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巴西红蜂胶口服摄入的遗传毒性和毒理学评价:一种临床前啮齿动物模型研究。

Genotoxicity and toxicological evaluations of Brazilian red propolis oral ingestion in a preclinical rodent model.

机构信息

School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Avenida do Café, s/nº, Ribeirão Preto, São Paulo, Brazil.

Nucleus of Research in Sciences and Technology, Laboratory of Mutagenesis, University of Franca, Av. Dr. Armando de Sáles Oliveira, 201 - Parque Universitario, Franca, São Paulo, Brazil.

出版信息

J Ethnopharmacol. 2023 Mar 1;303:115920. doi: 10.1016/j.jep.2022.115920. Epub 2022 Nov 11.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Brazilian red propolis is a natural product known due to its medicinal properties. The efficacy of this natural resin has been proved; however, few studies report the safety of its oral use. Some toxic effects of natural products may not be expressed in traditional use, and preclinical studies are necessary to guarantee their safety. Health regulatory agency currently requires these non-clinical studies to develop drugs and herbal medicines, including genotoxic and oral toxicity tests.

AIM OF THE STUDY

Accomplish the preclinical toxicity studies of Brazilian red propolis extract (BRP) in rodents, including genotoxicity, acute and sub-chronic toxicities.

MATERIAL AND METHODS

Genotoxicity assays followed the erythrocyte micronucleus test protocol in a range of 500-2000 mg/kg BRP oral treatment on male Swiss mice. After an up-and-down procedure, acute oral toxicity (single dose) was performed on female Wistar Hannover rats, reaching a 2000 mg/kg BRP oral gavage concentration. Animals were monitored periodically until 14 days and euthanized for a macroscopic necropsy analysis. The sub-chronic oral toxicity test (90 days) was achieved with 1000 mg/kg of BRP on Wistar Hannover rats (males/females). Animals were monitored to evaluated behavioral and biometrical changes, then were euthanized to perfomed hematological, biochemical, and histopathological analyses.

RESULTS

No genotoxic effect of the BRP was detected. The acute toxicity indicated no toxicity of a single oral dose of 2000 mg/kg of BRP. The long-term oral toxicity performed with 1000 mg/kg of BRP altered water and food intake and the biometrics, hematological and biochemical parameters. Biochemical alterations in hepatic and renal parameters were detected only in the males. Despite the detection of biochemical alterations, no histopathological changes were detected in the organs of any group.

CONCLUSIONS

BRP, at a higher dose, showed no signs of immediate toxicity. However, the obtained results suggest that the chemical composition and the intake of higher doses deserve special attention regarding possible toxicity.

摘要

民族药理学相关性

巴西红蜂胶是一种天然产物,以其药用特性而闻名。这种天然树脂的功效已得到证实;然而,很少有研究报告其口服使用的安全性。一些天然产物的毒性作用可能在传统用途中没有表现出来,因此需要进行临床前研究以保证其安全性。目前,健康监管机构要求这些非临床研究开发药物和草药,包括遗传毒性和口服毒性测试。

研究目的

完成巴西红蜂胶提取物(BRP)在啮齿动物中的临床前毒性研究,包括遗传毒性、急性毒性和亚慢性毒性。

材料和方法

遗传毒性试验遵循红细胞微核试验方案,对雄性瑞士小鼠进行 500-2000mg/kg BRP 口服治疗。在上下程序后,对雌性 Wistar 汉诺威大鼠进行急性口服毒性(单次剂量)试验,达到 2000mg/kg BRP 口服灌胃浓度。动物定期监测至 14 天,并进行大体解剖分析后安乐死。采用 1000mg/kg BRP 对 Wistar 汉诺威大鼠(雄性/雌性)进行亚慢性口服毒性试验(90 天)。监测动物以评估行为和生物计量变化,然后安乐死进行血液学、生化学和组织病理学分析。

结果

BRP 没有遗传毒性作用。单次口服 2000mg/kg BRP 的急性毒性试验表明无毒性。用 1000mg/kg BRP 进行长期口服毒性试验改变了水和食物的摄入以及生物计量、血液学和生化学参数。雄性动物的肝肾功能参数生化改变仅被检测到。尽管检测到生化改变,但任何组别的器官均未发现组织病理学变化。

结论

BRP 在较高剂量下没有表现出立即毒性的迹象。然而,所得结果表明,其化学成分和更高剂量的摄入值得特别注意可能的毒性。

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