Effects induced by Apis mellifera venom and its components in experimental models of nociceptive and inflammatory pain
The effects induced by Apis mellifera venom (AMV), melittin-free AMV, fraction with molecular mass < 10 kDa (F<10) or melittin in nociceptive and inflammatory pain models in mice were investigated. Subcutaneous administration of AMV (2, 4 or 6 mg/kg) or melittin-free AMV (1, 2 or 4 mg/kg) into...
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Published in: | Toxicon (Oxford) Vol. 57; no. 5; pp. 764 - 771 |
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Abstract | The effects induced by Apis mellifera venom (AMV), melittin-free AMV, fraction with molecular mass < 10 kDa (F<10) or melittin in nociceptive and inflammatory pain models in mice were investigated. Subcutaneous administration of AMV (2, 4 or 6 mg/kg) or melittin-free AMV (1, 2 or 4 mg/kg) into the dorsum of mice inhibited both phases of formaldehyde-induced nociception. However, F<10 (2, 4 or 6 mg/kg) or melittin (2 or 3 mg/kg) inhibited only the second phase. AMV (4 or 6 mg/kg), but not F<10, melittin-free AMV or melittin, induced antinociception in the hot-plate model. Paw injection of AMV (0.05 or 0.10 mg), F<10 (0.05 or 0.1 mg) or melittin (0.025 or 0.050 mg) induced a nociceptive response. In spite of inducing nociception after paw injection, scorpion (Tityus serrulatus) or snake (Bothrops jararaca) venom injected into the dorsum of mice did not inhibit formaldehyde-induced nociception. In addition, AMV (6 mg/kg), but not F<10 (6 mg/kg) or melittin (3 mg/kg), inhibited formaldehyde paw oedema. Concluding, AMV, F<10 and melittin induce two contrasting effects: nociception and antinociception. AMV antinociception involves the action of different components and does not result from non-specific activation of endogenous antinociceptive mechanisms activated by exposure to noxious stimuli. |
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AbstractList | The effects induced by Apis mellifera venom (AMV), melittin-free AMV, fraction with molecular mass < 10 kDa (F<₁₀) or melittin in nociceptive and inflammatory pain models in mice were investigated. Subcutaneous administration of AMV (2, 4 or 6 mg/kg) or melittin-free AMV (1, 2 or 4 mg/kg) into the dorsum of mice inhibited both phases of formaldehyde-induced nociception. However, F<₁₀ (2, 4 or 6 mg/kg) or melittin (2 or 3 mg/kg) inhibited only the second phase. AMV (4 or 6 mg/kg), but not F<₁₀, melittin-free AMV or melittin, induced antinociception in the hot-plate model. Paw injection of AMV (0.05 or 0.10 mg), F<₁₀ (0.05 or 0.1 mg) or melittin (0.025 or 0.050 mg) induced a nociceptive response. In spite of inducing nociception after paw injection, scorpion (Tityus serrulatus) or snake (Bothrops jararaca) venom injected into the dorsum of mice did not inhibit formaldehyde-induced nociception. In addition, AMV (6 mg/kg), but not F<₁₀ (6 mg/kg) or melittin (3 mg/kg), inhibited formaldehyde paw oedema. Concluding, AMV, F<₁₀ and melittin induce two contrasting effects: nociception and antinociception. AMV antinociception involves the action of different components and does not result from non-specific activation of endogenous antinociceptive mechanisms activated by exposure to noxious stimuli. The effects induced by Apis mellifera venom (AMV), melittin-free AMV, fraction with molecular mass < 10 kDa (F<₁₀) or melittin in nociceptive and inflammatory pain models in mice were investigated. Subcutaneous administration of AMV (2, 4 or 6 mg/kg) or melittin-free AMV (1, 2 or 4 mg/kg) into the dorsum of mice inhibited both phases of formaldehyde-induced nociception. However, F<₁₀ (2, 4 or 6 mg/kg) or melittin (2 or 3 mg/kg) inhibited only the second phase. AMV (4 or 6 mg/kg), but not F<₁₀, melittin-free AMV or melittin, induced antinociception in the hot-plate model. Paw injection of AMV (0.05 or 0.10 mg), F<₁₀ (0.05 or 0.1 mg) or melittin (0.025 or 0.050 mg) induced a nociceptive response. In spite of inducing nociception after paw injection, scorpion (Tityus serrulatus) or snake (Bothrops jararaca) venom injected into the dorsum of mice did not inhibit formaldehyde-induced