Wang Yu-Feng, Hatton Glenn I
Department of Cell Biology and Neuroscience, University of California, Riverside, California 92521, USA.
J Neurophysiol. 2004 May;91(5):2312-21. doi: 10.1152/jn.00697.2003. Epub 2004 Jan 14.
To examine the mechanisms underlying milk-ejection bursts of oxytocin (OT) neurons during suckling, both in vivo and in vitro studies were performed on supraoptic OT neurons from lactating rats. The bursts were first recorded extracellularly in anesthetized rats. Burst-related electrical parameters were essentially the same as previous reports except for a trend toward transient decreases in basal firing rates immediately preceding the burst. From putative OT neurons in slices with extracellular recordings, bursts that closely mimicked the in vivo bursts were elicited by phenylephrine, an alpha1-adrenoceptor agonist, in a low-Ca(2+) medium. Moreover, in whole cell patch-clamp recordings, the in vitro bursts were recorded from immunocytochemically identified OT neurons. After a transient decrease in the basal firing rate, the in vitro bursts started with a sudden increase in the firing rate, quickly reaching a peak level, then gradually decaying, and ended with a postburst inhibition. A brief depolarization of the membrane potential and an increase in membrane conductance appeared after the onset of the burst. Spikes during a burst were characterized by a significant increase in the duration and decrease in the amplitude around the peak rate firing. These bursts were significantly different from short-lasting burst firing of vasopressin neurons in membrane potential changes, time to reach peak firing rate, spike amplitude and duration during peak rate firing. Our extensive analysis of these results suggests that the in vitro burst is a useful model for further study of mechanisms underlying milk-ejection bursts of OT neurons in vivo.
为了研究哺乳期间催产素(OT)神经元射乳脉冲的潜在机制,对泌乳大鼠视上核OT神经元进行了体内和体外研究。首先在麻醉大鼠中进行细胞外记录这些脉冲。除了在脉冲即将开始前基础放电率有短暂下降的趋势外,与脉冲相关的电参数与先前报道基本相同。在低钙(2+)培养基中,通过α1肾上腺素能受体激动剂去氧肾上腺素,从细胞外记录切片中的假定OT神经元诱发了与体内脉冲非常相似的脉冲。此外,在全细胞膜片钳记录中,从免疫细胞化学鉴定的OT神经元记录到了体外脉冲。在基础放电率短暂下降后,体外脉冲以放电率突然增加开始,迅速达到峰值水平,然后逐渐衰减,并以脉冲后抑制结束。脉冲开始后出现膜电位的短暂去极化和膜电导增加。脉冲期间的动作电位特征是在峰值放电率附近持续时间显著增加,幅度减小。这些脉冲在膜电位变化、达到峰值放电率的时间、峰值放电率期间的动作电位幅度和持续时间方面与血管加压素神经元的短暂脉冲放电有显著差异。我们对这些结果的广泛分析表明,体外脉冲是进一步研究体内OT神经元射乳脉冲潜在机制的有用模型。