RESUMO
This paper describes the determination of strychnine and brucine in the seeds, root, stem and leaves of Strychnos species by HPLC. The analytical column used was ZY110 YNG-C18. The mobile phase was KH2PO4(0.01 mol.L-1)--MeOH(73:27), pH2.5, regulated by 10% H3PO4. Flow rate was 1.0 ml.min-1. The detection wavelength was 264 nm. The linear ranges of strychmine and brucine were 0.18-7.26 micrograms and 0.11-4.32 micrograms, respectively. The recoveries of strychnine and brucine were 98.27% and 98.04%, respectively. The analytical results showed that the contents of strychnine and brucine in samples showed great difference between different species. The contents of strychnine in the seeds of Strychnos wallichiana and S. ignatii were 5.6% and 3.9%, respectively. These results show that the two Strychnos species may be developed as the resources of strychnine.
Assuntos
Medicamentos de Ervas Chinesas/química , Plantas Medicinais/química , Estricnina/análogos & derivados , Estricnina/análise , Cromatografia Líquida de Alta Pressão , Magnoliopsida/químicaRESUMO
The effects of repeated cocaine administration on cochlear function were evaluated by measuring amplitude-intensity and latency-intensity functions of the whole-nerve action potential of the auditory nerve. Whole-nerve action potential input/output functions obtained using tone-pips of 0.5, 1, 2, 4 and 8 kHz in a group of cocaine-treated subjects were compared with those obtained in saline-treated animals. All measurements were made 24 h after the last treatment. Amplitudes of whole-nerve action potentials were enhanced in the cocaine-treated animals compared to the control group. No statistically significant differences in latency-intensity functions were seen after cocaine treatment. The effect of chronic cocaine exposure also was examined on catecholamine innervation in the cochlea using immunohistochemical techniques. The density of adrenergic innervation was reduced in the cocaine-treated animals.
Assuntos
Cocaína/farmacologia , Cóclea/efeitos dos fármacos , Estimulação Acústica , Fibras Adrenérgicas/efeitos dos fármacos , Animais , Chinchila , Cocaína/administração & dosagem , Cóclea/irrigação sanguínea , Cóclea/química , Cóclea/metabolismo , Cóclea/fisiologia , Dopamina beta-Hidroxilase/análise , Esquema de Medicação , Imuno-Histoquímica , Ketamina/farmacologia , Norepinefrina/metabolismo , Órgão Espiral/efeitos dos fármacos , Tirosina 3-Mono-Oxigenase/análiseRESUMO
This study was to examine the effects and mechanisms of injectio salviae miltiorrhizae (ISM) in preventing and treating fat embolism syndrome (FES), which was simulated by intravenous injection of homologous bone marrow fat in 16 dogs. PaO2, free fatty acids (FFAs), TXA2/PGI2, SOD/MDA were measured in different times combined with X-ray, conjunctiva microcirculation observation, radioisotope scanning and histologic examination. It was found that in the control group there were a significant fall in PaO alpha and rise in FFAs and MDA; blood clot stained with oil red O showed many fat droplets; radioisotope scanning revealed mild hypoperfusion or perfusion defects. In the treatment group, arterial oxygen levels were maintained, serum level of FFAS and MDA was reduced significantly. It is concluded that there is damage induced by oxygen-derived radicals in FES, LSM is an effective therapy for the FES, and 99mTc radioisotope scanning is a promising technique for noninvasive identification of FES in the early stage.
Assuntos
Medicamentos de Ervas Chinesas/uso terapêutico , Embolia Gordurosa/prevenção & controle , Animais , Túnica Conjuntiva/irrigação sanguínea , Cães , Embolia Gordurosa/tratamento farmacológico , Ácidos Graxos não Esterificados/sangue , Injeções Intravenosas , Pulmão/diagnóstico por imagem , Microcirculação , Extratos Vegetais , Cintilografia , Salvia miltiorrhiza , TecnécioRESUMO
The effects of a single administration of cocaine on the cochlea was evaluated by measuring amplitude-intensity functions of the N1 response of the auditory nerve. Amplitude-intensity functions of the N1 response to tone-pips of 500 Hz, 1, 2, 4 and 8 kHz were obtained before and after intraperitoneal injection of either saline, 3 mg/kg or 25 mg/kg of cocaine. N1 amplitudes were decreased after the administration of cocaine and this reduction was found to be dose dependent. The influence of cocaine on cochlear blood flow (CBF) was examined in order to test the possibility that cocaine induced reductions in CBF underlie these electro-physiological changes. Corresponding decreases in cochlear blood flow after cocaine exposure were observed.
Assuntos
Cocaína/toxicidade , Cóclea/efeitos dos fármacos , Nervo Vestibulococlear/efeitos dos fármacos , Estimulação Acústica , Animais , Limiar Auditivo/efeitos dos fármacos , Chinchila , Cocaína/administração & dosagem , Cóclea/irrigação sanguínea , Cóclea/fisiologia , Relação Dose-Resposta a Droga , Eletrofisiologia , Injeções Intraperitoneais , Fluxometria por Laser-Doppler , Distribuição Aleatória , Fluxo Sanguíneo Regional/efeitos dos fármacos , Nervo Vestibulococlear/fisiologiaRESUMO
Primary cultures of rat Leydig and Sertoli cells were used to evaluate the direct effects of GTW on testicular cells and to compare these to the effects of gossypol acetate. Both GTW and gossypol acetate can affect the survival of Leydig and Sertoli cells. But Sertoli cells are much more sensitive than Leydig cells, either to gossypol acetate or GTW. Leydig and Sertoli cells all died when they were exposed to gossypol acetate or GTW at a dose of 3.0 micrograms/ml or 30 micrograms/ml, respectively, for 24 hours. The cell survival-time course demonstrated that the cell numbers were decreased after 2 hours, and especially so after 8 hours. No significant changes were observed in testosterone production in Leydig cells after 24 hours of exposure to 1.0-20 micrograms/ml GTW. The forward motility of epididymal spermatozoa was completely lost and fertility of rat was significantly inhibited after the treatment of GTW in vivo. It is concluded that GTW does affect the fertility of rat and viability of cultured rat Leydig and Sertoli cells.