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Br J Pharmacol. 1995 Jun;115(3):534-8. doi: 10.1111/j.1476-5381.1995.tb16367.x.
2
Tyrosine kinase inhibitors block calcium channel currents in vascular smooth muscle cells.酪氨酸激酶抑制剂可阻断血管平滑肌细胞中的钙通道电流。
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Increase in tone and intracellular Ca2+ in rabbit isolated ear artery by platelet-derived growth factor.血小板衍生生长因子使兔离体耳动脉张力和细胞内钙离子增加。
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本文引用的文献

1
Vascular derived growth factors: cell biology, pathophysiology, and pharmacology.血管衍生生长因子:细胞生物学、病理生理学及药理学
Pharmacol Rev. 1993 Mar;45(1):1-42.
2
Effects of tyrosine kinase inhibitors on protein kinase-independent systems.酪氨酸激酶抑制剂对非蛋白激酶系统的作用。
FEBS Lett. 1993 Feb 1;316(3):278-82. doi: 10.1016/0014-5793(93)81308-m.
3
The acute actions of growth factors in smooth muscle systems.生长因子在平滑肌系统中的急性作用。
Life Sci. 1994;54(4):223-35. doi: 10.1016/0024-3205(94)00811-6.
4
Tyrphostin attenuates platelet-derived growth factor-induced contraction in aortic smooth muscle through inhibition of protein tyrosine kinase(s).tyrphostin 通过抑制蛋白酪氨酸激酶来减弱血小板衍生生长因子诱导的主动脉平滑肌收缩。
J Pharmacol Exp Ther. 1993 Dec;267(3):1119-25.
5
How receptor tyrosine kinases activate Ras.受体酪氨酸激酶如何激活Ras。
Trends Biochem Sci. 1993 Aug;18(8):273-5. doi: 10.1016/0968-0004(93)90031-h.
6
Insulin-like growth factor-I induces a rapid increase in calcium currents and spontaneous membrane activity in clonal pituitary cells.胰岛素样生长因子-I可使垂体克隆细胞中的钙电流和自发膜活性迅速增加。
Mol Pharmacol. 1994 Jun;45(6):1215-20.
7
Tyrosine kinase pathways and the regulation of smooth muscle contractility.酪氨酸激酶途径与平滑肌收缩性的调节
Trends Pharmacol Sci. 1994 Apr;15(4):108-14. doi: 10.1016/0165-6147(94)90046-9.
8
Increase in tone and intracellular Ca2+ in rabbit isolated ear artery by platelet-derived growth factor.血小板衍生生长因子使兔离体耳动脉张力和细胞内钙离子增加。
Br J Pharmacol. 1995 Jan;114(1):138-42. doi: 10.1111/j.1476-5381.1995.tb14917.x.
9
Channel regulation. Ion channel control by tyrosine phosphorylation.通道调节。酪氨酸磷酸化对离子通道的调控。
Curr Biol. 1994 Mar 1;4(3):242-5. doi: 10.1016/s0960-9822(00)00054-3.
10
Cytosolic Ca2+ transients are not required for platelet-derived growth factor to induce cell cycle progression of vascular smooth muscle cells in primary culture. Actions of tyrosine kinase.血小板衍生生长因子诱导原代培养的血管平滑肌细胞发生细胞周期进程并不需要胞质Ca2+瞬变。酪氨酸激酶的作用。
J Biol Chem. 1994 Mar 25;269(12):9011-8.

血小板衍生生长因子对兔离体耳动脉细胞电压门控钙通道的影响。

Effect of platelet-derived growth factor on voltage-operated calcium channels in rabbit isolated ear artery cells.

作者信息

Wijetunge S, Hughes A D

机构信息

Department of Clinical Pharmacology, St. Mary's Hospital Medical School, Imperial College of Science Technology & Medicine, London.

出版信息

Br J Pharmacol. 1995 Jun;115(3):534-8. doi: 10.1111/j.1476-5381.1995.tb16367.x.

DOI:10.1111/j.1476-5381.1995.tb16367.x
PMID:7582469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1908398/
Abstract
  1. Platelet derived growth factor (PDGF), AB and BB isoforms (100 pM) increased calcium channel currents measured by whole cell voltage clamp technique in single vascular smooth muscle cells isolated from rabbit ear arteries. 2. Tyrphostin-23 (100 microM) a selective inhibitor of protein tyrosine kinases, reduced calcium channel currents. Pre-incubation with tyrphostin-23 prevented PDGF-AB induced increase in calcium channel currents. However, in these same cells 10 nM (+)-202791, a dihydropyridine calcium channel agonist, did increase calcium channel currents. 3. Bistyrphostin (10 microM), a selective inhibitor of epidermal growth factor (EGF)-kinase also reduced calcium channel currents and inhibited PDGF-AB-induced increases in calcium channel currents. 4. Genistein (100 microM) a selective inhibitor of tyrosine kinases, structurally unrelated to the tryphostins, also inhibited calcium channel currents and pre-incubation with genistein prevented the PDGF-AB-induced rise in calcium channel currents. 5. These results indicate that PDGF increases calcium channel currents in vascular smooth muscle. This action of PDGF probably involves a tyrosine kinase.
摘要
  1. 血小板衍生生长因子(PDGF)的AB和BB亚型(100皮摩尔),通过全细胞电压钳技术测定,可增加从兔耳动脉分离出的单个血管平滑肌细胞中的钙通道电流。2. 酪氨酸磷酸化抑制剂-23(100微摩尔),一种蛋白酪氨酸激酶的选择性抑制剂,可降低钙通道电流。预先用酪氨酸磷酸化抑制剂-23孵育可阻止PDGF-AB诱导的钙通道电流增加。然而,在这些相同的细胞中,10纳摩尔(+)-202791,一种二氢吡啶钙通道激动剂,确实增加了钙通道电流。3. 双酪氨酸磷酸化抑制剂(10微摩尔),一种表皮生长因子(EGF)激酶的选择性抑制剂,也降低了钙通道电流,并抑制了PDGF-AB诱导的钙通道电流增加。4. 染料木黄酮(100微摩尔),一种与酪氨酸磷酸化抑制剂结构无关的酪氨酸激酶选择性抑制剂,也抑制了钙通道电流,预先用染料木黄酮孵育可阻止PDGF-AB诱导的钙通道电流升高。5. 这些结果表明,PDGF增加血管平滑肌中的钙通道电流。PDGF的这种作用可能涉及一种酪氨酸激酶。