鸡胚胎模型中内皮素-1诱导的持续性缺血

IF 1 Q3 BIOLOGY Bio-protocol Pub Date : 2024-09-05 DOI:10.21769/BioProtoc.5061
Neha Kumari, Ravi Prakash, Abu J Siddiqui, Arshi Waseem, Mohsin A Khan, Syed S Raza
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引用次数: 0

摘要

目前的缺血模型致力于复制缺血介导的损伤。然而,它们面临着重现性不足、难以将啮齿类动物的研究结果转化为人类研究结果,以及伦理、经济和实际限制等挑战,这些都限制了广泛研究的准确性。本研究介绍了一种利用内皮素-1诱导3日龄鸡胚胎持续缺血的新方法。该方案以右卵黄动脉为目标,并通过多普勒血流成像和分子生物学实验进行了验证。这种创新方法有助于利用 3 天大的鸡胚胎探索氧化应激、炎症反应、细胞死亡和潜在的药物筛选适宜性。主要特点 - 该模型可评估和研究与持续缺血有关的病理学 - 该模型可评估氧化应激、炎症和细胞死亡等参数 - 该模型可量化核酸和蛋白质水平的分子变化 - 该模型可有效筛选药物及其靶点 图表概览。
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Endothelin-1-Induced Persistent Ischemia in a Chicken Embryo Model.

Current ischemic models strive to replicate ischemia-mediated injury. However, they face challenges such as inadequate reproducibility, difficulties in translating rodent findings to humans, and ethical, financial, and practical constraints that limit the accuracy of extensive research. This study introduces a novel approach to inducing persistent ischemia in 3-day-old chicken embryos using endothelin-1. The protocol targets the right vitelline arteries, validated with Doppler blood flow imaging and molecular biology experiments. This innovative approach facilitates the exploration of oxidative stress, inflammatory responses, cellular death, and potential drug screening suitability utilizing a 3-day-old chicken embryo. Key features • This model enables the evaluation and investigation of the pathology related to persistent ischemia • This model allows for the assessment of parameters like oxidative stress, inflammation, and cellular death • This model enables quantification of molecular changes at the nucleic acid and protein levels • This model allows for the efficient screening of drugs and their targets Graphical overview.

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