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10.
J Physiol ; 195(3): 589-607, 1968 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-4296976

RESUMO

1. Both carotid bodies were removed from cats and placed in a small Perspex channel through which Locke solution was allowed to flow under a layer of paraffin oil. Stimulation of the upstream (;donor') organ elicited an increased sensory discharge in the downstream (;detector') preparation (Loewi effect).2. This effect was enhanced by eserine, depressed by hexamethonium and blocked by either mecamylamine or acetylcholinesterase. The Loewi effect did not disappear when chronically denervated (4 days) ;donor' carotid bodies were stimulated.3. These experiments led to the conclusion that ACh is released by the carotid body tissues (probably from the glomus cells) during stimulation and that this substance is responsible for the initiation of the chemosensory discharges.4. In single preparations the chemosensory endings proved to be very sensitive to ACh especially in the presence of eserine which, in all probability, inactivated the tissue cholinesterase. Curarizing agents such as mecamylamine, hexamethonium, (+)-tubocurarine and atropine blocked the response of the sensory endings to applied ACh in what appeared to be ;surmountable' antagonism.


Assuntos
Acetilcolina/metabolismo , Corpo Carotídeo/metabolismo , Células Quimiorreceptoras/efeitos dos fármacos , Parassimpatolíticos/farmacologia , Acetilcolina/antagonistas & inibidores , Acetilcolina/farmacologia , Acetilcolinesterase/farmacologia , Potenciais de Ação/efeitos dos fármacos , Animais , Atropina/farmacologia , Corpo Carotídeo/inervação , Gatos , Sinergismo Farmacológico , Compostos de Hexametônio/farmacologia , Mecamilamina/farmacologia , Músculos/antagonistas & inibidores , Perfusão , Fisostigmina/farmacologia , Transmissão Sináptica , Tubocurarina/farmacologia
17.
J Physiol ; 191(1): 59-90, 1967 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-4292958

RESUMO

1. The margin of safety for neuromuscular transmission in the tibialis and sartorius muscles of the cat has been determined by measuring the ratio by which end-plate depolarization produced by succinylcholine, decamethonium, octamethonium or iodocholine is antagonized, in the presence of neuromuscular block produced by tubocurarine, gallamine or DF-596. The estimate of the margin of safety was independent of the particular drugs chosen for the measurement.2. To produce threshold block to indirect stimulation once every 10 sec, a fractional occupancy by the antagonist of 0.76 +/- 0.05 (S.D.) was required; for nearly complete block, an occupancy of 0.917 +/- 0.16 (S.D.) was required. These figures correspond to factors of safety of 4.1 and 12 for the most sensitive and the most resistant groups of fibres respectively.3. The interaction between the agonists and the antagonists, when tested over a wide range of dosage, did not conform with the conditions of full competitive equilibrium. It was concluded that this arose, not because of some interfering non-competitive process, but because, during the relatively brief exposure to agonist, the equilibrium between the antagonist and the receptors is not significantly disturbed. An analysis of this condition of quasi-equilibrium is given. A correction downwards of the direct estimates of the margin of safety is required, but this proves to be small, about 8%, and may not be significant.4. The safety factor diminished when the motor nerve had been cut more than 5 hr; it is suggested that this represents an early sign of nerve degeneration.5. With dog sartorius muscle, results similar to those in the cat were obtained. But for deep block in the rabbit, the safety factor was only about 4.6. The existence of a substantial margin of safety influences considerably the interpretation of the time course of action of blocking drugs, and of comparisons between responses to nervous excitation and drug injection.


Assuntos
Trietiodeto de Galamina/farmacologia , Músculos/antagonistas & inibidores , Junção Neuromuscular/efeitos dos fármacos , Transmissão Sináptica/efeitos dos fármacos , Tubocurarina/farmacologia , Animais , Gatos , Compostos de Decametônio/antagonistas & inibidores , Antagonismo de Drogas , Succinilcolina/antagonistas & inibidores , Sinapses/efeitos dos fármacos
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