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Neuroanatomical and psychopharmacological evidence for interaction between opioid and GABAergic neural pathways in the modulation of fear and defense elicited by electrical and chemical stimulation of the deep layers of the superior colliculus and do

机译:神经解剖学和心理药理学证据表明阿片类药物和GABA能神经通路之间在上丘深层的深部电刺激和化学刺激引起的恐惧和防御调节中相互作用

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The effects of central administration of opioid antagonists on the aversive responses elicited by electrical (at the freezing and escape thresholds) or chemical stimulation (crossings, rearings, turnings and jumps, induced by microinjections of bicuculline) of the midbrain tectum were determined. Central microinjections of naloxone and naltrexone in the mesencephalic tectum caused a significant increase in the freezing and escape thresholds elicited by electrical midbrain tectum stimulation. Furthermore, both opioid antagonists caused a significant decrease in the mean incidence of aversive behavioral responses induced by microinjections of bicuculline in the deep layers of the superior colliculus (DLSC) and in dorsal aspects of the periaqueductal gray matter (DPAG), as compared with controls. These findings suggest an opioid modulation of the GABAergic inhibitory inputs controlling the aversive behavior elicited by midbrain tectum stimulation. In fact, immunohistochemical evidence suggests that the dorsal mesencephalon is rich in beta-endorphin-containing neurons and fibers with varicosities. Iontophoretical microinjections of the neurotracer biodextran in the substantia nigra, pars reticulata (SNpr), show nigro-tectal pathways connecting SNpr with the same neural substrate of the DPAG rich in neuronal cells immunoreactive for opioid peptides. Labeled neurons of the DLSC and periaqueductal gray matter send inputs with varsicosities to ipsi- and contralateral DPAG and ipsilateral SNpr. These findings, in addition to the psychopharmacological evidence for the interaction between opioid and GABAergic mechanisms, offer a neuroanatomical basis of a possible presynaptic opioid inhibition of GABAergic nigro-tectal neurons modulating the fear in aversive structures of the cranial mesencephalon, in a short link, and maybe through a major neural circuit, also in GABA-containing perikarya of nigro-tectal neurons.
机译:确定了中央给予阿片类药物拮抗剂对中脑皮层的电刺激(在冻结和逃逸阈值)或化学刺激(交叉注射,双尾cul的诱导,交叉,起伏和跳跃)引起的厌恶反应的影响。中脑皮层中央微量注射纳洛酮和纳曲酮导致中脑皮层电刺激引起的冻结和逃逸阈值显着增加。此外,与对照组相比,这两种阿片类药物拮抗剂均能显着降低上丘(DLSC)深层和导水管周围灰质(DPAG)背侧微注射双小分子诱导的厌恶行为反应的平均发生率。 。这些发现表明,阿片样物质调节了GABA能抑制性输入,从而控制了中脑顶盖刺激引起的厌恶行为。实际上,免疫组织化学证据表明背中脑富含富含β-内啡肽的神经元和具有静脉曲张的纤维。对黑质黑质(pars reticulata(SNpr))中神经示踪剂生物右旋糖酐的离子电渗显微注射显示,黑质-皮层通路将SNpr与DPAG的相同神经底物连接在一起,DPAG富含对阿片类肽具有免疫反应性的神经元细胞。标记的DLSC和导水管周围灰质神经元向同侧和对侧DPAG和同侧SNpr发送具有曲张性的输入。这些发现,除了阿片类药物与GABA能机制之间相互作用的心理药理学证据外,还为神经系统解剖学提供了可能的突触前阿片类药物抑制GABA能黑质顶神经元神经元的作用,该神经元可以在短期内调节颅内中脑的厌恶结构,并且可能通过一个主要的神经回路,也出现在含有GABA的黑果皮神经元周围核中。

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