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1.
Mol Psychiatry ; 23(6): 1466-1473, 2018 06.
Artículo en Inglés | MEDLINE | ID: mdl-28461696

RESUMEN

Aldosterone regulates electrolyte and fluid homeostasis through binding to the mineralocorticoid receptors (MRs). Previous work provides evidence for a role of aldosterone in alcohol use disorders (AUDs). We tested the hypothesis that high functional activity of the mineralocorticoid endocrine pathway contributes to vulnerability for AUDs. In Study 1, we investigated the relationship between plasma aldosterone levels, ethanol self-administration and the expression of CYP11B2 and MR (NR3C2) genes in the prefrontal cortex area (PFC) and central nucleus of the amygdala (CeA) in monkeys. Aldosterone significantly increased after 6- and 12-month ethanol self-administration. NR3C2 expression in the CeA was negatively correlated to average ethanol intake during the 12 months. In Study 2, we measured Nr3c2 mRNA levels in the PFC and CeA of dependent and nondependent rats and the correlates with ethanol drinking during acute withdrawal. Low Nr3c2 expression levels in the CeA were significantly associated with increased anxiety-like behavior and compulsive-like drinking in dependent rats. In Study 3, the relationship between plasma aldosterone levels, alcohol drinking and craving was investigated in alcohol-dependent patients. Non-abstinent patients had significantly higher aldosterone levels than abstinent patients. Aldosterone levels positively correlated with the number of drinks consumed, craving and anxiety scores. These findings support a relationship between ethanol drinking and the aldosterone/MR pathway in three different species.


Asunto(s)
Alcoholismo/metabolismo , Aldosterona/metabolismo , Receptores de Mineralocorticoides/metabolismo , Adulto , Consumo de Bebidas Alcohólicas/genética , Alcoholismo/genética , Amígdala del Cerebelo/metabolismo , Animales , Citocromo P-450 CYP11B2/genética , Citocromo P-450 CYP11B2/metabolismo , Modelos Animales de Enfermedad , Etanol/metabolismo , Humanos , Macaca mulatta/metabolismo , Masculino , Mineralocorticoides/metabolismo , Corteza Prefrontal/metabolismo , Datos Preliminares , Ratas , Ratas Wistar , Receptores de Mineralocorticoides/genética , Autoadministración
2.
Transl Psychiatry ; 5: e646, 2015 Sep 29.
Artículo en Inglés | MEDLINE | ID: mdl-26418274

RESUMEN

Increasing evidence supports the role of appetite-regulating pathways, including ghrelin and leptin, in alcoholism. This study tested the hypothesis that intravenous exogenous ghrelin administration acutely decreases endogenous serum leptin levels, and that changes in leptin levels negatively correlate with alcohol craving. This was a double-blind, placebo-controlled human laboratory study. Non-treatment-seeking, alcohol-dependent, heavy drinkers (n=45) were randomized to receive intravenous ghrelin or placebo, followed by a cue-reactivity procedure, during which participants were exposed to neutral (juice) and alcohol trial cues. There was a main effect for intravenous ghrelin administration, compared with placebo, in reducing serum leptin levels (P<0.01). Post hoc analysis showed significant differences in serum leptin levels at the alcohol trial (P<0.05) that persisted at the end of the experiment (P<0.05). By contrast, there were no significant differences in serum leptin levels at the juice trial (P=not significant (NS)). The change of serum leptin level at the alcohol trial correlated with the increase in alcohol urge (P<0.05), whereas urge to drink juice was not correlated with the leptin change at the juice trial (P=NS). These findings provide preliminary evidence of ghrelin-leptin cross-talk in alcoholic individuals and suggest that their relationship may have a role in alcohol craving.


Asunto(s)
Ansia , Etanol , Ghrelina , Leptina/sangre , Administración Intravenosa , Adulto , Consumo de Bebidas Alcohólicas/metabolismo , Consumo de Bebidas Alcohólicas/fisiopatología , Alcoholismo/metabolismo , Alcoholismo/fisiopatología , Depresores del Sistema Nervioso Central/metabolismo , Depresores del Sistema Nervioso Central/farmacología , Estimulantes del Sistema Nervioso Central/metabolismo , Estimulantes del Sistema Nervioso Central/farmacología , Ansia/efectos de los fármacos , Ansia/fisiología , Señales (Psicología) , Etanol/metabolismo , Etanol/farmacología , Femenino , Ghrelina/metabolismo , Ghrelina/farmacología , Humanos , Masculino , Estadística como Asunto
4.
Lupus ; 18(9): 845-7, 2009 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-19578111

RESUMEN

Familial Mediterranean fever (FMF) was recently associated with a hypercoagulable state. However, clinically overt thrombosis remains a rare event limited to patients with other predisposing factors. We herein present a child with FMF who experienced a stroke. An extensive thrombophilia work-up revealed multiple inherited and acquired risk factors. In areas with high prevalence of prothrombotic mutations and in children who are products of consanguineous marriages, early screening for concurrent thrombotic risk factors is warranted; as this may help design an optimal management plan and prevent unfavourable outcomes.


Asunto(s)
Fiebre Mediterránea Familiar/complicaciones , Fiebre Mediterránea Familiar/genética , Accidente Cerebrovascular/diagnóstico , Accidente Cerebrovascular/etiología , Adolescente , Consanguinidad , Factor V/genética , Femenino , Humanos , Metilenotetrahidrofolato Reductasa (NADPH2)/genética , Mutación/genética , Factores de Riesgo
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