ArticleFrontiers in pharmacology2026
Eliglustat prevents acute kidney injury caused by Shiga toxin 2 in lethal and sublethal rat models of hemolytic uremic syndrome.
Article in Frontiers in pharmacology, 2026. 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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Abstract
Background: Shiga toxin-producing Methods: Male juvenile Sprague-Dawley rats (∼100 g body weight (bw)) were intraperitoneally injected with lethal (5 ng/g bw) or sublethal (1 ng/g bw) doses of Stx2, or eluent. Some rats were orally treated with EG (15 mg/d or 25 mg/d) for 0-2 days, until 2 days or 3 days post-injection. Rat survival, renal Gb3 expression, renal function, histopathological observations, and aquaporin 1 (AQP1) and neutrophil gelatinase-associated lipocalin (NGAL) tubular expression were evaluated. Results: Rats injected with the Stx2 lethal dose showed significant kidney injury with extended tubular necrosis and some glomerular alterations at 3 days post-injection. The Stx2 sublethal dose caused significantly less renal injury extension than the lethal dose, showing only tubular damage. The expression of AQP1 and NGAL corroborated the tubular alteration in Stx2-injected rats. The oral treatment with EG reduced Gb3 renal levels and, therefore, significantly prevented the renal injury caused by lethal and sublethal doses of Stx2 in rats. Moreover, the pretreatment for 2 days with EG prevented the mortality in those rats injected with the Stx2 lethal dose. The EG treatment did not cause renal or systemic alterations. The effectiveness of EG treatment depended on the dose and the pretreatment time. Conclusion: The oral treatment with EG could be a therapeutic strategy to prevent the action of Stx2 and the development of acute kidney injury in diarrhea-associated HUS patients.
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