Effect of cold-dryness on pulmonary and immunologic function in chronic obstructive pulmonary disease model rats

OBJECTIVE: To study the effects of cold-dryness on pulmonary and immunologic function of peripheral T-lymphocytes in chronic obstructive pulmonary disease (COPD) model rats, and to provide references for the prevention and treatment of cold-dryness COPD in the Xinjiang region. METHODS: The COPD mode...

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Veröffentlicht in:Journal of Traditional Chinese Medicine 2014-04, Vol.34 (2), p.221-226
Hauptverfasser: Gao, Zhen, Li, Fengsen, Upur, Halmurat, Min, Jiang, Jing, Wang, Jing, Jing, Xu, Dan
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creator Gao, Zhen
Li, Fengsen
Upur, Halmurat
Min, Jiang
Jing, Wang
Jing, Jing
Xu, Dan
description OBJECTIVE: To study the effects of cold-dryness on pulmonary and immunologic function of peripheral T-lymphocytes in chronic obstructive pulmonary disease (COPD) model rats, and to provide references for the prevention and treatment of cold-dryness COPD in the Xinjiang region. METHODS: The COPD model was established with an elastase drip into the trachea combined with smoking. The cold-dryness COPD model was developed by stressing with a cold-dry environment. Success of the model was determined by observation of pathologic lung sections. Rats were sacrificed by exsanguination from the femoral artery and changes of peripheral blood CD4+, CD8+, and CD4+/CD8+ were detected by flow cytometryo Data were analyzed with SAS 11.5 statistical software. RESULTS: On the ninetieth day after ending the ex- periment, Peak expiratory flow in the cold-dryness COPD group was lower than that in the COPD and normal control groups (P〈0.01). The time of inspiration in the cold-dryness COPD group was higher than that in the COPD and normal groups (P〈0.05). Time of expiration (Te) in the cold-dryness COPD group was higher than that in the COPD and normal groups (P〈0.01). 50% tidal volume expiratory flow (EFS0) in the cold-dryness COPD group was lower than that in the COPD and normal groups (P〈 0.01), and EFS0 in the COPD group was lower than that in the normal group (P〈0.05). CD4+ content of peripheral blood in the cold-dryness COPD group was lower than that in the COPD and the normal groups (P〈0.05). CD8+ content in the cold-dryness COPD and COPD groups was higher than that in the normal control group (P〈0.01), and CD8+ content in the cold-dryness COPD group was higher than that in the COPD group (P〈0.01). CD4+/CD8+ in the cold-dryness COPD group and the COPD group was lower than that in the normal control group (P〈0.01), and CD4+/CD8+ in the cold-dryness COPD group was lower than that in the COPD group (P〈0.05). CONCLUSION: In the cold-dryness COPD model, CD8+ increased and CD4+/CD8+ decreased. Moreover, cold-dryness may aggravate this state. The effects of cold-dryness on pulmonary function main- ly manifested as prolongation of Te and decrease of EF50, which could be one of causes of cold-dryness environment in the northwest of China leading to COPD with region characteristics.
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METHODS: The COPD model was established with an elastase drip into the trachea combined with smoking. The cold-dryness COPD model was developed by stressing with a cold-dry environment. Success of the model was determined by observation of pathologic lung sections. Rats were sacrificed by exsanguination from the femoral artery and changes of peripheral blood CD4+, CD8+, and CD4+/CD8+ were detected by flow cytometryo Data were analyzed with SAS 11.5 statistical software. RESULTS: On the ninetieth day after ending the ex- periment, Peak expiratory flow in the cold-dryness COPD group was lower than that in the COPD and normal control groups (P〈0.01). The time of inspiration in the cold-dryness COPD group was higher than that in the COPD and normal groups (P〈0.05). Time of expiration (Te) in the cold-dryness COPD group was higher than that in the COPD and normal groups (P〈0.01). 