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ω-3在临床前试验中对降低阿霉素毒性的保护作用。

Protective effect of omega-3 on reducing doxorubicin toxicity in preclinical trials.

作者信息

de Paiva Marcelo Henrique, de Almeida-Junior Silvio, Garcia Cristiane Buzatto, Pereira Poliana Marques, Martins João Guilherme, Stante Flávio Henrique Rodrigues, Lucera Tiago Machado Carneiro, Dias Fernanda Gosuen Gonçalves, Furtado Ricardo Andrade, Junior Daniel Paulino

机构信息

Graduate Program in Animal Science, Animal Science Laboratory, University of Franca, Franca, São Paulo, Brazil.

出版信息

Toxicol Rep. 2025 May 22;14:102056. doi: 10.1016/j.toxrep.2025.102056. eCollection 2025 Jun.

Abstract

The use of chemotherapeutic agents, such as doxorubicin, is often associated with severe adverse effects, making it essential to develop therapeutic strategies that can attenuate or reduce their toxicity. This study aimed to investigate the effects of omega-3 in mitigating the damage induced by doxorubicin. Rabbits received doxorubicin (1 mg/kg, twice weekly for six weeks) with or without omega-3 (500, 1000, or 2000 mg/kg), administered concomitantly. An additional group received omega-3 alone (2000 mg/kg). Hematological, biochemical, genotoxic (micronucleus assay), cardiological (electrocardiogram, echocardiogram, and markers), and histopathological parameters were assessed. Os resultados mostraram que o tratamento com doxorrubicina isolada induziu caquexia nos animais. O tratamento com ômega-3 melhora parâmetros como ganho de peso, fração de ejeção cardíaca, encurtamento sistólico ventricular, marcadores cardíacos CK-MB e Troponina I, área do ventrículo esquerdo e parâmetros histopatológicos (inflamação, edema, dano celular e fibras musculares), sugerindo um efeito protetor. Além disso, o ômega-3 exibiu atividade antigenotóxica, evidenciada pela redução de micronúcleos. Esses achados indicam que o ômega-3 pode servir como um complemento eficaz à quimioterapia, reduzindo a toxicidade da doxorrubicina.

摘要

使用化疗药物,如阿霉素,通常会伴随严重的副作用,因此开发能够减轻或降低其毒性的治疗策略至关重要。本研究旨在调查ω-3对减轻阿霉素所致损伤的影响。兔子接受阿霉素(1毫克/千克,每周两次,共六周),同时给予或不给予ω-3(500、1000或2000毫克/千克)。另一组单独给予ω-3(2000毫克/千克)。评估血液学、生化、遗传毒性(微核试验)、心脏(心电图、超声心动图和标志物)和组织病理学参数。结果显示,单独使用阿霉素治疗可导致动物恶病质。ω-3治疗改善了体重增加、心脏射血分数、心室收缩期缩短、心脏标志物肌酸激酶同工酶(CK-MB)和肌钙蛋白I、左心室面积以及组织病理学参数(炎症、水肿、细胞损伤和肌肉纤维)等参数,提示具有保护作用。此外,ω-3表现出抗遗传毒性活性,微核减少证明了这一点。这些结果表明,ω-3可作为化疗的有效补充,降低阿霉素的毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7e3/12159444/950c7bfac43d/ga1.jpg

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