Differential responses of rat pineal thyroxine type II 5'-deiodinase and N-acetyltransferase activities to either light exposure, isoproterenol, phenylephrine, or propranolol

1. Compared to pineal N-acetyl transferase (NAT) activity, which exhibited a dramatic drop following acute light exposure at night, nocturnal rat pineal thyroxine type II 5'-deiodinase (5'-D) activity was minimally influenced by the same light exposure. The injection of cycloheximide, a po...

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Veröffentlicht in:Cellular and molecular neurobiology 1988-12, Vol.8 (4), p.447-458
Hauptverfasser: GUERRERO, J. M, PUIG-DOMINGO, M, SANTANA, C, MENENDEZ-PELAEZ, A, GONZALEZ-BRITO, A, REITER, R. J
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container_end_page 458
container_issue 4
container_start_page 447
container_title Cellular and molecular neurobiology
container_volume 8
creator GUERRERO, J. M
PUIG-DOMINGO, M
SANTANA, C
MENENDEZ-PELAEZ, A
GONZALEZ-BRITO, A
REITER, R. J
description 1. Compared to pineal N-acetyl transferase (NAT) activity, which exhibited a dramatic drop following acute light exposure at night, nocturnal rat pineal thyroxine type II 5'-deiodinase (5'-D) activity was minimally influenced by the same light exposure. The injection of cycloheximide, a potent inhibitor of protein synthesis, although it did curtail the rise in NAT activity for at least 2 hr, did not elicit decreases in the activities of either 5'-D or NAT enzymes. Propranolol, a beta-adrenergic blocker, either delayed the continued nocturnal rise in 5'-D activity when injected at 0000 hr or slightly enhanced the fall in 5'-D activity when injected at 0200 hr. These results suggest that interruption of the synthesis of proteins is responsible for the slow deterioration of 5'-D activity induced by either light or propranolol. 2. The slight fall in 5'-D activity induced by light at night was prevented by isoproterenol; phenylephrine, however, did not prevent the fall and the effect of isoproterenol + phenylephrine was similar to that obtained with isoproterenol alone. On the other hand, the light-inhibited NAT activity recovered after the injection of isoproterenol; phenylephrine did not elicit any effect, but the injection of both isoproterenol and phenylephrine simultaneously caused a greater NAT response than that induced by isoproterenol alone. 3. When injected during the day, phenylephrine had no effect on either pineal 5'-D or NAT activities; however, the injection of either isoproterenol alone or isoproterenol + phenylephrine elicited 5-fold and 10-fold increases in nocturnal, light-suppressed 5'-D and NAT activities, respectively. During the day, phenylephrine did not potentiate the effects of isoproterenol on NAT activity as it did at night. When the effects of isoproterenol on the 5'-D activity were compared to rats exposed to light during the day and at night, the activity of 5'-D reached a higher level at night than during the day.
doi_str_mv 10.1007/BF00711228
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M ; PUIG-DOMINGO, M ; SANTANA, C ; MENENDEZ-PELAEZ, A ; GONZALEZ-BRITO, A ; REITER, R. J</creator><creatorcontrib>GUERRERO, J. M ; PUIG-DOMINGO, M ; SANTANA, C ; MENENDEZ-PELAEZ, A ; GONZALEZ-BRITO, A ; REITER, R. J</creatorcontrib><description>1. Compared to pineal N-acetyl transferase (NAT) activity, which exhibited a dramatic drop following acute light exposure at night, nocturnal rat pineal thyroxine type II 5'-deiodinase (5'-D) activity was minimally influenced by the same light exposure. The injection of cycloheximide, a potent inhibitor of protein synthesis, although it did curtail the rise in NAT activity for at least 2 hr, did not elicit decreases in the activities of either 5'-D or NAT enzymes. Propranolol, a beta-adrenergic blocker, either delayed the continued nocturnal rise in 5'-D activity when injected at 0000 hr or slightly enhanced the fall in 5'-D activity when injected at 0200 hr. These results suggest that interruption of the synthesis of proteins is responsible for the slow deterioration of 5'-D activity induced by either light or propranolol. 2. The slight fall in 5'-D activity induced by light at night was prevented by isoproterenol; phenylephrine, however, did not prevent the fall and the effect of isoproterenol + phenylephrine was similar to that obtained with isoproterenol alone. On the other hand, the light-inhibited NAT activity recovered after the injection of isoproterenol; phenylephrine did not elicit any effect, but the injection of both isoproterenol and phenylephrine simultaneously caused a greater NAT response than that induced by isoproterenol alone. 3. When injected during the day, phenylephrine had no effect on either pineal 5'-D or NAT activities; however, the injection of either isoproterenol alone or isoproterenol + phenylephrine elicited 5-fold and 10-fold increases in nocturnal, light-suppressed 5'-D and NAT activities, respectively. During the day, phenylephrine did not potentiate the effects of isoproterenol on NAT activity as it did at night. When the effects of isoproterenol on the 5'-D activity were compared to rats exposed to light during the day and at night, the activity of 5'-D reached a higher level at night than during the day.</description><identifier>ISSN: 0272-4340</identifier><identifier>EISSN: 1573-6830</identifier><identifier>DOI: 10.1007/BF00711228</identifier><identifier>PMID: 3224360</identifier><identifier>CODEN: CMNEDI</identifier><language>eng</language><publisher>New York, NY: Springer</publisher><subject>Analytical, structural and metabolic biochemistry ; Animals ; Biological and medical sciences ; Circadian Rhythm ; Enzymes and enzyme inhibitors ; Fundamental and applied biological sciences. 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The injection of cycloheximide, a potent inhibitor of protein synthesis, although it did curtail the rise in NAT activity for at least 2 hr, did not elicit decreases in the activities of either 5'-D or NAT enzymes. Propranolol, a beta-adrenergic blocker, either delayed the continued nocturnal rise in 5'-D activity when injected at 0000 hr or slightly enhanced the fall in 5'-D activity when injected at 0200 hr. These results suggest that interruption of the synthesis of proteins is responsible for the slow deterioration of 5'-D activity induced by either light or propranolol. 