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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。

Presynaptic alpha 2-autoreceptors in brain cortex: alpha 2D in the rat and alpha 2A in the rabbit.

作者信息

Trendelenburg A U, Limberger N, Starke K

机构信息

Pharmakologisches Institut, Freiburg, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1993 Jul;348(1):35-45. doi: 10.1007/BF00168534.

Abstract

Presynaptic alpha 2-autoreceptors in rat and rabbit brain cortex were compared by means of antagonists and agonists. Brain cortex slices were preincubated with [3H]-noradrenaline and then superfused and stimulated by 3 (rat) or 4 (rabbit) pulses at a frequency of 100 Hz. The alpha 2-adrenoceptor agonist bromoxidine (UK 14304) reduced the electrically evoked overflow of tritium with EC50 values of 4.5 nmol/l in the rat and 0.7 nmol/l in the rabbit. The antagonists phentolamine, 2-[2H-(1-methyl-1,3-dihydroisoindole)methyl]-4,5-dihydroimidazo le (BRL 44408), rauwolscine, 1,2-dimethyl-2,3,9,13b-tetrahydro-1H-dibenzo(c,f)imidazo(1,5-a)aze pine (BRL 41992), 2-(2,6-dimethoxyphenoxyethyl)aminomethyl-1,4-benzodioxane (WB 4101), 6-chloro-9-[(3-methyl-2-butenyl)oxy]-3-methyl-1H-2,3,4, 5-tetrahydro-3-benzazepine (SKF 104078), imiloxan, prazosin and corynanthine did not per se increase the evoked overflow of tritium but shifted the concentration-inhibition curve of bromoxidine to the right in a manner compatible with competitive antagonism. Up to 4 concentrations of each antagonist were used to determine its dissociation constant KD. The KD values correlated only weakly between the rat and the rabbit. Dissociation constants KA of bromoxidine were calculated from equieffective concentrations in unpretreated brain slices and slices in which part of the alpha 2-adrenoceptors had been irreversibly blocked by phenoxybenzamine. The KA value was 123 nmol/l in the rat and 7.2 nmol/l in the rabbit. The results confirm the species difference between rat and rabbit brain presynaptic alpha 2-autoreceptors. Comparison with data from the literature indicates that the rat brain autoreceptors can be equated with the alpha 2D subtype as defined by radioligand binding, whereas the rabbit brain autoreceptors conform to the alpha 2A subtype. For example, the antagonist affinities for the rat autoreceptors correlate with their binding affinities for the gene product of alpha 2-RG20, the putative rat alpha 2D-adrenoceptor gene (r = 0.97; P < 0.01), but not with their binding affinities for the gene product of alpha 2-C10, the putative human alpha 2A-adrenoceptor gene. Conversely, the rabbit autoreceptors correlate with the alpha 2-C10 (r = 0.98; P < 0.001) but not with the alpha 2-RG20 gene product. Since presynaptic alpha 2-autoreceptors are also alpha 2D in rat submaxillary gland and perhaps vas deferens and alpha 2A in rabbit pulmonary artery, the possibility arises that the majority of alpha 2-autoreceptors generally are alpha 2D in the rat and alpha 2A in the rabbit. Moreover, receptors of the alpha 2A/D group generally may be the main mammalian alpha 2-autoreceptors.

摘要

通过拮抗剂和激动剂对大鼠和家兔大脑皮层中的突触前α2-自受体进行了比较。将大脑皮层切片与[3H]-去甲肾上腺素预孵育,然后以100Hz的频率用3个(大鼠)或4个(家兔)脉冲进行灌流和刺激。α2-肾上腺素能受体激动剂溴莫尼定(UK 14304)减少了电诱发的氚外流,大鼠的EC50值为4.5nmol/L,家兔为0.7nmol/L。拮抗剂酚妥拉明、2-[2H-(1-甲基-1,3-二氢异吲哚)甲基]-4,5-二氢咪唑(BRL 44408)、育亨宾、1,2-二甲基-2,3,9,13b-四氢-1H-二苯并(c,f)咪唑并(1,5-a)氮杂卓(BRL 41992)、2-(2,6-二甲氧基苯氧基乙基)氨基甲基-1,4-苯并二恶烷(WB 4101)、氯-9-[(3-甲基-2-丁烯基)氧基]-3-甲基-1H-2,3,4,5-四氢-3-苯并氮杂卓(SKF 104078)、咪洛昔生、哌唑嗪和可利那明本身不会增加诱发的氚外流,但以与竞争性拮抗作用相符的方式将溴莫尼定浓度-抑制曲线向右移动。使用每种拮抗剂的多达4个浓度来确定其解离常数KD。大鼠和家兔之间的KD值仅呈现微弱的相关性。根据未处理的大脑切片以及部分α2-肾上腺素能受体已被苯氧苄胺不可逆阻断的切片中的等效效应浓度计算溴莫尼定的解离常数KA。大鼠的KA值为123nmol/L,家兔为7.2nmol/L。结果证实了大鼠和家兔大脑突触前α2-自受体之间的种属差异。与文献数据比较表明,大鼠大脑自受体可等同于放射性配体结合所定义的α2D亚型,而家兔大脑自受体符合α2A亚型。例如,拮抗剂对大鼠自受体的亲和力与其对假定的大鼠α2D-肾上腺素能受体基因α2-RG20的基因产物的结合亲和力相关(r = 0.97;P < 0.01),但与其对假定的人α2A-肾上腺素能受体基因α2-C10的基因产物的结合亲和力无关。相反,家兔自受体与α2-C10相关(r = 0.98;P < 0.001),但与α2-RG20基因产物无关。由于大鼠颌下腺以及可能输精管中的突触前α2-自受体也是α2D,而家兔肺动脉中的是α2A,因此有可能大多数α2-自受体在大鼠中一般为α2D,在家兔中为α2A。此外,α2A/D组的受体通常可能是主要的哺乳动物α2-自受体。

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