Abd-Elhakim Yasmina M, Mohamed Amany Abdel-Rahman, Khamis Tarek, Metwally Mohamed M M, El-Shetry Eman S, Albaqami Amirah, Mawkili Wedad, Alosaimi Manal E, Alotaibi Badriyah S, ElAshmouny Naira, Dahran Naief, Alsharif Ghadi, Samak Mai A
Department of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt.
Department of Pharmacology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt; Laboratory of Biotechnology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt.
Tissue Cell. 2024 Dec;91:102574. doi: 10.1016/j.tice.2024.102574. Epub 2024 Sep 25.
Little is known about the effects of acrylamide (AMD) on the stomach. So, this study evaluated the effect of oral AMD exposure (20 mg/kg b.wt) on oxidative status, apoptotic, and inflammatory reactions in rat's stomach for 60 days. To explore novel targets of AMD toxicity, a more detailed molecular and immune-expression study was performed. Besides, the possible protective effect of green synthesized zinc oxide nanoparticles (G-ZNP) (10 mg/kg b.wt) was explored. The results revealed that AMD significantly provoked oxidative and lipid peroxidative damage of the stomach in terms of increased ROS and MDA but reduced SOD, CAT, GSH, and GSH/GSSG. Additionally, the stomachs of AMD-exposed rats showed a significant increment of PGE2 but reduced NO. Histopathologically, AMD induced a significant increase in PAS stain and the immunoexpression of iNOS and NF-κB in the glandular stomach. A significant upregulation of CART, VACHT, EGFR, caspase-3, NOS-1, and miR-27a-5p was evident in the stomach of the AMD group. Yet, G-ZNP oral dosing significantly rescued the AMD-induced oxidative damage, apoptotic reaction, inflammatory effect, and altered miR-27a-5p and gene expressions in the stomach. Conclusively, these findings demonstrated the efficacy of G-ZNP in protecting against the harmful impacts of acrylamide on stomach tissues.
关于丙烯酰胺(AMD)对胃的影响,人们了解甚少。因此,本研究评估了口服AMD(20毫克/千克体重)连续60天对大鼠胃的氧化状态、凋亡及炎症反应的影响。为探索AMD毒性的新靶点,进行了更详细的分子和免疫表达研究。此外,还探究了绿色合成氧化锌纳米颗粒(G-ZNP,10毫克/千克体重)可能的保护作用。结果显示,AMD显著引发胃的氧化和脂质过氧化损伤,表现为活性氧(ROS)和丙二醛(MDA)增加,但超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽(GSH)及谷胱甘肽/氧化型谷胱甘肽(GSH/GSSG)减少。此外,暴露于AMD的大鼠胃中前列腺素E2(PGE2)显著增加,但一氧化氮(NO)减少。组织病理学上,AMD导致腺胃中过碘酸雪夫氏(PAS)染色、诱导型一氧化氮合酶(iNOS)和核因子κB(NF-κB)的免疫表达显著增加。在AMD组大鼠的胃中,可卡因-安非他明调节转录肽(CART)、囊泡乙酰胆碱转运体(VACHT)、表皮生长因子受体(EGFR)、半胱天冬酶-3(caspase-3)、一氧化氮合酶-1(NOS-1)和微小RNA-27a-5p(miR-27a-5p)明显上调。然而,口服G-ZNP显著挽救了AMD诱导的氧化损伤、凋亡反应、炎症效应以及胃中miR-27a-5p和基因表达的改变。总之,这些发现证明了G-ZNP在预防丙烯酰胺对胃组织的有害影响方面的功效。