Effects of Nω-nitro-L-arginine methyl ester and aminoguanidine on lipopolysaccharide-induced airway hyperresponsiveness in guinea pigs
Background The down-regulation of constitutive nitric oxide synthase (cNOS) and up-regulation of inducible nitric oxide synthase (iNOS) are associated with the allergen-provocated airway hyperresponsiveness (AHR). This study aimed to determine whether their alteration also plays an important role in...
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Veröffentlicht in: | Chinese medical journal 2008-09, Vol.121 (17), p.1693-1697 |
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description | Background The down-regulation of constitutive nitric oxide synthase (cNOS) and up-regulation of inducible nitric oxide synthase (iNOS) are associated with the allergen-provocated airway hyperresponsiveness (AHR). This study aimed to determine whether their alteration also plays an important role in the AHR induced by lipopolysaccharide (LPS). Methods Hartley male guinea pigs, weighing between 250 g and 350 g, were injected with LPS at a dose of 1 mg/kg every 24 hours for three days. A non-selective NOS inhibitor, N~-nitro-L-arginine methyl ester (L-NAME), or a selective inducible NOS inhibitor, aminoguanidine (AG), were used thirty minutes before each injection of LPS. Airway reactions, nitric oxide (NO) production and inflammatory changes were detected 24 hours after the last dose of LPS. Results AG significantly decreased the NO production in the bronchoalveolar lavage fluid (BALF) and sharply reduced the intensity of bronchoconstdction to histamine challenge. L-NAME also significantly decreased the NO production in the BALF, but had no effect on airway reactions or, perhaps, a tendency to enhance the intensity of AHR. Conclusions The data suggest that inducible NOS contributes to the AHR induced by repetitive intraperitoneal LPS, and constitutive NOS was also involved. |
doi_str_mv | 10.1097/00029330-200809010-00020 |
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This study aimed to determine whether their alteration also plays an important role in the AHR induced by lipopolysaccharide (LPS). Methods Hartley male guinea pigs, weighing between 250 g and 350 g, were injected with LPS at a dose of 1 mg/kg every 24 hours for three days. A non-selective NOS inhibitor, N~-nitro-L-arginine methyl ester (L-NAME), or a selective inducible NOS inhibitor, aminoguanidine (AG), were used thirty minutes before each injection of LPS. Airway reactions, nitric oxide (NO) production and inflammatory changes were detected 24 hours after the last dose of LPS. Results AG significantly decreased the NO production in the bronchoalveolar lavage fluid (BALF) and sharply reduced the intensity of bronchoconstdction to histamine challenge. L-NAME also significantly decreased the NO production in the BALF, but had no effect on airway reactions or, perhaps, a tendency to enhance the intensity of AHR. Conclusions The data suggest that inducible NOS contributes to the AHR induced by repetitive intraperitoneal LPS, and constitutive NOS was also involved.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.1097/00029330-200809010-00020</identifier><language>eng</language><publisher>Department of Pulmonary Medicine,Huadong Hospital,Fudan University,Shanghai 200040,China%Department of Physiology and Pathophysiology,Medical College of Fudan University,Shanghai 200032,China</publisher><subject>氧化一氮 ; 氧化一氮合酶 ; 脂多糖</subject><ispartof>Chinese medical journal, 2008-09, Vol.121 (17), p.1693-1697</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c297t-ba98c935cd1ab50f0eb2580e12f6a95bb033f4217c32acbbd2a902776ad990823</citedby><cites>FETCH-LOGICAL-c297t-ba98c935cd1ab50f0eb2580e12f6a95bb033f4217c32acbbd2a902776ad990823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85656X/85656X.jpg</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>JIANG, Hong-ni</creatorcontrib><creatorcontrib>QU, Jie-ming</creatorcontrib><creatorcontrib>HE, Li-xian</creatorcontrib><creatorcontrib>CHEN, Xue-hua</creatorcontrib><creatorcontrib>PAN, Jue</creatorcontrib><creatorcontrib>LI, Li</creatorcontrib><creatorcontrib>ZHU, Da-nian</creatorcontrib><creatorcontrib>CAO, Yin-xiang</creatorcontrib><creatorcontrib>SHEN, Lin-lin</creatorcontrib><title>Effects of Nω-nitro-L-arginine methyl ester and aminoguanidine on lipopolysaccharide-induced airway hyperresponsiveness in guinea pigs</title><title>Chinese medical journal</title><addtitle>Chinese Medical Journal</addtitle><description>Background The down-regulation of constitutive nitric oxide synthase (cNOS) and up-regulation of inducible nitric oxide synthase (iNOS) are associated with the allergen-provocated airway hyperresponsiveness (AHR). This study aimed to determine whether their alteration also plays an important role in the AHR induced by lipopolysaccharide (LPS). Methods Hartley male guinea pigs, weighing between 250 g and 350 g, were injected with LPS at a dose of 1 mg/kg every 24 hours for three days. A non-selective NOS inhibitor, N~-nitro-L-arginine methyl ester (L-NAME), or a selective inducible NOS inhibitor, aminoguanidine (AG), were used thirty minutes before each injection of LPS. Airway reactions, nitric oxide (NO) production and inflammatory changes were detected 24 hours after the last dose of LPS. Results AG significantly decreased the NO production in the bronchoalveolar lavage fluid (BALF) and sharply reduced the intensity of bronchoconstdction to histamine challenge. L-NAME also significantly decreased the NO production in the BALF, but had no effect on airway reactions or, perhaps, a tendency to enhance the intensity of AHR. Conclusions The data suggest that inducible NOS contributes to the AHR induced by repetitive intraperitoneal LPS, and constitutive NOS was also involved.