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Métodos Terapéuticos y Terapias MTCI
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1.
Sci Rep ; 10(1): 20405, 2020 11 23.
Artículo en Inglés | MEDLINE | ID: mdl-33230154

RESUMEN

The Cannabis sativa plant contains more than 120 cannabinoids. With the exceptions of ∆9-tetrahydrocannabinol (∆9-THC) and cannabidiol (CBD), comparatively little is known about the pharmacology of the less-abundant plant-derived (phyto) cannabinoids. The best-studied transducers of cannabinoid-dependent effects are type 1 and type 2 cannabinoid receptors (CB1R, CB2R). Partial agonism of CB1R by ∆9-THC is known to bring about the 'high' associated with Cannabis use, as well as the pain-, appetite-, and anxiety-modulating effects that are potentially therapeutic. CB2R activation by certain cannabinoids has been associated with anti-inflammatory activities. We assessed the activity of 8 phytocannabinoids at human CB1R, and CB2R in Chinese hamster ovary (CHO) cells stably expressing these receptors and in C57BL/6 mice in an attempt to better understand their pharmacodynamics. Specifically, ∆9-THC, ∆9-tetrahydrocannabinolic acid (∆9-THCa), ∆9-tetrahydrocannabivarin (THCV), CBD, cannabidiolic acid (CBDa), cannabidivarin (CBDV), cannabigerol (CBG), and cannabichromene (CBC) were evaluated. Compounds were assessed for their affinity to receptors, ability to inhibit cAMP accumulation, ßarrestin2 recruitment, receptor selectivity, and ligand bias in cell culture; and cataleptic, hypothermic, anti-nociceptive, hypolocomotive, and anxiolytic effects in mice. Our data reveal partial agonist activity for many phytocannabinoids tested at CB1R and/or CB2R, as well as in vivo responses often associated with activation of CB1R. These data build on the growing body of literature showing cannabinoid receptor-dependent pharmacology for these less-abundant phytocannabinoids and are critical in understanding the complex and interactive pharmacology of Cannabis-derived molecules.


Asunto(s)
Analgésicos/farmacología , Ansiolíticos/farmacología , Agonistas de Receptores de Cannabinoides/farmacología , Cannabis/química , Psicotrópicos/farmacología , Receptor Cannabinoide CB1/genética , Receptor Cannabinoide CB2/genética , Analgésicos/aislamiento & purificación , Animales , Ansiolíticos/aislamiento & purificación , Células CHO , Cannabidiol/aislamiento & purificación , Cannabidiol/farmacología , Agonistas de Receptores de Cannabinoides/aislamiento & purificación , Cannabinoides/aislamiento & purificación , Cannabinoides/farmacología , Cricetulus , Dronabinol/análogos & derivados , Dronabinol/aislamiento & purificación , Dronabinol/farmacología , Expresión Génica , Humanos , Ratones Endogámicos C57BL , Extractos Vegetales/química , Psicotrópicos/aislamiento & purificación , Receptor Cannabinoide CB1/agonistas , Receptor Cannabinoide CB1/metabolismo , Receptor Cannabinoide CB2/agonistas , Receptor Cannabinoide CB2/metabolismo , Transgenes , Arrestina beta 2/genética , Arrestina beta 2/metabolismo
2.
J Clin Neurophysiol ; 37(1): 28-34, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31895187

RESUMEN

Posttraumatic Stress Disorder (PTSD) is a leading psychiatric disorder that mainly affects military and veteran populations but can occur in anyone affected by trauma. PTSD treatment remains difficult for physicians because most patients with PTSD do not respond to current pharmacological treatment. Psychotherapy is effective, but time consuming and expensive. Substance use disorder is often concurrent with PTSD, which leads to a significant challenge for PTSD treatment. Cannabis has recently received widespread attention for the potential to help many patient populations. Cannabis has been reported as a coping tool for patients with PTSD and preliminary legalization data indicate Cannabis use may reduce the use of more harmful drugs, such as opioids. Rigorous clinical studies of Cannabis could establish whether Cannabis-based medicines can be integrated into treatment regimens for both PTSD and substance use disorder patients.


Asunto(s)
Cannabinoides/uso terapéutico , Marihuana Medicinal/uso terapéutico , Trastornos por Estrés Postraumático/tratamiento farmacológico , Trastornos Relacionados con Sustancias/tratamiento farmacológico , Adulto , Femenino , Humanos , Masculino
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