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1.
Braz. j. med. biol. res ; 47(4): 328-333, 8/4/2014. graf
Artigo em Inglês | LILACS | ID: lil-705768

RESUMO

In cardiac and skeletal muscle, eugenol (μM range) blocks excitation-contraction coupling. In skeletal muscle, however, larger doses of eugenol (mM range) induce calcium release from the sarcoplasmic reticulum. The effects of eugenol are therefore dependent on its concentration. In this study, we evaluated the effects of eugenol on the contractility of isolated, quiescent atrial trabeculae from male Wistar rats (250-300 g; n=131) and measured atrial ATP content. Eugenol (1, 3, 5, 7, and 10 mM) increased resting tension in a dose-dependent manner. Ryanodine [100 µM; a specific ryanodine receptor (RyR) blocker] and procaine (30 mM; a nonspecific RyR blocker) did not block the increased resting tension induced by eugenol regardless of whether extracellular calcium was present. The myosin-specific inhibitor 2,3-butanedione monoxime (BDM), however, reversed the increase in resting tension induced by eugenol. In Triton-skinned atrial trabeculae, in which all membranes were solubilized, eugenol did not change resting tension, maximum force produced, or the force vs pCa relationship (pCa=-log [Ca2+]). Given that eugenol reduced ATP concentration, the increase in resting tension observed in this study may have resulted from cooperative activation of cardiac thin filaments by strongly attached cross-bridges (rigor state).


Assuntos
Animais , Masculino , Cálcio/fisiologia , Eugenol/farmacologia , Acoplamento Excitação-Contração/efeitos dos fármacos , Átrios do Coração/efeitos dos fármacos , Força Muscular/efeitos dos fármacos , Contração Miocárdica/efeitos dos fármacos , Trifosfato de Adenosina/análise , Anestésicos Locais/farmacologia , Eugenol/administração & dosagem , Técnicas In Vitro , Luciferases , Músculo Esquelético/efeitos dos fármacos , Procaína/farmacologia , Ratos Wistar , Rianodina/farmacologia
2.
Experimental & Molecular Medicine ; : 614-627, 2010.
Artigo em Inglês | WPRIM | ID: wpr-162255

RESUMO

During membrane depolarization associated with skeletal excitation-contraction (EC) coupling, dihydropyridine receptor [DHPR, a L-type Ca2+ channel in the transverse (t)-tubule membrane] undergoes conformational changes that are transmitted to ryanodine receptor 1 [RyR1, an internal Ca2+-release channel in the sarcoplasmic reticulum (SR) membrane] causing Ca2+ release from the SR. Canonical-type transient receptor potential cation channel 3 (TRPC3), an extracellular Ca2+-entry channel in the t-tubule and plasma membrane, is required for full-gain of skeletal EC coupling. To examine additional role(s) for TRPC3 in skeletal muscle other than mediation of EC coupling, in the present study, we created a stable myoblast line with reduced TRPC3 expression and without alpha1SDHPR (MDG/TRPC3 KD myoblast) by knock-down of TRPC3 in alpha1SDHPR-null muscular dysgenic (MDG) myoblasts using retrovirus-delivered small interference RNAs in order to eliminate any DHPR-associated EC coupling-related events. Unlike wild-type or alpha1SDHPR-null MDG myoblasts, MDG/TRPC3 KD myoblasts exhibited dramatic changes in cellular morphology (e.g., unusual expansion of both cell volume and the plasma membrane, and multi-nuclei) and failed to differentiate into myotubes possibly due to increased Ca2+ content in the SR. These results suggest that TRPC3 plays an important role in the maintenance of skeletal muscle myoblasts and myotubes.


