Abstract:The effects of four medicinal herbs (Arctium lappa, Plantago major, Mikania glomerata Spreng and Equisetum arvense) with anti-inflammatory properties were evaluated in a chronic obstructive pulmonary disease (COPD) model. Wistar rats were exposed to cigarette smoke during 8 weeks and one of the groups was orally given a solution containing 4% of each alcoholic herbal extracts during the exposure period. Control group was not exposed to smoke or treated. Histopathological, immunohistochemical and biochemical an… Show more
“…The equipment consists of an animal containment system and a cigarette smoke release system with an external cigarette holder connected to a dynamic suction pump. The pump can be programmed so that cigarette suction periods alternate with periods of clean air suction to prevent asphyxiation [32,33] (Supplementary Video 1). The exposures were standardized and performed twice a day using commercial cigarettes (containing 0.8 mg of nicotine, 10 mg of tar and 10 mg of carbon monoxide).…”
Section: Exposure To Cigarette Smoke and Treatment With Ac2-26 Mimetimentioning
confidence: 99%
“…The exposures were standardized and performed twice a day using commercial cigarettes (containing 0.8 mg of nicotine, 10 mg of tar and 10 mg of carbon monoxide). The animals were exposed to the burning of 10 cigarettes in the morning (7 a.m) and 10 cigarettes in the early evening (6 p.m.) [11,33], each exposure lasted approximately 1 h. The total exposure period was 5 uninterrupted weeks (35 days).…”
Section: Exposure To Cigarette Smoke and Treatment With Ac2-26 Mimetimentioning
confidence: 99%
“…The anti-inflammatory efficacy of Ac2-26 the AnxA1 mimetic peptide (Ac-AMVSEFLKQAWFIENEEQEYVQTVK, Thermo Fisher Scientific, Grand Island, NY, USA) in protecting against inflammatory processes caused by exposure to tobacco smoke was evaluated in one of the smoke-exposed groups (n = 10) by the intraperitoneal (ip) administration of Ac2-26 at the dosage of 1 mg/kg in 100 μL of phosphate buffered (PBS) solution [28][29][30][31][32][33], once a day and before the first exposure to cigarette smoke. The treatment protocol started along with the protocol of exposure to cigarette smoke and had the same duration of 5 weeks.…”
Section: Exposure To Cigarette Smoke and Treatment With Ac2-26 Mimetimentioning
confidence: 99%
“…The control group (n = 10) was kept in the same conditions but exposed only to compressed air, it was neither exposed to cigarette smoke nor treated [33]. The day after the end of the exposure protocol, the animals were euthanized by excessive dose of anesthetic (thiopental).…”
Section: Exposure To Cigarette Smoke and Treatment With Ac2-26 Mimetimentioning
confidence: 99%
“…Substrate diaminobenzidine (DAB Kit, Invitrogen, Cat No: P00-2020) was used for development and, thereafter, the sections were stained with Hematoxylin. Proteins were quantified by densitometry (arbitrary units 0 to 255) using the Leica Image Analysis Software [27,33,35]. The lung macrophages were quantified in 10 random images per slide under the 40× objective of the Leica microscope (DM500) and the tissue areas were obtained in the image analyzer.…”
Section: Histopathological and Immunohistochemical Studiesmentioning
Chronic obstructive pulmonary disease (COPD) is related to inflammatory process caused by smoking habit. In this scenario, the anti-inflammatory protein Annexin A1 (AnxA1) may represent a therapeutic alternative. We performed experiments to evaluate the effects of the AnxA1 mimetic peptide Ac2-26 in an initial COPD model by physiological, histopathological, biochemical and immunohistochemical analyses. Weight loss, increased blood pressure, reductions in the pulmonary frequency and ventilation, loss of tracheal cilia, enlargement of the pulmonary intra-alveolar spaces and lymphoid tissue found in untreated smoke-exposed group were attenuated by AnxA1 peptide treatment. The Ac2-26 administration also protected against leukocytes influx in bronchoalveolar lavage (BAL), lung and trachea, and it also led to decreased hemoglobin, glucose, cholesterol, gamma glutamyl transferase and aspartato aminotransferase levels. Similarly, reduction of proinflammatory mediators and higher concentration of anti-inflammatory cytokine were found in macerated lung supernatant, blood plasma and BAL in the treated animals. Besides Ac2-26 group showed reduced tissue expressions of AnxA1, cyclooxygenase-2 and metalloproteinase-9, but formylated peptide receptor 2 (FPR2) overexpression. Our results all together highlighted the protective role of the Ac2-26 mimetic peptide in COPD with promising perspectives.
