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1.
Angiol Sosud Khir ; 9(4): 125-6, 2003.
Article in Russian | MEDLINE | ID: mdl-14657923

ABSTRACT

Presented herein is a case of successful surgical treatment of infrarenal aortic aneurysm in a 95-year-old patient with coexistent pathology. The patient underwent replacement of the abdominal aorta with implantation of the inferior mesenteric artery. After treatment of complications which occurred in the postoperative period, the patient was discharged home in a satisfactory condition. The success of surgical treatment of infrarenal aortic aneurysm in elderly patients depends on the anesthesiological control and postoperative care of patients.


Subject(s)
Aortic Aneurysm, Abdominal/surgery , Vascular Surgical Procedures/methods , Aged , Aged, 80 and over , Humans , Male
3.
Fiziol Zh Im I M Sechenova ; 81(7): 27-32, 1995 Jul.
Article in Russian | MEDLINE | ID: mdl-8714372

ABSTRACT

Hexadecamethonium as well as its alkylating derivatives significantly decrease the effect of organophosphorous acetylcholinesterase inhibitor armine on the amplitude and duration of the EPPs. It seems possible that these substances prevent inhibition of acetylcholinesterase. This property of the substances seems to be due to a polymethelene chain with two nitrogens as the basic part of the molecule structure.


Subject(s)
Alkylating Agents/pharmacology , Armin/pharmacology , Cholinesterase Inhibitors/pharmacology , Decamethonium Compounds/pharmacology , Neuromuscular Junction/drug effects , Synaptic Transmission/drug effects , Animals , Drug Interactions , Electric Stimulation , In Vitro Techniques , Male , Microelectrodes , Neuromuscular Junction/physiology , Rana temporaria , Russia , Structure-Activity Relationship , Synaptic Transmission/physiology
4.
Fiziol Zh SSSR Im I M Sechenova ; 77(7): 22-8, 1991 Jul.
Article in Russian | MEDLINE | ID: mdl-1668154

ABSTRACT

The treatment of m. cutaneus pectoris-n. pectoralis preparations with 0.5 microM of alkylating derivate of hexadecamethonium, hexadecamethylene-bis-methylchloroethylamine, led to irreversible decrease of the amplitude of EPPs. The decrease was shown to be of a postsynaptic nature. After pretreatment of the neuromuscular preparations with alkylating derivate the effects of cholinesterase inhibitors were strongly diminished.


Subject(s)
Alkylating Agents/pharmacology , Decamethonium Compounds/pharmacology , Neuromuscular Junction/drug effects , Nitrogen Mustard Compounds/pharmacology , Synaptic Transmission/drug effects , Animals , Cholinesterase Inhibitors/pharmacology , Drug Interactions , In Vitro Techniques , Male , Membrane Potentials/drug effects , Membrane Potentials/physiology , Microelectrodes , Motor Endplate/drug effects , Motor Endplate/physiology , Neuromuscular Junction/physiology , Rana temporaria , Synapses/drug effects , Synapses/physiology , Synaptic Transmission/physiology
5.
Fiziol Zh SSSR Im I M Sechenova ; 75(1): 28-32, 1989 Jan.
Article in Russian | MEDLINE | ID: mdl-2538372

ABSTRACT

The dependence of the end-plate potentials inhibition upon the prevention of the muscle twitches either by tubocurarine, or alpha-neurotoxin, or cutting of the fibers was studied during nerve tetanization in the frog isolated cutaneous pectoral muscles. The decrease in end-plate potentials in the course of tetanization was the strongest under the effect of tubocurarine. The latter seems to inhibit the quantum release of acetylcholine during the nerve tetanization.


Subject(s)
Neuromuscular Junction/drug effects , Receptors, Cholinergic/drug effects , Synapses/drug effects , Tubocurarine/pharmacology , Acetylcholine/metabolism , Animals , In Vitro Techniques , Male , Neuromuscular Junction/physiology , Rana ridibunda , Synaptic Transmission/drug effects
6.
Fiziol Zh SSSR Im I M Sechenova ; 74(10): 1377-82, 1988 Oct.
Article in Russian | MEDLINE | ID: mdl-3265920

ABSTRACT

The effect of d-tubocurarine on quantal release of acetylcholine elicited with nerve pulses 0.5 to 1 Hz was studied in the frog isolated cutaneous pectoris muscle. The muscle twitches were prevented either by lowering Ca++ and raising Mg++ or by cutting the muscle fibers. In none of these cases d-tubocurarine (3.10(-7) to 5.10(-6) M) was found to affect quantal release of acetylcholine.


Subject(s)
Acetylcholine/metabolism , Motor Endplate/drug effects , Neuromuscular Junction/drug effects , Tubocurarine/pharmacology , Animals , Calcium/physiology , Dose-Response Relationship, Drug , Electric Stimulation , Magnesium/pharmacology , Male , Membrane Potentials/drug effects , Motor Endplate/physiology , Muscle Contraction/drug effects , Neuromuscular Junction/physiology , Rana temporaria
7.
Fiziol Zh SSSR Im I M Sechenova ; 74(9): 1228-34, 1988 Sep.
Article in Russian | MEDLINE | ID: mdl-2850942

ABSTRACT

The dependence of amplitude of synaptic potentials (EPP and mEPP) upon the d-tubocurarine concentration was studied in the frog cutaneous pectoral muscle. In the presence of d-tubocurarine up to 5 x 10(-7) M, the amplitude of EPP and mEPP decreased to the extent which strictly followed competitive action of d-tubocurarine. At a higher concentration, the inhibition of synaptic potentials was stronger than would be expected assuming that d-tubocurarine can only act as a competitive antagonist.


Subject(s)
Neuromuscular Junction/drug effects , Receptors, Neurotransmitter/drug effects , Tubocurarine/pharmacology , Animals , Dose-Response Relationship, Drug , Evoked Potentials/drug effects , In Vitro Techniques , Male , Microelectrodes , Motor Endplate/drug effects , Motor Endplate/physiology , Neuromuscular Junction/physiology , Rana temporaria , Receptors, Neurotransmitter/physiology
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