Evidence map›Paper›PMID 26950199›Full record

ArticleEndocrinology2016

Melatonin Synthesis: Acetylserotonin O-Methyltransferase (ASMT) Is Strongly Expressed in a Subpopulation of Pinealocytes in the Male Rat Pineal Gland.

Martin F Rath, Steven L Coon, Fernanda G Amaral, Joan L Weller, Morten Møller, David C Klein

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.1field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 76 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Martin F RathDepartment of Neuroscience and Pharmacology (M.F.R., M.M.), Faculty of Health and Medical Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark; and Section on Neuroendocrinology (M.F.R., S.L.C., F.G.A., J.L.W., D.C.K.), Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Steven L CoonDepartment of Neuroscience and Pharmacology (M.F.R., M.M.), Faculty of Health and Medical Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark; and Section on Neuroendocrinology (M.F.R., S.L.C., F.G.A., J.L.W., D.C.K.), Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Fernanda G AmaralDepartment of Neuroscience and Pharmacology (M.F.R., M.M.), Faculty of Health and Medical Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark; and Section on Neuroendocrinology (M.F.R., S.L.C., F.G.A., J.L.W., D.C.K.), Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Joan L WellerDepartment of Neuroscience and Pharmacology (M.F.R., M.M.), Faculty of Health and Medical Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark; and Section on Neuroendocrinology (M.F.R., S.L.C., F.G.A., J.L.W., D.C.K.), Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Morten MøllerDepartment of Neuroscience and Pharmacology (M.F.R., M.M.), Faculty of Health and Medical Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark; and Section on Neuroendocrinology (M.F.R., S.L.C., F.G.A., J.L.W., D.C.K.), Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
David C KleinDepartment of Neuroscience and Pharmacology (M.F.R., M.M.), Faculty of Health and Medical Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark; and Section on Neuroendocrinology (M.F.R., S.L.C., F.G.A., J.L.W., D.C.K.), Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Eunice Kennedy Shriver National Institute of Child Health and Human Development · USNational Institutes of Health · USUniversity of Copenhagen · DK

Funding

Pineal Regulation: Control of arylalkylamine N-acetyltransferaseZ01HD008836 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KLEIN, DAVID · 2007 to 2008
$2.0M
Pineal Regulation: Molecular basis of development Z01HD008837 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KLEIN, DAVID · 2007 to 2008
$1.2M
Pineal Regulation: Neural, transsynaptic and intracellular controlZ01HD008838 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KLEIN, DAVID · 2007 to 2008
$1.2M
Intramural NIH HHS Z01 HD008836Intramural NIH HHS Z01 HD008837Intramural NIH HHS Z01 HD008838
6 · The paper itself

Abstract

The rat pineal gland has been extensively used in studies of melatonin synthesis. However, the cellular localization of melatonin synthesis in this species has not been investigated. Here we focus on the localization of melatonin synthesis using immunohistochemical methods to detect the last enzyme in melatonin synthesis, acetylserotonin O-methyltransferase (ASMT), and in situ hybridization techniques to study transcripts encoding ASMT and two other enzymes in melatonin synthesis, tryptophan hydroxylase (TPH)-1 and aralkylamine N-acetyltransferase. In sections of the rat pineal gland, marked cell-to-cell differences were found in ASMT immunostaining intensity and in the abundance of Tph1, Aanat, and Asmt transcripts. ASMT immunoreactivity was localized to the cytoplasm in pinealocytes in the parenchyma of the superficial pineal gland, and immunopositive pinealocytes were also detected in the pineal stalk and in the deep pineal gland. ASMT was found to inconsistently colocalize with S-antigen, a widely used pinealocyte marker; this colocalization was seen in cells throughout the pineal complex and also in displaced pinealocyte-like cells of the medial habenular nucleus. Inconsistent colocalization between ASMT and TPH protein was also detected in the pineal gland. ASMT protein was not detected in extraepithalamic parts of the central nervous system or in peripheral tissues. The findings in this report are of special interest because they provide reason to suspect that melatonin synthesis varies significantly among individual pinealocytes.

Indexed as

Acetylserotonin O-MethyltransferaseAnimalsArylalkylamine N-AcetyltransferaseImmunohistochemistryMaleMelatoninPineal GlandRatsRats, Sprague-DawleyTryptophan HydroxylaseAcetylserotonin O-MethyltransferaseArylalkylamine N-AcetyltransferaseMelatoninTryptophan Hydroxylase

Identifiers

PMID26950199
PMCPMC4870883
OpenAlexW2300755804

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.