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突触前α2-肾上腺素能受体的亚分类:α2D-自身受体和调节豚鼠回肠乙酰胆碱释放的α2D-肾上腺素能受体。

Subclassification of presynaptic alpha 2-adrenoceptors: alpha 2D-autoreceptors and alpha 2D-adrenoceptors modulating release of acetylcholine in guinea-pig ileum.

作者信息

Funk L, Trendelenburg A U, Limberger N, Starke K

机构信息

Pharmakologisches Institut, Freiburg, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1995 Jul;352(1):58-66. doi: 10.1007/BF00169190.

DOI:10.1007/BF00169190
PMID:7477426
Abstract

The study was designed to classify in terms of alpha 2A, alpha 2B, alpha 2C and alpha 2D the presynaptic alpha 2-autoreceptors, as well as the alpha 2-receptors modulating the release of acetylcholine, in the myenteric plexus-longitudinal muscle (MPLM) preparation of the guinea-pig ileum. A set of antagonists was chosen that was able to discriminate between the four subtypes. Small pieces of the MPLM preparation were preincubated with 3H-noradrenaline or 3H-choline and then superfused and stimulated electrically. The stimulation periods used (3H-noradrenaline: 3 trains of 20 pulses, 50 Hz, train interval 60 s; 3H-choline: single trains of 30 pulses, 0.2 Hz) did not lead to alpha 2-autoinhibition or inhibition of 3H-acetylcholine release by endogenous noradrenaline. The alpha 2-selective agonist 5-bromo-6-(2-imidazolin-2-ylamino)-quinoxaline (UK 14,304) reduced the evoked overflow of tritium in both 3H-noradrenaline and 3H-choline experiments. Most (3H-noradrenaline) or all (3H-choline) of the 10 antagonists shifted the concentration-inhibition curves of UK 14,304 to the right. pKd values of the antagonists were calculated from the shifts. pKd values from 3H-noradrenaline experiments correlated with pKd values from 3H-choline experiments (r = 0.981). It is concluded that alpha 2-autoreceptors and alpha 2-heteroreceptors modulating the release of acetylcholine in the MPLM preparation are of the same subtype. Comparison with antagonist affinities for prototypic native alpha 2 binding sites, binding sites in cells transfected with alpha 2 subtype genes, and previously classified presynaptic alpha 2-adrenoceptors--all taken from the literature--indicates that both are alpha 2D.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

该研究旨在对豚鼠回肠肌间神经丛-纵肌(MPLM)标本中的突触前α2-自身受体以及调节乙酰胆碱释放的α2-受体,依据α2A、α2B、α2C和α2D进行分类。选用了一组能够区分这四种亚型的拮抗剂。将MPLM标本的小块组织先用3H-去甲肾上腺素或3H-胆碱进行预孵育,然后进行灌流并给予电刺激。所采用的刺激时段(3H-去甲肾上腺素:3组,每组20个脉冲,50Hz,组间间隔60秒;3H-胆碱:单组30个脉冲,0.2Hz)不会导致α2-自身抑制或内源性去甲肾上腺素对3H-乙酰胆碱释放的抑制。α2-选择性激动剂5-溴-6-(2-咪唑啉-2-基氨基)-喹喔啉(UK 14,304)在3H-去甲肾上腺素和3H-胆碱实验中均降低了诱发的氚外流。10种拮抗剂中的大多数(3H-去甲肾上腺素实验)或全部(3H-胆碱实验)使UK 14,304的浓度-抑制曲线右移。根据这些位移计算出拮抗剂的pKd值。3H-去甲肾上腺素实验的pKd值与3H-胆碱实验的pKd值相关(r = 0.981)。得出的结论是,MPLM标本中调节乙酰胆碱释放的α2-自身受体和α2-异源受体属于同一亚型。与文献中报道的针对原型天然α2结合位点、转染α2亚型基因的细胞中的结合位点以及先前分类的突触前α2-肾上腺素能受体的拮抗剂亲和力进行比较表明,两者均为α2D。(摘要截短于250字)

