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一种基于果蝇的方法来揭示导致肠病的药物。

A fruit fly-based approach to unraveling enteropathy-causing pharmaceuticals.

作者信息

Pratama Muhammad R, Wahyudin Elly, Putri Tenri Zad, Hardiyanti Widya, Fatiah Dewita, Chaeratunnisa Rizkya, Bapulo Nurdewi N, Latada Nadila P, Mudjahid Mukarram, Nainu Firzan

机构信息

Postgraduate Program in Pharmacy, Faculty of Pharmacy, Universitas Hasanuddin, Makassar, Indonesia.

Departmentof Pharmacy, Faculty of Pharmacy, Universitas Hasanuddin, Makassar, Indonesia.

出版信息

Narra J. 2024 Aug;4(2):e898. doi: 10.52225/narra.v4i2.898. Epub 2024 Aug 2.

Abstract

Enteropathy is a gastrointestinal disorder characterized by inflammation in the small intestine and one of the causes of enteropathy is the side effects of certain drugs, such as non-steroidal anti-inflammatory drugs (NSAIDs). The mechanism of NSAIDs, such as indomethacin, could inhibit prostaglandin synthesis, leading to a decrease in mucus production and small intestine integrity. To test the effects of a drug, it is necessary to undergo preclinical testing using animal models. Commonly used animal models such as mice and rats have several drawbacks including high cost, ethical issues, and long lifespan. Therefore, alternatives such as using invertebrate animals like as a more economical in vivo platform with genetic similarity to mammals and devoid of ethical concerns are needed. The aim of this study was to evaluate as an in vivo model organism in testing the side effects of pharmaceuticals that cause enteropathy. In this study, flies aged 3-5 days were starved and then placed into treatment vials comprising untreated control and indomethacin-treated (3.75 mM, 7.5 mM, and 15 mM). Survival analysis was conducted during the treatment period, followed by a Smurf assay test after seven days of treatment. Subsequently, the expression of pro-inflammatory cytokine-related genes ( and ), mitochondria stability-related genes (), and endogenous antioxidant-related genes (, and ) was performed using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Our data indicated that indomethacin did not impact lifespan or cause intestinal damage. However, we observed increased expression of pro-inflammatory cytokine-related genes, including , and a twofold increase in gene expression. Furthermore, there was a significant upregulation of mitochondrial stability gene , endogenous antioxidant genes and , and a threefold increase in at 15 mM indomethacin. Although no phenotypical changes in gut integrity were detected, the increased expression of pro-inflammatory cytokine genes suggests the occurrence of inflammation in the indomethacin-treated flies.

摘要

肠病是一种以小肠炎症为特征的胃肠道疾病,肠病的病因之一是某些药物的副作用,如非甾体抗炎药(NSAIDs)。吲哚美辛等NSAIDs的作用机制是抑制前列腺素合成,导致黏液分泌减少和小肠完整性受损。为了测试药物的效果,有必要使用动物模型进行临床前试验。常用的动物模型如小鼠和大鼠有几个缺点,包括成本高、伦理问题和寿命长。因此,需要使用无脊椎动物等替代方法,作为一种与哺乳动物具有遗传相似性且无伦理问题的更经济的体内平台。本研究的目的是评估 作为一种体内模型生物在测试导致肠病的药物副作用方面的作用。在本研究中,将3至5日龄的果蝇饥饿后放入包含未处理对照和吲哚美辛处理(3.75 mM、7.5 mM和15 mM)的处理瓶中。在处理期间进行生存分析,处理7天后进行Smurf分析测试。随后,使用逆转录定量聚合酶链反应(RT-qPCR)检测促炎细胞因子相关基因( 和 )、线粒体稳定性相关基因( )和内源性抗氧化相关基因( 、 和 )的表达。我们的数据表明,吲哚美辛不会影响寿命或导致肠道损伤。然而,我们观察到促炎细胞因子相关基因的表达增加,包括 ,并且 基因表达增加了两倍。此外,在15 mM吲哚美辛处理下,线粒体稳定性基因 、内源性抗氧化基因 和 显著上调, 增加了三倍。尽管未检测到肠道完整性的表型变化,但促炎细胞因子基因表达的增加表明吲哚美辛处理的果蝇中发生了炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b427/11394174/79a0903e7b18/NarraJ-4-e898-g001.jpg

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