Literature DB >> 12875868

Hemorrhagic activity of Bothrops venoms determined by two different methods and relationship with proteolytic activity on gelatin and lethality.

Adolfo Rafael de Roodt1, Silvana Litwin, Juan Carlos Vidal.   

Abstract

The changes in hemorrhagic activity, proteolytic activity on gelatin and the lethal potency of four Bothrops venoms treated at different pH values or with EDTA were studied. Venoms from B. alternatus, B. jararaca, B. moojeni and B. neuwiedii of Argentina were preincubated at pH 5.8, 5.1 or 3.8 or with EDTA and the hemorrhagic activity expressed as size of the hemorrhagic lesion or as the amount of hemoglobin extracted, the proteolytic activity on gelatin and the lethal potency were determined. Although the MHDs recorded in rats were 19-56 fold higher than those recorded in mice, the A(550) extracted per gram of hemorrhagic haloes was very similar in rats or mice independent of the venom dose. Inhibition of proteolytic activity after preincubation at pH 5.1 or 3.8, agrees with the decreased amount of hemoglobin extracted from the hemorrhagic haloes, and with the increase in mean survival time after the i.p. injection to mice. Preincubation with EDTA resulted in 80% inhibition of hemorrhagic activity of B. jararaca venom and complete inhibition with the other Bothrops venoms tested. Measurement of the amount of hemoglobin extracted gives significant information in comparative studies, not available by measurement of the size of hemorrhagic haloes.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12875868     DOI: 10.1016/s0041-0101(02)00392-6

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


  5 in total

1.  Purification and characterization of a metalloproteinase, Porthidin-1, from the venom of Lansberg's hog-nosed pitvipers (Porthidium lansbergii hutmanni).

Authors:  María E Girón; Amalid Estrella; Elda E Sánchez; Jacob Galán; W Andy Tao; Belsy Guerrero; Ana M Salazar; Alexis Rodríguez-Acosta
Journal:  Toxicon       Date:  2011-01-19       Impact factor: 3.033

2.  Strong myotoxic activity of Trimeresurus malabaricus venom: role of metalloproteases.

Authors:  C D Raghavendra Gowda; R Rajesh; A Nataraju; B L Dhananjaya; A R Raghupathi; T V Gowda; B K Sharath; B S Vishwanath
Journal:  Mol Cell Biochem       Date:  2006-01       Impact factor: 3.396

Review 3.  Inhibition of hemorragic snake venom components: old and new approaches.

Authors:  Isabella Panfoli; Daniela Calzia; Silvia Ravera; Alessandro Morelli
Journal:  Toxins (Basel)       Date:  2010-03-25       Impact factor: 4.546

4.  Human Monoclonal scFvs that Neutralize Fribrinogenolytic Activity of Kaouthiagin, a Zinc-Metalloproteinase in Cobra (Naja kaouthia) Venom.

Authors:  Jirawat Khanongnoi; Siratcha Phanthong; Onrapak Reamtong; Anchalee Tungtronchitr; Wanpen Chaicumpa; Nitat Sookrung
Journal:  Toxins (Basel)       Date:  2018-12-03       Impact factor: 4.546

5.  Comparative compositional and functional analyses of Bothrops moojeni specimens reveal several individual variations.

Authors:  Weslei da Silva Aguiar; Nathália da Costa Galizio; Caroline Serino-Silva; Sávio Stefanini Sant'Anna; Kathleen Fernandes Grego; Alexandre Keiji Tashima; Erika Sayuri Nishiduka; Karen de Morais-Zani; Anita Mitico Tanaka-Azevedo
Journal:  PLoS One       Date:  2019-09-12       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.