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1.
Usp Fiziol Nauk ; 42(4): 20-38, 2011.
Artigo em Russo | MEDLINE | ID: mdl-22145309

RESUMO

The paper reviews the information about the role of fast and slow potassium currents in electrical activity of amphibian myelinated nerve fibres. It demonstrates the importance of discovering of fast and slow potassium currents and their following pharmacological separation (by potassium channels blockers 4-aminopyridine and tetraethylammonium) in investigation of mechanisms of biological potentials generation. The information about the existence of fast and slow potassium channels in the nerve membrane and about the properties of 4-aminopyridine and tetraethylammonium action served as a base for determination the nature of biological potentials and discovering the mechanism of potential-dependent action of 4-aminopyridine that for tens of years suffered from the lack of adequate explanation.


Assuntos
Potenciais de Ação/fisiologia , Anfíbios/fisiologia , Bloqueadores dos Canais de Potássio/farmacologia , Canais de Potássio/fisiologia , Potássio/metabolismo , Potenciais Sinápticos/fisiologia , 4-Aminopiridina/farmacologia , Potenciais de Ação/efeitos dos fármacos , Animais , Decapodiformes/fisiologia , Fenômenos Eletrofisiológicos , Microeletrodos , Fibras Nervosas Mielinizadas/efeitos dos fármacos , Fibras Nervosas Mielinizadas/fisiologia , Canais de Potássio/classificação , Canais de Potássio/efeitos dos fármacos , Potenciais Sinápticos/efeitos dos fármacos , Compostos de Tetraetilamônio/farmacologia
2.
Fiziol Zh (1994) ; 53(3): 61-9, 2007.
Artigo em Russo | MEDLINE | ID: mdl-17725045

RESUMO

Myelinated nerve fibres of Rana ridibunda Pallas were studied by using extra-cellular recording technique. 4-aminopyridine, a blocker of fast potassium channels produced considerable changes in duration of the after-depolarization and increase in total membrane depolarization (evaluated by an action potential area). These effects were time-dependent. The after-depolarization duration under 4-aminopyridine (4-AP) treatment changes in 3 phases: at the beginning of the exposure its duration increased; then the increase stopped; and later duration of the after-depolarization start to decrease. The last phase was often followed by hyperpolarizing after-potential. The interchange of these phases accompanies by statistically significant increase of the action potential area (from 189.201 +/- 28.437 m x ms in normal solution to 489.945 +/- 41.75 m x ms in 5 minutes after 4-AP application). These observations are explained as a result of the increased activation of the slow potassium channels and decreased portion of fast potassium channels involved in membrane repolarization. The decrease in post-tetanic depolarization duration, the appearance of the post-tetanic hyperpolarization at low frequencies and increase of post-tetanic hyperpolarization at higher frequencies of stimulation under 4-AP treatment are dependent on activation of slow potassium channels.


Assuntos
4-Aminopiridina/farmacologia , Potenciais de Ação/fisiologia , Fibras Nervosas Mielinizadas/efeitos dos fármacos , Bloqueadores dos Canais de Potássio/farmacologia , Canais de Potássio/metabolismo , Potenciais de Ação/efeitos dos fármacos , Animais , Estimulação Elétrica , Eletrodos , Fibras Nervosas Mielinizadas/metabolismo , Fibras Nervosas Mielinizadas/fisiologia , Rana ridibunda , Fatores de Tempo
3.
Fiziol Zh (1994) ; 51(2): 96-103, 2005.
Artigo em Russo | MEDLINE | ID: mdl-15943238

RESUMO

Using the extracellular recording we studied the effect of 4-aminopyridine (4-AP), a potassium channel blocker on the electrical activity of the myelinated nerve fibres of amphibia Rana ridibunda Pallas. Two main types of the reaction on 4-AP were established: extension of the action potential and multi-spike response. In some cases the nerve fibres with multi-spike response generated spontaneous activity without stimulation in the form of bursts of action potentials. During repetitive stimulation 4-AP decreased after-depolarization (at the beginning of the stimulation), the posttetanic after-depolarization and the development of posttetanic after-hyperpolarization. Using the paired stimulation it was established that the spike and after-depolarization of the second action potential depended on the size of after-depolarization after the first action potential. The effects of 4-AP were strongly time-dependent.


Assuntos
4-Aminopiridina/farmacologia , Potenciais de Ação/efeitos dos fármacos , Fibras Nervosas Mielinizadas/efeitos dos fármacos , Bloqueadores dos Canais de Potássio/farmacologia , Animais , Estimulação Elétrica , Técnicas In Vitro , Fibras Nervosas Mielinizadas/fisiologia , Rana ridibunda
4.
Ross Fiziol Zh Im I M Sechenova ; 90(2): 181-6, 2004 Feb.
Artigo em Russo | MEDLINE | ID: mdl-15143505

RESUMO

When cathode subthreshold impulse was turned off, excitable membranes of isolated nerve fibres and nervous trunk show postelectrotonic depolarisation (PED), that is a slow recovery of membrane potential to the resting level. PED of the single nodes of Ranvier and nervous trunk is registered not only in normal conditions, but also after complete block of sodium channels. The size and duration of nervous trunk PED under subthreshold depolarising current increase along with duration of applied depolarisation: when cathode current 1 ms in duration was used, they were 0.093 +/- +/- 0.004 mV and 7.123 +/- 0.576 ms, respectively; when current was 5 ms in duration, they were 0.189 +/- 0.005 mV and 23.212 +/- 1.186 ms, whereas a 10-ms depolarisation yields values of 0.220 +/- 0.011 mV and 68.721 +/- 3.389 ms. Application of the train of catelectrotonic impulses leads to PED built-up. As PED is found not only in normal conditions but also after complete block of sodium channels, it is reasonable to suggest that the most probable reason for PED is an outward potassium current.


Assuntos
Fibras Nervosas/fisiologia , Potenciais de Ação , Animais , Técnicas In Vitro , Fibras Nervosas/efeitos dos fármacos , Canais de Potássio/fisiologia , Rana ridibunda , Nós Neurofibrosos/efeitos dos fármacos , Nós Neurofibrosos/fisiologia , Bloqueadores dos Canais de Sódio/farmacologia , Canais de Sódio/efeitos dos fármacos , Canais de Sódio/fisiologia , Tetrodotoxina/farmacologia
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