nociception. In addition, AMV (6 mg/kg), but not F<₁₀ (6 mg/kg) or melittin (3 mg/kg), inhibited formaldehyde paw oedema. Concluding, AMV, F<₁₀ and melittin induce two contrasting effects: nociception and antinociception. AMV antinociception involves the action of different components and does not result from non-specific activation of endogenous antinociceptive mechanisms activated by exposure to noxious stimuli. The effects induced by Apis mellifera venom (AMV), melittin-free AMV, fraction with molecular massANB<ANB10ANBkDa (F <10) or melittin in nociceptive and inflammatory pain models in mice were investigated. Subcutaneous administration of AMV (2, 4 or 6ANBmg/kg) or melittin-free AMV (1, 2 or 4ANBmg/kg) into the dorsum of mice inhibited both phases of formaldehyde-induced nociception. However, F <10 (2, 4 or 6ANBmg/kg) or melittin (2 or 3ANBmg/kg) inhibited only the second phase. AMV (4 or 6ANBmg/kg), but not F <10, melittin-free AMV or melittin, induced antinociception in the hot-plate model. Paw injection of AMV (0.05 or 0.10ANBmg), F <10 (0.05 or 0.1ANBmg) or melittin (0.025 or 0.050ANBmg) induced a nociceptive response. In spite of inducing nociception after paw injection, scorpion (Tityus serrulatus) or snake (Bothrops jararaca) venom injected into the dorsum of mice did not inhibit formaldehyde-induced nociception. In addition, AMV (6ANBmg/kg), but not F <10 (6ANBmg/kg) or melittin (3ANBmg/kg), inhibited formaldehyde paw oedema. Concluding, AMV, F <10 and melittin induce two contrasting effects: nociception and antinociception. AMV antinociception involves the action of different components and does not result from non-specific activation of endogenous antinociceptive mechanisms activated by exposure to noxious stimuli. The effects induced by Apis mellifera venom (AMV), melittin-free AMV, fraction with molecular mass < 10 kDa (F<10) or melittin in nociceptive and inflammatory pain models in mice were investigated. Subcutaneous administration of AMV (2, 4 or 6 mg/kg) or melittin-free AMV (1, 2 or 4 mg/kg) into the dorsum of mice inhibited both phases of formaldehyde-induced nociception. However, F<10 (2, 4 or 6 mg/kg) or melittin (2 or 3 mg/kg) inhibited only the second phase. AMV (4 or 6 mg/kg), but not F<10, melittin-free AMV or melittin, induced antinociception in the hot-plate model. Paw injection of AMV (0.05 or 0.10 mg), F<10 (0.05 or 0.1 mg) or melittin (0.025 or 0.050 mg) induced a nociceptive response. In spite of inducing nociception after paw injection, scorpion (Tityus serrulatus) or snake (Bothrops jararaca) venom injected into the dorsum of mice did not inhibit formaldehyde-induced nociception. In addition, AMV (6 mg/kg), but not F<10 (6 mg/kg) or melittin (3 mg/kg), inhibited formaldehyde paw oedema. Concluding, AMV, F<10 and melittin induce two contrasting effects: nociception and antinociception. AMV antinociception involves the action of different components and does not result from non-specific activation of endogenous antinociceptive mechanisms activated by exposure to noxious stimuli. The effects induced by Apis mellifera venom (AMV), melittin-free AMV, fraction with molecular mass < 10 kDa (F<₁₀) or melittin in nociceptive and inflammatory pain models in mice were investigated. Subcutaneous administration of AMV (2, 4 or 6 mg/kg) or melittin-free AMV (1, 2 or 4 mg/kg) into the dorsum of mice inhibited both phases of formaldehyde-induced nociception. However, F<₁₀ (2, 4 or 6 mg/kg) or melittin (2 or 3 mg/kg) inhibited only the second phase. AMV (4 or 6 mg/kg), but not F<₁₀, melittin-free AMV or melittin, induced antinociception in the hot-plate model. Paw injection of AMV (0.05 or 0.10 mg), F<₁₀ (0.05 or 0.1 mg) or melittin (0.025 or 0.050 mg) induced a nociceptive response. In spite of inducing nociception after paw injection, scorpion (Tityus serrulatus) or snake (Bothrops jararaca) venom injected into the dorsum of mice did not inhibit formaldehyde-induced nociception. In addition, AMV (6 mg/kg), but not F<₁₀ (6 mg/kg) or melittin (3 mg/kg), inhibited formaldehyde paw oedema. Concluding, AMV, F<₁₀ and melittin induce two contrasting effects: nociception and antinociception. AMV antinociception involves the action of different components and does not result from non-specific activation of endogenous antinociceptive mechanisms activated by exposure to noxious stimuli. |