2. The slight fall in 5'-D activity induced by light at night was prevented by isoproterenol; phenylephrine, however, did not prevent the fall and the effect of isoproterenol + phenylephrine was similar to that obtained with isoproterenol alone. On the other hand, the light-inhibited NAT activity recovered after the injection of isoproterenol; phenylephrine did not elicit any effect, but the injection of both isoproterenol and phenylephrine simultaneously caused a greater NAT response than that induced by isoproterenol alone. 3. When injected during the day, phenylephrine had no effect on either pineal 5'-D or NAT activities; however, the injection of either isoproterenol alone or isoproterenol + phenylephrine elicited 5-fold and 10-fold increases in nocturnal, light-suppressed 5'-D and NAT activities, respectively. During the day, phenylephrine did not potentiate the effects of isoproterenol on NAT activity as it did at night. 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J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-80ef7f431003a06a31e0fb3e87d74ac2c6a7f0c53b11da0bb370ec1c60d832c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Circadian Rhythm</topic><topic>Enzymes and enzyme inhibitors</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Iodide Peroxidase - metabolism</topic><topic>Iodide Peroxidase - physiology</topic><topic>Isoproterenol - pharmacology</topic><topic>Lighting</topic><topic>Male</topic><topic>Phenylephrine - pharmacology</topic><topic>Pineal Gland - drug effects</topic><topic>Pineal Gland - enzymology</topic><topic>Pineal Gland - physiology</topic><topic>Propranolol - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Receptors, Adrenergic - drug effects</topic><topic>Receptors, Adrenergic - physiology</topic><topic>Transferases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GUERRERO, J. M</creatorcontrib><creatorcontrib>PUIG-DOMINGO, M</creatorcontrib><creatorcontrib>SANTANA, C</creatorcontrib><creatorcontrib>MENENDEZ-PELAEZ, A</creatorcontrib><creatorcontrib>GONZALEZ-BRITO, A</creatorcontrib><creatorcontrib>REITER, R. 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J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential responses of rat pineal thyroxine type II 5'-deiodinase and N-acetyltransferase activities to either light exposure, isoproterenol, phenylephrine, or propranolol</atitle><jtitle>Cellular and molecular neurobiology</jtitle><addtitle>Cell Mol Neurobiol</addtitle><date>1988-12-01</date><risdate>1988</risdate><volume>8</volume><issue>4</issue><spage>447</spage><epage>458</epage><pages>447-458</pages><issn>0272-4340</issn><eissn>1573-6830</eissn><coden>CMNEDI</coden><abstract>1. Compared to pineal N-acetyl transferase (NAT) activity, which exhibited a dramatic drop following acute light exposure at night, nocturnal rat pineal thyroxine type II 5'-deiodinase (5'-D) activity was minimally influenced by the same light exposure. The injection of cycloheximide, a potent inhibitor of protein synthesis, although it did curtail the rise in NAT activity for at least 2 hr, did not elicit decreases in the activities of either 5'-D or NAT enzymes. Propranolol, a beta-adrenergic blocker, either delayed the continued nocturnal rise in 5'-D activity when injected at 0000 hr or slightly enhanced the fall in 5'-D activity when injected at 0200 hr. These results suggest that interruption of the synthesis of proteins is responsible for the slow deterioration of 5'-D activity induced by either light or propranolol. 2. The slight fall in 5'-D activity induced by light at night was prevented by isoproterenol; phenylephrine, however, did not prevent the fall and the effect of isoproterenol + phenylephrine was similar to that obtained with isoproterenol alone. On the other hand, the light-inhibited NAT activity recovered after the injection of isoproterenol; phenylephrine did not elicit any effect, but the injection of both isoproterenol and phenylephrine simultaneously caused a greater NAT response than that induced by isoproterenol alone. 3. When injected during the day, phenylephrine had no effect on either pineal 5'-D or NAT activities; however, the injection of either isoproterenol alone or isoproterenol + phenylephrine elicited 5-fold and 10-fold increases in nocturnal, light-suppressed 5'-D and NAT activities, respectively. During the day, phenylephrine did not potentiate the effects of isoproterenol on NAT activity as it did at night. When the effects of isoproterenol on the 5'-D activity were compared to rats exposed to light during the day and at night, the activity of 5'-D reached a higher level at night than during the day.</abstract><cop>New York, NY</cop><pub>Springer</pub><pmid>3224360</pmid><doi>10.1007/BF00711228</doi><tpages>12</tpages></addata></record>
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ispartof Cellular and molecular neurobiology, 1988-12, Vol.8 (4), p.447-458
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source MEDLINE; Springer Nature - Complete Springer Journals
subjects Analytical, structural and metabolic biochemistry
Animals
Biological and medical sciences
Circadian Rhythm
Enzymes and enzyme inhibitors
Fundamental and applied biological sciences. Psychology
Iodide Peroxidase - metabolism
Iodide Peroxidase - physiology
Isoproterenol - pharmacology
Lighting
Male
Phenylephrine - pharmacology
Pineal Gland - drug effects
Pineal Gland - enzymology
Pineal Gland - physiology
Propranolol - pharmacology
Rats
Rats, Inbred Strains
Receptors, Adrenergic - drug effects
Receptors, Adrenergic - physiology
Transferases
title Differential responses of rat pineal thyroxine type II 5'-deiodinase and N-acetyltransferase activities to either light exposure, isoproterenol, phenylephrine, or propranolol
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