El-Shehawi Ahmed M, Sayed Samy, Elseehy Mona M, Alotaibi Saqer, Alharthi Siraj B, Alsharif Ghadi, Soliman Mohamed
Department of Biotechnology, College of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Department of Economic Entomology and Pesticides, Faculty of Agriculture, Cairo University, Giza 12613, Egypt.
Toxicol Res (Camb). 2025 Mar 17;14(2):tfaf038. doi: 10.1093/toxres/tfaf038. eCollection 2025 Apr.
Acrylamide (A) is known for its biological toxicity and is recognized for its various biological activities. The leaf extract of was utilized as a protective approach from acrylamide-induced oxidative stress at the transcriptome level by analyzing global gene expression, biological processes and pathways. Three groups of rats were used to investigate the protective effect of leaf extract on the liver transcriptome: Group C (Control), group A (received acrylamide), and group A_S (received acrylamide and extract). Transcriptome analysis was conducted using RNAseq with the Illumina NovaSeq 6,000. The results identified 53 differentially expressed genes (DEGs) in A/C and 91 genes in A_S/C comparisons. Various GO terms were significantly enriched, with 19 terms in the A/C comparison and 6 terms in the A_S/C comparison. In addition, several pathways were enriched, including ATP biosynthesis, mitochondrial inner membrane, and iron binding. The extract of exhibited various effects, including A-like, A-antagonistic, or A-agonistic on gene expression. This explains the observed contradiction of extract on the global gene expression of rat liver. The identified DEGs in the current study are associated with various pathways, including electron transport chain, mitochondrial apoptosis, ribosome function, iron binding, and homeostasis. The findings indicate an A-like transcriptomic toxicity of although its previously reported antioxidant and anti-inflammatory activities. This raises concerns about the safety of medicinal plants and their widespread use in food supplements and alternative medicine, emphasizing the need for their assessment at various biological levels.
丙烯酰胺(A)以其生物毒性而闻名,并且因其多种生物活性而受到认可。通过分析全局基因表达、生物学过程和途径,[植物名称]的叶提取物被用作一种在转录组水平上抵御丙烯酰胺诱导的氧化应激的保护方法。使用三组大鼠来研究[植物名称]叶提取物对肝脏转录组的保护作用:C组(对照组)、A组(接受丙烯酰胺)和A_S组(接受丙烯酰胺和[植物名称]提取物)。使用Illumina NovaSeq 6000通过RNAseq进行转录组分析。结果在A/C比较中鉴定出53个差异表达基因(DEG),在A_S/C比较中鉴定出91个基因。各种基因本体(GO)术语显著富集,在A/C比较中有19个术语,在A_S/C比较中有6个术语。此外,还富集了几条途径,包括ATP生物合成、线粒体内膜和铁结合。[植物名称]提取物对基因表达表现出多种影响,包括类似A、拮抗A或激动A的作用。这解释了观察到的[植物名称]提取物对大鼠肝脏全局基因表达的矛盾现象。本研究中鉴定出的DEG与各种途径相关,包括电子传递链、线粒体凋亡、核糖体功能、铁结合和体内稳态。研究结果表明,尽管[植物名称]先前报道具有抗氧化和抗炎活性,但其具有类似A的转录组毒性。这引发了对药用植物安全性及其在食品补充剂和替代医学中广泛使用的担忧,强调了在不同生物学水平上对其进行评估的必要性。