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本文引用的文献

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[Relationship between the effects of analgesics and sympathomimetics on guinea pig small intestines].[镇痛药与拟交感神经药对豚鼠小肠作用的关系]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1958;233(1):112-24.
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Presynaptic alpha 2-autoreceptors in brain cortex: alpha 2D in the rat and alpha 2A in the rabbit.大脑皮层中的突触前α2 自身受体:大鼠中的α2D 和兔子中的α2A。
Naunyn Schmiedebergs Arch Pharmacol. 1993 Jul;348(1):35-45. doi: 10.1007/BF00168534.
3
Subtype classification of presynaptic alpha 2-adrenoceptors.突触前α2肾上腺素能受体的亚型分类
人近端胃中胆碱能神经传递的突触前调节
Br J Pharmacol. 2002 Jan;135(1):135-42. doi: 10.1038/sj.bjp.0704471.
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Effects of A1-adenosine receptor antagonists on purinergic transmission in the guinea-pig vas deferens in vitro.A1-腺苷受体拮抗剂对豚鼠离体输精管嘌呤能传递的影响。
Br J Pharmacol. 1999 Apr;126(8):1761-8. doi: 10.1038/sj.bjp.0702514.
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Presynaptic alpha 2-autoreceptors in mouse heart atria: evidence for the alpha 2D subtype.小鼠心房中的突触前α2-自身受体:α2D亚型的证据。
Naunyn Schmiedebergs Arch Pharmacol. 1996 Aug-Sep;354(3):253-61. doi: 10.1007/BF00171055.
6
Subclassification of presynaptic alpha 2-adrenoceptors: alpha 2D-autoreceptors in guinea-pig atria and brain.突触前α2肾上腺素能受体的亚分类:豚鼠心房和大脑中的α2D自身受体。
Naunyn Schmiedebergs Arch Pharmacol. 1995 Jul;352(1):49-57. doi: 10.1007/BF00169189.
7
Subclassification of presynaptic alpha 2-adrenoceptors: alpha 2A-autoreceptors in rabbit atria and kidney.突触前α2肾上腺素能受体的亚分类:兔心房和肾脏中的α2A自身受体
Naunyn Schmiedebergs Arch Pharmacol. 1995 Jul;352(1):31-42. doi: 10.1007/BF00169187.
Gen Pharmacol. 1993 Jan;24(1):1-8. doi: 10.1016/0306-3623(93)90003-g.
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International Union of Pharmacology nomenclature of adrenoceptors.国际药理学联合会肾上腺素能受体命名法
Pharmacol Rev. 1994 Jun;46(2):121-36.
5
Alpha 2-adrenergic receptors of the alpha 2c subtype mediate inhibition of norepinephrine release in human kidney cortex.α2c亚型的α2-肾上腺素能受体介导人肾皮质中去甲肾上腺素释放的抑制。
Mol Pharmacol. 1994 Jun;45(6):1168-76.
6
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Sympathoinhibition by rilmenidine in conscious rabbits: involvement of alpha 2-adrenoceptors.利美尼定对清醒家兔的交感神经抑制作用:α2肾上腺素能受体的参与
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8
Functional evidence that [3H]acetylcholine and [3H]noradrenaline release from guinea pig ileal myenteric plexus and noradrenergic terminals is modulated by different presynaptic alpha-2 adrenoceptor subtypes.功能证据表明,豚鼠回肠肌间神经丛和去甲肾上腺素能终末释放的[3H]乙酰胆碱和[3H]去甲肾上腺素受不同的突触前α-2肾上腺素能受体亚型调节。
J Pharmacol Exp Ther. 1993 Dec;267(3):1054-60.
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Heteroreceptor-mediated modulation of noradrenaline and acetylcholine release from peripheral nerves.异受体介导的外周神经去甲肾上腺素和乙酰胆碱释放的调节
Rev Physiol Biochem Pharmacol. 1995;126:265-412. doi: 10.1007/BFb0049778.
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Presynaptic alpha 2A-adrenoceptors inhibit the release of endogenous dopamine in rabbit caudate nucleus slices.突触前α2A肾上腺素能受体抑制兔尾状核切片中内源性多巴胺的释放。
Naunyn Schmiedebergs Arch Pharmacol. 1994 Nov;350(5):473-81. doi: 10.1007/BF00173016.