Literature DB >> 9237336

The dynamics of local tissue damage induced by Bothrops asper snake venom and myotoxin II on the mouse cremaster muscle: an intravital and electron microscopic study.

B Lomonte1, J Lundgren, B Johansson, U Bagge.   

Abstract

The acute tissue damaging effects of Bothrops asper snake venom and a myotoxic Lys-49 phospholipase A2 (myotoxin II) on the mouse cremaster muscle were studied by intravital and electron microscopy. Both venom and myotoxin induced local contractions of the muscle fibres within 10-60 sec after exposure, which disappeared after 1-2 min. This observation is consistent with the hypothesis that Bothrops myotoxins act initially at the sarcolemma by affecting its permeability and allowing an influx of calcium. The venom also induced an early but transient vasoconstriction of arterioles. The development of edema was monitored using i.v. FITC-dextran as a marker. Plasma leakage started after about 2 min of exposure to venom or myotoxin, was extensive by 4-5 min, and originated from small venules and their adjoining capillary segments. The venom induced formation of thrombi and emboli in venules, but not in arterioles. Haemorrhage appeared after 4-6 min of exposure, the bleedings always originating from capillaries and small venules. The microbleedings were explosive, appearing as rapid bursts of erythrocytes into the extravascular space, and suggesting a per rhexis type of haemorrhage. This was confirmed by electron microscopy evaluation of the same microvessels observed intravitally, which showed erythrocyte extravasation through gaps in damaged endothelial cells. Other phenomena in the microcirculation included blood-flow disturbances, crenation and sphering of erythrocytes, and stasis with dense packing of cells in capillary networks. Muscle necrosis, caused by either venom or myotoxin, started 3-4 min after application. The first sign of damage in the fibres was the development of a narrow, transverse band with local loss of striation. This was followed by slow retraction of myofibrils until there was a complete transverse rupture of the fibre. This process was often repeated along the same fibre, leaving a row of fragments separated by spaces apparently devoid of myofibrillar material. The results confirm the rapid tissue damaging effects of B. asper venom, implying that potentially useful blocking agents must be administered early and have the ability to diffuse rapidly into the tissues.

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Year:  1994        PMID: 9237336     DOI: 10.1016/0041-0101(94)90020-5

Source DB:  PubMed          Journal:  Toxicon        ISSN: 0041-0101            Impact factor:   3.033


  15 in total

Review 1.  Pharmacokinetic-pharmacodynamic relationships of immunoglobulin therapy for envenomation.

Authors:  José María Gutiérrez; Guillermo León; Bruno Lomonte
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

2.  Comparative analysis of membranotropic properties of various phospholipases A2 from venom of snakes of the family viperidae.

Authors:  N A Kazaryan; L Gulikyan; B Lomonte; T V Andreeva; V I Tsetlin; Yu N Utkin; N M Aivazyan
Journal:  Dokl Biochem Biophys       Date:  2014-08-30       Impact factor: 0.788

3.  Skeletal muscle necrosis and regeneration after injection of Thalassophryne nattereri (niquim) fish venom in mice.

Authors:  M Lopes-Ferreira; J Núñez; A Rucavado; S H Farsky; B Lomonte; Y Angulo; A M Moura Da Silva; J M Gutiérrez
Journal:  Int J Exp Pathol       Date:  2001-02       Impact factor: 1.925

4.  The anti-inflammatory action of Bothrops jararaca snake antithrombin on acute inflammation induced by carrageenan in mice.

Authors:  Karen de Morais-Zani; Fernanda Peixoto Barbosa Nunes; Jacilene Barbosa da Silva; Márcio José Ferreira; Kathleen Fernandes Grego; Mônica Lopes-Ferreira; Aparecida Sadae Tanaka; Anita Mitico Tanaka-Azevedo
Journal:  Inflamm Res       Date:  2013-05-12       Impact factor: 4.575

5.  Bothrops asper snake venom and its metalloproteinase BaP-1 activate the complement system. Role in leucocyte recruitment.

Authors:  S H Farsky; L R Gonçalves; J M Gutiérrez; A P Correa; A Rucavado; P Gasque; D V Tambourgi
Journal:  Mediators Inflamm       Date:  2000       Impact factor: 4.711

6.  Effects of PI and PIII Snake Venom Haemorrhagic Metalloproteinases on the Microvasculature: A Confocal Microscopy Study on the Mouse Cremaster Muscle.

Authors:  Cristina Herrera; Mathieu-Benoit Voisin; Teresa Escalante; Alexandra Rucavado; Sussan Nourshargh; José María Gutiérrez
Journal:  PLoS One       Date:  2016-12-16       Impact factor: 3.240

7.  Biochemical characterization, action on macrophages, and superoxide anion production of four basic phospholipases A2 from Panamanian Bothrops asper snake venom.

Authors:  Aristides Quintero Rueda; Isela González Rodríguez; Eliane C Arantes; Sulamita S Setúbal; Leonardo de A Calderon; Juliana P Zuliani; Rodrigo G Stábeli; Andreimar M Soares
Journal:  Biomed Res Int       Date:  2012-12-24       Impact factor: 3.411

8.  Effects of Bothrops asper snake venom on lymphatic vessels: insights into a hidden aspect of envenomation.

Authors:  Javier Mora; Rodrigo Mora; Bruno Lomonte; José María Gutiérrez
Journal:  PLoS Negl Trop Dis       Date:  2008-10-15

9.  Increments in cytokines and matrix metalloproteinases in skeletal muscle after injection of tissue-damaging toxins from the venom of the snake Bothrops asper.

Authors:  Alexandra Rucavado; Teresa Escalante; Catarina F P Teixeira; Cristina María Fernándes; Cecilia Diaz; José María Gutiérrez
Journal:  Mediators Inflamm       Date:  2002-04       Impact factor: 4.711

Review 10.  Hemorrhage Caused by Snake Venom Metalloproteinases: A Journey of Discovery and Understanding.

Authors:  José María Gutiérrez; Teresa Escalante; Alexandra Rucavado; Cristina Herrera
Journal:  Toxins (Basel)       Date:  2016-03-26       Impact factor: 4.546

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