</description><subject>氧化一氮</subject><subject>氧化一氮合酶</subject><subject>脂多糖</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNo9kM1u2zAQhIkiBeq4fQeih96YLknrh8fCcJICRnJJz8KKIiW6MqmScgPlBYI-XV8pcuzktMDsNzPAEEI5XHFQxXcAEEpKYAKgBAUc2FGCD2QhspVgWb7iF2QBMs9ZrpT6RC5T2s1ElhX5gjxvrDV6TDRYevf_H_NujIFtGcbWeecN3Zuxm3pq0mgiRd9Q3Dsf2gN61xz_wdPeDWEI_ZRQ6w6jawxzvjloM8MuPuJEu2kwMZo0BJ_cX-NNStR52h7mBKSDa9Nn8tFin8yX812SX9ebh_Ut297f_Fz_2DItVDGyGlWplcx0w7HOwIKpRVaC4cLmqLK6BintSvBCS4G6rhuBCkRR5NgoBaWQS_LtlPuI3qJvq104RD83Vk-d3u-OI_ICuJrB8gTqGFKKxlZDdHuMU8WhOi5fvS1fvS__KsFs_Xq2dsG3f9zcUqP-bV1vKlHyUqxyKV8A7POFlg</recordid><startdate>20080905</startdate><enddate>20080905</enddate><creator>JIANG, Hong-ni</creator><creator>QU, Jie-ming</creator><creator>HE, Li-xian</creator><creator>CHEN, Xue-hua</creator><creator>PAN, Jue</creator><creator>LI, Li</creator><creator>ZHU, Da-nian</creator><creator>CAO, Yin-xiang</creator><creator>SHEN, Lin-lin</creator><general>Department of Pulmonary Medicine,Huadong Hospital,Fudan University,Shanghai 200040,China%Department of Physiology and Pathophysiology,Medical College of Fudan University,Shanghai 200032,China</general><general>Department of Pulmonary Medicine,Research Institute of Respiratory Disease,Zhongshan Hospital,Fudan University,Shanghai 200032,China%Department of Pulmonary Medicine,Research Institute of Respiratory Disease,Zhongshan Hospital,Fudan University,Shanghai 200032,China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20080905</creationdate><title>Effects of Nω-nitro-L-arginine methyl ester and aminoguanidine on lipopolysaccharide-induced airway hyperresponsiveness in guinea pigs</title><author>JIANG, Hong-ni ; QU, Jie-ming ; HE, Li-xian ; CHEN, Xue-hua ; PAN, Jue ; LI, Li ; ZHU, Da-nian ; CAO, Yin-xiang ; SHEN, Lin-lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c297t-ba98c935cd1ab50f0eb2580e12f6a95bb033f4217c32acbbd2a902776ad990823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>氧化一氮</topic><topic>氧化一氮合酶</topic><topic>脂多糖</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>JIANG, Hong-ni</creatorcontrib><creatorcontrib>QU, Jie-ming</creatorcontrib><creatorcontrib>HE, Li-xian</creatorcontrib><creatorcontrib>CHEN, Xue-hua</creatorcontrib><creatorcontrib>PAN, Jue</creatorcontrib><creatorcontrib>LI, Li</creatorcontrib><creatorcontrib>ZHU, Da-nian</creatorcontrib><creatorcontrib>CAO, Yin-xiang</creatorcontrib><creatorcontrib>SHEN, Lin-lin</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>CrossRef</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>JIANG, Hong-ni</au><au>QU, Jie-ming</au><au>HE, Li-xian</au><au>CHEN, Xue-hua</au><au>PAN, Jue</au><au>LI, Li</au><au>ZHU, Da-nian</au><au>CAO, Yin-xiang</au><au>SHEN, Lin-lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Nω-nitro-L-arginine methyl ester and aminoguanidine on lipopolysaccharide-induced airway hyperresponsiveness in guinea pigs</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chinese Medical Journal</addtitle><date>2008-09-05</date><risdate>2008</risdate><volume>121</volume><issue>17</issue><spage>1693</spage><epage>1697</epage><pages>1693-1697</pages><issn>0366-6999</issn><eissn>2542-5641</eissn><abstract>Background The down-regulation of constitutive nitric oxide synthase (cNOS) and up-regulation of inducible nitric oxide synthase (iNOS) are associated with the allergen-provocated airway hyperresponsiveness (AHR). This study aimed to determine whether their alteration also plays an important role in the AHR induced by lipopolysaccharide (LPS). Methods Hartley male guinea pigs, weighing between 250 g and 350 g, were injected with LPS at a dose of 1 mg/kg every 24 hours for three days. A non-selective NOS inhibitor, N~-nitro-L-arginine methyl ester (L-NAME), or a selective inducible NOS inhibitor, aminoguanidine (AG), were used thirty minutes before each injection of LPS. Airway reactions, nitric oxide (NO) production and inflammatory changes were detected 24 hours after the last dose of LPS. Results AG significantly decreased the NO production in the bronchoalveolar lavage fluid (BALF) and sharply reduced the intensity of bronchoconstdction to histamine challenge. L-NAME also significantly decreased the NO production in the BALF, but had no effect on airway reactions or, perhaps, a tendency to enhance the intensity of AHR. Conclusions The data suggest that inducible NOS contributes to the AHR induced by repetitive intraperitoneal LPS, and constitutive NOS was also involved.</abstract><pub>Department of Pulmonary Medicine,Huadong Hospital,Fudan University,Shanghai 200040,China%Department of Physiology and Pathophysiology,Medical College of Fudan University,Shanghai 200032,China</pub><doi>10.1097/00029330-200809010-00020</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 氧化一氮 氧化一氮合酶 脂多糖 |
title | Effects of Nω-nitro-L-arginine methyl ester and aminoguanidine on lipopolysaccharide-induced airway hyperresponsiveness in guinea pigs |
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