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一种具有潜在抗 COVID-19 作用的抗疟植物药在短期毒性研究中对啮齿动物的物理、生物学和遗传毒性参数的影响。

Impacts of , an Antimalarial Phytomedicine With Potential Anti-COVID-19, on the Physical, Biological, and Genotoxicity Parameters of Rodents in Short-Term Toxicity Studies.

作者信息

Ouédraogo Joël, Ilboudo Sylvain, Ouédraogo Geoffroy Gueswindé, Dakuyo Virginie, Ouédraogo Salfo, Somda Gaétan D, Ouédraogo Jean Claude Romaric Pingdwindé, Ouédraogo Moussa, Semdé Rasmané, Ouédraogo Sylvin

机构信息

Department of Traditional Medicine-Pharmacopoeia and Pharmacy, Institute for Research in Health Sciences, National Center for Scientific and Technological Research (MEPHATRA-PH/IRSS/CNRST), Ouagadougou 03 BP 7047, Burkina Faso.

Laboratory for Drug Development, African Center of Excellence for Training, Research and Expertise in Pharmaceutical Sciences, Joseph KI-ZERBO University (LADME/CEA-CFOREM/UJKZ), Ouagadougou 03 BP 7021, Burkina Faso.

出版信息

J Toxicol. 2025 Jul 21;2025:7536185. doi: 10.1155/jt/7536185. eCollection 2025.

Abstract

In response to the COVID-19 pandemic and following the World Health Organization's call for action, several traditional medicine recipes were used without any scientific prerequisites concerning their safety. The current study investigated several short-term toxicity parameters of SAYE PLUS, an antimalarial phytomedicine used in COVID-19 patients in Burkina Faso. Following the guidelines of the Organisation for Economic Co-operation and Development (OECD), the safety profile of SAYE PLUS was investigated in a battery of tests in rats and mice. In an acute toxicity study, male and female rats received a single oral dose of 2000 mg/kg b.w. of the test substance. For the subacute toxicity test, male and female rats received daily oral doses of 250, 500, and 1000 mg/kg b.w. for 28 days. Acute and subacute toxicity tests were accompanied by food and water intake, body and organ relative weight, and blood chemistry of animals recording. In mutagenicity, sperm quality, and lipid peroxidation tests, mice were orally exposed to daily oral doses of 500, 1000, and 2000 mg/kg for seven days. Single dose of 2000 mg/kg b.w. of SAYE PLUS did not cause rats mortality. The LD is more than 2000 mg/kg b.w. Daily administration of SAYE PLUS for 28 days did not induce any significant change in the water or food intake and the body or organ relative weights of animals. Furthermore, no significant change was observed in biochemical parameters. In the test conditions, the recipe did not induce an increase of micronucleus or changes in sperm motility and number. However, all tested doses of SAYE PLUS induced a significant increase in MDA levels in mice serum. These results show that SAYE PLUS did not induce negative impacts on studied parameters, but the possible lipidic peroxidation observed must be further investigated for its mechanism and effects.

摘要

为应对新冠疫情,并响应世界卫生组织的行动呼吁,一些传统医学配方在未具备任何关于其安全性的科学前提条件下就被使用。本研究调查了SAYE PLUS的几个短期毒性参数,SAYE PLUS是布基纳法索用于新冠患者的一种抗疟植物药。遵循经济合作与发展组织(OECD)的指导方针,在一系列针对大鼠和小鼠的试验中研究了SAYE PLUS的安全性。在急性毒性研究中,雄性和雌性大鼠单次口服给予2000 mg/kg体重的受试物质。在亚急性毒性试验中,雄性和雌性大鼠每日口服给予250、500和1000 mg/kg体重,持续28天。急性和亚急性毒性试验同时记录动物的食物和水摄入量、身体和器官相对重量以及血液生化指标。在致突变性、精子质量和脂质过氧化试验中,小鼠每日口服给予500、1000和2000 mg/kg,持续7天。2000 mg/kg体重的SAYE PLUS单次给药未导致大鼠死亡。LD大于2000 mg/kg体重。SAYE PLUS连续给药28天未引起动物的水或食物摄入量以及身体或器官相对重量发生任何显著变化。此外,生化参数也未观察到显著变化。在试验条件下,该配方未诱导微核增加或精子活力和数量的改变。然而,所有测试剂量的SAYE PLUS均导致小鼠血清中MDA水平显著升高。这些结果表明,SAYE PLUS对所研究的参数未产生负面影响,但观察到的可能的脂质过氧化作用,其机制和影响必须进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1571/12303639/6e39b58d4ece/JT2025-7536185.001.jpg

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