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1.
Biochim Biophys Acta Biomembr ; 1865(1): 184057, 2023 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-36240866

RESUMO

Ts17 was purified from the venom of the scorpion Tityus serrulatus, the most dangerous scorpion species in Brazil. The activity on Nav1.1-Nav1.7 channels was electrophysiologically characterized by patch-clamp technique. Ts17 amino acid sequence indicated high similarity to alpha-scorpion toxins; however, it presented beta-toxin activity, altering the kinetics of the Na+-channels. The most affected subtypes during activation (with and without prepulse) and inactivation phases were Nav1.2 and Nav1.5, respectively. For recovery from inactivation, the most affected voltage-gated sodium channel was Nav1.5. Circular dichroism spectra showed that Ts17 presents mainly ß-sheet and unordered structures at all analyzed pHs, and the maximum value of α-helix was found at pH 4.0 (13.3 %). Based on the results, Ts17 might be used as a template to develop a new cardiac drug. Key contribution Purification of Ts17 from Tityus serrulatus, electrophysiological characterization of Ts17 on voltage-gated sodium channel subtypes, ß-toxin classification.


Assuntos
Venenos de Escorpião , Canais de Sódio Disparados por Voltagem , Animais , Escorpiões/química , Venenos de Escorpião/farmacologia , Venenos de Escorpião/química , Sequência de Aminoácidos , Técnicas de Patch-Clamp
2.
Biochim Biophys Acta Biomembr ; 1861(1): 142-150, 2019 01.
Artigo em Inglês | MEDLINE | ID: mdl-30463697

RESUMO

To1, previously named Tc49b, is a peptide neurotoxin isolated from venom of the scorpion Tityus obscurus that is responsible for lethal human poisoning cases in the Brazilian Amazonian region. Previously, To1 was shown to be lethal to mice and to change Na+ permeation in cerebellum granular neurons from rat brain. In addition, To1 did not affect Shaker B K+ channels. Based on sequence similarities, To1 was described as a ß-toxin. In the present work, To1 was purified from T. obscurus venom and submitted to an electrophysiological characterization in human and invertebrate NaV channels. The analysis of the electrophysiological experiments reveal that To1 enhances the open probability at more negative potentials of human NaV 1.3 and 1.6, of the insect channel BgNaV1 and of arachnid VdNaV1 channel. In addition, To1 reduces the peak of Na+ currents in some of the NaVs tested. These results support the classification of the To1 as a ß-toxin. A structure and functional comparison to other ß-toxins that share sequence similarity to To1 is also presented.


Assuntos
Canal de Sódio Disparado por Voltagem NAV1.3/química , Canal de Sódio Disparado por Voltagem NAV1.6/química , Venenos de Escorpião/química , Escorpiões/química , Canais de Sódio/química , Animais , Fenômenos Eletrofisiológicos , Células HEK293 , Humanos , Proteínas de Insetos/química , Cinética , Peptídeos , Probabilidade , Ligação Proteica , Sódio/química
3.
Toxins (Basel) ; 10(9)2018 08 22.
Artigo em Inglês | MEDLINE | ID: mdl-30131471

RESUMO

Scorpion venoms are a complex mixture of components. Among them the most important are peptides, which presents the capacity to interact and modulate several ion channel subtypes, including voltage-gated sodium channels (NaV). Screening the activity of scorpion toxins on different subtypes of NaV reveals the scope of modulatory activity and, in most cases, low channel selectivity. Until now there are approximately 60 scorpion toxins experimentally assayed on NaV channels. However, the molecular bases of interaction between scorpion toxins and NaV channels are not fully elucidated. The activity description of new scorpion toxins is crucial to enhance the predictive strength of the structural⁻function correlations of these NaV modulatory molecules. In the present work a new scorpion toxin (Tf1a) was purified from Tityus fasciolatus venom by RP-HPLC, and characterized using electrophysiological experiments on different types of voltage-gated sodium channels. Tf1a was able to modify the normal function of NaV tested, showing to be a typical ß-NaScTx. Tf1a also demonstrated an unusual capability to alter the kinetics of NaV1.5.


Assuntos
Venenos de Escorpião/toxicidade , Canais de Sódio Disparados por Voltagem/fisiologia , Sequência de Aminoácidos , Animais , Sequência de Bases , Linhagem Celular , Cricetulus , Humanos , Venenos de Escorpião/química , Escorpiões , Alinhamento de Sequência
4.
Peptides ; 95: 106-115, 2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28735770

RESUMO

Many scorpion toxins that act on sodium channels (NaScTxs) have been characterized till date. These toxins may act modulating the inactivation or the activation of sodium channels and are named α- or ß-types, respectively. Some venom toxins from Tityus obscurus (Buthidae), a scorpion widely distributed in the Brazilian Amazon, have been partially characterized in previous studies; however, little information about their electrophysiological role on sodium ion channels has been published. In the present study, we describe the purification, identification and electrophysiological characterization of a NaScTx, which was first described as Tc54 and further fully sequenced and renamed To4. This toxin shows a marked ß-type effect on different sodium channel subtypes (hNav1.1-hNav1.7) at low concentrations, and has more pronounced activity on hNav1.1, hNav1.2 and hNav1.4. By comparing To4 primary structure with other Tityus ß-toxins which have already been electrophysiologically tested, it is possible to establish some key amino acid residues for the sodium channel activity. Thus, To4 is the first toxin from T. obscurus fully electrophysiologically characterized on different human sodium channel isoforms.


