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1.
Acta Physiologica Sinica ; (6): 147-153, 2005.
Artigo em Chinês | WPRIM | ID: wpr-334193

RESUMO

The aim of the present study was to investigate the effect of tetramethylpyrazine (TMP) on the changes of respiration and expression of neuronal nitric oxide synthase (nNOS) in brainstem induced by hypoxia in the rats. Hypoxia was induced by inhalation of 8% O2-balanced N2.The electromyogram (EMG) of diaphragm was monitored to evaluate the respiratory response of the rats to hypoxia. The immunohistochemical staining technique was used to study the change of the expression of nNOS in the brainstem during hypoxia. In the rats of hypoxia group, a successive process of response, excitatory followed by inhibitory, was produced. Twenty min after hypoxia, a significant inhibition of respiration occurred, which was characterized with a marked decrease in the inspiratory duration, the respiratory frequency, and the amplitude of inspiration and a prolongation of expiratory duration (P<0.05). In the rats of pretreated with TMP, the respiratory activity was not obviously depressed (P>0.05). In the rats of hypoxia group, the level of nNOS immunoreactivity was enhanced remarkably in the lateral reticular nucleus, nucleus of trapezoid, hypoglossal nucleus and the facial nucleus compared with the control group (P<0.05). In the rats of pretreated with TMP, the nNOS level increased further in the nuclei mentioned above (P<0.05). The results obtained indicate that TMP can reverse the inhibitory effect of hypoxia on respiration in the rats and that nNOS may be involved in the respiratory protective action of TMP.


Assuntos
Animais , Feminino , Masculino , Ratos , Tronco Encefálico , Hipóxia , Óxido Nítrico Sintase Tipo I , Genética , Metabolismo , Pirazinas , Farmacologia , Distribuição Aleatória , Ratos Sprague-Dawley , Respiração , Insuficiência Respiratória
2.
Chinese Journal of Applied Physiology ; (6): 397-400, 2005.
Artigo em Chinês | WPRIM | ID: wpr-254649

RESUMO

<p><b>AIM</b>The protecting effect of human-derived neurotrophin-6 (NT-6) on injured neurons was investigated to test the neurobiological characteristics of human-derived NT-6.</p><p><b>METHODS</b>Adult SD rats were used and divided into two groups, normal control group and experiment group. The right facial nerve of the experimental rats was sectioned. The experimental animals were subdivided into three groups, blank control group, NT-6 group and saline control group. The rats were raised for two weeks. Brain stem of the rats was removed and transversely sliced. Nissle stain and ChAT immunohistochemical stain of the slices were carried out to observe the role of NT-6 in protecting facial motoneurons.</p><p><b>RESULTS</b>The number of the ChAT positive neurons and the intensity of Nissle stain in the facial nucleus of NT-6 group were significantly augmented compared with that of the blank and saline control groups.</p><p><b>CONCLUSION</b>The human-derived NT-6 could partially protect the facial motoneurons from retrograde degeneration induced by their axon damage.</p>


Assuntos
Animais , Humanos , Ratos , Modelos Animais de Doenças , Nervo Facial , Biologia Celular , Neurônios Motores , Patologia , Fatores de Crescimento Neural , Farmacologia , Fármacos Neuroprotetores , Farmacologia , Ratos Sprague-Dawley
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