50% tidal volume expiratory flow (EFS0) in the cold-dryness COPD group was lower than that in the COPD and normal groups (P〈 0.01), and EFS0 in the COPD group was lower than that in the normal group (P〈0.05). CD4+ content of peripheral blood in the cold-dryness COPD group was lower than that in the COPD and the normal groups (P〈0.05). CD8+ content in the cold-dryness COPD and COPD groups was higher than that in the normal control group (P〈0.01), and CD8+ content in the cold-dryness COPD group was higher than that in the COPD group (P〈0.01). CD4+/CD8+ in the cold-dryness COPD group and the COPD group was lower than that in the normal control group (P〈0.01), and CD4+/CD8+ in the cold-dryness COPD group was lower than that in the COPD group (P〈0.05). CONCLUSION: In the cold-dryness COPD model, CD8+ increased and CD4+/CD8+ decreased. Moreover, cold-dryness may aggravate this state. The effects of cold-dryness on pulmonary function main- ly manifested as prolongation of Te and decrease of EF50, which could be one of causes of cold-dryness environment in the northwest of China leading to COPD with region characteristics.</description><identifier>ISSN: 0255-2922</identifier><identifier>ISSN: 0254-6272</identifier><identifier>DOI: 10.1016/S0254-6272(14)60082-0</identifier><identifier>PMID: 24783937</identifier><language>eng</language><publisher>China</publisher><subject>Animals ; CD4-CD8 Ratio ; CD4-Positive T-Lymphocytes - cytology ; CD4-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - cytology ; CD8-Positive T-Lymphocytes - immunology ; Humans ; Lung - immunology ; Lung - pathology ; Lymphocyte Count ; Male ; Pulmonary Disease, Chronic Obstructive - immunology ; Pulmonary Disease, Chronic Obstructive - pathology ; Rats ; Rats, Wistar ; 免疫功能 ; 外周血T淋巴细胞 ; 寒冷 ; 干燥度 ; 慢性阻塞性肺疾病 ; 慢性阻塞性肺病 ; 疾病模型 ; 鼠肺</subject><ispartof>Journal of Traditional Chinese Medicine, 2014-04, Vol.34 (2), p.221-226</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-75d58c50308c9fcc7c67786c9685ffeef0b17be3d5699a9266e9fc3e54aabc313</citedby><cites>FETCH-LOGICAL-c438t-75d58c50308c9fcc7c67786c9685ffeef0b17be3d5699a9266e9fc3e54aabc313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/86801X/86801X.jpg</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24783937$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Zhen</creatorcontrib><creatorcontrib>Li, Fengsen</creatorcontrib><creatorcontrib>Upur, Halmurat</creatorcontrib><creatorcontrib>Min, Jiang</creatorcontrib><creatorcontrib>Jing, Wang</creatorcontrib><creatorcontrib>Jing, Jing</creatorcontrib><creatorcontrib>Xu, Dan</creatorcontrib><title>Effect of cold-dryness on pulmonary and immunologic function in chronic obstructive pulmonary disease model rats</title><title>Journal of Traditional Chinese Medicine</title><addtitle>Journal of Traditional Chinese Medicine</addtitle><description>OBJECTIVE: To study the effects of cold-dryness on pulmonary and immunologic function of peripheral T-lymphocytes in chronic obstructive pulmonary disease (COPD) model rats, and to provide references for the prevention and treatment of cold-dryness COPD in the Xinjiang region. METHODS: The COPD model was established with an elastase drip into the trachea combined with smoking. The cold-dryness COPD model was developed by stressing with a cold-dry environment. Success of the model was determined by observation of pathologic lung sections. Rats were sacrificed by exsanguination from the femoral artery and changes of peripheral blood CD4+, CD8+, and CD4+/CD8+ were detected by flow cytometryo Data were analyzed with SAS 11.5 statistical software. RESULTS: On the ninetieth day after ending the ex- periment, Peak expiratory flow in the cold-dryness COPD group was lower than that in the COPD and normal control groups (P〈0.01). The time of inspiration in the cold-dryness COPD group was higher than that in the COPD and normal groups (P〈0.05). Time of expiration (Te) in the cold-dryness COPD group was higher than that in the COPD and normal groups (P〈0.01). 50% tidal volume expiratory flow (EFS0) in the cold-dryness COPD group was lower than that in the COPD and normal groups (P〈 0.01), and EFS0 in the COPD group was lower than that in the normal group (P〈0.05). CD4+ content of peripheral blood in the cold-dryness COPD group was lower than that in the COPD and the normal groups (P〈0.05). CD8+ content in the cold-dryness COPD and COPD groups was higher than that in the normal control group (P〈0.01), and CD8+ content in the cold-dryness COPD group was higher than that in the COPD group (P〈0.01). CD4+/CD8+ in the cold-dryness COPD group and the COPD group was lower than that in the normal control group (P〈0.01), and CD4+/CD8+ in the cold-dryness COPD group was lower than that in the COPD group (P〈0.05). CONCLUSION: In the cold-dryness COPD model, CD8+ increased and CD4+/CD8+ decreased. Moreover, cold-dryness may aggravate this state. The effects of cold-dryness on pulmonary function main- ly manifested as prolongation of Te and decrease of EF50, which could be one of causes of cold-dryness environment in the northwest of China leading to COPD with region characteristics.