Evidence map›Paper›PMID 34998646›Full record

ArticleJournal of Ayurveda and integrative medicine

An in vivo acute toxicity and anti-shigellosis effect of designed formulation on rat.

Devendra Singh, Vishnu Agarwal

Abstract read
In one paragraph

Article in Journal of Ayurveda and integrative medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Devendra SinghDepartment of Biotechnology, Motilal Nehru National Institute of Technology, Allahabad 211004, Uttar Pradesh, India.
Vishnu AgarwalDepartment of Biotechnology, Motilal Nehru National Institute of Technology, Allahabad 211004, Uttar Pradesh, India. Electronic address: vishnua@mnnit.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionShigellosis is an intestinal disease and is one of the main causes of morbidity and mortality among children in India. The study aims to analyze the effect of the designed formulation on the hematological parameters in shigellosis-induced rats and assess the in vivo toxicity of this formulation.

methodsMale Wistar rats were housed in different groups. Group 1 is normal control; group 2 is diseased control; group 3 and group 4 diseased rats received 250 mg/kg formulation and 20 mg/kg body weight norfloxacin, respectively, orally once a day. Shigellosis was induced by a single intraperitoneal injection of Shigella flexneri, and bacterial load was calculated using the Shigella agar plate. On completion of the study, blood was collected for hematological as well as electrolyte analysis.

resultsThe in vivo acute toxicity results indicate that the formulation is safe up to 2000 mg/kg. Furthermore, formulation significantly (p < 0.05) decreases the bacterial load and increases the RBC, WBC, MCHC, platelet, hemoglobin, and electrolytes (Ca

conclusionThe results support the designed formulation's safety and therapeutic effects and support its use as an alternative medicine for treating shigellosis.

Indexed as

FormulationHematological parametersNorfloxacinRatsShigellosis

Identifiers

PMID34998646
PMCPMC10105236

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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.