Pulmonary mechanic and lung histology induced by Crotalus durissus cascavella snake venom

被引:8
作者
Neto, Joselito de Oliveira [1 ]
de Moraes Silveira, Joao Alison [2 ]
Serra, Daniel Silveira [3 ]
Viana, Daniel de Araujo [1 ]
Borges-Nojosa, Diva Maria [4 ]
Souza Sampaio, Celia Maria [5 ]
Azul Monteiro, Helena Serra [2 ]
Avila Cavalcante, Francisco Sales [3 ]
Azul Monteiro Evangelista, Janaina Serra [1 ]
机构
[1] Univ Estadual Ceara, Fac Vet, Postgrad Program Vet Sci, Fortaleza, Ceara, Brazil
[2] Univ Fed Ceara, Fac Med, Dept Physiol & Pharmacol, Fortaleza, Ceara, Brazil
[3] Univ Estadual Ceara, Postgrad Program Phys, Fortaleza, Ceara, Brazil
[4] Univ Fed Ceara, Dept Biol, Fortaleza, Ceara, Brazil
[5] Univ Estadual Ceara, Dept Biol, Fortaleza, Ceara, Brazil
关键词
Crotalus durissus cascavella; Pulmonary mechanics; Histopathology; Venom; Balb/C; AIRWAY SMOOTH-MUSCLE; BIOLOGICAL-ACTIVITIES; PHOSPHOLIPASE A(2); TERRIFICUS; ASTHMA; COLLILINEATUS; CROTOXIN; DISEASE; INJURY; VOLUME;
D O I
10.1016/j.toxicon.2017.07.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study have analyzed the pulmonary function in an experimental model of acute lung injury, induced by the Crotalus durissus cascavella venom (C. d. cascavella) (3.0 mu g/kg - i.p), in pulmonary mechanic and histology at 1 h, 3 h, 6 h, 12 h and 24 h after inoculation. The C d. cascavella venom led to an increase in Newtonian Resistance (R-N), Tissue Resistance (G) and Tissue Elastance (H) in all groups when compared to the control, particularly at 12 h and 24 h. The Histeresivity (eta) increased 6 h, 12 h and 24 h after inoculation. There was a decrease in Static Compliance (C-ST) at 6 h, 12 h and 24 h and inspiratory capacity (IC) at 3 h, 6 h, 12 h and 24 h. C d. cascavella venom showed significant morphological changes such as atelectasis, emphysema, hemorrhage, polymorphonuclear inflammatory infiltrate, edema and congestion. After a challenge with methacholine (MCh), R-N demonstrated significant changes at 6, 12 and 24 h. This venom caused mechanical and histopathological changes in the lung tissue; however, its mechanisms of action need further studies in order to better elucidate the morphofunctional lesions. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:144 / 149
页数:6
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