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1.
Front Psychiatry ; 12: 712110, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34366942

RESUMO

The treatment of patients with schizophrenia and substance use disorder poses a challenge for clinicians. Continued use of cannabis and cocaine can exacerbate psychotic symptoms and worsen the course of disease. To date, no pharmacotherapy is available for patients with cannabis use disorder (CUD). Cannabidiol (CBD) and Δ9-tetrahydrocannabinol (THC) are the main active constituents in Cannabis sativa, with the latter being linked to an increased risk of psychosis. We describe a clinical case of a male patient diagnosed with schizophrenia, combined personality disorder, CUD and cocaine use disorder. Over the course of 8 years, he was hospitalized 30 times due to psychotic relapses and continued substance use. Consequently, CBD cigarettes with a low THC content (<1%) were used as adjunctive therapy. Additionally, we established off-label treatment with methylphenidate to support abstinence. The patient reported to feel significantly less need to consume illegal cannabis with a high THC content. He stopped to use cocaine, for the time being, and has not been hospitalized since. This case report demonstrates the potential of smoked CBD as a substitute for severe and chronic CUD.

2.
J Parasitol ; 91(2): 307-15, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15986605

RESUMO

Organotypic slice culture explants of rat cortical tissue infected with Toxoplasma gondii tachyzoites were applied as an in vitro model to investigate host-pathogen interactions in cerebral toxoplasmosis. The kinetics of parasite proliferation and the effects of interferon-gamma (IFN-gamma) and tumor necrosis factor-alpha (TNF-alpha) in infected organotypic cultures were monitored by light microscopy, transmission electron microscopy (TEM), and quantitative polymerase chain reaction (PCR) assay. As assessed by the loss of the structural integrity of the glial fibrillary acidic protein-intermediate filament network, tachyzoites infected and proliferated mainly within astrocytes, whereas neurons and microglia remained largely unaffected. Toxoplasma gondii proliferation was severely inhibited by IFN-y. However, this inhibition was not linked to tachyzoite-to-bradyzoite stage conversion. In contrast, TNF-alpha treatment resulted in a dramatically enhanced proliferation rate of the parasite. The cellular integrity in IFN-gamma-treated organotypic slice cultures was severely impaired compared with untreated and TNF-alpha-treated cultures. Thus, on infection of organotypic neuronal cultures, IFN-gamma and TNF-alpha exhibit largely detrimental effects, which could contribute to either inhibition or acceleration of parasite proliferation during cerebral toxoplasmosis.


Assuntos
Córtex Cerebral/parasitologia , Interferon gama/farmacologia , Toxoplasma/crescimento & desenvolvimento , Fator de Necrose Tumoral alfa/farmacologia , Animais , Córtex Cerebral/citologia , Córtex Cerebral/ultraestrutura , Chlorocebus aethiops , Imunofluorescência , Interações Hospedeiro-Parasita/imunologia , Imuno-Histoquímica , Interferon gama/imunologia , Microscopia Eletrônica de Transmissão , Reação em Cadeia da Polimerase , Ratos , Ratos Wistar , Técnicas de Cultura de Tecidos , Toxoplasma/efeitos dos fármacos , Toxoplasma/ultraestrutura , Fator de Necrose Tumoral alfa/imunologia , Células Vero
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