Suppr超能文献

氨茶碱、色甘酸二钠和沙丁胺醇在小鼠胸膜炎模型中的抗炎作用

Anti-inflammatory effects of theophylline, cromolyn and salbutamol in a murine model of pleurisy.

作者信息

Saleh T S, Calixto J B, Medeiros Y S

机构信息

Department of Pharmacology, Centre of Biological Sciences, Universidade Federal de Santa Catarina, Brazil.

出版信息

Br J Pharmacol. 1996 Jun;118(3):811-9. doi: 10.1111/j.1476-5381.1996.tb15472.x.

Abstract
  1. The aim of this study was to examine the effect of theophylline, cromolyn and salbutamol, three well-known anti-asthmatic drugs, on the early (4 h) and late (48 h) phases of cell migration and fluid leakage induced by carrageenin in the pleural cavity of mice. 2. In the first set of experiments, animals were pretreated (30 min) with different doses of theophylline (0.5-50 mg kg-1, i.p.), cromolyn (0.02-0.2 mg per pleural cavity) or salbutamol (0.05-50 mg kg-1, i.p.); the total and differential cell content, and also the exudate were analysed 4 h after carrageenin (1%) administration. Afterwards, in order to evaluate the time course effects of these drugs on both phases of the inflammatory reaction, one dose employed in the above protocol was chosen, to pretreat (0.5-24 h) different groups of animals. The studied parameters were evaluated 4 and 48 h after pleurisy induction. 3. Acute administration of theophylline (1-50 mg kg-1, i.p.) cromolyn (0.02-0.2 mg per pleural cavity) and salbutamol (0.5-50 mg kg-1, i.p.), 30 min prior to carrageenin, caused significant inhibition of total cell and fluid leakage in the pleural cavity at 4 h (P < 0.01). All drugs exerted a long-lasting inhibitory effect on both exudation and cell migration (P < 0.01) when administered 0.5-8 h before pleurisy induction. However, the temporal profile of the inhibitory effect induced by these drugs on the first phase of the inflammatory reaction was clearly different. Thus, the inhibitory effect induced by theophylline and cromolyn on exudation was significantly longer (up to 24 h) in comparison to their effects on cell migration (only up to 8 h). In contrast, although salbutamol when administered 30 min before pleurisy induction abolished fluid leakage (P < 0.01), this effect was not sustained in the groups pretreated for 4-8 h. In these latter groups, a significant but much smaller reduction of exudation was observed (P < 0.01), whereas the magnitude of cell migration inhibition did not vary. 4. The second phase (48 h) of the inflammatory reaction induced by carrageenin (1%) was significantly inhibited by cromolyn (0.02 mg per pleural cavity) when this drug was administered 0.5-24 h before pleurisy induction (P < 0.01). Similar results were observed when theophylline (50 mg kg-1, i.p.) was administered 0.5-4 h before the injection of the phlogistic agent (P < 0.01). Treatment of the animals with salbutamol (5 mg kg-1, i.p.), 0.5-24 h before pleurisy induction, did not inhibit either cell migration or fluid leakage. In this condition, a significant increase of these parameters was observed in the group pretreated with salbutamol 8-24 h before pleurisy induction (P < 0.01). 5. These results indicate that theophylline and cromolyn were able to inhibit the early (4 h) and late (48 h) phases of the inflammatory reaction induced by carrageenin in a murine model of pleurisy. Salbutamol was effective only against the early phase. The inhibitory effects of theophylline, cromolyn and salbutamol on the early phase of this inflammatory reaction were long-lasting, although a distinct profile of inhibition was observed among them. These findings confirm and extend previous results described in other models of asthma and support both clinical and experimental evidence suggesting that these anti-asthmatic agents exhibit marked anti-inflammatory properties.
摘要
  1. 本研究的目的是考察三种著名的抗哮喘药物茶碱、色甘酸钠和沙丁胺醇对角叉菜胶诱导的小鼠胸腔细胞迁移和液体渗漏早期(4小时)和晚期(48小时)阶段的影响。2. 在第一组实验中,动物分别用不同剂量的茶碱(0.5 - 50毫克/千克,腹腔注射)、色甘酸钠(0.02 - 0.2毫克/胸腔)或沙丁胺醇(0.05 - 50毫克/千克,腹腔注射)进行预处理(30分钟);在给予角叉菜胶(1%)4小时后分析细胞总数、分类细胞含量以及渗出液。之后,为了评估这些药物对炎症反应两个阶段的时间进程影响,从上述方案中选取一个剂量,对不同组动物进行预处理(0.5 - 24小时)。在诱导胸膜炎4小时和48小时后评估所研究的参数。3. 在角叉菜胶注射前30分钟急性给予茶碱(1 - 50毫克/千克,腹腔注射)、色甘酸钠(0.02 - 0.2毫克/胸腔)和沙丁胺醇(0.5 - 50毫克/千克,腹腔注射),在4小时时可显著抑制胸腔内的细胞总数和液体渗漏(P < 0.01)。当在诱导胸膜炎前0.5 - 8小时给药时,所有药物对渗出和细胞迁移均产生持久的抑制作用(P < 0.01)。然而,这些药物对炎症反应第一阶段诱导的抑制作用的时间模式明显不同。因此,与它们对细胞迁移的作用(仅持续到8小时)相比,茶碱和色甘酸钠对渗出的抑制作用显著更长(长达24小时)。相比之下,虽然在诱导胸膜炎前30分钟给予沙丁胺醇可消除液体渗漏(P < 0.01),但在预处理4 - 8小时的组中这种作用未持续。在这些后一组中,观察到渗出有显著但小得多的减少(P < 0.01),而细胞迁移抑制的程度没有变化。4. 当在诱导胸膜炎前0.5 - 24小时给予色甘酸钠(0.02毫克/胸腔)时,角叉菜胶(1%)诱导的炎症反应的第二阶段(48小时)受到显著抑制(P < 0.01)。当在注射炎症剂前0.5 - 4小时给予茶碱(50毫克/千克,腹腔注射)时,观察到类似结果(P < 0.01)。在诱导胸膜炎前0.5 - 24小时用沙丁胺醇(5毫克/千克,腹腔注射)治疗动物,既不抑制细胞迁移也不抑制液体渗漏。在这种情况下,在诱导胸膜炎前8 - 24小时用沙丁胺醇预处理的组中观察到这些参数显著增加(P < 0.01)。5. 这些结果表明,在小鼠胸膜炎模型中,茶碱和色甘酸钠能够抑制角叉菜胶诱导的炎症反应的早期(4小时)和晚期(48小时)阶段。沙丁胺醇仅对早期阶段有效。茶碱、色甘酸钠和沙丁胺醇对这种炎症反应早期阶段的抑制作用是持久的,尽管在它们之间观察到不同的抑制模式。这些发现证实并扩展了在其他哮喘模型中描述的先前结果,并支持临床和实验证据,表明这些抗哮喘药物具有显著的抗炎特性。

