Potential Utilization of a Polysaccharide from the Marine Algae Gayralia oxysperma , as an Antivenom for Viperidae Snakebites
Worldwide, snakebites have serious implications for human health. The administration of antivenom is the official treatment used to reverse the toxic activities of envenomation. However, this therapy is not efficient to treat the local effects, leading to the amputation or deformity of affected limb...
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Published in: | Marine drugs Vol. 16; no. 11; p. 412 |
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Main Authors: | , , , , , , |
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Abstract | Worldwide, snakebites have serious implications for human health. The administration of antivenom is the official treatment used to reverse the toxic activities of envenomation. However, this therapy is not efficient to treat the local effects, leading to the amputation or deformity of affected limbs. As such, alternative treatments are needed. Here, we analyze the ability of a polysaccharide from the green marine alga
(Go3) to inhibit the effects of venom from
and
.
or
venoms were incubated together with sulfated heterorhamnans from Go3, and the in vitro (coagulation, proteolytic, and hemolytic) and in vivo (hemorrhagic, myotoxic, edematogenic, and lethal) activities of venoms were assessed. Additionally, Go3 was injected before and after the injection of venoms, and the toxic activities were further tested. When incubated with the venoms, Go3 inhibited all activities, though results varied with different potencies. Moreover, Go3 neutralized hemorrhagic, myotoxic, and edematogenic activities when injected before or after injection with
and
venom. Go3 also blocked the coagulation of plasma in mice caused by the venoms in an ex vivo test. Therefore, Go3 has the potential to be used as antivenom for
and
bites, notably exhibiting higher efficacy on
venom. |
---|---|
AbstractList | Worldwide, snakebites have serious implications for human health. The administration of antivenom is the official treatment used to reverse the toxic activities of envenomation. However, this therapy is not efficient to treat the local effects, leading to the amputation or deformity of affected limbs. As such, alternative treatments are needed. Here, we analyze the ability of a polysaccharide from the green marine alga Gayralia oxysperma (Go3) to inhibit the effects of venom from Bothrops jararaca and Lachesis muta. B. jararaca or L. muta venoms were incubated together with sulfated heterorhamnans from Go3, and the in vitro (coagulation, proteolytic, and hemolytic) and in vivo (hemorrhagic, myotoxic, edematogenic, and lethal) activities of venoms were assessed. Additionally, Go3 was injected before and after the injection of venoms, and the toxic activities were further tested. When incubated with the venoms, Go3 inhibited all activities, though results varied with different potencies. Moreover, Go3 neutralized hemorrhagic, myotoxic, and edematogenic activities when injected before or after injection with B. jararaca and L. muta venom. Go3 also blocked the coagulation of plasma in mice caused by the venoms in an ex vivo test. Therefore, Go3 has the potential to be used as antivenom for B. jararaca and L. muta bites, notably exhibiting higher efficacy on L. muta venom. Worldwide, snakebites have serious implications for human health. The administration of antivenom is the official treatment used to reverse the toxic activities of envenomation. However, this therapy is not efficient to treat the local effects, leading to the amputation or deformity of affected limbs. As such, alternative treatments are needed. Here, we analyze the ability of a polysaccharide from the green marine alga (Go3) to inhibit the effects of venom from and . or venoms were incubated together with sulfated heterorhamnans from Go3, and the in vitro (coagulation, proteolytic, and hemolytic) and in vivo (hemorrhagic, myotoxic, edematogenic, and lethal) activities of venoms were assessed. Additionally, Go3 was injected before and after the injection of venoms, and the toxic activities were further tested. When incubated with the venoms, Go3 inhibited all activities, though results varied with different potencies. Moreover, Go3 neutralized hemorrhagic, myotoxic, and edematogenic activities when injected before or after injection with and venom. Go3 also blocked the coagulation of plasma in mice caused by the venoms in an ex vivo test. Therefore, Go3 has the potential to be used as antivenom for and bites, notably exhibiting higher efficacy on venom. Worldwide, snakebites have serious implications for human health. The administration of antivenom is the official treatment used to reverse the toxic activities of envenomation. However, this therapy is not efficient to treat the local effects, leading to the amputation or deformity of affected limbs. As such, alternative treatments are needed. Here, we analyze the ability of a polysaccharide from the green marine alga Gayralia oxysperma (Go3) to inhibit the effects of venom from Bothrops jararaca and Lachesis muta . B. jararaca or L. muta venoms were incubated together with sulfated heterorhamnans from Go3, and the in vitro (coagulation, proteolytic, and hemolytic) and in vivo (hemorrhagic, myotoxic, edematogenic, and lethal) activities of venoms were assessed. Additionally, Go3 was injected before and after the injection of venoms, and the toxic activities were further tested. When incubated with the venoms, Go3 inhibited all activities, though results varied with different potencies. Moreover, Go3 neutralized hemorrhagic, myotoxic, and edematogenic activities when injected before or after injection with B. jararaca and L. muta venom. Go3 also blocked the coagulation of plasma in mice caused by the venoms in an ex vivo test. Therefore, Go3 has the potential to be used as antivenom for B. jararaca and L. muta bites, notably exhibiting higher efficacy on L. muta venom. |
