Evidence map›Paper›PMID 37814103›Full record

ArticleForensic toxicology2024

Alcohol spiked with zolpidem and midazolam potentiates inflammation, oxidative stress and organ damage in a mouse model.

Biwott Kipchumba, Francis Gitonga, Careen Jepchirchir, Grace Wairimu Gitau, Patrick W Okanya, Peris Wanza Amwayi, Alfred Orina Isaac, Nyariki James Nyabuga

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In one paragraph

Article in Forensic toxicology, 2024. 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
0.5field-weighted citation impact, top 30% 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. Trial
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Biwott KipchumbaDepartment of Biochemistry and Biotechnology, Technical University of Kenya, 52428, Nairobi, 00200, Kenya.
Francis GitongaDepartment of Biochemistry and Biotechnology, Technical University of Kenya, 52428, Nairobi, 00200, Kenya.
Careen JepchirchirDepartment of Biochemistry and Biotechnology, Technical University of Kenya, 52428, Nairobi, 00200, Kenya.
Grace Wairimu GitauDepartment of Biochemistry and Biotechnology, Technical University of Kenya, 52428, Nairobi, 00200, Kenya.
Patrick W OkanyaDepartment of Biochemistry and Biotechnology, Technical University of Kenya, 52428, Nairobi, 00200, Kenya.
Peris Wanza AmwayiDepartment of Biochemistry and Biotechnology, Technical University of Kenya, 52428, Nairobi, 00200, Kenya.
Alfred Orina IsaacDepartment of Pharmaceutical Technology, School of Health Sciences and Technology, Technical University of Kenya, 52428, Nairobi, 00200, Kenya.
Nyariki James NyabugaDepartment of Biochemistry and Biotechnology, Technical University of Kenya, 52428, Nairobi, 00200, Kenya. nyabukaj@tukenya.ac.ke.ORCID 0000-0002-3213-7824
Technical University of Kenya · KE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCrime-related spiking of alcoholic drinks with prescription drugs is quite common and has been happening for centuries. This study, therefore, evaluated the effects of oral administration of alcohol spiked with the zolpidem and midazolam potent sedatives on inflammation, oxidative stress and various organ damage in male Swiss albino mice.

methodsMice were randomly assigned into six treatment groups; the first group constituted the normal control, the second group received 50 mg/kg body weight of zolpidem only, the third group received 50 mg/kg body weight zolpidem dissolved in 5 g/kg alcohol, the fourth group received 50 mg/kg midazolam only, the fifth group received midazolam (50 mg/kg) dissolved in 5 g/kg alcohol and the sixth group received 5 g/kg alcohol.

resultsAlcohol-induced significant reduction in neurological function and altered blood hematological indicators. Such neurological impairment and negative effects on blood were exacerbated in mice administered with spiked alcohol. Additionally, midazolam and zolpidem enhanced alcohol-driven elevation of liver function markers; the serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) gamma glutamyltransferase (GGT), total bilirubin and alkaline phosphatase. Exposure to alcohol and/or spiked alcohol led to significant augmentation of nitric oxide and malonaldehyde, with concomitant depletion of liver glutathione (GSH) levels. Similarly, serum levels of pro-inflammatory cytokines tumor necrosis factor alpha and interferon-gamma were increased by co-exposure with midazolam or zolpidem. Alcohol-induced hepatotoxicity and nephrotoxicity were amplified by exposure to alcohol spiked with midazolam/zolpidem.

conclusionExposure to alcohol spiked with midazolam or zolpidem appears to exacerbate neurological deficits, inflammation, oxidative stress, and organ damage.

Indexed as

MidazolamOxidative StressAnimalsBody WeightEthanolGlutathioneInflammationMaleMiceZolpidemEthanolGlutathioneMidazolamZolpidemInflammationMiceMidazolamOxidative stressSpiked alcoholZolpidem

Identifiers

PMID37814103
OpenAlexW4387451731

What Socratic 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 Socratic graph.