Trendelenburg A U, Limberger N, Starke K
Pharmakologisches Institut, Freiburg, Germany.
J Pharmacol Exp Ther. 1996 Aug;278(2):462-7.
The presynaptic alpha-2 autoreceptors in pig brain cortex were subclassified in terms of alpha-2A, alpha-2B, alpha-2C and alpha-2D to test the hypothesis that alpha-2 autoreceptors belong predominantly to the alpha-2A/D pair of orthologous alpha-2 adrenoceptors. Slices of brain cortex were preincubated with [3H]norepinephrine and then superfused and stimulated electrically. pKd values of 13 alpha-2 adrenoceptor antagonists (including the partial agonist oxymetazoline) against the alpha-2 agoinst 5-bromo-6-(2-imidazolin-2-ylamino)quinoxaline (UK 14,304) were determined. The stimulation periods used (six pulses at 100 Hz) did not lead to alpha-2 autoinhibition, as shown by the failure of all but one of the alpha-2 antagonists to increase the stimulation-evoked overflow of tritium. UK 14,304 caused a concentration-dependent decrease of the evoked overflow of tritium, with an EC50 value of 0.90 nM and a maximal inhibition of 95.2%. All antagonists shifted the concentration-inhibition curve of UK 14,304 to the right in a parallel manner. Antagonist pKd values were calculated from the shifts. The pKd values at the presynaptic alpha-2 autoreceptors in pig brain cortex correlated excellently with pKd values at previously subclassified alpha-2A sites but did not correlate significantly or correlated much less well with pKd values at alpha-2B, alpha-2C and alpha-2D sites. Also, ratios of Kd values of the antagonists at the presynaptic alpha-2 autoreceptors in pig brain cortex agreed well with ratios at previously subclassified alpha-2A sites but not with those at previously subclassified alpha-2B-D sites. It is concluded that the alpha-2 autoreceptors in pig brain cortex are alpha-2A, in accordance with the hypothesis mentioned.
为了验证α-2自身受体主要属于α-2A/D这一对直系同源α-2肾上腺素能受体的假说,对猪脑皮质中的突触前α-2自身受体按照α-2A、α-2B、α-2C和α-2D进行了亚分类。将脑皮质切片与[3H]去甲肾上腺素预孵育,然后进行灌流并电刺激。测定了13种α-2肾上腺素能拮抗剂(包括部分激动剂氧甲唑啉)对α-2对抗剂5-溴-6-(2-咪唑啉-2-基氨基)喹喔啉(UK 14,304)的pKd值。所用的刺激周期(100 Hz下6个脉冲)并未导致α-2自身抑制,除一种α-2拮抗剂外,其他所有拮抗剂均未能增加刺激诱发的氚溢出,这表明了这一点。UK 14,304引起了刺激诱发的氚溢出的浓度依赖性降低,EC50值为0.90 nM,最大抑制率为95.2%。所有拮抗剂均以平行方式将UK 14,304的浓度-抑制曲线向右移动。根据移动情况计算拮抗剂的pKd值。猪脑皮质突触前α-2自身受体的pKd值与先前亚分类的α-2A位点的pKd值高度相关,但与α-2B、α-2C和α-2D位点的pKd值无显著相关性或相关性差得多。此外,猪脑皮质突触前α-2自身受体处拮抗剂的Kd值之比与先前亚分类的α-2A位点的比值吻合良好,但与先前亚分类的α-2B-D位点的比值不吻合。结论是,猪脑皮质中的α-2自身受体是α-2A,与上述假说一致。