Evidence map›Paper›PMID 41291971›Full record

ArticleBMC pharmacology & toxicology2025

Biochemical, histopathological, and immunohistochemical study on the ameliorative effect of crocin against lipopolysaccharide‑induced hippocampal toxicity in male albino rats.

Eatemad A Awadalla, Ola Mohamed, Ahmed Abdelsadik, Hoda S Sherkawy, Abd El-Kader M Abd El-Kader

Abstract read
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Article in BMC pharmacology & toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Eatemad A AwadallaDepartment of Zoology, Faculty of Science, Aswan University, Aswan, 81511, Egypt. Eatemad2000@aswu.edu.eg.ORCID 0000-0002-5470-3575
Ola MohamedDepartment of Zoology, Faculty of Science, Aswan University, Aswan, 81511, Egypt.
Ahmed AbdelsadikDepartment of Zoology, Faculty of Science, Aswan University, Aswan, 81511, Egypt.
Hoda S SherkawyDepartment of Medical Biochemistry, Faculty of Medicine, Aswan University, Aswan, 81511, Egypt.
Abd El-Kader M Abd El-KaderDepartment of Zoology, Faculty of Science, Aswan University, Aswan, 81511, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLipopolysaccharide (LPS)-induced neuroinflammation is widely used as an animal model for studying the mechanisms of neuroinflammation. Crocin, an active component of saffron (Crocus sativus L), possesses several beneficial properties. The present study aimed to investigate the role of crocin in alleviating hippocampal toxicity induced by LPS in rats.

methodForty male albino rats were randomly divided into five groups. Group I served as a control. Group II intraperitoneally (i.p.) injected with LPS (1 mg/kg/day) for a week. Groups III, IV, and V were treated by oral gavage with captopril (50 mg/kg/day), crocin (50 mg/kg/day), and a combination of both captopril (50 mg/kg/day) and crocin (50 mg/kg/day), respectively for 30 consecutive days, starting on the 8th day after LPS i.p. injection. During the therapy schedule, rats were tested for memory and learning abilities. Hippocampal samples were collected for biochemical, histological, immunohistochemical, and morphometric studies. Biochemical evaluation included nuclear factor kappa B, inflammatory cytokines (tumor necrosis factor-α and interleukin-1β), amyloid beta, angiotensin-converting enzyme, markers of the cholinergic system (acetylcholinesterase and choline acetyltransferase), antioxidant enzymes (catalase and superoxide dismutase) and an oxidative stress indicator (malondialdehyde). Histological examinations, as well as immunohistochemical and histomorphometric analysis, were also performed on hippocampal tissue.

resultsThe results revealed biochemical, histological, and immunohistochemical alterations in the hippocampus of the LPS group. Most of these alterations showed satisfactory improvements in hippocampal tissue when LPS-administered rats were treated with captopril and crocin, either separately or in combination.

conclusionThe present study suggests that crocin acts as a promising therapeutic agent for alleviating memory impairments and neuroinflammation induced by LPS.

Indexed as

Anti-Inflammatory AgentsCarotenoidsHippocampusLipopolysaccharidesNeuroprotective AgentsAnimalsAntioxidantsCaptoprilMaleNeuroinflammatory DiseasesOxidative StressRatsAnti-Inflammatory AgentsAntioxidantsCaptoprilCarotenoidscrocinLipopolysaccharidesNeuroprotective AgentsCaptoprilCrocinHippocampal toxicityLipopolysaccharideMemory impairments

Identifiers

PMID41291971
PMCPMC12648831

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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.