相似文献

1
Anti-inflammatory effects of theophylline, cromolyn and salbutamol in a murine model of pleurisy.
Br J Pharmacol. 1996 Jun;118(3):811-9. doi: 10.1111/j.1476-5381.1996.tb15472.x.
4
Analysis of the inflammatory response induced by substance P in the mouse pleural cavity.
Peptides. 1999;20(2):259-65. doi: 10.1016/s0196-9781(98)00170-3.
6
Effects of methotrexate upon inflammatory parameters induced by carrageenan in the mouse model of pleurisy.
Mediators Inflamm. 2002 Oct;11(5):299-306. doi: 10.1080/09629350210000015700.
10
Antiinflammatory effects of Tacrolimus in a mouse model of pleurisy.
Transpl Immunol. 2006 Aug;16(2):105-11. doi: 10.1016/j.trim.2006.04.001. Epub 2006 May 30.

引用本文的文献

1
Water-soluble tomato concentrate modulates shear-induced platelet aggregation and blood flow and .
Front Nutr. 2022 Sep 2;9:961301. doi: 10.3389/fnut.2022.961301. eCollection 2022.
2
Possible Treatment Approaches of Sulfur Mustard-Induced Lung Disorders, Experimental and Clinical Evidence, an Updated Review.
Front Med (Lausanne). 2022 Apr 29;9:791914. doi: 10.3389/fmed.2022.791914. eCollection 2022.
4
Characterization of -Octadecanoyl-5-hydroxytryptamide Anti-Inflammatory Effect.
Molecules. 2021 Jun 18;26(12):3709. doi: 10.3390/molecules26123709.
5
Acute toxicity, antinociceptive, and anti-inflammatory activities of the orally administered crotamine in mice.
Naunyn Schmiedebergs Arch Pharmacol. 2021 Aug;394(8):1703-1711. doi: 10.1007/s00210-021-02103-4. Epub 2021 May 20.
6
DNA damage, oxidative stress, and inflammation in children with celiac disease.
Genet Mol Biol. 2020 Jun 10;43(2):e20180390. doi: 10.1590/1678-4685-GMB-2018-0390. eCollection 2020.
7
Systemic Administration of Inhibits Inflammation Induced by Carrageenan in a Murine Model of Pulmonary Neutrophilia.
Mediators Inflamm. 2020 Jan 25;2020:4620251. doi: 10.1155/2020/4620251. eCollection 2020.
8
: Identification of the Anti-Inflammatory and Antinociceptive Effects.
Biomedicines. 2020 May 6;8(5):111. doi: 10.3390/biomedicines8050111.
9
Anti-Inflammatory Profile of Less. by Downregulation of Proinflammatory Mediators and Inhibition of NF-B and p38 Pathways.
Mediators Inflamm. 2020 Apr 11;2020:9078956. doi: 10.1155/2020/9078956. eCollection 2020.

本文引用的文献

1
Approaches to asthma management. Realities and recommendations.
Arch Intern Med. 1993 Apr 12;153(7):805-12.
2
Nedocromil sodium blocks the early and late phases of allergen challenge in a guinea pig model of asthma.
J Allergy Clin Immunol. 1993 Jul;92(1 Pt 2):177-82. doi: 10.1016/0091-6749(93)90102-l.
3
Immunohistology in bronchial asthma.
Respir Med. 1993 Aug;87 Suppl B:13-21. doi: 10.1016/0954-6111(93)90119-k.
6
Anti-inflammatory effects of low-dose oral theophylline in atopic asthma.
Lancet. 1994 Apr 23;343(8904):1006-8. doi: 10.1016/s0140-6736(94)90127-9.
7
Anti-inflammatory and bronchodilator properties of RP 73401, a novel and selective phosphodiesterase type IV inhibitor.
Br J Pharmacol. 1994 Dec;113(4):1423-31. doi: 10.1111/j.1476-5381.1994.tb17156.x.
8
K+ channel openers and suppression of airway hyperreactivity.
Trends Pharmacol Sci. 1994 Dec;15(12):463-8. doi: 10.1016/0165-6147(94)90060-4.
10
Bronchial responsiveness to histamine or methacholine in asthma: measurement and clinical significance.
J Allergy Clin Immunol. 1981 Nov;68(5):347-55. doi: 10.1016/0091-6749(81)90132-9.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验