RESUMO
Inhibitory action of some fatty acids on the visceral and vascular smooth muscle of guinea pig and rat was studied by the sucrose-gap method. Potency of the inhibitory effects of fatty acids depended both on the carbon chain length and degree of saturation of acid molecule. The revealed inhibitory effect of some fatty acids (caprinic and oleinic) can be of essential physiological significance in regulation of excitation of smooth muscles.
Assuntos
Ácidos Graxos não Esterificados/farmacologia , Contração Muscular/efeitos dos fármacos , Músculo Liso/efeitos dos fármacos , Animais , Depressão Química , Relação Dose-Resposta a Droga , Eletrofisiologia , Cobaias , Técnicas In Vitro , Contração Muscular/fisiologia , Músculo Liso/fisiologia , Músculo Liso Vascular/efeitos dos fármacos , Músculo Liso Vascular/fisiologia , Ratos , Relação Estrutura-AtividadeRESUMO
Nonadrenergic inhibitory junction potentials (IJPs) evoked by intramural stimulation were investigated in smooth muscle of guinea pig stomach, caecum and colon by means of sucrose-gap method. IJPs disappeared in the smooth muscle preexposed to K-free Krebs solution for 4-9 h and restored by addition 6mM Cs+. The amplitude of IJPs was half as much as one in normal conditions but the latency and duration were significantly prolonged. In most cases apamin blocks IJPs in these muscles. The results presented suggest that IJPs generation is due to Cs+ ions permeated through Ca(2+)-activated apamin-sensitive potassium channels of small conductance in these conditions. As the responses to ATP were affected in parallel with IJPs, these results are consistent with the purinergic hypothesis.
Assuntos
Césio/farmacologia , Músculo Liso/efeitos dos fármacos , Inibição Neural/efeitos dos fármacos , Potássio/farmacologia , Receptores Adrenérgicos/fisiologia , Sinapses/efeitos dos fármacos , Animais , Sistema Digestório/efeitos dos fármacos , Fenômenos Fisiológicos do Sistema Digestório , Cobaias , Técnicas In Vitro , Íons , Soluções Isotônicas , Potenciais da Membrana/efeitos dos fármacos , Potenciais da Membrana/fisiologia , Músculo Liso/fisiologia , Inibição Neural/fisiologia , Sinapses/fisiologiaAssuntos
Ácidos Graxos/análise , Águas Minerais/análise , Animais , Bactérias/enzimologia , Ácidos Graxos/síntese química , Ácidos Graxos/farmacologia , Cobaias , Hidrocarbonetos/metabolismo , Técnicas In Vitro , Contração Muscular/efeitos dos fármacos , Músculo Liso/efeitos dos fármacos , Músculo Liso/enzimologia , Oxirredução , Petróleo , Ranidae , Ratos , ATPase Trocadora de Sódio-Potássio/antagonistas & inibidores , Microbiologia da ÁguaRESUMO
The effect of the Krebs solution tonicity on the electrical and mechanical activity of smooth muscles has been studied while adding 1-5% volume of mineral water Naftusya, its artificial salt analog, and distilled water into the above solution. It is shown that effects observed are induced by the medium tonicity changes rather than by biologically active components of the mineral water. The smooth muscle cells of the rat portal vein are sensitive osmometers which affect hypotonic Krebs solution by 1%.
Assuntos
Águas Minerais , Contração Muscular , Músculo Liso Vascular/fisiologia , Veia Porta/fisiologia , Animais , Meios de Cultura , Técnicas In Vitro , Soluções Isotônicas , Músculo Liso Vascular/efeitos dos fármacos , Concentração Osmolar , Veia Porta/efeitos dos fármacos , Ratos , UcrâniaRESUMO
The ionic mechanism of nonadrenergic inhibition in smooth muscles of human intestine was studied by the sucrose-gap method. The results obtained suggest that calcium-dependent potassium conductance which consists of apamin-sensitive and -insensitive components is involved in the action of nonadrenergic transmitter in smooth muscles of human intestine.
Assuntos
Trifosfato de Adenosina/farmacologia , Bário/farmacologia , Manganês/farmacologia , Músculo Liso/efeitos dos fármacos , Estrôncio/farmacologia , Humanos , Técnicas In Vitro , Intestino Grosso/efeitos dos fármacos , Intestino Delgado/efeitos dos fármacos , Potenciais da Membrana/efeitos dos fármacos , Inibição Neural/efeitos dos fármacos , Transmissão Sináptica/efeitos dos fármacosRESUMO
Electrical responses of longitudinal and circular smooth muscles of human small intestine and colon to ATP, alpha, beta-methylene-ATP, beta, gamma-methylene-ATP and adenosine were studied by the sucrose-gap method. In most cases ATP induced the effect similar to that of stimulation of the nonadrenergic inhibitory nerves. Desensitization of the purinergic receptors by alpha, beta-methylene-ATP selectively decreased the amplitude of inhibitory junction potentials. The results confirm the purinergic hypothesis of the nonadrenergic inhibition in human intestine.