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牛磺酸选择性调节清醒大鼠中血管加压素神经元的分泌活动。

Taurine selectively modulates the secretory activity of vasopressin neurons in conscious rats.

作者信息

Engelmann M, Ludwig M, Singewald N, Ebner K, Sabatier N, Lubec G, Landgraf R, Wotjak C T

机构信息

Institut für Medizinische Neurobiologie, Otto-von-Guericke-Universität Magdeburg, Leipziger Str. 44. D-39120 Magdeburg, Germany.

出版信息

Eur J Neurosci. 2001 Oct;14(7):1047-55. doi: 10.1046/j.0953-816x.2001.01729.x.

Abstract

Previous experiments have shown that a 10-min forced swimming session triggers the release of vasopressin from somata and dendrites, but not axon terminals, of neurons of the hypothalamic-neurohypophysial system. To further investigate regulatory mechanisms underlying this dissociated release, we forced male Wistar rats to swim in warm (20 degrees C) water and monitored release of the potentially inhibitory amino acids gamma amino butyric acid (GABA) and taurine into the hypothalamic supraoptic nucleus using microdialysis. Forced swimming caused a significant increase in the release of taurine (up to 350%; P < 0.05 vs. prestress release), but not GABA. To reveal the physiological significance of centrally released taurine, the specific taurine antagonist 6-aminomethyl-3-methyl-4H-1,2,4-benzothiadiazine-1,1-dioxide was administered into the supraoptic nucleus via retrodialysis. Administration of this antagonist caused a significant increase in the release of vasopressin within the supraoptic nucleus and into the blood both under basal conditions and during stress (up to 800%; P < 0.05 vs. basal values), without affecting hypothalamic or plasma oxytocin. Local administration of the GABA(A) receptor antagonist bicuculline, in contrast, failed to influence vasopressin secretion at either time point. In a separate series of in vivo electrophysiological experiments, administration of the same dosage of the taurine antagonist into the supraoptic nucleus via microdialysis resulted in an increased electrical activity of identified vasopressinergic, but not oxytocinergic, neurons. Taken together our data demonstrate that taurine is released within the supraoptic nucleus during physical/emotional stress. Furthermore, at the level of the supraoptic nucleus, taurine inhibits not only the electrical activity of vasopressin neurons but also acts as an inhibitor of both central and peripheral vasopressin secretion during different physiological states.

摘要

先前的实验表明,10分钟的强迫游泳会促使下丘脑 - 神经垂体系统神经元的胞体和树突释放血管加压素,但轴突终末不会释放。为了进一步研究这种解离性释放背后的调节机制,我们迫使雄性Wistar大鼠在温(20摄氏度)水中游泳,并使用微透析监测潜在抑制性氨基酸γ-氨基丁酸(GABA)和牛磺酸向视上核的释放。强迫游泳导致牛磺酸释放显著增加(高达350%;与应激前释放相比,P < 0.05),但GABA没有增加。为了揭示中枢释放的牛磺酸的生理意义,通过逆向透析将特异性牛磺酸拮抗剂6-氨基甲基-3-甲基-4H-1,2,4-苯并噻二嗪-1,1-二氧化物注入视上核。在基础条件和应激期间,给予这种拮抗剂均导致视上核内和血液中血管加压素的释放显著增加(高达800%;与基础值相比,P < 0.05),而不影响下丘脑或血浆催产素。相比之下,在两个时间点局部给予GABA(A)受体拮抗剂荷包牡丹碱均未能影响血管加压素的分泌。在另一系列体内电生理实验中,通过微透析将相同剂量的牛磺酸拮抗剂注入视上核,导致已鉴定的血管加压素能神经元(而非催产素能神经元)的电活动增加。综合我们的数据表明,在身体/情绪应激期间,牛磺酸在视上核内释放。此外,在视上核水平,牛磺酸不仅抑制血管加压素神经元的电活动,而且在不同生理状态下作为中枢和外周血管加压素分泌的抑制剂。

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