首页> 外文会议>2011 International Conference on Human Health and Biomedical Engineering >Increased histamine by thioperamide exerts its neuronal protection effect through postsynaptic H1 receptor in neonatal hypoxic-ischemic encephalopathy rat model
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Increased histamine by thioperamide exerts its neuronal protection effect through postsynaptic H1 receptor in neonatal hypoxic-ischemic encephalopathy rat model

机译:硫代过酰胺增加组胺通过新生鼠缺氧缺血性脑病模型的突触后H1受体发挥其神经元保护作用

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Blocking histamine H3 receptor leads to increased histamine in the brain. The effects of H3 receptor antagonist in the rat model of neonatal hypoxic-ischemic encephalopathy (NHIE) and its mechanism is uncertain. In our study, we employed a NHIE model of postnatal 7 days rats and tested the brain water content, hippocampal histamine, cerebral MDA and SOD levels under the different combinations of H1, H2 and H3 antagnonists in order to investigate the effect of H3 antagonist and its mechanism in the NHIE model. H3 antagonist thioperamide decreased the brain water content and MDA and increased the hippocampal histamine and SOD level; H1 antagonist pyrilamine reversed the effects of thioperamide in the H3+H1 group, however, H2 antagonist has no significant influence on the effects of thioperamide as their combinational use. We deduce that thioperamide plays a neuronal protective role by increasing brain histamine through postsynaptic H1 receptor in the NHIE model.
机译:阻止组胺H3受体会导致大脑中组胺的增加。 H3受体拮抗剂在新生鼠缺氧缺血性脑病(NHIE)模型中的作用及其机制尚不确定。在我们的研究中,我们采用了出生后7天大鼠的NHIE模型,并测试了H1,H2和H3拮抗药在不同组合下的脑含水量,海马组胺,脑MDA和SOD水平,以研究H3拮抗剂和H3拮抗剂的作用。其机制在NHIE模型中。 H3拮抗剂thioperamide降低脑含水量和MDA并增加海马组胺和SOD水平; H1拮抗剂吡拉明逆转了H3 + H1组中硫代过酰胺的作用,但是,H2拮抗剂作为组合使用对硫代过酰胺的作用没有明显影响。我们推论出硫代过酰胺通过在NHIE模型中通过突触后H1受体增加脑组胺来发挥神经元保护作用。

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