京颗粒通过调节内质网膜应激信号通路来缓解OVA诱导的过敏性鼻炎
Zhikang Wang1, Shujun Liu2, Shirong Li3
1College of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, 250355, China; State Key Laboratory of Integration and Innovation of Classic Formula and Modern Chinese Medicine, Lunan Pharmaceutical Group Co. Ltd., Linyi, 276005, China.
Journal of ethnopharmacology
|November 7, 2024
概括
京颗粒 (JF) 通过减少炎症和改善鼻腔症状,有效治疗过敏性鼻炎 (AR). 这种草药化合物调节内质网膜应激通路,抑制关键的炎症过程,以获得治疗效益.
科学领域:
- 免疫学 免疫学 免疫学
- 药理学 药理学是指药理学的学科.
- 传统中国医药 传统中国医药
背景情况:
- 京芳颗粒 (JF) 是一种经验上用于治疗过敏疾病的草药制剂.
- 治疗过敏性鼻炎 (AR) 的JF的疗效和机制需要科学验证.
研究的目的:
- 在AR的小鼠模型中研究JF的治疗机制.
- 评估JF对鼻炎和相关分子通路的影响.
主要方法:
- 在ICR小鼠中建立了卵素 (OVA) /氧化诱导的AR模型.
- 通过监测行为症状,组织学变化,血清细胞因子水平 (ELISA) 和蛋白质表达 (Western blot) 来评估JF治疗效果.
- 用蛋白质组和代谢组分析来阐明JF的监管网络和分子目标.
主要成果:
- 在小鼠中,JF显著降低了AR症状,如鼻子和打喷.
- 结核病治疗降低了IgE,IL-4,IL-6,IL-13,TNF-α和组胺的水平,同时增加了IFN-γ.
- 结核菌抑制了内等质网膜 (ER) 压力标志物,并抑制了糖解/氨酸生物合成途径,从而减少了炎症.
结论:
- JF在治疗OVA/氧化诱导的鼻粘膜损伤和炎症方面表现出有效性.
- 通过调节ER应激信号通路,JF具有抗AR效应.
- JF抑制糖解和氨酸生物合成,有助于其在AR中的抗炎作用.
相关概念视频
GPCR Desensitization
5.8K
G protein-coupled receptor (GPCR) signaling plays a crucial role in cell functioning. GPCR desensitization is an equally essential process. It allows cells to respond to changing environments and regain sensitivity to new stimuli while preventing unnecessary stimulation when no longer needed. Prolonged exposure to stimuli leads to GPCR desensitization. It involves blocking the receptors from binding and activating additional G proteins. This inhibits activation of downstream effectors, thereby...
5.8K
Allergic Reactions
27.2K
Overview
27.2K
Endocrine Signaling
64.0K
Endocrine cells produce hormones to communicate with remote target cells found in other organs. The hormone reaches these distant areas using the circulatory system. This exposes the whole organism to the hormone but only those cells expressing hormone receptors or target cells are affected. Thus, endocrine signaling induces slow responses from its target cells but these effects also last longer.
64.0K
GPCRs Regulate Adenylyl Cylase Activity
5.3K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.3K
Regulation of the Unfolded Protein Response
2.4K
Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
2.4K
Antiasthma Drugs: Mast Cell Stabilizers and Anti-IgE Drugs
237
Asthma is a chronic respiratory condition for which new therapeutic avenues, including anti-inflammatory drugs like mast cell stabilizers and anti-IgE treatments, continue to be developed.
Mast cell stabilizers, such as cromolyn (also known as sodium cromoglycate) and nedocromil (Tilade), are effective drugs in asthma management. These stabilizers hinder histamine release by skillfully obstructing the activation of mast cells and other cellular entities. Notably, they navigate this task without...
Mast cell stabilizers, such as cromolyn (also known as sodium cromoglycate) and nedocromil (Tilade), are effective drugs in asthma management. These stabilizers hinder histamine release by skillfully obstructing the activation of mast cells and other cellular entities. Notably, they navigate this task without...
237


