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Métodos Terapéuticos y Terapias MTCI
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1.
Food Funct ; 5(8): 1819-28, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-24920211

RESUMEN

(E)-methyl isoeugenol (MIE) is a natural food flavour that constitutes 93.7% of an essential oil from Pimenta pseudocaryophyllus leaf. The leaf extracts of this species are used as a calming agent. As a ubiquitous food additive, the application of MIE for treating mood disorders appears to be globally attractive. Hence, we sought to evaluate general pharmacological activities, anticonvulsant, anxiolytic and antidepressant effects and the possible mechanisms of MIE actions. Administration of MIE was carried out prior to the exposure of a male Swiss mice to general behavioural tests, barbiturate sleep, PTZ-induced convulsion, light dark box (LDB), elevated plus maze (EPM), wire hanging, open field (OF) and forced swimming test (FST). The involvement of monoamine system was studied by mice pretreatment with WAY100635 (antagonist of 5-HT1A), α-methyl-p-tyrosine (AMPT; depletor of catecholamine) or p-chlorophenylalanine (PCPA; depletor of serotonin storage). There was no record of neurotoxic effect or animal's death during the course of general pharmacological tests. MIE at 250 and 500 mg kg(-1) potentiated the hypnotic effect of sodium pentobarbital. However, MIE did not protect against PTZ-induced convulsion. Except for MIE at 500 mg kg(-1), parameters evaluated in the LDB, EPM and OF demonstrated an anxiolytic like property of MIE. This effect was blocked by WAY100635 pretreatment. MIE at 500 mg kg(-1) elicited a reduction in locomotor activity of the mice in the OF. Anti-immobility effect of MIE 250 mg kg(-1) in the FST suggested an antidepressive like property. Unlike AMPT, pretreatment with PCPA reversed the antidepressant like effect of MIE. Our findings demonstrated anxiolytic and antidepressant like properties of (E)-methyl isoeugenol and suggested the participation of serotonergic pathways.


Asunto(s)
Anisoles/farmacología , Ansiolíticos/farmacología , Antidepresivos/farmacología , Aromatizantes/farmacología , Extractos Vegetales/farmacología , Animales , Relación Dosis-Respuesta a Droga , Fenclonina/efectos adversos , Masculino , Ratones , Condicionamiento Físico Animal , Piperazinas/efectos adversos , Piridinas/efectos adversos , Serotonina/sangre , Antagonistas de la Serotonina/efectos adversos , alfa-Metiltirosina/efectos adversos
2.
Zhong Yao Cai ; 36(10): 1635-9, 2013 Oct.
Artículo en Chino | MEDLINE | ID: mdl-24761674

RESUMEN

OBJECTIVE: To observe the effects of extract from Ziziphus Spinosa Semen and Schisandrae Chinensis Fructus on the content of amino acid neurotransmitter in the hypothalamus of insomnia rats induced by P-Chlorophenylalanine (PCPA) and its mechanism. METHODS: The model of insomnia rats were established by PCPA intraperitoneal injection, after the modeling, all the therapeutic group were treated with corresponding drug for one week. The hypothalamus pathological changes of the rats were observed. The contents of GABA, Glu in the hypothalamus were detected by Elisa. The GABA, Glu protein expression were detected by immunohistochemical. GABA(A), R(alpha1) and GABA(A)R(gamma2) mRNA expressions were detected by RT-PCR. RESULTS: Compared with model group, the content of GABA in the hypothalamus of rats increased obviously in the alcohol-water group (P < 0.05 or P < 0.01), while the content of Glu decreased obviously (P < 0.05 or P < 0.01). CONCLUSION: The extract from Ziziphus Spinosae Semen and Schisandrae Chinensis Fructus has obviously Sedative-hypnotic effect. Its mechanism may be related to regulating the content of amino acid neurotransmitter in the hypothalamus of rats.


Asunto(s)
Medicamentos Herbarios Chinos/uso terapéutico , Hipnóticos y Sedantes/uso terapéutico , Hipotálamo/metabolismo , Schisandra/química , Trastornos del Inicio y del Mantenimiento del Sueño/tratamiento farmacológico , Ziziphus/química , Animales , Modelos Animales de Enfermedad , Medicamentos Herbarios Chinos/farmacología , Femenino , Fenclonina/efectos adversos , Frutas/química , Ácido Glutámico/metabolismo , Hipnóticos y Sedantes/farmacología , Hipotálamo/patología , Masculino , ARN Mensajero/genética , ARN Mensajero/metabolismo , Ratas , Ratas Wistar , Receptores de GABA-A/genética , Receptores de GABA-A/metabolismo , Trastornos del Inicio y del Mantenimiento del Sueño/inducido químicamente , Trastornos del Inicio y del Mantenimiento del Sueño/metabolismo , Ácido gamma-Aminobutírico/genética , Ácido gamma-Aminobutírico/metabolismo
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