Minyan W, Dunn W R, Blaylock N A, Chan S L, Wilson V G
School of Biomedical Sciences, Queen's Medical Centre, Nottingham, NG7 2UH.
Br J Pharmacol. 2001 Apr;132(7):1359-63. doi: 10.1038/sj.bjp.0703949.
Imidazoline derivatives are known to elicit responses through both alpha(2)-adrenoceptor and non-adrenoceptor, imidazoline sites, though as yet there are no examples of the latter on vascular smooth muscle. In the presence of 0.3 microM prazosin, neither UK-14304 (0.01 - 3 microM) nor oxymetazoline (0.01 - 30 microM) caused a significant contraction of the porcine isolated rectal artery, a preparation with a low density of alpha(2)-adrenoceptors. In the presence of a combination of U46619 and forskolin, however, both agonists produced concentration-dependent contractions. Pretreatment with phenoxybenzamine (3 microM) abolished responses to UK-14304, but left those elicited by oxymetazoline largely unaffected. The putative I(3) imidazoline antagonist 2-(2,3 dihydro-2-benzofuranyl)-2-imidazole (KU-14R, 10 microM) caused a 6 fold rightward displacement of the phenoxybenzamine-insensitive concentration - response curve to oxymetazoline. Our data indicates that non-adrenoceptor, imidazoline sites, pharmacologically similar to the I(3) imidazoline site on islet cells, mediate vasoconstriction in the porcine isolated rectal artery.
已知咪唑啉衍生物可通过α(2)-肾上腺素能受体和非肾上腺素能咪唑啉位点引发反应,尽管目前在血管平滑肌上尚未发现后者的实例。在存在0.3微摩尔哌唑嗪的情况下,UK-14304(0.01 - 3微摩尔)和羟甲唑啉(0.01 - 30微摩尔)均未引起猪离体直肠动脉的显著收缩,该制剂的α(2)-肾上腺素能受体密度较低。然而,在存在U46619和福斯可林的组合时,两种激动剂均产生浓度依赖性收缩。用苯氧苄胺(3微摩尔)预处理可消除对UK-14304的反应,但对羟甲唑啉引发的反应基本无影响。推定的I(3)咪唑啉拮抗剂2-(2,3-二氢-2-苯并呋喃基)-2-咪唑(KU-14R,10微摩尔)使对羟甲唑啉的苯氧苄胺不敏感浓度-反应曲线向右位移6倍。我们的数据表明,非肾上腺素能咪唑啉位点,在药理学上类似于胰岛细胞上的I(3)咪唑啉位点,介导猪离体直肠动脉的血管收缩。