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豚鼠腹腔神经节中紧张性和位相性神经元上速激肽受体的亚型

Subtypes of tachykinin receptors on tonic and phasic neurones in coeliac ganglion of the guinea-pig.

作者信息

Zhao F Y, Saito K, Yoshioka K, Guo J Z, Murakoshi T, Konishi S, Otsuka M

机构信息

Department of Pharmacology, Faculty of Medicine, Tokyo Medical and Dental University, Japan.

出版信息

Br J Pharmacol. 1995 May;115(1):25-30. doi: 10.1111/j.1476-5381.1995.tb16315.x.

Abstract
  1. Intracellular recording techniques were used to investigate the characteristics of tachykinin receptors and their subtypes in tonic and phasic neurones, which constituted two major neuronal populations in the coeliac ganglion of the guinea-pig. 2. In 95% of phasic neurones a long-lasting after-hyperpolarization (LAH), 5-8 s in duration and 10-20 mV in amplitude, was observed following action potentials evoked by passing a train of depolarizing current pulses into the neurones. In contrast, LAH was observed in only 4% of tonic neurones. 3. In most tonic neurones, substance P (SP), neurokinin A (NKA) and senktide induced depolarizations, whereas in phasic neurones they usually inhibited LAH but rarely induced depolarization. 4. Tonic and phasic neurones were further classified into three groups based on their responses (depolarization for tonic neurones and LAH inhibition for phasic neurones) to these tachykinin receptor agonists: (1) neurones responsive to SP, NKA and senktide (71-78%); (2) those responsive to senktide but not to SP and NKA (12-23%) and (3) those not responsive to any of the three agonists (7-11%). 5. GR71251 (5 microM), an NK1-selective tachykinin receptor antagonist, depressed the depolarization in tonic neurones and the LAH inhibition in phasic neurones induced by SP and NKA, but not those induced by senktide. 6. Selective NK2 receptor agonists, [Nle10]NKA4-10, [beta-Ala8]NKA4-10 and GR64349, were without effect in both tonic and phasic neurones. Furthermore, an NK2 receptor antagonist, L659,877, did not inhibit the depolarization induced by NKA, SP or senktide in tonic neurones. 7. It is suggested that NK1 and NK3 receptors are present on a large proportion of coeliac ganglion neurones. In tonic neurones both subtypes of tachykinin receptors are coupled to membrane depolarization,whereas in phasic neurones activation of these receptors leads to inhibition of LAH. The present study also suggests that NKA evokes the depolarization in tonic neurones and the LAH inhibition in phasic neurones via NK1, but not NK2 receptors.
摘要
  1. 采用细胞内记录技术研究豚鼠腹腔神经节中构成两大主要神经元群的紧张性和位相性神经元中速激肽受体及其亚型的特性。2. 在95%的位相性神经元中,向神经元通入一串去极化电流脉冲诱发动作电位后,可观察到持续5 - 8秒、幅度为10 - 20毫伏的长时程超极化后电位(LAH)。相比之下,仅4%的紧张性神经元中观察到LAH。3. 在大多数紧张性神经元中,P物质(SP)、神经激肽A(NKA)和速激肽6均诱导去极化,而在位相性神经元中它们通常抑制LAH,但很少诱导去极化。4. 根据紧张性和位相性神经元对这些速激肽受体激动剂的反应(紧张性神经元为去极化,位相性神经元为LAH抑制),将其进一步分为三组:(1)对SP、NKA和速激肽6有反应的神经元(71 - 78%);(2)对速激肽6有反应但对SP和NKA无反应的神经元(12 - 23%);(3)对三种激动剂均无反应的神经元(7 - 11%)。5. NK1选择性速激肽受体拮抗剂GR71251(5微摩尔)可抑制SP和NKA诱导的紧张性神经元去极化以及位相性神经元的LAH抑制,但不抑制速激肽6诱导的反应。6. 选择性NK2受体激动剂[Nle10]NKA4 - 10、[β - Ala8]NKA4 - 10和GR64349对紧张性和位相性神经元均无作用。此外,NK2受体拮抗剂L659,877不抑制NKA、SP或速激肽6在紧张性神经元中诱导的去极化。7. 提示NK1和NK3受体存在于大部分腹腔神经节神经元上。在紧张性神经元中,两种速激肽受体亚型均与膜去极化偶联,而在位相性神经元中,这些受体的激活导致LAH抑制。本研究还提示NKA通过NK1而非NK2受体在紧张性神经元中诱发去极化,在位相性神经元中诱发LAH抑制。

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