Respiratory toxicity of direct lytic factor in the venom of the southern Chinese cobra (N-naja atra) in dogs

被引:1
作者
Huang, SJ
Fu, J
Sun, JJ
机构
[1] Pharmacology Department, Sun Yat-sen University of Medical Sciences, Guangzhou
来源
HUMAN & EXPERIMENTAL TOXICOLOGY | 1996年 / 15卷 / 08期
关键词
snake venoms; direct lytic factors; respiratory function tests; respiratory mechanics; pulmonary gas exchange; myocardial contraction;
D O I
10.1177/096032719601500806
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The effects of direct lytic factor (DLF) on respiratory ventilation, gas exchange as well as hemodynamics were studied in anesthetized dogs. After an intravenous DLF dose of 1 mg/kg, the initial manifestation of intoxication was observed as follows: (1) Increase in airway impedance characterized by slowed air flow rate and increased negative transpulmonary pressure, (2) Decrease in dynamic compliance, (3) Progressive increase in venoarterial shunt (Qs/Qt) and decrease in PaO2. (4) Elevation of pulmonary artery blood pressure and fall of mean systemic blood pressure and maximal left ventricular pressure. Above actions reached the peak values at 15 min and thereafter all respiratory functional parameters, except Qs/Qt and hypoxemia, returned gradually to approach the normal levels at 50 min. The tidal volume, PaCO2 and LVEDP remained unchanged until another DLF dose of 1.5 mg/kg was given. After a second dose of DLF (total 2.5 mg/kg), the respiratory functions and the cardiac performance deteriorated as follows: (1) Further increase in Qs/Qt and hypoxemia. (2) Appearance of hypercapnea and acidosis. (3) Fall of dP/dt(max) and elevation of LVEDP, widening of QRS complex of ECG. (4) Blood pressure run a downhill course, From above experimental evidence, we came to the conclusion that as well as the basic cardiotoxicity, respiratory toxicity of DLF must be considered as the primary, because of broad spectrum of action of DLF and early effect on respiratory function.
引用
收藏
页码:629 / 632
页数:4
相关论文
共 15 条
[1]   A NONTHROMBOGENIC DIFFUSION MEMBRANE FOR CONTINUOUS IN-VIVO MEASUREMENT OF BLOOD GASES BY MASS SPECTROMETRY [J].
BRANTIGA.JW ;
GOTT, VL ;
VESTAL, ML ;
FERGUSSO.GJ ;
JOHNSTON, WH .
JOURNAL OF APPLIED PHYSIOLOGY, 1970, 28 (03) :375-&
[2]  
CADE JF, 1988, ESSENTIALS RESPIRATO, P34
[3]  
Campbell CH, 1979, SNAKE VENOMS, P898
[4]   BRONCHOPULMONARY FUNCTION - REPORT OF THE MAIN WORKING PARTY [J].
CLARK, DG ;
BUCH, S ;
DOE, JE ;
FRITH, H ;
PULLINGER, DH .
PHARMACOLOGY & THERAPEUTICS, 1979, 5 (1-3) :149-179
[5]   MEMBRANE-ACTIVE POLYPEPTIDES FROM SNAKE-VENOM - CARDIOTOXINS AND HEMOCYTOTOXINS [J].
CONDREA, E .
EXPERIENTIA, 1974, 30 (02) :121-129
[6]   STRUCTURE AND PHARMACOLOGY OF ELAPID CYTOTOXINS [J].
DUFTON, MJ ;
HIDER, RC .
PHARMACOLOGY & THERAPEUTICS, 1988, 36 (01) :1-&
[7]   POSSIBLE MECHANISMS OF ACTION OF COBRA SNAKE-VENOM CARDIOTOXINS AND BEE VENOM MELITTIN [J].
FLETCHER, JE ;
JIANG, MS .
TOXICON, 1993, 31 (06) :669-695
[8]  
HANH HL, 1981, RESPIRATORY PHARM, P501
[9]  
HUANG SJ, 1991, ACTA PHARM SINIC, V12, P125
[10]   ISOLATION AND CHARACTERIZATION OF 2 PHOSPHOLIPASE AS FROM VENOM OF AGKISTRODON-HAYS-BLOMHOFFII [J].
KAWAUCHI, S ;
IWANAGA, S ;
SAMEJIMA, Y ;
SUZUKI, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1971, 236 (01) :142-&