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1.
Anaesthesia ; 56(4): 319-25, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11284817

RESUMO

We compared the effect of alfentanil 10 microg.kg-1 and esmolol 1.5 mg.kg-1 on the cardiovascular responses to laryngoscopy and double-lumen endobronchial intubation in two groups of 20 ASA 2-3 patients undergoing pulmonary surgery, in a randomised double-blind study. Arterial pressure and heart rate decreased after induction of anaesthesia and increased after intubation in both groups (p < 0.05) but remained at or below baseline values, and changes were comparable in both groups. Plasma catecholamine concentrations decreased after induction of anaesthesia in both groups (p < 0.05). Epinephrine concentrations increased in the esmolol group after intubation (p < 0.05) but remained below baseline in the alfentanil group (p < 0.05). Norepinephrine concentrations increased significantly in both groups after intubation but were higher in the esmolol group (p < 0.05). Although both esmolol 1.5 mg.kg-1 and alfentanil 10 microg.kg-1 similarly attenuated the arterial pressure and heart rate response to endobronchial intubation, plasma catecholamine concentrations increased in the esmolol group to values greater than previously reported after tracheal intubation.


Assuntos
Antagonistas Adrenérgicos beta/farmacologia , Alfentanil/farmacologia , Analgésicos Opioides/farmacologia , Hemodinâmica/efeitos dos fármacos , Intubação Intratraqueal , Propanolaminas/farmacologia , Adulto , Idoso , Pressão Sanguínea/efeitos dos fármacos , Método Duplo-Cego , Epinefrina/sangue , Feminino , Frequência Cardíaca/efeitos dos fármacos , Humanos , Laringoscopia , Pulmão/cirurgia , Masculino , Pessoa de Meia-Idade , Norepinefrina/sangue
2.
Br J Clin Pharmacol ; 51(4): 355-8, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11318773

RESUMO

AIMS: To examine the effects of nociceptin (NC) and endomorphin 1 (EM1) on electrical field stimulation (EFS)-induced contractions of the human vas deferens (hVD). METHODS: Concentration-response curves to NC and EM1 were constructed in the absence and in presence of peptidase inhibitors (PI). In some experiments a NC receptor antagonist, [Phe1psi(CH2-NH)Gly2]NC(1-13)NH2 [F/G], 10 microM) or naloxone (1 microM) were included. RESULTS: All data are mean(95%CI). In the presence of PI, NC inhibited twitches (Emax = 67(44,90)%; pEC50 = 7.28(6.95,7.61)). NC inhibition was sensitive to [F/G]. EM1 also inhibited twitches both in the absence (Emax = 82(73,91)% pEC50 = 7.07(6.92,7.22)) and presence (Emax = 83(76,90)%; pEC50 = 7.00(6.91, 7.09)) of PI. EM1 inhibition was sensitive to naloxone. CONCLUSIONS: These data suggest that hVD express NC and opioid receptors that inhibit neurogenic contractions.


Assuntos
Analgésicos Opioides/farmacologia , Oligopeptídeos/farmacologia , Peptídeos Opioides/farmacologia , Receptores Opioides/metabolismo , Ducto Deferente/efeitos dos fármacos , Relação Dose-Resposta a Droga , Estimulação Elétrica , Humanos , Técnicas In Vitro , Masculino , Naloxona/farmacologia , Antagonistas de Entorpecentes/farmacologia , Inibidores de Proteases/farmacologia , Receptores Opioides/agonistas , Ducto Deferente/metabolismo , Ducto Deferente/fisiologia , Vasodilatadores/farmacologia , Receptor de Nociceptina , Nociceptina
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