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二价阳离子敏感拮抗剂与心脏毒蕈碱受体的结合。

Divalent cation-sensitive antagonist binding to heart muscarinic receptors.

作者信息

Sulakhe P V, Jagadeesh G, Phan N T

机构信息

Department of Physiology, College of Medicine, University of Saskatchewan, Saskatoon, Canada.

出版信息

Gen Pharmacol. 1991;22(2):375-9. doi: 10.1016/0306-3623(91)90467-k.

Abstract
  1. The binding of (-) [3H]quinuclidinylbenzilate (QNB), a potent muscarinic antagonist, to cardiac muscarinic receptors was examined in washed particles and microsomes isolated from rat heart atria. 2. Addition of divalent cations (Mg2+, Mn2+ and Ca2+) to the binding assays increased (6 to 8-fold) the antagonist binding to microsomes but exerted little or only weak (up to 35%) stimulation of the antagonist binding to washed particles. 3. Mg2+ ions present only in the dilution and washing buffer prior to rapid filtration of the binding reaction were capable of markedly increasing the antagonist binding to microsomes but not to washed particles. 4. Such differential action of Mg2+ on antagonist binding to subcellular fractions was seen when fractions were either isolated and or incubated in media containing either 10 or 50 mM imidazole-Cl, Tris-phosphate or Tris-Cl buffer, each at pH 7.5. While the modulatory effect of Mg2+ was not seen in Na-K-phosphate buffer, pH 7.5, the antagonist binding per se was much higher in Na-K-phosphate buffer compared to other buffers.
摘要
  1. 研究了强效毒蕈碱拮抗剂(-)[3H]喹核醇基苯甲酸酯(QNB)与从大鼠心房分离的洗涤颗粒和微粒体中心脏毒蕈碱受体的结合情况。2. 在结合试验中添加二价阳离子(Mg2+、Mn2+和Ca2+)可使拮抗剂与微粒体的结合增加(6至8倍),但对拮抗剂与洗涤颗粒的结合几乎没有刺激作用或仅有微弱刺激(高达35%)。3. 在结合反应快速过滤之前仅存在于稀释和洗涤缓冲液中的Mg2+离子能够显著增加拮抗剂与微粒体的结合,但不能增加与洗涤颗粒的结合。4. 当在含有10或50 mM咪唑-Cl、磷酸三乙胺或Tris-Cl缓冲液(均为pH 7.5)的培养基中分离或孵育亚细胞组分时,可观察到Mg2+对拮抗剂与亚细胞组分结合的这种差异作用。虽然在pH 7.5的Na-K-磷酸盐缓冲液中未观察到Mg2+的调节作用,但与其他缓冲液相比,Na-K-磷酸盐缓冲液中拮抗剂的结合本身要高得多。

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