Abstract
The central nervous system is endowed with complex mechanisms of defense. However, these protection mechanisms fail in the presence of risk factors such as genetic mutations, environmental factors (bisphenol A, polycyclic aromatic hydrocarbons (PAHs), polyfluoroalkyl chemicals) or social stress and psychiatric disorders (anxiety, depression, psychosis, attention deficits) appear. Critical psychiatric conditions treatment consists in administration of antidepressants and antipsychotics drugs. These drugs are widely prescribed, but their efficiency in controlling mental symptoms is an important point in current clinical studies. Antidepressants and antipsychotics register several side effects and their interactions with other polycyclic aromatic hydrocarbons are well established. Research is focused upon reducing these side effects and understanding their pharmacodynamic and pharmacokinetic properties in order to develop advanced methods to predict induced pharmacological events. Here we intend to detail recent advances in the field of structure-activity relationship (QSAR) applied to antidepressants and antipsychotics with polycyclic aromatic structure as last generation drugs used in central nervous system disorders. We present the biological activity of large series of psychiatric drugs predicted by 2D and 3D-QSAR dependent and independent molecules alignment. Predicted biological activities were correlated with common pharmaceutical descriptors as steric, electronic hydrogen donor/acceptor bond but also new components of QSAR models as membrane ions’ contributions to the antagonism of these drugs at membrane receptors are presented. The paper refers both to preclinical tested molecules and to already known antidepressants and antipsychotics based on a large variety of polycyclic aromatic structure. Drug potency decrease in the presence of PAHs is also discussed. Keywords: Antidepressants, Antipsychotics, Membrane receptors, Polycyclic aromatic structure, QSAR, Pharmaceutical descriptors.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
