Chevaleyre V, Dayanithi G, Moos F C, Desarmenien M G
Centre National de la Recherche Scientifique Unité Propre de Recherche, Montpellier, France.
J Neurosci. 2000 Aug 1;20(15):5813-9. doi: 10.1523/JNEUROSCI.20-15-05813.2000.
Mature oxytocin (OT) and vasopressin (AVP) magnocellular neurons of the hypothalamic supraoptic nuclei (SON) autocontrol their electrical activity via somatodendritic release of their respective peptides. Because OT and AVP are synthesized early in development and could play an important role in the maturation of these neurons, we checked whether the peptides are released within the SON and act on their secreting neurons during 3 weeks of postnatal development. We used patch-clamp recordings from SON neurons in rat hypothalamic horizontal slices to show that the spontaneous electrical activity of immature SON neurons is blocked by OT or AVP receptor antagonists, demonstrating a basal somatodendritic release of the peptides. Application of OT or AVP depolarizes SON neurons and stimulates activity typical of the corresponding mature neurons. This effect is directly on SON neurons because it is recorded in dissociated neurons. Radioimmunoassays from isolated SON were used to show that each peptide facilitates its own release at a somatodendritic level, exhibiting a self-sustaining positive feedback loop. This autocontrol is not uniform during development because the proportion of neurons depolarized by the peptides, the amplitude of the depolarization, and the propensity of the peptides to facilitate their own release are maximal during the second postnatal week and decrease thereafter. These data are consistent with a role of autocontrol in the maturation of SON neurons because it is maximal during the delimited period of postnatal development that corresponds to the period of major synapse formation.
下丘脑视上核(SON)中成熟的催产素(OT)和血管加压素(AVP)大细胞神经元通过其各自肽段的树突体释放对自身电活动进行自动控制。由于OT和AVP在发育早期就已合成,且可能在这些神经元的成熟过程中发挥重要作用,因此我们研究了在出生后3周的发育过程中,这些肽段是否在SON内释放并作用于其分泌神经元。我们利用大鼠下丘脑水平切片中SON神经元的膜片钳记录来表明,未成熟SON神经元的自发电活动会被OT或AVP受体拮抗剂阻断,这证明了肽段存在基础的树突体释放。施加OT或AVP可使SON神经元去极化,并刺激相应成熟神经元的典型活动。这种效应直接作用于SON神经元,因为在分离的神经元中也能记录到。对分离出的SON进行放射免疫分析表明,每种肽段在树突体水平上都促进其自身的释放,呈现出一个自我维持的正反馈回路。这种自动控制在发育过程中并不一致,因为被肽段去极化的神经元比例、去极化幅度以及肽段促进自身释放的倾向在出生后第二周最大,此后逐渐降低。这些数据与自动控制在SON神经元成熟过程中的作用相一致,因为它在与主要突触形成期相对应的出生后发育限定时期最大。