Evidence map›Paper›PMID 33655408›Full record

ArticlePsychopharmacology2021

Co-administration of nalbuphine attenuates the morphine-induced anxiety and dopaminergic alterations in morphine-withdrawn rats.

Rahul Raghav, Raka Jain, Tony G Jacob, Anju Dhawan, Tara S Roy

Abstract read
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
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

5 authors at 1 institution in 1 country.

Rahul RaghavNational Drug Dependence Treatment Center, Department of Psychiatry, All India Institute of Medical Sciences, Room no. 4090, Teaching Block, New Delhi, 110029, India.
Raka JainNational Drug Dependence Treatment Center, Department of Psychiatry, All India Institute of Medical Sciences, Room no. 4090, Teaching Block, New Delhi, 110029, India. rakajain2009@gmail.com.
Tony G JacobDepartment of Anatomy, All India Institute of Medical Sciences, Room no. 1001, Teaching Block, New Delhi, 110029, India.
Anju DhawanNational Drug Dependence Treatment Center, Department of Psychiatry, All India Institute of Medical Sciences, Room no. 4090, Teaching Block, New Delhi, 110029, India.
Tara S RoyDepartment of Anatomy, All India Institute of Medical Sciences, Room no. 1001, Teaching Block, New Delhi, 110029, India.
All India Institute of Medical Sciences · IN

Funding

Indian Council of Medical Research, Govt. of India Grant, ID: 58/24/2011-BMS
6 · The paper itself

Abstract

introductionThe classical effects of exogenous opioids, such as morphine, are predominantly mediated through μ-opioid receptors. The chronic use of morphine induces anxiety-like behavior causing functional changes in the mesolimbic dopaminergic system. The mixed μ/κ-agonist, nalbuphine, used either as an analgesic or as an adjuvant with morphine, produces different and opposite effects. However, whether nalbuphine can be used to antagonize morphine-induced anxiety and dopaminergic alterations is not fully known.

objectiveThis study aimed to compare acute and chronic effects of nalbuphine on morphine-induced anxiety and dopaminergic alterations in rats.

methodsMale adult Wistar albino rats were made opioid-dependent by administering increasing doses of morphine (5-25 mg/kg; i.p.; b.i.d.). Withdrawal was induced by naloxone (1 mg/kg, i.p.), 4 h after the last morphine injection. Anxiety-like behavior was measured using Activity Monitor (Coulbourn Instruments, Inc. USA). Thereafter, the animals were sacrificed and the brain dissected out and the level of cAMP and the transcriptional and translational expression of TH was measured. Nalbuphine was co-administered with morphine, acutely and chronically, at various doses (0.1, 0.3, 1.0, 3.0 mg/kg, i.p.).

resultsMorphine-dependent rats showed a significant higher anxiety and cAMP levels and a significant decrease in the expression of TH. Co-administration of chronic doses of nalbuphine attenuates the higher anxiety, cAMP levels, and upregulates the TH expressions; however, the acute nalbuphine treatment does not attenuate the morphine-induced side effects.

conclusionTherefore, nalbuphine might have an important role in attenuating the anxiety and the effects of the dopaminergic pathway and may have potential in the treatment of opioid addiction.

Indexed as

Analgesics, OpioidAnimalsAnxietyCyclic AMPDopamineDose-Response Relationship, DrugMaleMorphineMotor ActivityNalbuphineNarcotic-Related DisordersRatsRats, WistarSubstance Withdrawal SyndromeTyrosine 3-MonooxygenaseAnalgesics, OpioidCyclic AMPDopamineMorphineNalbuphineTyrosine 3-MonooxygenaseAnxietyCo-administrationDopamineMorphineNalbuphineNaloxone

Identifiers

PMID33655408
OpenAlexW3133850360

What OpenQuestion holds

Textmetadata
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.