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内皮素诱导的大鼠气管平滑肌收缩及气管中特异性内皮素结合位点的鉴定。

Endothelin-induced contractions of tracheal smooth muscle and identification of specific endothelin binding sites in the trachea of the rat.

作者信息

Turner N C, Power R F, Polak J M, Bloom S R, Dollery C T

机构信息

Department of Clinical Pharmacology, Royal Postgraduate Medical School, Hammersmith Hospital, London.

出版信息

Br J Pharmacol. 1989 Oct;98(2):361-6. doi: 10.1111/j.1476-5381.1989.tb12605.x.

Abstract
  1. The presence of specific binding sites and the contractile activity of the novel peptide, endothelin have been investigated in rat trachea. 2. Endothelin (10(-8)-10(-5) M) induced long-lasting contraction of rat tracheal rings superfused with Krebs solution (EC50 5.4 x 10(-6) M). Contractions of the tissue to 10(-6) M endothelin were attenuated in Ca2+-free medium containing 0.1 mM EGTA but unaffected by nicardipine (10(-7) M). 3. After equilibration in Ca2+-free medium (without EGTA) a return to normal Ca2+ concentrations (2.5 mM), 30 min or 60 min following endothelin (10(-6) M), produced a sustained contraction of the tissue. 4. Specific binding sites for endothelin were identified on rat tracheal smooth muscle (KD 1.34 x 10(-10) M, maximal binding 1.2 fmol mm-2). Specific binding sites were also identified on nerve trunks. Endothelin binding was unaffected by co-incubation with nicardipine (10(-7) M) or verapamil (10(-7) M). 5. The discrepancy between the apparent KD for endothelin binding and the EC50 for endothelin-induced contraction suggests that the endothelin binding sites identified in this study may not be associated with the receptors mediating contraction. 6. These results indicate that endothelin binding sites are present on tracheal smooth muscle. The mechanism of endothelin-induced contraction, whilst being dependent on extracellular calcium, does not appear to involve binding to the dihydropyridine- or verapamil-sensitive sites on the voltage-dependent Ca2+ channel. Its long duration of action may be associated with a sustained increase in Ca2+ permeability.
摘要
  1. 已在大鼠气管中研究了新型肽内皮素的特异性结合位点及其收缩活性。2. 内皮素(10⁻⁸ - 10⁻⁵ M)可诱导用 Krebs 溶液灌流的大鼠气管环产生持久收缩(半数有效浓度 5.4×10⁻⁶ M)。在含 0.1 mM EGTA 的无钙培养基中,组织对 10⁻⁶ M 内皮素的收缩作用减弱,但不受尼卡地平(10⁻⁷ M)影响。3. 在无钙培养基(不含 EGTA)中平衡后,在给予内皮素(10⁻⁶ M)30 分钟或 60 分钟后恢复正常钙浓度(2.5 mM),可使组织产生持续收缩。4. 在大鼠气管平滑肌上鉴定出内皮素的特异性结合位点(解离常数 1.34×10⁻¹⁰ M,最大结合量 1.2 fmol·mm⁻²)。在神经干上也鉴定出特异性结合位点。内皮素结合不受与尼卡地平(10⁻⁷ M)或维拉帕米(10⁻⁷ M)共同孵育的影响。5. 内皮素结合的表观解离常数与内皮素诱导收缩的半数有效浓度之间的差异表明,本研究中鉴定出的内皮素结合位点可能与介导收缩的受体无关。6. 这些结果表明气管平滑肌上存在内皮素结合位点。内皮素诱导收缩的机制虽然依赖细胞外钙,但似乎不涉及与电压依赖性钙通道上的二氢吡啶或维拉帕米敏感位点结合。其作用持续时间长可能与钙通透性的持续增加有关。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f007/1854717/006523e94f3f/brjpharm00262-0035-a.jpg

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