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毒蕈碱对体外培养的兔虹膜中[3H]-去甲肾上腺素释放的抑制作用:刺激条件对乙酰甲胆碱和毛果芸香碱内在活性的影响。

Muscarinic inhibition of [3H]-noradrenaline release on rabbit iris in vitro: effects of stimulation conditions on intrinsic activity of methacholine and pilocarpine.

作者信息

Bognar I T, Pallas S, Fuder H, Muscholl E

机构信息

Pharmakologisches Institut der Universität, Mainz, Federal Republic of Germany.

出版信息

Br J Pharmacol. 1988 Jul;94(3):890-900. doi: 10.1111/j.1476-5381.1988.tb11601.x.

DOI:10.1111/j.1476-5381.1988.tb11601.x
PMID:3052680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1854025/
Abstract
  1. Rabbit isolated irides were loaded with [3H]-noradrenaline and superfused with Tyrode solution. The inhibition by the muscarinic agonists (+/-)-methacholine and pilocarpine of the [3H]-noradrenaline overflow into the superfusate evoked by field stimulation (pulses of 1 ms duration, 75 mA) was measured as an index of activation of presynaptic muscarinic receptors. 2. The fractional rate of release per pulse during the first stimulation period (S1) was low with 360 pulses at 3 Hz, intermediate with 360 pulses at 10 Hz and high with 1200 pulses at 10 Hz. Upon repetitive stimulation (7 periods at 20 min intervals), the fractional rates of release per pulse during S7 no longer differed, suggesting a 'long-term' regulation of [3H]-noradrenaline release depending on the stimulation conditions. 3. The evoked [3H]-noradrenaline overflow was depressed by (+/-)-methacholine in a concentration-dependent manner. The EC50 ranged from 0.29 to 0.42 microM. Methacholine nearly abolished the transmitter release evoked at 3 Hz but reduced that induced at 10 Hz by only 50%. Under the latter condition the methacholine concentration-inhibition curve was bell-shaped and no muscarinic inhibition was observed in the presence of methacholine 30 microM. After washout of methacholine the evoked [3H]-noradrenaline release was temporarily enhanced. 4. Atropine 0.1 microM enhanced the [3H]-noradrenaline overflow (evoked by stimulation with 360 or 1200 pulses at 10 Hz), probably antagonizing a presynaptic inhibition by endogenous acetylcholine. The inhibition by methacholine was competitively antagonized by atropine 0.1 microM (apparent -log KB = 8.5-9.0). 5. Depending on the concentration, pilocarpine reduced the [3H]-noradrenaline overflow evoked by 360 pulses at 3 Hz up to 63%. However, at 10 Hz stimulation frequency the compound was inactive as an agonist but competitively antagonized the presynaptic inhibition induced by methacholine. The KB under the latter condition (0.95 microM) was very close to the EC50 value determined at 3 Hz (0.85 microM). 6. The results demonstrate a muscarinic inhibition of noradrenaline release from the rabbit isolated iris. The activation by pilocarpine of the presynaptic receptors provides an alternative explanation for the miosis induced in the rabbit in vivo, which might be the result of a decreased sympathetic tone in the iris dilator muscle.
摘要
  1. 将兔离体虹膜用[3H]-去甲肾上腺素负载,并用台氏液进行灌流。通过测量毒蕈碱激动剂(±)-乙酰甲胆碱和毛果芸香碱对电场刺激(持续时间1毫秒、强度75毫安的脉冲)诱发的[3H]-去甲肾上腺素向灌流液中溢出的抑制作用,作为突触前毒蕈碱受体激活的指标。2. 在第一个刺激期(S1),3赫兹360个脉冲时每个脉冲的释放分数率较低,10赫兹360个脉冲时为中等,10赫兹1200个脉冲时较高。在重复刺激(每隔20分钟7个周期)时,S7期间每个脉冲的释放分数率不再有差异,表明[3H]-去甲肾上腺素释放存在取决于刺激条件的“长期”调节。3. (±)-乙酰甲胆碱以浓度依赖性方式抑制诱发的[3H]-去甲肾上腺素溢出。半数有效浓度(EC50)范围为0.29至0.42微摩尔。乙酰甲胆碱几乎完全抑制3赫兹诱发的递质释放,但仅将10赫兹诱发的释放减少50%。在后一种情况下,乙酰甲胆碱浓度-抑制曲线呈钟形,在30微摩尔乙酰甲胆碱存在时未观察到毒蕈碱抑制作用。洗脱乙酰甲胆碱后,诱发的[3H]-去甲肾上腺素释放暂时增强。4. 0.1微摩尔阿托品增强[3H]-去甲肾上腺素溢出(由10赫兹360或1200个脉冲刺激诱发),可能是拮抗内源性乙酰胆碱的突触前抑制作用。0.1微摩尔阿托品竞争性拮抗乙酰甲胆碱的抑制作用(表观-log KB = 8.5 - 9.0)。5. 根据浓度不同,毛果芸香碱将3赫兹360个脉冲诱发的[3H]-去甲肾上腺素溢出减少高达63%。然而,在10赫兹刺激频率下,该化合物作为激动剂无活性,但竞争性拮抗乙酰甲胆碱诱导的突触前抑制作用。在后一种情况下的解离常数(KB)(0.95微摩尔)非常接近在3赫兹测定的半数有效浓度(EC50)值(0.85微摩尔)。6. 结果表明毒蕈碱对兔离体虹膜去甲肾上腺素释放有抑制作用。毛果芸香碱对突触前受体的激活为兔体内诱导的瞳孔缩小提供了另一种解释,这可能是虹膜开大肌交感神经张力降低的结果。

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The effect of physostigmine on the vagally induced muscarinic inhibition of noradrenaline release from the isolated perfused rabbit atria.毒扁豆碱对迷走神经诱导的毒蕈碱抑制离体灌注兔心房去甲肾上腺素释放的影响。
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