Author | Heneine, Luiz Guilherme D. Nascimento, Elias B. Bastos, Leandro F.S. Godin, Adriana M. Moraes-Santos, Tasso Coelho, Márcio M. Merlo, Leonardo A. Rocha, Leonardo T.S. Paiva, André L.L. Zumpano, Antônio A.C. Bastos, Esther M.A.F. |
Author_xml | – sequence: 1 givenname: Leonardo A. surname: Merlo fullname: Merlo, Leonardo A. organization: Departamento de Produtos Farmacêuticos, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, 31270-901, Belo Horizonte, MG, Brazil – sequence: 2 givenname: Leandro F.S. surname: Bastos fullname: Bastos, Leandro F.S. organization: Departamento de Produtos Farmacêuticos, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, 31270-901, Belo Horizonte, MG, Brazil – sequence: 3 givenname: Adriana M. surname: Godin fullname: Godin, Adriana M. organization: Departamento de Produtos Farmacêuticos, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, 31270-901, Belo Horizonte, MG, Brazil – sequence: 4 givenname: Leonardo T.S. surname: Rocha fullname: Rocha, Leonardo T.S. organization: Departamento de Produtos Farmacêuticos, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, 31270-901, Belo Horizonte, MG, Brazil – sequence: 5 givenname: Elias B. surname: Nascimento fullname: Nascimento, Elias B. organization: Departamento de Produtos Farmacêuticos, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, 31270-901, Belo Horizonte, MG, Brazil – sequence: 6 givenname: André L.L. surname: Paiva fullname: Paiva, André L.L. organization: Departamento de Produtos Farmacêuticos, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, 31270-901, Belo Horizonte, MG, Brazil – sequence: 7 givenname: Tasso surname: Moraes-Santos fullname: Moraes-Santos, Tasso organization: Departamento de Alimentos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, 31270-901, Belo Horizonte, MG, Brazil – sequence: 8 givenname: Antônio A.C. surname: Zumpano fullname: Zumpano, Antônio A.C. organization: Laboratório de Imunologia e Bioprodutos do Centro de Pesquisa e Desenvolvimento da Fundação Ezequiel Dias (FUNED), Rua Conde Pereira Carneiro 80, 30510-010, Belo Horizonte, MG, Brazil – sequence: 9 givenname: Esther M.A.F. surname: Bastos fullname: Bastos, Esther M.A.F. organization: Laboratório de Imunologia e Bioprodutos do Centro de Pesquisa e Desenvolvimento da Fundação Ezequiel Dias (FUNED), Rua Conde Pereira Carneiro 80, 30510-010, Belo Horizonte, MG, Brazil – sequence: 10 givenname: Luiz Guilherme D. surname: Heneine fullname: Heneine, Luiz Guilherme D. organization: Laboratório de Imunologia e Bioprodutos do Centro de Pesquisa e Desenvolvimento da Fundação Ezequiel Dias (FUNED), Rua Conde Pereira Carneiro 80, 30510-010, Belo Horizonte, MG, Brazil – sequence: 11 givenname: Márcio M. surname: Coelho fullname: Coelho, Márcio M. email: mmcoelho@farmacia.ufmg.br organization: Departamento de Produtos Farmacêuticos, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, 31270-901, Belo Horizonte, MG, Brazil |
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Keywords | Nociception NO Melittin IL Bee venom TRPA s.c Inflammation AMV TNF Apis mellifera Pain F<10 PL Insecta Apidae Animal origin Apoidea Arthropoda Venom Models Hymenoptera Invertebrata Aculeata |
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SubjectTerms | Analysis of Variance animal models Animal poisons toxicology. Antivenoms Animals Apis mellifera Bee venom Bee Venoms - toxicity Biological and medical sciences Bothrops jararaca edema formaldehyde Formaldehyde - toxicity Inflammation Inflammation - chemically induced Male Medical sciences Melitten - toxicity Melittin Mice molecular weight Motor Activity - drug effects Nociception Pain Pain - chemically induced Pain Measurement snakes subcutaneous injection Tityus serrulatus Toxicology venoms |
Title | Effects induced by Apis mellifera venom and its components in experimental models of nociceptive and inflammatory pain |
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