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大鼠食管肌层黏膜中对河豚毒素敏感和不敏感的舒张反应

Tetrodotoxin-sensitive and -insensitive relaxations in the rat oesophageal tunica muscularis mucosae.

作者信息

Akbarali H I, Bieger D, Triggle C R

出版信息

J Physiol. 1986 Dec;381:49-63. doi: 10.1113/jphysiol.1986.sp016312.

Abstract
  1. Relaxation responses were produced by vagal and field stimulation, respectively, of the whole oesophagus preparation from the rat and of the isolated tunica muscularis mucosae (t.m.m.) preparation from the rat. These relaxation responses persisted in the presence of antagonists of histamine, serotonin, noradrenaline and acetylcholine. 2. Unlike vagally evoked relaxation, that evoked by low-frequency field stimulation, i.e. field-stimulated relaxation (f.s.r.) was generally resistant to tetrodotoxin (TTX). 3. Both types of relaxations exhibited remarkable temperature sensitivity and were abolished by lowering the bath temperature from 37 to 28 degrees C. 4. TTX-resistant relaxations were also produced by scorpion (Leiurus quinquestriatus) venom, the calcium ionophore, A23187 (calimycin) and by increasing the extracellular potassium by 2 mM. The failure of these agents to inhibit f.s.r. is inconsistent with a releasing and/or depleting action on any endogenous mediator. 5. Relaxations produced by vasoactive intestinal peptide (VIP) could be blocked by alpha-chymotrypsin which, however, failed to abolish f.s.r., suggesting that VIP is not the mediator of f.s.r. 6. F.s.r. was completely blocked by the calcium channel antagonists, verapamil (10(-6) M), nifedipine (10(-7) M), and by magnesium (20 mM). 7. Our results indicate that TTX-insensitive relaxations in the isolated t.m.m. are dependent upon extracellular calcium, are due to activation of potential-operated calcium channels and are not mediated by VIP.
摘要
  1. 分别通过对大鼠整个食管标本的迷走神经刺激和对大鼠离体黏膜肌层(t.m.m.)标本的电场刺激产生松弛反应。这些松弛反应在组胺、5-羟色胺、去甲肾上腺素和乙酰胆碱拮抗剂存在的情况下仍然持续存在。2. 与迷走神经诱发的松弛不同,低频电场刺激诱发的松弛,即电场刺激松弛(f.s.r.)通常对河豚毒素(TTX)具有抗性。3. 两种类型的松弛都表现出显著的温度敏感性,并且当浴温从37℃降至28℃时松弛反应消失。4. 蝎毒(Leiurus quinquestriatus)、钙离子载体A23187(钙霉素)以及将细胞外钾离子浓度增加2 mM也能产生对TTX抗性的松弛。这些药剂未能抑制f.s.r.,这与它们对任何内源性介质的释放和/或消耗作用不一致。5. 血管活性肠肽(VIP)产生的松弛可被α-糜蛋白酶阻断,然而,α-糜蛋白酶未能消除f.s.r.,这表明VIP不是f.s.r.的介质。6. f.s.r. 被钙通道拮抗剂维拉帕米(10⁻⁶ M)、硝苯地平(10⁻⁷ M)以及镁离子(20 mM)完全阻断。7. 我们的结果表明,离体t.m.m.中对TTX不敏感的松弛依赖于细胞外钙,是由电压门控钙通道的激活引起的,且不是由VIP介导的。

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5-Hydroxytryptamine in scorpion venom.蝎毒中的5-羟色胺
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The muscularis mucosae of the oesophagus of the cat, rabbit and rat.猫、兔和大鼠食管的黏膜肌层。
J Physiol. 1955 Oct 28;130(1):123-30. doi: 10.1113/jphysiol.1955.sp005398.
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Relaxation of rat tail artery to electrical stimulation.大鼠尾动脉对电刺激的舒张反应。
Life Sci. 1983 Jul 25;33(4):303-9. doi: 10.1016/s0024-3205(83)80001-0.

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