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首页> 外文期刊>Japanese Journal of Pharmacology >Relationship between muscarinic autoinhibition and the inhibitory effect of morphine on acetylcholine release from myenteric plexus of guinea pig ileum.
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Relationship between muscarinic autoinhibition and the inhibitory effect of morphine on acetylcholine release from myenteric plexus of guinea pig ileum.

机译:毒蕈碱自身抑制作用与吗啡抑制作用对豚鼠回肠肌层神经丛乙酰胆碱释放的影响。

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摘要

The relationship between muscarinic autoinhibition and the inhibitory effect of morphine on acetylcholine (ACh) release was investigated in a longitudinal muscle with myenteric plexus (LMMP) preparation of guinea pig ileum. Morphine (10 microM) inhibited spontaneous and evoked ACh release by electrical field stimulation (EFS) at 1 Hz but not at 10 Hz. Atropine (1 microM) did not affect the resting ACh release, but it significantly increased EFS-evoked release, suggesting activation of muscarinic autoreceptors by ACh released during EFS. Only when the autoinhibition was weakened by atropine, morphine exhibited an inhibitory effect on the EFS-evoked release at 10 Hz. Bethanechol (300 microM) inhibited the EFS-evoked release at 1 Hz but not 10 Hz, suggesting that muscarinic autoreceptors are partially or almost fully activated at 1 or 10 Hz stimulation, respectively. After bethanechol treatment, morphine did not exhibit its inhibitory effect on the EFS-evoked release at 1 Hz. Naloxone (1 microM) increased spontaneous and EFS-evoked ACh release at 1 Hz but not at 10 Hz. Following treatment with atropine, naloxone also increased ACh release at 10-Hz stimulation. These results suggest that morphine and an endogenous opioid inhibit ACh release from LMMP preparations when muscarinic autoinhibition mechanism does not fully work. This inhibitory effect of morphine is discussed in relation to the calcium sensitivity of the preparations in ACh release.
机译:研究了豚鼠回肠肌间神经丛(LMMP)制备的纵肌中毒蕈碱自身抑制与吗啡对乙酰胆碱(ACh)释放抑制作用的关系。吗啡(10 microM)通过1 Hz的电场刺激(EFS)抑制自发的和诱发的ACh释放,但不抑制10 Hz的释放。阿托品(1 microM)不会影响静止的ACh释放,但会显着增加EFS诱发的释放,表明EFS期间释放的ACh激活了毒蕈碱自受体。仅当阿托品减弱了自身抑制作用时,吗啡才对10 Hz下的EFS诱发的释放表现出抑制作用。 Bethanechol(300 microM)在1 Hz时抑制EFS诱发的释放,但在10 Hz时不抑制,这表明毒蕈碱自身受体分别在1或10 Hz刺激下被部分或几乎完全激活。在苯乙二酚处理后,吗啡在1 Hz下对EFS诱发的释放没有抑制作用。纳洛酮(1 microM)在1 Hz时增加自发和EFS诱发的ACh释放,但在10 Hz时则没有。用阿托品治疗后,纳洛酮在10 Hz刺激下还增加了ACh的释放。这些结果表明,当毒蕈碱自抑制机制不能完全发挥作用时,吗啡和内源性阿片类药物会抑制LMMP制剂中的ACh释放。讨论了吗啡的这种抑制作用与制剂在ACh释放中的钙敏感性有关。

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