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Major Hemothorax Induced Hypovolemic Shock Fallowing Administration of Intrapleural Urokinase

Tuberculosis & Respiratory Diseases / Tuberculosis & Respiratory Diseases,
2004, v.57 no.5, pp.465-469







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Abstract

Background : Induction of oral tolerance (OT) has been known to prevent allergic inflammation in acute asthma model within 4 weeks. However it is remained whether induction of OT may effectively prevent allergic inflammation in chronic asthma model over 4 weeks. We observed the effect of induction of OT on allergic inflammation and airway remodeling in chronic asthma model up to 8 weeks. Methods : 5-week-old female BALB/c mice divided into 4 groups-control group, asthma group, low dose OT group, and high dose OT group. To induce oral tolerance mice were fed ovalbumin (OVA) before sensitization with OVA and aluminum hydroxide-1 mg for 6 consecutive days in the low dose OT group and 25 mg once in the high dose OT group. Mice in the asthma group were fed phosphate buffered saline instead of OVA. After sensitization followed by repeated challenge with aerosolized 1% OVA during 6 weeks, enhanced pause (Penh), inflammatory cells, IL-13, and IFN-γ levels in bronchoalveolar lavage (BAL) fluids as well as OVA-specific IgE, IgG1, and IgG2a levels in serum were measured. In addition the degree of goblet cell hyperplasia and peribronchial fibrosis were observed from lung tissues by PAS and Masson's trichrome stain. Results : Both OT groups showed a significant decrease in Penh, inflammatory cells, IL-13, and IFN-γ levels in BAL fluids as well as OVA-specific IgE, IgG1, and IgG2a levels in serum compared with the asthma group (P<0.05). In addition, the degree of goblet cell hyperplasia and peribronchial fibrosis were significantly attenuated in both OT groups compared with the asthma group (P<0.01). Conclusion : These results suggest that induction of OT may effectively prevent allergic inflammation as well as airway remodeling even in chronic asthma model up to 8 weeks.(Tuberc Respir Dis 2004; 57:425-433)

keywords
Urokinase, Hemothorax, Hypovolemic shock, Pleural effusion.늑막강내 Urokinase 주입후 발생된 Major Hemothorax에 기인된 Hypovolemic shock건양대학교 의과대학 내과학교실1, 건양대학교 의과대학 영상의학교실2김정규1, 정인범1, 손지웅1, 최유진1, 나문준1, 이원영1, 조영준2Major Hemothorax Induced Hypovolemic Shock Fallowin, Urokinase, Hemothorax, Hypovolemic shock, Pleural effusion.늑막강내 Urokinase 주입후 발생된 Major Hemothorax에 기인된 Hypovolemic shock건양대학교 의과대학 내과학교실1, 건양대학교 의과대학 영상의학교실2김정규1, 정인범1, 손지웅1, 최유진1, 나문준1, 이원영1, 조영준2Major Hemothorax Induced Hypovolemic Shock Fallowin

Reference

1.

Sohn DH, (2000) Effects of Intracavitary Urokinase Instillation in Complicated Pleural Effusion,

2.

Temes RT, (1996) Intrapleural fibrinolytics in management of empyema thoracis,

3.

Landay MJ, (1980) Anaerobic pleural and pulmonary infections,

4.

Widstrom O, (1986) Measurements of enzymatic activities in pleural exudates with chromogenic substrates.Thromb Res,

5.

Agrenius V, (1989) Pleural fibrinolytic activity is decreased in inflammation as demonstrated in quinacrine pleurodesis treatment of malignant pleural effusion,

6.

Glauser FL, (1975) In vitro pleural fluid clottability and fibrinogen content,

7.

Widstrom O, (1983) Fibrinolytic and coagulation mechanisms in stages of inflammation;a study of BCG-induced pleural exudate in guinea pig,

8.

Tillet WS, (inverst1949) The effect in patients of streptococcal fibrinolysis and streptococcal deoxyribonuclease on fibrinous purulent,

9.

Moulton JS, (1989) Treatment of loculated pleural effusions with transcatheter intracavitary urokinase,

10.

Robinson LA, (1994) Intrapleural fibrinolytic treatment of multiloculated thoracic empyemas,

11.

Jung TG, (1989) Acute and Long-term effect of intraluminal urokinase in Korean empyema patients.J Korean Radiol Soc,

12.

Lee KS, (1991) Treatment of thoracic multiloculated empyemas with intracavitary urokinase,

13.

Godley PJ, (1984) Major hemorrhage following administration of intrapleural streptokinase,

14.

Porter J, (1998) Intrapleural streptokinase,

Tuberculosis & Respiratory Diseases