</description><subject>Animals</subject><subject>CD4-CD8 Ratio</subject><subject>CD4-Positive T-Lymphocytes - cytology</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - cytology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Humans</subject><subject>Lung - immunology</subject><subject>Lung - pathology</subject><subject>Lymphocyte Count</subject><subject>Male</subject><subject>Pulmonary Disease, Chronic Obstructive - immunology</subject><subject>Pulmonary Disease, Chronic Obstructive - pathology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>免疫功能</subject><subject>外周血T淋巴细胞</subject><subject>寒冷</subject><subject>干燥度</subject><subject>慢性阻塞性肺疾病</subject><subject>慢性阻塞性肺病</subject><subject>疾病模型</subject><subject>鼠肺</subject><issn>0255-2922</issn><issn>0254-6272</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkMtOwzAQRb0AUSh8AsjsYBHw284SVeUhVWIBrC3HcdqgxC52gtS_x6WlYjXS1bkzowPAJUZ3GGFx_4YIZ4UgktxgdisQUqRAR-A0x7wgJSETcJbSJ0Jcca5OwIQwqWhJ5SlYz5vG2QGGBtrQ1UUdN96lBIOH67HrgzdxA42vYdv3ow9dWLYWNqO3Q5uR1kO7isHnLFRpiGOOv92_Zt0mZ5KDfahdB6MZ0jk4bkyX3MV-TsHH4_x99lwsXp9eZg-LwjKqhkLymivLEUXKlo210goplbClUDx_7BpUYVk5WnNRlqYkQriMUceZMZWlmE7BzW7vOoav0aVB922yruuMd2FMGnOCJGVMiIzyHWpjSCm6Rq9j2-f3NUZ6K1j_CtZbwRrnuRWsUe5d7U-MVe_qQ-vPbgau94tXwS-_Wr88MKxkkglK6Q-ebYZ2</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Gao, Zhen</creator><creator>Li, Fengsen</creator><creator>Upur, Halmurat</creator><creator>Min, Jiang</creator><creator>Jing, Wang</creator><creator>Jing, Jing</creator><creator>Xu, Dan</creator><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201404</creationdate><title>Effect of cold-dryness on pulmonary and immunologic function in chronic obstructive pulmonary disease model rats</title><author>Gao, Zhen ; 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METHODS: The COPD model was established with an elastase drip into the trachea combined with smoking. The cold-dryness COPD model was developed by stressing with a cold-dry environment. Success of the model was determined by observation of pathologic lung sections. Rats were sacrificed by exsanguination from the femoral artery and changes of peripheral blood CD4+, CD8+, and CD4+/CD8+ were detected by flow cytometryo Data were analyzed with SAS 11.5 statistical software. RESULTS: On the ninetieth day after ending the ex- periment, Peak expiratory flow in the cold-dryness COPD group was lower than that in the COPD and normal control groups (P〈0.01). The time of inspiration in the cold-dryness COPD group was higher than that in the COPD and normal groups (P〈0.05). Time of expiration (Te) in the cold-dryness COPD group was higher than that in the COPD and normal groups (P〈0.01). 50% tidal volume expiratory flow (EFS0) in the cold-dryness COPD group was lower than that in the COPD and normal groups (P〈 0.01), and EFS0 in the COPD group was lower than that in the normal group (P〈0.05). CD4+ content of peripheral blood in the cold-dryness COPD group was lower than that in the COPD and the normal groups (P〈0.05). CD8+ content in the cold-dryness COPD and COPD groups was higher than that in the normal control group (P〈0.01), and CD8+ content in the cold-dryness COPD group was higher than that in the COPD group (P〈0.01). CD4+/CD8+ in the cold-dryness COPD group and the COPD group was lower than that in the normal control group (P〈0.01), and CD4+/CD8+ in the cold-dryness COPD group was lower than that in the COPD group (P〈0.05). CONCLUSION: In the cold-dryness COPD model, CD8+ increased and CD4+/CD8+ decreased. Moreover, cold-dryness may aggravate this state. The effects of cold-dryness on pulmonary function main- ly manifested as prolongation of Te and decrease of EF50, which could be one of causes of cold-dryness environment in the northwest of China leading to COPD with region characteristics.</abstract><cop>China</cop><pmid>24783937</pmid><doi>10.1016/S0254-6272(14)60082-0</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
CD4-CD8 Ratio
CD4-Positive T-Lymphocytes - cytology
CD4-Positive T-Lymphocytes - immunology
CD8-Positive T-Lymphocytes - cytology
CD8-Positive T-Lymphocytes - immunology
Humans
Lung - immunology
Lung - pathology
Lymphocyte Count
Male
Pulmonary Disease, Chronic Obstructive - immunology
Pulmonary Disease, Chronic Obstructive - pathology
Rats
Rats, Wistar
免疫功能
外周血T淋巴细胞
寒冷
干燥度
慢性阻塞性肺疾病
慢性阻塞性肺病
疾病模型
鼠肺
title Effect of cold-dryness on pulmonary and immunologic function in chronic obstructive pulmonary disease model rats
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