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介导血管紧张素II在大鼠延髓背侧神经元效应的受体亚型。

Receptor subtype that mediates the neuronal effects of angiotensin II in the rat dorsal medulla.

作者信息

Barnes K L, McQueeney A J, Ferrario C M

机构信息

Department of Neurosciences, Cleveland Clinic Foundation, OH 44195-5286.

出版信息

Brain Res Bull. 1993;31(1-2):195-200. doi: 10.1016/0361-9230(93)90025-7.

Abstract

We have shown previously that many neurons in the caudal medial nucleus tractus solitarii (nTS) are excited by angiotensin (Ang) II. The selective Ang II receptor antagonists losartan (AT1; DuP 753) and CGP 42112A or PD 123177 (AT2) were used to evaluate the receptor subtype that mediates excitation of medial nTS neurons by Ang II (1 microM) in rat medulla in vitro slices. Neither losartan nor the AT2 antagonists altered the baseline firing of either Ang II-sensitive or Ang II-unresponsive neurons. However, in six cells with low-frequency spontaneous activity that remained above baseline after excitation by Ang II, subsequent administration of losartan reversed the firing pattern to the initial low-frequency activity. Losartan (10 microM) blocked the excitation by Ang II in 29 medial nTS neurons. The Ang II-induced excitation recovered from Type I blockade in 1 h. In contrast, both CGP 42112A (10 and 100 microM, n = 12) and PD 123177 (100 microM, n = 7) failed to block excitation by Ang II in all neurons tested. Furthermore, the AT2 antagonists were ineffective in preventing Ang II-induced neuronal excitation both when they were the first antagonist tested and when they were evaluated after the neuron had recovered from AT1 receptor blockade. These studies suggest that the Ang II-induced excitation of caudal medial nTS neurons is mediated by AT1 Ang II receptors.

摘要

我们之前已经表明,尾侧孤束核内侧部(nTS)中的许多神经元会被血管紧张素(Ang)II激活。使用选择性Ang II受体拮抗剂氯沙坦(AT1;DuP 753)和CGP 42112A或PD 123177(AT2)来评估介导体外培养的大鼠延髓内侧nTS神经元被1微摩尔Ang II激活的受体亚型。氯沙坦和AT2拮抗剂均未改变Ang II敏感或不敏感神经元的基础放电。然而,在六个具有低频自发活动的细胞中,这些细胞在被Ang II激活后仍高于基线水平,随后给予氯沙坦可使放电模式恢复到最初的低频活动。10微摩尔的氯沙坦可阻断29个内侧nTS神经元被Ang II激活。Ang II诱导的激活在1小时后从I型阻断中恢复。相比之下,CGP 42112A(10和100微摩尔,n = 12)和PD 123177(100微摩尔,n = 7)在所有测试的神经元中均未能阻断Ang II诱导的激活。此外,当AT2拮抗剂作为第一个测试的拮抗剂以及在神经元从AT1受体阻断中恢复后进行评估时均无法有效阻止Ang II诱导的神经元激活。这些研究表明,Ang II诱导的尾侧内侧nTS神经元激活是由AT1 Ang II受体介导的。

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