280 research outputs found
Cellular and molecular mechanisms involved in the neurotoxicity of opioid and psychostimulant drugs
Substance abuse and addiction are the most costly of all the neuropsychiatric disorders. In the last decades, much progress has been achieved in understanding the effects of the drugs of abuse in the brain. However, efficient treatments that prevent relapse have not been developed. Drug addiction is now considered a brain disease, because the abuse of drugs affects several brain functions. Neurological impairments observed in drug addicts may reflect drug-induced neuronal dysfunction and neurotoxicity. The drugs of abuse directly or indirectly affect neurotransmitter systems, particularly dopaminergic and glutamatergic neurons. This review explores the literature reporting cellular and molecular alterations reflecting the cytotoxicity induced by amphetamines, cocaine and opiates in neuronal systems. The neurotoxic effects of drugs of abuse are often associated with oxidative stress, mitochondrial dysfunction, apoptosis and inhibition of neurogenesis, among other mechanisms. Understanding the mechanisms that underlie brain dysfunction observed in drug-addicted individuals may contribute to improve the treatment of drug addiction, which may have social and economic consequences.http://www.sciencedirect.com/science/article/B6SYS-4S50K2J-1/1/7d11c902193bfa3f1f57030572f7034
Altering APP Proteolysis: Increasing sAPPalpha Production by Targeting Dimerization of the APP Ectodomain
One of the events associated with Alzheimer's disease is the dysregulation of Ī±- versus Ī²-cleavage of the amyloid precursor protein (APP). The product of Ī±-cleavage (sAPPĪ±) has neuroprotective properties, while AĪ²1-42 peptide, a product of Ī²-cleavage, is neurotoxic. Dimerization of APP has been shown to influence the relative rate of Ī±- and Ī²- cleavage of APP. Thus finding compounds that interfere with dimerization of the APP ectodomain and increase the Ī±-cleavage of APP could lead to the development of new therapies for Alzheimer's disease. Examining the intrinsic fluorescence of a fragment of the ectodomain of APP, which dimerizes through the E2 and AĪ²-cognate domains, revealed significant changes in the fluorescence of the fragment upon binding of AĪ² oligomersāwhich bind to dimers of the ectodomainā and AĪ² fragmentsāwhich destabilize dimers of the ectodomain. This technique was extended to show that RERMS-containing peptides (APP695 328ā332), disulfiram, and sulfiram also inhibit dimerization of the ectodomain fragment. This activity was confirmed with small angle x-ray scattering. Analysis of the activity of disulfiram and sulfiram in an AlphaLISA assay indicated that both compounds significantly enhance the production of sAPPĪ± by 7W-CHO and B103 neuroblastoma cells. These observations demonstrate that there is a class of compounds that modulates the conformation of the APP ectodomain and influences the ratio of Ī±- to Ī²-cleavage of APP. These compounds provide a rationale for the development of a new class of therapeutics for Alzheimer's disease
RESOLUTION OF OVERLAPPING BANDS IN THE NEARāUV ABSORPTION SPECTRUM OF INDOLE DERIVATIVES
Abstractā The second derivative spectra of tryptophan in water and in ethylene glycol at 22Ā°C have been integrated in order to obtain the corresponding primitive functions. The integration was carried out by making use of Tchebychev polynomials. The results show that the integrated primitive functions do not correspond to the original absorption spectra of tryptophan in various solvents, but they reflect only the contributions of the 1Lb bands of the indolic chromophore. The identification of the electronic component, which generates the second derivative spectrum, was based on the solvent insensitivity of the derivative peaks. The comparison between the absorption spectra reported in this paper and those calculated for the 1Lbā1A electronic transition of indole confirmed the assumption that the derivation process eliminates the broad, although more intense, contributions coming from the 1Laā1A electronic transition. Copyright Ā© 1985, Wiley Blackwell. All rights reserve
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