Evidence map›Paper›PMID 30018992›Full record

ArticleJournal of arthropod-borne diseases2018

Hemodynamic Changes in Experimentally Envenomed Anaesthetized Rats by Intravenous Injection of

Khalil Pourkhalili, Hossein Fatemikia, Euikyung Kim, Navid Reza Mashayekhy, Naser Mohammadpour Dounighi, Abdollah Hajivandi, Yaghoob Hassan, Ramin Seyedian

Open access · greenAbstract read
In one paragraph

Article in Journal of arthropod-borne diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Serological, pathological, and scintigraphic assessment ofIranian journal of basic medical sciences · 2018
    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

8 authors at 5 institutions in 2 countries.

Khalil PourkhaliliDepartment of Physiology, Faculty of Medicine, Bushehr University of Medical Sciences, Bushehr, Iran.
Hossein FatemikiaDepartment of Physiology, Faculty of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Euikyung KimCollege of Veterinary Medicine, Gyeongsang National University, Jinju, South Korea.
Navid Reza MashayekhyDepartment of Cardiology, Amir Kabir Hospital, Arak University of Medical Sciences, Arak, Iran.
Naser Mohammadpour DounighiDepartment of Human Vaccine and Serum, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization, Karaj, Iran.
Abdollah HajivandiDepartment of Biostatistics, Faculty of Health, Bushehr University of Medical Sciences, Bushehr, Iran.
Yaghoob HassanStudent Research Committee, Bushehr University of Medical Sciences, Bushehr, Iran.
Ramin SeyedianDepartment of Pharmacology, Bushehr University of Medical Sciences, Bushehr, Iran.
Bushehr University of Medical Sciences · IRAgricultural Research & Education Organization · IRArak University of Medical Sciences · IRGyeongsang National University · KRShiraz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe investigated the hemodynamic changes (Inotropic, chronotropic and arrhythmogenic) in intravenously envenomed anesthetized rats with

methodsDifferent doses of the crude venom (100, 200 and 400μg/rat) were injected during five minutes via the femoral vein and cardiovascular changes were recorded in rats in Razi Institute Corporation, Karaj, Iran in 2017. The drugs (Atropine, lidocaine, propranolol and prazosin) were injected before the venom for determination of the counteracting effects. Different volumes (100, 500 and 1000μl) of the antivenom were pre envenomed to neutralize cardiovascular changes.

resultsTemporary hypertension and bradycardia with no arrhythmogenic effects were depicted within twenty minutes. There was a difference in arterial pressure between the venom (400μg/rat) and the vehicle at 8 minutes (114.68±5.1mmHg versus 70.2±4.3mmHg). Elevation of the mean arterial pressure was inhibited by propranolol (2 mg/kg) and neutralized by prazosin (1mg/kg) while lidocaine (4mg/kg) and atropine (1mg/kg) had no effects. Premedication with Iranian commercial antivenom (1000μl) produced surprisingly temporary hypertension compared to the vehicle (140.84±4.5 versus 84.3±3.2). It had no neutralizing properties on blood pressure variation before the venom injection. Volume-expanded hypertension phenomenon was ruled out in a parallel study.

conclusionThis venom has vasoconstrictive effects in rats probably due to the presence of norepinephrine like materials in its content or liberated from adrenal gland inhibited by prazosin premedication. The neutralizing effects of antivenom on venom-induced hypertension are questionable.

Indexed as

Hemiscorpius lepturusPolyvalent antivenomVasoconstriction

Identifiers

PMID30018992
PMCPMC6046103
OpenAlexW2801422720

What OpenQuestion holds

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LicenceCC BY
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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.