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首页> 外文期刊>Neurochemical Research >Clozapine Administration Modifies Neurotensin Effect on Synaptosomal Membrane Na+, K+ -ATPase Activity
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Clozapine Administration Modifies Neurotensin Effect on Synaptosomal Membrane Na+, K+ -ATPase Activity

机译:氯氮平给药可改善神经降压素对突触膜Na + ,K + -ATPase活性的影响

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摘要

Na+, K+-ATPase is inhibited by neurotensin, an effect which involves the peptide high affinity receptor (NTS1). Neurotensin effect on cerebral cortex synaptosomal membrane Na+, K+-ATPase activity of rats injected i.p. with antipsychotic clozapine was studied. Whereas 3.5 × 10−6 M neurotensin decreased 44% Na+, K+-ATPase activity in the controls, the peptide failed to modify enzyme activity 30 min after a single 3.0, 10.0 and 30.0 mg/kg clozapine dose. Neurotensin decreased Na+, K+-ATPase activity 40 or 20% 18 h after 3.0 or 5.6 mg/kg clozapine administration, respectively, and lacked inhibitory effect 18 h after 17.8 and 30.0 mg/kg clozapine doses. Results indicated that the clozapine treatment differentially modifies the further effect of neurotensin on synaptosomal membrane Na+, K+-ATPase activity according to time and dose conditions employed. Taken into account that clozapine blocks the dopaminergic D2 receptor, findings obtained favor the view of an interplay among neurotensinergic receptor, dopaminergic D2 receptor and Na+, K+-ATPase at synaptic membranes.
机译:Na + ,K + -ATPase被神经降压素抑制,这种作用涉及肽高亲和力受体(NTS1)。神经降压素对腹腔注射大鼠脑皮质突触小体膜Na + ,K + -ATPase活性的影响。与抗精神病药氯氮平一起进行了研究。对照中3.5×10 −6 M神经降压素使Na + ,K + -ATPase活性降低44%,而该肽无法修饰酶服用氯氮平3.0、10.0和30.0 mg / kg一次后30分钟进行活性测定。服用氯氮平3.0或5.6 mg / kg后18小时,神经降压素分别降低Na + ,K + -ATPase活性40或20%,而在17.8后18 h则无抑制作用和30.0 mg / kg的氯氮平剂量。结果表明,氯氮平治疗根据使用的时间和剂量条件,不同程度地改变了神经降压素对突触体膜Na + ,K + -ATPase活性的进一步影响。考虑到氯氮平会阻断多巴胺能D2受体,因此获得的研究结果支持了神经降压能受体,多巴胺能D2受体和Na + ,K + -ATPase在突触之间相互作用的观点。膜。

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