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1.
Neurobiol Dis ; 191: 106408, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-38199274

RESUMO

Excitotoxicity arises from unusually excessive activation of excitatory amino acid receptors such as glutamate receptors. Following an energy crisis, excitotoxicity is a major cause for neuronal death in neurological disorders. Many glutamate antagonists have been examined for their efficacy in mitigating excitotoxicity, but failed to generate beneficial outcome due to their side effects on healthy neurons where glutamate receptors are also blocked. In this study, we found that during chronic hypoxia there is upregulation and activation of a nonselective cation channel TRPM4 that contributes to the depolarized neuronal membrane potential and enhanced glutamate-induced calcium entry. TRPM4 is involved in modulating neuronal membrane excitability and calcium signaling, with a complex and multifaceted role in the brain. Here, we inhibited TRPM4 using a newly developed blocking antibody M4P, which could repolarize the resting membrane potential and ameliorate calcium influx upon glutamate stimulation. Importantly, M4P did not affect the functions of healthy neurons as the activity of TRPM4 channel is not upregulated under normoxia. Using a rat model of chronic hypoxia with both common carotid arteries occluded, we found that M4P treatment could reduce apoptosis in the neurons within the hippocampus, attenuate long-term potentiation impairment and improve the functions of learning and memory in this rat model. With specificity to hypoxic neurons, TRPM4 blocking antibody can be a novel way of controlling excitotoxicity with minimal side effects that are common among direct blockers of glutamate receptors.


Assuntos
Ácido Glutâmico , Canais de Cátion TRPM , Ratos , Animais , Ácido Glutâmico/metabolismo , Cálcio/metabolismo , Receptores de Glutamato/metabolismo , Neurônios/metabolismo , Hipóxia/metabolismo , Canais de Cátion TRPM/metabolismo
2.
BMC Complement Altern Med ; 9: 46, 2009 Nov 21.
Artigo em Inglês | MEDLINE | ID: mdl-19930582

RESUMO

BACKGROUND: Endophytes, microorganisms which reside in plant tissues, have potential in producing novel metabolites for exploitation in medicine. Cytotoxic and antibacterial activities of a total of 300 endophytic fungi were investigated. METHODS: Endophytic fungi were isolated from various parts of 43 plants from the National Park Pahang, Malaysia. Extracts from solid state culture were tested for cytotoxicity against a number of cancer cell lines using the MTT assay. Antibacterial activity was determined using the disc diffusion method. RESULTS: A total of 300 endophytes were isolated from various parts of plants from the National Park, Pahang. 3.3% of extracts showed potent (IC50 < 0.01 microg/ml) cytotoxic activity against the murine leukemic P388 cell line and 1.7% against a human chronic myeloid leukemic cell line K562. Sporothrix sp. (KK29FL1) isolated from Costus speciosus showed strong cytotoxicity against colorectal carcinoma (HCT116) and human breast adenocarcinoma (MCF7) cell lines with IC50 values of 0.05 microg/ml and 0.02 microg/ml, respectively. Antibacterial activity was demonstrated for 8% of the extracts. CONCLUSION: Results indicate the potential for production of bioactive agents from endophytes of the tropical rainforest flora.


Assuntos
Antibacterianos/uso terapêutico , Antineoplásicos Fitogênicos/uso terapêutico , Fungos/isolamento & purificação , Neoplasias/terapia , Plantas/microbiologia , Animais , Antibacterianos/farmacologia , Antineoplásicos Fitogênicos/farmacologia , Linhagem Celular Tumoral , Humanos , Malásia , Camundongos
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