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(哈拉蒙汀)可预防大鼠中暴露于丙烯菊酯所致的肺部损伤:机制性白细胞介素

(haramonting) protects against allethrin-exposed pulmo damage in rats: mechanistic interleukins.

作者信息

Situmorang Putri Cahaya, Ilyas Syafruddin, Syahputra Rony Abdi, Nugraha Alexander Patera, Putri Mimmy Sari Syah, Rumahorbo Cheryl Grace Pratiwi

机构信息

Study Program of Biology, Faculty of Mathematics and Natural Sciences, Universitas Sumatera Utara, Medan, Indonesia.

Department of Pharmacology, Faculty of Pharmacy, Universitas Sumatera Utara, Medan, Indonesia.

出版信息

Front Pharmacol. 2024 Feb 6;15:1343936. doi: 10.3389/fphar.2024.1343936. eCollection 2024.

DOI:10.3389/fphar.2024.1343936
PMID:38379903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10877004/
Abstract

Inhaling Allethrin (C19H26O3) may induce oxidative stress in lung cells by causing the formation of free radi-cals. Interleukins (IL) are a group of secreted cytokines or proteins and signaling molecules initially produced as an immune response by leukocytes. (haramonting) contains antioxidants that may prevent lung damage induced by allethrin-containing electric mosquito repellents. In this study, six groups of rats were exposed to allethrin via an electric mosquito repellent, including positive, negative, and comparison control groups and three groups were administered Rhodomyrtus tomentosa (Aiton) Hassk at 100 mg/kg BW, 200 mg/kg BW, and 300 mg/kg BW. After 30 days, the pulmonary tissue and the blood were taken for immunohisto-chemical and ELISA analysis. The accumulation of inflammatory cells causes the thickening of the alveolar wall structures. Injuries were more prevalent in the A+ group than in the other groups. The connection between the alveoli and blood capillaries, which can interfere with alveolar gas exchange, is not regulated, and the lu-minal morphology is aberrant, causing damage to the alveolar epithelial cells. Exposure to electric mosquito coils containing allethrin can increase the expression of interleukin-1, interleukin-8, interleukin-9, and interleu-kin-18 in blood serum and tissues while decreasing the expression of interleukin-6 and interleukin-10. Like the Vitamin C group, Rhodomyrtus tomentosa can increase alveolar histological alterations by decreasing the ex-pression of IL-1β, IL-8, IL-9, and IL-18 while increasing IL-6 and IL-10. So that this plant can be developed in the future as a drug to prevent lung harm from exposure.

摘要

吸入丙烯菊酯(C19H26O3)可能通过导致自由基的形成在肺细胞中诱导氧化应激。白细胞介素(IL)是一组分泌的细胞因子或蛋白质以及信号分子,最初由白细胞作为免疫反应产生。(毛稔)含有抗氧化剂,可能预防含丙烯菊酯的电蚊香引起的肺损伤。在本研究中,六组大鼠通过电蚊香接触丙烯菊酯,包括阳性、阴性和比较对照组,三组分别以100mg/kg体重、200mg/kg体重和300mg/kg体重给予毛稔。30天后,采集肺组织和血液进行免疫组织化学和酶联免疫吸附测定分析。炎症细胞的积聚导致肺泡壁结构增厚。A+组的损伤比其他组更普遍。肺泡与血毛细血管之间的连接未得到调节,这可能会干扰肺泡气体交换,管腔形态异常,导致肺泡上皮细胞受损。接触含丙烯菊酯的电蚊香可增加血清和组织中白细胞介素-1、白细胞介素-8、白细胞介素-9和白细胞介素-18的表达,同时降低白细胞介素-6和白细胞介素-10的表达。与维生素C组一样,毛稔可通过降低IL-1β、IL-8、IL-9和IL-18的表达,同时增加IL-6和IL-10来增加肺泡组织学改变。因此,这种植物未来可开发成一种预防暴露引起的肺损伤的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/25c9191c21d4/fphar-15-1343936-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/487b32167e1e/fphar-15-1343936-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/f757ccc64dc7/fphar-15-1343936-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/5ba55bd71656/fphar-15-1343936-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/730616e8524c/fphar-15-1343936-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/2102a3f3a936/fphar-15-1343936-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/74b1e5da2f40/fphar-15-1343936-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/790bd1cbed01/fphar-15-1343936-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/acf2eb83afc5/fphar-15-1343936-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/25c9191c21d4/fphar-15-1343936-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/487b32167e1e/fphar-15-1343936-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/f757ccc64dc7/fphar-15-1343936-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/5ba55bd71656/fphar-15-1343936-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/730616e8524c/fphar-15-1343936-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/2102a3f3a936/fphar-15-1343936-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/74b1e5da2f40/fphar-15-1343936-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/790bd1cbed01/fphar-15-1343936-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/acf2eb83afc5/fphar-15-1343936-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0a/10877004/25c9191c21d4/fphar-15-1343936-g009.jpg

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