Zobrazeno 1 - 9
of 9
pro vyhledávání: '"S V, Tam"'
Autor:
N V, Solenkova, L N, Maslov, Iu B, Lishmanov, V Iu, Serebrov, S A, Bogomaz, G G, Gross, J B, Stefano, S V, Tam
Publikováno v:
Eksperimental'naia i klinicheskaia farmakologiia. 65(1)
Preliminary administration of the delta 1-opioid receptor (delta 1-OR) selective peptide agonist DPDPE (0.1 mg/kg, i.v.) increased the ventricular fibrillation threshold (VFT) in postinfarction cardiosclerosis in rats. Pretreatment with the selective
Autor:
L N, Maslov, T V, Lasukova, N V, Solenkova, A Iu, Lishmanov, S A, Bogomaz, S V, Tam, G J, Gross
Publikováno v:
Eksperimental'naia i klinicheskaia farmakologiia. 64(5)
Preliminary administration of the mu-opioid receptor (mu-OR) agonist DAMGO (0.1 mg/kg) 15 min before heart isolation led to attenuation of the postischemic systolic and diastolic contractility dysfunction in isolated perfused rat heart. In addition,
Publikováno v:
Eksperimental'naia i klinicheskaia farmakologiia. 64(1)
Peripheral administration of the mu- or kappa-receptor agonists or sigma-receptor antagonists produced a significant receptor-dependent increase in the ventricular fibrillation threshold in rats with postinfarction cardiosclerosis. The effect was not
Publikováno v:
Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova. 87(5)
Activation of mu-opioid receptor (OR) in rats prevented development of reperfusion-induced myocardial cell damage. In contrast, direct cardiac mu-OR stimulation with the opioid receptor agonist DAMGO decreased cardiac contractility in normal oxygenat
Publikováno v:
Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova. 87(5)
I.v. administration of the delta-opioid (OR) receptors' agonists DSLET or DTLET prevented creatine kinase leakage from the rat isolated heart in oxidative stress damage and abolished an increase in myocardial levels of conjugated diens and malondiald
Publikováno v:
Biochemistry. Biokhimiia. 66(4)
Preliminary intravenous injection of delta-opiate receptor (OR) agonists DSLET (0.1 mg/kg) or DTLET (0.1 mg/kg) increased tolerance of isolated perfused myocardium to damage by oxidative stress simulated in vivo with FeSO4 + ascorbic acid. This manif
Autor:
Iu B, Lishmanov, L N, Maslov, A V, Krylatov, S A, Afanas'ev, V Iu, Timofeev, P, Gilligan, S V, Tam
Publikováno v:
Eksperimental'naia i klinicheskaia farmakologiia. 63(6)
It has been found that in vivo pretreatment of rats with the sigma receptor antagonist DuP 734 (1 mg/kg) resulted in an increase in the heart tolerance to ischemic and reperfusion arrhythmias both in vivo and ex vivo. Administration of DuP 734 (1 mg/
Publikováno v:
Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova. 86(2)
In vivo pre-treatment with the opioid receptor antagonist D,L-naloxone completely eliminated the reperfusion-induced creatine kinase (CK) leakage from the rat isolated perfused haert. The inactive isomer L-naloxone decreased the CK release by half. T
Publikováno v:
Scopus-Elsevier
Intravenous injection of the selective mu-opiate receptor agonist DAMGO (0.1 mg/kg, 15 min before isolation of the heart) improved resistance of isolated perfused rat heart to ischemia (45 min) and reperfusion (60 min) damages. In vivo administration