Evidence map›Paper›PMID 35047129›Full record

ArticleAddiction & health2021

Tramadol Treatment Induces Change in Phospho-Cyclic Adenosine Monophosphate Response Element-Binding Protein and Delta and Mu Opioid Receptors within Hippocampus and Amygdala Areas of Rat Brain.

Hamid Ahmadian-Moghadam, Mitra Sadat Sadat-Shirazi, Somaiyeh Azmoun, Reza Vafadoost, Solmaz Khalifeh, Mohammad Reza Zarrindast

Open access · greenAbstract read
In one paragraph

Article in Addiction & health, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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.

Hamid Ahmadian-MoghadamIranian National Center for Addiction Studies, Tehran University of Medical Sciences, Tehran, Iran.
Mitra Sadat Sadat-ShiraziCognitive and Neuroscience Research Center, Amir-Almomenin Hospital, Tehran Medical Branch, Islamic Azad University, Tehran, Iran.
Somaiyeh AzmounDepartment of Environmental Health Sciences, Florida International University, Florida, USA.
Reza VafadoostDepartment of Pathology, School of Dentistry, Islamic Azad University, Tehran Medical Branch, Tehran, Iran.
Solmaz KhalifehCognitive and Neuroscience Research Center, Amir-Almomenin Hospital, Tehran Medical Branch, Islamic Azad University, Tehran, Iran.
Mohammad Reza ZarrindastDepartment of Pharmacology, School of Medicine AND Iranian National Center for Addiction Studies AND Endocrinology and Metabolism Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Islamic Azad University Medical Branch of Tehran · IRTehran University of Medical Sciences · IRFlorida International University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTramadol induces its unique effects through opioid pathways, but the exact mechanism is not known. The study aims to evaluate changes in the level of mu-opioid receptor (µOR), delta-opioid receptor (δOR), and phosphorylated cyclic adenosine monophosphate (cAMP) response element-binding protein (p-CREB) in the hippocampus (HPC) and amygdala (AL) areas of tramadol-treated rats.

methodsFor this purpose, a total of 36 male rats were divided into two main groups for chronic or acute tramadol exposure. The animals were then exposed to 5 mg.kg-1 of tramadol, 10 mg.kg-1 of tramadol, and normal saline. The HPC and AL areas of the animals were dissected upon completion of the period. The levels of p-CREB and µOR were quantified using the western blotting technique. The data were subjected to analysis of variance (ANOVA) followed by Tukey's post-hoc analysis. The differences with the P-value lower than 0.05 were considered as significant.

findingsIn the HPC and AL areas of the brain, the level of µOR was decreased by acute tramadol exposure, while no significant difference was observed by chronic tramadol exposure. Moreover, results showed that the level of p-CREB dose-dependently increased by acute and chronic tramadol exposure.

conclusionHPC and AL are essential in the control of tramadol abuse. Tramadol abuse affects gene expression and transcription factors such as CREB. With acute drug tramadol treatments, the level of cAMP response element-binding protein (CREB) rapidly increases, while by chronic tramadol treatment, "peak and trough pattern is observing". The activation of the rewarding mechanism is a precise instance of addictive behavior in tramadol-treated individuals.

Indexed as

AmygdalaCyclic adenosine monophosphate response element-binding protein AHippocampusOpioid receptorTramadol

Identifiers

PMID35047129
PMCPMC8730448
OpenAlexW3208004438

What OpenQuestion holds

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Registered trials

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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.