“…The equipment consists of an animal containment system and a cigarette smoke release system with an external cigarette holder connected to a dynamic suction pump. The pump can be programmed so that cigarette suction periods alternate with periods of clean air suction to prevent asphyxiation [32,33] (Supplementary Video 1). The exposures were standardized and performed twice a day using commercial cigarettes (containing 0.8 mg of nicotine, 10 mg of tar and 10 mg of carbon monoxide).…”
Section: Exposure To Cigarette Smoke and Treatment With Ac2-26 Mimetimentioning
confidence: 99%
“…The exposures were standardized and performed twice a day using commercial cigarettes (containing 0.8 mg of nicotine, 10 mg of tar and 10 mg of carbon monoxide). The animals were exposed to the burning of 10 cigarettes in the morning (7 a.m) and 10 cigarettes in the early evening (6 p.m.) [11,33], each exposure lasted approximately 1 h. The total exposure period was 5 uninterrupted weeks (35 days).…”
Section: Exposure To Cigarette Smoke and Treatment With Ac2-26 Mimetimentioning
confidence: 99%
“…The anti-inflammatory efficacy of Ac2-26 the AnxA1 mimetic peptide (Ac-AMVSEFLKQAWFIENEEQEYVQTVK, Thermo Fisher Scientific, Grand Island, NY, USA) in protecting against inflammatory processes caused by exposure to tobacco smoke was evaluated in one of the smoke-exposed groups (n = 10) by the intraperitoneal (ip) administration of Ac2-26 at the dosage of 1 mg/kg in 100 μL of phosphate buffered (PBS) solution [28][29][30][31][32][33], once a day and before the first exposure to cigarette smoke. The treatment protocol started along with the protocol of exposure to cigarette smoke and had the same duration of 5 weeks.…”
Section: Exposure To Cigarette Smoke and Treatment With Ac2-26 Mimetimentioning
confidence: 99%
“…The control group (n = 10) was kept in the same conditions but exposed only to compressed air, it was neither exposed to cigarette smoke nor treated [33]. The day after the end of the exposure protocol, the animals were euthanized by excessive dose of anesthetic (thiopental).…”
Section: Exposure To Cigarette Smoke and Treatment With Ac2-26 Mimetimentioning
confidence: 99%
“…Substrate diaminobenzidine (DAB Kit, Invitrogen, Cat No: P00-2020) was used for development and, thereafter, the sections were stained with Hematoxylin. Proteins were quantified by densitometry (arbitrary units 0 to 255) using the Leica Image Analysis Software [27,33,35]. The lung macrophages were quantified in 10 random images per slide under the 40× objective of the Leica microscope (DM500) and the tissue areas were obtained in the image analyzer.…”
Section: Histopathological and Immunohistochemical Studiesmentioning
Chronic obstructive pulmonary disease (COPD) is related to inflammatory process caused by smoking habit. In this scenario, the anti-inflammatory protein Annexin A1 (AnxA1) may represent a therapeutic alternative. We performed experiments to evaluate the effects of the AnxA1 mimetic peptide Ac2-26 in an initial COPD model by physiological, histopathological, biochemical and immunohistochemical analyses. Weight loss, increased blood pressure, reductions in the pulmonary frequency and ventilation, loss of tracheal cilia, enlargement of the pulmonary intra-alveolar spaces and lymphoid tissue found in untreated smoke-exposed group were attenuated by AnxA1 peptide treatment. The Ac2-26 administration also protected against leukocytes influx in bronchoalveolar lavage (BAL), lung and trachea, and it also led to decreased hemoglobin, glucose, cholesterol, gamma glutamyl transferase and aspartato aminotransferase levels. Similarly, reduction of proinflammatory mediators and higher concentration of anti-inflammatory cytokine were found in macerated lung supernatant, blood plasma and BAL in the treated animals. Besides Ac2-26 group showed reduced tissue expressions of AnxA1, cyclooxygenase-2 and metalloproteinase-9, but formylated peptide receptor 2 (FPR2) overexpression. Our results all together highlighted the protective role of the Ac2-26 mimetic peptide in COPD with promising perspectives.
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