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1.
Zhonghua Yi Shi Za Zhi ; 47(2): 70-72, 2017 Mar 28.
Artigo em Chinês | MEDLINE | ID: mdl-28468106

RESUMO

The first material recorded about hair charcoal is seen in Nei jing (Inner Canon). It has a history of over 2 000 years for the carbonization of Chinese materia medica. There were controversies on this matter and its clinical application was seldom seen and underdeveloped. After the Yuan Dynasty, the main theory of carbonic herbs for hemostasis, and keeping the nature of the medicines after carbonization was gradually formed, and physicians of generations began to conduct in-depth research. Through repeated practice and verification, people summed up the suitable species of Chinese materia medica and its principle for carbonization. The methods and degree of carbonization of Chinese materia medica are reasonably discussed, with its principle and basis for application primarily interpreted.


Assuntos
Medicamentos de Ervas Chinesas/história , Materia Medica/história , Medicina Tradicional Chinesa/história , Carvão Vegetal , China , História Antiga , História Medieval , Humanos
2.
J Cardiovasc Pharmacol ; 38(2): 232-9, 2001 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-11483873

RESUMO

To explore the signaling mechanisms of the negative modulation of beta-adrenoceptors by kappa-Opioid receptors (kappa-OR) in the heart, the possibility of the interaction at the level of G protein and receptor was determined. Cholera toxin, an activator of the stimulatory G protein (Gs), elevated electrically induced intracellular Ca2+ ([Ca2+]i) transients and induced ribosylation of the alpha-subunit of Gs (Gsalpha) in rat ventricular myocytes. The effects were significantly attenuated by U50,488H, a specific agonist of kappa-OR, and were abolished by nor-binaltorphimine, a selective kappa-OR antagonist. The content of Gsalpha, however, was not affected by U50,488H. Receptor binding experiments showed that neither Bmax nor Kd of the binding of [3H]CGP-12177, a beta-adrenoceptor antagonist, was affected by U50,488H. The current study provides the first evidence that kappa-OR stimulation inhibits the ribosylation of the alpha-subunit of the Gs protein, thus inhibiting the action of cholera toxin on the protein.


Assuntos
Toxina da Cólera/farmacologia , Subunidades alfa Gs de Proteínas de Ligação ao GTP/antagonistas & inibidores , Subunidades alfa Gs de Proteínas de Ligação ao GTP/metabolismo , Miocárdio/metabolismo , Receptores Opioides kappa/agonistas , Receptores Opioides kappa/fisiologia , (trans)-Isômero de 3,4-dicloro-N-metil-N-(2-(1-pirrolidinil)-ciclo-hexil)-benzenoacetamida/farmacologia , Analgésicos não Narcóticos/farmacologia , Animais , Sítios de Ligação , Cálcio/metabolismo , Estimulação Elétrica , Ventrículos do Coração/citologia , Ventrículos do Coração/efeitos dos fármacos , Miocárdio/citologia , Propanolaminas/metabolismo , Ratos , Ratos Sprague-Dawley , Receptores Adrenérgicos beta/metabolismo , Receptores Opioides kappa/metabolismo
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