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纵行肌-肠肌丛切除及吲哚美辛对豚鼠回肠环行肌对速激肽NK-2和NK-3受体激动剂反应的影响。

Effect of longitudinal muscle-myenteric plexus removal and indomethacin on the response to tachykinin NK-2 and NK-3 receptor agonists in the circular muscle of the guinea-pig ileum.

作者信息

Maggi C A, Patacchini R, Meini S, Giuliani S

机构信息

Pharmacology Department, A. Menarini Pharmaceuticals, Florence, Italy.

出版信息

J Auton Pharmacol. 1994 Feb;14(1):49-60. doi: 10.1111/j.1474-8673.1994.tb00589.x.

DOI:10.1111/j.1474-8673.1994.tb00589.x
PMID:7512089
Abstract
  1. The effect of removal of the longitudinal muscle-myenteric plexus (LM-MP) and/or indomethacin (10 microM) on the response to the tachykinin NK-2 receptor selective agonist, [beta Ala8]NKA(4-10), or to the NK-3 receptor selective agonist, senktide, was investigated by measuring mechanical activity (isotonic recording) of circular muscle (ring preparation) of the guinea-pig ileum. 2. Indomethacin (10 microM) increased the percentage of ileal rings displaying spontaneous activity, either intact or LM-MP-free. The response to senktide (10 nM and 1 microM) was lower in LM-MP-free than in intact ileal rings, either in the absence or presence of indomethacin. The response to a low concentration (10 nM) of [beta Ala8] NKA (4-10) was enhanced in LM-MP-free rings and by indomethacin. 3. In intact ileal rings, the response to senktide was unaffected by atropine (3 microM) alone or by the tachykinin NK-2 receptor antagonist MEN 10,376 (10 microM) alone while it was reduced by the combined administration of the two antagonists. The response to senktide was greatly reduced by tetrodotoxin (TTX, 1 microM). Senktide-induced contractions (10 nM) were also reduced by the blocker of N-type voltage-sensitive calcium channels, omega-contoxin (CTX, 0.1 microM). 4. In about 30% of preparations tested, an inhibitory response (decrease in spontaneous activity) to 10 nM senktide, was disclosed in CTX-treated intact ileal rings. This inhibitory effect was TTX-sensitive. 5. In LM-MP-free ileal rings, the response to senktide was abolished or reduced by atropine and MEN 10,376, alone or in combination, and was also reduced or abolished by TTX and CTX. 6. The response to [beta Ala8]NKA (4-10) was inhibited by MEN 10,376, in both intact and LM-MP-free ileal rings while it was unaffected by atropine, TTX or CTX. 7. These results indicate that indomethacin pretreatment induces a regular background activity for studying the motor response to tachykinins in the circular muscle of the ileum, probably by blocking the formation of relaxant prostanoids. A further increase in sensitivity to direct smooth muscle stimulation (NK-2 receptor agonist) can be obtained by removal of the LM-MP. The response to NK-3 receptor stimulation is diminished but not abolished by removal of the LM-MP, suggesting that NK-3 receptors are located on neuronal bodies of myenteric neurons, but possibly also at other sites (possibly, nerve terminals).(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 通过测量豚鼠回肠环形肌(肠段标本)的机械活动(等张记录),研究去除纵行肌 - 肌间神经丛(LM - MP)和/或吲哚美辛(10微摩尔)对速激肽NK - 2受体选择性激动剂[β丙氨酸8]NKA(4 - 10)或NK - 3受体选择性激动剂senktide反应的影响。2. 吲哚美辛(10微摩尔)增加了完整或无LM - MP的回肠肠段出现自发活动的百分比。在无LM - MP的回肠肠段中,无论有无吲哚美辛,对senktide(10纳摩尔和1微摩尔)的反应均低于完整回肠肠段。在无LM - MP的肠段中以及吲哚美辛存在时,对低浓度(10纳摩尔)的[β丙氨酸8]NKA(4 - 10)的反应增强。3. 在完整回肠肠段中,单独使用阿托品(3微摩尔)或速激肽NK - 2受体拮抗剂MEN 10,376(10微摩尔)时,对senktide的反应不受影响,而联合使用这两种拮抗剂时反应降低。对senktide的反应被河豚毒素(TTX,1微摩尔)大大降低。senktide诱导的收缩(10纳摩尔)也被N型电压敏感性钙通道阻滞剂ω - 芋螺毒素(CTX,0.1微摩尔)降低。4. 在约30%的测试标本中,在CTX处理的完整回肠肠段中发现了对10纳摩尔senktide的抑制反应(自发活动减少)。这种抑制作用对TTX敏感。5. 在无LM - MP的回肠肠段中,单独或联合使用阿托品和MEN 10,376可消除或降低对senktide的反应,TTX和CTX也可降低或消除该反应。6. 对[β丙氨酸8]NKA(4 - 10)的反应在完整和无LM - MP的回肠肠段中均被MEN 10,376抑制,而不受阿托品、TTX或CTX的影响。7. 这些结果表明,吲哚美辛预处理诱导了一种规律的背景活动,用于研究回肠环形肌对速激肽的运动反应,可能是通过阻断舒张性前列腺素的形成。去除LM - MP可进一步提高对直接平滑肌刺激(NK - 2受体激动剂)的敏感性。去除LM - MP会使对NK - 3受体刺激的反应减弱但未消除,这表明NK - 3受体位于肌间神经元的神经元体上,但也可能位于其他部位(可能是神经末梢)。(摘要截断于400字)

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