Evidence map›Paper›PMID 39315284›Full record

ArticleMolecular biology research communications2024

The hepatoprotective effects of sitagliptin against cyclophosphamide-induced hepatotoxicity in rat.

Reza Maleki, Mohammad Foad Noorbakhsh, Nasrin Kazemipour, Maliheh Masoudian, Fatemeh Namazi, Saeed Nazifi

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Article in Molecular biology research communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Reza MalekiDepartment of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Mohammad Foad NoorbakhshDepartment of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Nasrin KazemipourDepartment of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Maliheh MasoudianMolecular Department of Central Laboratory, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Fatemeh NamaziDepartment of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Saeed NazifiDepartment of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatotoxicity is a serious side effects of cyclophosphamide. Thus, the present research investigates the protective properties of sitagliptin against cyclophosphamide-induced hepatotoxicity. Fifty male rats were randomly divided into five groups. They were pre-treated with either sitagliptin or normal saline once a day for the first ten days of the study. To induce acute hepatotoxicity, cyclophosphamide (200 mg/kg, i.p) was injected only one time and 45 min after the last dose of sitagliptin. The rats were sacrificed on the 11th day, and their blood and liver were collected for biochemical, gene expression, and histopathological assessments. Our results showed that cyclophosphamide induced obvious liver toxicity as marked by an increase in serum levels of alanine transaminase and aspartate transaminase, reduced serum albumin and total protein levels, in addition to histopathological changes. The malondialdehyde, tumor necrosis factor-α, and interleukin-6 levels were also elevated and total antioxidant capacity declined in serum and hepatic homogenates. Sitagliptin magnificently attenuated the cylophosphamide-induced histological alterations, improved liver function tests, enhanced total antioxidant capacity, and decreased malondialdehyde, tumor necrosis factor-α, and interleukin-6 in the blood and hepatic tissues. These findings suggest that sitagliptin has hepatoprotective activity against cyclophosphamide toxicity, which may be due to its antioxidant and anti-inflammatory effects.

Indexed as

CyclophosphamideHepatotoxicityOxidative StressSitagliptin

Identifiers

PMID39315284
PMCPMC11416847

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