for 6 h in tissue culture 199 medium with 1–1000 nM PGE1, PGE2) or PGF2n. Melatonin concentration in pin...
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1982
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00137227_v111_n2_p530_Cardinali http://hdl.handle.net/20.500.12110/paper_00137227_v111_n2_p530_Cardinali |
| Aporte de: |
| Sumario: | The effects of prostaglandins (PGs) on melatonin secretion and norepinephrine (NE) release in rat pineal gland were examined in vitro. To study melatonin secretion, pineal explants were incubated for 6 h in tissue culture 199 medium with 1–1000 nM PGE1, PGE2) or PGF2n. Melatonin concentration in pineal glands and media was determined by RIA. PGE2 increased pineal and medium melatonin at all concentrations tested, with a maximum of 1 nM; PGE1 was effective only at concentrations 100–1000 times greater, whereas 100 nM PGF2n decreased melatonin concentration in media but not in pineal gland. Exposure of pineal explants to 10 μM NE brought about a 20-fold increase in melatonin release to the medium. This effect was impaired significantly, but not blocked, by prior exposure to indomethacin, acetylsalicylic acid, or mefenamic acid at supramaximal concentrations to inhibit PG synthesis (100 μM). TO examine the effects of PGs on NE release, endogenous NE stores in pineal nerve endings were labeled in vitro by incubating rat pineals with [3H]NE for 30 min. Fifty minutes later, at the time when spontaneous radioactivity efflux had leveled off, transmitter release was elicited by a 1-min exposure to 80 mM K+ (S1), and the stimulus was repeated 35 min later (S2). PGs (10–100 nM) were added to the medium 20 min before S2. Ratios between fractional release of the two consecutive stimulations (S2/S1) varied between 0.84 and 1.16 in control pineals. Only 100 nM PGE2 impaired significantly transmitter release by 40%. These results suggest that PGE2 can play a role in NE-stimulated melatonin synthesis. At greater concentrations PGE2 inhibits NE release from pineal nerve endings. © 1982 by The Endocrine Society. |
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