Publications by authors named "R P Ureshino"

Article Synopsis
  • * Researchers tested over 1,400 approved drugs in zebrafish models of tauopathy and found that carbonic anhydrase (CA) inhibitors helped protect against tau toxicity.
  • * One specific CA inhibitor, methazolamide, showed promise in reducing tau levels and improving neuron survival in mouse models, indicating potential for using CA inhibitors as treatments for tauopathies.
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COVID-19, caused by SARS-CoV-2, affects neuronal cells, causing several symptoms such as memory loss, anosmia and brain inflammation. Curcuminoids (Me08 e Me23) and curcumin (CUR) are derived from Curcuma Longa extract (EXT). Many therapeutic actions have been linked to these compounds, including antiviral action.

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Parkinson's disease (PD) is a progressive neurodegenerative disease characterized by resting tremor, bradykinesia, rigidity, and postural instability that also includes non-motor symptoms such as mood dysregulation. Dopamine (DA) is the primary neurotransmitter involved in this disease, but cholinergic imbalance has also been implicated. Current intervention in PD is focused on replenishing central DA, which provides remarkable temporary symptomatic relief but does not address neuronal loss and the progression of the disease.

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COVID-19, along with most respiratory diseases in the medical field, demonstrates significant ability to take its toll on global population. There is a particular difficulty in studying these conditions, which stems especially from the short supply of models for detailed investigation, the specific therapeutic knowledge required for disease scrutinization and the occasional need of BSL-3 [Biosafety Level 3] laboratories for research. Based on this, the process of drug development is hampered to a great extent.

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Huntington's disease (HD) is a progressive neurodegenerative disease characterized by mutations in the huntingtin gene (mHtt), causing an unstable repeat of the CAG trinucleotide, leading to abnormal long repeats of polyglutamine (poly-Q) in the N-terminal region of the huntingtin, which form abnormal conformations and aggregates. Alterations in Ca signaling are involved in HD models and the accumulation of mutated huntingtin interferes with Ca homeostasis. Lysosomes are intracellular Ca storages that participate in endocytic and lysosomal degradation processes, including autophagy.

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