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电刺激小脑顶核对大鼠胃缺血-再灌注损伤的神经调控被引量:4
2009年
本实验采用夹闭大鼠腹腔动脉30min后松开动脉夹血流复灌1h的方法建立胃缺血-再灌注(gastric ischemia-reperfusion,GI-R)损伤模型,在此模型基础上观察电刺激小脑顶核(fastigial nucleus,FN)对大鼠GI-R损伤的影响,并对其可能的神经调控机制进行初步的探讨。胃黏膜损伤检测显示,电刺激小脑FN使GI-R损伤显著减轻,且有强度-效应依赖关系;另外,电刺激小脑FN使胃黏膜细胞的凋亡率降低。预先化学损毁小脑FN,则可消除电刺激对GI-R损伤的减轻作用。内脏大神经放电检测分析显示,电刺激小脑FN使内脏大神经放电频率减少和放电幅度降低,而化学损毁双侧下丘脑外侧区(lateral hypothalamic area,LHA),再电刺激FN,内脏大神经的放电频率、幅度与刺激FN前相比都无明显变化。剪断双侧内脏大神经,再电刺激小脑FN,同样可使GI-R损伤减轻。化学损毁双侧LHA能取消电刺激小脑FN对GI-R损伤的减轻作用。氧化应激方面,电刺激小脑FN使缺血-再灌注的胃黏膜内超氧化物歧化酶(SOD)活性升高、丙二醛(MDA)含量降低。以上结果提示:电刺激小脑FN对大鼠缺血-再灌注的胃黏膜具有保护作用,小脑FN可能是对大鼠GI-R损伤具有调控作用的中枢部位,其神经机制可能是通过LHA介导,降低了交感神经的兴奋性实现的,此外可能还与其抗氧化作用有关。
蒋信伟杜东书张建福张咏梅周晓燕马小波
关键词:小脑顶核下丘脑外侧区内脏大神经
Excitatory effect of histamine on neuronal activity of rat cerebellar fastigial nucleus in vitro被引量:1
2007年
The cerebellar fastigial nucleus (FN) holds an important role in motor control and body balance. Previous studies have revealed that the nucleus is innervated by direct hypothalamocerebellar histaminergic fibers. However, the functional role of histaminergic projection in cerebellar FN has never been established. In this study, we investigated the effect of histamine on neuronal firing of cerebellar FN by using slice preparations. Sixty-five FN cells were recorded from 47 cerebellar slices, and a vast majority of the cells responded to histamine stimulation with an excitatory response (58/65, 89.2%). Perfusing slices with low-Ca2+/high-Mg2+ medium did not block the histamine-induced excitation (n=10), supporting a direct postsynaptic action of histamine on the cells. Furthermore, the excitatory effect of histamine on FN neurons was not blocked by selective histamine H1 receptor antagonist triprolidine (n=15) or chlorpheniramine (n=10), but was effectively suppressed by ranitidine (n=15), a highly selective histamine H2 receptor antagonist. On the other hand, highly selective histamine H2 receptor agonist dimaprit (n=20) instead of histamine H1 receptor agonist 2-pyridylethylamine (n=16) mimicked the ex- citatory effect of histamine on FN neurons. The dimaprit-induced FN neuronal excitation was effectively antagonized by selective histamine H2 receptor antagonist ranitidine (n=13) but not influenced by se- lective histamine H1 receptor antagonist triprolidine (n=15). These results demonstrate that histamine excites cerebellar FN cells via the histamine H2 receptor mechanism and suggest that the hypotha- lamocerebellar histaminergic fibers may modulate cerebellar FN-mediated sensorimotor integration through their excitatory innervations on FN neurons.
TANG BiaoZHANG JunLI HongZhaoZHU JingNingWANG JianJun
关键词:小脑顶核神经活动组胺受体
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