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大鼠肠道中功能性α2D肾上腺素能受体的证据。

Evidence for functional alpha 2D-adrenoceptors in the rat intestine.

作者信息

Liu L, Coupar I M

机构信息

Department of Pharmaceutical Biology and Pharmacology, Monash University, Parkville, Vic, Australia.

出版信息

Br J Pharmacol. 1996 Mar;117(5):787-92. doi: 10.1111/j.1476-5381.1996.tb15261.x.

Abstract
  1. Peristaltic contractions were induced in segments of rat ileum by raising the intramural pressure. A mean pressure of 4.3 +/- 0.2 cmH2O (n = 112) was required to initiate rhythmic contractions of the longitudinal muscle (preparatory phase) and associated volume expulsions caused by circular muscle contraction. The frequency of peristalsis remained constant over two 15 min periods of stimulation. 2. The alpha 2-adreoceptor agonists, clonidine, UK 14,304, B-HT 920, B-HT 933 and the selective alpha 2A-agonists, oxymetazoline and guanfacine, caused concentration-dependent inhibition of peristaltic contractions. The potency order and IC50 values (nM) were: clonidine (2.81) > or = oxymetazoline (4.23) > or = UK 14,304 (4.48) > or = guanfacine (5.51) > B-HT 920 (78.72) > B-HT 933 (442.48). 3. High concentrations of clonidine, amounting to more than 10 and 100 times the IC50 value in the peristaltic reflex (30 and 300 nM respectively), failed to inhibit the cholinergic contractile response to transmural electrical stimulation over the range of 2.5 to 40 Hz. 4. alpha 2-Adrenoceptor antagonists were used to determine the subtype of presynaptic alpha 2-adrenoceptor in rat ileum. All the antagonists tested caused parallel shifts to the right of the concentration-response regression line to clonidine and none, except ARC 239, influenced the rate of peristalsis. However, ARC 239 significantly decreased the frequency of control period peristaltic contractions. The order of affinity of the antagonists against clonidine (pKB values in parentheses) was RX 821002 (8.99) > phentolamine (8.07) > BRL 44408 (7.43) > or = rauwolscine (7.41) > or = yohimbine (7.28) > prazosin (5.86) > or = ARC 239 (5.74). 5. These results, when compared with binding and functional data from various other tissues and cell lines, are consistent with the presence of presynaptic alpha 2D-adrenoceptors in rat ileum. Further evidence is provided that this subtype of alpha 2-adrenoceptor is probably located proximal to the final cholinergic neurones in the reflex arc.
摘要
  1. 通过升高肠壁内压力在大鼠回肠段诱导蠕动收缩。启动纵肌节律性收缩(准备阶段)和由环肌收缩引起的相关容积排出需要平均压力4.3±0.2 cmH₂O(n = 112)。在两个15分钟的刺激期内,蠕动频率保持恒定。2. α₂肾上腺素能受体激动剂可乐定、UK 14,304、B-HT 920、B-HT 933以及选择性α₂A激动剂奥昔肾上腺素和胍法辛引起蠕动收缩的浓度依赖性抑制。效价顺序和IC₅₀值(nM)为:可乐定(2.81)≥奥昔肾上腺素(4.23)≥UK 14,304(4.48)≥胍法辛(5.51)>B-HT 920(78.72)>B-HT 933(442.48)。3. 高浓度的可乐定,分别相当于蠕动反射中IC₅₀值的10倍和100倍以上(分别为30和300 nM),在2.5至40 Hz范围内未能抑制对跨壁电刺激的胆碱能收缩反应。4. 使用α₂肾上腺素能受体拮抗剂来确定大鼠回肠中突触前α₂肾上腺素能受体的亚型。所有测试的拮抗剂均使可乐定的浓度 - 反应回归线平行右移,除ARC 239外,均不影响蠕动速率。然而,ARC 239显著降低了对照期蠕动收缩的频率。拮抗剂对可乐定的亲和力顺序(括号内为pKB值)为:RX 821002(8.99)>酚妥拉明(8.07)>BRL 44408(7.43)≥萝芙辛(7.41)≥育亨宾(7.28)>哌唑嗪(5.86)≥ARC 239(5.74)。5. 这些结果与来自其他各种组织和细胞系的结合及功能数据相比,与大鼠回肠中存在突触前α₂D肾上腺素能受体一致。进一步的证据表明,这种α₂肾上腺素能受体亚型可能位于反射弧中最终胆碱能神经元的近端。

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