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1.
Neuroscience ; 315: 1-17, 2016 Feb 19.
Artículo en Inglés | MEDLINE | ID: mdl-26691962

RESUMEN

Syrian hamsters exposed to anabolic/androgenic steroids (AAS) during adolescence consistently show increased aggressive behavior across studies. Although the behavioral and anatomical profiles of AAS-induced alterations have been well characterized, there is a lack of data describing physiological changes that accompany these alterations. For instance, behavioral pharmacology and neuroanatomical studies show that AAS-induced changes in the vasopressin (AVP) neural system within the latero-anterior hypothalamus (LAH) interact with the serotonin (5HT) and dopamine (DA) systems to modulate aggression. To characterize the electrophysiological profile of the AAS aggression circuit, we recorded LAH neurons in adolescent male hamsters in vivo and microiontophoretically applied agonists and antagonists of aggressive behavior. The interspike interval (ISI) of neurons from AAS-treated animals correlated positively with aggressive behaviors, and adolescent AAS exposure altered parameters of activity in regular firing neurons while also changing the proportion of neuron types (i.e., bursting, regular, irregular). AAS-treated animals had more responsive neurons that were excited by AVP application, while cells from control animals showed the opposite effect and were predominantly inhibited by AVP. Both DA D2 antagonists and 5HT increased the firing frequency of AVP-responsive cells from AAS animals and dual application of AVP and D2 antagonists doubled the excitatory effect of AVP or D2 antagonist administration alone. These data suggest that multiple DA circuits in the LAH modulate AAS-induced aggressive responding. More broadly, these data show that multiple neurochemical interactions at the neurophysiological level are altered by adolescent AAS exposure.


Asunto(s)
Agresión/efectos de los fármacos , Anabolizantes/toxicidad , Área Hipotalámica Lateral/efectos de los fármacos , Hipotálamo Anterior/efectos de los fármacos , Neuronas/efectos de los fármacos , Esteroides/toxicidad , Potenciales de Acción/efectos de los fármacos , Potenciales de Acción/fisiología , Agresión/fisiología , Animales , Antagonistas de los Receptores de Dopamina D2/farmacología , Área Hipotalámica Lateral/fisiopatología , Hipotálamo Anterior/fisiopatología , Masculino , Mesocricetus , Neuronas/fisiología , Receptores de Dopamina D2/metabolismo , Salicilamidas/farmacología , Serotonina/administración & dosificación , Serotonina/metabolismo , Vasopresinas/administración & dosificación , Vasopresinas/metabolismo
2.
J Assoc Off Anal Chem ; 70(4): 626-30, 1987.
Artículo en Inglés | MEDLINE | ID: mdl-3624165

RESUMEN

A simple and rapid method is described for the determination of dimetridazole (DMZ) and ipronidazole (IPR) in swine feeds at various levels (0.11-110 ppm). The drugs are released from feed by prewetting with a buffer, followed by extraction with either methanol or methylene chloride, depending on the drug level; if necessary, an acid-base cleanup is used before the liquid chromatographic analysis. The analytes are separated on a C18 column and monitored at 320 nm for detection and quantitation. Recoveries of DMZ from several feed formulations averaged 108% at the 92.8 ppm level with a standard deviation (SD) of 4.00% and a coefficient of variation (CV) of 3.70%, 101% at the 11.2 ppm level with an SD of 11.9% and a CV of 11.8%, and 100% at the 0.112 ppm level with an SD of 9.27% and a CV of 9.25%. Recoveries of IPR averaged 77.1% at the 12.9 ppm level with an SD of 1.75% and a CV of 2.27%; IPR recoveries averaged 35.2% at the 0.129 ppm level with an SD of 3.39% and a CV of 9.63%.


Asunto(s)
Alimentación Animal/análisis , Dimetridazol/análisis , Ipronidazol/análisis , Nitroimidazoles/análisis , Animales , Cromatografía Liquida , Solventes , Porcinos
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