Author | Sanchez, Eladio Flores Fuly, Andre Lopes Cassolato, Juliana Emanuela Fogari da Silva, Ana Cláudia Rodrigues Noseda, Miguel Daniel Duarte, Maria Eugenia Rabello Ferreira, Luciana Garcia |
AuthorAffiliation | 2 Department of Biochemistry and Molecular Biology, Federal University of Paraná, Curitiba, Paraná 81531-980, Brazil; mdn@ufpr.br (M.D.N.); lugarciaferreira@gmail.com (L.G.F.); jcassolato@yahoo.com.br (J.E.F.C.) 3 Laboratory of Biochemistry of Proteins from Animal Venoms, Research and Development Center, Ezequiel Dias Foundation, Belo Horizonte, Minas Gerais 30510-010, Brazil; eladiooswaldo@gmail.com 1 Department of Molecular and Cellular Biology, Federal Fluminense University, Niterói, Rio de Janeiro 24020-141, Brazil; anacrs1@yahoo.com.br |
AuthorAffiliation_xml | – name: 1 Department of Molecular and Cellular Biology, Federal Fluminense University, Niterói, Rio de Janeiro 24020-141, Brazil; anacrs1@yahoo.com.br – name: 2 Department of Biochemistry and Molecular Biology, Federal University of Paraná, Curitiba, Paraná 81531-980, Brazil; mdn@ufpr.br (M.D.N.); lugarciaferreira@gmail.com (L.G.F.); jcassolato@yahoo.com.br (J.E.F.C.) – name: 3 Laboratory of Biochemistry of Proteins from Animal Venoms, Research and Development Center, Ezequiel Dias Foundation, Belo Horizonte, Minas Gerais 30510-010, Brazil; eladiooswaldo@gmail.com |
Author_xml | – sequence: 1 givenname: Ana Cláudia Rodrigues surname: da Silva fullname: da Silva, Ana Cláudia Rodrigues email: anacrs1@yahoo.com.br organization: Department of Molecular and Cellular Biology, Federal Fluminense University, Niterói, Rio de Janeiro 24020-141, Brazil. anacrs1@yahoo.com.br – sequence: 2 givenname: Maria Eugenia Rabello surname: Duarte fullname: Duarte, Maria Eugenia Rabello email: nosedaeu@ufpr.br organization: Department of Biochemistry and Molecular Biology, Federal University of Paraná, Curitiba, Paraná 81531-980, Brazil. nosedaeu@ufpr.br – sequence: 3 givenname: Miguel Daniel surname: Noseda fullname: Noseda, Miguel Daniel email: mdn@ufpr.br organization: Department of Biochemistry and Molecular Biology, Federal University of Paraná, Curitiba, Paraná 81531-980, Brazil. mdn@ufpr.br – sequence: 4 givenname: Luciana Garcia surname: Ferreira fullname: Ferreira, Luciana Garcia email: lugarciaferreira@gmail.com organization: Department of Biochemistry and Molecular Biology, Federal University of Paraná, Curitiba, Paraná 81531-980, Brazil. lugarciaferreira@gmail.com – sequence: 5 givenname: Juliana Emanuela Fogari surname: Cassolato fullname: Cassolato, Juliana Emanuela Fogari email: jcassolato@yahoo.com.br organization: Department of Biochemistry and Molecular Biology, Federal University of Paraná, Curitiba, Paraná 81531-980, Brazil. jcassolato@yahoo.com.br – sequence: 6 givenname: Eladio Flores surname: Sanchez fullname: Sanchez, Eladio Flores email: eladiooswaldo@gmail.com organization: Laboratory of Biochemistry of Proteins from Animal Venoms, Research and Development Center, Ezequiel Dias Foundation, Belo Horizonte, Minas Gerais 30510-010, Brazil. eladiooswaldo@gmail.com – sequence: 7 givenname: Andre Lopes orcidid: 0000-0002-5265-5258 surname: Fuly fullname: Fuly, Andre Lopes email: andrefuly@id.uff.br organization: Department of Molecular and Cellular Biology, Federal Fluminense University, Niterói, Rio de Janeiro 24020-141, Brazil. andrefuly@id.uff.br |
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CitedBy_id | crossref_primary_10_1007_s13399_023_03922_6 crossref_primary_10_1016_j_carbpol_2018_12_054 crossref_primary_10_1515_znc_2022_0010 crossref_primary_10_3390_md18100514 crossref_primary_10_3390_toxins16040188 crossref_primary_10_1016_j_aquaculture_2022_738596 |
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Keywords | polysaccharide Bothrops jararaca Lachesis muta antivenom green marine alga neutralization snake venom Gayralia oxysperma |
Language | English |
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SubjectTerms | Algae Amputation Animals Antivenins - isolation & purification Antivenins - pharmacology Antivenins - therapeutic use Antivenom Aquatic Organisms - chemistry Biocompatibility Blood Coagulation - drug effects Bothrops Bothrops jararaca Chlorophyta - chemistry Coagulation Crotalid Venoms - antagonists & inhibitors Crotalid Venoms - pharmacology Cytotoxicity Deformation effects Deoxy Sugars - isolation & purification Deoxy Sugars - pharmacology Deoxy Sugars - therapeutic use Disease Models, Animal Gayralia oxysperma green marine alga Haemorrhage Hemolysis - drug effects Hemorrhage Humans In vivo methods and tests Injection Lachesis muta Mannans - isolation & purification Mannans - pharmacology Mannans - therapeutic use Mice Mice, Inbred BALB C neutralization Plant resistance Plasma polysaccharide Polysaccharides Proteolysis Snake bites Snake Bites - blood Snake Bites - drug therapy snake venom Toxicity testing Venom |
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Title | Potential Utilization of a Polysaccharide from the Marine Algae Gayralia oxysperma , as an Antivenom for Viperidae Snakebites |
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