PMID- 26398389 OWN - NLM STAT- MEDLINE DCOM- 20160706 LR - 20200106 IS - 2299-5684 (Electronic) IS - 1734-1140 (Linking) VI - 67 IP - 5 DP - 2015 Oct TI - The potential effect of the angiotensin II receptor blocker telmisartan in regulating OVA-induced airway remodeling in experimental rats. PG - 943-51 LID - S1734-1140(15)00039-0 [pii] LID - 10.1016/j.pharep.2015.02.010 [doi] AB - BACKGROUND: Bronchial asthma is a true ascending clinical problem. Angiotensin II is now accused to be potentially implicated in its pathogenesis, being a potent pro-inflammatory mediator with remodeling effects. OBJECTIVE: This study aims to evaluate the possible protective effect of telmisartan, an angiotensin II receptor blocker, on experimentally-induced bronchial asthma. METHODS: Animals were divided into 5 groups; a normal control group, an asthma control group, a reference treatment group, receiving dexamethasone, and two treatment groups, receiving telmisartan in two dose levels. Bronchial asthma was induced by intraperitoneal sensitization followed by intranasal challenge with ovalbumin (OVA). Test agents were administered prior to each intranasal OVA challenge. Lung function tests, namely tidal volume (TV) and peak expiratory flow rate (PEF) were assessed 1h after the last challenge. One day after the last challenge, absolute eosinophil counts (AEC) in blood and bronchoalveolar lavage fluids (BALF) were assessed. Serum immunoglobulin E (IgE) as well as BALF total nitrate/nitrite (NOx) were assessed. Oxidative and inflammatory biomarkers, namely lung tissue superoxide dismutase (SOD), glutathione reduced (GSH), tumor necrosis factor-alpha (TNF-alpha) and interleukin-5 (IL-5), were also assessed, in addition to histopathological study. RESULTS: Telmisartan administration in both doses significantly improved TV, PEF, AEC, IgE, NOx, GSH, SOD, TNF-alpha and IL-5 values compared to asthma control values. Histopathological study strongly supported the results of biochemical estimations, particularly regarding airway remodeling. CONCLUSION: These results suggest that telmisartan may have potential protecting effects against experimental bronchial asthma, probably due to its bronchodilator, antioxidant and anti-inflammatory effects. CI - Copyright (c) 2015 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier Urban & Partner Sp. z o.o. All rights reserved. FAU - Abdel-Fattah, Maha M AU - Abdel-Fattah MM AD - Department of Pharmacology and Toxicology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt. Electronic address: dr.mahamohammed@yahoo.com. FAU - Salama, Abeer A A AU - Salama AA AD - Department of Pharmacology, National Research Center, Giza, Egypt. FAU - Shehata, Basim A AU - Shehata BA AD - Department of Pharmacology and Toxicology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt. FAU - Ismaiel, Ismaiel E AU - Ismaiel IE AD - Department of Pharmacology, National Research Center, Giza, Egypt. LA - eng PT - Journal Article DEP - 20150316 PL - Switzerland TA - Pharmacol Rep JT - Pharmacological reports : PR JID - 101234999 RN - 0 (Angiotensin II Type 1 Receptor Blockers) RN - 0 (Benzimidazoles) RN - 0 (Benzoates) RN - 0 (Biomarkers) RN - 0 (Serine Proteinase Inhibitors) RN - 9006-59-1 (Ovalbumin) RN - U5SYW473RQ (Telmisartan) SB - IM MH - Airway Remodeling/*drug effects MH - Angiotensin II Type 1 Receptor Blockers/*pharmacology MH - Animals MH - Asthma/pathology/*prevention & control MH - Benzimidazoles/*pharmacology MH - Benzoates/*pharmacology MH - Biomarkers MH - Bronchoalveolar Lavage Fluid/chemistry MH - Immunization MH - Male MH - Ovalbumin/*toxicity MH - Peak Expiratory Flow Rate/drug effects MH - Rats MH - Rats, Wistar MH - Respiratory Function Tests MH - Serine Proteinase Inhibitors/*toxicity MH - Telmisartan MH - Tidal Volume/drug effects OTO - NOTNLM OT - Airway remodeling OT - Angiotensin II OT - Bronchial asthma OT - Rat OT - Telmisartan EDAT- 2015/09/24 06:00 MHDA- 2016/07/07 06:00 CRDT- 2015/09/24 06:00 PHST- 2014/12/05 00:00 [received] PHST- 2015/02/12 00:00 [revised] PHST- 2015/02/23 00:00 [accepted] PHST- 2015/09/24 06:00 [entrez] PHST- 2015/09/24 06:00 [pubmed] PHST- 2016/07/07 06:00 [medline] AID - S1734-1140(15)00039-0 [pii] AID - 10.1016/j.pharep.2015.02.010 [doi] PST - ppublish SO - Pharmacol Rep. 2015 Oct;67(5):943-51. doi: 10.1016/j.pharep.2015.02.010. Epub 2015 Mar 16.