Assuntos
Canal de Sódio Disparado por Voltagem NAV1.1/efeitos dos fármacos , Canal de Sódio Disparado por Voltagem NAV1.7/efeitos dos fármacos , Isoformas de Proteínas/efeitos dos fármacos , Venenos de Escorpião/farmacologia , Sequência de Aminoácidos/efeitos dos fármacos , Animais , Eletrofisiologia , Humanos , Canal de Sódio Disparado por Voltagem NAV1.1/química , Canal de Sódio Disparado por Voltagem NAV1.7/química , Isoformas de Proteínas/química , Venenos de Escorpião/química , Escorpiões/química
5.
Behav Processes ; 118: 102-10, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26049017

RESUMO

Ayahuasca, a psychoactive beverage used by indigenous and religious groups, is generally prepared by the coction of Psychotria viridis and Banisteriopsis caapi plants containing N,N-dimethyltryptamine (DMT) and ß-carboline alkaloids, respectively. To investigate the acute toxicity of ayahuasca, the infusion was administered by gavage to female Wistar rats at doses of 30X and 50X the dose taken during a religious ritual, and the animals observed for 14 days. Behavioural functions were investigated one hour after dosing at 15X and 30X using the open field, elevated plus maze, and forced swimming tests. Neuronal activation (c-fos marked neurons) and toxicity (Fluoro-Jade B and Nissl/Cresyl staining) were investigated in the dorsal raphe nuclei (DRN), amygdaloid nucleus, and hippocampal formation brain areas of rats treated with a 30X ayahuasca dose. The actual lethal oral dose in female Wistar rats could not be determined in this study, but was shown to be higher than the 50X (which corresponds to 15.1mg/kg bw DMT). The ayahuasca and fluoxetine treated groups showed a significant decrease in locomotion in the open field and elevated plus-maze tests compared to controls. In the forced swimming test, ayahuasca treated animals swam more than controls, a behaviour that was not significant in the fluoxetine group. Treated animals showed higher neuronal activation in all brain areas involved in serotoninergic neurotransmission. Although this led to some brain injury, no permanent damage was detected. These results suggest that ayahuasca has antidepressant properties in Wistar female at high doses, an effect that should be further investigated.


Assuntos
Banisteriopsis/toxicidade , Preparações de Plantas/toxicidade , Animais , Comportamento Animal/efeitos dos fármacos , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Relação Dose-Resposta a Droga , Feminino , Locomoção/efeitos dos fármacos , Modelos Animais , Ratos , Ratos Wistar
6.
Toxicon ; 101: 55-62, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25911957

RESUMO

Injuries caused by aquatic animals in Brazil in most cases are provoked by marine and freshwater catfish. Pimelodus maculatus is a freshwater catfish very common in Brazilian basins that causes frequent accidents mainly amongst fishermen, and whose venom characteristics and pathological mechanisms of the venom are poorly known. In the present study for the first time, we have characterized the main pathophysiological mechanisms associated with the clinical manifestation (pain, local inflammation and edema) of the envenomations caused by P. maculatus crude venom. It was estimated that the crude venom of one P. maculatus stinger contains approximately 100 µg of protein, likely the quantity involved in the envenomation. P. maculatus crude venom induced marked nociceptive and edematogenic effects and caused vascular permeability alterations at doses from 30 to 100 µg/animal. Additionally, P. maculatus crude venom caused a decrease in the contraction force in in situ frog heart, did not cause hemorrhage or alterations in clotting times (prothrombin time and activated partial thromboplastin time), but induced significant changes in the levels of CK and its isoenzyme CK-MB in mice. In the present work, we present a correlation between the effects obtained experimentally and the main symptoms observed in the human accidents provoked by P. maculatus.


Assuntos
Mordeduras e Picadas/fisiopatologia , Peixes-Gato/metabolismo , Edema/fisiopatologia , Venenos de Peixe/toxicidade , Inflamação/fisiopatologia , Dor/fisiopatologia , Animais , Brasil , Permeabilidade Capilar/efeitos dos fármacos , Creatina Quinase/metabolismo , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Edema/etiologia , Feminino , Venenos de Peixe/química , Água Doce , Hemorragia/etiologia , Hemorragia/fisiopatologia , Inflamação/etiologia , Isoenzimas/metabolismo , Masculino , Camundongos , Nociceptores/efeitos dos fármacos , Nociceptores/patologia , Dor/etiologia , Tempo de Tromboplastina Parcial , Tempo de Protrombina , Ratos , Ratos Wistar
7.
Zootaxa ; 3750: 321-47, 2013 Dec 20.
Artigo em Inglês | MEDLINE | ID: mdl-25113702

RESUMO

Based on the analyses of specimens collected at several areas in the Cerrado domain from Central Brazil and others housed in scientific collections and on specimens collected at the type-locality, herein we describe three new species belonging to the P. cristiceps group: Proceratophrys bagnoi sp. nov., from UHE Serra da Mesa power plant (13°49'47.5"S, 48°19'17"W; 570 m a.s.l.; WGS84 datum), Municipality of Minaçu, State of Goiás; Proceratophrys branti sp. nov., from Jalapão, Municipality of Mateiros (05o15'25"S, 48o12'00"W; 109 m a.s.l.; WGS84 datum), State of Tocantins; and Proceratophrys dibernardoi sp. nov., Municipality of Mineiros (17o33'52"S, 52o33'20"W; 803 m a.s.l.; WGS84 datum), State of Goiás. The diversity of Proceratophrys in Brazilian Cerrado is still underscored and several species will be described in the following years.


Assuntos
Anuros/classificação , Distribuição Animal , Estruturas Animais/anatomia & histologia , Animais , Anuros/anatomia & histologia , Brasil , Ecossistema , Feminino , Masculino
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