Pathology of experimental arsenic toxicity in rats and investigation of protective effect of simultaneously administered <i>Cistus laurifolius</i> L. (Cistaceae)

Sodium arsenite is abundantly available in the environment, and arsenic toxicity is a public health problem that raises concerns worldwide. In this study, the protective effect of Cistus laurifolius L. (Cistaceae) against sodium arsenite-induced oxidative stress in rats was investigated. The 108 male Sprague-Dawley rats were divided into 12 equal groups. Group 1 was the negative control, and no treatment was given to the rats in this group. Group 2 was the normal control, and only carboxymethyl cellulose (CMC) was given as the solvent of the plant extract. Group 3 received 5 mg/kg sodium arsenite. Groups 4, 5, 6, and 7 were given 500 mg/kg/day doses of n-hexane, diethyl ether, ethyl acetate, and methanolic extracts of Cistus laurifolius L. (Cistaceae), respectively. Groups 8, 9, 10, and 11 were given a 500 mg/kg/day doses of sodium arsenite (5 mg/kg) and respectively the n-hexane, diethyl ether, ethyl acetate, and methanolic extracts of Cistus laurifolius L. simultaneously. Group 12 was given sodium arsenite (5 mg/kg), as well as alpha lipoic acid (70 mg/kg) as a standard control. All treatments were given for 32 days through gastric gavage. Cistus laurifolius extracts and alpha-lipoic acid reduced oxidative stress and protected tissues from histopathological damage, while ethyl acetate extract showed a greater reduction in metallothionein positivity. In conclusion, it was determined that Cistus laurifolius L. extracts, especially its ethyl acetate extract, had protective effects against sodium arsenite-induced oxidative damage in rats.

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Journal
Toxicology Research
Published
2025-07-05
DOI
https://doi.org/10.1093/toxres/tfaf085
Primary Topic
Drug-Induced Hepatotoxicity and Protection
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article
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article

Pathology of experimental arsenic toxicity in rats and investigation of protective effect of simultaneously administered Cistus laurifolius L. (Cistaceae)

Hasan Hüseyin Demirel, Erkan Karadaş, Esra Küpeli-Akkol
Toxicology Research
Drug-Induced Hepatotoxicity and Protection
article

Pathology of experimental arsenic toxicity in rats and investigation of protective effect of simultaneously administered Cistus laurifolius L. (Cistaceae)

Hasan Hüseyin Demirel, Erkan Karadaş, Esra Küpeli-Akkol
article en

Abstract

Sodium arsenite is abundantly available in the environment, and arsenic toxicity is a public health problem that raises concerns worldwide. In this study, the protective effect of Cistus laurifolius L. (Cistaceae) against sodium arsenite-induced oxidative stress in rats was investigated. The 108 male Sprague-Dawley rats were divided into 12 equal groups. Group 1 was the negative control, and no treatment was given to the rats in this group. Group 2 was the normal control, and only carboxymethyl cellulose (CMC) was given as the solvent of the plant extract. Group 3 received 5 mg/kg sodium arsenite. Groups 4, 5, 6, and 7 were given 500 mg/kg/day doses of n-hexane, diethyl ether, ethyl acetate, and methanolic extracts of Cistus laurifolius L. (Cistaceae), respectively. Groups 8, 9, 10, and 11 were given a 500 mg/kg/day doses of sodium arsenite (5 mg/kg) and respectively the n-hexane, diethyl ether, ethyl acetate, and methanolic extracts of Cistus laurifolius L. simultaneously. Group 12 was given sodium arsenite (5 mg/kg), as well as alpha lipoic acid (70 mg/kg) as a standard control. All treatments were given for 32 days through gastric gavage. Cistus laurifolius extracts and alpha-lipoic acid reduced oxidative stress and protected tissues from histopathological damage, while ethyl acetate extract showed a greater reduction in metallothionein positivity. In conclusion, it was determined that Cistus laurifolius L. extracts, especially its ethyl acetate extract, had protective effects against sodium arsenite-induced oxidative damage in rats.

Toxicology ResearchVol. 14(4)
Dokuz Eylül University (TR), Afyon Kocatepe University (TR), Gazi University (TR)
Openalex Percentile: Top 78%
Drug-Induced Hepatotoxicity and Protection
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