Literature DB >> 10665801

Effect of crotapotin and heparin on the rat paw oedema induced by different secretory phospholipases A2.

E C Landucci1, M Toyama, S Marangoni, B Oliveira, G Cirino, E Antunes, G de Nucci.   

Abstract

The effects of crotapotin (a non-toxic and non-enzymatic acid polypeptide naturally complexed with phospholipase A2) and heparin on rat paw edema induced by different secretory phospholipases A2 (sPLA2) have been investigated. The ability of crotapotin to affect the enzymatic activity of the sPLA2(s) have also been evaluated. Secretory PLA2(s) obtained from both snake (Naja naja, Naja mocambique mocambique, Crotalus adamanteus and Crotalus durissus terrificus) and bee (Apis mellifera) venoms as well as that from bovine pancreas were used in this study. Rat paw oedema was induced by a single subplantar injection of the sPLA2s (5-30 microg/paw) in absence and presence of either crotapotin (10-100 microg/paw) or heparin (50 U/paw). Paw volume was measured using a hydroplethysmometer. Phospholipase A2 from Naja naja, Naja mocambique mocambique, Apis mellifera venoms and the basic component of Crotalus durissus terrificus venom all induced dose-dependent rat paw oedema whereas those from Crotalus adamanteus venom and bovine pancreas were ineffective. Paw oedema induced by PLA2(s) from both Naja naja and Apis mellifera venoms was significantly (P < 0.05) inhibited by crotapotin (0.1-100 microg/site) whereas the Naja mocambique mocambique venom PLA2-induced oedema was significantly potentiated (P < 0.05) by this polypeptide (40 microg/site). On the other hand, heparin (50 U/paw) had no effect on the paw oedema induced by PLA2 from Naja naja and Apis mellifera venoms but significantly inhibited the Naja mocambique mocambique venom PLA2-induced oedema. The measurement of the in vitro phospholipasic activity revealed that crotapotin inhibited by 60-70% the enzymatic activities of PLA2(s) from Crotalus adamanteus, Naja mocambique mocambique, Apis mellifera venoms and bovine pancreas. Our results suggest that despite the great homology between the various types of sPLA2 they interact with crotapotin on cell surfaces in different ways leading to either inhibition or potentiation of the paw oedema by a mechanism unrelated to their enzymatic activities. Since heparin reduced paw oedema induced by PLA2 from Naja mocambique mocambique venom it is likely that this sPLA2 is similar to the novel heparin-sensitive PLA2 found in mast cells.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10665801     DOI: 10.1016/s0041-0101(99)00143-9

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


  15 in total

1.  Crystallization and preliminary X-ray crystallographic analysis of the heterodimeric crotoxin complex and the isolated subunits crotapotin and phospholipase A2.

Authors:  K F Santos; M T Murakami; A C O Cintra; M H Toyama; S Marangoni; V P Forrer; J R Brandão Neto; I Polikarpov; R K Arni
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2007-03-12

Review 2.  The nociceptive and anti-nociceptive effects of bee venom injection and therapy: a double-edged sword.

Authors:  Jun Chen; William R Lariviere
Journal:  Prog Neurobiol       Date:  2010-06-15       Impact factor: 11.685

3.  Hydrogen sulphide induces mouse paw oedema through activation of phospholipase A2.

Authors:  Roberta d'Emmanuele di Villa Bianca; Ciro Coletta; Emma Mitidieri; Gianfranco De Dominicis; Antonietta Rossi; Lidia Sautebin; Giuseppe Cirino; Mariarosaria Bucci; Raffaella Sorrentino
Journal:  Br J Pharmacol       Date:  2010-12       Impact factor: 8.739

4.  Effects of low molecular weight sulfated galactan fragments from Botryocladia occidentalis on the pharmacological and enzymatic activity of sPLA2 from Crotalus durissus cascavella.

Authors:  M H Toyama; D O Toyama; V M Torres; G C Pontes; W R L Farias; F R Melo; S C B Oliveira; F H R Fagundes; E B S Diz Filho; B S Cavada
Journal:  Protein J       Date:  2010-11       Impact factor: 2.371

5.  PhTX-II a basic myotoxic phospholipase A₂ from Porthidium hyoprora snake venom, pharmacological characterization and amino acid sequence by mass spectrometry.

Authors:  Salomón Huancahuire-Vega; Luis Alberto Ponce-Soto; Sergio Marangoni
Journal:  Toxins (Basel)       Date:  2014-10-31       Impact factor: 4.546

Review 6.  Bee Venom Phospholipase A2: Yesterday's Enemy Becomes Today's Friend.

Authors:  Gihyun Lee; Hyunsu Bae
Journal:  Toxins (Basel)       Date:  2016-02-22       Impact factor: 4.546

7.  Articular inflammation induced by an enzymatically-inactive Lys49 phospholipase A2: activation of endogenous phospholipases contributes to the pronociceptive effect.

Authors:  Renata Gonçalves Dias; Sandra Coccuzzo Sampaio; Morena Brazil Sant'Anna; Fernando Queiroz Cunha; José María Gutiérrez; Bruno Lomonte; Yara Cury; Gisele Picolo
Journal:  J Venom Anim Toxins Incl Trop Dis       Date:  2017-03-23

8.  Effect of Vipera ammodytes ammodytes Snake Venom on the Human Cytokine Network.

Authors:  Francisc Boda; Krisztina Banfai; Kitti Garai; Augustin Curticapean; Lavinia Berta; Emese Sipos; Krisztian Kvell
Journal:  Toxins (Basel)       Date:  2018-06-25       Impact factor: 4.546

9.  Biochemical, pharmacological, and structural characterization of new basic PLA2 Bbil-TX from Bothriopsis bilineata snake venom.

Authors:  Victor Corasolla Carregari; Rafael Stuani Floriano; Lea Rodrigues-Simioni; Flavia V Winck; Paulo Aparecido Baldasso; Luis Alberto Ponce-Soto; Sergio Marangoni
Journal:  Biomed Res Int       Date:  2012-12-30       Impact factor: 3.411

10.  Crotalus durissus terrificus crotapotin naturally displays preferred positions for amino acid substitutions.

Authors:  Laudicéia Alves de Oliveira; Rui Seabra Ferreira; Benedito Barraviera; Francilene Capel Tavares de Carvalho; Luciana Curtolo de Barros; Lucilene Delazari Dos Santos; Daniel Carvalho Pimenta
Journal:  J Venom Anim Toxins Incl Trop Dis       Date:  2017-11-28
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.