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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Autores principales: Cardinali, D.P., Ritta, M.N., Pereyra, E., Solveyra, C.G.
Formato: JOUR
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rat
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00137227_v111_n2_p530_Cardinali
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spelling todo:paper_00137227_v111_n2_p530_Cardinali2023-10-03T14:11:07Z Role of prostaglandins in rat pineal neuroeffector junction. changes in melatonin and norepinephrine release in vitro Cardinali, D.P. Ritta, M.N. Pereyra, E. Solveyra, C.G. acetylsalicylic acid indometacin mefenamic acid melatonin noradrenalin potassium prostaglandin prostaglandin E prostaglandin E1 prostaglandin E2 prostaglandin F prostaglandin F2 alpha animal article drug effect male metabolism pineal body rat rat strain Alprostadil Animal Aspirin Dinoprost Dinoprostone Indomethacin Male Mefenamic Acid Melatonin Norepinephrine Pineal Gland Potassium Prostaglandins Prostaglandins E Prostaglandins F Rats Rats, Inbred Strains Support, Non-U.S. Gov't 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00137227_v111_n2_p530_Cardinali
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic acetylsalicylic acid
indometacin
mefenamic acid
melatonin
noradrenalin
potassium
prostaglandin
prostaglandin E
prostaglandin E1
prostaglandin E2
prostaglandin F
prostaglandin F2 alpha
animal
article
drug effect
male
metabolism
pineal body
rat
rat strain
Alprostadil
Animal
Aspirin
Dinoprost
Dinoprostone
Indomethacin
Male
Mefenamic Acid
Melatonin
Norepinephrine
Pineal Gland
Potassium
Prostaglandins
Prostaglandins E
Prostaglandins F
Rats
Rats, Inbred Strains
Support, Non-U.S. Gov't
spellingShingle acetylsalicylic acid
indometacin
mefenamic acid
melatonin
noradrenalin
potassium
prostaglandin
prostaglandin E
prostaglandin E1
prostaglandin E2
prostaglandin F
prostaglandin F2 alpha
animal
article
drug effect
male
metabolism
pineal body
rat
rat strain
Alprostadil
Animal
Aspirin
Dinoprost
Dinoprostone
Indomethacin
Male
Mefenamic Acid
Melatonin
Norepinephrine
Pineal Gland
Potassium
Prostaglandins
Prostaglandins E
Prostaglandins F
Rats
Rats, Inbred Strains
Support, Non-U.S. Gov't
Cardinali, D.P.
Ritta, M.N.
Pereyra, E.
Solveyra, C.G.
Role of prostaglandins in rat pineal neuroeffector junction. changes in melatonin and norepinephrine release in vitro
topic_facet acetylsalicylic acid
indometacin
mefenamic acid
melatonin
noradrenalin
potassium
prostaglandin
prostaglandin E
prostaglandin E1
prostaglandin E2
prostaglandin F
prostaglandin F2 alpha
animal
article
drug effect
male
metabolism
pineal body
rat
rat strain
Alprostadil
Animal
Aspirin
Dinoprost
Dinoprostone
Indomethacin
Male
Mefenamic Acid
Melatonin
Norepinephrine
Pineal Gland
Potassium
Prostaglandins
Prostaglandins E
Prostaglandins F
Rats
Rats, Inbred Strains
Support, Non-U.S. Gov't
description 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.
format JOUR
author Cardinali, D.P.
Ritta, M.N.
Pereyra, E.
Solveyra, C.G.
author_facet Cardinali, D.P.
Ritta, M.N.
Pereyra, E.
Solveyra, C.G.
author_sort Cardinali, D.P.
title Role of prostaglandins in rat pineal neuroeffector junction. changes in melatonin and norepinephrine release in vitro
title_short Role of prostaglandins in rat pineal neuroeffector junction. changes in melatonin and norepinephrine release in vitro
title_full Role of prostaglandins in rat pineal neuroeffector junction. changes in melatonin and norepinephrine release in vitro
title_fullStr Role of prostaglandins in rat pineal neuroeffector junction. changes in melatonin and norepinephrine release in vitro
title_full_unstemmed Role of prostaglandins in rat pineal neuroeffector junction. changes in melatonin and norepinephrine release in vitro
title_sort role of prostaglandins in rat pineal neuroeffector junction. changes in melatonin and norepinephrine release in vitro
url http://hdl.handle.net/20.500.12110/paper_00137227_v111_n2_p530_Cardinali
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AT pereyrae roleofprostaglandinsinratpinealneuroeffectorjunctionchangesinmelatoninandnorepinephrinereleaseinvitro
AT solveyracg roleofprostaglandinsinratpinealneuroeffectorjunctionchangesinmelatoninandnorepinephrinereleaseinvitro
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