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5-羟色胺从豚鼠回肠肌间神经丛分离出的神经膨体中释放三磷酸腺苷。

5-hydroxytryptamine releases adenosine 5'-triphosphate from nerve varicosities isolated from the myenteric plexus of guinea-pig ileum.

作者信息

Al-Humayyd M, White T D

出版信息

Br J Pharmacol. 1985 Jan;84(1):27-34.

Abstract

5-Hydroxytryptamine (5-HT)-evoked release of ATP from nerve varicosities isolated from the myenteric plexus of guinea pig ileum was investigated. 5-HT released ATP from myenteric varicosities by a Ca2+-dependent mechanism. The EC50 for release of ATP was 7 X 10(-7) M 5-HT. 5-HT-evoked release of ATP was not blocked by tetrodotoxin (TTX), indicating that release was not initiated by the opening of Na+-channels in the isolated myenteric varicosities. Release of ATP by 5-HT was diminished to 56% of control values by in vivo pretreatment of the guinea-pig with 6-hydroxydopamine (6-OHDA, 250 mg kg-1, i.p.) for 24 h. 6-OHDA pretreatment caused extensive destruction of noradrenergic varicosities as indicated by an 87% loss of noradrenaline content. Quipazine (5 X 10(-6) M) and methysergide (10(-4) M) caused a small release of ATP and blocked subsequent 5-HT-induced release of ATP. Metergoline (2.5 X 10(-5) M), (+)-tubocurarine (7 X 10(-5) M) and cocaine (10(-4) M) decreased 5-HT-induced ATP release. 5-Methoxytryptamine (10(-4) M), picrotoxin (3.5 X 10(-6) M), spiroperidol (10(-6) M), morphine (1.3 X 10(-6) M) and phenoxybenzamine (3.7 X 10(-7) M) were ineffective. The results demonstrate a 5-HT-receptor-mediated release of ATP from noradrenergic and possibly non-adrenergic varicosities in the myenteric plexus of guinea-pig ileum. The 5-HT-induced release of ATP is consistent with a possible transmitter, cotransmitter or modulatory role for ATP in the myenteric plexus.

摘要

研究了5-羟色胺(5-HT)诱发的豚鼠回肠肌间神经丛分离的神经膨体中ATP的释放。5-HT通过钙依赖机制从肌间神经膨体释放ATP。ATP释放的半数有效浓度(EC50)为7×10⁻⁷ M 5-HT。5-HT诱发的ATP释放不受河豚毒素(TTX)阻断,表明在分离的肌间神经膨体中,释放不是由钠通道开放引发的。用6-羟基多巴胺(6-OHDA,250 mg/kg,腹腔注射)对豚鼠进行24小时的体内预处理后,5-HT诱发的ATP释放减少至对照值的56%。如去甲肾上腺素含量损失87%所示,6-OHDA预处理导致去甲肾上腺素能神经膨体广泛破坏。喹哌嗪(5×10⁻⁶ M)和麦角酰二乙胺(10⁻⁴ M)引起少量ATP释放,并阻断随后5-HT诱导的ATP释放。麦角新碱(2.5×10⁻⁵ M)、(+)-筒箭毒碱(7×10⁻⁵ M)和可卡因(10⁻⁴ M)减少5-HT诱导的ATP释放。5-甲氧基色胺(10⁻⁴ M)、印防己毒素(3.5×10⁻⁶ M)、螺哌啶醇(10⁻⁶ M)、吗啡(1.3×10⁻⁶ M)和酚苄明(3.7×10⁻⁷ M)无效。结果表明,5-HT受体介导豚鼠回肠肌间神经丛中去甲肾上腺素能和可能的非肾上腺素能神经膨体释放ATP。5-HT诱导的ATP释放与ATP在肌间神经丛中可能作为递质、共递质或调节剂的作用一致。

相似文献

本文引用的文献

1
Two kinds of tryptamine receptor.两种色胺受体。
Br J Pharmacol Chemother. 1957 Sep;12(3):323-8. doi: 10.1111/j.1476-5381.1957.tb00142.x.
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Antagonism by picrotoxin of 5-hydroxytryptamine-induced excitation of primary afferent neurons.
Brain Res. 1980 Jun 23;192(2):592-1. doi: 10.1016/0006-8993(80)90913-0.

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