首页> 外文期刊>Psychology >Buspirone Ameliorates the Morphine Withdrawal-Induced Anxiety through Synaptic Ultrastructural Changes in Hippocampus of Rat
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Buspirone Ameliorates the Morphine Withdrawal-Induced Anxiety through Synaptic Ultrastructural Changes in Hippocampus of Rat

机译:丁螺环酮通过大鼠海马突触超微结构变化缓解吗啡戒断所致的焦虑

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Morphine administration causes long-lasting neural changes in the brain that underpin the behavioral abnormalities, and the relationship between structural changes and behavioral symptoms is obscure. In present study, the elevated plus-maze and transmission electron microscope were applied to validate the anxiety-like behaviors and synaptic ultrastructural changes in the hippocampi of rats among the morphine group (morphine administration only), the buspirone group (morphine plus buspirone administration) and the vehicle (saline treated only). As compared with the vehicle group, lower values of OE (times of entering into the open arms), OE% (percentage of entries into the open arms), OT (time spent in the open arms), OT% (percentage of time stayed in the open arms), Ns (surface density (Sv)umerical density (Nv)) and S (surface area) of synapses were observed in the morphine group , but significantly, behavior higher scores of RR (rearing), HD (head-dipping), FBA (flat back approach), and higher Nv, Sv, PSD (postsynaptic density), LPT (length of postsynaptic thickening), WCJ (widths in synaptic cleft on junctions) and CCR (curvature of the cleft region) of synapses appeared in the morphine group. However, no significant differences in values of most of those parameters above were detected between the vehicle group and the buspirone group. These results supported that anxiety-like symptoms of rats significantly occurred to the rats after acute morphine withdrawal, but buspirone administration could reverse these indexes. It also proved that the appearance/disappearance of anxiety-related symptoms was related to the ultrastructural changes/reversibility of synapses in the hippocampus with morphine and buspirone administrations. So, it suggested that anxiety-related symptoms were modified in rats subjected to the synaptic ultrastructural changes in hippocampus by morphine acute withdrawal and were further rehabilitated by buspirone administration. It is helpful to pursue the effective therapeutic methods of morphine addiction.
机译:服用吗啡会导致大脑中持久的神经变化,从而助长行为异常,而且结构变化与行为症状之间的关系也不清楚。在本研究中,高架迷宫和透射电子显微镜用于验证吗啡组(仅吗啡给药),丁螺环酮组(吗啡加丁螺环酮给药)之间大鼠海马的焦虑样行为和突触超微结构变化。和车辆(仅盐水处理)。与车辆组相比,OE(进入开放式武器的时间),OE %(进入开放式武器的百分比),OT(开放式武器所花费的时间),OT %(占开放式武器的百分比)的值较低在吗啡组中观察到Ns(表面密度(Sv)/数值密度(Nv))和S(表面积)的突触,但显着地,RR(抚养),HD的行为得分更高(头部浸入),FBA(向后平放)和更高的Nv,Sv,PSD(突触后密度),LPT(突触后增厚的长度),WCJ(交界处突触裂缝的宽度)和CCR(裂缝区域的曲率)吗啡组出现突触。但是,在车辆组和丁螺环酮组之间未检测到上述大多数参数的值存在显着差异。这些结果支持在急性吗啡戒断后大鼠明显出现了焦虑样症状,但是使用丁螺环酮可以逆转这些指标。还证明了与焦虑有关的症状的出现/消失与吗啡和丁螺环酮给药后海马突触的超微结构变化/可逆性有关。因此,这表明通过吗啡急性停药可减轻海马突触超微结构变化大鼠的焦虑相关症状,并通过使用丁螺环酮进一步缓解这种症状。寻求有效的吗啡成瘾治疗方法是有帮助的。

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