The Prophylactic and Therapeutic Effects of Cholinolytics on Perfluoroisobutylene Inhalation Induced Acute Lung Injury
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概要
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Perfluoroisobutylene (PEIB) is a kind of fluoro-olefin that is ten times more toxic than phosgene. The mechanisms of the acute lung injury (ALI) induced by PEIB inhalation remain unclear. To find possible pharmacological interventions, mice and rats were exposed to PEIB, and the prophylactic or therapeutic effects of 3-quinuclidinyl benzilate (QNB) and anisodamine were studied and confirmed. It was observed that the wet lung/body weight and the dry lung/body weight ratios at 24 h after PEIB exposure (130 mg/m^3 for 5 min) were significantly decreased when a single dose of QNB (5 mg/kg) was administered intraperitoneally either 30 min before exposure or 10 h after exposure. Anisodamine was without any prophylactic or therapeutic effects at single doses below 30 mg/kg. The effects of QNB against PEIB inhalation induced ALI were well evidenced by the significantly decreased mice mortality at 72 h, the total protein concentration in bronchoalveolar lavage fluid at 24 h after the PEIB exposure, as well as the ultrastructural observations. The analysis of the time courses of lung sulfhydryl concentration, myeloperoxidase (MPO) activity and hemorheology assay showed that the toxicity of PEIB may be due to consumption of lung protein sulfhydryl, influx of polymorphonuclear leukocytes (PMNs) into the lung, and increased peripheral blood viscosity at a low shear rate, all of which were partially blocked by QNB intervention except for PMN influx. The results suggest that cholinolytics might have prophylactic and therapeutic roles in PEIB inhalation induced ALI.
- 社団法人日本産業衛生学会の論文
著者
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Xu Jin
Juhua Hospital Juhua Group Cooperation The China Pla P.r.
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SHAO Zhihua
Juhua Hospital, Juhua Group Cooperation, the China PLA, P.R.
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ZHANG Xigang
307 Hospital, the China PLA, P.R.
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DING Rigao
Beijing Institute of Pharmacology and Toxicology, the China PLA, P.R.
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RUAN Jinxiu
Beijing Institute of Pharmacology and Toxicology, the China PLA, P.R.
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SUN Xiaohong
Beijing Institute of Pharmacology and Toxicology, the China PLA, P.R.
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HUANG Chunqian
Beijing Institute of Pharmacology and Toxicology, the China PLA, P.R.
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DING Rigao
Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences
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RUAN Jinxiu
Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences
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SUN Xiaohong
Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences
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Ruan Jinxiu
Beijing Institute Of Pharmacology And Toxicology The China Pla P.r.
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Ding Rigao
Beijing Institute Of Pharmacology And Toxicology The China Pla P.r.
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Shao Zhihua
Juhua Hospital Juhua Group Cooperation The China Pla P.r.
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Sun Xiaohong
Beijing Institute Of Pharmacology And Toxicology The China Pla P.r.
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Zhang Xigang
307 Hospital The China Pla P.r.
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Huang Chunqian
Beijing Institute Of Pharmacology And Toxicology The China Pla P.r.
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ZHANG Tianhong
Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences
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SHAO Zhihua
Quhua Hospital, Quhua Group Corporation, P. R. China
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YANG Shunjiang
Quhua Hospital, Quhua Group Corporation, P. R. China
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Xu Jin
Quhua Hospital, Quhua Group Corporation, P. R. China
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HUANG Chunqian
Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences
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Hu Zuliang
Quhua Hospital, Quhua Group Corporation, P. R. China
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ZHANG Xianchang
Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences
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Hu Zuliang
Quhua Hospital Quhua Group Corporation P. R. China
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Zhang Tianhong
Institute Of Pharmacology And Toxicology Academy Of Military Medical Sciences
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YANG Shunjiang
Quhua Hospital, Quhua Group Corporation
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