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1.
Am J Psychother ; 77(1): 23-29, 2024 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-37670578

RESUMEN

Bipolar disorder and borderline personality disorder commonly co-occur. Each disorder is associated with substantial morbidity and mortality, which are worsened by co-occurrence of the disorders. Emotional dysregulation, suicidality, and disrupted circadian rhythm are key aspects of psychopathology associated with both conditions. A novel psychotherapy combining elements of two evidence-based treatments (i.e., dialectical behavior therapy [DBT] for borderline personality disorder and social rhythm therapy [SRT] for bipolar disorder) is described. Unlike either treatment alone, the new therapy, called dialectical behavior and social rhythm therapy (DBSRT), targets all three disease-relevant processes and therefore may represent a promising new approach to treatment for individuals with these two conditions. DBSRT may also have utility for individuals with overlapping characteristics of bipolar disorder and borderline personality disorder or for those whose illness manifestation includes a mix of bipolar and borderline personality disorder traits. Strategies associated with DBSRT are described, and a brief case vignette illustrates its application.


Asunto(s)
Trastorno Bipolar , Trastorno de Personalidad Limítrofe , Terapia Conductual Dialéctica , Humanos , Terapia Conductista , Trastorno Bipolar/complicaciones , Trastorno Bipolar/epidemiología , Trastorno Bipolar/terapia , Trastorno de Personalidad Limítrofe/complicaciones , Trastorno de Personalidad Limítrofe/epidemiología , Trastorno de Personalidad Limítrofe/terapia , Psicoterapia , Resultado del Tratamiento
2.
Bioorg Med Chem Lett ; 19(22): 6376-8, 2009 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-19815410

RESUMEN

In the previous article we demonstrated how certain CCK2R-selective anthranilic amides could be structurally modified to afford high-affinity, selective CCK1R activity. We now describe our efforts at modulating and optimizing the CCK1R and CCK2R affinities aimed at producing compounds with good pharmacokinetics properties and in vivo efficacy in rat models of gastric acid and pancreatic amylase secretion.


Asunto(s)
Isoxazoles/química , Receptor de Colecistoquinina A/antagonistas & inhibidores , Receptor de Colecistoquinina B/antagonistas & inhibidores , Transducción de Señal/efectos de los fármacos , Sulfonamidas/farmacología , Sustitución de Aminoácidos , Animales , Modelos Moleculares , Ratas , Ratas Wistar , Resultado del Tratamiento
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