Assuntos
Animais , Camundongos , Cálcio/metabolismo , Canais de Cálcio/metabolismo , Canais de Cálcio Tipo L/genética , Cátions/metabolismo , Diferenciação Celular , Proliferação de Células , Células Cultivadas , Acoplamento Excitação-Contração , Técnicas de Silenciamento de Genes , Potenciais da Membrana , Fibras Musculares Esqueléticas/metabolismo , Proteínas Musculares/metabolismo , Mioblastos Esqueléticos/metabolismo , Canal de Liberação de Cálcio do Receptor de Rianodina/metabolismo , Retículo Sarcoplasmático/fisiologia , Sinaptofisina/metabolismo , Canais de Cátion TRPC/genética , Canais de Potencial de Receptor Transitório/metabolismo
3.
Neotrop. ichthyol ; 7(3): 471-478, Sept. 2009. tab, graf
Artigo em Inglês | LILACS, VETINDEX | ID: lil-530312

RESUMO

This study analyzed the physiological role of the cardiac sarcoplasmic reticulum (SR) of two neotropical teleosts, the jeju, Hoplerythrinus unitaeniatus (Erythrinidae), and the acara, Geophagus brasiliensis (Cichlidae). While the in vivo heart frequency (fH - bpm) of acara (79.6 ± 6.6) was higher than that of the jeju (50.3 ± 2.7), the opposite was observed for the ventricular inotropism (Fc - mN/mm²) at 12 bpm (acara = 28.66 ± 1.86 vs. jeju = 36.09 ± 1.67). A 5 min diastolic pause resulted in a strong potentiation of Fc (≅ 90 percent) of strips from jeju, which was completely abolished by ryanodine. Ryanodine also resulted in a ≅ 20 percent decrease in the Fc developed by strips from jeju at both subphysiological (12 bpm) and physiological (in vivo) frequencies. However, this effect of ryanodine reducing the Fc from jeju was completely compensated by adrenaline increments (10-9 and 10-6 M). In contrast, strips from acara were irresponsive to ryanodine, irrespective of the stimulation frequency, and increases in adrenaline concentration (to 10-9 and 10-6 M) further increased Fc. These results reinforce the hypothesis of the functionality of the SR as a common trait in neotropical ostariophysian (as jeju), while in acanthopterygians (as acara) it seems to be functional mainly in 'athletic' species.(AU)


O presente estudo analisou o papel fisiológico desempenhado pelo retículo sarcoplasmático (RS) de duas espécies de teleósteos neotropicais, o jeju, Hoplerythrinus unitaeniatus (Erythrinidae), e o acará, Geophagus brasiliensis (Cichlidae). Enquanto a frequência cardíaca registrada in vivo (fH - bpm) para o acará (79.6 ± 6.6) foi superior àquela observada para o jeju (50.3 ± 2.7), resposta inversa foi verificada para o inotropismo ventricular (Fc - mN/mm²) na frequência de estimulação de 12 bpm (acará = 28.66 ± 1.86 vs. jeju = 36.09 ± 1.67). Uma pausa diastólica de 5 min resultou em uma expressiva potenciação da Fc (≅ 90 por cento) das tiras de jeju, a qual foi completamente abolida pela rianodina. A rianodina também resultou em um decréscimo de ≅ 20 por cento na Fc desenvolvida pelas tiras de jeju tanto a frequências sub-fisiológicas (12 bpm) quanto fisiológicas (in vivo). No entanto, o decréscimo da Fc promovido pela rianodina foi completamente compensado pela adição de adrenalina (10-9 e 10-6 M). Em contraste, as tiras de acará foram irresponsivas à rianodina, independentemente da frequência de estimulação utilizada, fazendo com que a adição de adrenalina (10-9 e 10-6 M) resultasse em incrementos ainda maiores da Fc. Esses resultados reforçam a hipótese de que a funcionalidade do RS seja uma característica comum aos ostariofíseos neotropicais (como o jeju), enquanto nos acantopterígios (como o acará) esta organela parece ser funcional principalmente em espécies ativas.(AU)


Assuntos
Animais , Acoplamento Excitação-Contração , Caraciformes/anatomia & histologia , Ventrículos do Coração/química , Contração Miocárdica/fisiologia
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